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Profil bibliographique

Sibğatullah Ali Orak

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

28Publications signalées
41Citations signalées
2Affiliations récentes

Les institutions déclarées

Les domaines associés

Epilepsy research and treatmentMultiple Sclerosis Research StudiesAutoimmune Neurological Disorders and TreatmentsPeripheral Neuropathies and DisordersTuberous Sclerosis Complex Research

Les publications récentes

2026 article OpenAlex

Electrophysiological, neurocognitive, and GFAP biomarker responses to corticosteroid therapy in children with ESES/CSWS

Celil Yılmaz, Sibğatullah Ali Orak, Muzaffer Polat, Tugce Ozer et autres

Developmental and/or epileptic encephalopathy with spike–wave activation during sleep (DE SWAS), including electrical status epilepticus during sleep (ESES/CSWS), is associated with seizures, neurocognitive regression, and characteristic electroencephalographic abnormalities. This study aimed to evaluate the clinical, electrophysiological, neurocognitive, and molecular response to corticosteroid …

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0 citations Applied Neuropsychology Child
2026 article OpenAlex

Cognitive disengagement syndrome and learning difficulty symptoms in children with epilepsy: A case–control study

Çisil Çerçi Kubur, Beyhan Cengiz Özyurt, Öznur Bılaç, Sibğatullah Ali Orak et autres

Objective Cognitive Disengagement Syndrome (CDS) is an attentional construct characterized by excessive daydreaming, mental fogginess, and slowed behavior. This study examined CDS/SCT symptoms and their association with learning difficulties in children with epilepsy.Methods In this cross-sectional case–control study, 400 children aged 6–16 …

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0 citations Applied Neuropsychology Child
Accès ouvert 2026 article OpenAlex

Early Normal EEG and Seizure-Free Long-Term Follow-Up in Deletion-Positive Angelman Syndrome: A Case Series

Çisil Çerçi Kubur, Dilek Gün Bilgiç, Sibğatullah Ali Orak, Aslı Kübra Atasever et autres

A bstract Angelman syndrome (AS) is a rare neurogenetic disorder characterized by global developmental delay, absent or severely impaired speech, movement abnormalities, and distinct behavioral features. The most common genetic mechanism involves maternal deletion of the 15q11–q13 region. We report the case …

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0 citations Journal of Pediatric Neurosciences
2026 article OpenAlex

Clinical, Radiological, and Prognostic Features of Pediatric Clinically Isolated Syndrome and Risk of Conversion to Multiple Sclerosis: A Single-center Cohort Study

Çisil Çerçi Kubur, Beyhan Cengiz Özyurt, Sibğatullah Ali Orak, Aslı Kübra Atasever et autres

Abstract Pediatric clinically isolated syndrome (CIS) is the first inflammatory demyelinating event of the central nervous system and may progress to multiple sclerosis (MS). Data on relapse patterns and predictors of MS conversion in children remain limited. To evaluate the clinical, radiological, …

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0 citations Neuropediatrics
Accès ouvert 2026 article OpenAlex

Retrospective evaluation of patients followed with a diagnosis of dystonia: A single-center experience

Çisil Çerçi Kubur, Sibğatullah Ali Orak, Aslı Kübra Atasever, Muzaffer Polat

Background: This study aimed to evaluate the clinical and etiological characteristics of pediatric patients followed with a diagnosis of dystonia at a tertiary pediatric neurology center. Materials and Methods: Patients under the age of 18 who presented to our clinic between January …

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0 citations Journal of Parkinson’s Disease and Movement Disorders
Accès ouvert 2025 article OpenAlex

Acute cerebellitis in SARS-CoV-2 infection: A case report

Çisil Çerçi Kubur, Sibğatullah Ali Orak, Muzaffer Polat

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), first identified in Wuhan, China, in December 2019, has emerged as a major global public health threat. The literature on the severe neurological manifestations of coronavirus disease 2019 (COVID-19) has expanded substantially, with numerous studies …

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0 citations Journal of Parkinson’s Disease and Movement Disorders
Accès ouvert 2025 article OpenAlex

Can serum neuropeptide levels help diagnose pediatric migraine? A prospective case–control study

Sibğatullah Ali Orak, Muzaffer Polat, Çisil Çerçi Kubur, Aslı Kübra Atasever et autres

OBJECTIVE: The objective of this study was to examine the serum levels of vasoactive neuropeptides (calcitonin gene-related peptide [CGRP], pituitary adenylate cyclase-activating peptide-38 [PACAP-38], substance P [SP], and vasoactive intestinal peptide [VIP], which have been linked to the pathophysiology of migraine in …

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7 citations Headache The Journal of Head and Face Pain
Accès ouvert 2025 article OpenAlex

Tuberoskleroz Tanısı ile İzlenen Hastaların Klinik Özellikleri: Tek Merkez Deneyimi

Çisil Çerçi Kubur, Sibğatullah Ali Orak, Aslı Kübra Atasever, Muzaffer Polat et autres

Özet Amaç: Nörokutanöz sendromlar sinir sistemini, cildi tutan hastalık grubudur. Bunların arasında en sık görülenlerden biri de tuberoskleroz’dur (TS). Bu çalışmanın amacı Celal Bayar Üniversitesi Çocuk Nörolojisi Polikliniğinde izlenen TS tanılı hastaların klinik özelliklerini değerlendirmektir. Gereç ve Yöntemler: Ocak 2005-Ocak 2023 tarihleri …

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0 citations Celal Bayar Üniversitesi Sağlık Bilimleri Enstitüsü Dergisi
2024 book-chapter OpenAlex

Değişken Odaklı Familyal Fokal Epilepsi (Çocukluktan Erişkin Döneme Kadar)

Sibğatullah Ali Orak, Çisil Çerçi Kubur, Muzaffer Polat

Değişken odaklara sahip ailesel fokal epilepsi (FFEVF), fokal epilepsili birden fazla aile üyesi ile karakterize, nöbet odağının aile üyeleri arasında farklılık gösterebilen ancak aynı bireyde sabit kaldığı ailesel epilepsi sendromudur. Değişken odaklı ailesel fokal epilepsi genetik nedenli epilepsi sendromları arasında yer almaktadır. …

0 citations
2024 article OpenAlex

Evaluation of GFAP, S100B, and UCHL-1 Levels in Children With Refractory Epilepsy

Halil Aksoy, Celil Yılmaz, Sibğatullah Ali Orak, Senem Ayça et autres

Introduction A number of biomarkers are used to evaluate the duration of the epileptic seizure and the interictal period following neuronal injury. Invasive diagnostic methods are increasingly being replaced by peripheral or minimally invasive biomarkers that give results faster and are more …

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10 citations Journal of Child Neurology

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