Mehmet Canpolat
Erciyes, Turkey
Last Updated: 09/26/2026
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Found 70 publications
From Leukaemia to MOGAD, From Refractive Error to Dural Fistula: Torticollis as the Presenting Sign of Serious Disease in Children.
Journal: Journal of paediatrics and child health
Published: April 07, 2026
Blended Hereditary Neuropathy Phenotype Caused by Biallelic PRX and SCN9A Variants: A Case Report.
Journal: Molecular syndromology
Published: March 20, 2026
The efficacy and tolerability of lacosamide adjunctive therapy in children with drug-refractory epilepsy: A nationwide Turkish cohort study.
Journal: Epilepsy & behavior : E&B
Published: December 14, 2025
Neonatal-onset genetic epilepsies: Insights from a large multicentre cohort.
Journal: Seizure
Published: October 28, 2025
The genetic landscape of childhood-onset dystonia in a nationwide Turkish cohort: Clinical spectrum, molecular diagnostics, and therapeutic implications.
Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
Published: June 30, 2025
Acute Disseminated Encephalomyelitis in Children and Adolescents: A Multicenter Retrospective Study of Relapse and Outcome.
Journal: Journal of child neurology
Published: May 09, 2025
Nusinersen for children with type I spinal muscular atrophy: 4 years' clinical experience in Turkish cohort.
Journal: Frontiers in neurology
Published: December 07, 2024
Corrigendum to "Re-examining the characteristics of pediatric multiple sclerosis in the era of antibody-associated demyelinating syndromes" [Europ. J. Paediatr. Neurol. 41 (2022) 8-18 doi.org/10.1016/j.ejpn.2022.08.006].
Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
Published: December 03, 2024
Molecular analysis of SMN2, NAIP, and GTF2H2 gene deletions and relationships with clinical subtypes of spinal muscular atrophy.
Journal: Journal of neurogenetics
Published: September 25, 2024
Blended Phenotypes of Sexual Development Disorder and Coenzyme Q10 Deficiency, Together with a Sibling with Homozygous Variants in the AHI1 Gene.
Journal: Molecular syndromology
Published: March 02, 2024
The Assessment and Management of Childhood Masturbation: An Analysis of 90 Cases.
Journal: Neuropediatrics
Published: October 12, 2023
Optic neuritis in Turkish children and adolescents: A multicenter retrospective study.
Journal: Multiple sclerosis and related disorders
Published: September 14, 2023
Last Updated: 09/26/2026