The Effects of Neurokinin B upon Gonadotrophin Release in Male Rodents von Corander, M. P., Challis, B. G., Thompson, E. L., Jovanovic, Z., Loraine Tung, Y. C., Rimmington, D., Huhtaniemi, I. T., Murphy, K. G., Topaloglu, A. K., Yeo, G. S. H., O'Rahilly, S., Dhillo, W. S., Semple, R. K., Coll, A. P.

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Novel inactivating mutations of the DCAF17 gene in American and Turkish families cause male infertility and female subfertility in the mouse model von Gurbuz, F., Desai, S., Diao, F., Turkkahraman, D., Wranitz, F., Wood‐Trageser, M., Shin, Y.‐H., Kotan, L.D., Jiang, H., Witchel, S., Gurtunca, N., Yatsenko, S., Mysliwec, D., Topaloglu, K., Rajkovic, A.

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The Investigation of Plasma Glucagon-like Peptide-1 Levels in Newly Diagnosed Type 1 Diabetic Children von Uslu, B, Gurbuz, F, Temiz, F, Yuksel, B, Mungan, N, Topaloglu, A K

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Ambulatory Blood Pressure Monitoring and Serum Nitric Oxide Concentration in Type 1 Diabetic Children von HOROZ, Ozden O, YUKSEL, Bilgin, BAYAZIT, Aysun K, ATTILA, Gulen, SERTDEMIR, Yasar, MUNGAN, Neslihan O, TOPALOGLU, Ali K, OZER, Guler

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Twenty novel mutations in the alpha-galactosidase A gene causing Fabry disease von Topaloglu, A K, Ashley, G A, Tong, B, Shabbeer, J, Astrin, K H, Eng, C M, Desnick, R J

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Neurokinin B Signalling in Human Puberty von Topaloglu, A. K., Kotan, L. D., Yuksel, B.

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Growth hormone and insulin-like growth factor 1 levels and their relation to survival in children with bacterial sepsis and septic shock von Önenli-Mungan, N, Yildizdas, D, Yapicioglu, H, Topaloglu, AK, Yüksel, B, Özer, G

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Crigler-Najjar syndrome type II caused by a homozygous triple mutation [T-3279G, A(TA)7TAA, and H39D] of UGT1A1 von MARUO, Yoshihiro, TOPALOGLU, Ali K, TAKAHASHI, Hiroko, MORI, Asami, IWAI, Masaru, DUZOVALI, Oznur, YAMAMOTO, Kazuo, MATUI, Katsuyuki, SATO, Hiroshi, TAKEUCHI, Yoshihiro

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Urinary N-acetyl-beta-D-glucosaminidase activity in type I diabetes mellitus von MUNGAN, N, YUKSEL, B, BAKMAN, M, TOPALOGLU, A. K, OZER, G

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Bone calcium changes during diabetic ketoacidosis: A comparison with lactic acidosis due to volume depletion von Topaloglu, A. Kemal, Yildizdas, Dincer, Yilmaz, H. Levent, Mungan, Neslihan O., Yuksel, Bilgin, Ozer, Guler

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S119: Which must be prefered to provide better comfort for both patient and doctor? Flexible or rigid cystoscopy von Erdem, M.R, Topaloglu, K, Yucebas, O.E, Sengor, F, Aslan, A.R, Tosun, C

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Prenatal molecular diagnosis of severe ornithine carbamoyltransferase deficiency due to a novel mutation, E181G von Topaloglu, A. K., Sansaricq, C., Fox, J. E., Bale, A. E., Tuchman, M., Desnick, R. J.

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Lack of association between plasma leptin levels and appetite in children with iron deficiency von Topaloglu, A.Kemal, Hallioglu, Olgu, Canim, Ali, Duzovali, Oznur, Yilgor, Esat

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Congenital Adrenal Hyperplasia and Bilateral Ovarian Cysts in a Neonate von Topaloglu, A. Kemal, Vade, Aruna, Zeller, W. Patrick

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Evaluation of Cerebral Maturation by Visual and Quantitative Analysis of Resting Electroencephalography in Children With Primary Nocturnal Enuresis von Hallioglu, Olgu, Ozge, Aynur, Comelekoglu, Ulku, Topaloglu, Ali Kemal, Kanik, Arzu, Duzovali, Oznur, Yilgor, Esat

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Influence of metabolic control on growth in homocystinuria due to cystathionine B-synthase deficiency von TOPALOGLU, Ali Kemal, SANSARICQ, Claude, SNYDERMAN, Selma E

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Wolcott-rallison syndrome: Clinical, genetic, and functional study of EIF2AK3 mutations and suggestion of genetic heterogeneity von SENEE, Valérie, VATTEM, Krishna M, MICHAUD, Jacques L, BIN-ABBAS, Bassan, TAHA, Doris, ZABEL, Bernard, FRANCESCHINI, Piergiorgio, TOPALOGLU, A. Kemal, LATHROP, G. Mark, BARRETT, Timothy G, NICOLINO, Marc, WEK, Ronald C, DELEPINE, Marc, JULIER, Cécile, RAINBOW, Lynn A, HATON, Céline, LECOQ, Annick, SHAW, Nick J, ROBERT, Jean-Jacques, ROOMAN, Raoul, DIATLOFF-ZITO, Catherine

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Chronic mercury intoxication simulating pheochromocytoma: Effect of captopril on urinary mercury excretion von Kosan, Celalettin, Topaloglu, A Kemal, Ozkan, Behzat

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Neurokinin B Signalling in Human Puberty: The 7th International Congress of NEUROENDOCRINOLOGY, July, 11-15, 2010, Rouen, France: Special issue containing reviews based on: Plenary... von TOPALOGLU, A. K, KOTAN, L. D, YUKSEL, B

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Molecular Genetic Analysis of Normosmic Hypogonadotropic Hypogonadism in a Turkish Population: Identification and Detailed Functional Characterization of a Novel Mutation in the Go... von Topaloglu, A. Kemal, Lu, Zhi-Liang, Farooqi, I. Sadaf, Mungan, Neslihan O., Yuksel, Bilgin, O'Rahilly, Stephen, Millar, Robert P.

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