McArdle's syndrome: a review and a preliminary report of four further cases
Open Access
- 1 May 1967
- journal article
- review article
- Published by Oxford University Press (OUP)
- Vol. 43 (499) , 365-371
- https://doi.org/10.1136/pgmj.43.499.365
Abstract
No abstract availableThis publication has 14 references indexed in Scilit:
- Histopathology of Voluntary MusclePublished by Oxford University Press (OUP) ,1965
- A Family Study of Phosphorylase Deficiency in MuscleAnnals of Internal Medicine, 1965
- McArdle's Syndrome with Previously Unreported Electrocardiographic and Serum Enzyme AbnormalitiesAnnals of Internal Medicine, 1965
- A case of McArdle's syndrome with a positive family historyJournal of Neurology, Neurosurgery & Psychiatry, 1964
- Glycogen storage disease of myocardiumAmerican Heart Journal, 1963
- McARDLE'S SYNDROME: PHOSPHORYLASE-DEFICIENT MYOPATHYThe Lancet, 1962
- A metabolic myopathy due to absence of muscle phosphorylaseThe American Journal of Medicine, 1961
- Hereditary Absence of Muscle Phosphorylase (McArdle's Syndrome)New England 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