Mert Altıntas
Ankara, Turkey
Last Updated: 09/26/2026
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Found 12 publications
A Case of Paroxysmal Exercise-Induced Dyskinesia Expands the Phenotypic spectrum of NAXE-Related Encephalopathy.
Journal: Journal of child neurology
Published: July 24, 2026
Genotypic and phenotypic heterogeneity in tubulinopathies: insights from a Turkish multicenter cohort.
Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: April 29, 2026
Status Epilepticus in Children With Hemophagocytic Lymphohistiocytosis: Literature Review.
Journal: Journal of child neurology
Published: February 05, 2026
Pontocerebellar Hypoplasia Type 11 Case with a Novel Variant of TBC1D23 Gene: Case Report and Literature Review.
Journal: Cerebellum (London, England)
Published: February 02, 2026
ANO3-related tremulous dystonia: case report.
Journal: Acta neurologica Belgica
Published: October 27, 2025
A rare cause of persistent hiccups: familial cerebral cavernous malformations associated with mutation of the KRIT1 gene.
Journal: Acta neurologica Belgica
Published: April 08, 2025
Central Nervous System Involvement in Pediatric Juvenile Idiopathic Arthritis: A Case Report of Cerebellitis and Literature Review.
Journal: Journal of child neurology
Published: January 19, 2025
Clinical and Prognostic Characteristics in Childhood Osteosarcoma: A Single-Center Experience in Türkiye.
Journal: Turkish archives of pediatrics
Published: October 23, 2024
Progressive Myoclonus Epilepsy and Beyond: A Systematic Review of SEMA6B-related Disorders.
Journal: Neuropediatrics
Published: October 17, 2024
Predictors of medical intractability in children with epilepsy onset during the first two years of life, excluding infantile epileptic spasm syndrome.
Journal: Seizure
Published: December 27, 2023
Ketogenic diet-responsive drug-resistant epilepsy in a case of asparagine synthetase deficiency with a novel compound heterozygous missense variant.
Journal: Clinical neurology and neurosurgery
Published: March 06, 2023
The diagnostic challenges of congenital mirror movements and hand stereotypies in a case with TUBB3-associated tubulinopathy.
Journal: Acta neurologica Belgica
Published: June 07, 2021
Showing 1-12 of 12
Last Updated: 09/26/2026