Evaluation of the etiology of epilepsy and/or developmental delay in children via next-generation sequencing: a single-center experience by Handan Kava, Ozlem Akgun-Dogan, Ozlem Akgun-Dogan, Ozlem Akgun-Dogan, Ahmet Yesilyurt, Yasemin Alanay, Yasemin Alanay, Yasemin Alanay, Ugur Isik

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Clinical findings and molecular diagnosis in children with Bardet-Biedl Syndrome in Turkey: Identification of novel variants by Özlem Akgün Doğan, Nihat Buğra Ağaoğlu

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Varicella-Related Hospitalizations Among Immunocompetent and Immunocompromised Children in Pre-Vaccine Era: A Tertiary Care Center Experience in Turkey by Özlem Akgün Doğan, Seda Topçu, Naciye Gönül Tanır

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Anauxetic dysplasia: A rare clinical entity by Özlem Akgün-Doğan, Pelin Özlem Şimsek-Kiper, Gülen Eda Utine, Koray Boduroğlu

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Impact of deep phenotyping: high diagnostic yield in a diverse pediatric population of 172 patients through clinical whole-genome sequencing at a single center by Ozlem Akgun-Dogan, Ozlem Akgun-Dogan, Ozlem Akgun-Dogan, Ecenur Tuc Bengur, Ecenur Tuc Bengur, Beril Ay, Gulsah Sebnem Ozkose, Gulsah Sebnem Ozkose, Emre Kar, Fuat Baris Bengur, Aybike S. Bulut, Aybike S. Bulut, Ayca Yigit, Ayca Yigit, Eylul Aydin, Eylul Aydin, Fatma Nisa Esen, Ozkan Ozdemir, Ozkan Ozdemir, Ahmet Yesilyurt, Yasemin Alanay, Yasemin Alanay, Yasemin Alanay

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Peters Plus syndrome: a recognizable clinical entity by Gizem Ürel Demir, Naz Güleray Lafcı, Özlem Akgün Doğan, Pelin Özlem Şimşek-Kiper, Gülen Eda Utine

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Responding to COVID-19 in Istanbul: Perspective from genomic laboratory by Levent Doganay, Nihat Bugra Agaoglu, Arzu Irvem, Gizem Alkurt, Jale Yildiz, Betsi Kose, Yasemin Kendir, Ozlem Akgun Dogan, Gizem Dinler Doganay

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Obstacles and expectations of rare disease patients and their families in Türkiye: ISTisNA project survey results by Ozden Hatirnaz Ng, Ozden Hatirnaz Ng, Ozden Hatirnaz Ng, Ilayda Sahin, Yucel Erbilgin, Ozkan Ozdemir, Ozkan Ozdemir, Emrah Yucesan, Nazli Erturk, Merve Yemenici, Ozlem Akgun Dogan, Ozlem Akgun Dogan, Sibel Aylin Ugur Iseri, Ilhan Satman, Ilhan Satman, Yasemin Alanay, Yasemin Alanay, Yasemin Alanay, Ugur Ozbek, Ugur Ozbek, Ugur Ozbek

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Rapid genome sequencing for critically ill infants: an inaugural pilot study from Turkey by Bengisu Guner Yilmaz, Ozlem Akgun-Dogan, Ozlem Akgun-Dogan, Ozlem Akgun-Dogan, Ozkan Ozdemir, Ozkan Ozdemir, Ozkan Ozdemir, Bayram Yuksel, Ozden Hatirnaz Ng, Ozden Hatirnaz Ng, Kaya Bilguvar, Kaya Bilguvar, Beril Ay, Gulsah Sebnem Ozkose, Eylul Aydin, Ayca Yigit, Aybike Bulut, Fatma Nisa Esen, Serdar Beken, Selma Aktas, Atalay Demirel, Baran Cengiz Arcagok, Ebru Kazanci, İbrahim Bingol, Ozge Umur, Guntulu Sik, Ugur Isik, Melike Ersoy, Ayse Korkmaz, Agop Citak, Adil Mardinoglu, Adil Mardinoglu, Adil Mardinoglu, Ugur Ozbek, Ugur Ozbek, Ugur Ozbek, Yasemin Alanay, Yasemin Alanay, Yasemin Alanay

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Magnetic resonance imaging based kidney volume assessment for risk stratification in pediatric autosomal dominant polycystic kidney disease by Kubra Yilmaz, Seha Saygili, Nur Canpolat, Ozlem Akgun-Dogan, Zeynep Nagehan Yuruk Yildirim, Rumeysa Yasemin Cicek-Oksuz, Huseyin Adil Oner, Bagdagul Aksu, Nazli Gulsum Akyel, Ozge Oguzhan-Hamis, Hasan Dursun, Sevgi Yavuz, Neslihan Cicek, Nurver Akinci, Esra Karabag Yilmaz, Ayse Agbas, Ahmet Nevzat Nayir, Dildar Konukoglu, Sebuh Kurugoglu, Lale Sever, Salim Caliskan

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