Did you mean: Dilshad Turkdogan

PRRT2 Mutations are the major cause of benign familial infantile seizures

…, P Striano, J Teichler, D Turkdogan… - Human …, 2012 - Wiley Online Library
Mutations in PRRT2 have been described in paroxysmal kinesigenic dyskinesia (PKD) and
infantile convulsions with choreoathetosis (PKD with infantile seizures), and recently also in …

A prevalence study of restless legs syndrome in Turkish children and adolescents

D Turkdogan, N Bekiroglu, S Zaimoglu - Sleep medicine, 2011 - Elsevier
OBJECTIVE: To determine the prevalence of the restless legs syndrome (RLS) in Turkish
school children and adolescents during the past 12months. METHODS: A cross-sectional …

Auditory neuropathy in hyperbilirubinemia: is there a correlation between serum bilirubin, neuron-specific enolase levels and auditory neuropathy?

İ Akman, E Özek, S Kulekci, D Türkdogˇan… - … journal of audiology, 2004 - Taylor & Francis
This study evaluated whether a correlation exists between increased serum bilirubin and
neuron-specific enolase (NSE) assays (a biochemical index of neuronal damage) and auditory …

Characteristic and overlapping features of migraine and tension‐type headache

D Turkdogan, S Cagirici, D Soylemez… - … : The Journal of …, 2006 - Wiley Online Library
Objective.—This epidemiological survey was conducted to investigate comprehensive
characteristic and overlapping features of migraine and tension‐type headache (TTH) disorders …

The effects of neurodevelopmental therapy on feeding and swallowing activities in children with cerebral palsy

G Acar, N Ejraei, D Turkdoğan, N Enver, G Öztürk… - Dysphagia, 2022 - Springer
This study investigated the effect of the structured Neurodevelopmental Therapy Method-Bobath
(NDT-B) approach on the feeding and swallowing activity of patients with cerebral palsy …

Lipid peroxidation and antioxidative enzyme activities in childhood epilepsy

D Turkdogan, S Toplan… - Journal of child …, 2002 - journals.sagepub.com
This study aimed to investigate the relationship among lipid peroxidation, subsequent
activation of scavenger enzymes (superoxide dismutase and glutathione peroxidase), and the …

Genome‐wide linkage meta‐analysis identifies susceptibility loci at 2q34 and 13q31. 3 for genetic generalized epilepsies

…, R Kaneva, H Caglayan, D Turkdogan… - …, 2012 - Wiley Online Library
Purpose: Genetic generalized epilepsies (GGEs) have a lifetime prevalence of 0.3% with
heritability estimates of 80%. A considerable proportion of families with siblings affected by …

[HTML][HTML] The burden of primary caregivers of spinal muscular atrophy patients and their needs

…, Y Gökdemir, G Özel, D Türkdoğan - Turkish archives of …, 2021 - ncbi.nlm.nih.gov
Aim: This study aims to reveal the problems faced by families of children with spinal muscular
atrophy (SMA), by evaluating their care burden, needs, and expectations. Materials and …

De novo FZR1 loss-of-function variants cause developmental and epileptic encephalopathies

…, J Roovers, N Smal, CT Myers, D Turkdogan… - Brain, 2022 - academic.oup.com
FZR1, which encodes the Cdh1 subunit of the anaphase-promoting complex, plays an
important role in neurodevelopment by regulating the cell cycle and by its multiple post-mitotic …

Subdural EEG patterns in children with taylor-type cortical dysplasia: comparison with nondysplastic lesions

D Turkdogan, M Duchowny, T Resnick… - Journal of clinical …, 2005 - journals.lww.com
The authors compared interictal and ictal abnormalities from chronic intracranial recordings
in children with Taylor-type cortical dysplasia (TTCD) and nondysplastic lesions. Interictal …
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