41 results on '"Isiklar I"'
Search Results
2. Spleen Size Changes in Pediatric Liver Transplant Recipients With Functioning Grafts
- Author
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Tutar, N.U., Isiklar, I., Ulu, E.M. Kayahan, and Haberal, M.
- Published
- 2007
- Full Text
- View/download PDF
3. Osteoarthritis in hemodialysis patients: relationships with bone mineral density and other clinical and laboratory parameters
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Kart-Köseoglu, Hamide, Yucel, A. E., Niron, E. A., Köseoglu, H., Isiklar, I., and Ozdemir, F. N.
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- 2005
- Full Text
- View/download PDF
4. Localized Fluid Collections After Liver Transplantation
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Akin, K., Ozturk, A., Guvenc, Z., Isiklar, I., and Haberal, M.
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- 2006
- Full Text
- View/download PDF
5. Venous Complications After Orthotopic Liver Transplantation
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Karakayali, H., Boyvat, F., Coskun, M., Isıklar, I., Sözen, H., Filik, L., Yılmaz, U., Gür, G., and Haberal, M.
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- 2006
- Full Text
- View/download PDF
6. P358The effect of myocardial fibrosis on left ventricular torsion / twist in patients with non-ischemic dilated cardiomyopathy: a cardiovascular magnetic resonance imaging and echocardiography study
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Gurel, E, Karaahmet, T, Tigen, K, Kirma, C, Dundar, C, Pala, S, Isiklar, I, Cevik, C, Kilicgedik, A, and Basaran, Y
- Published
- 2011
7. P1267 Negative baseline diagnostic imaging does not exclude pulmonary embolism in patients with reccurrent syncope
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Kocabas, U, primary, Altay, H, additional, Ozkalayci, F, additional, Isiklar, I, additional, and Pehlivanoglu, S, additional
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- 2020
- Full Text
- View/download PDF
8. Relationship Between Leptin and Bone Mineral Density in Renal Transplant Recipients
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Agras, P.I., Baskin, E., Saatci, U., Colak, T., Cengiz, N., Kinik, S.T., Isiklar, I., Haberal, A., Mert, I., and Haberal, M.
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- 2005
- Full Text
- View/download PDF
9. FROM DONOR TO RECIPIENT: Doppler US, power US and scintigraphy of kidney perfusion before and after transplantation
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Isiklar, I, Aktas, A, Akgun, S, and Karakayali, H
- Published
- 2000
10. HEPATIC ALVEOLAR ECHINOCOCCOSIS: A case report
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Akin, O. and Isiklar, I.
- Published
- 1999
11. Type A intramural hematoma in a patient with acute coronary syndrome mimicking acute Type A aortic dissection
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Gülmez, Ö, primary, Saritas, B, additional, and Isiklar, I, additional
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- 2017
- Full Text
- View/download PDF
12. Poster Session 1: Thursday 8 December 2011, 08:30-12:30 * Location: Poster Area
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Vijayan, S., primary, Khanji, M., additional, Ionescu, A., additional, Vijayan, S., additional, Podoleanu, C., additional, Frigy, A., additional, Ugri, A., additional, Varga, A., additional, Podoleanu, D., additional, Incze, A., additional, Carasca, E., additional, Dobreanu, D., additional, Mjolstad, O., additional, Dalen, H., additional, Graven, T., additional, Kleinau, J., additional, Hagen, B., additional, Fu, H., additional, Liu, T., additional, Li, J., additional, Liu, C., additional, Zhou, C., additional, Li, G., additional, Bordese, R., additional, Capriolo, M., additional, Brero, D., additional, Salvetti, I., additional, Cannillo, M., additional, Antolini, M., additional, Grosso Marra, W., additional, Frea, S., additional, Morello, M., additional, Gaita, F., additional, Maffessanti, F., additional, Caiani, E., additional, Muraru, D., additional, Tuveri, F., additional, Dal Bianco, L., additional, Badano, L., additional, Majid, A., additional, Soesanto, A., additional, Ario Suryo Kuncoro, B., additional, Sukmawan, R., additional, Ganesja, M. H., additional, Benedek, T., additional, Chitu, M., additional, Beata, J., additional, Suciu, Z., additional, Kovacs, I., additional, Bucur, O., additional, Benedek, I., additional, Hrynkiewicz-Szymanska, A., additional, Szymanski, F., additional, Karpinski, G., additional, Filipiak, K., additional, Radunovic, Z., additional, Lande Wekre, L., additional, Steine, K., additional, Bech-Hanssen, O., additional, Rundqvist, B., additional, Lindgren, F., additional, Selimovic, N., additional, Jedrzychowska-Baraniak, J., additional, Jozwa, R., additional, Larysz, B., additional, Kasprzak, J., additional, Ripp, T., additional, Mordovin, V., additional, Ripp, E., additional, Ciobanu, A., additional, Dulgheru, R., additional, Dragoi, R., additional, Magda, S., additional, Florescu, M., additional, Mihaila, S., additional, Rimbas, R., additional, Cinteza, M., additional, Vinereanu, D., additional, Benavides-Vallve, C., additional, Pelacho, B., additional, Iglesias, O., additional, Castano, S., additional, Munoz-Barrutia, A., additional, Prosper, F., additional, Ortiz De Solorzano, C., additional, Manouras, A., additional, Sahlen, A., additional, Winter, R., additional, Vardas, P., additional, Brodin, L., additional, Sarvari, S. I., additional, Haugaa, K. H., additional, Zahid, W., additional, Bendz, B., additional, Aaberge, L., additional, Edvardsen, T., additional, Di Bella, G., additional, Pedri, S., additional, Donato, R., additional, Madaffari, A., additional, Zito, C., additional, Stapf, D., additional, Schreckenberg, M., additional, Carerj, S., additional, Yoshikawa, H., additional, Suzuki, M., additional, Kusunose, Y., additional, Hashimoto, G., additional, Otsuka, T., additional, Nakamura, M., additional, Sugi, K., additional, Grapsa, J., additional, Dawson, D., additional, Gin-Sing, W., additional, Howard, L., additional, Gibbs, J., additional, Nihoyannopoulos, P., additional, Smith, B., additional, Coulter, T., additional, Rendon, A., additional, Gorissen, W., additional, Shiran, A., additional, Asmer, I., additional, Adawi, S., additional, Ganaeem, M., additional, Shehadeh, J., additional, Cameli, M., additional, Lisi, M., additional, Righini, F., additional, Maccherini, M., additional, Sani, G., additional, Galderisi, M., additional, Mondillo, S., additional, Kalimanovska-Ostric, D., additional, Nastasovic, T., additional, Jovanovic, I., additional, Milakovic, B., additional, Dostanic, M., additional, Stosic, M., additional, Sasic, I., additional, Sveen, K., additional, Nerdrum, T., additional, Hanssen, K., additional, Dahl-Jorgensen, K., additional, Holte, E., additional, Vegsundvaag, J., additional, Hole, T., additional, Hegbom, K., additional, Wiseth, R., additional, Ikonomidis, I., additional, Lekakis, J., additional, Tritakis, V., additional, Papadakis, I., additional, Kadoglou, N., additional, Tzortzis, S., additional, Trivilou, P., additional, Koukoulis, C., additional, Paraskevaidis, I., additional, Anastasiou-Nana, M., additional, Smedsrud, M. K., additional, Sarvari, S., additional, Gjesdal, O., additional, Beraldo, M., additional, Solda', E., additional, Cucchini, U., additional, Peluso, D., additional, Tuveri, M., additional, Al Mamary, A., additional, Iliceto, S., additional, Dores, H., additional, Abecasis, J., additional, Carvalho, M., additional, Santos, M., additional, Andrade, M., additional, Ribeiras, R., additional, Reis, C., additional, Horta, E., additional, Gouveia, R., additional, Mendes, M., additional, Zaliaduonyte-Peksiene, D., additional, Mizariene, V., additional, Cesnaite, G., additional, Tamuleviciute, E., additional, Jurkevicius, R., additional, Vaskelyte, J., additional, Zaliunas, R., additional, Smarz, K., additional, Zaborska, B., additional, Jaxa-Chamiec, T., additional, Maciejewski, P., additional, Budaj, A., additional, Trifunovic, D., additional, Sobic-Saranovic, D., additional, Stankovic, S., additional, Ostojic, M., additional, Vujisic-Tesic, B., additional, Petrovic, M., additional, Nedeljkovic, I., additional, Banovic, M., additional, Tesic, M., additional, Petrovic, I., additional, Peovska, I., additional, Srbinovska, E., additional, Maksimovic, J., additional, Andova, V., additional, Arnaudova, F., additional, Hristova, E., additional, Otljanska, M., additional, Vavlukis, M., additional, Jovanova, S., additional, Tamborini, G., additional, Fusini, L., additional, Gripari, P., additional, Muratori, M., additional, Pontone, G., additional, Andreini, D., additional, Bertella, E., additional, Ghulam Ali, S., additional, Bartorelli, A., additional, Pepi, M., additional, Cusma-Piccione, M., additional, Salvia, J., additional, Antonini-Canterin, F., additional, Lentini, S., additional, Donato, D., additional, Miceli, M., additional, Oreto, G., additional, Sachner, R., additional, Rubinshtein, R., additional, Shnapp, M., additional, Gaspar, T., additional, Marchese, A., additional, Deste, W., additional, Sanfilippo, A., additional, Aruta, P., additional, Patane, M., additional, Millan, G., additional, Ussia, G., additional, Tamburino, C., additional, Kujacic, V., additional, Obradovic, S., additional, Crkvenac, Z., additional, Bernard, A., additional, Piquemal, M., additional, Muller, G., additional, Arbeille, P., additional, Charbonnier, B., additional, Broyd, C., additional, Davies, J., additional, Mikhail, G., additional, Mayet, J., additional, Francis, D., additional, Rosca, M., additional, Magne, J., additional, Szymanski, C., additional, Popescu, B., additional, Ginghina, C., additional, Pierard, L., additional, Lancellotti, P., additional, Gonzalez-Mansilla, A., additional, Solis, J., additional, Angulo, R., additional, Perez-David, E., additional, Madrid, G., additional, Garcia-Robles, J., additional, Yotti, R., additional, Prieto, R., additional, Bermejo, J., additional, Fernandez-Aviles, F., additional, Ishikawa, Y., additional, Ishida, T., additional, Osaki, T., additional, Matsuyama, M., additional, Yamashita, H., additional, Ozaki, S., additional, Stevanella, M., additional, Votta, E., additional, Veronesi, F., additional, Alamanni, F., additional, Redaelli, A., additional, Park, S. D., additional, Lee, J., additional, Shin, S., additional, Woo, S., additional, Kim, D., additional, Park, K., additional, Kwan, J., additional, Tsang, W., additional, Chandra, S., additional, Weinert, L., additional, Gayat, E., additional, Djelassi, M., additional, Balbach, T., additional, Mor-Avi, V., additional, Lang, R., additional, De Meester, P., additional, Van De Bruaene, A., additional, Delcroix, M., additional, Budts, W., additional, Abid, L., additional, Frikha, Z., additional, Makni, K., additional, Rekik, H., additional, Znazen, A., additional, Mourad, H., additional, Kammoun, S., additional, Sargento, L., additional, Satendra, M., additional, Sousa, C., additional, Lopes, S., additional, Longo, S., additional, Lousada, N., additional, Palma Reis, R., additional, Fouad, D., additional, Shams Eldeen, R., additional, Beladan, C., additional, Calin, A., additional, Voinea, F., additional, Enache, R., additional, Jurcut, R., additional, Coman, I., additional, Ghionea, M., additional, Djordjevic-Dikic, A., additional, Petrovic, O., additional, Boricic, M., additional, Giga, V., additional, Pisciella, L., additional, Lanzillo, C., additional, Minati, M., additional, Caselli, S., additional, Di Roma, M., additional, Fratini, S., additional, Romano, S., additional, Calo', L., additional, Lioy, E., additional, Penco, M., additional, Finocchiaro, G., additional, Pinamonti, B., additional, Merlo, M., additional, Barbati, G., additional, Sinagra, G., additional, Dilenarda, A., additional, Comenale Pinto, S., additional, Ancona, R., additional, Caso, P., additional, Cavallaro, C., additional, Vecchione, F., additional, D'onofrio, A., additional, Fero', M., additional, Calabro', R., additional, Gustafsson, S., additional, Ihse, E., additional, Henein, M., additional, Westermark, P., additional, Suhr, O., additional, Lindqvist, P., additional, Oliva Sandoval, M., additional, Gonzalez Carrillo, M., additional, Garcia Navarro, M., additional, Garcia-Molina Saez, E., additional, Sabater Molina, M., additional, Saura Espin, D., additional, Lacunza Ruiz, J., additional, Gimeno Blanes, J., additional, De La Morena Valenzuela, G., additional, Valdes Chavarri, M., additional, Prinz, C., additional, Faber, L., additional, Horstkotte, D., additional, Hoetz, H., additional, Voigt, J., additional, Gandara, F., additional, Correia, M., additional, Rosario, I., additional, Fonseca, C., additional, Arroja, I., additional, Aleixo, A., additional, Martins, A., additional, Radulescu, L., additional, Dan Radulescu, D., additional, Parv Andreea, P., additional, Duncea Caius, D., additional, Ciuleanu T, C., additional, Mitrea Paulina, M., additional, Cali Quaglia, F., additional, Ribezzo, M., additional, Boffini, M., additional, Rinaldi, M., additional, Maceira Gonzalez, A. M., additional, Cosin-Sales, J., additional, Dalli, E., additional, Diago, J., additional, Aguilar, J., additional, Ruvira, J., additional, Goncalves, S., additional, Gomes, A., additional, Pinto, F., additional, Tsai, W.-C., additional, Liu, Y.-W., additional, Shih, J.-Y., additional, Huang, Y.-Y., additional, Chen, J.-Y., additional, Tsai, L.-M., additional, Chen, J.-H., additional, Ribeiro, S., additional, Doroteia, D., additional, Santos, L., additional, David, C., additional, Vinhas De Sousa, G., additional, Almeida, A., additional, Iwase, M., additional, Itou, Y., additional, Yasukochi, S., additional, Shiino, K., additional, Inuzuka, H., additional, Sugimoto, K., additional, Ozaki, Y., additional, Gieszczyk-Strozik, K., additional, Sikora-Puz, A., additional, Mizia, M., additional, Lasota, B., additional, Chmiel, A., additional, Lis-Swiety, A., additional, Michna, J., additional, Brzezinska-Wcislo, L., additional, Mizia-Stec, K., additional, Gasior, Z., additional, Luijendijk, P., additional, De Bruin-Bon, H., additional, Zwiers, C., additional, Vriend, J., additional, Van Den Brink, R., additional, Mulder, B., additional, Bouma, B., additional, Brigido, S., additional, Gianfagna, P., additional, Proclemer, A., additional, Plicht, B., additional, Kahlert, P., additional, Kaelsch, H., additional, Buck, T., additional, Erbel, R., additional, Konorza, T., additional, Yoon, H., additional, Kim, K., additional, Ahn, Y., additional, Jeong, M., additional, Cho, J., additional, Park, J., additional, Kang, J., additional, Rha, W., additional, Jansen Klomp, W. W., additional, Brandon Bravo Bruinsma, G., additional, Van 'T Hof, A., additional, Spanjersberg, S., additional, Nierich, A., additional, Bombardini, T., additional, Gherardi, S., additional, Picano, E., additional, Ciarka, A., additional, Herbots, L., additional, Eroglu, E., additional, Van Cleemput, J., additional, Droogne, W., additional, Jasityte, R., additional, Meyns, B., additional, D'hooge, J., additional, Vanhaecke, J., additional, Al Barjas, M., additional, Iskreva, R., additional, Morris, R., additional, Davar, J., additional, Zhao, Y., additional, Holmgren, A., additional, Morner, S., additional, Stepanovic, J., additional, Beleslin, B., additional, Nedeljkovic, M., additional, Mazic, S., additional, Stojanov, V., additional, Piatkowski, R., additional, Kochanowski, J., additional, Scislo, P., additional, Grabowski, M., additional, Marchel, M., additional, Roik, M., additional, Kosior, D., additional, Opolski, G., additional, Tomaszewski, A., additional, Kutarski, A., additional, Tomaszewski, M., additional, Eibel, S., additional, Hasheminejad, E., additional, Mukherjee, C., additional, Tschernich, H., additional, Ender, J., additional, Delithanasis, I., additional, Celutkiene, J., additional, Kenny, C., additional, Monaghan, M., additional, Van Den Oord, S., additional, Ten Kate, G., additional, Akkus, Z., additional, Renaud, G., additional, Sijbrands, E., additional, Ten Cate, F., additional, De Jong, N., additional, Bosch, J., additional, Van Der Steen, A., additional, Schinkel, A., additional, Lisowska, A., additional, Knapp, M., additional, Tycinska, A., additional, Sawicki, R., additional, Kralisz, P., additional, Sobkowicz, B., additional, Chang, S.-A., additional, Lee, S.-C., additional, Kim, E.-Y., additional, Hahm, S.-H., additional, Ahn, G.-T., additional, Sohn, M.-K., additional, Park, S.-J., additional, Choi, J.-O., additional, Park, S.-W., additional, Oh, J.-K., additional, Gursoy, M. O., additional, Gokdeniz, T., additional, Astarcioglu, M., additional, Bayram, Z., additional, Cakal, B., additional, Karakoyun, S., additional, Kalcik, M., additional, Kahveci, G., additional, Yildiz, M., additional, Ozkan, M., additional, Skidan, V., additional, Borowski, A., additional, Park, M., additional, Thomas, J., additional, Ranjbar, S., additional, Hassantash, S., additional, Karvandi, M., additional, Foroughi, M., additional, Davidsen, E. S., additional, Cramariuc, D., additional, Bleie, O., additional, Gerdts, E., additional, Matre, K., additional, Cusma' Piccione, M., additional, Bagnato, G., additional, Mohammed, M., additional, Piluso, S., additional, Oreto, L., additional, Bitter, T., additional, Carvalho, S., additional, Canada, M., additional, Santisteban Sanchez De Puerta, M., additional, Mesa Rubio, M. D., additional, Ruiz Ortiz, M., additional, Delgado Ortega, M., additional, Pena Pena, M. L., additional, Puentes Chiachio, M., additional, Suarez De Lezo Cruz-Conde, J., additional, Pan Alvarez-Ossorio, M., additional, Mazuelos Bellido, F., additional, Suarez De Lezo Herreros De Tejada, J., additional, Altekin, E., additional, Yanikoglu, A., additional, Karakas, S., additional, Oncel, C., additional, Akdemir, B., additional, Belgi Yildirim, A., additional, Cilli, A., additional, Yilmaz, H., additional, Lenartowska, L., additional, Furdal, M., additional, Knysz, B., additional, Konieczny, A., additional, Lewczuk, J., additional, Severino, S., additional, Cavallaro, M., additional, Coppola, M., additional, Motoki, H., additional, To, A., additional, Bhargava, M., additional, Wazni, O., additional, Marwick, T., additional, Klein, A., additional, Sinkovskaya, E., additional, Horton, S., additional, Abuhamad, A., additional, Mingo Santos, S., additional, Monivas Palomero, V., additional, Beltran Correas, B., additional, Mitroi, C., additional, Gutierrez Landaluce, C., additional, Garcia Lunar, I., additional, Gonzalez Mirelis, J., additional, Cavero, M., additional, Segovia Cubero, J., additional, Alonso Pulpon, L., additional, Gurel, E., additional, Karaahmet, T., additional, Tigen, K., additional, Kirma, C., additional, Dundar, C., additional, Pala, S., additional, Isiklar, I., additional, Cevik, C., additional, Kilicgedik, A., additional, Basaran, Y., additional, Brambatti, M., additional, Romandini, A., additional, Barbarossa, A., additional, Molini, S., additional, Urbinati, A., additional, Giovagnoli, A., additional, Cipolletta, L., additional, Capucci, A., additional, Park, S., additional, Choi, E., additional, Ahn, C., additional, Hong, S., additional, Kim, M., additional, Lim, D., additional, Shim, W., additional, Xie, J., additional, Fang, F., additional, Zhang, Q., additional, Chan, J., additional, Yip, G., additional, Sanderson, J., additional, Lam, Y., additional, Yan, B., additional, Yu, C., additional, Jorge Perez, P., additional, De La Rosa Hernandez, A., additional, Hernandez Garcia, C., additional, Duque Garcia, A., additional, Barragan Acea, A., additional, Arroyo Ucar, E., additional, Jimenez Rivera, J., additional, Lacalzada Almeida, J., additional, Laynez Cerdena, I., additional, Carminati, C., additional, Capoulade, R., additional, Larose, E., additional, Clavel, M., additional, Dumesnil, J., additional, Arsenault, M., additional, Bedard, E., additional, Mathieu, P., additional, Pibarot, P., additional, Gargani, L., additional, Baldi, G., additional, Forfori, F., additional, Caramella, D., additional, D'errico, L., additional, Abramo, A., additional, Sicari, R., additional, Giunta, F., additional, Lee, W.-N., additional, Larrat, B., additional, Messas, E., additional, Pernot, M., additional, Tanter, M., additional, Velagic, V., additional, Cikes, M., additional, Matasic, R., additional, Skorak, I., additional, Samardzic, J., additional, Puljevic, D., additional, Lovric Bencic, M., additional, Biocina, B., additional, Milicic, D., additional, Roosens, B., additional, Bala, G., additional, Droogmans, S., additional, Hostens, J., additional, Somja, J., additional, Delvenne, E., additional, Schiettecatte, J., additional, Lahoutte, T., additional, Van Camp, G., additional, Cosyns, B., additional, Ghosh, A., additional, Hardy, R., additional, Chaturvedi, N., additional, Deanfield, J., additional, Pellerin, D., additional, Kuh, D., additional, Hughes, A., additional, Malmgren, A., additional, Dencker, M., additional, Stagmo, M., additional, Gudmundsson, P., additional, Seo, Y., additional, Ishizu, T., additional, Aonuma, K., additional, Schuuring, M. J., additional, Vis, J., additional, Van Dijk, A., additional, Van Melle, J., additional, Pieper, P., additional, Vliegen, H., additional, Sieswerda, G., additional, Foukarakis, E., additional, Pitarokilis, A., additional, Kafarakis, P., additional, Kiritsi, A., additional, Klironomos, E., additional, Manousakis, A., additional, Fragiadaki, X., additional, Papadakis, E., additional, and Dermitzakis, A., additional
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- 2011
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13. Comparison of continuous spinal, continuous epidural and general anaesthesia in patients undergoing total hip arthroplasty: perioperative complications and stress response
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Karaaslan, P., primary, Pirat, A., additional, Kocay, A. M., additional, Tandogan, R., additional, and Isiklar, I., additional
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- 2006
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14. Osteoarthritis in hemodialysis patients: relationships with bone mineral density and other clinical and laboratory parameters
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Kart-Köseoglu, Hamide, primary, Yucel, A. E., additional, Niron, E. A., additional, Köseoglu, H., additional, Isiklar, I., additional, and Ozdemir, F. N., additional
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- 2004
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15. Bone Mineral Density in Patients on Maintenance Hemodialysis and Effect of Chronic Hepatitis C Virus Infection
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Yücel, A. Eftal, primary, Kart‐Köseoglu, H., additional, Isiklar, I., additional, Kuruinci, E., additional, Özdemir, F. N., additional, and Arslan, H., additional
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- 2004
- Full Text
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16. Power Doppler ultrasonography compared with scintigraphy in the diagnosis of renal allograft dysfunction
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Isiklar, I, primary, Aktas, A, additional, Uzuner, O, additional, Demirag, A, additional, and Haberal, M, additional
- Published
- 1999
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17. Early postoperative ultrasound of normally functioning transplanted kidneys: abnormal findings and their significance
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Isiklar, I, primary, Uzuner, O, additional, Demirag, A, additional, and Haberal, M, additional
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- 1999
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18. Is common femoral artery flow affected by the ipsilateral transplanted kidney?
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Isiklar, I, primary, Uzuner, O, additional, Demirag, A, additional, Akin, O, additional, and Haberal, M, additional
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- 1999
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19. Hepatic Alveolar Echinococcosis
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Akin, O., primary and Isiklar, I., additional
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- 1999
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20. An unusual sonographic finding in Caroli's disease.
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Akin, O, primary, Isiklar, I, additional, Baysal, C, additional, and Bilginoglu, S E, additional
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- 1998
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21. Intracranial metastatic melanoma: correlation between MR imaging characteristics and melanin content.
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Isiklar, I, primary, Leeds, N E, additional, Fuller, G N, additional, and Kumar, A J, additional
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- 1995
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22. Prognostic value of the PAI-1 4G/5G polymorphism in invasive ductal carcinoma of the breast
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Yagmurdur, M. C., Atac, F. B., Tutar, N. U., Verdi, H., Isiklar, I., Ozdemir, B. H., Ozbek, N., Karakayali, H., and Mehmet Haberal
23. The effect of cisapride on gallbladder contractility in type II diabetic patients
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Gursoy, M., Guvener, N., Isiklar, I., Tutal, E., Ozin, B., and Ahmet Sedat Boyacioglu
- Subjects
Adult ,Glycated Hemoglobin ,Male ,Cisapride ,Gallbladder Emptying ,Treatment Outcome ,Diabetes Mellitus, Type 2 ,Image Processing, Computer-Assisted ,Humans ,Female ,Middle Aged ,Biliary Dyskinesia ,Ultrasonography - Abstract
To investigate whether diabetics have altered gallbladder motility, and whether cisapride has any effect on gallbladder motility in these patients. The factors associated with abnormal gallbladder contractility, and with the effects of cisapride on gallbladder contractility in diabetics were also evaluated.The gallbladder contractility parameters of 20 diabetics and 20 controls were assessed by real time ultrasonography. The same measurements were made after cisapride treatment in diabetics.Fasting gallbladder volume and residual gallbladder volume were statistically higher in the diabetic group than in the controls (P = 0.018 and P = 0.022, respectively). Multivariate analysis also showed a significant association between fasting gallbladder volume and existing diabetes (P = 0.0002). There was a significant positive correlation between level of hemoglobin A1c and fasting gallbladder volume (r = 0.48, P = 0.031). Responders to cisapride treatment had significantly higher hemoglobin A1c levels than nonresponders (6.6 +/- 1.3 vs. 9.1 +/- 1.8, respectively; P = 0.004). Logistic multiple regression analysis revealed that hemoglobin A1c level was the only independent factor that was predictive for efficacy of cisapride treatment.This study demonstrates that diabetics have impaired gallbladder contractility, and that control of diabetes is predictive for gallbladder contractility and response to cisapride therapy in these patients.
24. Management of bilateral breast carcinoma: Long-term results
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Goksel, H. A., Yagmurdur, M. C., Karakayali, H., Gökhan Moray, Demirhan, B., Isiklar, I., Bilgin, N., and Haberal, M.
25. Prognostic value of the PAI-1 4G/5G polymorphism in invasive ductal carcinoma of the breast
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Mc, Yagmurdur, Fb, Atac, Nu, Tutar, Verdi H, Isiklar I, B.Handan Özdemir, Ozbek N, Karakayali H, and Haberal M
- Subjects
Polymorphism, Genetic ,Genotype ,Turkey ,Carcinoma, Ductal, Breast ,Breast Neoplasms ,Prognosis ,Disease-Free Survival ,Statistics, Nonparametric ,Plasminogen Activator Inhibitor 1 ,Humans ,Female ,Neoplasm Invasiveness ,Neoplasm Recurrence, Local ,Alleles ,Retrospective Studies - Abstract
The study group was derived from the archive materials of 55 invasive ductal breast cancer (IDC) patients who had undergone breast-preserving surgery (partial mastectomy/ axillary dissection). All patients included in the study had clinically T(1)-2, N0-M0 invasive ductal carcinoma. Genomic DNA species were extracted from paraffin-embedded blocks, and plasminogen activator inhibitor type-1 (PAI-1) gene 4G/5G genotyping was done by polymerase chain reaction (PCR)-restriction fragment length polymorphism (RFLP). Patient demographics, axillary metastasis status, metastatic lymph nodi/total dissected lymph nodes from axilla, histopathologic characteristics of tumors, local recurrences, and survival ratio were assessed. PAI-1 4G/5G genotype frequencies were 4G/4G (64%), 4G/5G (31%), and 5G/5G (5%) in the patient group. According to the results based on frequencies, the demographics were not different. Five-year local recurrence rate of 4G/5G patients was the lowest (2/17, 12%) (P = 0.02). Also five-year distant metastases ratio of 4G/5G patients was the highest (18%) (P = 0.01). Five- and 10-year disease-free survival rates for the 4G/4G, 4G/5G, and 5G/5G groups were 97% and 94%, 82% and 77%, and 100% and 94%, respectively (P = 0.004). The results of this study indicate that the 4G allele in the PAI 1 gene had a negative impact on local recurrence and disease-free survival of patients with clinical T(1)-2N0M0 IDC.
26. Influence of Various Living Donor Kidney Measurements in Relation to Recipient Body Measurements on Posttransplant Allograft Functional Outcomes.
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Kulah E, Ozcelik U, Isiklar I, Cevik H, Bircan HY, Y Karakayali F, and Haberal M
- Subjects
- Adult, Age Factors, Allografts, Computed Tomography Angiography, Female, Humans, Kidney Transplantation adverse effects, Linear Models, Male, Middle Aged, Multivariate Analysis, Organ Size, Predictive Value of Tests, Risk Factors, Time Factors, Treatment Outcome, Body Mass Index, Glomerular Filtration Rate, Kidney diagnostic imaging, Kidney physiopathology, Kidney surgery, Kidney Transplantation methods, Living Donors
- Abstract
Objectives: Donor kidney measurements may affect outcomes of transplanted allografts. We tested allograft and recipient measurements on kidney allograft outcomes. In this study, we compared the effects of kidney allograft volumes, which were measured using computed tomographic angiography before transplant, and allograft weight, which was measured during surgery, in relation to the recipient's body weight and body mass index on kidney function at 6 and 12 months after transplant., Material and Methods: We included 74 patients (40 female and 34 male patients, mean age of 50.42 ± 9.75 y) in this study., Results: Intraoperative allograft weight was 182.68 ± 40.33 g (range, 104-266 g). The allograft volume measured using computed tomographic angiography scanning was 123.34 ± 24.26 mL (range, 78-181 mL). The estimated glomerular filtration rates of the recipients at 6 and 12 months after transplant correlated negatively with age and recipient body mass index but correlated positively with allograft volume/recipient body weight, allograft volume/recipient body mass index, allograft weight, allograft weight/recipient body weight, and allograft weight/recipient body mass index values, as concluded by univariate analyses. From multivariate analyses, we found variables of interest presumed to significantly affect the 12-month estimated glomerular filtration rates, including recipient age, allograft volume/recipient body weight, allograft volume/recipient body mass index, allograft weight, allograft weight/recipient body weight, and allograft weight/recipient body mass index., Conclusions: Transplanted allograft and recipient body values may be used as predictors of estimated glomerular filtration rates 6 and 12 months after transplant.
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- 2018
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27. Penile Plexiform Neurofibroma in a Patient with Neurofibromatosis I.
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Koseoglu H, Demiralay E, and Isiklar I
- Subjects
- Adult, Humans, Male, Neurofibroma, Plexiform pathology, Neurofibromatosis 1 pathology, Penile Neoplasms pathology
- Published
- 2016
28. Fragmented QRS complexes are associated with cardiac fibrosis and significant intraventricular systolic dyssynchrony in nonischemic dilated cardiomyopathy patients with a narrow QRS interval.
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Basaran Y, Tigen K, Karaahmet T, Isiklar I, Cevik C, Gurel E, Dundar C, Pala S, Mahmutyazicioglu K, and Basaran O
- Subjects
- Adult, Cardiomyopathy, Dilated diagnosis, Diagnosis, Differential, Endomyocardial Fibrosis physiopathology, Female, Humans, Ischemia diagnosis, Ischemia diagnostic imaging, Magnetic Resonance Angiography, Male, Radiography, Ventricular Dysfunction diagnosis, Cardiomyopathy, Dilated diagnostic imaging, Echocardiography methods, Endomyocardial Fibrosis diagnostic imaging, Ventricular Dysfunction diagnostic imaging
- Abstract
Background: Myocardial scar causes heterogeneous ventricular activation, which results in fragmentation of QRS complexes on ECG. Myocardial fibrosis in patients with nonischemic cardiomyopathy (NDCM) can be identified as late gadolinium enhancement (LGE) areas on cardiac magnetic resonance (CMR) studies. We investigated the association of fragmented QRS (fQRS) complexes with systolic dyssynchrony and myocardial fibrosis in patients with NDCM., Methods: Twenty patients with NDCM and sinus rhythm who had fQRS complexes were evaluated with CMR. The association of fQRS complexes with LGE and systolic dyssynchrony was investigated., Results: Nineteen patients had significant systolic dyssynchrony with echocardiography. Among 19 patients with significant dyssynchrony, 14 (74%) patients had fQRS complexes in the most delayed contracting segment or one of the dyssynchronous segments, whereas five patients (26%) had fQRS complexes in a lead which is discordant with the dyssynchronous segment on echocardiography. Seventeen patients had LGE in their CMR. Among the 17 patients with LGE; 13 patients (76%) had fQRS complexes concordant with LGE present segments., Conclusion: Fragmentation of QRS complexes on ECG is associated with intraventricular systolic dyssynchrony and subendocardial fibrosis in NDCM patients with a narrow QRS interval and sinus rhythm., (© 2010, Wiley Periodicals, Inc.)
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- 2011
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29. The effect of cardiac fibrosis on left ventricular remodeling, diastolic function, and N-terminal pro-B-type natriuretic peptide levels in patients with nonischemic dilated cardiomyopathy.
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Karaahmet T, Tigen K, Dundar C, Pala S, Guler A, Kilicgedik A, Cevik C, Mahmutyazicioglu K, Isiklar I, and Basaran Y
- Subjects
- Cardiomyopathy, Dilated complications, Echocardiography, Endomyocardial Fibrosis complications, Female, Humans, Male, Middle Aged, Myocardial Ischemia blood, Myocardial Ischemia complications, Myocardial Ischemia diagnosis, Reproducibility of Results, Sensitivity and Specificity, Ventricular Dysfunction, Left complications, Ventricular Remodeling, Cardiomyopathy, Dilated blood, Cardiomyopathy, Dilated diagnosis, Endomyocardial Fibrosis blood, Endomyocardial Fibrosis diagnosis, Natriuretic Peptide, Brain blood, Peptide Fragments blood, Ventricular Dysfunction, Left blood, Ventricular Dysfunction, Left diagnosis
- Abstract
Background: Cardiac fibrosis is common and associated with poor prognosis in patients with heart failure. We investigated the effect of cardiac fibrosis on the left ventricular (LV) diastolic function, functional capacity, LV remodeling, and biochemical parameters in patients with nonischemic dilated cardiomyopathy (NIDC). In addition, we investigated the biochemical and echocardiographic predictors of cardiac fibrosis in this group., Methods and Results: Forty patients with NIDC were enrolled. Cardiac fibrosis was evaluated according to the presence of late gadolinium enhancement (LGE) on cardiac magnetic resonance (CMR) imaging. Nineteen patients had cardiac fibrosis (Group I) and 21 patients did not have cardiac fibrosis (Group II). LV systolic and diastolic parameters were assessed with conventional and tissue Doppler echocardiography. N-terminal pro-B-type natriuretic peptide (NT-pro BNP) levels of each patient were recorded. Patients with cardiac fibrosis had impaired diastolic function, higher functional class and NT-pro BNP levels, and significant LV remodeling than the patients without cardiac fibrosis. A correlation analysis revealed that the cardiac fibrosis severity was associated with functional class, cardiac chamber sizes, NT-pro BNP levels, diastolic parameters such as E/Se. A linear regression analysis demonstrated that NT-pro BNP and E/Se were the independent predictors of cardiac fibrosis., Conclusion: Cardiac fibrosis correlates with impaired LV diastolic function and functional capacity, elevated NT-proBNP levels, and adverse cardiac remodeling in patients with NIDC. Therefore, the assessment of cardiac fibrosis can be useful in the management of these patients., (© 2010, Wiley Periodicals, Inc.)
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- 2010
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30. Diffuse late gadolinium enhancement by cardiovascular magnetic resonance predicts significant intraventricular systolic dyssynchrony in patients with non-ischemic dilated cardiomyopathy.
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Tigen K, Karaahmet T, Kirma C, Dundar C, Pala S, Isiklar I, Cevik C, Kilicgedik A, and Basaran Y
- Subjects
- Cardiomyopathy, Dilated pathology, Echocardiography, Doppler, Female, Fibrosis pathology, Gadolinium, Humans, Image Enhancement, Male, Middle Aged, Myocardium pathology, Systole, Cardiomyopathy, Dilated physiopathology, Magnetic Resonance Imaging, Ventricular Dysfunction, Left physiopathology
- Abstract
Background: Left ventricular dyssynchrony and myocardial fibrosis are common findings in patients with nonischemic dilated cardiomyopathy (NDCM). The aim of this study was to investigate the association between myocardial fibrosis and intraventricular systolic dyssynchrony (DYS-sys) in patients with NDCM., Methods: Thirty-nine patients with NDCM and sinus rhythm were enrolled. Intraventricular DYS-sys was evaluated using Doppler tissue imaging, and cardiac fibrosis was assessed with cardiovascular magnetic resonance imaging with a 17-segment cardiac model. Each segment was graded on a 2-point scale (segmental fibrosis score): 0 = absence of late gadolinium enhancement, and 1 = presence of late gadolinium enhancement. A cardiac fibrosis index was calculated as 17/(17 - sum of fibrotic segments). Receiver operating characteristic analysis was performed to determine the utility of the cardiac fibrosis index to predict intraventricular systolic dyssynchrony., Results: Patients with DYS-sys had larger left atrial size (P = .004) and left ventricular end-systolic (P = .028) and end-diastolic (P = .034) volumes and lower tricuspid annular Doppler tissue imaging peak systolic velocities (P = .037) compared with patients without DYS-sys. A cardiac fibrosis index > or = 1.4 predicted significant DYS-sys with 92% sensitivity and 60% specificity (area under the receiver operating characteristic curve, 0.703; 95% confidence interval, 0.512-0.893; P = .035). Patients with cardiac fibrosis indexes > or = 1.4 (group 1) had larger left ventricular end-systolic (P = .044) and end-diastolic (P = .034) volumes than those with cardiac fibrosis indexes < 1.4 (group 2). Nine of 11 patients (82%) in group 1 and 6 of 28 patients (21%) in group 2 had significant DYS-sys (Pearson's chi(2) = 12.169, P < .0001). Logistic regression analysis revealed that cardiac fibrosis index > or = 1.4 (odds ratio, 11.2; 95% confidence interval, 1.72-71.4; P = .012) was an independent predictor of DYS-sys., Conclusion: Patients with NDCM and prominent cardiac fibrosis have significant DYS-sys. The cardiac fibrosis index is a useful tool to predict DYS-sys., (Copyright 2010 American Society of Echocardiography. Published by Mosby, Inc. All rights reserved.)
- Published
- 2010
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31. Prognostic value of the PAI-1 4G/5G polymorphism in invasive ductal carcinoma of the breast.
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Yagmurdur MC, Atac FB, Tutar NU, Verdi H, Isiklar I, Ozdemir BH, Ozbek N, Karakayali H, and Haberal M
- Subjects
- Alleles, Breast Neoplasms surgery, Carcinoma, Ductal, Breast surgery, Disease-Free Survival, Female, Genotype, Humans, Neoplasm Invasiveness, Neoplasm Recurrence, Local genetics, Prognosis, Retrospective Studies, Statistics, Nonparametric, Turkey, Breast Neoplasms genetics, Carcinoma, Ductal, Breast genetics, Plasminogen Activator Inhibitor 1 genetics, Polymorphism, Genetic
- Abstract
The study group was derived from the archive materials of 55 invasive ductal breast cancer (IDC) patients who had undergone breast-preserving surgery (partial mastectomy/ axillary dissection). All patients included in the study had clinically T(1)-2, N0-M0 invasive ductal carcinoma. Genomic DNA species were extracted from paraffin-embedded blocks, and plasminogen activator inhibitor type-1 (PAI-1) gene 4G/5G genotyping was done by polymerase chain reaction (PCR)-restriction fragment length polymorphism (RFLP). Patient demographics, axillary metastasis status, metastatic lymph nodi/total dissected lymph nodes from axilla, histopathologic characteristics of tumors, local recurrences, and survival ratio were assessed. PAI-1 4G/5G genotype frequencies were 4G/4G (64%), 4G/5G (31%), and 5G/5G (5%) in the patient group. According to the results based on frequencies, the demographics were not different. Five-year local recurrence rate of 4G/5G patients was the lowest (2/17, 12%) (P = 0.02). Also five-year distant metastases ratio of 4G/5G patients was the highest (18%) (P = 0.01). Five- and 10-year disease-free survival rates for the 4G/4G, 4G/5G, and 5G/5G groups were 97% and 94%, 82% and 77%, and 100% and 94%, respectively (P = 0.004). The results of this study indicate that the 4G allele in the PAI 1 gene had a negative impact on local recurrence and disease-free survival of patients with clinical T(1)-2N0M0 IDC.
- Published
- 2008
32. Unusual MDCT and sonography findings in fulminant hepatic failure resulting from hepatitis A infection.
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Cakir B, Teksam M, Tarhan NC, Isiklar I, Tutar NU, Ozcay F, Coskun M, Bilezikci B, and Demirhan B
- Subjects
- Child, Preschool, Diagnosis, Differential, Humans, Liver Failure, Acute diagnostic imaging, Male, Tomography, X-Ray Computed, Ultrasonography, Hepatitis A complications, Liver Failure, Acute virology
- Published
- 2005
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33. Management strategies for patients with nipple discharge.
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Goksel HA, Yagmurdur MC, Demirhan B, Isiklar I, Karakayali H, Bilgin N, and Haberal M
- Subjects
- Adult, Biopsy, Breast pathology, Breast Diseases epidemiology, Breast Neoplasms epidemiology, Case-Control Studies, Endoscopy, Female, Humans, Lactation, Parity, Pregnancy, Risk Factors, Breast Diseases diagnosis, Breast Diseases surgery, Breast Neoplasms diagnosis, Breast Neoplasms surgery, Nipples metabolism
- Abstract
Background and Aims: The aim of this study was to assess management strategies for patients with nipple discharge (ND)., Patients and Methods: The records of 13,443 women with breast-related complaints who were examined by the same surgeon between 1 January 1960 and 31 December 2000 were retrospectively assessed. Patients with ND were grouped according to whether they had had a spontaneous or provoked discharge. The parameters investigated in each group were age, physical findings, number of pregnancies, duration of lactation, duration of discharge, colour of discharge, and histopathological features. Chi-square and Mann-Whitney U-tests were used for statistical analysis., Results: ND was the presenting symptom in 603 (4.5%) of the cases. Two hundred and eighty-seven (48%) of the 603 patients showed spontaneous nipple discharge (SND group) and the other 316 (52%) showed provoked nipple discharge (PND group). In the SND group, 124 (43%) tissue specimens were obtained by either biopsy or sub-areolar exploration. Histopathological examination revealed that the most frequent causes of ND in these cases were intraductal papilloma (49 patients; 40%), intraductal carcinoma (35 patients; 28%), and cystic disease (15 patients; 12%). Twenty tissue specimens were obtained from the group with PND. In these cases, the most frequently identified causes of ND were cystic disease (seven patients; 35%), intraductal papilloma (six patients; 30%), ductal ectasia (two patients; 10%), and carcinoma (one patient; 5%). The SND and PND groups differed significantly with respect to age (P = 0.001) and duration of ND (P = 0.008). The incidence of cancer was higher in the SND specimens than in the PND specimens (28% vs 5%, respectively; P = 0.01). The number of pregnancies was significantly higher and the duration of lactation was significantly longer in the SND group (P = 0.03 and P = 0.02, respectively)., Conclusion: The study confirms previous reports that patients with SND have a higher incidence of carcinoma than those with PND. The results suggest that older age, higher number of pregnancies, and longer duration of lactation may predispose to cancer development in patients with SND. The possibility of breast cancer should also be kept in mind when one is assessing patients with PND. Careful physical examination and close follow-up is the optimal management strategy for patients with any type of ND.
- Published
- 2005
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34. Value of the D-dimer test in diagnosing deep vein thrombosis in rehabilitation inpatients.
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Akman MN, Cetin N, Bayramoglu M, Isiklar I, and Kilinc S
- Subjects
- Arthroplasty, Replacement, Hip adverse effects, Brain Injuries complications, Female, Humans, Male, Prospective Studies, Sensitivity and Specificity, Stroke complications, Ultrasonography, Doppler, Color, Venous Thrombosis diagnostic imaging, Venous Thrombosis etiology, Arthroplasty, Replacement, Hip rehabilitation, Brain Injuries rehabilitation, Fibrin Fibrinogen Degradation Products analysis, Stroke Rehabilitation, Venous Thrombosis diagnosis
- Abstract
Objective: To assess the utility of the D-dimer test-a widely available, less costly, and less time-consuming test than others used to diagnose or exclude deep vein thrombosis (DVT) and pulmonary embolism., Design: Blind comparison., Setting: An inpatient rehabilitation facility in Turkey., Participants: Sixty-eight consecutive inpatients being rehabilitated after stroke, spinal cord injury, hip arthroplasty, or traumatic brain injury., Interventions: A latex D-dimer assay was performed on each patient at admission and then weekly throughout the hospital stay. Color Doppler ultrasonography of the lower limbs was also done for each patient at admission and was repeated when indicated by clinical signs and symptoms of DVT or by elevated D-dimer levels. Main outcome measures Patients' clinical findings, D-dimer test results, and ultrasonography results were recorded. Sensitivity, specificity, and positive and negative predictive values were calculated for the D-dimer test, each clinical finding, and combinations of D-dimer results and clinical findings in relation to DVT diagnosis., Results: The sensitivity and negative predictive value of the D-dimer test were high, at 95.2% and 96.2%, respectively. The specificity and positive predictive value were low, at 55.3% and 48.7%, respectively. No single clinical finding was reliably diagnostic for DVT., Conclusions: The D-dimer assay is a reliable method for ruling out DVT. In the rehabilitation setting, it can be used as a routine screening test or to assess cases of suspected DVT. D-dimer testing may reduce the need for sophisticated, time-consuming, and expensive diagnostic workup of rehabilitation inpatients, a group that is at increased risk for DVT.
- Published
- 2004
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35. Management of bilateral breast carcinoma: long-term results.
- Author
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Goksel HA, Yagmurdur MC, Karakayali H, Moray G, Demirhan B, Isiklar I, Bilgin N, and Haberal M
- Subjects
- Breast Neoplasms diagnosis, Breast Neoplasms mortality, Carcinoma, Ductal mortality, Carcinoma, Ductal surgery, Carcinoma, Lobular mortality, Carcinoma, Lobular surgery, Carcinoma, Papillary mortality, Carcinoma, Papillary surgery, Disease-Free Survival, Female, Humans, Lactation, Lymphatic Metastasis, Middle Aged, Neoplasm Recurrence, Local, Neoplasms, Second Primary diagnosis, Neoplasms, Second Primary mortality, Risk Factors, Breast Neoplasms surgery, Neoplasms, Second Primary surgery
- Abstract
The aim of this study was to document the clinical features and long-term outcomes in 43 cases of bilateral breast carcinoma. All the women were diagnosed by a single surgeon who had evaluated 13,443 patients with breast-related complaints over a 40-year period. At the initial cancer diagnosis, 28 patients (65%) were of premenopausal age (< or = 46 years; group 1) and 15 (35%) were postmenopausal (> 46 years; group 2). The median interval between initial and subsequent cancer was 24 months (range, 12-288 months) in group 1 and 20 months (range, 14-252 months) in group 2 (P > 0.05). The distribution of initial cancer types based on pathological examination was ductal adenocarcinoma in 28 (65%) cases; lobular carcinoma in 5 (12%) cases; comedocarcinoma in 5 (12%) cases; papillary carcinoma in 2 (4.5%) cases; papillary combined with squamous cell carcinoma in 1 (2%) case; and lobular combined with medullary carcinoma in 2 (4.5%) cases. There were no significant differences between the groups with respect to the distribution of types of surgery used for the initial and subsequent carcinomas. Tumor locations were symmetrical in 26 (60%) patients. The mean palpable mass sizes for the initial and subsequent tumors in group 1 were 3 +/- 1.4 (range, 1-8 cm) and 1.3 +/- 0.5 cm (range, 1-2 cm), respectively. The corresponding means for group 2 were 2.3 +/- 1.8 (range, 0.9-7 cm) and 1.3 +/- 0.5 cm (range, 1-2 cm). The 10- and 20-year disease-free survival rates for group 1 versus group 2 were 32% versus 27% and 10% versus 8%, respectively. The rates of axillary lymph node metastasis from the primary cancer in groups 1 and 2 were statistically similar; however, the rate of axillary lymph node metastasis from subsequent cancer in group 1 was significantly higher than that in group 2 (P = 0.02). The lactation period (after each child born) in group 1 was significantly longer than that in group 2 (P = 0.04). Group 1 had a higher rate of distant metastasis at 20 years (P = 0.03), but the groups' local recurrence rates at this stage were similar. Log-rank analysis revealed no significant differences between the groups' 10- and 20-year patient survival rates. Subsequent breast cancer was not detected on mammography in 4 (9%) of the 43 patients. In these cases, the tumors were diagnosed by ultrasonography after physical examination revealed suspicious findings at symmetrical locations. The findings suggest that women who are diagnosed with primary cancer before menopause are at greater risk for distant metastasis than postmenopausal women, when subsequent cancer is detected in the contralateral breast. Herein, the risk for metastasis is only assessed after cancer is detected in the other breast. The premenopausal women had a significantly longer mean lactation period. Extended lactation may be a risk factor for breast cancer development in this age group, but this needs further investigation.
- Published
- 2004
36. Joint pain and arthritis in renal transplant recipients and correlation with cyclosporine therapy.
- Author
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Kart-Köseoglu H, Yücel AE, Isiklar I, Türker I, Akçali Z, and Haberal M
- Subjects
- Adult, Arthralgia chemically induced, Arthralgia epidemiology, Arthritis chemically induced, Arthritis epidemiology, Child, Cyclosporine blood, Female, Humans, Immunosuppressive Agents blood, Kidney Failure, Chronic surgery, Male, Middle Aged, Prevalence, Retrospective Studies, Arthralgia etiology, Arthritis etiology, Cyclosporine adverse effects, Immunosuppressive Agents adverse effects, Kidney Failure, Chronic complications, Kidney Transplantation adverse effects
- Abstract
Objective: The aim of this study was to determine the prevalence of joint pain and arthritis in renal transplant recipients and to investigate relationships with various laboratory and clinical parameters., Methods: Eighty-two patients who underwent renal transplantation (RT) had joint examinations and reported by questionnaire on levels of joint pain and arthritis. Each individual was then followed by the rheumatology department for 1 year, with joint examination and laboratory tests every 3 months., Results: Thirty-one of 82 patients (37.8%) complained of joint pain before RT, of whom seven reported pain continuing after the operation. Seventeen of the 82 (20.7%) began to suffer joint pain after RT. Six (7.3%) and three (3.7%) of the 82 patients, respectively, developed arthritis before and after transplantation., Conclusion: The study showed that joint pain is common before and after RT. In renal transplant recipients, joint pain significantly correlated with serum cyclosporine levels higher than 200 ng/ml.
- Published
- 2003
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37. The effect of cisapride on gallbladder contractility in type II diabetic patients.
- Author
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Gürsoy M, Güvener N, Isiklar I, Tutal E, Ozin B, and Boyacioglu S
- Subjects
- Adult, Biliary Dyskinesia blood, Biliary Dyskinesia diagnostic imaging, Cisapride adverse effects, Diabetes Mellitus, Type 2 blood, Diabetes Mellitus, Type 2 diagnostic imaging, Female, Glycated Hemoglobin metabolism, Humans, Image Processing, Computer-Assisted, Male, Middle Aged, Treatment Outcome, Ultrasonography, Biliary Dyskinesia drug therapy, Cisapride therapeutic use, Diabetes Mellitus, Type 2 drug therapy, Gallbladder Emptying drug effects
- Abstract
Background/aims: To investigate whether diabetics have altered gallbladder motility, and whether cisapride has any effect on gallbladder motility in these patients. The factors associated with abnormal gallbladder contractility, and with the effects of cisapride on gallbladder contractility in diabetics were also evaluated., Methodology: The gallbladder contractility parameters of 20 diabetics and 20 controls were assessed by real time ultrasonography. The same measurements were made after cisapride treatment in diabetics., Results: Fasting gallbladder volume and residual gallbladder volume were statistically higher in the diabetic group than in the controls (P = 0.018 and P = 0.022, respectively). Multivariate analysis also showed a significant association between fasting gallbladder volume and existing diabetes (P = 0.0002). There was a significant positive correlation between level of hemoglobin A1c and fasting gallbladder volume (r = 0.48, P = 0.031). Responders to cisapride treatment had significantly higher hemoglobin A1c levels than nonresponders (6.6 +/- 1.3 vs. 9.1 +/- 1.8, respectively; P = 0.004). Logistic multiple regression analysis revealed that hemoglobin A1c level was the only independent factor that was predictive for efficacy of cisapride treatment., Conclusions: This study demonstrates that diabetics have impaired gallbladder contractility, and that control of diabetes is predictive for gallbladder contractility and response to cisapride therapy in these patients.
- Published
- 2001
38. An unusual sonographic finding in Caroli's disease.
- Author
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Akin O, Isiklar I, Baysal C, and Bilginoglu SE
- Subjects
- Adult, Bile, Cholangiopancreatography, Endoscopic Retrograde, Humans, Male, Ultrasonography, Caroli Disease diagnostic imaging
- Published
- 1998
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39. Radiation-induced rhabdomyosarcoma.
- Author
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Isiklar I and Libshitz HI
- Subjects
- Aged, Aged, 80 and over, Female, Humans, Male, Muscle Neoplasms diagnosis, Muscle Neoplasms etiology, Muscle, Skeletal radiation effects, Radiotherapy adverse effects, Rhabdomyosarcoma diagnosis, Testicular Neoplasms radiotherapy, Time Factors, Neoplasms, Radiation-Induced diagnosis, Rhabdomyosarcoma etiology
- Published
- 1996
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40. Intracranial metastatic melanoma: correlation between MR imaging characteristics and melanin content.
- Author
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Isiklar I, Leeds NE, Fuller GN, and Kumar AJ
- Subjects
- Adult, Aged, Brain metabolism, Brain pathology, Brain Neoplasms pathology, Female, Humans, Immunohistochemistry, Male, Melanoma pathology, Middle Aged, Retrospective Studies, Time Factors, Brain Neoplasms diagnosis, Brain Neoplasms secondary, Magnetic Resonance Imaging instrumentation, Magnetic Resonance Imaging methods, Melanins metabolism, Melanoma diagnosis, Melanoma secondary
- Abstract
Objective: Preliminary reports based on limited numbers of cases have proposed that specific MR imaging patterns may permit a distinction between melanotic and amelanotic brain metastases in melanoma patients. The purpose of this study was to test this hypothesis by categorizing MR images obtained from a large series of patients and correlating the results with the percentage of melanin-containing cells in surgically resected metastases., Subjects and Methods: The MR images of 30 patients with histologically proven intracerebral melanoma were reviewed retrospectively. Precontrast MR images were obtained with T1-weighted spin-echo sequences in axial and sagittal sections and with proton density-weighted and T2-weighted sequences in axial sections. After IV injection of gadopentetate dimeglumine (0.1 mmol/kg of body weight), T1-weighted images were obtained in axial and coronal sections. All patients had undergone gross total resection of the evaluated lesions. MR images of the metastases were reviewed and sorted into four groups on the basis of putative patterns: (1) melanotic pattern--hyperintense in relation to cortex on T1-weighted images, hypointense in relation to cortex on T2-weighted images, and isointense or hyperintense in relation to cortex on proton density-weighted images; (2) amelanotic pattern--hypointense or isointense in relation to cortex on T1-weighted images and hyperintense or isointense in relation to cortex on T2-weighted and proton density-weighted images; (3) indeterminate, or mixed, pattern--MR imaging characteristics that did not conform to those of one of the first two categories; and (4) hematoma pattern--MR imaging features that exhibited only hematoma characteristics. Tissue sections from all evaluated lesions were independently reviewed by a neuropathologist (G.N.F.), and the percentage of melanin-containing tumor cells in each resected metastatic lesion was estimated. The MR imaging data and histologic data were then compared to assess the predictive value of the MR imaging patterns., Results: Forty-two metastatic lesions were identified and categorized by MR imaging pattern as follows: 10 melanotic, 11 indeterminate (mixed), 16 amelanotic, and five hematoma. Correlation with histologic findings revealed that a majority (7/10) of lesions that exhibited a melanotic MR imaging pattern had more than 10% melanin-containing cells, over half (9/16) of lesions that exhibited an amelanotic MR imaging pattern contained histologically identifiable melanin (but always in less than 10% of cells), and lesions that exhibited a mixed MR imaging pattern were either amelanotic or contained less than 10% melanotic cells. Conversely, a majority of lesions containing more than 10% melanotic cells (7/8) demonstrated the typical melanotic MR imaging pattern, lesions with less than 10% melanin-containing cells exhibited a variety of MR imaging patterns, and only about half of patients with amelanotic lesions (6/13) showed the characteristic amelanotic MR imaging pattern. For five lesions, potentially informative imaging data on melanin content was obscured by histologically documented hematoma formation., Conclusion: Only a minority of melanoma metastases have the anticipated MR imaging findings of melanotic melanoma, which consist of high signal intensity relative to that of cortex on T1-weighted images and low signal intensity relative to that of cortex on T2-weighted images. Of tumors that do exhibit this melanotic pattern, the majority have more than 10% melanin-containing cells. The putative MR imaging pattern for amelanotic melanoma is nonspecific, as over half of tumors with this pattern contain melanin.
- Published
- 1995
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41. Different biologic features of desmoid tumors in adult and juvenile patients: MR demonstration.
- Author
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Romero JA, Kim EE, Kim CG, Chung WK, and Isiklar I
- Subjects
- Adolescent, Adult, Biology, Child, Contrast Media, Disease-Free Survival, Follow-Up Studies, Humans, Image Enhancement, Middle Aged, Necrosis, Neoplasm Invasiveness, Neoplasm Recurrence, Local pathology, Retrospective Studies, Fibromatosis, Aggressive pathology, Magnetic Resonance Imaging
- Abstract
Objective: To demonstrate different biologic features of desmoid tumors on MRI between juvenile and adult patients., Materials and Methods: We have retrospectively analyzed clinical records and 121 MRI findings in 40 patients (8 juveniles and 32 adults) with proven desmoid tumors. The Fisher exact test and Kaplan-Meier curve were utilized for statistical analysis., Results: Recurrences in the juvenile patients were more multiple (50 vs 12%) and appeared significantly earlier than in the adult patients. Adult patients demonstrate a much greater recurrence-free rate (p = 0.0001). Infiltrative pattern was significantly predominant in the juvenile patients (63%) whereas the nodular pattern was more frequent in the adult patients (81%). Low-signal intensity zones on T1- and T2-weighted imaging as well as the type of contrast enhancement did not show any significant relationship with biological behavior. Four cases with no significant contrast enhancement showed low signal intensities on T2-weighted imaging., Conclusion: Magnetic resonance demonstrates different biologic features between juvenile and adult patients with histologically same desmoid tumors. These differences may be useful in consideration of MRI follow-up studies.
- Published
- 1995
- Full Text
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