Mehmet Gunduz

Irfan Bastug St
Ankara, Turkey

Last Updated: 09/26/2026

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Found 28 publications

Diverse clinical spectrum of Niemann-Pick C: insights from a single center.

Diverse clinical spectrum of Niemann-Pick C: insights from a single center.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: February 26, 2026

Awareness and knowledge of obstetricians about prenatal findings of inherited metabolic disorders.

Awareness and knowledge of obstetricians about prenatal findings of inherited metabolic disorders.

Journal: Scientific reports

Published: February 09, 2026

Correction: Investigation of the Oxidative Process by Measuring Total Antioxidant Capacity and Total Oxidant Capacity in Patients with Gaucher Disease.

Correction: Investigation of the Oxidative Process by Measuring Total Antioxidant Capacity and Total Oxidant Capacity in Patients with Gaucher Disease.

Journal: Klinische Padiatrie

Published: June 02, 2025

Investigation of the Oxidative Process by Measuring Total Antioxidant Capacity and Total Oxidant Capacity in Patients with Gaucher Disease.

Investigation of the Oxidative Process by Measuring Total Antioxidant Capacity and Total Oxidant Capacity in Patients with Gaucher Disease.

Journal: Klinische Padiatrie

Published: May 05, 2025

Genetic, neuroimaging, and clinical characteristics of a cohort of individuals with L-2-hydroxyglutaric aciduria from Türkiye.

Genetic, neuroimaging, and clinical characteristics of a cohort of individuals with L-2-hydroxyglutaric aciduria from Türkiye.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: January 09, 2025

Evaluation of Lysosphingolipid Analysis for the Diagnosis of Lysosomal Storage Disease.

Evaluation of Lysosphingolipid Analysis for the Diagnosis of Lysosomal Storage Disease.

Journal: Klinische Padiatrie

Published: September 25, 2024

Clinical and Radiological Profile of Nine Patients with Metachromatic Leukodystrophy.

Clinical and Radiological Profile of Nine Patients with Metachromatic Leukodystrophy.

Journal: Molecular syndromology

Published: June 01, 2024

Evaluation of clinical, laboratory, and molecular genetic features of patients with biotinidase deficiency.

Evaluation of clinical, laboratory, and molecular genetic features of patients with biotinidase deficiency.

Journal: European journal of pediatrics

Published: September 04, 2023

The assessment of the knowledge and practices of healthcare providers regarding paroxysmal non-epileptic events (PNES) in children: A cross-sectional study.

The assessment of the knowledge and practices of healthcare providers regarding paroxysmal non-epileptic events (PNES) in children: A cross-sectional study.

Journal: Epileptic disorders : international epilepsy journal with videotape

Published: June 12, 2023

Out-of-pocket health expenditures in patients living with ınborn errors of metabolism.

Out-of-pocket health expenditures in patients living with ınborn errors of metabolism.

Journal: Orphanet journal of rare diseases

Published: August 24, 2022

CLN3-Associated NCL Case with a Preliminary Diagnosis of Niemann Pick Type C.

CLN3-Associated NCL Case with a Preliminary Diagnosis of Niemann Pick Type C.

Journal: Molecular syndromology

Published: February 19, 2022

Frequency and status of depression and anxiety in mothers of children with inborn errors of metabolism with restricted diet, with and without risk of metabolic crises.

Frequency and status of depression and anxiety in mothers of children with inborn errors of metabolism with restricted diet, with and without risk of metabolic crises.

Journal: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie

Published: October 08, 2021

Showing 1-12 of 28

Last Updated: 09/26/2026