DEFECTS OF THE RESPIRATORY-CHAIN

[71] SUBACUTE NECROTIZING ENCEPHALOMYELOPATHY IN AN INFANT [J]. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1951, 14 (03) : 216 - 221

[72] LJUNGDAHL PO, 1989, J BIOL CHEM, V264, P3723

[73] TISSUE-SPECIFIC GENES FOR RESPIRATORY PROTEINS [J]. TRENDS IN BIOCHEMICAL SCIENCES, 1989, 14 (12) : 501 - 503

[74] A CASE OF SEVERE HYPERMETABOLISM OF NONTHYROID ORIGIN WITH A DEFECT IN MAINTENANCE OF MITOCHONDRIAL RESPIRATORY CONTROL - A CORRELATED CLINICAL, BIOCHEMICAL, AND MORPHOLOGICAL STUDY [J]. JOURNAL OF CLINICAL INVESTIGATION, 1962, 41 (09) : 1776 - &

[75] A NEW TYPE OF MITOCHONDRIAL ENCEPHALOMYOPATHY WITH STROKE-LIKE EPISODES DUE TO CYTOCHROME-OXIDASE DEFICIENCY [J]. JOURNAL OF INHERITED METABOLIC DISEASE, 1988, 11 : 186 - 188

[76] DEFECT IN SUCCINATE OXIDATION BY ISOLATED MUSCLE MITOCHONDRIA IN A PATIENT WITH SYMMETRICAL LESIONS IN THE BASAL GANGLIA [J]. JOURNAL OF THE NEUROLOGICAL SCIENCES, 1988, 84 (2-3) : 189 - 200

[77] MENDELL JR, 1987, ANN NEUROL, V22, P128

[78] FATAL INFANTILE MITOCHONDRIAL MYOPATHY DUE TO CYTOCHROME-C OXIDASE DEFICIENCY [J]. JOURNAL OF THE NEUROLOGICAL SCIENCES, 1983, 60 (03) : 453 - 463

[79] CYTOCHROME-C OXIDASE DEFICIENCY IN LEIGHS SYNDROME - GENETIC-EVIDENCE FOR A NUCLEAR DNA-ENCODED MUTATION [J]. NEUROLOGY, 1989, 39 (05) : 697 - 702

[80] 2 SIBLINGS WITH CYTOCHROME-C OXIDASE DEFICIENCY [J]. JOURNAL OF INHERITED METABOLIC DISEASE, 1983, 6 (03) : 121 - 122

[71] SUBACUTE NECROTIZING ENCEPHALOMYELOPATHY IN AN INFANT [J]. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1951, 14 (03) : 216 - 221

[72] LJUNGDAHL PO, 1989, J BIOL CHEM, V264, P3723

[73] TISSUE-SPECIFIC GENES FOR RESPIRATORY PROTEINS [J]. TRENDS IN BIOCHEMICAL SCIENCES, 1989, 14 (12) : 501 - 503

[74] A CASE OF SEVERE HYPERMETABOLISM OF NONTHYROID ORIGIN WITH A DEFECT IN MAINTENANCE OF MITOCHONDRIAL RESPIRATORY CONTROL - A CORRELATED CLINICAL, BIOCHEMICAL, AND MORPHOLOGICAL STUDY [J]. JOURNAL OF CLINICAL INVESTIGATION, 1962, 41 (09) : 1776 - &

[75] A NEW TYPE OF MITOCHONDRIAL ENCEPHALOMYOPATHY WITH STROKE-LIKE EPISODES DUE TO CYTOCHROME-OXIDASE DEFICIENCY [J]. JOURNAL OF INHERITED METABOLIC DISEASE, 1988, 11 : 186 - 188

[76] DEFECT IN SUCCINATE OXIDATION BY ISOLATED MUSCLE MITOCHONDRIA IN A PATIENT WITH SYMMETRICAL LESIONS IN THE BASAL GANGLIA [J]. JOURNAL OF THE NEUROLOGICAL SCIENCES, 1988, 84 (2-3) : 189 - 200

[77] MENDELL JR, 1987, ANN NEUROL, V22, P128

[78] FATAL INFANTILE MITOCHONDRIAL MYOPATHY DUE TO CYTOCHROME-C OXIDASE DEFICIENCY [J]. JOURNAL OF THE NEUROLOGICAL SCIENCES, 1983, 60 (03) : 453 - 463

[79] CYTOCHROME-C OXIDASE DEFICIENCY IN LEIGHS SYNDROME - GENETIC-EVIDENCE FOR A NUCLEAR DNA-ENCODED MUTATION [J]. NEUROLOGY, 1989, 39 (05) : 697 - 702

[80] 2 SIBLINGS WITH CYTOCHROME-C OXIDASE DEFICIENCY [J]. JOURNAL OF INHERITED METABOLIC DISEASE, 1983, 6 (03) : 121 - 122