Mirac S. Yıldırım-Yildirim

Ankara, Turkey

Last Updated: 09/26/2026

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Found 72 publications

A Case of Paroxysmal Exercise-Induced Dyskinesia Expands the Phenotypic spectrum of NAXE-Related Encephalopathy.

A Case of Paroxysmal Exercise-Induced Dyskinesia Expands the Phenotypic spectrum of NAXE-Related Encephalopathy.

Journal: Journal of child neurology

Published: July 24, 2026

The Diagnostic Dilemma: Seronegative Autoimmune Encephalitis or Isolated Anti-Zic4 Antibody-Positive Autoimmune Encephalitis Without an Underlying Malignancy.

The Diagnostic Dilemma: Seronegative Autoimmune Encephalitis or Isolated Anti-Zic4 Antibody-Positive Autoimmune Encephalitis Without an Underlying Malignancy.

Journal: Turkish archives of pediatrics

Published: July 02, 2026

Genotypic and phenotypic heterogeneity in tubulinopathies: insights from a Turkish multicenter cohort.

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

Correction: Prognostic Differences Between P190 and P210 BCR::ABL1 in Patients with Philadelphia-Positive B-cell Acute Lymphoblastic Leukemia.

Correction: Prognostic Differences Between P190 and P210 BCR::ABL1 in Patients with Philadelphia-Positive B-cell Acute Lymphoblastic Leukemia.

Journal: Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion

Published: April 27, 2026

The Cases of Acute Necrotizing Encephalopathy Due to Human Herpes Virus-6.

The Cases of Acute Necrotizing Encephalopathy Due to Human Herpes Virus-6.

Journal: The Pediatric infectious disease journal

Published: February 19, 2026

A missed clinical clue: congenital mydriasis and broomstick-like cerebrovascular imaging in ACTA2 mutation.

A missed clinical clue: congenital mydriasis and broomstick-like cerebrovascular imaging in ACTA2 mutation.

Journal: Acta neurologica Belgica

Published: February 11, 2026

Status Epilepticus in Children With Hemophagocytic Lymphohistiocytosis: Literature Review.

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.

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

Neonatal-onset genetic epilepsies: Insights from a large multicentre cohort.

Neonatal-onset genetic epilepsies: Insights from a large multicentre cohort.

Journal: Seizure

Published: October 28, 2025

ANO3-related tremulous dystonia: case report.

ANO3-related tremulous dystonia: case report.

Journal: Acta neurologica Belgica

Published: October 27, 2025

Two Siblings with LRPPRC Mutation: Mitochondrial Complex IV Deficiency: Case Report.

Two Siblings with LRPPRC Mutation: Mitochondrial Complex IV Deficiency: Case Report.

Journal: Molecular syndromology

Published: August 13, 2025

Predictors Associated with Motor and Cognitive Impairment in Children with Corpus Callosum Malformation.

Predictors Associated with Motor and Cognitive Impairment in Children with Corpus Callosum Malformation.

Journal: Neuropediatrics

Published: July 16, 2025

Showing 1-12 of 72

Last Updated: 09/26/2026