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25. 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]
26. Deficiency of the iron-sulfur clusters of mitochondrial reduced nicotinamide-adenine dinucleotide-ubiquinone oxidoreductase (complex I) in an infant with congenital lactic acidosis. Moreadith RW; Batshaw ML; Ohnishi T; Kerr D; Knox B; Jackson D; Hruban R; Olson J; Reynafarje B; Lehninger AL J Clin Invest; 1984 Sep; 74(3):685-97. PubMed ID: 6432847 [TBL] [Abstract][Full Text] [Related]
27. Experimental thiamine deficiency. Neuropathic and mitochondrial changes induced in rat muscle. Kark RA; Brown WJ; Edgerton VR; Reynolds SF; Gibson G Arch Neurol; 1975 Dec; 32(12):818-25. PubMed ID: 54158 [TBL] [Abstract][Full Text] [Related]
28. Neuromuscular disorders with abnormal muscle mitochondria. Kamieniecka Z; Schmalbruch H Int Rev Cytol; 1980; 65():321-57. PubMed ID: 6993406 [No Abstract] [Full Text] [Related]
29. High-Resolution FluoRespirometry and OXPHOS Protocols for Human Cells, Permeabilized Fibers from Small Biopsies of Muscle, and Isolated Mitochondria. Doerrier C; Garcia-Souza LF; Krumschnabel G; Wohlfarter Y; Mészáros AT; Gnaiger E Methods Mol Biol; 2018; 1782():31-70. PubMed ID: 29850993 [TBL] [Abstract][Full Text] [Related]
30. Histochemical and biochemical investigations of adenosine triphosphatase in vertebrate mixed muscles. Khan MA; Kleine TO Acta Histochem Suppl; 1977; Suppl 18():245-58. PubMed ID: 45633 [TBL] [Abstract][Full Text] [Related]
31. A familial mitochondrial myopathy with central defect in neural transmission. Barron SA; Heffner RR; Zwirecki R Arch Neurol; 1979 Sep; 36(9):553-6. PubMed ID: 224846 [TBL] [Abstract][Full Text] [Related]
32. Early biochemical consequences of denervation in fast and slow skeletal muscles and their relationship to neural control over muscle differentiation. Margreth A; Salviati G; Di Mauro S; Turati G Biochem J; 1972 Mar; 126(5):1099-110. PubMed ID: 4262959 [TBL] [Abstract][Full Text] [Related]
33. Morphogenesis of the mitochondrial alterations in muscle diseases. Shah AJ; Sahgal V; Muschler G; Subramani V; Singh H J Neurol Sci; 1982 Jul; 55(1):25-37. PubMed ID: 7108562 [TBL] [Abstract][Full Text] [Related]
34. [Mitochondrial myopathies and encephalomyopathies. Neuromuscular and central nervous system diseases caused by defects in mitochondrial oxidative metabolism]. Siemes H Monatsschr Kinderheilkd; 1985 Nov; 133(11):798-805. PubMed ID: 3935918 [TBL] [Abstract][Full Text] [Related]
35. Patterns of neuromuscular disease. As related to stages of normal embryogenesis in voluntary muscle. Korényi-Both A; Marosán G Am J Pathol; 1979 May; 95(2):359-78. PubMed ID: 156504 [TBL] [Abstract][Full Text] [Related]
36. Biochemical functioning of mitochondria in normal and denervated mammalian skeletal muscle. Joffe M; Savage N; Isaacs H Muscle Nerve; 1981; 4(6):514-9. PubMed ID: 6273720 [TBL] [Abstract][Full Text] [Related]
37. Mitochondrial functions in five cases of human neuromuscular disorders. Gimeno A; Trueba JL; Blanco M; Gosalvez M J Neurol Neurosurg Psychiatry; 1973 Oct; 36(5):806-12. PubMed ID: 4753876 [TBL] [Abstract][Full Text] [Related]
38. 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]