Gulden F. Gokcay
Istanbul, Turkey
Last Updated: 09/26/2026
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Found 63 publications
Familial hypercholesterolaemia in children: diagnostic profile and factors influencing diagnosis in a tertiary referral centre.
Journal: Cardiology in the young
Published: June 25, 2026
The silent threat in mucopolysaccharidosis: assessment of sleep quality and disorders.
Journal: Journal of pediatric endocrinology & metabolism : JPEM
Published: March 19, 2026
Harmonizing Perspectives on MPS II Care in Türkiye: A Delphi Study Towards Treatment Management Consensus.
Journal: Healthcare (Basel, Switzerland)
Published: February 20, 2026
Factors affecting the success of follow-up and treatment of adults with phenylketonuria diagnosed by newborn screening.
Journal: Journal of pediatric endocrinology & metabolism : JPEM
Published: February 17, 2026
Glutaric acidemia type 1 in a non-newborn-screened cohort: clinical, biochemical, and molecular features and neurologic outcomes.
Journal: Italian journal of pediatrics
Published: January 12, 2026
Shifting Towards Empagliflozin First-Line Therapy in Glycogen Storage Disease Type Ib: A Nationwide Real-World Study.
Journal: Journal of inherited metabolic disease
Published: December 22, 2025
Correction: Choline supplementation in classic homocystinuria: impact on homocysteine and hepatic steatosis.
Journal: Pediatric research
Published: November 01, 2025
Response to the letter by Schmitt et al.
Journal: European journal of endocrinology
Published: August 07, 2025
Evaluation of Serum FGF21 Levels in Patients with Mitochondrial Aminoacyl-tRNA Synthetase Deficiency.
Journal: International journal of molecular sciences
Published: July 28, 2025
Profiles of paediatric patients experiencing stroke-like episodes associated with mitochondrial disease.
Journal: Frontiers in neurology
Published: July 01, 2025
The genotypic and phenotypic landscape of PDHA1-related pyruvate dehydrogenase complex deficiency.
Journal: Brain : a journal of neurology
Published: July 01, 2025
Last Updated: 09/26/2026