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Journal of Inherited Metabolic Disease|January 1, 1995
Clinical, biochemical, and molecular analysis of a maternally inherited case of Leigh syndrome (MILS) associated with the mtDNA T8993G point mutationF Degoul, M Diry, D Rodriguez, et al.
Annals of Neurology|June 1, 1991
Zidovudine myopathy: a distinctive disorder associated with mitochondrial dysfunctionC Mhiri, M Baudrimont, G Bonne, et al.
American Journal of Human Genetics|January 1, 1987
The French and North American phenotypes of pyruvate carboxylase deficiency, correlation with biotin containing protein by 3H-biotin incorporation, 35S-streptavidin labeling, and Northern blotting with a cloned cDNA probeB H Robinson, J Oei, J M Saudubray, et al.
The British Journal of Surgery|September 1, 1996
Homocysteine: an independent risk factor for the failure of vascular interventionI C Currie, Y G Wilson, J Scott, et al.
Human Molecular Genetics|April 18, 1998
Isoleucylation properties of native human mitochondrial tRNAIle and tRNAIle transcripts. Implications for cardiomyopathy-related point mutations (4269, 4317) in the tRNAIle geneF Degoul, H Brulé, C Cepanec, et al.
Free Radical Research|November 8, 2001
UV-A irradiation induces a decrease in the mitochondrial respiratory activity of human NCTC 2544 keratinocytesM Djavaheri-Mergny, C Marsac, C Mazière, et al.
Neuropediatrics|November 5, 2003
Infantile spasms with basal ganglia MRI hypersignal may reveal mitochondrial disorder due to T8993G MT DNA mutationI Desguerre, F Pinton, R Nabbout, et al.
European Journal of Vascular and Endovascular Surgery : the Official Journal of the European Society for Vascular Surgery|October 1, 1996
Hyperhomocysteinaemia is a risk factor for vein graft stenosisC Irvine, Y G Wilson, I C Currie, et al.
Revue Neurologique|January 1, 1991
[Familial mitochondrial encephalopathy. A clinicopathologic study]B Estournet, C Duyckaerts, C Marsac, et al.
European Neurology|January 1, 1991
Histological, enzymatic and mitochondrial DNA studies in patients with Kearns-Sayre syndrome and chronic progressive external ophthalmoplegiaH Reichmann, F Degoul, R Gold, et al.
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