Familial association of metabolic myopathy, lactic acidosis and sideroblastic anemia
Authors:
- J.M. RawlesJRJ.M. Rawles
- R.O. WellerRWR.O. Weller
- 1 June 1974
- journal article
- research article
- Published by Elsevier in The American Journal of Medicine
- Vol. 56 (6) , 891-897
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
- Familial “mitochondrial” myopathyJournal of the Neurological Sciences, 1972
- Chronic lactic acidosis in an adultThe American Journal of Medicine, 1970
- HEREDITARY ABNORMAL MUSCLE METABOLISM WITH HYPERKINETIC CIRCULATION DURING EXERCISEActa Medica Scandinavica, 1969
- SKELETAL MUSCLE DISEASE WITH ABNORMAL MITOCHONDRIABrain, 1967
- TWO CHILDHOOD MYOPATHIES WITH ABNORMAL MITOCHONDRIABrain, 1966
- Hereditary metabolic myopathy with paroxysmal myoglobinuria due to abnormal glycolysisJournal of Neurology, Neurosurgery & Psychiatry, 1964
- A CASE OF SEVERE HYPERMETABOLISM OF NONTHYROID ORIGIN WITH A DEFECT IN THE MAINTENANCE OF MITOCHONDRIAL RESPIRATORY CONTROL: A CORRELATED CLINICAL, BIOCHEMICAL, AND MORPHOLOGICAL STUDYJournal of Clinical Investigation, 1962