Browsing by Author "Işıkay, Sedat"
Now showing items 1-8 of 8
-
Foreign Body in the Scalp: A Rare Cause of Recurrent Headache
Işıkay, Sedat (Springer, 2016-08)To the Editor: A 9-y-old boy was admitted to the hospital with a complaint of continuous headache, starting from left part of his head and radiating through all parts. He was localizing the beginning and maximal point of ... -
Gastrointestinal findings in children with Down syndrome: Is there an early sign for Celiac disease?
Kocamaz, Halil; Işıkay, Sedat (2018)Aim: To investigate the prevalence of celiac disease (CD) among children with Down’s syndrome (DS) and its association with gastrointestinal symptoms and other accompanying diseases. Methods: The study was consisted of ... -
Gastrointestinal findings in children with Down syndrome: Is there an early sign for Celiac disease?
Kocamaz, Halil; Işıkay, Sedat (Doç.Dr. Mustafa Hasbahçeci, 2018)Aim: To investigate the prevalence of celiac disease (CD) among children with Down’s syndrome (DS) and its association with gastrointestinal symptoms and other accompanying diseases. Methods: The study was consisted of ... -
Katılma nöbeti, febril konvülziyon ve anemi bir yap-bozun parçaları mı? Çölyak hastalığı
Kocamaz, Halil; Işıkay, Sedat (2017)Çölyak hastalığı epilepsi, ataksi, nöropati, miyopati ve baş ağrısı gibi birçok nörolojik hastalık ile ilişkili olup, febril konvülziyon ile birlikteliği enderdir. Bununla birlikte, demir eksikliği anemisi olan olgularda ... -
Katılma nöbeti, febril konvülziyon ve anemi bir yap-bozun parçaları mı? Çölyak hastalığı
Kocamaz, Halil; Işıkay, Sedat (Erkan Mor, 2017)Çölyak hastalığı epilepsi, ataksi, nöropati, miyopati ve baş ağrısı gibi birçok nörolojik hastalık ile ilişkili olup, febril konvülziyon ile birlikteliği enderdir. Bununla birlikte, demir eksikliği anemisi olan olgularda ... -
RANBP2 Mutation in Clinically Undiagnosed Acute Necrotizing Encephalopathy
Işıkay, Sedat; Şahin, Yavuz (Springer, 2018-09-01) -
Spontaneous Pneumocephalus Secondary to Positive Ventilation in an Infant
Işıkay, Sedat (Springer, 2019-04-10) -
Williams-Beuren Syndrome with Mirror Movements
Işıkay, Sedat; Sezer, Sadettin; Kırık, Serkan; Güngör, Olcay (Springer India, 2016-06)To the Editor: Williams-Beuren Syndrome (WBS) is a rare neurodevelopmental disorder caused by deletion of chromosome 7 at q11.23. It is characterized by distinctive facies, congenital cardiovascular malformations, intellectual ...