Meral Topcu

Ankara, Turkey

Last Updated: 09/26/2026

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Found 49 publications

Clinical and radiological evaluation of children with hemimegalencephaly and epilepsy: A single-center study.

Clinical and radiological evaluation of children with hemimegalencephaly and epilepsy: A single-center study.

Journal: Seizure

Published: June 14, 2025

Evaluation of the Patients with the Diagnosis of Pontocerebellar Hypoplasia: A Multicenter National Study.

Evaluation of the Patients with the Diagnosis of Pontocerebellar Hypoplasia: A Multicenter National Study.

Journal: Cerebellum (London, England)

Published: March 27, 2024

Electro-clinical features and long-term outcomes in guanidinoacetate methyltransferase (GAMT) deficiency.

Electro-clinical features and long-term outcomes in guanidinoacetate methyltransferase (GAMT) deficiency.

Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society

Published: November 21, 2023

Non-epileptic paroxysmal events at pediatric video-electroencephalography monitoring unit over a 15-year period.

Non-epileptic paroxysmal events at pediatric video-electroencephalography monitoring unit over a 15-year period.

Journal: Seizure

Published: December 05, 2022

Sepiapterin Reductase Deficiency Misdiagnosed as Neurological Sequelae of Meningitis.

Sepiapterin Reductase Deficiency Misdiagnosed as Neurological Sequelae of Meningitis.

Journal: Molecular syndromology

Published: November 06, 2022

Myelin oligodendrocyte glycoprotein antibodies in genetic leukodystrophies.

Myelin oligodendrocyte glycoprotein antibodies in genetic leukodystrophies.

Journal: Journal of neuroimmunology

Published: December 18, 2021

Lesional resective epilepsy surgery in childhood: Comparison of two decades and long-term seizure outcome from a single center.

Lesional resective epilepsy surgery in childhood: Comparison of two decades and long-term seizure outcome from a single center.

Journal: Epilepsy research

Published: November 27, 2021

Unraveling neuronal ceroid lipofuscinosis type 2 (CLN2) disease: A tertiary center experience for determinants of diagnostic delay.

Unraveling neuronal ceroid lipofuscinosis type 2 (CLN2) disease: A tertiary center experience for determinants of diagnostic delay.

Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society

Published: December 15, 2020

The Complex Genetic Landscape of Hereditary Ataxias in Turkey and Implications in Clinical Practice.

The Complex Genetic Landscape of Hereditary Ataxias in Turkey and Implications in Clinical Practice.

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: October 13, 2020

Management of CLN1 Disease: International Clinical Consensus.

Management of CLN1 Disease: International Clinical Consensus.

Journal: Pediatric neurology

Published: September 04, 2020

Comprehensive clinical, biochemical, radiological and genetic analysis of 28 Turkish cases with suspected metachromatic leukodystrophy and their relatives.

Comprehensive clinical, biochemical, radiological and genetic analysis of 28 Turkish cases with suspected metachromatic leukodystrophy and their relatives.

Journal: Molecular genetics and metabolism reports

Published: August 11, 2020

International consensus classification of hippocampal sclerosis and etiologic diversity in children with temporal lobectomy.

International consensus classification of hippocampal sclerosis and etiologic diversity in children with temporal lobectomy.

Journal: Epilepsy & behavior : E&B

Published: April 08, 2020

Showing 1-12 of 49

Last Updated: 09/26/2026