Gunes Sager

Kartal, Turkey

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 14 publications

Experience with the Ketogenic Diet in a Boy with CLCN4 Related Neurodevelopmental Disorder.

Experience with the Ketogenic Diet in a Boy with CLCN4 Related Neurodevelopmental Disorder.

Journal: Balkan journal of medical genetics : BJMG

Published: March 14, 2024

Novel, homozygous RAB3GAP1 c.2606 + 1G>A, p.Glu830ValfsTer9 variant and chromosome 3q29 duplication in a Turkish individual with Warburg micro syndrome.

Novel, homozygous RAB3GAP1 c.2606 + 1G>A, p.Glu830ValfsTer9 variant and chromosome 3q29 duplication in a Turkish individual with Warburg micro syndrome.

Journal: Clinical dysmorphology

Published: March 06, 2023

Novel guanosine diphosphate-mannose pyrophosphorylase A variant in an individual with achalasia, alacrima, and intellectual disability.

Novel guanosine diphosphate-mannose pyrophosphorylase A variant in an individual with achalasia, alacrima, and intellectual disability.

Journal: Clinical dysmorphology

Published: December 12, 2022

The course of sleep habits in newly diagnosed epilepsy in children: A prospective study.

The course of sleep habits in newly diagnosed epilepsy in children: A prospective study.

Journal: Epilepsy & behavior : E&B

Published: December 09, 2022

Molecular characterization of Turkish patients with demyelinating Charcot-Marie-Tooth disease.

Molecular characterization of Turkish patients with demyelinating Charcot-Marie-Tooth disease.

Journal: Neurogenetics

Published: March 10, 2022

Chromosomal microarray and exome sequencing in unexplained early infantile epileptic encephalopathies in a highly consanguineous population.

Chromosomal microarray and exome sequencing in unexplained early infantile epileptic encephalopathies in a highly consanguineous population.

Journal: The International journal of neuroscience

Published: August 11, 2021

Evaluation of the signs and symptoms of pseudotumor cerebri syndrome in pediatric population.

Evaluation of the signs and symptoms of pseudotumor cerebri syndrome in pediatric population.

Journal: Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery

Published: March 20, 2021

Active Giant Cell Vasculitis Diagnosis with 68Ga PSMA PET/CT Imaging.

Active Giant Cell Vasculitis Diagnosis with 68Ga PSMA PET/CT Imaging.

Journal: Molecular imaging and radionuclide therapy

Published: February 15, 2021

Comparison of brain F-18 FDG PET/MRI with PET/CT imaging in pediatric patients.

Comparison of brain F-18 FDG PET/MRI with PET/CT imaging in pediatric patients.

Journal: Clinical neurology and neurosurgery

Published: February 04, 2021

A Novel ELP2 Compound Heterozygous Mutation in a Boy with Severe Intellectual Disability, Spastic Diplegia, Stereotypic Behavior and Review of the Current Literature.

A Novel ELP2 Compound Heterozygous Mutation in a Boy with Severe Intellectual Disability, Spastic Diplegia, Stereotypic Behavior and Review of the Current Literature.

Journal: Molecular syndromology

Published: July 05, 2020

Acute flaccid myelitis outbreak through 2016-2018: A multicenter experience from Turkey.

Acute flaccid myelitis outbreak through 2016-2018: A multicenter experience from Turkey.

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

Published: June 15, 2020

A novel truncating mutation of DOCK7 gene with an early-onset non-encephalopathic epilepsy.

A novel truncating mutation of DOCK7 gene with an early-onset non-encephalopathic epilepsy.

Journal: Seizure

Published: October 05, 2018

Showing 1-12 of 14

Last Updated: 09/26/2026