Can Scoliosis Help the Early Diagnosis of Congenital Myasthenic Syndrome?

por Kaya, Oğuz, Kirik, Serkan
Publicado 2023

Congenital mirror movement associated with migraine: A case report

por Kirik, Serkan, Sahin, Hamza
Publicado 2018

Vitamin B12 Deficiency Observed in Children With First Afebrile Seizures

por Kirik, Serkan, Çatak, Zekiye
Publicado 2021

Importance of targeted next-generation sequencing in pediatric patients with developmental epileptic encephalopathy

por Bariş, Savaş, Kırık, Serkan, Balasar, Özgür
Publicado 2023

Importance of Streptococci Infections in Childhood Neuropsychiatric Disorders

por Kırık, Serkan, Güngör, Olcay, Kırık, Yasemin
Publicado 2019

A Novel SCN1A Mutation: A Case Report

por Aslan, Mahmut, Ozgor, Bilge, Kirik, Serkan, Gungor, Serdal
Publicado 2020

A hereditary angioedema screening in two villages, based on an index case, and identification of a novel mutation, “1033G>T”, at the SERPING1 gene

por Ozkars, Mehmet Yasar, Keskın, Ozlem, Bayram, Nazan, Onay, Huseyin, Keskın, Mehmet, Bayram, Hasan, Sahın, Yavuz, Küçükosmanoğlu, Ercan, Kırık, Serkan
Publicado 2019