Moraes CT - Search Results

1

Mitochondrial DNA depletion: mutations in thymidine kinase gene with myopathy and SMA.

Mancuso M, Salviati L, Sacconi S, Otaegui D, Camaño P, Marina A, Bacman S, Moraes CT, Carlo JR, Garcia M, Garcia-Alvarez M, Monzon L, Naini AB, Hirano M, Bonilla E, Taratuto AL, DiMauro S, Vu TH. Mancuso M, et al. Among authors: moraes ct. Neurology. 2002 Oct 22;59(8):1197-202. doi: 10.1212/01.wnl.0000028689.93049.9a. Neurology. 2002. PMID: 12391347

2

Molecular analysis of the muscle pathology associated with mitochondrial DNA deletions.

Moraes CT, Ricci E, Petruzzella V, Shanske S, DiMauro S, Schon EA, Bonilla E. Moraes CT, et al. Nat Genet. 1992 Aug;1(5):359-67. doi: 10.1038/ng0892-359. Nat Genet. 1992. PMID: 1284549

3

The mitochondrial tRNA(Leu(UUR)) mutation in mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes (MELAS): genetic, biochemical, and morphological correlations in skeletal muscle.

Moraes CT, Ricci E, Bonilla E, DiMauro S, Schon EA. Moraes CT, et al. Am J Hum Genet. 1992 May;50(5):934-49. Am J Hum Genet. 1992. PMID: 1315123 Free PMC article.

4

New morphological approaches to the study of mitochondrial encephalomyopathies.

Bonilla E, Sciacco M, Tanji K, Sparaco M, Petruzzella V, Moraes CT. Bonilla E, et al. Among authors: moraes ct. Brain Pathol. 1992 Apr;2(2):113-9. doi: 10.1111/j.1750-3639.1992.tb00679.x. Brain Pathol. 1992. PMID: 1341952 Review.

5

Disorders associated with depletion of mitochondrial DNA.

Ricci E, Moraes CT, Servidei S, Tonali P, Bonilla E, DiMauro S. Ricci E, et al. Among authors: moraes ct. Brain Pathol. 1992 Apr;2(2):141-7. doi: 10.1111/j.1750-3639.1992.tb00682.x. Brain Pathol. 1992. PMID: 1341955 Review.

6

A new mtDNA mutation in the tRNA(Lys) gene associated with myoclonic epilepsy and ragged-red fibers (MERRF).

Silvestri G, Moraes CT, Shanske S, Oh SJ, DiMauro S. Silvestri G, et al. Among authors: moraes ct. Am J Hum Genet. 1992 Dec;51(6):1213-7. Am J Hum Genet. 1992. PMID: 1361099 Free PMC article.

7

MELAS: clinical features, biochemistry, and molecular genetics.

Ciafaloni E, Ricci E, Shanske S, Moraes CT, Silvestri G, Hirano M, Simonetti S, Angelini C, Donati MA, Garcia C, et al. Ciafaloni E, et al. Among authors: moraes ct. Ann Neurol. 1992 Apr;31(4):391-8. doi: 10.1002/ana.410310408. Ann Neurol. 1992. PMID: 1586140

8

Mitochondrial encephalomyopathies: biochemical approach.

Dimauro S, Moraes CT, Shanske S, Lombes A, Nakase H, Mita S, Tritschler HJ, Bonilla E, Miranda AF, Schon EA. Dimauro S, et al. Among authors: moraes ct. Rev Neurol (Paris). 1991;147(6-7):443-9. Rev Neurol (Paris). 1991. PMID: 1660180 Review.

9

Depletion of muscle mitochondrial DNA in AIDS patients with zidovudine-induced myopathy.

Arnaudo E, Dalakas M, Shanske S, Moraes CT, DiMauro S, Schon EA. Arnaudo E, et al. Among authors: moraes ct. Lancet. 1991 Mar 2;337(8740):508-10. doi: 10.1016/0140-6736(91)91294-5. Lancet. 1991. PMID: 1671889 Free article. Clinical Trial.

10

Transcription and translation of deleted mitochondrial genomes in Kearns-Sayre syndrome: implications for pathogenesis.

Nakase H, Moraes CT, Rizzuto R, Lombes A, DiMauro S, Schon EA. Nakase H, et al. Among authors: moraes ct. Am J Hum Genet. 1990 Mar;46(3):418-27. Am J Hum Genet. 1990. PMID: 1689952 Free PMC article.

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