Familial association of metabolic myopathy, lactic acidosis and sideroblastic anemia
- 1 June 1974
- journal article
- research article
- Published by Elsevier in American Journal Of Medicine
- Vol. 56 (6), 891-897
- https://doi.org/10.1016/0002-9343(74)90820-1
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
- Familial “mitochondrial” myopathy: A myopathy associated with disordered oxidative metabolism in muscle fibres Part 1. Clinical, electrophysiological and pathological findingsJournal of the Neurological Sciences, 1972
- Chronic lactic acidosis in an adult: A new syndrome associated with an altered redox state of certain NAD/NADH coupled reactionsAmerican 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 STUDYJCI Insight, 1962