Related Experiment Videos
Detection of inborn errors of metabolism. II. Defects in propionic acid metabolism
Clinical Genetics
|January 1, 1974
Abstract
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
Guideline for the diagnosis and management of glutaryl-CoA dehydrogenase deficiency (glutaric aciduria type I).
Journal of inherited metabolic disease·2007
Infant mice with glutaric acidaemia type I have increased vulnerability to 3-nitropropionic acid toxicity.
Journal of inherited metabolic disease·2006
Vascular dysfunction as an additional pathomechanism in glutaric aciduria type I.
Journal of inherited metabolic disease·2004
Glutaric aciduria type I: outcome in the Republic of Ireland.
Journal of inherited metabolic disease·2004
Development of pathogenic concepts in glutaryl-CoA dehydrogenase deficiency: the challenge.
Journal of inherited metabolic disease·2004
A Homozygous Variant in DMRTB1 Is Associated With Non-Obstructive Azoospermia in Humans.
Clinical genetics·2026
Advancing insights into fibromyalgia: an updated review of diagnosis and differential diagnosis.
Expert review of neurotherapeutics·2026
Fibromyalgia beyond pain: a multisystemic dysregulation framework.
Pain management·2026
MMP-9 and non-invasive markers in evaluating MASLD and atherosclerosis.
Journal, genetic engineering & biotechnology·2026
[Research progress in diagnosis and treatment of multiple ligament knee injuries].
Zhongguo xiu fu chong jian wai ke za zhi = Zhongguo xiufu chongjian waike zazhi = Chinese journal of reparative and reconstructive surgery·2026
Metaproteomics in the Study of Marine Microbial Processes: Opportunities in Ocean Research and Diagnosis.
Annual review of marine science·2026