First Genetic Screening for Maternal Uniparental Disomy of Chromosome 7 in Turkish Silver-Russell Syndrome Patients

por Karaca, Emin, Tuysuz, Beyhan, Pehlivan, Sacide, Ozkinay, Ferda
Publicado 2012

Response to a letter to the editor regarding ‘ the comparison of seroconversion rates among different varicella vaccines administered Turkish children; MAV/06 and vOka’

por Sahbudak Bal, Zumrut, Zeytinoglu, Aysin, Ozkinay, Ferda, Kurugol, Zafer
Publicado 2022

Comprehensive Analysis of Deafness Genes in Families with Autosomal Recessive Nonsyndromic Hearing Loss

por Atik, Tahir, Onay, Huseyin, Aykut, Ayca, Bademci, Guney, Kirazli, Tayfun, Tekin, Mustafa, Ozkinay, Ferda
Publicado 2015

Molecular Genetic Analysis of Survival Motor Neuron Gene in 460 Turkish Cases with Suspicious Spinal Muscular Atrophy Disease

por RASHNONEJAD, Afrooz, ONAY, Huseyin, ATIK, Tahir, ATAN SAHIN, Ozlem, GOKBEN, Sarenur, TEKGUL, Hasan, OZKINAY, Ferda
Publicado 2016

A Novel Missense Mutation in BRAF Caused Cardio-Facio-Cutaneous Syndrome

por Hazan, Filiz, Karaca, Emin, Koker, Sultan Aydin, Korkmaz, Huseyin Anil, Mese, Timur, Onay, Huseyin, Ozkinay, Ferda
Publicado 2013

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

por Özen, Samim, Atik, Tahir, Korkmaz, Özlem, Onay, Hüseyin, Gökşen, Damla, Özkınay, Ferda, Çoğulu, Özgür, Darcan, Şükran
Publicado 2020

Melanocortin 4 receptor (MC4R) gene variants in children and adolescents having familial early-onset obesity: genetic and clinical characteristics

por Aykut, Ayça, Özen, Samim, Gökşen, Damla, Ata, Aysun, Onay, Hüseyin, Atik, Tahir, Darcan, Şükran, Özkinay, Ferda
Publicado 2020

Cervical abscess caused by methicillin-susceptible Staphylococcus aureus in an infant infected with SARS-CoV-2: Diagnostic dilemma

por Yildirim Arslan, Sema, Sahbudak Bal, Zumrut, Guner Ozenen, Gizem, Bilen, Nimet Melis, Kurugol, Zafer, Ozkinay, Ferda
Publicado 2021

A Neurofibromatosis Noonan Syndrome Patient Presenting with Abnormal External Genitalia

por Işık, Esra, Onay, Hüseyin, Atik, Tahir, Solmaz, Aslı Ece, Özen, Samim, Çoğulu, Özgür, Darcan, Şükran, Özkınay, Ferda
Publicado 2020

The Change of Perinatal Mortality Over Three Decades in a Reference Centre in the Aegean Region: Neonatal Mortality has decreased but Foetal Mortality Remains Unchanged

por Kültürsay, Nilgün, Aşkar, Niyazi, Terek, Demet, Yeniel, Ahmet Özgür, Altun Köroğlu, Özge, Yalaz, Mehmet, Özkınay, Ferda, Akısü, Mete
Publicado 2017

415. Misdiagnosis of multisystem inflammatory syndrome in children: A diagnostic challenge

por Avcu, Gülhadiye, Arslan, Aslı, Arslan, Sema Yildirim, Sahbudak, Zumrut, Turan, Caner, Ersayoglu, Irem, Cebeci, Kübra, Kurugol, Zafer, Ozkınay, Ferda
Publicado 2023

Izmir Mental Health Cohort for Gene-Environment Interaction in Psychosis (TürkSch): Assessment of the Extended and Transdiagnostic Psychosis Phenotype and Analysis of Attrition in...

por Kırlı, Umut, Binbay, Tolga, Elbi, Hayriye, Drukker, Marjan, Kayahan, Bülent, Özkınay, Ferda, Onay, Hüseyin, Alptekin, Köksal, van Os, Jim
Publicado 2019

2272. Evaluation of Clinical Features, Carbapenem Resistance and Risk Factors of Klebsiella Species: A 4-Year Retrospective Study in Turkey

por Umit, Zuhal, Sahbudak Bal, Zumrut, Guner, Gizem, Avcu, Gulhadiye, Bozkurt, Duygu, Kurugol, Zafer, Vardar, Fadil, Cilli, Feriha, Ozkinay, Ferda
Publicado 2019

290. Quantitative Antibody Levels Against SARS-CoV-2 Spike Protein in Children with COVID-19 and MIS-C

por Avcu, Gulhadiye, Arslan, Sema Yıldırım, Soylu, Mehmet, Bilen, Melis, Çiçek, Candan, Bal, Zümrüt Şahbudak, Kurugöl, Nuri Zafer, Ozkinay, Ferda
Publicado 2022

Persistent Müllerian Duct Syndrome with Transverse Testicular Ectopia: A Novel Anti-Müllerian Hormone Receptor Mutation

por Korkmaz, Özlem, Özen, Samim, Özcan, Nurhan, Bayındır, Petek, Şen, Sait, Onay, Hüseyin, Gökşen, Damla, Avanoğlu, Ali, Özkınay, Ferda, Darcan, Şükran
Publicado 2017

A New Cause of Obesity Syndrome Associated with a Mutation in the Carboxypeptidase Gene Detected in Three Siblings with Obesity, Intellectual Disability and Hypogonadotropic Hypogo...

por Durmaz, Asude, Aykut, Ayça, Atik, Tahir, Özen, Samim, Ayyıldız Emecen, Durdugül, Ata, Aysun, Işık, Esra, Gökşen, Damla, Çoğulu, Özgür, Özkınay, Ferda
Publicado 2021

Intracranial Bleeding in a Female Hemophilia Patient: Molecular Analysis of the Factor 8 Gene and Determination of a Novel Mutation

por Tatlı Güneş, Burçak, Önder Siviş, Zühal, Ataseven, Eda, Malbora, Barış, Türker, Meral, Belen, Fatma Burcu, Atabay, Berna, Atik, Tahir, Işık, Esra, Özkınay, Ferda
Publicado 2018

Psychiatric Approaches for Disorders of Sex Development: Experience of a Multidisciplinary Team

por Özbaran, Burcu, Özen, Samim, Gökşen, Damla, Korkmaz, Özlem, Onay, Hüseyin, Özkınay, Ferda, Çoğulu, Özgür, Erermiş, Serpil, Köse, Sezen, Avanoğlu, Ali, Ulman, İbrahim, Darcan, Şükran
Publicado 2013

Prospective Evaluation of Whole Genome MicroRNA Expression Profiling in Childhood Acute Lymphoblastic Leukemia

por Duyu, Muhterem, Durmaz, Burak, Gunduz, Cumhur, Vergin, Canan, Yilmaz Karapinar, Deniz, Aksoylar, Serap, Kavakli, Kaan, Cetingul, Nazan, Irken, Gulersu, Yaman, Yontem, Ozkinay, Ferda, Cogulu, Ozgur
Publicado 2014

Quality of Life and Psychological Well-being in Children and Adolescents with Disorders of Sex Development

por Şentürk Pilan, Birsen, Özbaran, Burcu, Çelik, Didem, Özcan, Tuğçe, Özen, Samim, Gökşen, Damla, Ulman, İbrahim, Avanoğlu, Ali, Tiryaki, Sibel, Onay, Hüseyin, Çoğulu, Özgür, Özkınay, Ferda, Darcan, Şükran
Publicado 2021