HISTORICAL AND CURRENT CONCEPTS IN MITOCHONDRIAL MYOPATHIES

[1] SEQUENCE AND ORGANIZATION OF THE HUMAN MITOCHONDRIAL GENOME [J]. NATURE, 1981, 290 (5806) : 457 - 465

[2] DISORDER OF MUSCLE LIPID-METABOLISM AND MYOGLOBINURIA - ABSENCE OF CARNITINE PALMITYL TRANSFERASE [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1975, 292 (09) : 443 - 449

[3] BLASS J P, 1970, Journal of Clinical Investigation, V49, P423, DOI 10.1172/JCI106251

[4] LOW ACTIVITIES OF PYRUVATE AND OXOGLUTARATE DEHYDROGENASE COMPLEXES IN 5 PATIENTS WITH FRIEDREICHS ATAXIA [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1976, 295 (02) : 62 - 67

[5] ELECTRON CYTOCHEMISTRY OF CRYSTALLINE INCLUSIONS IN HUMAN SKELETAL-MUSCLE MITOCHONDRIA [J]. JOURNAL OF ULTRASTRUCTURE RESEARCH, 1975, 51 (03): : 404 - 408

[6] Byrne E, UNPUB

[7] MEGACONIAL MITOCHONDRIA OBSERVED IN A CASE OF CHRONIC POLYMYOSITIS [J]. ACTA NEUROPATHOLOGICA, 1969, 12 (01) : 68 - +

[8] NEW MYOPATHY WITH MITOCHONDRIAL ENZYME HYPERACTIVITY - HISTOCHEMICAL DEMONSTRATION [J]. JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1967, 199 (09): : 624 - &

[9] FATAL CASES OF LIPID STORAGE MYOPATHY WITH CARNITINE DEFICIENCY [J]. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1977, 40 (02) : 170 - 178

[10] ABRUPT NEUROLOGICAL DETERIORATION IN CHILDREN WITH KEARNS-SAYRE SYNDROME [J]. ARCHIVES OF NEUROLOGY, 1981, 38 (04) : 247 - 250

[1] SEQUENCE AND ORGANIZATION OF THE HUMAN MITOCHONDRIAL GENOME [J]. NATURE, 1981, 290 (5806) : 457 - 465

[2] DISORDER OF MUSCLE LIPID-METABOLISM AND MYOGLOBINURIA - ABSENCE OF CARNITINE PALMITYL TRANSFERASE [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1975, 292 (09) : 443 - 449

[3] BLASS J P, 1970, Journal of Clinical Investigation, V49, P423, DOI 10.1172/JCI106251

[4] LOW ACTIVITIES OF PYRUVATE AND OXOGLUTARATE DEHYDROGENASE COMPLEXES IN 5 PATIENTS WITH FRIEDREICHS ATAXIA [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1976, 295 (02) : 62 - 67

[5] ELECTRON CYTOCHEMISTRY OF CRYSTALLINE INCLUSIONS IN HUMAN SKELETAL-MUSCLE MITOCHONDRIA [J]. JOURNAL OF ULTRASTRUCTURE RESEARCH, 1975, 51 (03): : 404 - 408

[6] Byrne E, UNPUB

[7] MEGACONIAL MITOCHONDRIA OBSERVED IN A CASE OF CHRONIC POLYMYOSITIS [J]. ACTA NEUROPATHOLOGICA, 1969, 12 (01) : 68 - +

[8] NEW MYOPATHY WITH MITOCHONDRIAL ENZYME HYPERACTIVITY - HISTOCHEMICAL DEMONSTRATION [J]. JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1967, 199 (09): : 624 - &

[9] FATAL CASES OF LIPID STORAGE MYOPATHY WITH CARNITINE DEFICIENCY [J]. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1977, 40 (02) : 170 - 178

[10] ABRUPT NEUROLOGICAL DETERIORATION IN CHILDREN WITH KEARNS-SAYRE SYNDROME [J]. ARCHIVES OF NEUROLOGY, 1981, 38 (04) : 247 - 250