Growth Hormone Therapy in Children with Chronic Renal Failure

von Cayir, Atilla, Kosan, Celalettin
Veröffentlicht in Eurasian J Med (2015)

Evaluation of Hearing in Children with Metabolic Syndrome

von Kılıç, Korhan, Sakat, Muhammed Sedat, Çayır, Atilla
Veröffentlicht in Turk Arch Otorhinolaryngol (2018)

Cystinosis Presenting with Findings of Bartter Syndrome

von Özkan, Behzat, Çayır, Atilla, Koşan, Celalettin, Alp, Handan
Veröffentlicht 2011

Anogenital Distance in Turkish Newborns

von Özkan, Behzat, Konak, Belkıs, Çayır, Atilla, Konak, Murat
Veröffentlicht 2011

Plasma Kisspeptin Levels in Newborn Infants with Breast Enlargement

von Kaya, Avni, Orbak, Zerrin, Polat, Harun, Çayır, Atilla, Erdil, Abdullah, Döneray, Hakan
Veröffentlicht in J Clin Res Pediatr Endocrinol (2015)

Bone mineral density and vitamin K status in children with celiac disease: Is there a relation?

von Volkan, Burcu, Fettah, Ali, İşlek, Ali, Kara, Soner Sertan, Kurt, Nezahat, Çayır, Atilla
Veröffentlicht in Turk J Gastroenterol (2018)

The Relationship between Psychopathology, Self-esteem, Body Perception and Serum Sex Steroids in Pubertal Gynecomastia

von Arslan, Semiha Comertoglu, Esin, Ibrahim Selcuk, Cayır, Atilla, Orbak, Zerrin, Dursun, Onur Burak
Veröffentlicht in Clin Psychopharmacol Neurosci (2021)

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

von Fettah, Ali, Reis, Gökçe Pınar, Kara, Soner Sertan, Aksu, Tekin, Durur Karakaya, Afak, Subaşı, Mahmut, Çayır, Atilla
Veröffentlicht in Turk J Haematol (2016)

Identification of Three Novel and One Known Mutation in the WFS1 Gene in Four Unrelated Turkish Families: The Role of Homozygosity Mapping in the Early Diagnosis

von Sherif, Maha, Demirbilek, Hüseyin, Çayır, Atilla, Tahir, Sophia, Çavdarlı, Büşra, Demiral, Meliha, Cebeci, Ayşe Nurcan, Vurallı, Doğuş, Rahman, Sofia Asim, Unal, Edip, Büyükyılmaz, Gönül, Baran, Riza Taner, Özbek, Mehmet Nuri, Hussain, Khalid
Veröffentlicht in J Clin Res Pediatr Endocrinol (2021)

Comparison of Treatment Regimens in Management of Severe Hypercalcemia Due to Vitamin D Intoxication in Children

von Demir, Korcan, Döneray, Hakan, Kara, Cengiz, Atay, Zeynep, Çetinkaya, Semra, Çayır, Atilla, Anık, Ahmet, Eren, Erdal, Uçaktürk, Ahmet, Can Yılmaz, Gülay, Törel Ergür, Ayça, Kendirci, Mustafa, Aycan, Zehra, Bereket, Abdullah, Aydın, Murat, Orbak, Zerrin, Özkan, Behzat
Veröffentlicht in J Clin Res Pediatr Endocrinol (2019)

Novel Mutations in Obesity-related Genes in Turkish Children with Non-syndromic Early Onset Severe Obesity: A Multicentre Study

von Akıncı, Ayşehan, Türkkahraman, Doğa, Tekedereli, İbrahim, Özer, Leyla, Evren, Bahri, Şahin, İbrahim, Kalkan, Tarkan, Çürek, Yusuf, Çamtosun, Emine, Döğer, Esra, Bideci, Aysun, Güven, Ayla, Eren, Erdal, Sangün, Özlem, Çayır, Atilla, Bilir, Pelin, Törel Ergür, Ayça, Ercan, Oya
Veröffentlicht in J Clin Res Pediatr Endocrinol (2019)

Management of Thyrotoxicosis in Children and Adolescents: A Turkish Multi-center Experience

von Esen, İhsan, Bayramoğlu, Elvan, Yıldız, Melek, Aydın, Murat, Karakılıç Özturhan, Esin, Aycan, Zehra, Bolu, Semih, Önal, Hasan, Kör, Yılmaz, Ökdemir, Deniz, Ünal, Edip, Önder, Aşan, Evliyaoğlu, Olcay, Çayır, Atilla, Taştan, Mehmet, Yüksel, Ayşegül, Kılınç, Aylin, Büyükinan, Muammer, Özcabı, Bahar, Akın, Onur, Binay, Çiğdem, Kılınç, Suna, Yıldırım, Ruken, Hatun Aytaç, Emel, Sağsak, Elif
Veröffentlicht in J Clin Res Pediatr Endocrinol (2019)

Clinical Characteristics and Long-term Follow-up of Patients with Diabetes Due To PTF1A Enhancer Mutations

von Demirbilek, Huseyin, Cayir, Atilla, Flanagan, Sarah E, Yıldırım, Ruken, Kor, Yılmaz, Gurbuz, Fatih, Haliloğlu, Belma, Yıldız, Melek, Baran, Rıza Taner, Akbas, Emine Demet, Demiral, Meliha, Ünal, Edip, Arslan, Gulcin, Vuralli, Dogus, Buyukyilmaz, Gonul, Al-Khawaga, Sara, Saeed, Amira, Al Maadheed, Maryam, Khalifa, Amel, Onal, Hasan, Yuksel, Bilgin, Ozbek, Mehmet Nuri, Bereket, Abdullah, Hattersley, Andrew T, Hussain, Khalid, De Franco, Elisa
Veröffentlicht in J Clin Endocrinol Metab (2020)

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

von 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
Veröffentlicht in 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

von 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
Veröffentlicht in J Hum Genet (2014)

Nationwide Turkish Cohort Study of Hypophosphatemic Rickets

von Şıklar, Zeynep, Turan, Serap, Bereket, Abdullah, Baş, Firdevs, Güran, Tülay, Akberzade, Azad, Abacı, Ayhan, Demir, Korcan, Böber, Ece, Özbek, Mehmet Nuri, Kara, Cengiz, Poyrazoğlu, Şükran, Aydın, Murat, Kardelen, Aslı, Tarım, Ömer, Eren, Erdal, Hatipoğlu, Nihal, Büyükinan, Muammer, Akyürek, Nesibe, Çetinkaya, Semra, Bayramoğlu, Elvan, Selver Eklioğlu, Beray, Uçaktürk, Ahmet, Abalı, Saygın, Gökşen, Damla, Kor, Yılmaz, Ünal, Edip, Esen, İhsan, Yıldırım, Ruken, Akın, Onur, Çayır, Atilla, Dilek, Emine, Kırel, Birgül, Anık, Ahmet, Çatlı, Gönül, Berberoğlu, Merih
Veröffentlicht in J Clin Res Pediatr Endocrinol (2020)

WNT Signaling Perturbations Underlie the Genetic Heterogeneity of Robinow Syndrome

von 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.
Veröffentlicht in Am J Hum Genet (2018)