Related Experiment Videos
Heparin and false-positive tests for mucopolysacchariduria
Lancet (London, England)
|August 5, 1972
Summary
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
Mitochondrial encephalomyopathy and complex III deficiency associated with a stop-codon mutation in the cytochrome b gene.
American journal of human genetics·2000
Cardiomyopathy in childhood, mitochondrial dysfunction, and the role of L-carnitine.
American heart journal·2000
D-2-Hydroxyglutaric aciduria: biochemical marker or clinical disease entity?
Annals of neurology·1999
Mutations in the liver glycogen synthase gene in children with hypoglycemia due to glycogen storage disease type 0.
The Journal of clinical investigation·1998
Inborn errors of metabolism: medical and administrative "orphans".
The American journal of managed care·1998
Early metastatic BRAFV600E mutation melanoma without known primary lesion: a case report.
Annals of medicine and surgery (2012)·2026
Dermatofibrosarcoma protuberans mimicking hemorrhoids: a rare case report.
International journal of surgery case reports·2026
Successful resection of a giant pericardial myolipoma in a resource-limited setting: a case report.
International journal of surgery case reports·2026
Metastatic Gastrointestinal Neuroectodermal Tumor Mimicking a Benign Hepatic Hemangioma on MRI: Role of 18F-FDG PET/CT.
Clinical nuclear medicine·2026