Relationship Between Oxytocin and Attention Deficit Hyperactivity Disorder by Tuğba Kalyoncu, Burcu Özbaran, Sezen Köse, Hüseyin Onay

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Griscelli Syndrome Presented with Status Epilepticus and Hemophagocytic Lymphohistiocytosis by Fatih Demircioğlu, Hilal Aydın, Mustafa Erkoçoğlu, Hüseyin Önay, Emine Dağıstan

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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

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Lipemia Retinalis Diagnosed Incidentally After Laser Photocoagulation Treatment for Retinopathy of Prematurity by Taylan Öztürk, Ezgi Karataş Yiğitaslan, Pelin Teke Kısa, Hüseyin Onay, Ali Osman Saatci

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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

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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

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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

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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

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Metreleptin Treatment in a Boy with Congenital Generalized Lipodystrophy due to Homozygous c.465_468delGACT (p.T156Rfs*8) Mutation in the BSCL2 Gene: Results From the First-year by Şervan Özalkak, Meliha Demiral, Edip Ünal, Funda Feryal Taş, Hüseyin Onay, Hüseyin Demirbilek, Mehmet Nuri Ozbek

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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

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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

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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

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Investigation of the molecular genetic causes of non-syndromic primary ovarian ınsufficiency by next generation sequencing analysis by Eren Er, Semih Aşıkovalı, Hatice Özışık, Elif Sağsak, Damla Gökşen, Hüseyin Onay, Füsun Saygılı, Şükran Darcan, Samim Özen

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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

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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

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Clinical spectrum of early onset “Mediterranean” (homozygous p.P131L mutation) mitochondrial neurogastrointestinal encephalomyopathy by Sema Kalkan Uçar, Havva Yazıcı, Ebru Canda, Esra Er, Fatma Derya Bulut, Cenk Eraslan, Hüseyin Onay, Bridget Elizabeth Bax, Mahmut Çoker

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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

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Epidemiological analysis of Leishmania tropica strains and giemsa-stained smears from Syrian and Turkish leishmaniasis patients using multilocus microsatellite typing (MLMT). by Mehmet Karakuş, Abed Nasereddin, Hüseyin Onay, Emin Karaca, Ahmet Özkeklikçi, Charles L Jaffe, Katrin Kuhls, Ahmet Özbilgin, Hatice Ertabaklar, Samiye Demir, Yusuf Özbel, Seray Töz

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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

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Quality of Life and Psychological Well-being in Children and Adolescents with Disorders of Sex Development by Birsen Şentürk Pilan, Burcu Özbaran, Didem Çelik, Tuğçe Özcan, Samim Özen, Damla Gökşen, İbrahim Ulman, Ali Avanoğlu, Sibel Tiryaki, Hüseyin Onay, Özgür Çoğulu, Ferda Özkınay, Şükran Darcan

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