M O. Herguner
Adana, Turkey
Last Updated: 09/26/2026
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Found 53 publications
Acute Disseminated Encephalomyelitis in Children and Adolescents: A Multicenter Retrospective Study of Relapse and Outcome.
Journal: Journal of child neurology
Published: May 09, 2025
Diagnosing missed cases of spinal muscular atrophy in genome, exome, and panel sequencing data sets.
Diagnosing missed cases of spinal muscular atrophy in genome, exome, and panel sequencing data sets.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: July 08, 2024
Diagnosing missed cases of spinal muscular atrophy in genome, exome, and panel sequencing datasets.
Journal: medRxiv : the preprint server for health sciences
Published: February 26, 2024
The Prognostic Factors in Children With Status Epilepticus and Status Epilepticus Severity Score Scales.
Journal: Behavioural neurology
Published: January 29, 2024
Clinical and Genetic Spectrum of Myotonia Congenita in Turkish Children.
Journal: Journal of neuromuscular diseases
Published: June 25, 2023
Can bispectral index be an early marker in the diagnosis of brain death?
Journal: Acta neurologica Belgica
Published: August 17, 2022
Clinical, radiological, and genetic variation in pontocerebellar hypoplasia disorder and our clinical experience.
Journal: Italian journal of pediatrics
Published: May 16, 2022
A Cytogenetic Study of Turkish Children with Global Developmental Delay.
Journal: Journal of pediatric genetics
Published: November 26, 2021
Glycogen storage disease type XII; an ultra rare cause of hemolytic anemia and rhabdomyolysis: one new case report.
Journal: Journal of pediatric endocrinology & metabolism : JPEM
Published: February 02, 2021
A homozygote frameshift mutation in OCLN gene result in Pseudo-TORCH syndrome type I: A case report extending the phenotype with central diabetes insipidus and renal dysfunction.
Journal: European journal of medical genetics
Published: January 21, 2020
Dysarthria, Ataxia, and Dystonia Associated with COX20 (FAM36A) Gene Mutation: A Case Report of a Turkish Child.
Journal: Annals of Indian Academy of Neurology
Published: October 23, 2019
Mitochondrial Membrane Protein-Associated Neurodegeneration: A Case Series of Six Children.
Journal: Annals of Indian Academy of Neurology
Published: May 14, 2019
Last Updated: 09/26/2026