MCARDLES SYNDROME (MYOPHOSPHORYLASE DEFICIENCY) - A STUDY OF A FAMILY
- 1 January 1967
- journal article
- research article
- Vol. 36 (144), 565-+
Abstract
No abstract availableThis publication has 11 references indexed in Scilit:
- McArdle's Syndrome with Previously Unreported Electrocardiographic and Serum Enzyme AbnormalitiesAnnals of Internal Medicine, 1965
- A Family Study of Phosphorylase Deficiency in MuscleAnnals of Internal Medicine, 1965
- A case of McArdle's syndrome with a positive family historyJournal of Neurology, Neurosurgery & Psychiatry, 1964
- McArdle's DiseaseArchives of Neurology, 1963
- CYTOCHEMISTRY AND ELECTRON MICROSCOPYThe Journal of cell biology, 1963
- A metabolic myopathy due to absence of muscle phosphorylaseAmerican Journal Of Medicine, 1961
- CHRONIC PROGRESSIVE MYOPATHY WITH MYOGLOBINURIA: DEMONSTRATION OF A GLYCOGENOLYTIC DEFECT IN THE MUSCLE*Journal of Clinical Investigation, 1959
- A FUNCTIONAL DISORDER OF MUSCLE ASSOCIATED WITH THE ABSENCE OF PHOSPHORYLASEProceedings of the National Academy of Sciences, 1959
- A STUDY OF FIXATION FOR ELECTRON MICROSCOPYThe Journal of Experimental Medicine, 1952
- MYOPATHY DUE TO A DEFECT IN MUSCLE GLYCOGEN BREAKDOWN1951