Clinical and Molecular Genetic Analysis in Three Children with Wolfram Syndrome: A Novel WFS1 Mutation (c.2534T>A)

por Çelmeli, Gamze, Türkkahraman, Doğa, Çürek, Yusuf, Houghton, Jayne, Akçurin, Sema, Bircan, İffet
Publicado 2017

Pyridoxine-Responsive Seizures in Infantile Hypophosphatasia and a Novel Homozygous Mutation in ALPL Gene

por Güzel Nur, Banu, Çelmeli, Gamze, Manguoğlu, Esra, Soyucen, Erdoğan, Bircan, İffet, Mıhçı, Ercan
Publicado 2016

Basal Serum Neurokinin B Levels in Differentiating Idiopathic Central Precocious Puberty from Premature Thelarche

por Parlak, Mesut, Türkkahraman, Doğa, Ellidağ, Hamit Yaşar, Çelmeli, Gamze, Parlak, Ayşe Eda, Yılmaz, Necat
Publicado 2017

Remarkable Increase in the Prevalence of Overweight and Obesity Among School Age Children in Antalya, Turkey, Between 2003 and 2015

por Çelmeli, Gamze, Çürek, Yusuf, Arslan Gülten, Zümrüt, Yardımsever, Mehmet, Koyun, Mustafa, Akçurin, Sema, Bircan, İffet
Publicado 2019

The Results of 16 Years of Iodization: Assessment of Iodine Deficiency Among School-age Children in Antalya, Turkey

por Çelmeli, Gamze, Çürek, Yusuf, Özen Kücükçetin, İkbal, Arslan Gülten, Zümrüt, Özdem, Sebahat, Akçurin, Sema, Bircan, İffet
Publicado 2020

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 2016