Doç. Dr. Sevgi Yimenicioğlu

Epilepsi tanılı çocuğu olan ebeveynlerin epilepsiye ilişkin bilgi düzeyleri ve damgalanma algılarının değerlendirilmesi: Tanımlayıcı bir çalışma

Ağrı Tıp Fakültesi Dergisi, 2026

DOI 10.61845/agrimedical.1798384 Texte intégral en libre accèsSource : ORCID

Clinical and molecular spectrum of TSC1 and TSC2 mutations in pediatric tuberous sclerosis complex: Report of five novel variants

Neurology Asia, 2026

DOI 10.54029/2026jwy Texte intégral en libre accèsSource : ORCID

Concomitant Antiseizure Medications' Influence on Valproic Acid and Levetiracetam Pharmacokinetics in Pediatric Patients

Pediatrics International, 2026

DOI 10.1111/ped.70510 PMID 42590959 Texte intégral en libre accèsSource : ORCID

Prenatal diagnosis of fetal left transverse venous sinus thrombosis with intracranial hemorrhage: imaging findings and short-term outcome

Pediatric Radiology, 2025

DOI 10.1007/s00247-025-06475-0 PMID 41258972 1 citation (OpenAlex) Source : OpenAlex

Hypomagnesemia as a primary clue for the diagnosis of 17q12 deletion syndrome associated with spinal syringomyelia: a case report

The Turkish Journal of Pediatrics, 2025

DOI 10.24953/turkjpediatr.2025.6246 PMID 41636192 Texte intégral en libre accèsSource : ORCID

NEURODEVELOPMENTAL OUTCOMES IN PRETERM INFANTS

Eskisehir Medical Journal, Eskisehir City Hospital, 2024

DOI 10.48176/esmj.2024.163 Texte intégral en libre accèsSource : ORCID

Interstitial 3p25.3 deletion syndrome: 13 years'-long follow-up of an affected individual

Clinical Dysmorphology, 2024

DOI 10.1097/mcd.0000000000000503 PMID 38856647 1 citation (Scopus) Source : Scopus

Hot water epilepsy with alone and spontaneous seizures in childhood

Epilepsy Research, 2024

DOI 10.1016/j.eplepsyres.2024.107418 PMID 39003967 Source : Scopus

Case report: Pai syndrome with multiple ventricular septal defect and without cleft palate

Clinical Neurology and Neurosurgery, 2024

DOI 10.1016/j.clineuro.2023.108045 PMID 38091702 Source : Scopus

Temel Pediatrik Nöroloji: Tanı ve Tedavi 4. Cilt

Akademisyen Kitabevi eBooks, 2023

DOI 10.37609/akya.2033 Texte intégral en libre accèsSource : OpenAlex

First report of tethered cord syndrome in a patient with Verheij syndrome

Ophthalmic Genetics, 2023

DOI 10.1080/13816810.2022.2121968 PMID 36134573 3 citations (Europe PMC) Source : ORCID

The factors affecting neurodevelopmental outcomes in HIE

Acta Neurologica Belgica, 2023

DOI 10.1007/s13760-022-02126-5 PMID 36352199 5 citations (Scopus) Source : ORCID

De novo STXBP1 mutation in a child with hypotonia, intellectual disability, tremor and without epilepsy

Neurology Asia, 2023

DOI 10.54029/2023mru Texte intégral en libre accèsSource : ORCID

Clinical, neuroimaging and genetic findings in children with hereditary ataxia: single center study

Molecular Biology Reports, 2023

DOI 10.1007/s11033-022-08148-9 PMID 36462087 Source : ORCID

Identification of Novel Gene Variants in Children With Drug-Resistant Epilepsy: Expanding the Genetic Spectrum

Pediatric Neurology, 2023

DOI 10.1016/j.pediatrneurol.2022.11.005 PMID 36493596 10 citations (Scopus) Source : ORCID

A p.Val412Serfs pathogenic variant associated with Wolfram-like syndrome and leukodystrophy

The Egyptian Journal of Neurology, Psychiatry and Neurosurgery, 2023

DOI 10.1186/s41983-023-00608-8 1 citation (Scopus) Texte intégral en libre accèsSource : ORCID

Evaluation of Molecular and Clinical Findings in Children With Neurofibromatosis Type 1: Identification of 15 Novel Variants

Pediatric Neurology, 2023

DOI 10.1016/j.pediatrneurol.2023.08.036 PMID 37806041 7 citations (Scopus) Source : Scopus

A randomized controlled study: Evaluating the efficacy of a mobile application developed for mothers who have children with epilepsy in Turkiye

Journal of Pediatric Nursing, 2023

DOI 10.1016/j.pedn.2023.02.010 PMID 36870141 8 citations (Scopus) Source : Scopus

A rare case of Coffin–Lowry syndrome accompanied by a copper-beaten skull appearance

Neurology Asia, 2023

DOI 10.54029/2023jyx 1 citation (Scopus) Texte intégral en libre accèsSource : Scopus

The Novel Homozygous ADCY6 c.413G>A; p.R138H gene Variant Associated with Lethal Congenital Contracture Syndrome 8 in a Female Patient with Epilepsy and Pachygyria

Hong Kong Journal of Paediatrics, 2023

1 citation (Scopus) Source : Scopus

Antiepileptic Drug Adverse Cutaneous Reaction in Childhood

Journal of Pediatric Epilepsy, 2022

DOI 10.1055/s-0042-1749344 1 citation (OpenAlex) Source : ORCID

Is Levetiracetam Monotherapy Effective And Safe In Children With Epilepsy

Eskisehir Medical Journal, Eskisehir City Hospital, 2022

DOI 10.48176/esmj.2022.86 Texte intégral en libre accèsSource : ORCID

Generalized tetanus in an eight-year-old girl: a case report

The European Research Journal, 2022

DOI 10.18621/eurj.1049854 1 citation (OpenAlex) Texte intégral en libre accèsSource : ORCID

Case Report Presentation: Measles as the Cause of Cerebral Venous Sinus Thrombosis in Childhood

Pediatric Academic Case Reports, 2022

DOI 10.61107/pacr.2022.023 Texte intégral en libre accèsSource : ORCID

A Novel Mutation in the TBC1D20 Gene with Associated Warburg Micro Syndrome

Batı Karadeniz Tıp Dergisi, 2022

DOI 10.29058/mjwbs.1024327 Texte intégral en libre accèsSource : ORCID

Presentation of an Infant with Chromosome 18p Deletion Syndrome and Asymmetric Septal Hypertrophy

Global Medical Genetics, 2022

DOI 10.1055/s-0042-1743261 PMID 35707779 3 citations (Europe PMC) Texte intégral en libre accèsSource : ORCID

COVID-19 Symptoms with Pre-Existing and Not Pre-Existing Neurological Disorders in Pediatrics

Journal of Pediatric Infectious Diseases, 2022

DOI 10.1055/s-0042-1748921 Source : ORCID

Koolen-de Vries syndrome: A de novo missense KANSL1 variant

Clinical Neurology and Neurosurgery, 2022

DOI 10.1016/j.clineuro.2022.107444 PMID 36150256 2 citations (Scopus) Source : Scopus

Novel NR2F1 variant identified by whole-exome sequencing in a patient with Bosch-Boonstra-Schaaf optic atrophy syndrome

Indian Journal of Ophthalmology, 2022

DOI 10.4103/ijo.ijo_1061_22 PMID 35791240 3 citations (Scopus) Texte intégral en libre accèsSource : Scopus

A novel splice-site variant in the MCPH1 gene manifests with autosomal recessive primary microcephaly

Neurology Asia, 2022

DOI 10.54029/2022vtk Texte intégral en libre accèsSource : Scopus

Response to “SARS-CoV-2 related encephalitis requires documentation of the virus in the cerebrospinal fluid”

Turkish Journal of Pediatrics, 2022

DOI 10.24953/turkjped.2022.759-1 PMID 36583905 Texte intégral en libre accèsSource : Scopus

Lethal encephalitis in a pediatric patient with SARS-CoV-2

Turkish Journal of Pediatrics, 2022

DOI 10.24953/turkjped.2021.1142 PMID 35899571 4 citations (Scopus) Texte intégral en libre accèsSource : Scopus

Acute cerebellar ataxia in a child: Rotavirus coinfection with SARS-CoV-2

Zeynep Kamil Medical Journal, 2022

DOI 10.14744/zkmj.2022.00921 Source : OpenAlex

A Novel KMT2D mutation in Kabuki syndrome with elevated liver enzymes and congenital bilateral hip dislocation

Neurology Asia, 2021

DOI 10.54029/2021ryp 1 citation (Scopus) Texte intégral en libre accèsSource : ORCID

Case report: a de-novo 7p12.3 microduplication detected in an infant with perineal hamartoma and imperforate anus

Egyptian Journal of Medical Human Genetics, 2021

DOI 10.1186/s43042-021-00205-5 Texte intégral en libre accèsSource : Scopus

Evaluation of clinical findings and treatment options of Sydenham chorea patients

Journal of Surgery and Medicine, 2021

DOI 10.28982/josam.804833 3 citations (OpenAlex) Texte intégral en libre accèsSource : OpenAlex

Nörokütan Hastalıkların Tarihi ve Sınıflandırması

2021

Source : OpenAlex

Allen-Herndon-Dudley Sendromunda yeni Bir Hemizigot SLC16A2 nonsense mutasyonu

DergiPark (Istanbul University), 2021

Texte intégral en libre accèsSource : OpenAlex

Çocukluk Çağında Narkolepsi

2020

Source : OpenAlex

Viral etiological causes of febrile seizures for respiratory pathogens (EFES Study)

Human Vaccines and Immunotherapeutics, 2019

DOI 10.1080/21645515.2018.1526588 PMID 30235060 65 citations (Scopus) Texte intégral en libre accèsSource : ORCID

Tüberoskleroz Kompleksi Hastalarının Klinik ve Demografik Özellikleri

OSMANGAZİ JOURNAL OF MEDICINE, 2019

DOI 10.20515/otd.594858 1 citation (OpenAlex) Texte intégral en libre accèsSource : OpenAlex

Diagnostic effectiveness of muscle biopsy in neuromuscular diseases; Four years retrospective critical review

The Anatolian Journal of General Medical Research, 2019

DOI 10.5222/terh.2019.99267 2 citations (OpenAlex) Texte intégral en libre accèsSource : OpenAlex

Febril Nöbet Geçiren Çocuklarda Akuaporin 4 Gen Polimorfizmi

OSMANGAZİ JOURNAL OF MEDICINE, 2018

DOI 10.20515/otd.469491 Texte intégral en libre accèsSource : OpenAlex

Hot Water Epilepsy Successfully Treated with Daily Clobazam

Pediatric Emergency Care, 2017

DOI 10.1097/pec.0000000000000659 PMID 26959518 3 citations (Scopus) Source : ORCID

Microcephaly-Lymphedema-Chorioretinal Dysplasia Syndrome: Two Case Reports

International Journal of Clinical Pediatrics, 2017

DOI 10.14740/ijcp275w 1 citation (OpenAlex) Texte intégral en libre accèsSource : OpenAlex

Nörofibromatozis Tip 1: 49 Olgunun Değerlendirilmesi

Haydarpaşa Numune Eğitim ve Araştırma Hastanesi Tıp Dergisi, 2017

1 citation (OpenAlex) Source : OpenAlex

The evaluation of epilepsy and other contributing disorders in patients with cerebral palsy using the Gross Motor Function Classification System

The European Research Journal, 2017

DOI 10.18621/eurj.294051 2 citations (OpenAlex) Texte intégral en libre accèsSource : OpenAlex

Griscelli Syndrome with neurological deterioration: A case report.

The Medical Journal of Okmeydani Training and Research Hospital, 2017

DOI 10.5222/otd.2017.1117 1 citation (OpenAlex) Source : OpenAlex

Hemi-meningitis with hemophagocytic lymphohistiocytosis

Annals of Indian Academy of Neurology, 2016

DOI 10.4103/0972-2327.165458 PMID 27570395 1 citation (Scopus) Texte intégral en libre accèsSource : ORCID

Subcutaneous Fat Necrosis Associated with hypo/Hypercalcemia and Brachiall Plexopathy

Journal of Dr Behcet Uz Children s Hospital, 2016

DOI 10.5222/buchd.2016.081 Texte intégral en libre accèsSource : OpenAlex