Recurrent myoglobinuria and muscle carnitine palmityltransferase deficiency
- 31 August 1977
- journal article
- case report
- Published by Elsevier in The Journal of Pediatrics
- Vol. 91 (2), 247-250
- https://doi.org/10.1016/s0022-3476(77)80821-4
Abstract
No abstract availableKeywords
This publication has 16 references indexed in Scilit:
- A Disorder of Muscle Lipid Metabolism and MyoglobinuriaNew England Journal of Medicine, 1975
- Muscle Carnitine Palmityltransferase Deficiency and MyoglobinuriaScience, 1973
- The activities of lipases and carnitine palmitoyl-transferase in muscles from vertebrates and invertebratesBiochemical Journal, 1972
- A Skeletal-Muscle Disorder Associated with Intermittent Symptoms and a Possible Defect of Lipid MetabolismNew England Journal of Medicine, 1970
- [55] The assay of (−)-carnitine and its o-acyl derivativesMethods in Enzymology, 1969
- Contracture in McArdle's DiseaseArchives of Neurology, 1965
- Phosphofructokinase deficiency in skeletal muscle. A new type of glycogenosisBiochemical and Biophysical Research Communications, 1965
- McArdle's DiseaseArchives of Neurology, 1963
- A metabolic myopathy due to absence of muscle phosphorylaseAmerican Journal Of Medicine, 1961
- [7] Chemical procedures for analysis of polysaccharidesMethods in Enzymology, 1957