Nezir Ozgun

Mardin, Turkey

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 23 publications

Effects of newborn screening and nusinersen on survival and functional outcomes in spinal muscular atrophy with two SMN2 copies: A nationwide multicentre real-world study from Turkey.

Effects of newborn screening and nusinersen on survival and functional outcomes in spinal muscular atrophy with two SMN2 copies: A nationwide multicentre real-world study from Turkey.

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

Published: March 15, 2026

Not Just for Adults: Transient Global Amnesia is Rare-But Possible-in Children.

Not Just for Adults: Transient Global Amnesia is Rare-But Possible-in Children.

Journal: Cognitive and behavioral neurology : official journal of the Society for Behavioral and Cognitive Neurology

Published: September 28, 2025

Evaluation of Children and Adolescents with Thalassemia Major in Terms of Osteoporosis: A Single-Centre Experience.

Evaluation of Children and Adolescents with Thalassemia Major in Terms of Osteoporosis: A Single-Centre Experience.

Journal: Journal of clinical medicine

Published: February 01, 2025

An Unexpected Presentation of Pertussis: Pneumomediastinum and Subcutaneous Emphysema.

An Unexpected Presentation of Pertussis: Pneumomediastinum and Subcutaneous Emphysema.

Journal: Pediatric pulmonology

Published: October 29, 2024

Effectiveness of Valproic Acid in the Treatment of Sydenham's Chorea and a Literature Review.

Effectiveness of Valproic Acid in the Treatment of Sydenham's Chorea and a Literature Review.

Journal: Clinical pediatrics

Published: August 18, 2023

Clinical and Genetic Spectrum of Myotonia Congenita in Turkish Children.

Clinical and Genetic Spectrum of Myotonia Congenita in Turkish Children.

Journal: Journal of neuromuscular diseases

Published: June 25, 2023

Rafiq Syndrome: Old Variant in MAN1B1 Gene and Some New Phenotypic Features.

Rafiq Syndrome: Old Variant in MAN1B1 Gene and Some New Phenotypic Features.

Journal: Iranian journal of child neurology

Published: June 04, 2023

The role of metabolic diseases in neonatal convulsions.

The role of metabolic diseases in neonatal convulsions.

Journal: European review for medical and pharmacological sciences

Published: March 06, 2023

Shared Biological Pathways and Processes in Patients with Intellectual Disability: A Multicenter Study.

Shared Biological Pathways and Processes in Patients with Intellectual Disability: A Multicenter Study.

Journal: Neuropediatrics

Published: February 14, 2023

Thirteen-year surveillance results of acute flaccid paralysis cases in Southeast Turkey and the effect of refugee movements on surveillance results.

Thirteen-year surveillance results of acute flaccid paralysis cases in Southeast Turkey and the effect of refugee movements on surveillance results.

Journal: Central European journal of public health

Published: September 25, 2022

A case with congenital disorder of glycosylation with defective fucosylation 2 and new mutation in FUK gene.

A case with congenital disorder of glycosylation with defective fucosylation 2 and new mutation in FUK gene.

Journal: Brain & development

Published: July 08, 2021

Congenital myotonia: a review of twenty cases and a new splice-site mutation in the CLCN1 gene.

Congenital myotonia: a review of twenty cases and a new splice-site mutation in the CLCN1 gene.

Journal: The Turkish journal of pediatrics

Published: June 20, 2020

Showing 1-12 of 23

Last Updated: 09/26/2026