DiMauro S - Search Results

1

Mitochondrial disorders in the nervous system.

DiMauro S, Schon EA. DiMauro S, et al. Annu Rev Neurosci. 2008;31:91-123. doi: 10.1146/annurev.neuro.30.051606.094302. Annu Rev Neurosci. 2008. PMID: 18333761 Review.

2

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. Among authors: dimauro s. Am J Hum Genet. 1992 May;50(5):934-49. Am J Hum Genet. 1992. PMID: 1315123 Free PMC article.

3

Mitochondrial encephalomyopathies.

DiMauro S. DiMauro S. Brain Pathol. 1992 Apr;2(2):111-2. doi: 10.1111/j.1750-3639.1992.tb00678.x. Brain Pathol. 1992. PMID: 1341951 Review. No abstract available.

4

Use of single strand conformation polymorphism analysis to detect point mutations in human mitochondrial DNA.

Suomalainen A, Ciafaloni E, Koga Y, Peltonen L, DiMauro S, Schon EA. Suomalainen A, et al. Among authors: dimauro s. J Neurol Sci. 1992 Sep;111(2):222-6. doi: 10.1016/0022-510x(92)90074-u. J Neurol Sci. 1992. PMID: 1431990

5

Accumulation of deletions in human mitochondrial DNA during normal aging: analysis by quantitative PCR.

Simonetti S, Chen X, DiMauro S, Schon EA. Simonetti S, et al. Among authors: dimauro s. Biochim Biophys Acta. 1992 Dec 10;1180(2):113-22. doi: 10.1016/0925-4439(92)90059-v. Biochim Biophys Acta. 1992. PMID: 1463763

6

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. Rev Neurol (Paris). 1991;147(6-7):443-9. Rev Neurol (Paris). 1991. PMID: 1660180 Review.

7

Localization of mitochondrial DNA in normal and pathological muscle using immunological probes: a new approach to the study of mitochondrial myopathies.

Andreetta F, Tritschler HJ, Schon EA, DiMauro S, Bonilla E. Andreetta F, et al. Among authors: dimauro s. J Neurol Sci. 1991 Sep;105(1):88-92. doi: 10.1016/0022-510x(91)90123-o. J Neurol Sci. 1991. PMID: 1665507

8

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: dimauro s. Lancet. 1991 Mar 2;337(8740):508-10. doi: 10.1016/0140-6736(91)91294-5. Lancet. 1991. PMID: 1671889 Clinical Trial.

9

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: dimauro s. Am J Hum Genet. 1990 Mar;46(3):418-27. Am J Hum Genet. 1990. PMID: 1689952 Free PMC article.

10

Mitochondrial DNA deletion in a girl with manifestations of Kearns-Sayre and Lowe syndromes: an example of phenotypic mimicry?

Moraes CT, Zeviani M, Schon EA, Hickman RO, Vlcek BW, DiMauro S. Moraes CT, et al. Among authors: dimauro s. Am J Med Genet. 1991 Dec 1;41(3):301-5. doi: 10.1002/ajmg.1320410308. Am J Med Genet. 1991. PMID: 1789283

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