116 results on '"Oberwittler C"'
Search Results
2. Ophthalmoneurology
- Author
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Kömpf, D., Fetter, M., Tweed, D., Koenig, E., Thier, P., Dichgans, J., Mergner, Th., Maurer, Ch., Becker, W., Fischer, D., Misslisch, H., Härtung, Hans-Peter, Toyka, Klaus V., Büttner, Th., Kuhn, W., Klotz, P., Steinberg, R., Langkafel, M., Przuntek, H., Wöbker, G., Cramer, S., Ferbert, A., Konstanzer, A., Ceballos-Baumann, A.-O., Kornhuber, M., Dressnandt, J., Conrad, B., Erbguth, F., Hilz, M.-J., Kilian, K.-D., Rechlin, Th., Claus, D., Neundörfer, B., Klostermann, W., Verleger, R., Heide, W., Wauschkuhn, B., Seyfert, T., Mierisch, C., Moser, A., Matzke, M., Heinze, H. J., Dorfmüller, G., Münte, T. F., Dietz, H., Masur, H., Papke, K., Oberwittler, C., Müller, M., Kessler, Ch., Wessel, K., Mehdorn, E., Baez, K. A., Hamann, G., Höh, H., Ruprecht, K. W., Schumacher, M., Schmidt, D., Wakhloo, A. K., Wittich, I., Klingelhöfer, J., Matzander, G., Lagrèze, H. L., Hartmann, A., Anzinger, G., Petrovici, J.-N., Niklaus, K., Schulz, J. B., Klockgether, T., Faiss, J., Rosengart, A., Kaplan, R. F., Hedges, T. R., Eisner, A. E., Caplan, L. R., Barry, J. C., Effert, R., Kaupp, A., Jerusalem, F., Nüssgens, Z., Roggenkämper, P., Wittkämper, A., Wilhelm, H., Schierer, U., Zrenner, E., Kölmel, Hans W., Schoepf, Dieter, Zangemeister, W. H., Collmann, H., Sörensen, N., Krauß, J., Sold, J., Mühling, J., and Schimrigk, K.
- Published
- 1992
- Full Text
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3. Ophthalmoneurology
- Author
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Papke, K., Masur, H., Oberwittler, C., Verleger, R., Wascher, E., Kömpf, D., Mielke, R., Kessler, J., Fink, G. R., Herholz, K., Heiss, W.-D., Moser, A., Olschinka, J., Seyer, H., Fahlbusch, R., Küchle, M., Awe, B., König, H.-J., Gerding, H., Schuierer, G., Brune, G. G., Trabert, W., Grundmann, M., Drescher, S., Heide, W., Fischer, D., Fetter, M., Tweed, D., Misslisch, H., Koenig, E., Lortz, Katja, Zangemeister, W. H., Moschner, C., Rüttinger, H., Krekel, Ch., Schimrigk, K., Herbst, H., Thier, P., Dichgans, J., Scharein, Sigrid, Hartard, Christiane, Kunze, Klaus, Sievers, C., Knappertz, V., Rothacher, G., Krämer, G., Klingelhöfer, J., Wittich, I., Sander, D., Conrad, B., v. Maravic, M., Kessler, Ch., Böhning, A., Speisberg, B., Carvajal-Lizano, M., Thie, A., Schmitt, T., Erbguth, F., Taghavy, A., Reichmann, H., Gold, R., Beck, A., Maas, J., Seibel, P., Naumann, M., Schubert, M., Zierz, S., Elek, J., Dengler, R., Breul, Petra, Zierz, Stephan, Jerusalem, Felix, Schneider, Ch., Lindner, A., Klopstock, Th., Toyka, K.-V., Hansen, H. C., Lueck, C. J., Kennard, C., Krieg, P., Jost, W., Richter, J., Loew, S., Mielke, U., Ruprecht, K. W., Remberger, K., and Schimrigk, K.
- Published
- 1992
- Full Text
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4. MR-tomographische und elektrophysiologische Befunde bei 10 Patienten mit Syringomyelie: Eine Verlaufsuntersuchung über 2 Jahre
- Author
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Masur, H., Oberwittler, C., Reuther, G., Brune, G. G., Steudel, W. I., editor, Lumenta, C. B., editor, and Klug, N., editor
- Published
- 1993
- Full Text
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5. Klinische und elektrophysiologische (SEP, MEP) Verlaufsuntersuchungen (3 Jahre) bei Patienten mit engem zervikalen Spinalkanal
- Author
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Masur, H., Oberwittler, C., Seifert, D., Brune, G. G., Steudel, W. I., editor, Lumenta, C. B., editor, and Klug, N., editor
- Published
- 1993
- Full Text
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6. Klinische Differentialdiagnostik der Myasthenia gravis
- Author
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Oberwittler, C.
- Published
- 1998
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7. Die X-chromosomal rezessive spinobulbäre Muskelatrophie (Typ Kennedy) Beschreibung einer Familie, Klinik, molekulare Genetik, Differentialdiagnose und Therapie: Beschreibung einer Familie, Klinik, molekulare Genetik, Differentialdiagnose und Therapie
- Author
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Kuhlenbäumer, G., Bocchicchio, M., Kreß, W., Young, P., Oberwittler, C., and Stögbauer, F.
- Published
- 1998
- Full Text
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8. Effect of l-dopa on visual evoked potentials and neuropsychological tests in adult phenylketonuria patients
- Author
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Ullrich, K., Weglage, J., Pietsch, M., Fünders, B., Oberwittler, C., von Eckardstein, H., and Colombo, J. P.
- Published
- 1996
- Full Text
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9. Fourth meeting of the European Neurological Society 25–29 June 1994 Barcelona, Spain: Abstracts of Symposia and free communications
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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. J., Kohncke, G., Castellli, E., Linssen, W., Stegeman, D., Binkhorst, R., Notermans, S., Jaspert, A., Fahsold, R., de Munain, A. Lopez, Cobo, A., Martorell, L., Poza, J. J., Navarrete Palau, D., Emparanza, J. I., Sanchez-Roy, R., Vilchez, J. J., Hernandez, M., Tena, J. Garcia, Perla, C., Koutroumanidis, M., Papathanasopoulos, P., Papadimitriou, A., Papapetropoulos, T. H., Divari, R., Hadjigeorgiou, G. M., Anastasopoulos, I., Sansone, V., Rotondo, G., Meola, G., Rigoletto, C., Messina, S., Szwabowska-Orzeszko, E., Jozwiak, S., Michalowicz, R., Szaplyko, W., Petrella, M. A., Della Marca, G., Masullo, G., Mennuni, G. F., Kompf, D., Wascher, E., Verleger, R., Kaido, M., Soga, F., Toyooka, H., Bayon, C., Rubio, J., Carlomagno, S., Parlato, V., Santoro, A., Lavarone, A., Bonavita, V., Pentore, R., Venneri, A., Pasquier, F., Lebert, F., Grymonprez, L., Lefebvre, C., Van der Linden, M., Derouesné, C., Renault, B., Lacomblez, L., Homeyer, P., Ouss, L., Neuman, E., Malbezin, M., Barrandon, S., Guez, D., Stevens, M., van Swieten, J. C., Franke, C. L., Sanchez, A., Castellvirel, S., Mila, M., Jimenez, D., Pallesta, F., Ruiz, P. J. Garcia, Barrio, A., Barroso, T., Benitez, J., de Yebenes, J. Garcia, Manubens, J. M., Martinez-Lage, J. M., Larumbe, R., Muruzabal, J., Lacruz, F., Quesada, Pedro, Gallego, J., Ferini-Strambi, L., Marcone, A., Garancini, P., Tedesi, B., Jacob, B., Rozewicz, L., Langdon, D., Davie, C., Ron, M., Thompson, A., Koepp, M. J., Hansen, M. L., Guldin, B., Pressler, R. M., Ried, S., Scholz, C., Monaco, F., Gianelli, M., Schiavalla, M. P., Naldi, P., Cantello, R., Torta, R., Verze, L., Mutani, R., Knott, H., Ferbert, A., Schulze-Bonhage, A., Aust, W., Di Mascio, R., Marchioli, R., Vitullo, F., Di Pasquale, A., Sciulli, L., Kramer, V., Tognoni, G., Santacruz, P., Lopez, R., Marti, M. J., Charques, I., Catafau, A., Lomeila, F., Peila, J., Bertran, I., Blesa, R., Krendel, D. A., Costiga, D. A., Koeppen, S., Korn, W. M., Brugge, S., Schmitz, D., Scheulen, M. E., King, R. H. M., Robertson, A. M., Thomas, P. K., Kerkhofs, A., Vermersch, P., Dereeper, O., Daems Monpeun, C., Parent, M., Deplanque, D., Petit, H., Campero, M., Serra, J., Ochoa, J. L., Martinez-Matos, J. A., Montero, J., Olivé, M., Rene, R., Vidaller, A., Gugenheim, M., Gouider, R., Le Guern, E., Brice, A., Agid, Y., Bouche, P., Grisold, W., Ziflo, U., Drlicek, M., Budka, H., Jellinger, K., Zielinski, C. H., Ginsberg, L., King, R. H. M., Workman, J., Platts, A. D., Thomas, P. K., Gherardi, R. K., Florea-Strat, A., Poron, F., Sabourin, J. -C., Fazio, R., Nemni, R., Franceschi, M., Lorenzetti, I., Rinaldi, L., Canal, N., Weilbach, F. X., Sennlaub, A., Jung, S., Gold, R., Toyka, K. V., Hartung, H. P., Giegerich, G., Ellie, E., Vital, A., Steck, A. J., Vital, C., Julien, J., Doneda, P., Pizzul, S., Scarpini, E., Chiodi, P., Ramacci, M. T., Livraghi, S., Maimone, D., Annunziata, P., Salvadori, C., Guazzi, G. C., Arne-Bes, M. C., Delisle, M. B., Fabre, N., Hurtevent, J. F., Bes, A., Baudoin-Martin, D., Laborde, E., Viallet, F., Creisson, C., Crespi, V., Bogliun, G., Marzorati, L., Zincone, A., D'Angelo, L., Liberani, A., Merlini, M., Rivolta, R., Creange, A., Sabourin, J. -C., Theodorou, I., Gherardi, R. K., Conti, A. M., Malosio, M. L., Baron, P. L., Scarlato, G., Chorao, R., Rosas, M. J., Leite, I., Callea, L., Donati, E., Bargnani, C., Bud, M., Verdu, E., Navarro, X., Braun, S., Einius, S., Poindron, P., Warier, J. M., Bradley, J., Bekkelund, S. I., Torbergsen, T., Mellgren, S. I., Carlomagno, S., Parlato, V., Santoro, A., Lavarone, A., Boller, F., Bonavita, V., Engelhardt, A., Lörler, H., Robeck, S., Kluglein, C., Comi, G., Avoledo, V., Locatelli, T., Leocani, L., Galardi, G., Magnani, G., Medaglini, S., Chkhikvishvili, T. S., Zangaladze, A., Bratoeva, M., Kovachev, P., Chavdarov, D., Artemis, N., Karacostas, D., Milonas, I., Arpa, J., Lopez-Pajares, R., Cruz-Matinez, A., Sarria, J., Palomo, F., Alonso, M., Rodriguez-Al-barino, A., Lacasa, T., Nos, J., Barreiro, P., Martinez, A. Cruz, Villoslada, C., Alons, M., Taghavy, A., Hamer, H., Kratzer, A., Dethy, S., Pauwels, T., Monclus, M., Luxen, A., Goldman, S., Ziegler, M., Crambes, O., Ragueneau, I., Arnaud, F., Zappia, M., Montesanti, R., Colao, R., Palmieri, A., Branca, D., Nicoletti, G., Rizzo, M., Parlato, G., Quattrone, A., Vanacore, N., Zuchegna, P., Bonifati, V., Meco, G., Scholz, J., Friedrich, H. -J., Rohl, A., Ulm, G., Vieregge, P., Savettieri, G., Rocca, W. 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M., Krauseneck P., Meyding-Lamadé, U., Krieger, D., Sartor, K., Hacke, W., Maugard-Louboutin, C., Fayet, G., Sagan, C., Martin, S., Ménégalli, D., Lajat, Y., Resche, F., Koriech, O. M., Al Moutaery, K., Yaqub, B., Jochens, R., Wolters, A., Venz, S., Cordes, M., Hecht, B. K., Chatel, M., Gaudray, P., Turc-Carel, C., Gioanni, J., Ayraud, N., Hecht, F., Rumbach, L., Racadot, E., Bataillard, M., Billot, M., Pariset, J., Wijdenes, J., Montalban, Rio J., Tintoré, M., Galan, I., Acarin, N., Rapaport, S., Huberman, M., Shechtcr, D., Karabudak, R., Kilinc, M., Boyacigil, S., Cila, A., Polo, J. M., Setien, S., Sanchez, R., Figols, J., Zubimendi, A., Nadareishvili, Z. G., Massot, R., Marés, R., Gallecho, F., Richart, C., Hernandez, M. A., Garcia, M. R., Lorenzo, J. N., Leon, C., Muros, M., Togores, J., Kutluk, K., Damlacik, G. A., Tekinsoy, B., Obuz, O., Baklan, B., Idiman, E., Genc, K., Zielasek, J., Schmidt, B., Liew, F. Y., Gulay, Z., Yulug, N., Wong, K. S., Wong, T. W., Yu, T. 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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
- Published
- 1994
- Full Text
- View/download PDF
10. Effect ofl-DOPA on pattern visual evoked potentials (P-100) and neuropsychological tests in untreated adult patients with phenylketonuria
- Author
-
Ullrich, K., Weglage, J., Oberwittler, C., Pietsch, M., Fünders, B., van Eckhardstein, H., and Colombo, J. P.
- Published
- 1994
- Full Text
- View/download PDF
11. White matter abnormalities in patients with treated hyperphenylalaninaemia: Magnetic resonance relaxometry and proton spectroscopy findings
- Author
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Bick, U., Ullrich, K., Stöber, U., Möller, H., Schuierer, G., Ludolph, A. C., Oberwittler, C., Weglage, J., and Wendel, U.
- Published
- 1993
- Full Text
- View/download PDF
12. Spontane Remission eines Massenprolaps C5/C6 bei einer erwachsenen Frau - ein Äquivalent zur Discitis calcarea bei Kindern?
- Author
-
Masur, H., Fahrendorf, G., Oberwittler, C., Nedjat, S., Hilker, E., Firnhaber, Wolfgang, editor, Dworschak, Kurt, editor, Lauer, Klaus, editor, and Nichtweiß, Michael, editor
- Published
- 1991
- Full Text
- View/download PDF
13. Gibt es spezifische MR-tomographische Befunde bei der Amyotrophen Lateralsklerose (ALS) ?
- Author
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Oberwittler, C., Bick, U., Ludolph, A. C., Fahrendorf, G., Masur, H., Brune, G. G., Firnhaber, Wolfgang, editor, Dworschak, Kurt, editor, Lauer, Klaus, editor, and Nichtweiß, Michael, editor
- Published
- 1991
- Full Text
- View/download PDF
14. Neurological deterioration in adult phenylketonuria
- Author
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Weglage, J., Oberwittler, C., Marquardt, T., Schellscheidt, J., v. Teeffelen-Heithoff, A., Koch, G., and Gerding, H.
- Published
- 2000
15. Gibt es spezifische MR-tomographische Befunde bei der Amyotrophen Lateralsklerose (ALS) ?
- Author
-
Oberwittler, C., primary, Bick, U., additional, Ludolph, A. C., additional, Fahrendorf, G., additional, Masur, H., additional, and Brune, G. G., additional
- Published
- 1991
- Full Text
- View/download PDF
16. Spontane Remission eines Massenprolaps C5/C6 bei einer erwachsenen Frau - ein Äquivalent zur Discitis calcarea bei Kindern?
- Author
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Masur, H., primary, Fahrendorf, G., additional, Oberwittler, C., additional, Nedjat, S., additional, and Hilker, E., additional
- Published
- 1991
- Full Text
- View/download PDF
17. Giant Axonal Neuropathy (GAN) caused by mutations in the Gigaxonin gene
- Author
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Kuhlenbaumer, G., Young, P., Oberwittler, C., Ringelstein, B., and Stogbauer, F.
- Subjects
Human genetics -- Research ,Peripheral nerve diseases -- Genetic aspects ,Genetic disorders -- Physiological aspects ,Biological sciences - Published
- 2001
18. Sensory neuropathy and vitamin B6 treatment in homocystinuria
- Author
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Ludolph, A. C., Masur, H., Oberwittler, C., Koch, H. G., and Ullrich, K.
- Published
- 1993
- Full Text
- View/download PDF
19. Magnetische Stimulation zur Erzeugung somatosensorisch evozierter Potentiale und ein Vergleich mit der konventionellen Elektrostimulation
- Author
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F. Klostermann, H. Masur, Oberwittler C, and Papke K
- Subjects
Biomedical Engineering - Published
- 2009
- Full Text
- View/download PDF
20. The X-chromosomal recessive spinobulbar muscular atrophy (type Kennedy) : description of a family, clinical features, molecular genetics, differential diagnosis and therapy
- Author
-
Kuhlenbaumer, G., Bocchicchio, M., Kress, W., Young, P., Oberwittler, C., and Stogbauer, F.
- Subjects
Human medicine - Abstract
The Kennedy-Syndrome is a X-linked recessive bulbospinal muscular atrophy, in some cases associated with endocrinological disturbances such as androgen resistance and diabetes mellitus. The age of onset is usually between 20 and 40. Presenting symptoms are proximal flaccid weakness,fasciculations, cramps or tremor. Disease progression is usually slow and live expectancy is normal. It is important to distinguish the Kennedy-Syndrome from amyotrophic lateral sclerosis, spinal muscular atrophy, muscular dystrophies and other types of motor neuron disease. Kennedy disease is caused by an expanded trinucleotide repeat in the androgen receptor gene. Genetic analysis allows a precise diagnosis on an individual basis and reliable genetic counselling. An effective medical treatment does not yet exist.
- Published
- 1998
21. Magnetische Stimulation zur Erzeugung somatosensorisch evozierter Potentiale und ein Vergleich mit der konventionellen Elektrostimulation
- Author
-
Klostermann, F., primary, Masur, H., additional, Papke, K., additional, and Oberwittler, C., additional
- Published
- 2009
- Full Text
- View/download PDF
22. Utilization and perceived effectiveness of complementary and alternative medicine in patients with dystonia
- Author
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Junker, J., primary, Oberwittler, C., additional, Jackson, D., additional, and Berger, Klaus, additional
- Published
- 2004
- Full Text
- View/download PDF
23. Giant axonal neuropathy (GAN): Case report and two novel mutations in the gigaxonin gene
- Author
-
Kuhlenbäumer, G., primary, Young, P., additional, Oberwittler, C., additional, Hünermund, G., additional, Schirmacher, A., additional, Domschke, K., additional, Ringelstein, B., additional, and Stögbauer, F., additional
- Published
- 2002
- Full Text
- View/download PDF
24. Botulinum toxin a in the treatment of spastic equinus feet. Clinical, electromyographic and functional results
- Author
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Rosenbaum, D., primary, Senst, S., additional, Hafkemeier, U., additional, Oberwittler, C., additional, and Young, P., additional
- Published
- 1999
- Full Text
- View/download PDF
25. Syringomyelia in Chiari Malformation
- Author
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Masur H and Oberwittler C
- Subjects
business.industry ,Medicine ,Surgery ,Neurology (clinical) ,Anatomy ,business ,medicine.disease ,Syringomyelia ,Chiari malformation - Published
- 1993
- Full Text
- View/download PDF
26. Dopplersonographisches Monitoring einer A. carotis interna - Dissektion unter ungünstigen Kollateralisationsbedingungen
- Author
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Haase, C., primary, Vollmer-Haase, J., additional, Oberwittler, C., additional, and Lüdemann, P., additional
- Published
- 1998
- Full Text
- View/download PDF
27. Postexcitatory inhibition after transcranial magnetic stimulation of the motor cortex in patients with drug-induced parkinsonism and in healthy individuals
- Author
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Masur, H., primary, Althoff, S., additional, Erim, Y., additional, Oberwittler, C., additional, and Hornung, W. P, additional
- Published
- 1998
- Full Text
- View/download PDF
28. Letters to the editor
- Author
-
Preston, David C., primary, Logigian, Eric L., additional, Uncini, A., additional, Krarup, C., additional, Trojaborg, W., additional, Liguori, R., additional, Phillips, Lawrence H., additional, Masur, H., additional, Schulte‐Oversohl, U., additional, Oberwittler, C., additional, Dettmers, Christian, additional, Jerusalem, Felix, additional, Anghinah, Renato, additional, Oliveira, Acary S. B., additional, and Gabbai, Alberto A., additional
- Published
- 1994
- Full Text
- View/download PDF
29. D2-Rezeptorszintigraphie (123J-IBZM) im Vergleich zur zerebralen Perfusion (99mTc-HMPAO) bei extrapyramidalen Erkrankungen
- Author
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Bartenstein, P., primary, Schober, O., primary, Oberwittler, C., primary, Lerch, H., primary, Masur, H., primary, and Saur, H.-B., additional
- Published
- 1994
- Full Text
- View/download PDF
30. Letters to the editor
- Author
-
Singer, Carlos, primary, Weiner, William J., additional, Lange, Dale J., additional, Brain, Mitchell F., additional, Greene, Paul, additional, Lovelace, Robert E., additional, Fahn, Stanley, additional, Radecki, Patrick L., additional, Campbell, William W., additional, Pridgeon, Rhonda M., additional, Citak, Kenneth A., additional, Dickoff, David J., additional, Simpson, David M., additional, Palace, Jackie, additional, Losseff, Nick, additional, Clough, Chris, additional, Masur, H., additional, and Oberwittler, C., additional
- Published
- 1993
- Full Text
- View/download PDF
31. Suppression of visual perception by transcranial magnetic stimulation — experimental findings in healthy subjects and patients with optic neuritis
- Author
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Masur, H., primary, Papke, K., additional, and Oberwittler, C., additional
- Published
- 1993
- Full Text
- View/download PDF
32. MRI in ALS
- Author
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Oberwittler, C., primary, Masur, H., additional, Ludolph, A. C., additional, and Fahrendorf, G., additional
- Published
- 1992
- Full Text
- View/download PDF
33. MS and syringomyelia
- Author
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Masur, H., primary and Oberwittler, C., additional
- Published
- 1992
- Full Text
- View/download PDF
34. Cerebellar atrophy following acute intoxication with phenytoin
- Author
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Masur, H., primary, Fahrendorf, G., additional, Oberwittler, C., additional, and Reuther, G., additional
- Published
- 1990
- Full Text
- View/download PDF
35. Postexcitatory inhibition after transcranial magnetic stimulation of the motor cortex in patients with druginduced parkinsonism and in healthy individuals
- Author
-
Masur, H., Althoff, S., Erim, Y., Oberwittler, C., and Hornung, W. P
- Abstract
The duration of the postexcitatory inhibition after transcranial magnetic stimulation was investigated in 16 patients with drug-induced parkinsonism and in 20 healthy control individuals. In the patients, the chlorpromazine-equivalent of the neuroleptic medication was determined, and the severity of the drug-induced parkinsonism was measured using the Simpson-Ångus Scale score. Group comparison (U-test) revealed a significant shorter postexcitatory inhibition in patients than in control individuals. Regression analyses showed a negative correlation between the Simpson-Ångus scale score and the duration of the postexcitatory inhibition. The correlation only reached significance for a group of patients who received at least one butyrophenone derivate. No clear-cut relation was found between the chlorpromazine equivalent and the postexcitatory inhibition. These results indicate that drug-induced parkinsonism shares features of genuine Parkinson's disease. Furthermore, it seems possible to assess the extrapyramidal side effect of butyrophenone derivates, but not for other neuroleptic drugs, by means of the method described.
- Published
- 1998
36. D2-Rezeptorszintigraphie (123J-IBZM) im Vergleich zur zerebralen Perfusion (99mTc-HMPAO) bei extrapyramidalen Erkrankungen
- Author
-
Saur, H.-B., Bartenstein, P., Schober, O., Oberwittler, C., Lerch, H., and Masur, H.
- Published
- 1994
- Full Text
- View/download PDF
37. Magnetische Stimulation zur Erzeugung somatosensorisch evozierter Potentiale und ein Vergleich mit der konventionellen Elektrostimulation.
- Author
-
Klostermann, F., Masur, H., Papke, K., and Oberwittler, C.
- Published
- 1995
38. 576P High precision quantification of ICAM-1 highlights similarities and differences between subgroups of Idiopathic inflammatory myopathies.
- Author
-
Nishimura, A., Nelke, C., Huber, M., Mensch, A., Roth, A., Oberwittler, C., Zimmerlein, B., Krämer, H., Neuen-Jacob, E., Stenzel, W., Müller-Ladner, U., Ruck, T., and Schänzer, A.
- Subjects
- *
INCLUSION body myositis , *CD54 antigen , *MAJOR histocompatibility complex , *MEMBRANE proteins , *IDIOPATHIC diseases - Abstract
The integrated classification of myositis includes a distinct morphologic characterization of skeletal muscle pathology. For the diagnosis of myositis subtypes, the evaluation of proteins associated with the underlying immune signature, such as major histocompatibility complex 1 (MHC-1) and MHC-2, is recommended. However, diagnosis can be difficult and additional markers are needed. Intercellular adhesion molecule 1 (ICAM-1) is a transmembrane protein important for immunological processes. ICAM-1 has not been yet established as a diagnostic marker for myositis. The aim of our study was to establish an automated morphometric analysis to quantify ICAM-1 protein expression on myofibers and on endomysial vessels on digitalized whole muscle sections using immunofluorescence. We included 58 biopsies from patients with Dermatomyositis (DM; n=9), Anti-synthetase syndrome (ASyS; n=6), Inclusion body myositis (IBM; n=11), Immune mediated necrotizing myopathy (IMNM; n=7), Dysferlinopathy (DYSF; n=5), COVID-19 associated myopathy (COVID-19; n=7), non-diseased controls (NDC; n=8) and neurogenic atrophy (NA; n=5). On muscle fibers, ICAM-1 expression was significantly higher in ASyS, IBM, IMNM, and COVID-19, compared to NDC. ICAM-1 expression on endomysial capillaries was significantly higher in ASyS, DM, and COVID-19 compared to NDC, IBM, and IMNM. ICAM-1 showed a strong discriminatory ability for ASyS and DM compared to NDC, IBM, and IMNM. Our study presents a method to accurately detect proteins on muscle fibers and vessels separately. We identified ICAM-1 as a new diagnostic marker for the classification of myositis. Notably, endothelial expression of ICAM-1 is increased in ASyS, DM and COVID-19, suggesting its involvement in endothelial activation in these conditions. [ABSTRACT FROM AUTHOR]
- Published
- 2024
- Full Text
- View/download PDF
39. Differentiating idiopathic inflammatory myopathies by automated morphometric analysis of MHC-1, MHC-2 and ICAM-1 in muscle tissue.
- Author
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Nishimura A, Nelke C, Huber M, Mensch A, Roth A, Oberwittler C, Zimmerlein B, Krämer HH, Neuen-Jacob E, Stenzel W, Müller-Ladner U, Ruck T, and Schänzer A
- Subjects
- Humans, COVID-19 pathology, COVID-19 diagnosis, Male, Female, Diagnosis, Differential, Histocompatibility Antigens Class II metabolism, Intercellular Adhesion Molecule-1 metabolism, Myositis pathology, Myositis diagnosis, Myositis metabolism, Muscle, Skeletal pathology, Muscle, Skeletal metabolism
- Abstract
Aims: Diagnosis of idiopathic inflammatory myopathies (IIM) is based on morphological characteristics and the evaluation of disease-related proteins. However, although broadly applied, substantial bias is imposed by the respective methods, observers and individual staining approaches. We aimed to quantify the protein levels of major histocompatibility complex (MHC)-1, (MHC)-2 and intercellular adhesion molecule (ICAM)-1 using an automated morphometric method to mitigate bias., Methods: Double immunofluorescence staining was performed on whole muscle sections to study differences in protein expression in myofibre and endomysial vessels. We analysed all IIM subtypes including dermatomyositis (DM), anti-synthetase syndrome (ASyS), inclusion body myositis (IBM), immune-mediated-necrotising myopathy (IMNM), dysferlinopathy (DYSF), SARS-CoV-2 infection and vaccination-associated myopathy. Biopsies with neurogenic atrophy (NA) and normal morphology served as controls. Bulk RNA-Sequencing (RNA-Seq) was performed on a subset of samples., Results: Our study highlights the significance of MHC-1, MHC-2 and ICAM-1 in diagnosing IIM subtypes and reveals distinct immunological profiles. RNASeq confirmed the precision of our method and identified specific gene pathways in the disease subtypes. Notably, ASyS, DM and SARS-CoV-2-associated myopathy showed increased ICAM-1 expression in the endomysial capillaries, indicating ICAM-1-associated vascular activation in these conditions. In addition, ICAM-1 showed high discrimination between different subgroups with high sensitivity and specificity., Conclusions: Automated morphometric analysis provides precise quantitative data on immune-associated proteins that can be integrated into our pathophysiological understanding of IIM. Further, ICAM-1 holds diagnostic value for the detection of IIM pathology., (© 2024 The Author(s). Neuropathology and Applied Neurobiology published by John Wiley & Sons Ltd on behalf of British Neuropathological Society.)
- Published
- 2024
- Full Text
- View/download PDF
40. Disease reactivation after switching from natalizumab to daclizumab.
- Author
-
Uphaus T, Oberwittler C, Groppa S, Zipp F, and Bittner S
- Subjects
- Adult, Anti-Inflammatory Agents therapeutic use, Daclizumab, Humans, Magnetic Resonance Imaging, Male, Methylprednisolone therapeutic use, Multiple Sclerosis, Relapsing-Remitting diagnostic imaging, Antibodies, Monoclonal, Humanized adverse effects, Drug Substitution adverse effects, Immunoglobulin G adverse effects, Immunologic Factors therapeutic use, Multiple Sclerosis, Relapsing-Remitting chemically induced, Multiple Sclerosis, Relapsing-Remitting drug therapy, Natalizumab therapeutic use
- Abstract
Discontinuation of natalizumab can lead to severe rebound of disease activity in patients with relapsing-remitting multiple sclerosis (RRMS); nevertheless, the treatment regimen in this clinical situation remains controversial. We report the case of a 25-year-old male patient with RRMS who was clinically stable under 3 years of natalizumab before treatment was stopped due to progressive multifocal leucencephalopathy (PML) safety concerns. After initiation of daclizumab, the patient suffered from disease reactivation, which was ultimately controlled by intravenous methylprednisolone and alemtuzumab treatment. Therefore, in some patients, daclizumab might not be sufficient to control disease activity after discontinuing natalizumab treatment.
- Published
- 2017
- Full Text
- View/download PDF
41. Recessively inherited amyotrophic lateral sclerosis: a Germany family with the D90A CuZn-SOD mutation.
- Author
-
Winter SM, Claus A, Oberwittler C, Völkel H, Wenzler S, and Ludolph AC
- Subjects
- Adult, Aged, DNA Mutational Analysis, Exons, Female, Genes, Recessive, Genetics, Population, Humans, Male, Middle Aged, Pedigree, Phenotype, Amyotrophic Lateral Sclerosis genetics, Point Mutation, Superoxide Dismutase genetics
- Abstract
Mutations of the SOD1 gene encoding the free radical scavenging enzyme copper-zinc superoxide dismutase (CuZn-SOD) occur in patients with familial amyotrophic lateral sclerosis (ALS). Recent reports have shown homozygosity for a CuZn-SOD mutation in exon 4, the D90A (Asp90A1a) mutation. Other mutations described to date show an autosomal dominant pattern of inheritance. This is the first description of autosomal recessively inherited ALS in an out-bred population in central Europe. This study confirms the earlier described characteristic phenotype reported in D90A homozygous ALS patients in Scandinavia and supports the theory of the existence of a strong modifying factor in some cases of ALS associated with mutations in the CuZn-SOD gene.
- Published
- 2000
- Full Text
- View/download PDF
42. [X-chromosomal recessive spinobulbar muscular atrophy (Kennedy type). Description of a family, clinical aspects, molecular genetics, differential diagnosis and therapy].
- Author
-
Kuhlenbäumer G, Bocchicchio M, Kress W, Young P, Oberwittler C, and Stögbauer F
- Subjects
- Diagnosis, Differential, Humans, Muscular Atrophy, Spinal diagnosis, Neurologic Examination, Pedigree, Receptors, Androgen genetics, Sex Chromosome Aberrations diagnosis, Syndrome, Trinucleotide Repeats genetics, Genes, Recessive genetics, Medulla Oblongata, Muscular Atrophy, Spinal genetics, Sex Chromosome Aberrations genetics, X Chromosome
- Abstract
The Kennedy-Syndrome is a X-linked recessive bulbospinal muscular atrophy, in some cases associated with endocrinological disturbances such as androgen resistance and diabetes mellitus. The age of onset is usually between 20 and 40. Presenting symptoms are proximal flaccid weakness, fasciculations, cramps or tremor. Disease progression is usually slow and live expectancy is normal. It is important to distinguish the Kennedy-Syndrome from amyotrophic lateral sclerosis, spinal muscular atrophy, muscular dystrophies and other types of motor neuron disease. Kennedy disease is caused by an expanded trinucleotide repeat in the androgen receptor gene. Genetic analysis allows a precise-diagnosis on an individual basis and reliable genetic counselling. An effective medical treatment does not yet exist.
- Published
- 1998
- Full Text
- View/download PDF
43. Early elevation of cerebrospinal fluid neuron-specific enolase in Creutzfeldt-Jakob disease.
- Author
-
Evers S, Droste DW, Lüdemann P, and Oberwittler C
- Subjects
- Creutzfeldt-Jakob Syndrome enzymology, Female, Humans, Middle Aged, Time Factors, Creutzfeldt-Jakob Syndrome cerebrospinal fluid, Phosphopyruvate Hydratase cerebrospinal fluid
- Published
- 1998
- Full Text
- View/download PDF
44. Variation of reaction time can be reduced by the time locked application of magnetic stimulation of the motor cortex.
- Author
-
Masur H, Schneider U, Papke K, and Oberwittler C
- Subjects
- Evoked Potentials, Humans, Movement, Muscle, Skeletal physiology, Thumb physiology, Magnetics, Motor Cortex physiology, Reaction Time physiology
- Abstract
It was the aim of this study to determine the influence of non-invasive magnetic stimulation on the performance of a visually induced reaction task. The experiment was performed in 8 healthy volunteers. After a visual stimulus subjects had to move their thumbs as soon as possible. The muscular reaction was recorded with surface EMG on both sides. After the visual go-signal a magnetic stimulus (Fig. 8 coil) was applied above the right or left motor cortex at varying time intervals (30 and 110 ms). The magnetic stimulus was randomly given or not. Short time intervals between visual and magnetic stimulus induced a shortening, long intervals induced a prolongation of the reaction time. The contralateral reaction time was always longer than the ipsilateral one. Compared with the reaction times without magnetic stimulation, the intraindividual standard deviation of the reaction times was markedly reduced by the application of the magnetic stimulation. This reduction was greater in ipsilateral than in contralateral recordings. The kind of the instruction had additional modifying effects.
- Published
- 1996
45. Somatosensory evoked potentials after magnetic stimulation at different points of the body in normal subjects and in patients with syringomyelia.
- Author
-
Masur H, Klostermann F, Oberwittler C, and Papke K
- Subjects
- Adult, Electric Stimulation, Female, Humans, Magnetic Resonance Imaging, Magnetics, Male, Middle Aged, Reaction Time, Reference Values, Syringomyelia diagnosis, Evoked Potentials, Somatosensory, Syringomyelia physiopathology
- Abstract
Somatosensory evoked potentials (SEPs) were elicited by magnetic stimulation of the tibial nerve, gastrocnemic muscle and by stimulation over the spinous processes of lumbar vertebra 5 (L 5), thoracic vertebra 9 (Th 9) and cervical vertebra 7 (C 7). The first SEP-positivity (P1-latency) was measured in a group of 20 controls and in another group of 18 patients with syringomyelia. The P1-latencies of the latter group following the stimulations over Th 9 and C 7 were significantly longer than those of the controls. Furthermore a correlation between electrophysiological findings and clinical data of the patients could be proven. Thus the method emerged as an appropriate tool for the investigation of the central part of the sensory system and for the diagnosis of spinal abnormalities.
- Published
- 1996
46. Involvement of the autonomic nervous system in patients with syringomyelia--a study with the sympathetic skin response.
- Author
-
Masur H, Schulte-Oversohl U, Papke K, Oberwittler C, and Vollmer J
- Subjects
- Adult, Aged, Autonomic Nervous System Diseases diagnosis, Female, Foot innervation, Hand innervation, Humans, Male, Middle Aged, Reaction Time physiology, Reference Values, Syringomyelia diagnosis, Autonomic Nervous System Diseases physiopathology, Galvanic Skin Response physiology, Skin innervation, Sympathetic Nervous System physiopathology, Syringomyelia physiopathology
- Abstract
In order to determine the function of the autonomic nervous system in syringomyelia, the sympathetic skin response (SSR) was performed in 13 patients with syringomyelia and 20 healthy controls. SSR was recorded from both palms and soles. In patients with syringomyelia, we found absent responses, prolonged latencies and reduced amplitudes. SSRs could be recorded in 15 out of the examined 26 upper extremities. The latencies were prolonged in 12 of these cases. In the lower limbs, 11 SSRs could be obtained. In 4 of these cases the latencies were prolonged. The SSR latencies recorded from the palms and soles were both significantly prolonged (p < 0.05) and the amplitudes were reduced (p < 0.05) as compared to normal persons. Our data strongly suggest involvement of the autonomic nervous system in syringomyelia as assessed by the SSR response (in upper and lower extremities). In our patients, the extent of autonomic dysfunction was not related to the stage or the duration of disease.
- Published
- 1996
47. Sympathetic skin response in patients with amyotrophic lateral sclerosis.
- Author
-
Masur H, Schulte-Oversohl U, Papke K, Oberwittler C, and Vollmer J
- Subjects
- Adult, Aged, Autonomic Nervous System Diseases diagnosis, Female, Humans, Male, Middle Aged, Severity of Illness Index, Amyotrophic Lateral Sclerosis complications, Autonomic Nervous System Diseases complications, Galvanic Skin Response
- Abstract
To determine a possible involvement of the autonomic nervous system in amyotrophic lateral sclerosis (ALS), measurement of the sympathetic skin response (SSR) was performed in 15 patients with definite ALS. Findings were compared with those in 20 normal controls. In ALS patients the mean SSR latencies recorded from the palms and soles were both significantly prolonged (p < 0.05) and the amplitudes were reduced as compared with normal persons. In 5 patients, SSR potentials were completely lacking in one or even more extremities. Our data strongly suggest subclinical involvement of the autonomic nervous system in ALS as assessed by the SSR response. In our patients the extent of autonomic dysfunction was not related to the stage or the duration of disease.
- Published
- 1995
48. [The idiopathic QT syndrome as the cause of epileptic and nonepileptic seizures].
- Author
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Hördt M, Haverkamp W, Oberwittler C, Lüdemann P, Borggrefe M, Ringelstein EB, and Breithardt G
- Subjects
- Adolescent, Adult, Child, Diagnosis, Differential, Electrocardiography, Electroencephalography, Epilepsy physiopathology, Fatal Outcome, Female, Heart Conduction System physiopathology, Humans, Long QT Syndrome diagnosis, Long QT Syndrome physiopathology, Prognosis, Seizures physiopathology, Syncope etiology, Syncope physiopathology, Syndrome, Torsades de Pointes complications, Torsades de Pointes physiopathology, Epilepsy etiology, Long QT Syndrome complications, Seizures etiology
- Abstract
The long QT syndrome (LQTS) is characterized by a pathological lengthening of the corrected QT interval on the surface ECG and the occurrence of syncopal attacks, sometimes presenting as a seizure disorder. They are caused by ventricular tachycardia of the torsade de pointes type, an arrhythmia that is also responsible for the high incidence of sudden death among these patients. Besides the acquired forms of LQTS which are transient (e.g. therapy with QT-prolonging drugs), congenital variants (Romano-Ward syndrome, Jervell/Lange-Nielsen syndrome, sporadic form) can occur as well. The latter mostly become manifest during childhood or adolescence. Because the syndrome is rare, it is often not included in the primary differential diagnosis of syncope. Thus, misinterpretation as epilepsy may occur. Especially if siblings are affected, a genetic epilepsy may be diagnosed. However, the correct diagnosis can be made by standard ECG methods. Early recognition of the syndrome is very importance because of prognostic and therapeutic consequences. In this article, two cases of idiopathic LQTS are presented. Problems regarding differential diagnosis and therapy are discussed.
- Published
- 1995
49. Inhibitory period and late muscular responses after transcranial magnetic stimulation in healthy children.
- Author
-
Masur H, Althoff S, Kurlemann G, Sträter R, and Oberwittler C
- Subjects
- Adolescent, Aging, Child, Child, Preschool, Electromyography, Female, Humans, Male, Motor Cortex radiation effects, Muscle, Skeletal radiation effects, Reference Values, Time Factors, Motor Cortex physiology, Muscle, Skeletal physiology, Transcranial Magnetic Stimulation
- Abstract
Transcranial magnetic stimulation (TMS) was investigated in 24 healthy children between the ages of 3 and 14 years in order to study late muscular responses (as they are observed in adults) as a function of age and maturation. Muscular responses were recorded bilaterally from the biceps muscle. An early muscular response and several late phenomena can be elicited in children. (i) An inhibitory period following the primary response could preferentially be recorded contralaterally. (ii) During facilitation, a late response was recorded bilaterally. (iii) Without facilitation (during 'relaxation'), late responses were recorded bilaterally with a latency of between 50-400 ms. The latency of the latter responses depended on the age of the children, and may therefore be useful in monitoring the maturation of the central motor system in infants. Due to small side-to-side differences, the inhibitory period may be of diagnostic value in children for detection of unilateral dysfunction of the central nervous system.
- Published
- 1995
- Full Text
- View/download PDF
50. Cerebellar herniation in syringomyelia: relation between tonsillar herniation and the dimensions of the syrinx and the remaining spinal cord. A quantitative MRI study.
- Author
-
Masur H, Oberwittler C, Reuther G, and Heyen P
- Subjects
- Adolescent, Adult, Aged, Cerebellar Diseases pathology, Encephalocele pathology, Female, Humans, Male, Middle Aged, Motor Neuron Disease diagnosis, Motor Neuron Disease pathology, Neurologic Examination, Prognosis, Sensation Disorders diagnosis, Sensation Disorders pathology, Syringomyelia pathology, Cerebellar Diseases diagnosis, Cerebellum pathology, Encephalocele diagnosis, Image Processing, Computer-Assisted, Magnetic Resonance Imaging methods, Spinal Cord pathology, Syringomyelia diagnosis
- Abstract
The dimensions of the syrinx, the remaining spinal cord and the degree of cerebellar herniation were analyzed by one- and two-dimensional MRI studies in 22 patients with syringomyelia. A deep and/or broad cyst tends to be a long one. The dimensions of the syrinx and the spinal cord have an inverse relationship. The degree of cerebellar herniation is not related to the longitudinal or transverse extension of the cyst or the ratio cyst/cord or the remaining spinal cord (neither for diameters nor for cross-sectional areas). The dimensions of cysts are not significantly greater in patients with tonsillar herniation than in patients without. We conclude that cerebellar herniation is not a major prognostic factor and should not be overestimated for the development and progression of the disease.
- Published
- 1995
- Full Text
- View/download PDF
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