MITOCHONDRIAL MYOPATHIES

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

[2] TREATMENT OF MITOCHONDRIAL MYOPATHY DUE TO COMPLEX-III DEFICIENCY WITH VITAMINS K3 AND C - A P-31-NMR FOLLOW-UP-STUDY [J]. ANNALS OF NEUROLOGY, 1986, 19 (06) : 598 - 602

[3] ARTS WFM, 1983, LANCET, V2, P581

[4] MITOCHONDRIAL MYOPATHY WITH LACTIC-ACIDOSIS AND DEFICIENT ACTIVITY OF MUSCLE SUCCINATE CYTOCHROME-C-OXIDOREDUCTASE [J]. EUROPEAN JOURNAL OF PEDIATRICS, 1984, 143 (01) : 67 - 71

[5] FASTING HYPOGLYCEMIA RESULTING FROM HEPATIC CARNITINE PALMITOYL TRANSFERASE DEFICIENCY [J]. JOURNAL OF PEDIATRICS, 1981, 98 (05) : 742 - 746

[6] MITOCHONDRIAL CYTOCHROME DEFICIENCY PRESENTING AS A MYOPATHY WITH HYPOTONIA, EXTERNAL OPHTHALMOPLEGIA, AND LACTIC-ACIDOSIS IN AN INFANT AND AS FATAL HEPATOPATHY IN A 2ND COUSIN [J]. ANNALS OF NEUROLOGY, 1983, 14 (04) : 462 - 470

[7] FATAL INFANTILE CYTOCHROME-C OXIDASE DEFICIENCY - DECREASE OF IMMUNOLOGICALLY DETECTABLE ENZYME IN MUSCLE [J]. NEUROLOGY, 1985, 35 (06) : 802 - 812

[8] PARTIAL CYTOCHROME-OXIDASE (AA3) DEFICIENCY IN CHRONIC PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA - HISTOCHEMICAL AND BIOCHEMICAL-STUDIES [J]. JOURNAL OF THE NEUROLOGICAL SCIENCES, 1985, 71 (2-3) : 257 - 271

[9] CHRISTENSEN E, 1986, 24TH P ANN S AM, P72

[10] MITOCHONDRIAL MYOPATHIES - DEFECTS IN MITOCHONDRIAL METABOLISM IN HUMAN SKELETAL-MUSCLE [J]. BIOCHEMICAL SOCIETY TRANSACTIONS, 1983, 11 (06) : 626 - 627

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

[2] TREATMENT OF MITOCHONDRIAL MYOPATHY DUE TO COMPLEX-III DEFICIENCY WITH VITAMINS K3 AND C - A P-31-NMR FOLLOW-UP-STUDY [J]. ANNALS OF NEUROLOGY, 1986, 19 (06) : 598 - 602

[3] ARTS WFM, 1983, LANCET, V2, P581

[4] MITOCHONDRIAL MYOPATHY WITH LACTIC-ACIDOSIS AND DEFICIENT ACTIVITY OF MUSCLE SUCCINATE CYTOCHROME-C-OXIDOREDUCTASE [J]. EUROPEAN JOURNAL OF PEDIATRICS, 1984, 143 (01) : 67 - 71

[5] FASTING HYPOGLYCEMIA RESULTING FROM HEPATIC CARNITINE PALMITOYL TRANSFERASE DEFICIENCY [J]. JOURNAL OF PEDIATRICS, 1981, 98 (05) : 742 - 746

[6] MITOCHONDRIAL CYTOCHROME DEFICIENCY PRESENTING AS A MYOPATHY WITH HYPOTONIA, EXTERNAL OPHTHALMOPLEGIA, AND LACTIC-ACIDOSIS IN AN INFANT AND AS FATAL HEPATOPATHY IN A 2ND COUSIN [J]. ANNALS OF NEUROLOGY, 1983, 14 (04) : 462 - 470

[7] FATAL INFANTILE CYTOCHROME-C OXIDASE DEFICIENCY - DECREASE OF IMMUNOLOGICALLY DETECTABLE ENZYME IN MUSCLE [J]. NEUROLOGY, 1985, 35 (06) : 802 - 812

[8] PARTIAL CYTOCHROME-OXIDASE (AA3) DEFICIENCY IN CHRONIC PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA - HISTOCHEMICAL AND BIOCHEMICAL-STUDIES [J]. JOURNAL OF THE NEUROLOGICAL SCIENCES, 1985, 71 (2-3) : 257 - 271

[9] CHRISTENSEN E, 1986, 24TH P ANN S AM, P72

[10] MITOCHONDRIAL MYOPATHIES - DEFECTS IN MITOCHONDRIAL METABOLISM IN HUMAN SKELETAL-MUSCLE [J]. BIOCHEMICAL SOCIETY TRANSACTIONS, 1983, 11 (06) : 626 - 627