Bilge Özgör

High diagnostic rate of trio exome sequencing in consanguineous families with neurogenetic diseases

P. Chinnery, H. Lochmüller, R. Horvath, 2021, Brain : a journal of neurology.

A Retrospective Evaluation of Children Diagnosed with Dermatomyositis: A Single-center Study

Y. Tabel, S. Güngör, Mahmut Aslan, 2022, Bakirkoy Tip Dergisi / Medical Journal of Bakirkoy.

Re-examining the characteristics of pediatric multiple sclerosis in the era of antibody-associated demyelinating syndromes.

H. Per, M. Canpolat, D. Yalnızoǧlu, 2022, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Severe Complications of Varicella Zoster Virus Infection in Two Children

S. Güngör, Mahmut Aslan, S. Kırık, 2018 .

Evaluation of seizures and clinical features of pediatric patients diagnosed with Rett Syndrome who were detected to have MECP2 mutation

S. Güngör, Mahmut Aslan, S. Kırık, 2020 .

Evaluation of pediatric patients presenting with vertigo

M. Özkars, S. Kırık, Bilge Özgör, 2021, Journal of Health Sciences and Medicine.

Acute Ataxia in Childhood: Clinical Presentation, Etiology, and Prognosis of Single-Center Experience.

S. Güngör, Mahmut Aslan, S. Kırık, 2020, Pediatric emergency care.

Autosomal recessive variants in TUBGCP2 alter the γ-tubulin ring complex leading to neurodevelopmental disease

D. MacArthur, I. Vernos, S. Beltran, 2020, iScience.

Coeliac disease and reproductive disorders

M. Selimoğlu, Bilge Özgör, 2010, Scandinavian journal of gastroenterology.

Prevalence of celiac disease in parents of preterm or low birthweight newborns

I. Temel, Y. Seckin, M. Selimoğlu, 2011, The journal of obstetrics and gynaecology research.

The PURPLE N study: objective and perceived nutritional status in children and adolescents with cerebral palsy

S. Yılmaz, A. Smorenburg, S. Bertoli, 2021, Disability and rehabilitation.