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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Mannose-binding lectin gene codon 54 polymorphism susceptible to brucellosis in Turkish children by Nuri Bayram, Ferda Ozkinay, Hüseyin Onay, Dilek Yilmaz-Ciftdoğan, Senem Tufan, Fadil Vardar

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Persistent moderate methylmalonic aciduria in a patient with methylmalonyl CoA epimerase deficiency by Havva Yazıcı, Ebru Canda, Hüseyin Onay, Sema Kalkan Uçar, Sara Habif, Mahmut Çoker

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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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Association of Helicobacter pylori-associated Duodenal Ulcer and Precancerous Findings with Toll-like Receptor-4 Asp299Gly and Toll-like Receptor-9 123T/C Polymorphism and Cag-A, V... by Ayşegül Cebe Tok, Hasan Erhun Kasırga, Hörü Gazi, Hüseyin Onay, Ferda Özkınay, Semin Ayhan

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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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Ocular Manifestations of Fabry Disease: Report from a Tertiary Eye Care Center in Türkiye by İlayda Korkmaz, Sema Kalkan Uçar, Hüseyin Onay, Eser Yıldırım Sözmen, Mahmut Çoker, Melis Palamar

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Association between mannose binding lectin polymorphisms and predisposition to bacterial meningitis by Fadil Vardar, Sacide Pehlivan, Hüseyin Onay, Füsun Atlihan, Nesrin Güliz, Cihangir Ozkinay, 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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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

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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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Evaluation of Coronavirus Disease 2019-Related Morbidity and Mortality in Lipodystrophy Patients During the Pandemic Period by Gökçen Güngör Semiz, Tevfik Demir, Ilgın Yıldırım Şimşir, İsmail Selimoğlu, Müge Yılmaz, Hülya Ellidokuz, Hüseyin Onay, Ramazan Gen, Bahri Evren

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Mannose-binding lectin may affect pregnancy outcome by Şebnem Çalkavur, Fuat Akercan, Ferda Özkınay, Güzide Aksu, Osman Zekioğlu, Mehmet Yalaz, Özge Altun Köroğlu, Hüseyin Onay, Gülin Erdemir, Nilgün Kültürsay

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Congenital Disorder of Glycosylation: Clinical and Molecular Characteristics of 9 Patients from Turkey by Melis Kose, Engin Kose, Mehtap Kagnici, Hande Gazeteci Tekin, Burçin Ozen, Taha Reşid Ozdemir, Özgür Kirbiyik, Huseyin Onay, Ünsal Yilmaz, Aycan Unalp

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