Hasil Pencarian - Hüseyin Önay

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  1. 1
    Relationship Between Oxytocin and Attention Deficit Hyperactivity Disorder

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

    Diterbitkan 2017-09-01
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  2. 2
    Griscelli Syndrome Presented with Status Epilepticus and Hemophagocytic Lymphohistiocytosis

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

    Diterbitkan 2017-03-01
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  3. 3
    Association of vitamin D receptor polymorphisms and type 1 diabetes susceptibility in children: a meta-analysis

    Association of vitamin D receptor polymorphisms and type 1 diabetes susceptibility in children: a meta-analysis oleh Ozlem Atan Sahin, Damla Goksen, Aysel Ozpinar, Muhittin Serdar, Huseyin Onay

    Diterbitkan 2017-03-01
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  4. 4
    Lipemia Retinalis Diagnosed Incidentally After Laser Photocoagulation Treatment for Retinopathy of Prematurity

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

    Diterbitkan 2021-10-01
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  5. 5
    Mannose-binding lectin gene polymorphism and chronic hepatitis B infection in children

    Mannose-binding lectin gene polymorphism and chronic hepatitis B infection in children oleh Gulin Erdemir, Tanju B Ozkan, Taner Ozgur, Ferah Budak, Sara S Kilic, Huseyin Onay

    Diterbitkan 2015-01-01
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  6. 6
    Bannayan-Riley-Ruvalcaba Syndrome in a Case Evaluated Due to Multinodular Goiter

    Bannayan-Riley-Ruvalcaba Syndrome in a Case Evaluated Due to Multinodular Goiter oleh Özlem Korkmaz, Samim Özen, Hüseyin Onay, Ahmet Çelik, Yeşim Ertan, Damla Gökşen, Şükran Darcan

    Diterbitkan 2018-12-01
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  7. 7
    Comprehensive Analysis of Deafness Genes in Families with Autosomal Recessive Nonsyndromic Hearing Loss.

    Comprehensive Analysis of Deafness Genes in Families with Autosomal Recessive Nonsyndromic Hearing Loss. oleh Tahir Atik, Huseyin Onay, Ayca Aykut, Guney Bademci, Tayfun Kirazli, Mustafa Tekin, Ferda Ozkinay

    Diterbitkan 2015-01-01
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  8. 8
    Ocular Manifestations of Fabry Disease: Report from a Tertiary Eye Care Center in Türkiye

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

    Diterbitkan 2024-06-01
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  9. 9
    Fabry disease: An overlooked diagnosis in adult cardiac patients

    Fabry disease: An overlooked diagnosis in adult cardiac patients oleh Meral Kayıkçıoğlu, Evrim Şimşek, Sema Kalkan Uçar, Selen Bayraktaroğlu, Hüseyin Onay, Eser Sözmen, Mahmut Çoker

    Diterbitkan 2017-09-01
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  10. 10
    Clinical, Biochemical and Molecular Characteristics of Fifteen Patients with Mucopolysaccharidosis Type II in Western Turkey

    Clinical, Biochemical and Molecular Characteristics of Fifteen Patients with Mucopolysaccharidosis Type II in Western Turkey oleh Havva Yazıcı, Ebru Canda, Esra Er, Sema Kalkan Uçar, Hüseyin Onay, Ferda Özkınay, Mahmut Çoker

    Diterbitkan 2018-03-01
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  11. 11
    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

    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 oleh Şervan Özalkak, Meliha Demiral, Edip Ünal, Funda Feryal Taş, Hüseyin Onay, Hüseyin Demirbilek, Mehmet Nuri Ozbek

    Diterbitkan 2023-09-01
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  12. 12
    Aromatase Deficiency in Two Siblings with 46,XX Karyotype Raised as Different Genders: A Novel Mutation (p.R115X) in the CYP19A1 Gene

    Aromatase Deficiency in Two Siblings with 46,XX Karyotype Raised as Different Genders: A Novel Mutation (p.R115X) in the CYP19A1 Gene oleh Samim Özen, Tahir Atik, Özlem Korkmaz, Hüseyin Onay, Damla Gökşen, Ferda Özkınay, Özgür Çoğulu, Şükran Darcan

    Diterbitkan 2020-03-01
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  13. 13
    A Neurofibromatosis Noonan Syndrome Patient Presenting with Abnormal External Genitalia

    A Neurofibromatosis Noonan Syndrome Patient Presenting with Abnormal External Genitalia oleh Esra Işık, Hüseyin Onay, Tahir Atik, Aslı Ece Solmaz, Samim Özen, Özgür Çoğulu, Şükran Darcan, Ferda Özkınay

    Diterbitkan 2020-03-01
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  14. 14
    A Remarkable Coexistence of Systemic Capillary Leak Syndrome and Diabetes in an 11-Year-Old Boy: A Case Report and Review of the Literature

    A Remarkable Coexistence of Systemic Capillary Leak Syndrome and Diabetes in an 11-Year-Old Boy: A Case Report and Review of the Literature oleh Aysun Ata, Samim Özen, Damla Gökşen, Neslihan Edeer Karaca, Güzide Aksu, Necil Kütükçüler, Hüseyin Onay, Şükran Darcan

    Diterbitkan 2020-01-01
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  15. 15
    Initial and Final Status of the Patients with Niemann Pick A and B: Ege University Experience

    Initial and Final Status of the Patients with Niemann Pick A and B: Ege University Experience oleh Ebru Canda, Havva Yazıcı, Esra Er, Sema Kalkan Uçar, Hüseyin Onay, Eser Sözmen, Ferda Özkınay, Mahmut Çoker

    Diterbitkan 2018-03-01
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  16. 16
    Investigation of the molecular genetic causes of non-syndromic primary ovarian ınsufficiency by next generation sequencing analysis

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

    Diterbitkan 2024-02-01
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  17. 17
    A Novel Androgen Receptor Gene Mutation in a 46,XY Patient: Complete Androgen Insensitivity Syndrome

    A Novel Androgen Receptor Gene Mutation in a 46,XY Patient: Complete Androgen Insensitivity Syndrome oleh Hale Tuhan, MD, Ayhan Abaci, MD, Ayca Aykut, MD, Ahmet Anik, MD, Hüseyin Onay, MD, Ece Bober, MD

    Diterbitkan 2016-01-01
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  18. 18
    Pregnancy-associated plasma protein A gene polymorphism in pregnant women with preeclampsia and intrauterine growth restriction

    Pregnancy-associated plasma protein A gene polymorphism in pregnant women with preeclampsia and intrauterine growth restriction oleh Sultan Ozkan, Cem Yasar Sanhal, Ozgur Yeniel, Esra Arslan Ates, Mete Ergenoglu, Birol Bınbır, Huseyin Onay, Ferda Ozkınay, Sermet Sagol

    Diterbitkan 2015-10-01
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  19. 19
    Homozygous LMNA p.R582H pathogenic variant reveals increasing effect on the severity of fat loss in lipodystrophy

    Homozygous LMNA p.R582H pathogenic variant reveals increasing effect on the severity of fat loss in lipodystrophy oleh Utku Erdem Soyaltin, Ilgin Yildirim Simsir, Baris Akinci, Canan Altay, Suleyman Cem Adiyaman, Kristen Lee, Huseyin Onay, Elif Arioglu Oral

    Diterbitkan 2020-07-01
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  20. 20
    Expert opinion on the recognition, diagnosis and management of children and adults with Fabry disease: a multidisciplinary Turkey perspective

    Expert opinion on the recognition, diagnosis and management of children and adults with Fabry disease: a multidisciplinary Turkey perspective oleh Fatih Ezgu, Erkan Alpsoy, Zerrin Bicik Bahcebasi, Ozgur Kasapcopur, Melis Palamar, Huseyin Onay, Binnaz Handan Ozdemir, Mehmet Akif Topcuoglu, Omac Tufekcioglu

    Diterbitkan 2022-03-01
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