Relationship Between Oxytocin and Attention Deficit Hyperactivity Disorder

by Tuğba Kalyoncu, Burcu Özbaran, Sezen Köse, Hüseyin Onay
Published 2017-09-01

Pompe disease: A case report

by Abdullah Çim, Salih Coşkun, Ahmet Yılmaz, Hüseyin Onay
Published 2015-12-01

Association of vitamin D receptor polymorphisms and type 1 diabetes susceptibility in children: a meta-analysis

by Ozlem Atan Sahin, Damla Goksen, Aysel Ozpinar, Muhittin Serdar, Huseyin Onay
Published 2017-03-01

Mannose-binding lectin gene polymorphism and chronic hepatitis B infection in children

by Gulin Erdemir, Tanju B Ozkan, Taner Ozgur, Ferah Budak, Sara S Kilic, Huseyin Onay
Published 2015-01-01

Bannayan-Riley-Ruvalcaba Syndrome in a Case Evaluated Due to Multinodular Goiter

by Özlem Korkmaz, Samim Özen, Hüseyin Onay, Ahmet Çelik, Yeşim Ertan, Damla Gökşen, Şükran Darcan
Published 2018-12-01

Comprehensive Analysis of Deafness Genes in Families with Autosomal Recessive Nonsyndromic Hearing Loss.

by Tahir Atik, Huseyin Onay, Ayca Aykut, Guney Bademci, Tayfun Kirazli, Mustafa Tekin, Ferda Ozkinay
Published 2015-01-01

Fabry disease: An overlooked diagnosis in adult cardiac patients

by Meral Kayıkçıoğlu, Evrim Şimşek, Sema Kalkan Uçar, Selen Bayraktaroğlu, Hüseyin Onay, Eser Sözmen, Mahmut Çoker
Published 2017-09-01

Clinical, Biochemical and Molecular Characteristics of Fifteen Patients with Mucopolysaccharidosis Type II in Western Turkey

by Havva Yazıcı, Ebru Canda, Esra Er, Sema Kalkan Uçar, Hüseyin Onay, Ferda Özkınay, Mahmut Çoker
Published 2018-03-01

A novel mutation and in vivo confocal microscopic findings in Fabry disease

by Cumali Degirmenci, Suzan Guven Yilmaz, Huseyin Onay, Melis Palamar, Sema Kalkan Ucar, Meral Kayikcioglu, Mahmut Coker
Published 2017-01-01

Aromatase Deficiency in Two Siblings with 46,XX Karyotype Raised as Different Genders: A Novel Mutation (p.R115X) in the CYP19A1 Gene

by Samim Özen, Tahir Atik, Özlem Korkmaz, Hüseyin Onay, Damla Gökşen, Ferda Özkınay, Özgür Çoğulu, Şükran Darcan
Published 2020-03-01

A Remarkable Coexistence of Systemic Capillary Leak Syndrome and Diabetes in an 11-Year-Old Boy: A Case Report and Review of the Literature

by Aysun Ata, Samim Özen, Damla Gökşen, Neslihan Edeer Karaca, Güzide Aksu, Necil Kütükçüler, Hüseyin Onay, Şükran Darcan
Published 2020-01-01

A Neurofibromatosis Noonan Syndrome Patient Presenting with Abnormal External Genitalia

by Esra Işık, Hüseyin Onay, Tahir Atik, Aslı Ece Solmaz, Samim Özen, Özgür Çoğulu, Şükran Darcan, Ferda Özkınay
Published 2020-03-01

Initial and Final Status of the Patients with Niemann Pick A and B: Ege University Experience

by Ebru Canda, Havva Yazıcı, Esra Er, Sema Kalkan Uçar, Hüseyin Onay, Eser Sözmen, Ferda Özkınay, Mahmut Çoker
Published 2018-03-01

A hereditary angioedema screening in two villages, based on an index case, and identification of a novel mutation, “1033G>T”, at the SERPING1 gene

by Mehmet Ozkars, Ozlem Keskın, Nazan Bayram, Huseyin Onay, Mehmet Keskın, Hasan Bayram, Yavuz Sahın, Ercan Küçükosmanoğlu, Serkan Kırık
Published 2019-08-01

A Novel Androgen Receptor Gene Mutation in a 46,XY Patient: Complete Androgen Insensitivity Syndrome

by Hale Tuhan, MD, Ayhan Abaci, MD, Ayca Aykut, MD, Ahmet Anik, MD, Hüseyin Onay, MD, Ece Bober, MD
Published 2016-01-01

Homozygous LMNA p.R582H pathogenic variant reveals increasing effect on the severity of fat loss in lipodystrophy

by Utku Erdem Soyaltin, Ilgin Yildirim Simsir, Baris Akinci, Canan Altay, Suleyman Cem Adiyaman, Kristen Lee, Huseyin Onay, Elif Arioglu Oral
Published 2020-07-01

Pregnancy-associated plasma protein A gene polymorphism in pregnant women with preeclampsia and intrauterine growth restriction

by Sultan Ozkan, Cem Yasar Sanhal, Ozgur Yeniel, Esra Arslan Ates, Mete Ergenoglu, Birol Bınbır, Huseyin Onay, Ferda Ozkınay, Sermet Sagol
Published 2015-10-01

Clinical, Neuroimaging, and Genetic Features of the Patients with L-2-Hydroxyglutaric Aciduria

by Ebru Canda, Melis Köse, Havva Yazıcı, Esra Er, Cenk Eraslan, Ferda Özkınay, Mahmut Çoker, Sema Kalkan Uçar, Sara Habif, Emin Karaca, Hüseyin Onay
Published 2018-03-01

Tetrahydrobiopterin deficiencies: Lesson from clinical experience

by Ayse Ergul Bozaci, Esra Er, Havva Yazici, Ebru Canda, Sema Kalkan Uçar, Merve Güvenc Saka, Cenk Eraslan, Hüseyin Onay, Sara Habif, Beat Thöny, Mahmut Coker
Published 2021-05-01

Clinical and Molecular Spectrum of Tuberous Sclerosis Complex Patients: Identification of Three Novel Mutations

by Esra Işık, Hüseyin Onay, Tahir Atık, Aslı Ece Solmaz, Demet Terek, Sarenur Gökben, Hasan Tekgül, Ertürk Levent, Mehmet Kantar, Nilgün Kültürsay, Özgür Çoğulu, Ferda Özkınay
Published 2020-12-01