Hidde Huidekoper

Dr. Hidde Huidekoper is a researcher in the Department of Pediatrics at Erasmus MC, affiliated with the Faculty of Medicine. His work focuses on inherited metabolic disorders, particularly in newborn screening, glycogen storage diseases, urea cycle disorders, and folate metabolism.

His research spans clinical studies, cohort analyses, and European collaborative efforts such as MetabERN, contributing to clinical pathway development and treatment accessibility for rare metabolic conditions.

Key research areas include:

• Glycogen Storage Disease Type II (Pompe Disease)
• Enzyme Replacement Therapy
• Newborn Screening Programs
• Metabolic Biochemistry and Blood Plasma Analysis
• Quality of Life in Pediatric Metabolic Disorders
• Folate and Carnitine Metabolism Defects

Recent publications highlight trends in evaluating treatment accessibility, developing clinical guidelines, and assessing long-term outcomes in rare diseases. His work is frequently published in high-impact journals such as Orphanet Journal of Rare Diseases and Journal of Inherited Metabolic Disease.

He has no listed scientific awards in the provided text.

Dr. Huidekoper actively collaborates with European experts in metabolic diseases and contributes to multidisciplinary research networks. While no formal advisees are listed, his role involves significant research leadership and clinical investigation. There is no mention of specific labs or teams, but his involvement in MetabERN indicates integration into large-scale clinical research infrastructure.