Huseyin Onay - Medical Faculty, Ege University

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Papers共 365 篇Author StatisticsCo-AuthorSimilar Experts

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A case of alström syndrome with a novel variant in alms1 gene presenting with cone rod dystrophy as first finding

Busra Yen,Mukaddes Damla Ciftci,Filiz Afrashi,Huseyin Onay,Damla Goksen

Retinal cases & brief reports (2024)

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Multinational experience with next-generation sequencing: opportunity to identify transthyretin cardiac amyloidosis and Fabry disease

Sandra Marques E Silva, Andrea Virginia Ferreira Chaves, Murillo Antunes, Juan Pablo Costabel, Armando Alves da Fonseca, Adriana Furtado,Juan Esteban Gomez-Mesa, Francisco Javier Marin Gutiérrez, Oren Caspi,Irina Maksimova,Manish Maski,Cecilia Micheletti,

Cardiovascular diagnosis and therapyno. 2 (2024): 294-303

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Investigation of the molecular genetic causes of non-syndromic primary ovarian insufficiency by next generation sequencing analysis

Eren Er,Semih Asikovali,Hatice Ozisik,Elif Sagsak,Damla Goksen,Huseyin Onay,Fusun Saygili,Sukran Darcan,Samim Ozen

ARCHIVES OF ENDOCRINOLOGY METABOLISM（2024）

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Congenital sucrase-isomaltase deficiency in Trkiye; a single center experience

Dogan Barut,Ezgi Kiran Tasci, Bora Kunay,Burcu Guven,Betul Aksoy,Yeliz Cagan Appak,Miray Karakoyun,Funda Cetin,Ayse Selimoglu,Huseyin Onay,Sema Aydogdu

SCANDINAVIAN JOURNAL OF GASTROENTEROLOGYno. 6 (2024): 647-651

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Ocular Manifestations of Fabry Disease: Report from a Tertiary Eye Care Center in Türkiye

İlayda Korkmaz,Sema Kalkan Uçar,Hüseyin Onay,Eser Yıldırım Sözmen,Mahmut Çoker,Melis Palamar

Turkish journal of ophthalmologyno. 3 (2024): 127-132

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Molecular Genetic Diagnosis with Targeted Next Generation Sequencing in a Cohort of Turkish Osteogenesis Imperfecta Patients and Their Genotype-phenotype Correlation

Samim Özen,Damla Gökşen,Ferda Evin,Esra Işık,Hüseyin Onay,Bilçağ Akgün,Aysun Ata,Tahir Atik, Füsun Düzcan,Ferda Özkınay,Şükran Darcan,Özgür Çoğulu

Journal of clinical research in pediatric endocrinology (2024)

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Facilitating intrafamily communication to enable earlier diagnosis of Fabry disease in relatives: Expert opinion

Dominique P. Germain, Fathiya Al Murshedi,Fatma Al Jasmi,Gheona Altarescu,Olga Azevedo,Fellype C. Barreto,Fatih Ezgu,Dawn A. Laney,Sergey Moiseev,Kotaro Nochioka,Yan Ouyang,Huseyin Onay,

MOLECULAR GENETICS AND METABOLISMno. 2 (2024)

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Effectiveness of whole exome sequencing analyses in the molecular diagnosis of osteogenesis imperfecta

Ferda Evin,Tahir Atik,Huseyin Onay,Damla Goksen,Sukran Darcan,Ozgur Cogulu,Samim Ozen

Journal of pediatric endocrinology & metabolism : JPEM（2024）

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Ferda Evin,Esra Isik,Huseyin Onay,Samim Ozen,Sukran Darcan,Damla Goksen

Journal of pediatric endocrinology & metabolism : JPEMno. 0 (2023)

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COVID-19 infection in lipodystrophy syndromes

Gökçen Güngör Semiz,Tevfik Demir,Ilgın Yildirim Şimşir, İsmail Selimoğlu, Muge Yılmaz,Mehmet Cağrı Unal, Hulya Ellidıkuz,Hüseyin Önay,Ramazan Gen, Bahri Evren

Endocrine Abstracts (2023)

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