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Neuromuscular Disorders : NMD|January 1, 1993
Atypical clinical presentations associated with the MELAS mutation at position 3243 of human mitochondrial DNAC T Moraes, F Ciacci, G Silvestri, et al.
American Journal of Human Genetics|March 1, 1991
mtDNA depletion with variable tissue expression: a novel genetic abnormality in mitochondrial diseasesC T Moraes, S Shanske, H J Tritschler, et al.
The Journal of Biological Chemistry|October 5, 1990
Purification and substrate specificity of heparitinase I and heparitinase II from Flavobacterium heparinum. Analyses of the heparin and heparan sulfate degradation products by 13C NMR spectroscopyH B Nader, M A Porcionatto, I L Tersariol, et al.
Neuroscience Letters|February 28, 2001
Dysfunctional mitochondrial respiration in the wobbler mouse brainG P Xu, K R Dave, C T Moraes, et al.
Nucleic Acids Research|February 11, 1990
Recombination via flanking direct repeats is a major cause of large-scale deletions of human mitochondrial DNAS Mita, R Rizzuto, C T Moraes, et al.
Annals of Neurology|April 1, 1992
MELAS: clinical features, biochemistry, and molecular geneticsE Ciafaloni, E Ricci, S Shanske, et al.
Neurology|January 1, 1990
Widespread tissue distribution of mitochondrial DNA deletions in Kearns-Sayre syndromeS Shanske, C T Moraes, A Lombes, et al.
The New England Journal of Medicine|May 18, 1989
Mitochondrial DNA deletions in progressive external ophthalmoplegia and Kearns-Sayre syndromeC T Moraes, S DiMauro, M Zeviani, et al.
The Journal of Clinical Investigation|December 1, 1993
Two novel pathogenic mitochondrial DNA mutations affecting organelle number and protein synthesis. Is the tRNA(Leu(UUR)) gene an etiologic hot spot?C T Moraes, F Ciacci, E Bonilla, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas|September 1, 1994
Sequencing of heparan sulfate proteoglycans: identification of variable and constant oligosaccharide regions in eight heparan sulfate proteoglycans of different originsI L Tersariol, T M Ferreira, M G Medeiros, et al.
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