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52. [A case of familial mitochondrial myopathy associated with peripheral neuropathy and optic atrophy]. Watanabe M; Mizusawa H; Kanazawa I; Nakanisi T Rinsho Shinkeigaku; 1987 Sep; 27(9):1163-6. PubMed ID: 2831006 [No Abstract] [Full Text] [Related]
53. Mitochondrial defects of brain and muscle. De Vivo DC; DiMauro S Biol Neonate; 1990; 58 Suppl 1():54-69. PubMed ID: 2265220 [TBL] [Abstract][Full Text] [Related]
54. An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytes. Barth PG; Scholte HR; Berden JA; Van der Klei-Van Moorsel JM; Luyt-Houwen IE; Van 't Veer-Korthof ET; Van der Harten JJ; Sobotka-Plojhar MA J Neurol Sci; 1983 Dec; 62(1-3):327-55. PubMed ID: 6142097 [TBL] [Abstract][Full Text] [Related]
55. Muscle coenzyme Q deficiency in familial mitochondrial encephalomyopathy. Ogasahara S; Engel AG; Frens D; Mack D Proc Natl Acad Sci U S A; 1989 Apr; 86(7):2379-82. PubMed ID: 2928337 [TBL] [Abstract][Full Text] [Related]
56. Myopathy with mitochondrial inclusion bodies: histological and metabolic studies. Sulaiman WR; Doyle D; Johnson RH; Jennett S J Neurol Neurosurg Psychiatry; 1974 Nov; 37(11):1236-46. PubMed ID: 4376164 [TBL] [Abstract][Full Text] [Related]
57. Familial "mitochondrial" myopathy. A myopathy associated with disordered oxidative metabolism in muscle fibres. 2. Biochemical findings. Worsfold M; Park DC; Pennington RJ J Neurol Sci; 1973 Jul; 19(3):261-74. PubMed ID: 4716844 [No Abstract] [Full Text] [Related]
58. [A case of mitochondrial encephalomyopathy (MELAS) with abnormality of the electron transfer chain]. Utatsu Y; Nakagawa M; Yamano T; Osame M; Igata A Rinsho Shinkeigaku; 1987 Sep; 27(9):1109-16. PubMed ID: 3440355 [No Abstract] [Full Text] [Related]
59. A study of a family with inherited disease of cardiac and skeletal muscle. Part II. Skeletal muscle morphology and mitochondrial oxidative phosphorylation. Lochner A; Hewlett RH; O'Kennedy A; van der Walt JJ; Tiedt FA; Hoffman H; de Graaf AS; Przybojewski JZ; Torrington M S Afr Med J; 1981 Mar; 59(13):453-61. PubMed ID: 6259763 [TBL] [Abstract][Full Text] [Related]
60. Simultaneous metabolic profile studies of three patients with fatal infantile mitochondrial myopathy-de Toni-Fanconi-Debré syndrome by GC/MS. Ning C; Kuhara T; Matsumoto I Clin Chim Acta; 1996 Mar; 247(1-2):197-200. PubMed ID: 8920239 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]