HYPOCARNITINAEMIA IN DISORDERS OF ORGANIC ACID METABOLISM
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference15 articles.
1. Progressive neonatal leukoencephalomyopathy due to absent 5,10-methylenetetrahydrofolate reductase, responsive to treatment;Allen;Ann Neurol,1980
2. An improved and simplified radioisotopic assay for the determination of free and esterified carnitine;McGarry;J Lipid Res,1976
3. Disorders of lipid metabolism;DiMauro;Muscle Nerve,1980
4. Defective propionate carboxylation m ketotic hyperglycinemia;Hsia;Lancet,1969
5. Carnitine deficiency induced during intermittent haemodialysis for renal failure;Bohmer;Lancet,1978
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1. Characterization of acylcarnitines using fast atom bombardment mass spectrometry and gas chromatography/mass spectrometry;Journal of Mass Spectrometry;1995-01
2. Is Carnitine Essential in Children?;Journal of International Medical Research;1991-03
3. Progressive renal insufficiency in methylmalonic acidemia;Pediatric Nephrology;1991
4. Les triglycérides à chaînes moyennes en nutrition clinique;Nutrition Clinique et Métabolisme;1989-01
5. Cardiac manifestations in disorders of fat and carnitine metabolism in infancy;Journal of the American College of Cardiology;1988-06
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