Halil I. Aydin
Ankara, Turkey
Last Updated: 09/26/2026
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Found 26 publications
Evaluation of food rejection and swallowing function in inherited metabolic diseases on diet therapy.
Journal: European journal of clinical nutrition
Published: July 22, 2025
Effect of empagliflozin treatment on laboratory and clinical findings of patients with glycogen storage disease type Ib: first study from Türkiye.
Journal: Journal of pediatric endocrinology & metabolism : JPEM
Published: November 20, 2024
Short and Long-Term Outcomes of Liver Transplantation in Pediatric Patients With Inborn Errors of Metabolism: A Single-Center Study.
Journal: Pediatric transplantation
Published: August 14, 2024
Expert opinion on clinical presentation, diagnosis, and treatment of infantile-onset Pompe disease: a Delphi study in Türkiye.
Journal: Turkish journal of medical sciences
Published: May 23, 2024
Three-Country Snapshot of Ornithine Transcarbamylase Deficiency.
Journal: Life (Basel, Switzerland)
Published: September 22, 2022
A novel mutation in TRMT5 associated with idiopathic non-cirrhotic portal hypertension and hepatopulmonary syndrome: Case report of two siblings.
Journal: Clinics and research in hepatology and gastroenterology
Published: December 18, 2021
Severe isolated sulfide oxidase deficiency with a novel mutation.
Journal: The Turkish journal of pediatrics
Published: August 27, 2021
Bi-allelic loss-of-function OBSCN variants predispose individuals to severe recurrent rhabdomyolysis.
Journal: Brain : a journal of neurology
Published: June 04, 2021
The Relationship between Daily Fructose Consumption and Oxidized Low-Density Lipoprotein and Low-Density Lipoprotein Particle Size in Children with Obesity.
Journal: Pediatric gastroenterology, hepatology & nutrition
Published: March 04, 2021
Retrospective evaluation of patients with X-linked adrenoleukodystrophy with a wide range of clinical presentations: a single center experience.
Journal: Journal of pediatric endocrinology & metabolism : JPEM
Published: January 15, 2021
Coexistence of guanidinoacetate methyltransferase (GAMT) deficiency and neuroleptic malignant syndrome without creatine kinase elevation.
Journal: Brain & development
Published: October 14, 2019
A novel mutation in two cousins with guanidinoacetate methyltransferase (GAMT) deficiency presented with autism.
Journal: The Turkish journal of pediatrics
Published: September 28, 2019
Last Updated: 09/26/2026