DiMauro S - Search Results

1

A mitochondrial DNA duplication as a marker of skeletal muscle specific mutations in the mitochondrial genome.

Mancuso M, Vives-Bauza C, Filosto M, Marti R, Solano A, Montoya J, Gamez J, DiMauro S, Andreu AL. Mancuso M, et al. Among authors: dimauro s. J Med Genet. 2004 Jun;41(6):e73. doi: 10.1136/jmg.2003.012278. J Med Genet. 2004. PMID: 15173239 Free PMC article. No abstract available.

2

Lack of paternal inheritance of muscle mitochondrial DNA in sporadic mitochondrial myopathies.

Filosto M, Mancuso M, Vives-Bauza C, Vilà MR, Shanske S, Hirano M, Andreu AL, DiMauro S. Filosto M, et al. Among authors: dimauro s. Ann Neurol. 2003 Oct;54(4):524-6. doi: 10.1002/ana.10709. Ann Neurol. 2003. PMID: 14520667

3

Mutations in mitochondrial DNA as a cause of exercise intolerance.

DiMauro S, Andreu AL. DiMauro S, et al. Ann Med. 2001 Oct;33(7):472-6. doi: 10.3109/07853890109002096. Ann Med. 2001. PMID: 11680795 Free article. Review.

4

Current classification of mitochondrial disorders.

Andreu AL, DiMauro S. Andreu AL, et al. Among authors: dimauro s. J Neurol. 2003 Dec;250(12):1403-6. doi: 10.1007/s00415-003-0281-3. J Neurol. 2003. PMID: 14673571 Review. No abstract available.

5

Mitochondrial disorders.

DiMauro S, Andreu AL, De Vivo DC. DiMauro S, et al. J Child Neurol. 2002 Dec;17 Suppl 3:3S35-45; discussion 3S46-7. J Child Neurol. 2002. PMID: 12597054 Review.

6

[Mitochondrial encephalopathies: where are we going?].

DiMauro S, Andreu AL, Bonilla E. DiMauro S, et al. Rev Neurol. 1999 Jan 16-31;28(2):164-8. Rev Neurol. 1999. PMID: 10101786 Review. Spanish.

7

Mutations in mtDNA: are we scraping the bottom of the barrel?

DiMauro S, Andreu AL. DiMauro S, et al. Brain Pathol. 2000 Jul;10(3):431-41. doi: 10.1111/j.1750-3639.2000.tb00275.x. Brain Pathol. 2000. PMID: 10885662 Free PMC article. Review.

8

The A8344G mutation in mitochondrial DNA associated with stroke-like episodes and gastrointestinal dysfunction.

Tanji K, Gamez J, Cervera C, Mearin F, Ortega A, de la Torre J, Montoya J, Andreu AL, DiMauro S, Bonilla E. Tanji K, et al. Among authors: dimauro s. Acta Neuropathol. 2003 Jan;105(1):69-75. doi: 10.1007/s00401-002-0604-y. Epub 2002 Sep 7. Acta Neuropathol. 2003. PMID: 12471464

9

Spinal muscular atrophy and mitochondrial DNA depletion. Response to Berber et al. (2003) Acta Neuropathol 105:245-251.

Mancuso M, Filosto M, Hirano M, DiMauro S. Mancuso M, et al. Among authors: dimauro s. Acta Neuropathol. 2003 Jun;105(6):621-2. doi: 10.1007/s00401-003-0699-9. Epub 2003 Apr 10. Acta Neuropathol. 2003. PMID: 12687391 No abstract available.

10

A novel mitochondrial tRNAPhe mutation causes MERRF syndrome.

Mancuso M, Filosto M, Mootha VK, Rocchi A, Pistolesi S, Murri L, DiMauro S, Siciliano G. Mancuso M, et al. Among authors: dimauro s. Neurology. 2004 Jun 8;62(11):2119-21. doi: 10.1212/01.wnl.0000127608.48406.f1. Neurology. 2004. PMID: 15184630

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