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22. Mosaicism of mitochondria in mitochondrial myopathy: an electronmicroscopic analysis of cytochrome c oxidase. Haginoya K; Miyabayashi S; Iinuma K; Tada K Acta Neuropathol; 1990; 80(6):642-8. PubMed ID: 2177307 [TBL] [Abstract][Full Text] [Related]
23. Biochemical studies in mitochondrial encephalomyopathy. Goda S; Ishimoto S; Goto I; Kuroiwa Y; Koike K; Koike M; Nakagawa M; Reichmann H; DiMauro S J Neurol Neurosurg Psychiatry; 1987 Oct; 50(10):1348-52. PubMed ID: 3681314 [TBL] [Abstract][Full Text] [Related]
24. The syndrome of systemic carnitine deficiency. Clinical, morphologic, biochemical, and pathophysiologic features. Karpati G; Carpenter S; Engel AG; Watters G; Allen J; Rothman S; Klassen G; Mamer OA Neurology; 1975 Jan; 25(1):16-24. PubMed ID: 234182 [TBL] [Abstract][Full Text] [Related]
25. Reversible mitochondrial myopathy with cytochrome c oxidase deficiency. Salo MK; Rapola J; Somer H; Pihko H; Koivikko M; Tritschler HJ; DiMauro S Arch Dis Child; 1992 Aug; 67(8):1033-5. PubMed ID: 1325759 [TBL] [Abstract][Full Text] [Related]
26. Myopathy in vitamin E deficient rats: muscle fibre necrosis associated with disturbances of mitochondrial function. Thomas PK; Cooper JM; King RH; Workman JM; Schapira AH; Goss-Sampson MA; Muller DP J Anat; 1993 Dec; 183 ( Pt 3)(Pt 3):451-61. PubMed ID: 8300427 [TBL] [Abstract][Full Text] [Related]
27. A mitochondrial encephalomyopathy with cardiomyopathy. A case revealing a defect of complex I in the respiratory chain. Nishizawa M; Tanaka K; Shinozawa K; Kuwabara T; Atsumi T; Miyatake T; Ohama E J Neurol Sci; 1987 Apr; 78(2):189-201. PubMed ID: 3106581 [TBL] [Abstract][Full Text] [Related]
28. 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]
29. Mitochondrial cytochrome deficiency presenting as a myopathy with hypotonia, external ophthalmoplegia, and lactic acidosis in an infant and as fatal hepatopathy in a second cousin. Boustany RN; Aprille JR; Halperin J; Levy H; DeLong GR Ann Neurol; 1983 Oct; 14(4):462-70. PubMed ID: 6314875 [TBL] [Abstract][Full Text] [Related]
30. Infantile familial cardiomyopathy due to mitochondrial complex I and IV associated deficiency. Romero NB; Marsac C; Paturneau-Jouas M; Ogier H; Magnier S; Fardeau M Neuromuscul Disord; 1993 Jan; 3(1):31-42. PubMed ID: 8392409 [TBL] [Abstract][Full Text] [Related]
31. Childhood mitochondrial myopathy with ophthalmoplegia. Land JM; Hockaday JM; Hughes JT; Ross BD J Neurol Sci; 1981 Sep; 51(3):371-82. PubMed ID: 7276984 [TBL] [Abstract][Full Text] [Related]
32. Two cases of NADH-coenzyme Q reductase deficiency: relationship to MELAS syndrome. Kobayashi M; Morishita H; Sugiyama N; Yokochi K; Nakano M; Wada Y; Hotta Y; Terauchi A; Nonaka I J Pediatr; 1987 Feb; 110(2):223-7. PubMed ID: 3100753 [TBL] [Abstract][Full Text] [Related]
34. A mitochondrial encephalomyopathy: the first case with an established defect at the level of coenzyme Q. Fischer JC; Ruitenbeek W; Gabreƫls FJ; Janssen AJ; Renier WO; Sengers RC; Stadhouders AM; ter Laak HJ; Trijbels JM; Veerkamp JH Eur J Pediatr; 1986 Feb; 144(5):441-4. PubMed ID: 3956532 [TBL] [Abstract][Full Text] [Related]
35. Mitochondria-lipid-glycogen myopathy, hyperlactacidemia, and carnitine deficiency. Di Donato S; Cornelio F; Balestrini MR; Bertagnolio B; Peluchetti D Neurology; 1978 Nov; 28(11):1110-6. PubMed ID: 568729 [TBL] [Abstract][Full Text] [Related]
36. [A clinical, histochemical and ultrastructural study of mitochondrial myopathy]. Jiang XM Zhonghua Shen Jing Jing Shen Ke Za Zhi; 1990 Oct; 23(5):297-9, 320. PubMed ID: 2178086 [TBL] [Abstract][Full Text] [Related]
37. Fatal infantile mitochondrial myopathy due to cytochrome c oxidase deficiency. Minchom PE; Dormer RL; Hughes IA; Stansbie D; Cross AR; Hendry GA; Jones OT; Johnson MA; Sherratt HS; Turnbull DM J Neurol Sci; 1983; 60(3):453-63. PubMed ID: 6313867 [TBL] [Abstract][Full Text] [Related]
38. Lipid storage myopathy in multiple acyl-CoA dehydrogenase deficiency: an adult case. Mongini T; Doriguzzi C; Palmucci L; De Francesco A; Bet L; Manfredi L; Ponzetto C; Bresolin N Eur Neurol; 1992; 32(3):170-6. PubMed ID: 1592075 [TBL] [Abstract][Full Text] [Related]
39. Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes with recurrent abdominal symptoms and coenzyme Q10 administration. Yamamoto M; Sato T; Anno M; Ujike H; Takemoto M J Neurol Neurosurg Psychiatry; 1987 Nov; 50(11):1475-81. PubMed ID: 2826704 [TBL] [Abstract][Full Text] [Related]
40. [Ergometric and pathologic study of a family with complex I deficiency]. Tojo M; Ogawa N; Takeuchi M; Toyama J; Torigoe K; Sato S; Takahashi R; Koga Y; Nonaka I No To Hattatsu; 1992 Jan; 24(1):20-6. PubMed ID: 1731824 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]