TISSUE-SPECIFICITY IN CYTOCHROME-C OXIDASE DEFICIENT MYOPATHY

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

[2] 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

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

[4] PROGRESSIVE CYTOCHROME-C-OXIDASE DEFICIENCY IN A CASE OF KEARNS-SAYRE SYNDROME - MORPHOLOGICAL, IMMUNOLOGICAL, AND BIOCHEMICAL-STUDIES IN MUSCLE BIOPSIES AND AUTOPSY TISSUES [J]. ANNALS OF NEUROLOGY, 1987, 21 (06) : 564 - 572

[5] DARLEYUSMAR VM, 1986, CLIN CHIM ACTA, V158, P253, DOI 10.1016/0009-8981(86)90289-5

[6] BENIGN INFANTILE MITOCHONDRIAL MYOPATHY DUE TO REVERSIBLE CYTOCHROME-C OXIDASE DEFICIENCY [J]. ANNALS OF NEUROLOGY, 1983, 14 (02) : 226 - 234

[7] DIMAURO S, 1986, ANN NY ACAD SCI, V488, P19

[8] CYTOCHROME-C-OXIDASE DEFICIENCY IN LEIGH SYNDROME [J]. ANNALS OF NEUROLOGY, 1987, 22 (04) : 498 - 506

[9] MITOCHONDRIAL MYOPATHIES [J]. ANNALS OF NEUROLOGY, 1985, 17 (06) : 521 - 538

[10] RETRIEVAL OF CRYOSTAT SECTIONS FOR COMPARISON OF HISTOCHEMISTRY AND QUANTITATIVE ELECTRON-MICROSCOPY IN A MUSCLE-FIBER [J]. JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1977, 25 (10) : 1169 - 1177

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

[2] 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

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

[4] PROGRESSIVE CYTOCHROME-C-OXIDASE DEFICIENCY IN A CASE OF KEARNS-SAYRE SYNDROME - MORPHOLOGICAL, IMMUNOLOGICAL, AND BIOCHEMICAL-STUDIES IN MUSCLE BIOPSIES AND AUTOPSY TISSUES [J]. ANNALS OF NEUROLOGY, 1987, 21 (06) : 564 - 572

[5] DARLEYUSMAR VM, 1986, CLIN CHIM ACTA, V158, P253, DOI 10.1016/0009-8981(86)90289-5

[6] BENIGN INFANTILE MITOCHONDRIAL MYOPATHY DUE TO REVERSIBLE CYTOCHROME-C OXIDASE DEFICIENCY [J]. ANNALS OF NEUROLOGY, 1983, 14 (02) : 226 - 234

[7] DIMAURO S, 1986, ANN NY ACAD SCI, V488, P19

[8] CYTOCHROME-C-OXIDASE DEFICIENCY IN LEIGH SYNDROME [J]. ANNALS OF NEUROLOGY, 1987, 22 (04) : 498 - 506

[9] MITOCHONDRIAL MYOPATHIES [J]. ANNALS OF NEUROLOGY, 1985, 17 (06) : 521 - 538

[10] RETRIEVAL OF CRYOSTAT SECTIONS FOR COMPARISON OF HISTOCHEMISTRY AND QUANTITATIVE ELECTRON-MICROSCOPY IN A MUSCLE-FIBER [J]. JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1977, 25 (10) : 1169 - 1177