122 results on '"Tex S"'
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2. Values for Triglycerides, Insulin, Cortisol, and ACTH in a Herd of Normal Donkeys
- Author
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Dugat, Susan L., Taylor, Tex S., Matthews, Nora S., and Gold, Jenifer R.
- Published
- 2010
3. Guaifenesin-Ketamine-Xylazine Infusions to Provide Anesthesia in Donkeys
- Author
-
Taylor, Ethel V., Baetge, Courtney L., Matthews, Nora S., Taylor, Tex S., and Barling, Kerry S.
- Published
- 2008
4. Fourth meeting of the European Neurological Society 25–29 June 1994 Barcelona, Spain: Abstracts of Symposia and free communications
- Author
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Harms, L., Bock, A., JÄnisch, W., Valdueza, J., Weber, J., Link, I., De Keyser, J., Goossens, A., Wilczak, N., Vedeler, C., Bjorge, L., Uvestad, E., Conti, G., Williams, K., Ginsberg, L., Rafique, S., Rapoport, S. I., Gershfeld, N. L., De La Meilleure, G., Crevits, L., Faiss, J. H., Heye, N., Blanke, J., Sackmann, A., Kastrup, O., Doornbos, R., van der Worp, H. B., Kappelle, L. J., Bar, P. R., Davie, C. A., Barker, G. J., Brenton, D., Miller, D. H., Thompson, A. J., Block, F., Schwarz, M., Delodovici, L., Baruzzi, F., Bonaldi, G., Dario, A., Marra, A., Mercuri, A., Dworzak, F., Cavallari, P., Confalonieri, P., Zuffi, M., Antozzi, C., Cornelio, F., Baldissera, F., Chassande, B., Ameri, A., Eymard, B., Poisson, M., Vérier, A., Brunet, P., Congia, S., Murgia, P. L., Cannas, A., Borghero, G., Uselli, S., Mellino, G., Ferrai, R., Lampis, R., Massa, R., Muzzetto, B., Giannini, F., Rossi, S., Cioni, R., d'Aniello, C., Guarneri, A., Battistini, N., Ceriani, F., Del Santo, A., Poloni, M., Campo, J. F., Iglesias, F., Guitera, M. V., Farinas, C., Pascual, J., Leno, C., Berciano, J., Thorpe, I. W., Kendall, B. E., McDonald, W. I., Moulignier, A., Dromer, F., Baudrimont, M., Dupont, B., Gozlan, J., El Amrani, M., Petit, J. C., Roullet, E., Sterzi, R., Causaran, R., Protti, A., Riva, M., Erminio, F., Arena, O., Villa, F., Maccagnano, E., Miletta, M., Spinelli, F., Ben-Hur, T., Weidenfeldl, J., Rao, N. S., Chari, C. C., Laforet, P., Matheron, S., Adams, D., Chemouilli, Ph., Desi, M., Said, G., Davous, P., Lionnet, F., Pulik, M., Genet, P., Rozenberg, F., Cartier, L. M., Castillo, J. L., Cea, J. G., Villagra, R., de Saint Martin, L., Mahieux, F., Manifacier, M. J., Mattos, K., Queiros, C., Publio, L., Vinhas, V., PeÇanha-Martins, A. C., Melo, A., Liska, U., Zifko, U., Budka, H., Drlicek, M., Grisold, W., Kaufmann, R., Kaiser, R., Czygan, M., Gomes, I., Jones, N., Cunha, S., EmbiruÇu, E. Katiane, Vieira, V., Araujo, I., Alexandra, M., Ferreira, A., Goes, J., Chemouilli, P., Israel-Biet, Masson, H., Lacroix, C., Gasnault, J., Hildebrandt-Müller, B., Oschmann, P., Krack, P., Willems, W. R., Dorndorf, W., Freitas, V., Bittencourt, A., Fernandes, D., Nascimento, M. H., Severo, M., Moraes, D., Muller, M., Hasert, K., Merkelbach, S., Schimrigk, K., van Oosten, B. W., Lai, M., Polman, C. H., Bertelsmann, F. W., Hodgkinson, S., Cabre, P. H., Volpe, L., Smadja, D., Vernant, J. P., Villaroya, H., Violleau, K., Younes-Chennoufi, A. Ben, Baumann, N., Villanueva-Hemandez, P., Ballabriga, J., Basart, E., Arbizu, T. X., Perez-Serra, J., Vinuels, F., Giron, J. M., Castilla, J. M., Redondo, L., Izquierdo, G., Lauer, K., Henneberg, A., Bittmann, N., Link, D., Wollinsky, K. H., Mobner, R., Fassbender, K., Kuhnen, J., Schwartz, A., Hennerici, M., Miller, A., Lider, O., Abramsky, O., Weiner, H. L., Offner, H., Vanderbark, A. A., Paoino, E., Fainardi, E., Addonizio, M. C., Ruppi, P., Tola, M. R., Granieri, E., Carreras, M., Sazdovitch, V., Joutel, A., Verdier-taillefer, M. H., Heinzlef, O., Radder, C., Tournier-Lasserve, E., Brenner, R. E., Munro, P. M. G., Williams, S. C. R., Bell, J. D., Hawkins, C. P., Filippi, M., Campi, A., Dousset, V., Canal, N., Comi, G., Zhu, J., Weber, F., Retska, R., List, J., Zhang, L., Brock, M., Taphoorn, M. J. B., Heimans, J. J., van der Veen, E. A., Karim, A. B. M. F., Sarazin, M., Argentino, N., Delattre, J. Y., Derkinderen, P., Buchwald, B., Schroter, G., Serve, G., Franke, C. H., Conrad, B., Kitchen, N. D., Thomas, D. G. T., Forman, A. D., Ang, Kie- Kian, Price, R., Stephens, C., Salmaggi, A., Nermni, R., Silvani, A., Forno, M. G., Luksch, R., Boiardi, A., Grzelec, H., Fryze, C., Nowacki, P., Zdziarska, B., Sanson, M., Merel, P., Richard, S., Rouleau, G., Thomas, G., Olsen, N. K., Pfeiffer, P., Egund, N., Bentzen, S. M., Johannesen, L., Mondrup, K., Rose, C., Zyluk, B., Wondrusch, E., Berger, O., Fast, N., Jellinger, K., Lindner, K., Urman, A., Thibault, J. L., Duyckaerts, Ch., Strik, H., Muller, B., Richter, E., Krauseneck, P., Steinbrecher, A., Schabet, M., Hess, C., Bamberg, M., Dichgans, J., Counsell, C. E., McLeod, M., Grant, R., Creel, G. B., Claus, D., Sieber, E., Engelhardt, A., Rechlin, T., Thierauf, P., Neubauer, U., Peresson, M., Di Giovacchino, G., Romani, G. L., Di Silverio, F., Danek, A., Kuffner, M., Hoermann, R., Schopohl, J., Laska, M., Heye, B., Zangaladze, A. T., Valls-SoIè, J., Cammarota, A., Alvarez, R., Tolosa, E., Hallett, M., Ulbricht, D., Ganslandt, O., Kober, H., Vieth, J., Grummich, P., Pongratz, H., Brigel, C., Fahlbusch, R., Serra, F. P., Palma, V., Nolfe, G., Buscaino, G. A., Rothstein, T. L., Gibson J. M., Morrison P. M., Collins A. D., Eiselt, M., Wagnur, H., Zwiener, U., Schindler, T., Efendi, H., Ertekin, C., Erfas, M., Larsson, L. E., Sirin, H., AraÇ, N., Toygar, A., Demir, Y., Seddigh, S., Vogt, T. H., Hundemer, H., Visbeck, A., Pastena, L., Faralli, F., Mainardi, G., Gagliardi, R., Linden, D., Berlit, P., Lopez, O. L., Becker, J. T., Jungreis, C., Brenner, R., Rezek, D., Dekesky, S. T., Estol, C., Boller, F., Fernandez, J. M., Mederer, S., Batlle, J., Turon, A., Codina, A., Hitzenberger, P., Vila, N., Valls-SolÇ, J., Chamorro, A., Pouget, J., Schmied, A., Morin, D., Azulay, J. Ph., Vedel, J. P., Montalt, J., Escudero, J., Barona, R., Campos, A., Varli, K., Ertem, E., Uludag, B., Yagiz, A., Privorkin, Z., Steinvil, Y., Kott, E., Combarros, O., Sanchez-Pernaute, R., Orizaola, P., Mokrusch, Th., Kutluaye, E., Selcuki, D., Ertikin, C., Zettl, U., Gold, R., Harvey, G. K., Hartung, H. P., Toyka, K. V., Wokke, J. H. J., Oey, P. L., Ippel, P. F., Jansen, G. H., Franssen, H., Toyooka, K., Fujimura, H., Ueno, S., Yoshikawa, H., Yorifuji, S., Yanagihara, T., Talamon, C., Tzourio, C., Kiefer, R., Jung, S., Toyka, K., Ruolt, I., Tranchant, C., Mohr, M., Warter, J. M., Younger, D. S., Rosoklija, G., Hays, A. P., Kurita, R., Hasegawa, O., Matsumto, M., Komiyama, A., Nara, Y., Oueslati, S., Belal, S., Turki, I., Ben Hamida, C., Hentati, F., Ben Hamida, M., Kwiecinski, H., Krolicki, L., Domzal-Stryga, A., Dellemijn, P. L. I., van Deventer, P., van Moll, B., Drogendijk, T., Vecht, Ch. J., Nemni S., Amadio, Fazio, R., Galardin, G., Delodovici, M. L., Peghi, E., Monticelli, M. L., Sessa, A., Viguera, M. L., Palomar, M., Gamez, J., Cervera, C., Navarro, C., Serena, J., Duran, I., Fernandez, A. L., Comabella, M., Nos, C., Rio, J., Montalban, J., Navarro, X., Verdu, E., Darbra, S., Buti, M., Mrabet, A., Fredj, M., Gouider, R., Tounsi, H., Khalfallah, N., Haddad, A., Dbaiss, T., Ghnassia, R., Rouillet, E., Chedru, F., Porsche, H., Strenge, H., Li, S. W., Young, Y. P., Garcia, A. A., Baron, P., Scarpini, E., Bianchi, R., Conti, A., Livraghi, S., Rees, J. H., Gregson, N. A., Hughes, R. A. C., Sedano, M. J., Calleja, J., Canga, E., Bahou, Y., Biary, N., Al Deeb, S. M., Guern, E. L. E., Gugenheim, M., Tardieu, S., Aisonobe, T. M., Agid, Y., Bouche, P., Brice, A., Rautenstrauss, B., Nelis, E., Grehl, H., Van Broeckhoven, C., Pfeiffer, R. A., Liehr, T., Ganzmann, E., Gehring, C., Neundörfer, B., Geremia, L., Doronzo, R., Sacilotto, G., Sergi, P., Pastorino, G. C., Scarlato, G., Planté-Bordeneuve, V., Mantel, A., Baas, F., Moser, H., Antonini, A., Psylla, M., Günther, I., Vontobell, P., Beer, H. F., Leenders, K. L., Chaudhuri, K. Ray, Parker, J., Pye, I. F., Millac, P. A. H., Abbott, R. J., Sutter, M., Albani, C., de Rijk, M. C., Breteler, M. M. B., Graveland, G. A., van der Mechè, F. G. A., Hofman, A., Keipes, M., Hilger, Ch., Diederich, N., Metz, H., Hentges, F., Pollak, P., Benabid, A. L., Limousin, P., Hoffmann, D., Benazzouz, A., Perret, J., Laihinen, A., Rinne, J. O., Ruottinen, H., Nagren, K., Lehikoinen, P., Oikonen, V., Ruotsalainen, U., Rinne, U. K., Cocozza, S., Pizzuti, A., Cavalcanti, F., Monticelli, A., Pianese, L., Redolfi, E., Paiau, F., Di Donato, S., Pandolfo, M., Palau, F., Monros, E., De Michele, G., Smeyers, P., Lopez-ArLandis, J., Uilchez, J., Filla, A., Genis, D., Matilla, T., Volpini, V., Blanchs, M. I., Davalos, A., Molins, A., Rosell, J., Estivill, X., De Jonghe, P., Smeyers, G., Krols, L., Mercelis, R., Hazan, J., Weissenbach, J., Martin, J. J., Warner, T. A. T., Williams, L., Orb, A. S., Harding, A. E., Giunti, P., Sweeney, M. G., Spadaro, M., Jodice, C., Novelletto, A., Malaspina, P., Frontali, M., Salmon, E., Gregoire, Del Fiore, Comar, Franck, G., Scheltens, P. H., Siegfried, K., Dartigues, E., De Deyn, P., Horn, R., Nelson, I., Hanna, M. G., Morgan-Hughes, J. A., Collinge, J., Palmer, M. S., Campbell, T., Mahal, S., Sidle, K., Humphreys, C., Tavitian, B., Pappata, S., Jobert, A., Crouzel, A. M., DiGiamberardino, L., Steimetz, G., Barbanti, P., Fabbrini, G., Salvatore, M., Buzzi, M. G., Di Piero, V., Petraroli, R., Sbriccoli, A., Pocchiari, M., Macchi, G., Lenzi, G. L., Spiegel, R., Maguire, P., Schmid, W., Ott, A., Bots, M. L., Grobbe, D. E., Hofman, A., Howard, R. S., Russell, S., Losseff, N., Hirsch, N. P., Couderc, R., Bailleul, S., Nargeot, M. C., Touchon, J., Picot, M. C., Rizzo, M., Watson, G., McGehee, D., Dingus, T., Kappos, L., Radü, E. W., Haas, J., Hartard, C. H., Spuler, S., Yousry, T., Voltz, R., Scheller, A., Holler, E., Hohlfeld, R., Scolding, N. J., Sussman, J., Kolar, O. J., Farlow, M. R., Rice, P. H., Zipp, F., Sotgiu, S., Weiss, E. H., Wekerle, H., Chalmers, R., Robertson, N., Compston, D. A. S., Martino, G., Clementi, E., Brambilla, E., Moiola, L., Martinelli, V., Colombo, B., Poggi, A., Rovaris, M., Grimaldi, L. M. E., Roth, M. P., Descoins, P., Ballivet, S., Ruidavets, J. B., Waubant, E., Nogueira, L., Cambon-Thomsen, A., Clanet, M., Leppert, D., Hauser, S., Lugaresi, A., Tartaro, A., D'aurelio, P., Befalo, L. L. O., Thomas, A., Malatesta, G., Gambi, D., Benedikz, J. E. G., Magnusson, H., Poser, C. M., Guomundsson, G., Bates, T. E., Davies, S. E. C., Clark, J. B., Landon, D. N., ùther, J. R., Rautenberg, W., Overgaard, K., Sereghy, T., Pedersen, H., Boysen, G., Diez-Tejedor, E., Carceller, F., Gutierrez, M., Lopez-Pajares, R., Roda, J. M., Chandra, B., Ricart, W., Gonzalez-Huix, F., Molina, A., Rundek, T., Demarin, V., De Reuck, J., Boon, P., Decoq, D., Strijckmans, K., Goethals, P., Lemahieu, I., Nibbio, A., Chabriat, H., Vahedi, K., Nagy, T., Verin, M., Mas, J. L., Julien, J., Ducrocq, X., Iba-Zizen, M. T., Cabanis, E. A., Bousser, M. G., Rolland, Y., Landgraf, F., Bompais, B., Lemaitre, M. H., Edan, G., Vorstrup, S., Knudsen, L., Olsen, K. Skovgaard, Videbaek, C., Schroeder, T., van Gijn, J., Jansen, H. M. L., Pruim, J., Paans, A. M. J., Willemsen, A. T. M., Hew, J. M., vd Vliet, A. M., Haaxma, R., Vaalburg, W., Minderhoud, J. M., Korf, J., Soudain, S. E., Ho, T. W., Mishu, B., Li, C. Y., Nachainkin, I., Gao, C. Y., Cornblath, D. R., Griffin, J. W., Asbury, A. K., Blaser, M. J., McKhann, G. M., Ho, T., Macko, C., Xue, P., Stadlan, E. M., Ramos-Alvarez, M., Valenciano, L., Visser, L. H., van der Meché, F. G. A., van Darn, P. A., Meulstee, J., Schmitz, P. I. M., Jacobs, B., Oomes, P. G., Kleyweg, R. P., Jacobs, B. C., Endtz, H. P., van Doorn, P. A., van der Mech, F. G. A., Van den Berg, L. H., Mollee, I., Logtenberg, T., Thomas, P. K., Plant, G., Baxter, P. J., Luis, R. Santiago, Matsumoto, M., Notermans, N. C., Wokke, J. H. J., Lokhorst, H. M., van der Graaf, Y., Jennekens, F. G. I., Azulay, J. P., Bille-Turg, F., Valentin, P., Farnarier, G. G., Pellissier, J. F., Serratrice, G., Quasthoff, S., Schneider, U., Grafe, P., Hilkens, P. H. E., Moll, J. W. B., van der Burg, M. E. L., Planting, A. S. T., van Putten, W. L. J., van den Bent, M. J., Birklein, F., Spitzer, A., Lang, E., Neundorfer, B., Diehl, R. R., Lücke, D., Smith, G. D. P., Mathias, C. J., Serra, J., Campera, M., Ochoa, J. L., Ray Chaudhuri, K., Pavitt, D., Alam, M., Handwerker, H. O., Bleasdale-Barr, K., Smith, G., Murray, N. M. F., Hawkins, P., Pepys, M., Gellera, C., DiDonato, S., Taroni, F., Uncini, A., Di Muzio, A., Servidei, S., Silvestri, G., Lodi, R., Iotti, S., Barbiroli, B., Morrissey, S. P., Borruat, F. X., Francis, D., Mosely, I., Hansen, H. C., Helmke, K., Kunze, K., Sadzot, B., Maquet, P., Lemaire, Plenevaux, Damhaut, Sommer, C., Myers, R. R., Berta, E., Mantegazza, R., Argov, Z., Shapira, Y., Wirguin, I., Beuuer, J., Franke, C., Roberts, M., Willison, H., Vincent, A., Newsom-Davis, J., Morrison, K. E., Damels, R., Francis, M., Campbell, L., Davies, K. E., Kohler, W., Bucka, C., Hertel, G., Kanovsky, P., Auer, D., Ackermann, H., Klose, U., Naegele, Th., Bien, S., Voigt, K., Fink, G. R., Stephan, K. M., Wise, R. J. S., Mullatti, N., Hewer, L., Frackowiak, R. S. J., Weiller, C. S., Rijnites, M., Jueptner, M., Bauermann, T., Krams, M., Diener, H. C., van Walderveen, M. A. A., Barkhof, F., Hommes, O. R., Valk, J., Willmer, J. P., Guzman, D. A., Passingham, R. E., Silbersweig, D., Ceballos-Baumann, A., Frith, C. D., Frackowiak, R., Lucas, C. H., Goullard, L., Marchau, M. J., Godefroy, O., Rondepierre, P. H., Chamas, E., Mounier-Vehier, F., Leys, D., Renato, J., Verdugo, M. S. C., Campero, M., Jose, L., Ochoa, D. S. C., Vivancos, F., Tejedor, E. Diez, Martinez, N., Roda, J., Frank, A., Barreiro, P., Satoh, Y., Nagata, K., Maeda, T., Hirata, Y., YalÇinerner, B., Ozkara, C., Ozer, F., Ozer, S., Hanoglu, L., Zunker, P., Pozo, J. L., Oberwittler, C., Schick, A., Buschmann, H. -Ch., Ringelstein, E. Bernd, Lara, M., Anzola, G. P., Magoni, M., Volta, G. Dalla, Tarasov, A., Feigin, V., Beaudry, M. G., Carrier, S., Chicoutimi, Henriques, I. L., Bogoussslavsky, J., van Melle, G., Mathieu, J., Perusse, L., Allard, P., Prevost, C., Cantin, L., Bouchard, J. M., De Braekeleer, M., Agbo, C., Neau, J. P., Tantot, A. M., Dary-Auriol, M., Ingrand, P., Gil, R., Baltadjiev, D., Zekin, D., Sabey, K., Gennaula, C. P., Pope, B. A., Caparros-Lefebvre, D., Girard-Buttaz, I., Pruvo, J. P., Petit, H., Hipola, D., Martin, M., Giménez-Roldan, S., Ivanez, V., Japaridze, G., Carrasco, J. L., Picomell, I., Herranz, J. L., Macias, J. A., Nieto, M., Noya, M., Oller, L., Kiteva-Trencevska, G., Delgado, M. R., Liu, H., Luengo, A., Parra, J., Colas, J., Fernandez, M. J., Manzanares, R., Kornhuber, M. E., Malashkhia, V., Orkodashili, G., Martinez, M., Bonaventura, I., Porta, G., Martinez, I., Fernandez, A., Aguilar, M., Masnou, P., Drouet, A., Dreyfus, M., Cartron, J., Morel-Kopp, M. C., Tchernia, G., Kaplan, C., Lammers, M. W., Hekster, Y. A., Keyser, A., Meinardi, H., Renier, W. O., Boon, P. A. J. M., Have, M. D., Kint, B., Cruz, P., Cadilha, A., Almeida, R., Goncalves, M., Pimenta, M., Ramos, L. M. P., Polder, T. W., Broere, C. A., Polman, L., Rother, I., Rother, M., Schlaug, G., Arnold, S., Holthausen, H., Wunderlich, G., Ebner, A., Luders, H., Witte, O. W., Seitz, R. J., Serra, L. L., Gallicchio, B., Rotondi, F., Wieshmann, U., Meierkord, H., Sabev, K., Di Carlo, V., Gueguen, B., Derouesné, Ch., Ancri, D., Bourdel, M. C., Guillou, S., Aliaga, R., Chornet, M. A., Rodrigo, A., Pascual, A. Pascual -Leone, Catala, M. D., Pascual-Leone, A., Benbadis, S. R., Dinner, D. S., Chelune, G. J., Lüders, H. O., Piedmonte, M. R., Blanco, T., Lopez, M. P., Romero, B., Deltoro, A., Pascual, A., Pascual, Leone, Bolgert, F., Josse, M. O., Tassan, P., Touze, E., Laplane, D., Godenberg, F., Brizioli, E., Del Gobbo, M., Pelliccioni, G., Scarpino, O., Durak, H., Damlacik, G., Tunca, Z., Fidaner, H., Yurekli, Y., Yemez, B., Kaygisiz, A., Anllo, E. A., Esperet, E., Giovagnoli, A. R., Casazza, M., Spreafico, R., Avanzini, G., Mascheroni, S., Vecchio, I., Tornali, C., Antonuzzo, A., Grasso, A. A., Bella, R., Pennisi, G., Raffaele, R., Broeckx, J., Schildermans, F., Hospers, W., Deberdt, W., Carney, J. M., Aksenova, M., Chen, M. S., Juncadella, M., Busquets, N., De la Fuente, I., Rodriguez, A., Rubio, F., Soler, R., Khati, C., Pillon, B., Deweer, B., Malapani, C., Malichard, N., Dubois, B., Rancurel, G., Lopez, D. L., Jungreia, G., DeKosky, S. T., Boiler, F., Weiller, C., Rijntjes, M., Mueller, S. P., Maguire, E. A., Burke, E. T., Staunton, H., Phillips, J., Rousseaux, M., Pena, J., Bertran, I., Santacruz, P., Lopez, R., Catafau, A., Lomena, F., Blesa, R., Rampello, L., Nicoletti, A., Cabaret, M., Lesoin, F., Steinling, M., Tournev, I., Maier-Hauff, K., Schroeder, M., Wolf, A., Cochin, J. P., Noel, I., Augustin, P., Auzou, P., Hannequin, D., Maria, V., Lopez-Bresnahan, Danielle, D. M., Antin-Ozerkis B. A., Bartels, E., Rodiek, S. O., Flugel, K. A., Campos, D. M., Salas-Puig, J., Del Rio, J. Sanhez, Vidal, J. A., Lahoz, C. H., Eraksoy, M., Barlas, O., Barlas, M., Bayindir, C., Ozcan, H., Birbamer, G., Gerstenbrand, F., Felber, S., Luz, G., Aichner, F., Seidel, G., Kaps, M., Hutzelmann, A., Gerriets, T., Kruggel, F., Martin, P. J., Gaunt, M. E., Abbot, R. J., Naylor, A. R., Meary, E., Dilouya, A., Meder, J. F., De Recondo, J., Lebtahi, R., Neff, K. W., Meairs, S., Viola, S., Matta, E., Aquilone, L., Rise, I. R., Authier, F. J., Kondo, H., Ghnassia, R. T., Degos, J. D., Gherardi, R. K., Bardoni A., Ciafaloni E., Comi G. P., Bresolin N., Robotti M., Moggio M., Rigoletto C., Roses A., Scarlato G., Castelli, E., Turconi, A., Bresolin, N., Perani, D., Felisari, G., Chariot, P., de Pinieux, G., Astier, A., Jacotot, B., Gherardi, R., Fischer-Gagnepain, V., Louboutin, J. P., Crespo, F., Florea-Strat, A., Fromont, G., Sabourin, J. -C., Gonano, E. -F., Moroni, I., Prelle, A., Iannaccone, S., Quattrini, A., deRino, F., Sessa, M., Golzi, V., Smirne, S., Nemni, R., Turpin, J. C., Lucotte, G., Jacobs, S. C. J. M., Willems, P. W. A., Bootsma, A. L., Lasa, A., Calaf, M., Baiget, M., Gallano, B., Fichter-Gagnepain, V., Mazzucchelli, F., D'Angelo, M. G., Velicogna, M., Bet, L., Comi, G. P., Bordoni, A., Gonano, E. F., Bazzi, P., Rapuzzi, S., Moggio, M., Fagiolari, G., Ciscato, P., Messina, A., Battistel, A., Ryniewicz, B., Sangla, I., Desnuelle, C., Paquis, V., Cozzone, P. J., Bendahan, D., Sturenburg, H. 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Garcia, Prados, C., Gomez, L., Munoz, J., Bouchard, C., Barrett, M. J., Coulton, G. R., Casadevall, J., Sala, R. Alvarez, Garcia, J. M. Pino, Dupuis, M. J. M., Mezt, R., Jean, D., Maes, E., Smits, R. C. F., Emmen, H. H., Kulig, B. M., van Loenen, A. C., de Waal, R., van Diemen, H. A. M., Koetsier, J. C., Ince, D., Ferri, R., Durelli, L., Bangioanni, M. R., Ferrero, B., Riva, A., Bergaasco, B., Stenager, E., Stenager, E. N., Jensen, K., De Andres, C., Anaya, F., Dimova, V., Hansen, A. W., Norby, S., Edal, A. L., Rosenberg, T., Thorpe, J. W., Filippi, M., Horsfleld, M. A., Reganati, P., Baratti, C., Bressi, S., Ozurk, V., Yeil, S., Rodegher, M., Sirabian, G., Alberoni, M., Eoli, M., La Mantia, L., Manetti, E., Zaffaroni, M., Milanese, C., Corsini, E., de Castro, P., Carreno, M., Iriarte, J., Heide, W., Barado, J., Echaniz, P., Cuadrado, E., Baykan-Kurt, B., Oktem-Tanor, O., Bahar, S., Konyalioglu, R., Tumac, A., Gok, S., Gurvit, H., Gursoy, G., Henderson, C. E., Westarp, M. E., Perron, H., Hoff-Jörgensen, R., Rasmussen, H., Schraff, S., Kornhuber, H. H., Moseley, I. F., Colangelo, A. M., Fetoni, V., Parati, E., Austoni, L., DiGiovanni, A., Meucci, N., Nobile-Orazio, E., Scarlato, G., Goi, G., Lombardo, A., Bairati, C., Aversa, E., Caputo, D., Ferrarese, C., Canafoglia, L., Frigo, M., Pecora, N., Riva, R., Frattola, L., Carpo, M., Gamba, M., Meussi, N., Barbieri, S., Ostermeyer, B., Patten, B. M., Abeta, S., Inoue, N., Matsui, H., Yoshino, Y., Pizzi, C. Delli, Ragno, M., Losseff, N. A., Fletcher, N. A., Thorpe, J., Droogan, A. G., Harper, R., Hawkins, S. A., Patterson, V. H., Bell, P., Soeterboek, A. A. J., Koehler, P. J., Urtasun, M., Vilchez, J., Castel-lvi-Rel, S., Gine, R., Villa, M., Koehler, W., Kumar, A. J., Edwin, D., Moser, H. W., Guidetti, D., Ferlini, A., Motti, L., Bondavalli, M., Patrosso, M. C., Ghidoni, E., Alfaro, A., Giros, M. L., Barcelo, A., Piqueras, A., Martinez, V., Rango, M., Bamonti, F., Greco, F., Spagnoli, D., Tomei, G., Zetta, L., Honczarenko, K., Jezewski, T., Kojder, I., Verlooy, J., Reempts, Jos V., Deuren, B. V., Borgers, M., Gajda, J. U., Ley-Pozo, J., Louwen, P., Happe, S., Buschmann, H. C., Ringelstein, E. B., Yamawaki, T., Takao, M., Suzuki, N., WeilBenborn, K., Schellong, S., Ehrenheim, C., Wollenhaupt, J., Goetz, C., Lubach, D., Vion-Dury, J., Nicoli, F., Confort-Gouny, S. O., Dhiver, C. O., Lamoureux, S., Salvan, A. M., Gastaut, J. -A., Gastaut, J. -L., Cozzone, P., Ribalta, T., Santamaria, J., Drewes, A. M., Taagholt, S. J., van den Berg, J. S. P., Limburg, M., Valldeoriola, F., Valls-Solé, J., Marti, M. J., Trenkwalder, C., Stiasny, K., Collado-Scidel, V., Wetter, T., Kazenwadel, J., Kohnen, R., Ramm, S., Oertel, W. H., Thajeb, P., Starck, M., Albrecht, H., Pollmann, W., Konic, N., Split, W., Sulkowski, W., Kowalska, S., Sawradewicz-Rybak, M., Musior, M., Scaioli, V., Brock, S., Ciano, C., Palazzini, E., Servan, J., Aoba, S., Yamaguchi, S., Johkura, K., Rosin, L., Solimena, M., De Camilli, P., Meinck, H. -M., Roquer, J., Marti, N., Cano, A., Pou-Serradell, A., Robeck, S., Enqelhardt, A., Kalden, J. R., Dhaenens, G., Tyrdal, S., Broere, C. A. J., Polman, L. J., Gomez, R., Alberdi, M., Delgado, J. M., Kansu, E., Saribas, O., Zileli, T., Proust, F., Freger, P., Creissard, P., Proano, J., Patrignani, J., Castro, J., Ugarte, A., Giros, Ma. L., Pampols, Ta., Sabev, C., Gikova, S., Antonova, N., Georgieva, L., Stanev, V., Popova, G., Kostadinova, S., Pepeliarska, M., Pierre-Jerome, C., Bekkelund, S. I., Husby, G., Mellgren, S. I., Attaccalite, A., Guidi, M., Passero, S., Caruso, V., HÄgele, J., Lohmeyer, J., Heilmann, M., Ohly, A., Ceballos-Baumann, A. O., Joussen, K., Sonka, K., Chave, B., Confort-Gouny, S., Houallah, T., Neundoerfer, B., Tex, S., Seeber, C., Mokrusch, T., Urdiain, T. X. Arbizu, Yelamos, S. M., Villanueva, P., Serra, J. Peres, Braghi, S., Bonifacio, E., Natali-Sora, M. G., Debbink, Y. N., Marra, T. R., Mossman, S., Timmings, P., Seitz-Dertinger, S., Solbach, W., Mainz, A., Manfredini, E., Calabrese, E., Allaria, S., Mariani, C., Sinaki, M., Lynn, S., Westerlind, K., Ossege, L. M., Voss, B., Wiethege, Th., Sindern, E., Malin, J. p., Le Doze, F., Chapon, F., de la Sayette, V., Schaeffer, S., Dary, M., Lechevalier, B., Viader, F., de Pommery, J., Weill-Fulazza, J., Menetrey, M., Lazzarino, L. G., Nicolai, A., Nappo, A., Blin, J., Mazetti, P., Mazoyer, B., Ayed, S. Ben, Rivaud, S., Vidailhet, M., Pierrot-Deseilligny, C., Chase, T., Jordan, K. G., Gergaud, J. M., Breux, J. P., Roblot, P., Grollier, G., Giraudon, B. Becq, Dobato, J. L., Gilabert, Y. Perez, Blanco, J. L. Munoz, de Kruijk, J., Twijnstra, A., Wilmink, J., Leffers, P., Iniguez, C., Jimenez-Escrig, A., Nocito, M., Villar, M. L., Gonzalez-Porque, P., Gobernado, J. M., Chandler, H. C., Crockard, H. A., Henderson, F., Rossi, T., Maidani, M., Pujol, A., Rimola, A., Beltran, J., Garcia-Valdecasas, J. C., Navasa, M., Grande, L., Galofre, J., Visa, J., Rodes, J., Ruiz, M., Pampols, T., Bruce, L., Tanner, M. J. A., Lefaucheur, J. P., Verroust, J., Taghavy, A., Hamer, H., Benomar, A., Cancel, G., Stevanin, G., Durr, A., Labaune, C., Desnizza, V., Widjaja-Cramer, B., Schulze-Bonhage, A., Kott, H., Ferbert, A., Sanz-Sebastian, C., Pascual, L. F., Alegria, F. Abad, Kushnir, M., Groozman, G. B., Korczyn, A. D., Drory, Ve., Korczyn, A., Guggenheim, H., Baykouchev, St., Struppler, A., Tchalucova, N., Jotova, J., Mokri, B., Parisi, J. E., Scheithauer, B. W., Piepgras, D. G., Miller, M., Kornhuber, A. W., Köhler, A., Hülser, P. J., Kriebel, J., Alonso-Villaverde, C., Castro, A., Masana, L., Urda, A. Martin, Fernandez, J., Mares, R., Torre, L., Mayayo, E., Lossos, A., Gomori, M., Libson, E., Goldfarb, A., Seigal, T., de Louw, A., Praamstra, P., Horstink, M., Cools, A., Tarrats, E. Basart, Calopa, M., Martinez, S., Ballabrina, J., Taussig, D., Marion, M. -H., Mallecourt, J., Ranoux, D., Gasser, T., Kabus, C., Ozelius, L., Wenzel, R., Breakefield, X. O., Boot, H., Poublon, R. M. L., Bogaard, J. M., GinaÏ, A. Z., Cabezas, C., Scholz, J., Nitschke, N., Vieregge, P., Wirk, B., Hochberg, F. H., Hefter, H., Kessler, K., Wirrwar, A., Stocklin, G., Tournier-Lasserves, E., Agundez, J. Garcia, Ruiz, E., Li, X. P., Hedlund, P. B., Fuxe, K., Kulisevsky, J., Avila, A., Berthier, M. L., Gerard, J. -M., Cambier, J., Caucheteur, C., Deuschl, G., Köster, B., Scheidt, C., Lücking, C. H., Mena, M. A., Chedru, F., Oubary, P., Rondot, P., Anagnostou, C. N., Panagopoulos, C. P., Ziogas, D. E., Vermersch, P., Robitaille, Y., Gauvreau, D., Destée, A., Delacourte, A., Ficola, U., Marozzi, P., Piccoli, F., Janelidze, M., Shakarishvili, R., Gagoshidze, T., Vashadze, T., Tsiskaridze, A., Djannelidze, M., Trullen, J. M. Perez, Pardo, P. J. Modrego, Vazquez-Andre, M. L., Bail, L., Naccache, L., Gauvrit, J. L., Panisset, M., Boller, A. F., Giannini, M., Zanette, E., Di Cesare, S., Altieri, M., Maloteaux, J. M., Delwaide, C., Sciaky, M., Newman, S. K., Kennedy, A. M., Frackowiack, R. S. J., Warrington, E. K., Rossor, M. N., Martinez-Lage, Pablo, Martinez Lage, J. Manuel, Manubens, JosÇ M., Lacruz, Francisco, Larumbe, Rosa, Muruzabal, Javier, Locatelli, T., Cursi, M., Mauri, M., Liberati, D., Fornada, C., Iriarte, L. M., Lopez, M., Grilo, A., Repeto, M., Brasic, J. R., Barnett, J. Y., Sheitman, B. B., Young, J. G., Shalit, F., Brodie, C., Sredni, B., Engelien, A., Stern, E., Huber, W., Frith, C., Miralles, F., Albadalejo, M. D., Antem, M., Pastor, I., Estelies, M. A., Del Ser, T., Ochoa, H. Severo, Munoz, D., Hachinski, V., Cucinotta, D., Senin, U., Girardello, R., Crepaldi, G., Croria, F., Schens, D. B., Vigo-Pelfrey, C., SempereE, A. P., Ortega, M. P., Bava, L., Magni, E., Aronovich, B. D., Treves, T. A., Bornstein, N. M., Van Blercom, N., Blecic, S., Violon, Ph., Hildebrand, J., Zamboni, M., Ambrosoli, L., Poli, A., Kuehnen, J., Tilgner, C., Raltzig, M., Moering, B., Faiss, J., Deeb, S. M. Al, Daif, A., Sharif, H., Tatay, J., Caroeller, F., Avendano, C., Vinogradova, T., Pinto, A. N., Canhao, P., Neau, J. -Ph., Pacquereau, J., Meurice, J. -C., Schwab, M., Bauer, R., Deeb, M. AL, Tjan, T. J., Aabed, M., Berges, S., Crepin-Leblond, T., Chavot, D., Cattin, F., Snidaro, M. H., Chopard, J. L., Ley, C. Oliveras, Alameda, F., Alfonso, S., Podobnik-Sarkanji, S., Pniewski, J., Torbicki, A., Mieszkowski, J., Plaza, I., Petrunjashev, V., Velcheva, I., Hadjiev, D., Yancheva, S., Petrov, L., Karakaneva, S., Petkov, A., Nikolov, E., Niehaus, L., Sacchetti, M. L., Toni, D., Fiorelli, M., Gori, C., Argentino, C., Lyrer, Ph., Radu, E. W., Gratzl, O., Rondepierre, Ph., Leclerc, X., Marchau, Jr, M., Scheltens, Ph., Hamon, M., Janssens, E., Henon, H., Lucas, C., KuÇukoglu, H., Baybas, S., Dervis, A., YalÇiner, B., Yilmaz, N., Ozturk, M., Arpaci, B., Navarro, J. A., Arenas, J., Perez-Sempere, A., Egido, J. A., Soriano-Soriano, C., Beau, P., Gergaud, J. -M., Coudero, C., Dierckx, R. A., Dobbeleir, A., Timmermans, E., Vandevivere, J., Lucas, C. H., Gomez, M., Aguirre, J., Berenguer, A., Duran, C., Parrilla, J., Gonzalez, F., Gironell, A., Rey, A., Marti-Vilalta, J. L., de Lecinana, M. Alonso, Federico, F., Conte, C., Simone, I. L., Giannini, P., Liguori, M., Lucivero, V., Picciola, E., Tortorella, C., Drislane, F., Wang, A. Ming, Di Mascio, R., Marchioli, R., Vitullo, F., Di Pasquale, A., Sciulli, L., Kramer, V., Tognoni, G., Levivier, M., del Olmo, A., Caballero, E., Degaey, I., de Bruijn, S. F. T. M., Tchaoussoglou, I., Bastianello, S., Pozzilli, C., Cervello, A., Catala, N., Koskas, F., Kieffer, E., Botia, E., Vivancos, J., Leon, T., Segura, T., Ramo, C., Lopez, F., Karepov, V. G., Gur, A. J., Berlanga, B., Gracia, V., Fiol, C., Kurtel, H., Ozkutlu, U., Yegen, B., Grau, A. J., Buggle, F., Heindle, S., Steichen-Wiehn, C., Banerjee, T., Maiwald, M., Becher, H., Villafana, W., Medina, F., Fernandez-Real, J. M., Soler, S., Planas, E., Iceman, E., Doganer, I., Badlan, G., Genc, B., Yulug, K., Ideman, E., Dural, H., Kutlul, K., Damalik, G., Baklan, Y., Metin, B., Tekinsoy, E., Iriarte, I., Subira, M. L., Crockar, A. D., Treacy, M., McNell, T. A., Grazzi, L., Ediboglu, N., Bilgin, H., Ertas, S., Goument, J. -P., Basset, C., Campos, Y., Garcia-Silva, T., Cabello, A., Bussaglia, E., Tizzano, E., Colomer, J., Gimbergues, P., Campagne, D., Bommelaer, C., Delaguillaume, B., Ramtami, H., Ait-Kaci-Ahmed, M., Pascual L. F., Fernandez T., Hortells M., Sanz C., Morales F., Lauritzen, L., Picard, F., Sellal, F., Collard, M., Avramidis, T., Alexiou, E., Anastopoulos, T., Frongillo, D., Delfino, F. A., Cannata, M., Calo, L., Vichi, R., Antonini, G., Fragola, V., Cannata, D., Salas, M., Ruiz, C., Angelard, B., Lacau, J., Guily, St., Sendtner, M., Goadsby, Peter J., Quin, N. P., Gadian, D. G., Roland, P. E., Seitz, Rudiger J., Frackowiak, Richard S. J., Becker, G., Krone, A., Schmidt, K., Hofmann, E., Bogdahn, U., Rosenfeld, M. R., Meneses, P., Kaplitt, M. G., Dalmau, J., Posner, J., Cordon-Cardon, C., Hoang-Xuan, K., Vega, F., Nishisho, I., Moisan, J. P., Theillet, C., Delattre, O., Zhu, Jiahong, Walther, W., Posner, J. B., Roelcke, U., von Ammon, K., Pellikka, R., Lucking, C. H., Walon, C., Boucquey, D., -Van Rijckevorsel, K. Harmant, Lannoy, N., Verellen-Dunoulin, Ch., Liszka, U., Cavaletti, G., Casati, B., Kolig, C., Bogliun, G., Marzorati, L., Johannsen, L., Chio, A., Ruda, R., Vigliani, M. C., Sciolla, R., Seliak, D., Hoang-Xuang, K., Villanueva, J. A., Montalban, X., Arboix, A., Colosimo, C., Albanese, A., Hughes, A. J., de Bruin, V., Lees, A. J., Kowalski, J. W., Banfi, S., Santoro, L., Perretti, A., Castaldo, I., Barbieri, F., Campanella, G., Bhatia, K. P., Mardsen, C. D., de Bruin, V. S., Machedo, C., Ceballos-Baumann, D., Marsden, C. D., Brooks, D. B. J., Wennlng, G. K., Quinn, N., McDonald, W. l., Warner, T. T., Bain, P. C., Davis, M. B., Conway, D., Shaunak, S., O'Sullivan, E., Crawford, T., Lawden, M., Blunt, S., Rapoport, A., Sarova-Pinchas, I., de Beyl, D. Zegers, Mavroudakis, N., Blanc, S., Godinot, C., Lenoir, G., Barkhof, M. S. F., Tas, M. W., Baron, P. L., Constantin, C., Cassatella, M. A., Langdon, D. W., Webb, S., Gasparini, P., Zeviani, A., Kidd, D., Mammi, S., Cahalon, L., Hershkoviz, R., Lahat, N., Wallach, D., Annunziata, P., Martino, T., Maimone, D., Guazzi, G. C., Porrini, A. M., Dell'Arciprete, L., Rothwell, P. M., Stewart, R. R. C., Cull, R. E., Willmes, K., Poeck, K., Russell, D., Braekken, S. K., Brucher, R., Svennevig, J., Hermesl, M., Bruckmann, H., Biraben, A., Sliwka, U., Meyer, B., Schondube, F., Noth, J., Lavenu, I., Lammers, C., Waldecker, B., Haberbosch, W., Stam, J., Schneider, R., Gautier, J. C., Berlit, T. P., Fauser, B., Kuhne, D., Geraud, G., Danielli, A., Larrue, V., Bes, A., Timmerman, E., Bono, F., Bruni, A. C., Valalentino, P., Montesi, M. P., Talerico, G., Zappia, M., Sabatelli, M., Quattrone, A., Pareyson, D., Lorenzetti, D., Sghirlanzoni, A., Castellotti, B., Lupski, J. R., Archidiacono, N., Antonacci, R., Marzella, R., Rocchi, M., Samuel, D., Goulon-Goeau, C., Costa, P. P., Bismuth, H., Said, G., De Jongh P., Lofgren A., Timmerman V., Vance J. M., Van Broeckhoven C., Martin J. -J., Martinez, A. Cruz, Bort, S., Arpa, J., Misra, P., King, R. H. M., Badhia, K., Anderson, M., Caballo, A., Vichez, J., Gabriel, J. M., Erne, B., Miescher, G. C., Ulrich, J., Vital, A., Vital, C., Steck, A., Petry, K., Labatut, I., Hilmi, S., Ellie, E., Ferrini-Strambi, L., Zucconl, M., Marchettini, P., Palazzi, S., Oehlschlager, M., Pepinsky, R. B., Gemignani, F., Marbini, A., Pavesi, G., Di Vittorio, S., Manganelli, P., Mancia, D., Vermersh, P., Roche, J., Durocher, A. M., Dewailly, Ph., Dettmers, C., Fink, G., Lemon, R., Stephan, K., Passingham, D., Weder, B., Knorr, U., Huang, Y., Butterfield, D. A., Peris, M. L., Peiro, C., Pascual, A. Pascual-Leone, Bottini, G., Folnegovic-Smalc, V., Knezevic, S., Bokonjic, R., Ersmark, B., Torres, M. Gonzalez, Guiraud-Chaumeil, B., Haugaard, K., Jovicic, A., Chr, Lang, Levic, Z., Parra, C. Martinez, Ochoa, J. Patrignani, Titlbach, O., Wikkelso, C., Caparros-Lefevre, D., Debachy, B., Verier, A., Cantinho, G., Santos, A. I., Godinho, F., Bagunya, J., Roig, T., Ensenyat, A., Santiag, O., Trabucchi, H., De Leo, D., Koch, Ch., Zeumer, H., Matkovic, Z., Morris, P., Donaghy, M., Köhler, W., Kammer, T., Röther, J., Navon, R., Fontaine, B., Wu, Y., Capdevila, A., Guardiola, M. J., van Dijk, G. W., Notermans, N. C., Kruize, A. A., Kater, L., Bertelt, C., Hesse, S., Friedrich, H., Mauritz, K. -H., Giron, L. T., Watanabe, I. S., Ewing, D., Koepp, M., Lempert, T., Sander, B., Kauerz, U., Mehdorn, H. M., Hezel, J., Eickhoff, W., Kryst, T., Timsit, S., Gardeur, D., Reis, Mitermayer Galvao dos, Secor, E., Filho, A. Andrade, Silva, M. Cardoso, Santos, S. R. Silveira, Vasilaski, G., Reis, E. A. dos, Velupillai, P., Harn, D. A., Tigera, J. Garcia, Dreke, R. Martinez, Crespo, R. Piedra, Besses, C., Acin, P., Massons, J., Florensa, L., Oliveres, M., Sans-Sabrafen, J., Wicklein, E. M., Pleiffer, G., Kunre, K., Dieterich, M., Brandt, Th., Guarino, M., Stracciari, A., Pazzaglia, P., D'Alessandro, R., Santilli, I., Donato, M., The European Velnacrine Study Group, The Dutch Guillain-Barré study group, The COP-1 Multicenter Clinical and Research Group Study, and European Study Group
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- 1994
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5. Management of difficult common bile duct stones
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Hochberger, J, Tex, S, Maiss, J, and Hahn, E.G
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- 2003
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6. A comparison of three combinations of injectable anesthetics in miniature donkeys
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Matthews, Nora S, Taylor, Tex S, and Sullivan, Jennifer A
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- 2002
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7. Nephrectomy Via Ventral Median Celiotomy in Equids
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John P. Caron, Harold C. Schott, Tex S. Taylor, Carolyn E. Arnold, and M. Keith Chaffin
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medicine.medical_specialty ,General Veterinary ,business.industry ,medicine.medical_treatment ,Peritonitis ,medicine.disease ,Nephrectomy ,Surgery ,Ureter ,medicine.anatomical_structure ,Blunt dissection ,medicine.artery ,Laparotomy ,medicine ,Ascending colon ,Ectopic ureter ,Renal artery ,business - Abstract
Objective To report technique for, and outcome after, nephrectomy through a ventral median celiotomy in equids. Study Design Case series. Animals Equids with unilateral renal disease (n = 6), aged 2 months to 18 years, weighing 90–434 kg. Methods A ventral median celiotomy was used to access the left or right kidney. To facilitate surgical exposure, the small intestine was reflected towards the diaphragm using laparotomy sponges and the ascending colon was exteriorized and in some cases evacuated. The peritoneum over the affected kidney was incised and blunt dissection used to free the kidney from the retroperitoneal fat, then the renal artery, vein, and ureter were isolated and ligated. Abdominal lavage with sterile saline solution was performed before abdominal closure. Results Four horses, 1 donkey, and 1 mule had unilateral nephrectomy to treat verminous nephritis (1), idiopathic hematuria (1), and ectopic ureter (4). A ventral median approach provided adequate access to the kidney in all 6 cases. Two horses had postoperative complications (peritonitis, chylous abdominal effusion) that resolved with medical therapy. No complications attributable to nephrectomy were reported by the owners upon follow-up 1–8 years after surgery. Conclusions A ventral median approach for nephrectomy can be used for unilateral nephrectomy in equids weighing up to 434 kg.
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- 2013
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8. Treatment of rectal tears in 85 horses presented to the Texas Veterinary Medical Center
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T. G. Eastman, R. N. Hooper, Tex S. Taylor, and Clifford M. Honnas
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medicine.medical_specialty ,Veterinary medicine ,Rectal tears ,Equine ,business.industry ,medicine ,Center (algebra and category theory) ,business ,Surgery - Published
- 2010
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9. Guaifenesin-Ketamine-Xylazine Infusions to Provide Anesthesia in Donkeys
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Kerry S. Barling, Ethel V. Taylor, Nora S. Matthews, Tex S. Taylor, and Courtney L. Baetge
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Guaifenesin ,Equine ,business.industry ,Arterial oxygen ,Xylazine ,Intravenous anesthesia ,Anesthesia ,Anesthetic ,Heart rate ,Ketamine xylazine ,medicine ,Ketamine ,business ,medicine.drug - Abstract
The purpose of this study was to determine a satisfactory combination of guaifenesin, ketamine, and xylazine (GKX) that would produce safe and satisfactory total intravenous anesthesia in donkeys for use under field conditions. Donkeys require higher amounts of ketamine in GKX to achieve satisfactory anesthetic levels without producing excessive depression with guaifenesin. Five adult standard donkeys (average weight, 264 kg) were anesthetized with 1.5 mg/mL ketamine, 0.5 mg/mL xylazine, 50 mg/mL guaifenesin (GKX-1); 2.0 mg/mL ketamine, 0.5 mg/mL xylazine, 50 mg/mL guaifenesin (GKX-2); or 2.0 mg/mL ketamine, 0.75 mg/mL xylazine, 50 mg/mL guaifenesin (GKX-3). For the first trial, two donkeys received GKX-1, two received GKX-2, and one received GKX-3. One donkey received GKX-1, one received GKX-2, and three received GKX-3 for the second trial. In the final trial, two received GKX-1, two received GKX-2, and one received GKX-3. Donkeys were sedated with xylazine (1.1 mg/kg body weight) intravenously, and anesthesia was induced using intravenous GKX-1, GKX-2, or GKX-3. Anesthesia was maintained for 45 minutes; temperature, respiration rate, heart rate, hemoglobin saturation, partial pressure of arterial oxygen (PaO2), partial pressure of carbon dioxide in arterial gas (PaCO2), and pH were measured. There was no significant difference between combinations for temperature, respiration rate, heart rate, hemoglobin saturation, PaCO2, or pH. At 30 and 45 minutes, GKX-3 produced significantly (P
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- 2008
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10. Comparative pharmacokinetics of meloxicam in clinically normal horses and donkeys
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Nora S. Matthews, Melissa Sinclair, Ken E. Peck, Brad S. Bennett, Tex S. Taylor, and Katrina L. Mealey
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Male ,Veterinary medicine ,Thiazines ,Meloxicam ,Bolus (medicine) ,Species Specificity ,Pharmacokinetics ,Animals ,Medicine ,Horses ,Volume of distribution ,General Veterinary ,business.industry ,Anti-Inflammatory Agents, Non-Steroidal ,Area under the curve ,Horse ,Total body ,Equidae ,General Medicine ,Thiazoles ,Health ,Area Under Curve ,Female ,Donkey ,business ,medicine.drug - Abstract
Objective—To determine the disposition of a bolus of meloxicam (administered IV) in horses and donkeys (Equus asinus) and compare the relative pharmacokinetic variables between the species. Animals—5 clinically normal horses and 5 clinically normal donkeys. Procedures—Blood samples were collected before and after IV administration of a bolus of meloxicam (0.6 mg/kg). Serum meloxicam concentrations were determined in triplicate via high-performance liquid chromatography. The serum concentration-time curve for each horse and donkey was analyzed separately to estimate standard noncompartmental pharmacokinetic variables. Results—In horses and donkeys, mean ± SD area under the curve was 18.8 ± 7.31 μg/mL/h and 4.6 ± 2.55 μg/mL/h, respectively; mean residence time (MRT) was 9.6 ± 9.24 hours and 0.6 ± 0.36 hours, respectively. Total body clearance (CLT) was 34.7 ± 9.21 mL/kg/h in horses and 187.9 ± 147.26 mL/kg/h in donkeys. Volume of distribution at steady state (VDSS) was 270 ± 160.5 mL/kg in horses and 93.2 ± 33.74 mL/kg in donkeys. All values, except VDSS, were significantly different between donkeys and horses. Conclusions and Clinical Relevance—The small VDSS of meloxicam in horses and donkeys (attributed to high protein binding) was similar to values determined for other nonsteroidal anti-inflammatory drugs. Compared with other species, horses had a much shorter MRT and greater CLT for meloxicam, indicating a rapid elimination of the drug from plasma; the even shorter MRT and greater CLT of meloxicam in donkeys, compared with horses, may make the use of the drug in this species impractical.
- Published
- 2006
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11. Spiral colon bypass in a geriatric Vietnamese potbellied pig
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Michael Walker, D. Bruce Lawhorn, Tex S. Taylor, and Mark A. Gallardo
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medicine.medical_specialty ,Colon ,Swine ,Exploratory laparotomy ,medicine.medical_treatment ,Constriction, Pathologic ,Anastomosis ,Gastroenterology ,Colonic Diseases ,Cecum ,Internal medicine ,otorhinolaryngologic diseases ,medicine ,Animals ,Abscess ,Swine Diseases ,General Veterinary ,Megacolon ,business.industry ,Impaction ,Anastomosis, Surgical ,Abdominal distension ,medicine.disease ,digestive system diseases ,Surgery ,medicine.anatomical_structure ,Spiral Colon ,Female ,sense organs ,medicine.symptom ,business ,Intestinal Obstruction - Abstract
An 8-year-old potbellied pig was evaluated for anorexia, decreased fecal production, signs of depression, inappetence, and abdominal distension. During hospitalization, a tooth root impaction and abscess were diagnosed, and abdominal radiography revealed severely distended, gas-filled large and small intestines. Exploratory laparotomy revealed a stricture of the proximal centripetal loop of the spiral colon and megacolon of the proximal portion of the spiral colon and cecum. A side-to-side spiral colon anastomosis was performed to create a partial bypass of the spiral colon. The success of this procedure suggests that spiral colon bypass is a treatment option for spiral colon stricture formation in potbellied pigs. Spiral colon stricture formation should be considered as a differential diagnosis in geriatric potbellied pigs that are anorectic, have abdominal distension, and have decreased fecal production.
- Published
- 2003
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12. Evaluation of a vessel-sealing device for use in laparoscopic ovariectomy in mares
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Peter C. Rakestraw, Tex S. Taylor, and Reese Hand
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medicine.medical_specialty ,Ovariectomy ,medicine.medical_treatment ,Electrocoagulation ,medicine ,Animals ,Horses ,Prospective Studies ,High current ,Prospective cohort study ,Ligature ,General Veterinary ,business.industry ,Major Operative ,Vessel sealing ,Equipment Design ,Surgical Instruments ,Hemostasis, Surgical ,Surgery ,Dissection ,medicine.anatomical_structure ,Hemostasis ,Abdomen ,Female ,Laparoscopy ,business - Abstract
Objective— To evaluate a vessel-sealing instrument (LigaSure™) as a method for hemostasis of the ovarian vasculature. Study design— Prospective study. Animals or sample population— Thirteen mares (8 experimental, 5 patients), aged 2 to 20 years and weighing 405 to 500 kg. Methods— Thirteen mares had standing bilateral laparoscopic ovariectomy using a vessel-sealing device (LigaSure) to provide hemostasis. Eight reproductively normal experimental mares were divided into 2 groups: 1 group was re-examined laparoscopically 72 hours and the other group 10 days after the initial standing laparoscopic ovariectomy. The vessel-sealing device uses high current and low voltage, along with pressure, to reorganize the collagen into a translucent seal to achieve hemostasis of the ovarian vasculature. Results— No major operative or postoperative complications were encountered. Complete hemostasis of the ovarian pedicle was accomplished. One mare had a fever for 24 hours' postoperatively; this responded to a single dose of flunixin meglumine. Conclusions— The LigaSure appears to be a safe method for hemostasis of the ovarian vasculature. Clinical relevance— Benefits of the LigaSure include no foreign material remaining in the abdomen and minimal to no need for surgical dissection before application. The LigaSure eliminates complications with potential ligature slippage and bleeding during dissection.
- Published
- 2002
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13. Pharmacokinetics of sulfamethoxazole and trimethoprim in donkeys, mules, and horses
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Katrina L. Mealey, Tex S. Taylor, Kenneth E. Peck, and Nora S. Matthews
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Male ,Veterinary medicine ,General Veterinary ,biology ,business.industry ,Sulfamethoxazole ,Equidae ,General Medicine ,Trimethoprim ,Anti-Infective Agents ,Pharmacokinetics ,Area Under Curve ,biology.animal ,Trimethoprim, Sulfamethoxazole Drug Combination ,Trimethoprim-Sulfamethoxazole Combination ,Area under curve ,medicine ,Animals ,Female ,Horses ,business ,medicine.drug - Abstract
Objective—To compare serum disposition of sulfamethoxazole and trimethoprim after IV administration to donkeys, mules, and horses. Animals—5 donkeys, 5 mules, and 3 horses. Procedure—Blood samples were collected before (time 0) and 5, 15, 30, and 45 minutes and 1, 1.25, 1.5, 1.75, 2, 2.5, 3, 3.5, 4, 4.5, 5, 6, 8, 10, and 24 hours after IV administration of sulfamethoxazole (12.5 mg/kg) and trimethoprim (2.5 mg/kg). Serum was analyzed in triplicate with high-performance liquid chromatography for determination of sulfamethoxazole and trimethoprim concentrations. Serum concentration-time curve for each animal was analyzed separately to estimate noncompartmental pharmacokinetic variables. Results—Clearance of trimethoprim and sulfamethoxazole in donkeys was significantly faster than in mules or horses. In donkeys, mean residence time (MRT) of sulfamethoxazole (2.5 hours) was less than half the MRT in mules (6.2 hours); MRT of trimethoprim in donkeys (0.8 hours) was half that in horses (1.5 hours). Volume of distribution at steady state (Vdss) for sulfamethoxazole did not differ, but Vdss of trimethoprim was significantly greater in horses than mules or donkeys. Area under the curve for sulfamethoxazole and trimethoprim was higher in mules than in horses or donkeys. Conclusions and Clinical Relevance—Dosing intervals for IV administration of trimethoprim-sulfamethoxazole in horses may not be appropriate for use in donkeys or mules. Donkeys eliminate the drugs rapidly, compared with horses. Ratios of trimethoprim and sulfamethoxazole optimum for antibacterial activity are maintained for only a short duration in horses, donkeys, and mules. (Am J Vet Res 2002;63:349–353)
- Published
- 2002
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14. Physiological responses of donkeys to treadmill exercise and conditioning: a pilot study
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Tex S. Taylor, R. E. Welfare, Gary D. Potter, John D. Williams, Erica L. Foster, S. W. Erickson, and Nora S. Matthews
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Veterinary medicine ,Respiratory rate ,Triglyceride ,business.industry ,Horse ,Treadmill exercise ,General Medicine ,Physiological responses ,chemistry.chemical_compound ,chemistry ,Anesthesia ,Heart rate ,Medicine ,Conditioning ,Treadmill ,business - Abstract
Summary Five healthy standard donkeys were subjected to exercise tests on a treadmill before and after conditioning. After the pre-conditioning trial, the donkeys worked 3 days/week for 60 min pulling a cart at increasing trot duration and 2 days/week for 20 min in a round pen for the 28 day conditioning period. During the trial, donkeys worked at 1.5–2 m/s on an 11% grade for a distance of 1830 m. Heart rate, respiratory rate and body temperature were recorded before, 10 min into exercise, immediately following and 1, 5, 10, 20, 30, and 60 min after exercise. Arterial samples for blood gas measurements and venous samples for measurement of lactate [La−], glucose and triglyceride concentrations also were collected. Mean blood [La−] in unconditioned donkeys increased from 1.25 mmol/l at rest to 3.48 mmol/l at 1 min after exercise. Conditioning resulted in decreased heart rate and lactate and blood glucose concentrations during recovery. There were no effects of exercise or conditioning on triglyceride concentrations or blood gas values.
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- 2010
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15. Treatment of grade 3 rectal tears in horses by direct suturing per rectum
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Brent A. Hague, T. G. Eastman, R. N. Hooper, and Tex S. Taylor
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medicine.medical_specialty ,medicine.anatomical_structure ,Rectal tears ,Equine ,business.industry ,General surgery ,Medicine ,Rectum ,business ,Surgery - Published
- 2010
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16. Mammoth asses—selected behavioural considerations for the veterinarian
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Nora S. Matthews and Tex S. Taylor
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medicine.medical_specialty ,Food Animals ,Family medicine ,medicine ,Animal Science and Zoology ,Biology ,biology.organism_classification ,Herd health ,Archaeology ,Mammoth - Abstract
Observations of the behaviour of domestic mammoth and standard asses (donkeys) receiving routine herd health and therapeutic procedures are described. These procedures include capture, physical examination, restraint, medicating, adapting to hospitalization and training for interspecies breeding.
- Published
- 1998
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17. Physiologic responses during an exhaustive driving test in donkeys: effect of conditioning
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Nora S. Matthews, Gary D. Potter, and Tex S. Taylor
- Subjects
Cart ,medicine.medical_specialty ,Respiratory rate ,business.industry ,Rectal temperature ,Body weight ,Surgery ,Animal science ,Food Animals ,Heart rate ,medicine ,Conditioning ,Animal Science and Zoology ,Donkey ,business ,Time to exhaustion - Abstract
Improvement in performance following a 1-month conditioning period was tested in five donkeys. The two females and three geldings weighed 235 kg (SD, 54) and were 4 to 8 years old. The donkeys had previously been trained to pull a cart and were accustomed to wearing heart rate monitors. Following resting readings of heart rate (HR), respiratory rate (RR), rectal temperature (T), and venous lactate samples, the donkeys were driven to the cart with a draft load equal to 21% body weight, at a trot, until exhausted (defined as when they would not continue trotting). Time to exhaustion, distance and speed were measured. HR was recorded at 5-min intervals during the test and at 1, 5, 10, 20, 30 and 60 min after the test ended. T, RR and lactate were measured at 30-min intervals during the test and at 1, 5, 10, 20, 30 and 60 min post-test. The donkeys were then conditioned for 1 month by being driven 3×/week for 90 min, with a draft load equal to 15% body weight, and weekly increases in trotting time. Donkeys were then re-tested as before conditioning. Resting HR decreased significantly post-conditioning. Working HR values were lower and post-exercise HR decreased to resting rate post-conditioning. Lactate increased 3-fold pre-conditioning, but only by 50% post-conditioning. Average distance covered post-conditioning was increased by 67% (from 12.7 to 21.2 km), while time to exhaustion increased by 86% (from 84 to 155 min). Donkeys worked under conditions of high ambient temperate and humidity: temperatures ranged from 29 to 34°C while humidity ranged from 43 to 65%. Conditioning significantly increased the donkeys apparent productivity (as measured by distance covered).
- Published
- 1998
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18. Anaesthesia of donkeys and mules
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Nora S. Matthews, Sandee M. Hartsfield, and Tex S. Taylor
- Subjects
Intoxicative inhalant ,Anaesthetic management ,Equine ,business.industry ,Anesthesia ,Medicine ,Donkey ,business - Abstract
Summary Great variabilities in the sizes and types of donkeys and mules affects the choice of drugs and anaesthetic management of these equids. Most of the difference between donkeys, mules and horses is apparent when using injectable anaesthetic regimens, since these drugs are distributed and metabolised at rates different from the horse. With inhalant anaesthesia few differences are seen between equids. However, it is helpful for the clinician to recognise behavioural differences between donkeys, mules and horses which impact on anaesthetic management.
- Published
- 1997
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19. RADIOGRAPHIC APPEARANCE OF THE FEET OF MAMMOTH DONKEYS AND THE FINDING OF SUBCLINICAL LAMINITIS
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Margaret R. Slater, Tex S. Taylor, David M. Hood, Vicki A. Weir, Michael Walker, and Jonelle Elslander
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animal structures ,General Veterinary ,biology ,business.industry ,Hoof ,Radiography ,Anatomy ,Laminitis ,Phalanx ,biology.organism_classification ,body regions ,Pedal osteitis ,Medicine ,Donkey ,business ,Mammoth ,Subclinical infection - Abstract
All feet of 10 clinically sound mammoth donkeys (Group I) were radiographed to determine the appearance of the distal phalanx. The distal phalanges had blunted to concave-shaped dorsal solar margins which varied in appearance from slight to pronounced. The distal phalanges of the forefeet were wider than those of the hindfeet, and also were positioned a greater distance from the dorsal aspect of the hoof wall. The greater distance between the dorsal aspect of the hoof wall and the distal phalanges seemed related to the presence of a periosteal-like bony proliferation on the dorsum of the distal phalanx. This bony proliferation occurred in those distal phalanges which also had radiographic findings consistent with pedal osteitis. Next, all feet of 5 additional mammoth donkeys (Group 11) that were to be necropsied for various reasons, were examined similarly to Group I, necropsied and found to have laminitis. Only 2 of these 5 donkeys had been lame; only one had rotation of the distal phalanges (in the forefeet). Radiographic data from the 4 donkeys without rotation seemed most similar to that found in those Group I donkeys which had periosteal reactions on their distal phalanges. Conclusions from this study were that: 1) feet of mammoth donkeys have some anatomic differences from those of domestic horses, 2) subclinical laminitis and pedal osteitis can occur in mammoth donkeys, 3) rotation of the distal phalanx occurs in some, but not all laminitic donkeys, 4) laminitic changes may be more pronounced in their fore than in their hindfeet, and 5) additional studies of donkeys need to be done, examining both proven normal and confirmed laminitic feet. Veterinary Radiology & Uttrasound, Vol.
- Published
- 1995
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20. Evaluation of a laryngotomy approach for near-total resection of the nasal septum in the horse
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Ricardo J, Loinaz, Christopher P, Boutros, Peter C, Rakestraw, and Tex S, Taylor
- Subjects
Treatment Outcome ,Nasal Surgical Procedures ,Animals ,Horses ,Nasal Cavity ,Bone Wires ,Nasal Septum - Abstract
To report a laryngotomy approach for the removal of the nasal septum in adult horses.Descriptive study.Horses (n = 10).Near-total resection of the nasal septum was made using a modification of a previously reported 3-wire technique using a trephination approach and a 2-wire technique using a laryngotomy approach. Surgical time, ease of technique, complications, and outcome were recorded. At 45 days, horses were euthanatized and septal measurements made.Near-total resection of the nasal septum was accomplished with both techniques without complications. Incisional complications occurred in the trephination group and transient granulation tissue formation near the rostral stump occurred in the laryngotomy group. The laryngotomy technique was technically easier and resulted in a more cosmetic outcome.A laryngotomy approach is safe and expedient for near-total resection of the nasal septum with minimal complications.
- Published
- 2012
21. Pharmacokinetics of gentamicin in Mammoth asses
- Author
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K. L. Mealey, S. M. Miller, Gordon W. Brumbaugh, Tex S. Taylor, and Nora S. Matthews
- Subjects
Pharmacology ,General Veterinary ,biology ,business.industry ,Equidae ,biology.organism_classification ,Models, Biological ,Pharmacokinetics ,Anesthesia ,Injections, Intravenous ,medicine ,Animals ,Female ,Gentamicin ,Gentamicins ,business ,medicine.drug ,Mammoth - Published
- 1994
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22. The relationship of daily sperm production with number of Sertoli cells and testicular size in adult horses: role of primitive spermatogonia
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Terry L. Blanchard, G.K. Carter, Tex S. Taylor, Dickson D. Varner, M. S. Rembert, and Larry Johnson
- Subjects
Male ,endocrine system ,Embryology ,Cell type ,Cell Count ,Semen ,Stereology ,Biology ,Testicle ,Andrology ,Endocrinology ,Testis ,medicine ,Animals ,Horses ,Spermatogenesis ,reproductive and urinary physiology ,Sertoli Cells ,urogenital system ,Obstetrics and Gynecology ,Organ Size ,Cell Biology ,Sertoli cell ,Spermatogonia ,medicine.anatomical_structure ,Reproductive Medicine ,Spermatocytogenesis ,Germ cell - Abstract
correlations between the number of Sertoli cells and the number of germ cells observed as early as type B2 spermatogonia in the horse. However, the stage within spermatocytogenesis at which these relationships first occur is unclear. The relationships between the number of Sertoli cells and parenchymal weight and the number of germ cells during the mitosis of spermatogenesis were determined in 184 adult horses to identify the developmental stage (that is, the earliest germ cell) at which significant relationships are established. The total numbers of all types of A spermatogonia and of specific subtypes (A1, A2, A3, B1 or B2) of spermatogonia were correlated with the number of Sertoli cells and with parenchymal weight. The number of each cell type was calculated using stereology. The number of Sertoli cells was correlated (P < 0.01) with parenchymal weight (r = 0.85) and with daily sperm production (r = 0.83), and parenchymal weight was correlated (P < 0.01) with daily sperm production (r = 0.89). The number of Sertoli cells was correlated (P < 0.01) with the number of type A (r = 0.81) and A1 (r = 0.74) spermatogonia. Parenchymal weight was correlated with the number of type A (r = 0.80) spermatogonia and with the number of A1 (r = 0.67) spermatogonia. These data are consistent with the hypotheses that the number of Sertoli cells is important in determining testicular size and daily sperm production and that the relationship of daily sperm production to the number of Sertoli cells or to parenchymal weight has already been established at the level of primitive spermatogonia.
- Published
- 1994
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23. Use of an Ecraseur for Ovariohysterectomy in Mares
- Author
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R. Neil Hooper, Eddy Behrens, Dickson D. Varner, and Tex S. Taylor
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endocrine system ,medicine.medical_specialty ,Ovariectomy ,animal diseases ,medicine.medical_treatment ,Vaginal Diseases ,Uterus ,Hemorrhage ,Hysterectomy ,Ovarian artery ,Palpation ,Postoperative Complications ,Hematoma ,Estrus ,medicine.artery ,medicine ,Animals ,Vaginal bleeding ,Horses ,Ovarian Diseases ,Intraoperative Complications ,reproductive and urinary physiology ,Gynecology ,General Veterinary ,medicine.diagnostic_test ,urogenital system ,business.industry ,Suspensory ligament ,medicine.disease ,Intraoperative Hemorrhage ,Surgery ,surgical procedures, operative ,medicine.anatomical_structure ,Female ,medicine.symptom ,business - Abstract
Ovariohysterectomy was performed in 20 mares at three stages of estrus. An ecraseur was used to severe the ovarian branch of the ovarian artery and vein and the ovarian suspensory ligament en masse. All other vessels supplying the ovaries and uterus were doubly ligated and transected. All mares survived. Complications were intraoperative hemorrhage in three mares, postoperative vaginal bleeding in two mares, and a hematoma in the remnant of the broad ligament in one mare. No adhesions between the uterine stump or remnants of the broad ligament and abdominal structures were detected by palpation per rectum.
- Published
- 1992
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24. Disseminated Intravascular Coagulation Associated with Colic in 23 Horses (1984-1989)
- Author
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G. K. Carter, Tex S. Taylor, Noah D. Cohen, Robert D. Welch, and Jeffrey P. Watkins
- Subjects
medicine.medical_specialty ,Colic ,Antithrombin III ,Anastomosis ,Gastroenterology ,Fibrin ,Fibrin Fibrinogen Degradation Products ,Internal medicine ,medicine ,Coagulopathy ,Animals ,Horses ,Retrospective Studies ,Whole blood ,Disseminated intravascular coagulation ,Duodenitis ,General Veterinary ,biology ,medicine.diagnostic_test ,Platelet Count ,business.industry ,Anastomosis, Surgical ,Horse ,Jejunal Diseases ,Heparin ,Disseminated Intravascular Coagulation ,Colitis ,medicine.disease ,Thrombocytopenia ,Enteritis ,Surgery ,Intestines ,Prothrombin Time ,biology.protein ,Horse Diseases ,Partial Thromboplastin Time ,Gastrointestinal Hemorrhage ,business ,Intestinal Obstruction ,medicine.drug ,Partial thromboplastin time - Abstract
Disseminated intravascular coagulation (DIC) secondary to colic was diagnosed in 23 horses. Each horse was categorized retrospectively as to the cause of the colic based on surgical and/or necropsy findings: group 1 consisted of 14 horses with compromised intestine that required resection and anastomosis; group 2 consisted of 3 horses with nonstrangulating intestinal displacement and/or impactions; and group 3 consisted of 6 horses with colic associated with enteritis and/or colitis. Horses were considered to be affected with DIC if at least three of five hemostatic parameters were significantly abnormal: decreased antithrombin III (AT III) values, increased level of fibrin degradation products (FDP), thrombocytopenia, prolonged activated partial thromboplastin time, and prolonged prothrombin time. The most consistent hemostatic abnormalities were decreased AT III activity, increased FDP titers, and thrombocytopenia. Clotting times were more variable and did not always correlate with the presence of excessive hemorrhage. Excessive hemorrhage was present during surgery in seven horses and occurred within 1 to 12 hours after surgery in nine other horses. In addition to treatment of the primary disease, 19 horses received treatment for DIC consisting of heparin and/or plasma or fresh whole blood transfusions. Heparin alone was used in 12 horses. Heparin, in addition to fresh whole blood transfusions or fresh plasma, was administered to four horses. Three horses were treated with plasma alone. Four other horses were not treated specifically for the DIC. Eight horses (34%) survived the acute coagulopathy. Although a greater proportion of the surviving horses received heparin therapy (87.5%; 7/8) than did those that died (60%; 9/15), the difference was not statistically significant (P = 0.345).(ABSTRACT TRUNCATED AT 250 WORDS)
- Published
- 1992
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25. Pharmacokinetics of R(-) and S(+) carprofen after administration of racemic carprofen in donkeys and horses
- Author
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Melissa L Burchfield, Nora S. Matthews, Brad S. Bennett, Kenneth E. Peck, Tex S. Taylor, and Katrina L. Mealey
- Subjects
Time Factors ,General Veterinary ,business.industry ,Anti-Inflammatory Agents, Non-Steroidal ,Carbazoles ,Horse ,General Medicine ,Equidae ,Pharmacology ,Bolus (medicine) ,Pharmacokinetics ,Isomerism ,Area Under Curve ,Plasma concentration ,Medicine ,Animals ,Time curve ,Donkey ,Carprofen ,Horses ,Enantiomer ,business ,Chromatography, High Pressure Liquid ,medicine.drug - Abstract
Objective—To compare plasma disposition of the R(–) and S(+) enantiomers of carprofen after IV administration of a bolus dose to donkeys and horses. Animals—5 clinically normal donkeys and 3 clinically normal horses. Procedure—Blood samples were collected from all animals at time 0 (before) and at 10, 15, 20, 30, and 45 minutes and 1, 1.5, 2, 2.5, 3, 4, 5, 6, 8, 10, 24, 28, 32, and 48 hours after IV administration of a bolus of carprofen (0.7 mg/kg). Plasma was analyzed in triplicate via high-performance liquid chromatography to determine the concentrations of the carprofen enantiomers. A plasma concentration-time curve for each donkey and horse was analyzed separately to estimate noncompartmental pharmacokinetic variables. Results—In donkeys and horses, the area under the plasma concentration versus time curve (AUC) was greater for the R(–) carprofen enantiomer than it was for the S(+) carprofen enantiomer. For the R(–) carprofen enantiomer, the AUC and mean residence time (MRT) were significantly less and total body clearance (ClT) was significantly greater in horses, compared with donkeys. For the S(+) carprofen enantiomer, AUC and MRT were significantly less and ClT and apparent volume of distribution at steady state were significantly greater in horses, compared with donkeys. Conclusions and Clinical Relevance—Results have suggested that the dosing intervals for carprofen that are used in horses may not be appropriate for use in donkeys. (Am J Vet Res 2004;65:1479–1482)
- Published
- 2004
26. Pharmacokinetics of ketamine in mules and mammoth asses premedicated with xylazine
- Author
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Nora S. Matthews, W. L. Hayton, Tex S. Taylor, D. H. Jones, and Sandee M. Hartsfield
- Subjects
Xylazine ,medicine.medical_specialty ,Time Factors ,Pharmacokinetics ,biology.animal ,medicine ,Animals ,Ketamine ,Anesthetics ,Mammoth ,Anesthetics, Dissociative ,Dose-Response Relationship, Drug ,biology ,business.industry ,Equidae ,General Medicine ,biology.organism_classification ,Surgery ,Anesthesia ,Injections, Intravenous ,business ,Half-Life ,medicine.drug - Published
- 1994
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27. Lungworms in donkeys: Evaluation of Anthelmintics Under Field Conditions
- Author
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Tex S. Taylor and Thomas M. Craig
- Subjects
Veterinary medicine ,Equine ,business.industry ,Animal science ,Ivermectin ,medicine ,Herd ,Fenbendazole ,Dictyocaulus arnfieldi ,business ,Lungworm ,Feces ,medicine.drug ,Field conditions - Abstract
Summary In a herd of large donkeys, 30 (86%) were lungworm positive by the Baermann fecal technique. Eleven donkeys treated with fenbendazole (50 mg/kg) and 11 donkeys treated with thiabendazole were still lungworm positive 2-weeks posttreatment (PT). Subsequent treatment of 21 donkeys with ivermectin resulted in negative lungworm evaluations 2-weeks PT. At 20 weeks PT, all 8 donkeys evaluated were negative, while 7 of 12 donkeys evaluated were lungworm negative at 35-40 weeks PT. Five donkeys, given oral ivermectin paste at 6-8 month intervals after the 20-week evaluation were lungworm negative 4-5 years later.
- Published
- 1993
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28. Pharmacokinetics of phenylbutazone and its metabolite oxyphenbutazone in miniature donkeys
- Author
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Tex S. Taylor, Nora S. Matthews, Katrina L. Mealey, and Kenneth E. Peck
- Subjects
Male ,General Veterinary ,Chemistry ,Metabolite ,Anti-Inflammatory Agents, Non-Steroidal ,Oxyphenbutazone ,Total body ,General Medicine ,Equidae ,Pharmacology ,Body weight ,chemistry.chemical_compound ,Animal science ,Pharmacokinetics ,Phenylbutazone ,Area Under Curve ,medicine ,Animals ,Donkey ,medicine.drug - Abstract
Objective—To describe the pharmacokinetics of phenylbutazone and oxyphenbutazone after IV administration in miniature donkeys. Animals—6 clinically normal miniature donkeys. Procedure—Blood samples were collected before and 5, 10, 20, 30, 45, 60, 90, 120, 180, 240, 300, 360, and 480 minutes after IV administration of phenylbutazone (4.4 mg/kg of body weight). Serum was analyzed in triplicate by use of high-performance liquid chromatography for determination of phenylbutazone and oxyphenbutazone concentrations. The serum concentration-time curve for each donkey was analyzed separately to estimate model-independent pharmacokinetic variables. Results—Serum concentrations decreased rapidly after IV administration of phenylbutazone, and they reached undetectable concentrations within 4 hours. Values for mean residence time ranged from 0.5 to 3.0 hours (median, 1.1 hour), whereas total body clearance ranged from 4.2 to 7.5 ml/kg/ min (mean, 5.8 ml/kg/ min). Oxyphenbutazone appeared rapidly in the serum; time to peak concentration ranged from 13 to 41 minutes (mean, 26.4 minutes), and peak concentration in serum ranged from 2.8 to 4.0 mg/ml (mean, 3.5 μg/ml). Conclusion and Clinical Relevance—Clearance of phenylbutazone in miniature donkeys after injection of a single dose (4.4 mg/kg, IV) is rapid. Compared with horses, miniature donkeys may require more frequent administration of phenylbutazone to achieve therapeutic efficacy. (Am J Vet Res 2001;62:673–675)
- Published
- 2001
29. Techniques for evaluating selected reproductive disorders of stallions
- Author
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C.C. Love, Steven P. Brinsko, Tex S. Taylor, Terry L. Blanchard, Larry Johnson, and Dickson D. Varner
- Subjects
Infertility ,Male ,medicine.medical_specialty ,Physiology ,Semen ,Male infertility ,Endocrinology ,Food Animals ,Testicular Neoplasms ,Biopsy ,medicine ,Animals ,Horses ,Infertility, Male ,Ultrasonography ,Azoospermia ,Gynecology ,medicine.diagnostic_test ,business.industry ,Hemospermia ,General Medicine ,medicine.disease ,Sperm ,Urethra ,medicine.anatomical_structure ,Animal Science and Zoology ,Horse Diseases ,business - Abstract
Numerous techniques may be used for evaluation of the different reproductive disorders of the stallion. Approaches may vary from real-time ultrasonography and biopsy for evaluating testicular tumors to use of special assays for evaluating sperm or plasma for presence of antisperm antibodies. This communication addresses techniques used to evaluate five relatively uncommon, but perplexing, disorders of breeding stallions: (1) seminal vesiculitis, (2) hemospermia associated with idiopathic urethral defects, (3) acrosomal dysfunction, (4) abnormal spermatozoal chromatin, and (5) azoospermia.
- Published
- 2000
30. A comparison of three combinations of injectable anesthetics in miniature donkeys
- Author
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Nora S. Matthews, Jennifer A Sullivan, and Tex S. Taylor
- Subjects
Random order ,Blood pressure ,Muscle relaxation ,General Veterinary ,business.industry ,Anesthesia ,Arterial blood ,Medicine ,Respiratory system ,business ,Miniature donkey ,Short duration ,Hemoglobin Saturation - Abstract
Objective To compare three combinations of injectable anesthetics in miniature donkeys for quality of induction, recovery, muscle relaxation, cardiopulmonary changes during anesthesia and duration of recumbency. Design Prospective, randomized experimental study. Animals Six miniature donkeys ( Materials and methods The drug combinations were: xylazine−butorphanol−ketamine (XBK), xylazine−butorphanol−tiletamine−zolazepam (XBT) and xylazine−propofol (XP). Each miniature donkey was anesthetized with each combination at 1–week intervals in random order. Heart and respiratory rates, indirect blood pressure and temperature were measured before and at 5–minute intervals during recumbency. Arterial blood samples were drawn for blood–gas analysis before and at 5, 15 and 30 minutes of anesthesia when samples could be collected. Recumbency time to sternal and time to standing were recorded and a subjective evaluation of induction, muscle relaxation and recovery were made. Results Mean recumbency time ± SD was 14.7 ± 9.4, 33.8 ± 6.3 and 14.6 ± 1.9 minutes with XBK, XBT and XP, respectively. Mean time to standing ± SD was 28.4 ± 11.3, 43.7 ± 7.2 and 26.3 ± 2.9 minutes with XBK, XBT and XP, respectively. Heart and respiratory rates and blood pressures varied from baseline but were always within normal ranges. Hemoglobin saturation, pH and PaO 2 tended to be lower with these doses of XBT and XP. Conclusions and clinical relevance Overall quality of anesthesia was poor with XBK. At the doses used this combination did not provide sufficient anesthesia compared with the combinations of XBT and XP, which appeared to provide acceptable anesthesia of short duration in miniature donkeys.
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- 2000
31. Paranasal sinus surgery through a frontonasal flap in sedated, standing horses
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David J. Murphy, Brent A. Hague, David M. Dutton, James Schumacher, and Tex S. Taylor
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Male ,Xylazine ,medicine.medical_specialty ,Posture ,Hematoma ,Frontal Sinusitis ,otorhinolaryngologic diseases ,medicine ,Animals ,Hypnotics and Sedatives ,Nasal Bone ,Horses ,Anesthetics, Local ,Osteoma ,Sinus (anatomy) ,Nose ,Postoperative Care ,General Veterinary ,business.industry ,Imidazoles ,Lidocaine ,Anatomy ,medicine.disease ,Nasal bone ,Surgery ,Analgesics, Opioid ,medicine.anatomical_structure ,Frontal bone ,Paranasal sinuses ,Treatment Outcome ,Butorphanol ,Frontal Bone ,Mepivacaine ,Female ,Horse Diseases ,Analgesia ,business ,Anesthesia, Local - Abstract
Objective— To report experience with paranasal sinus surgery through a frontonasal flap in sedated, standing horses. Study Design— Treatment of 10 horses with naturally occurring paranasal sinus disease through a frontonasal bone flap created with the horses standing. Animals Ten adult horses. Methods— After restraint and sedation, local anesthetic was injected subcutaneously along the proposed incision line over the conchofrontal sinus and was instilled into the sinuses through a small hole created in the frontal bone. A 3-sided, rectangular, cutaneous incision that extended through the periosteum was created over the frontal and nasal bones. The incision was extended into the conchofrontal sinus using a bone saw, and the base of the flap, on the midline of the face, was fractured. The sinuses were explored, and the horse was treated for the disease encountered. The flap was repositioned; subcutaneous tissue and skin were sutured separately. Results— The horses had few signs of discomfort during creation of the bone flap and during disease treatment. Diseases encountered included inspissated exudate in the ventral conchal sinus (five horses), feed and exudate throughout the sinuses (one horse), occlusion of the nasomaxillary aperature (one horse), polyp (one horse), osteoma (one horse), and progressive ethmoidal hematoma (one horse). Conclusion In selected cases, surgery of the paranasal sinuses can be performed safely on sedated and standing horses through a frontonasal bone flap. Clinical Relevance— Performing surgery through a frontonasal bone flap with the horse standing and sedated, rather than anesthetized, eliminates risks and expense of general anesthesia.
- Published
- 2000
32. SEQUESTRUM FORMATION AND OSTEOMYELITIS IN A BULL
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R. Neil Hooper, Michael Walker, and Tex S. Taylor
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medicine.medical_specialty ,General Veterinary ,business.industry ,Soft tissue swelling ,Radiography ,Osteomyelitis ,Soft tissue ,Anatomy ,Pelvic limb ,medicine.disease ,Sequestrum ,Surgery ,medicine ,Tibia ,business ,Abscess - Abstract
A four-year-old Hereford bull was admitted to The Texas Veterinary Medical Center for evaluation of a left pelvic limb injury. In initial radiographs there was extensive soft tissue swelling but no significant osseous involvement. Additional radiographs made six weeks later identified a sequestrum on the cranial surface of the tibia and an area caudal to the tibia suggestive of an abscess. The sequestrum was removed surgically but did not communicate with the abscess in the adjacent soft tissue. Reports on bony sequestration in food animals are rare.
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- 1991
- Full Text
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33. Pharmacokinetics and cardiopulmonary effects of guaifenesin in donkeys
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K. L. Mealey, Kenneth E. Peck, Nora S. Matthews, Tex S. Taylor, and A.c. Ray
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Guaifenesin ,Male ,Respiratory rate ,Pharmacokinetics ,Species Specificity ,Computer software ,medicine ,Animals ,Horses ,Expectorants ,Pharmacology ,Volume of distribution ,General Veterinary ,business.industry ,Pulmonary Gas Exchange ,Respiration ,Hemodynamics ,Equidae ,Anesthesia ,Area Under Curve ,Injections, Intravenous ,Arterial blood ,Female ,business ,medicine.drug ,Clearance ,Half-Life - Abstract
Five donkeys and three horses were given guaifenesin, intravenously, by gravity administration, until recumbency was produced. The time and dose required to produce recumbency, recovery time to sternal and standing were recorded. Blood samples were collected for guaifenesin assay at 10, 20, 30, 40, 50, 60 min, and 2, 3, 4 and 6 h after guaifenesin administration. Serum was analysed for guaifenesin using HPLC and pharmacokinetic values were calculated using a computer software package (RSTRIP). In donkeys, heart and respiratory rates and blood pressures were recorded before and at 5-min intervals during recumbency. Arterial blood samples were collected before and at 5 and 15 min intervals during recumbency for analysis of pH, CO2, and O2. ANOVA was used to evaluate dynamic data, while t-tests were used for kinetic values. Respiratory rate was decreased significantly during recumbency, but no other significant changes from baseline occurred. The mean (+/- SD) recumbency dose of guaifenesin was 131 mg/kg (27) for donkeys and 211 mg/kg (8) for horses. Recovery time to sternal (min) was 15 (SD, 11) for donkeys and 34 (SD, 1.4) for horses. Time to standing was 32 min for donkeys and 36 min for horses. Calculation of AUC (area under the concentration-time curve) microgram/mL) (dose-dependent variable) was 231 (SD, 33) for donkeys and 688 (SD, 110) for horses. The clearance (CL) (mL/h.kg) was 546 (SD, 73) for donkeys, which was significantly different from 313 (SD, 62) for horses. Mean residence time (MRT) (h) was 1.2 (SD, 0.1) for donkeys and 2.6 (SD, 0.5) for horses. Volume of distribution Vd(area) (mL/kg) was 678 (SD, 92) for donkeys and 794 (SD, 25) for horses. At the rate of administration used in this study, donkeys required less guaifenesin than horses to produce recumbency, but cleared it more rapidly.
- Published
- 1998
34. Pharmacokinetics of gentamicin in donkeys
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Tex S. Taylor, K. L. Mealey, R. E. Welfare, and Nora S. Matthews
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Pharmacology ,Male ,Blood Specimen Collection ,General Veterinary ,Dose-Response Relationship, Drug ,business.industry ,Fluorescence Polarization ,Equidae ,Reference Standards ,Models, Biological ,Anti-Bacterial Agents ,Pharmacokinetics ,Injections, Intravenous ,Medicine ,Animals ,Gentamicin ,Female ,Gentamicins ,business ,medicine.drug - Published
- 1996
35. Permanent tracheostomy in standing horses: technique and results
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M. K. Chaffin, Clifford M. Honnas, S R McClure, James Schumacher, Tex S. Taylor, and Anton G. Hoffman
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Male ,medicine.medical_specialty ,Posture ,Tracheal mucosa ,Tracheostomy ,Suture (anatomy) ,Cricoid cartilage ,medicine ,Animals ,Local anesthesia ,Horses ,Permanent tracheostomy ,General Veterinary ,business.industry ,Suture Techniques ,Anatomy ,respiratory system ,Airway obstruction ,medicine.disease ,Prognosis ,Surgery ,Airway Obstruction ,medicine.anatomical_structure ,Female ,Horse Diseases ,business ,Anesthesia, Local - Abstract
Permanent tracheal stomas were created in seven sedated, standing horses with severe upper airway obstruction. After local anesthesia, a 3-cm by 6-cm rectangle of skin was removed from the ventral surface of the neck, 3 cm distal to the cricoid cartilage. The sternothyrohyoideus muscles were clamped proximally and distally, then transected to expose the tracheal rings. The ventral third of four tracheal rings was dissected from the tracheal mucosa that was then incised in a double "Y." Two layers of suture were used to achieve mucocutaneous closure. Stomas healed without serious complications; two mares subsequently foaled, and three horses were used for riding.
- Published
- 1995
36. Lateral thoracotomy for management of recurrent or refractory thoracic abscesses associated with equine pleuropneumonia
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Tracy E. Norman, G.K. Carter, M. K. Chaffin, Carolyn E. Arnold, and Tex S. Taylor
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Florfenicol ,Pathology ,medicine.medical_specialty ,Cefotaxime ,Equine ,Tetracycline ,medicine.drug_class ,Antibiotics ,Biology ,medicine.disease ,Microbiology ,Penicillin ,Agar plate ,chemistry.chemical_compound ,chemistry ,medicine ,Pleuropneumonia ,Enrofloxacin ,medicine.drug - Abstract
isolated 3 strains with different colonies sizes on the blood agar plate, UBA8Ch (0.5mm), UBA8Md (2mm) andUBA8Gd (4 mm). Expression of capsule was observed by negative staining with India ink solution and with electron microscopywith fosfotungstic acid.Diskdiffusion testwereusedas recommended by Clinical and Laboratory Standards Institute (CLSI). The antibiotic tested were: erithromycin (ERY), penicillin (PEN), ciprofloxacine (CIP), enrofloxacin (ENR), tetracycline (TET) trimethoprim-sulfamethoxazole (TMS), cefotaxime (CTX) and florfenicol (FFC). Results were categorized by using the guidelines recommended by the CLSI 2008, 2010 [3]. The capsule was observed in the 3 strains with optical microscope and with electron microscope. The strains expressed different levels of capsule, UBA8Ch: small sized, UBA8Md:medium sized andUBA8Gd: high sized. The UBA8Ch and UBA8Gd strains were susceptible for all the antimicrobials tested. The UBA8Md strain was intermedia susceptibility for ERY, ENR and TMS. The immune status of the host and the guttural pouch environment could influence in the phenotypic characteristics variation of the strains. Itwas isolated three strains froma same sample that expressed different levels of capsule, different colonies sizes on the blood agar plate and antibiotic sensibility. This suggests the presence of different clones of See in carriers.
- Published
- 2012
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37. Klinische Ergebnisse mit einem neuen Frequenzverdoppelten Doppelpuls Nd:YAG Laser (FREDDY) für die Lithotripsie bei komplizierter Choledocholithiasis
- Author
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HOCHBERGER, J., primary, BAYER, J., additional, MAISS, J., additional, TEX, S., additional, and HAHN, E.G., additional
- Published
- 2009
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38. KLINISCHE ERGEBNISSE MIT EINEM NEUEN FREQUENZVERDOPPELTEN DOPPELPULS ND:YAG LASER (FREDDY) FÜR DIE LITHOTRIPSIE KOMPLIZIERTER GALLENGANGSSTEINE AN 22 PATIENTEN
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Maiss, J., primary, Tex, S., additional, Bayer, J., additional, Hahn, E.G., additional, and Hochberger, J., additional
- Published
- 2009
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39. KLINISCHE ERGEBNISSE MIT EINEM NEUEN FREQUENZVERDOPPELTEN DOPPELPULS ND:YAG LASER (FREDDY) FÜR DIE LITHOTRIPSIE KOMPLIZIERTER GALLENGANGSTEINE AN 17 PATIENTEN
- Author
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Hochberger, J., primary, Maiss, J., additional, Tex, S., additional, Bayer, J., additional, and Hahn, E.G., additional
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- 2009
- Full Text
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40. A comparison of injectable anaesthetic regimens in mules
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J. D. Williams, Tex S. Taylor, Cindy L. Skrobarcek, and Nora S. Matthews
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Male ,Xylazine ,Butorphanol ,Muscle Relaxation ,Partial Pressure ,Respiratory chain ,Blood Pressure ,Heart Rate ,Catheterization, Peripheral ,medicine ,Animals ,Tiletamine ,business.industry ,Respiration ,Zolazepam ,General Medicine ,Equidae ,Carbon Dioxide ,Hydrogen-Ion Concentration ,Oxygen ,Muscle relaxation ,Blood pressure ,Anesthesia ,Injections, Intravenous ,Anesthesia, Intravenous ,Arterial blood ,Female ,Ketamine ,business ,Anesthetics, Intravenous ,medicine.drug - Abstract
Three combinations of injectable anaesthetic agents were compared in nine adult mules. The combinations were xylazine/ketamine (X/K), xylazine/butorphanol/ketamine (X/B/K), and xylazine/tiletamine-zolazepam (X/T). Measured variables were heart rate, respiratory rate, systolic blood pressure, arterial blood pH, PCO2 and PO2, recumbency time and number of attempts to stand. Quality of induction and recovery, muscle relaxation and response to stimulus were evaluated subjectively. Recumbency time was significantly (P < 0.05) longer with X/B/K and X/T than with X/K. Mules required significantly more attempts to stand under the influence of X/T than X/K or X/B/K. No statistically significant (P < 0.05) differences in heart rate, respiratory rate, blood pressure or arterial pH, PCO2 and PO2 were detected between groups.
- Published
- 1992
41. Surgical correction of strictures of the large colon in three horses
- Author
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Patricia L. Rose, James Schumacher, and Tex S. Taylor
- Subjects
Male ,medicine.medical_specialty ,General Veterinary ,Colic ,business.industry ,Colon ,Anastomosis, Surgical ,Constriction, Pathologic ,Surgical correction ,Pyloroplasty ,Surgery ,medicine ,Large Colon ,Animals ,Female ,Horse Diseases ,Horses ,business ,Left dorsal colon ,Intestinal Obstruction - Abstract
An extensive stricture of the left dorsal colon in a Thoroughbred colt was resected and the colon was anastomosed. In two horses, circumferential strictures at the pelvic flexure 2.5 to 3 cm long were corrected with a modified Heineke-Mikulicz pyloroplasty technique. The horses were reported to be doing well at 6, 8, and 45 months, respectively.
- Published
- 1991
42. Comparative pharmacokinetics of meloxicam in clinically normal horses and donkeys
- Author
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Sinclair, Melissa D., primary, Mealey, Katrina L., additional, Matthews, Nora S., additional, Peck, Ken E., additional, Taylor, Tex S., additional, and Bennett, Brad S., additional
- Published
- 2006
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43. Pharmacokinetics of R(–) and S(+) carprofen after administration of racemic carprofen in donkeys and horses
- Author
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Mealey, Katrina L., primary, Matthews, Nora S., additional, Peck, Kenneth E., additional, Burchfield, Melissa L., additional, Bennett, Brad S., additional, and Taylor, Tex S., additional
- Published
- 2004
- Full Text
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44. Spiral colon bypass in a geriatric Vietnamese potbellied pig
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Gallardo, Mark A., primary, Lawhorn, D. Bruce, additional, Taylor, Tex S., additional, and Walker, Michael A., additional
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- 2003
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45. Pharmacokinetics of sulfamethoxazole and trimethoprim in donkeys, mules, and horses
- Author
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Peck, Kenneth E., primary, Matthews, Nora S., additional, Taylor, Tex S., additional, and Mealey, Katrina L., additional
- Published
- 2002
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46. Pharmacokinetics of phenylbutazone and its metabolite oxyphenbutazone in miniature donkeys
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Matthews, Nora S., primary, Peck, Kenneth E., additional, Taylor, Tex S., additional, and Mealey, Katrina L., additional
- Published
- 2001
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47. FREQUENZVERDOPPELTER DOPPELPULS ND:YAG LASER (FREDDY) FÜR DIE GALLENSTEINLITHOTRIPSIE - PRÄKLINISCHE VERGLEICHSUNTERSUCHUNGEN MIT ETABLIERTEN LASERSYSTEMEN
- Author
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Tex, S., primary, Magdeburg, B., additional, Maiss, J., additional, Neizamy, E., additional, Köbnick, C., additional, Hahn, E.G., additional, and Hochberger, J., additional
- Published
- 2001
- Full Text
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48. ENDOSKOPISCHE IMPLANTATION VON ENTERYX IN DEN UNTEREN ÖSOPHAGUSSPINKTER ZUR BEHANDLUNG DER GASTROÖSOPHAGEALEN REFLUXKRANKHEIT
- Author
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Hochberger, J., primary, Tex, S., additional, Maiss, J., additional, Mühldorfer, S., additional, and Hahn, E.G., additional
- Published
- 2001
- Full Text
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49. Paranasal Sinus Surgery Through a Frontonasal Flap in Sedated, Standing Horses
- Author
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Schumacher, Jim, primary, Dutton, David M., additional, Murphy, David J., additional, Hague, Brent A., additional, and Taylor, Tex S., additional
- Published
- 2000
- Full Text
- View/download PDF
50. Pharmacokinetics of flunixin meglumine in donkeys, mules, and horses
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Coakley, Mariah, primary, Peck, Kenneth E., additional, Taylor, Tex S., additional, Matthews, Nora S., additional, and Mealey, Katrina L., additional
- Published
- 1999
- Full Text
- View/download PDF
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