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Profil bibliographique

Aslı Kübra Atasever

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

22Publications signalées
23Citations signalées
2Affiliations récentes

Les institutions déclarées

Les domaines associés

Epilepsy research and treatmentMultiple Sclerosis Research StudiesGenomics and Rare DiseasesTuberous Sclerosis Complex ResearchAttention Deficit Hyperactivity Disorder

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

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
2025 article OpenAlex

Acute Disseminated Encephalomyelitis in Children and Adolescents: A Multicenter Retrospective Study of Relapse and Outcome

Seda Kanmaz, Sanem Keskin Yılmaz, Nihal Olgaç Dündar, Ayşe Aksoy et autres

Objectives To evaluate the demographic, clinical, laboratory, and prognostic data of children with acute disseminated encephalomyelitis with respect to anti-myelin oligodendrocyte glycoprotein (MOG) antibody status. Methods Acute disseminated encephalomyelitis patients (n = 245) from 24 centers followed up between 2010 and 2022 …

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0 citations Journal of Child Neurology
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

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