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Human Genetics|March 1, 1996
Fatal mitochondrial myopathy, lactic acidosis, and complex I deficiency associated with a heteroplasmic A --> G mutation at position 3251 in the mitochondrial tRNALeu(UUR) gneM Houshmand, N G Larsson, A Oldfors, et al.Archives of Biochemistry and Biophysics|May 1, 1990
The influence of pH on substrate form specificity of phosphoenolpyruvate carboxylase purified from Crassula argenteaC R Meyer, P Rustin, M K Black, et al.Acta Neuropathologica|January 1, 1990
Neuropathology in Kearns-Sayre syndromeA Oldfors, I M Fyhr, E Holme, et al.The Journal of Pediatrics|August 1, 1991
Mitochondrial encephalomyopathies in childhood. I. Biochemical and morphologic investigationsM H Tulinius, E Holme, B Kristiansson, et al.The Journal of Pediatrics|August 1, 1991
Mitochondrial encephalomyopathies in childhood. II. Clinical manifestations and syndromesM H Tulinius, E Holme, B Kristiansson, et al.Journal of Neuroscience Methods|May 30, 1998
Cytochrome c oxidase assay in minute amounts of human skeletal muscle using single wavelength spectrophotometersO Miró, F Cardellach, A Barrientos, et al.Human Genetics|December 24, 1997
No mitochondrial cytochrome oxidase (COX) gene mutations in 18 cases of COX deficiencyB Parfait, A Percheron, D Chretien, et al.Brain & Development|November 1, 1992
Deficiency in complex II of the respiratory chain, presenting as a leukodystrophy in two sisters with Leigh syndromeM Burgeois, F Goutieres, D Chretien, et al.Biochimica Et Biophysica Acta|July 10, 1997
Sequence and structure of the human OXA1L gene and its upstream elementsA Rötig, B Parfait, L Heidet, et al.European Journal of Pediatrics|February 1, 1994
Valproate-induced hepatic failure in a case of cytochrome c oxidase deficiencyB Chabrol, J Mancini, D Chretien, et al.Pageof 18