Leman Orgun-Tekin

Kosekoy, Turkey

Last Updated: 09/26/2026

Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 13 publications

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

WWOX Mutation as a Rare Cause of Neonatal-Infantile Parkinsonism Mimicking a Neurotransmitter Disorder: A Case Report.

WWOX Mutation as a Rare Cause of Neonatal-Infantile Parkinsonism Mimicking a Neurotransmitter Disorder: A Case Report.

Journal: Journal of paediatrics and child health
Published: February 07, 2026

A gentle and colorful touch of epilepsy surgery on a young painter's art and life: a case report with dramatic paintings.

A gentle and colorful touch of epilepsy surgery on a young painter's art and life: a case report with dramatic paintings.

Journal: Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery
Published: October 05, 2025

Leber hereditary optic neuropathy (LHON) in a 6-year-old boy with a transient spinal cord lesion.

Leber hereditary optic neuropathy (LHON) in a 6-year-old boy with a transient spinal cord lesion.

Journal: The Turkish journal of pediatrics
Published: August 24, 2025

Diagnosis of Congenital Cytomegalovirus in a 14-Month-Old Patient Presenting with Sensorineural Hearing Loss: Storing Dry Blood Samples.

Diagnosis of Congenital Cytomegalovirus in a 14-Month-Old Patient Presenting with Sensorineural Hearing Loss: Storing Dry Blood Samples.

Journal: Turkish archives of pediatrics
Published: January 13, 2025

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

First pediatric case with primary familial brain calcification due to a novel variant on the MYORG gene and review of the literature.

First pediatric case with primary familial brain calcification due to a novel variant on the MYORG gene and review of the literature.

Journal: Brain & development
Published: November 25, 2020

Reply to "Ultrasound evaluation of optic nerve sheath diameter to assess treatment efficacy in pediatric idiopathic intracranial hypertension".

Reply to "Ultrasound evaluation of optic nerve sheath diameter to assess treatment efficacy in pediatric idiopathic intracranial hypertension".

Journal: Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery
Published: February 24, 2020

Optic nerve ultrasonography in monitoring treatment efficacy in pediatric idiopathic intracranial hypertension.

Optic nerve ultrasonography in monitoring treatment efficacy in pediatric idiopathic intracranial hypertension.

Journal: Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery
Published: May 29, 2019

Decrease in Cerebral Oxygen Saturation During the 6-Minute Walk Test in Pediatric Pulmonary Arterial Hypertension.

Decrease in Cerebral Oxygen Saturation During the 6-Minute Walk Test in Pediatric Pulmonary Arterial Hypertension.

Journal: Pediatric cardiology
Published: April 14, 2019

Effects of robotic rehabilitation on walking and balance in pediatric patients with hemiparetic cerebral palsy.

Effects of robotic rehabilitation on walking and balance in pediatric patients with hemiparetic cerebral palsy.

Journal: Gait & posture
Published: September 24, 2018

What has changed in the utility of pediatric EEG over the last decade?

What has changed in the utility of pediatric EEG over the last decade?

Journal: Turkish journal of medical sciences
Published: August 18, 2018
Showing 1-12 of 13

Last Updated: 09/26/2026