Related Experiment Videos
First trimester prenatal exclusion of glutaryl-CoA dehydrogenase deficiency (glutaric aciduria type 1)
1University Department of Paediatrics, Rigshospitalet, Copenhagen, Denmark.
Journal of Inherited Metabolic Disease
|January 1, 1989
Abstract
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
An evaluation of initiatives to enhance hospital rotations during GP speciality training in Denmark.
Education for primary care : an official publication of the Association of Course Organisers, National Association of GP Tutors, World Organisation of Family Doctors·2025
Physics performance of a low-luminosity low energy neutrino factory.
Physical review letters·2013
Plasma osteopontin as a biomarker of prostate cancer aggression: relationship to risk category and treatment response.
British journal of cancer·2012
Randomised clinical trial: identification of responders to short-term treatment with esomeprazole for dyspepsia in primary care - a randomised, placebo-controlled study.
Alimentary pharmacology & therapeutics·2010
Consensus Guidelines for Diagnosis and Management of Pyruvate Dehydrogenase Complex Deficiency.
Journal of inherited metabolic disease·2026
Essential Oral Single Nutritional Therapy Products for Inherited Metabolic Diseases: Evidence and Consensus Assessment Using a Modified Delphi Method.
Journal of inherited metabolic disease·2026
Congenital Disorders of Glycosylation (CDG): State of the Art in 2026.
Journal of inherited metabolic disease·2026
Treatment of Fatty Acid Oxidation Disorders Today: Emerging Personalized Treatment Strategies.
Journal of inherited metabolic disease·2026
International Guideline on the Diagnosis, Treatment, and Monitoring of Long-Chain Fatty Acid Oxidation Disorders (LC-FAOD).
Journal of inherited metabolic disease·2026
Evaluation of genetic parameters affecting the reliability and effectiveness of kinship reconstruction in Forest and Tundra Nenets populations using X-STR markers.
Vavilovskii zhurnal genetiki i selektsii·2026
A novel variant c.1185_1196dup (p.(Gly396_Ser399dup)) in the SLC26A4 gene associated with recessive hearing loss.
Vavilovskii zhurnal genetiki i selektsii·2026