DEFECTS OF THE RESPIRATORY-CHAIN

[1] ACKRELL BAC, 1984, J BIOL CHEM, V159, P10053

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

[3] CHILDHOOD ENCEPHALOMYOPATHY WITH CYTOCHROME-C-OXIDASE DEFICIENCY, ATAXIA, MUSCLE WASTING, AND MENTAL IMPAIRMENT [J]. NEUROLOGY, 1986, 36 (08) : 1048 - 1052

[4] 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

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

[6] CYTOCHROME-C-OXIDASE DEFICIENCY IN SUBACUTE NECROTIZING ENCEPHALOMYELOPATHY [J]. JOURNAL OF THE NEUROLOGICAL SCIENCES, 1987, 77 (01) : 103 - 115

[7] BASTIAENSEN LAK, 1978, ACTA NEUROL SCAND, V58, P9

[8] BIOTINIDASE DEFICIENCY - A CAUSE OF SUBACUTE NECROTIZING ENCEPHALOMYELOPATHY (LEIGH SYNDROME) - REPORT OF A CASE WITH LETHAL OUTCOME [J]. PEDIATRIC RESEARCH, 1989, 26 (03) : 260 - 266

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

[10] LUMPING OR SPLITTING - OPHTHALMOPLEGIA-PLUS OR KEARNS-SAYRE SYNDROME [J]. ANNALS OF NEUROLOGY, 1977, 1 (01) : 37 - 54

[1] ACKRELL BAC, 1984, J BIOL CHEM, V159, P10053

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

[3] CHILDHOOD ENCEPHALOMYOPATHY WITH CYTOCHROME-C-OXIDASE DEFICIENCY, ATAXIA, MUSCLE WASTING, AND MENTAL IMPAIRMENT [J]. NEUROLOGY, 1986, 36 (08) : 1048 - 1052

[4] 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

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

[6] CYTOCHROME-C-OXIDASE DEFICIENCY IN SUBACUTE NECROTIZING ENCEPHALOMYELOPATHY [J]. JOURNAL OF THE NEUROLOGICAL SCIENCES, 1987, 77 (01) : 103 - 115

[7] BASTIAENSEN LAK, 1978, ACTA NEUROL SCAND, V58, P9

[8] BIOTINIDASE DEFICIENCY - A CAUSE OF SUBACUTE NECROTIZING ENCEPHALOMYELOPATHY (LEIGH SYNDROME) - REPORT OF A CASE WITH LETHAL OUTCOME [J]. PEDIATRIC RESEARCH, 1989, 26 (03) : 260 - 266

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

[10] LUMPING OR SPLITTING - OPHTHALMOPLEGIA-PLUS OR KEARNS-SAYRE SYNDROME [J]. ANNALS OF NEUROLOGY, 1977, 1 (01) : 37 - 54