Growth Hormone Therapy in Children with Chronic Renal Failure

Por Cayir, Atilla, Kosan, Celalettin
Publicado no Eurasian J Med (2015)

Cystinosis Presenting with Findings of Bartter Syndrome

Por Özkan, Behzat, Çayır, Atilla, Koşan, Celalettin, Alp, Handan
Publicado em 2011

Anogenital Distance in Turkish Newborns

Por Özkan, Behzat, Konak, Belkıs, Çayır, Atilla, Konak, Murat
Publicado em 2011

Plasma Kisspeptin Levels in Newborn Infants with Breast Enlargement

Por Kaya, Avni, Orbak, Zerrin, Polat, Harun, Çayır, Atilla, Erdil, Abdullah, Döneray, Hakan
Publicado no J Clin Res Pediatr Endocrinol (2015)

An Unusual Congenital Anomaly in Fanconi Aplastic Anemia: Congenital Lobar Emphysema

Por Fettah, Ali, Reis, Gökçe Pınar, Kara, Soner Sertan, Aksu, Tekin, Durur Karakaya, Afak, Subaşı, Mahmut, Çayır, Atilla
Publicado no Turk J Haematol (2016)

The Growth Characteristics of Patients with Noonan Syndrome: Results of Three Years of Growth Hormone Treatment: A Nationwide Multicenter Study

Por Şıklar, Zeynep, Genens, Mikayir, Poyrazoğlu, Şükran, Baş, Firdevs, Darendeliler, Feyza, Bundak, Rüveyde, Aycan, Zehra, Savaş Erdeve, Şenay, Çetinkaya, Semra, Güven, Ayla, Abalı, Saygın, Atay, Zeynep, Turan, Serap, Kara, Cengiz, Can Yılmaz, Gülay, Akyürek, Nesibe, Abacı, Ayhan, Çelmeli, Gamze, Sarı, Erkan, Bolu, Semih, Korkmaz, Hüseyin Anıl, Şimşek, Enver, Çatlı, Gönül, Büyükinan, Muammer, Çayır, Atilla, Evliyaoğlu, Olcay, İşgüven, Pınar, Özgen, Tolga, Hatipoğlu, Nihal, Elhan, Atilla Halil, Berberoğlu, Merih
Publicado no J Clin Res Pediatr Endocrinol (2016)

The phenotypic and molecular genetic spectrum of Alström Syndrome in 44 Turkish kindreds and a literature review of Alström Syndrome in Turkey

Por Ozantürk, Ayşegül, Marshall, Jan D, Collin, Gayle B, Düzenli, Selma, Marshall, Robert P, Candan, Şükrü, Tos, Tülay, Esen, İhsan, Taşkesen, Mustafa, Çayır, Atilla, Öztürk, Şükrü, Üstün, İhsan, Ataman, Esra, Karaca, Emin, Özdemir, Taha Reşid, Erol, İlknur, Eroğlu, Fehime Kara, Torun, Deniz, Parıltay, Erhan, Yılmaz-Güleç, Elif, Karaca, Ender, Atabek, M. Emre, Elçioğlu, Nursel, Satman, İlhan, Möller, Claes, Müller, Jean, Naggert, Jürgen K, Özgül, Rıza Köksal
Publicado no J Hum Genet (2014)

WNT Signaling Perturbations Underlie the Genetic Heterogeneity of Robinow Syndrome

Por White, Janson J., Mazzeu, Juliana F., Coban-Akdemir, Zeynep, Bayram, Yavuz, Bahrambeigi, Vahid, Hoischen, Alexander, van Bon, Bregje W.M., Gezdirici, Alper, Gulec, Elif Yilmaz, Ramond, Francis, Touraine, Renaud, Thevenon, Julien, Shinawi, Marwan, Beaver, Erin, Heeley, Jennifer, Hoover-Fong, Julie, Durmaz, Ceren D., Karabulut, Halil Gurhan, Marzioglu-Ozdemir, Ebru, Cayir, Atilla, Duz, Mehmet B., Seven, Mehmet, Price, Susan, Ferreira, Barbara Merfort, Vianna-Morgante, Angela M., Ellard, Sian, Parrish, Andrew, Stals, Karen, Flores-Daboub, Josue, Jhangiani, Shalini N., Gibbs, Richard A., Brunner, Han G., Sutton, V. Reid, Lupski, James R., Carvalho, Claudia M.B.
Publicado no Am J Hum Genet (2018)