Selahattin Tekes

Dicle, Turkey

Last Updated: 09/26/2026

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Found 15 publications

Genotypic and phenotypic spectrum of congenital myasthenic syndrome: Insights from Southeastern Türkiye.

Genotypic and phenotypic spectrum of congenital myasthenic syndrome: Insights from Southeastern Türkiye.

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

Published: April 24, 2026

Phenotypic variability in Klinefelter syndrome: clinical findings including reported fatherhood.

Phenotypic variability in Klinefelter syndrome: clinical findings including reported fatherhood.

Journal: Endocrine

Published: November 18, 2025

A Comprehensive Perspective on Febrile Seizures in Children: A Prospective Cohort Study with Evaluation of Clinical, Laboratory, and Genetic Features.

A Comprehensive Perspective on Febrile Seizures in Children: A Prospective Cohort Study with Evaluation of Clinical, Laboratory, and Genetic Features.

Journal: Journal of clinical medicine

Published: August 28, 2025

Clinical application of whole-exome sequencing analysis in childhood epilepsy.

Clinical application of whole-exome sequencing analysis in childhood epilepsy.

Journal: Journal of neurogenetics

Published: December 10, 2024

Clinical, biochemical, and genotypical characteristics in urea cycle mitochondrial transporter disorders.

Clinical, biochemical, and genotypical characteristics in urea cycle mitochondrial transporter disorders.

Journal: European review for medical and pharmacological sciences

Published: March 18, 2024

COMPARISON OF C-PEPTIDE LEVELS IN MONOGENIC FORMS OF DIABETES WITH OTHER TYPES OF DIABETES: A SINGLE-CENTER STUDY.

COMPARISON OF C-PEPTIDE LEVELS IN MONOGENIC FORMS OF DIABETES WITH OTHER TYPES OF DIABETES: A SINGLE-CENTER STUDY.

Journal: Acta endocrinologica (Bucharest, Romania : 2005)

Published: February 15, 2024

The clinical and demographic characteristics of patients with late-diagnosed cerebrotendinous xanthomatosis in a Turkish population.

The clinical and demographic characteristics of patients with late-diagnosed cerebrotendinous xanthomatosis in a Turkish population.

Journal: Journal of clinical lipidology

Published: January 06, 2024

Prevalence of HLA B27 in Patients Diagnosed with Ankylosing Spondylitis (AS) in Diyarbakır, Southeastern Region of Turkey.

Prevalence of HLA B27 in Patients Diagnosed with Ankylosing Spondylitis (AS) in Diyarbakır, Southeastern Region of Turkey.

Journal: Nigerian journal of clinical practice

Published: April 05, 2023

Crystalline gene mutations in Turkish children with congenital cataracts.

Crystalline gene mutations in Turkish children with congenital cataracts.

Journal: International ophthalmology

Published: September 11, 2020

Early-infantile onset epilepsy and developmental delay caused by bi-allelic GAD1 variants.

Early-infantile onset epilepsy and developmental delay caused by bi-allelic GAD1 variants.

Journal: Brain : a journal of neurology

Published: November 29, 2019

Clinical characteristics and molecular genetic analysis of 22 patients with neonatal diabetes from the South-Eastern region of Turkey: predominance of non-KATP channel mutations.

Clinical characteristics and molecular genetic analysis of 22 patients with neonatal diabetes from the South-Eastern region of Turkey: predominance of non-KATP channel mutations.

Journal: European journal of endocrinology

Published: October 08, 2014

Seroprevalence of serum HBsAg positivity and hepatitis delta virus infection among blood donors in Southeastern Turkey.

Seroprevalence of serum HBsAg positivity and hepatitis delta virus infection among blood donors in Southeastern Turkey.

Journal: La Clinica terapeutica

Published: April 29, 2014

Showing 1-12 of 15

Last Updated: 09/26/2026