Oliveira AS - Search Results

1

Frequency of duplications in the D-loop in patients with mitochondrial DNA deletions.

Tengan CH, Ferreiro-Barros C, Cardeal M, Fireman MA, Oliveira AS, Kiyomoto BH, Gabbai AA. Tengan CH, et al. Among authors: oliveira as. Biochim Biophys Acta. 2002 Oct 9;1588(1):65-70. doi: 10.1016/s0925-4439(02)00140-0. Biochim Biophys Acta. 2002. PMID: 12379315 Free article.

2

Fukuyama-type congenital muscular dystrophy: a case report in the Japanese population living in Brazil.

Zanoteli E, Rocha JC, Narumia LK, Fireman MA, Moura LS, Oliveira AS, Gabbai AA, Fukuda Y, Kinoshita M, Toda T. Zanoteli E, et al. Among authors: oliveira as. Acta Neurol Scand. 2002 Aug;106(2):117-21. doi: 10.1034/j.1600-0404.2002.01318.x. Acta Neurol Scand. 2002. PMID: 12100373

3

Temporomandibular joint and masticatory muscle involvement in myotonic dystrophy: a study by magnetic resonance imaging.

Zanoteli E, Yamashita HK, Suzuki H, Oliveira AS, Gabbai AA. Zanoteli E, et al. Among authors: oliveira as. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2002 Aug;94(2):262-71. doi: 10.1067/moe.2002.124580. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2002. PMID: 12221397

4

Rod distribution and muscle fiber type modification in the progression of nemaline myopathy.

Gurgel-Giannetti J, Reed UC, Marie SK, Zanoteli E, Fireman MA, Oliveira AS, Werneck LC, Beggs AH, Zatz M, Vainzof M. Gurgel-Giannetti J, et al. Among authors: oliveira as. J Child Neurol. 2003 Mar;18(3):235-40. doi: 10.1177/08830738030180031501. J Child Neurol. 2003. PMID: 12731651

5

Deletion of both MTM1 and MTMR1 genes in a boy with myotubular myopathy.

Zanoteli E, Laporte J, Rocha JC, Kretz C, Oliveira AS, Mandel JL, Perez AB, Gabbai AA, Buj-Bello A. Zanoteli E, et al. Among authors: oliveira as. Am J Med Genet A. 2005 Apr 30;134(3):338-40. doi: 10.1002/ajmg.a.30574. Am J Med Genet A. 2005. PMID: 15690409 No abstract available.

6

The role of nitric oxide in muscle fibers with oxidative phosphorylation defects.

Tengan CH, Kiyomoto BH, Godinho RO, Gamba J, Neves AC, Schmidt B, Oliveira AS, Gabbai AA. Tengan CH, et al. Among authors: oliveira as. Biochem Biophys Res Commun. 2007 Aug 3;359(3):771-7. doi: 10.1016/j.bbrc.2007.05.184. Epub 2007 Jun 4. Biochem Biophys Res Commun. 2007. PMID: 17560547

7

Age-related mitochondrial DNA point mutations in patients with mitochondrial myopathy.

da Costa CK, Kiyomoto BH, Schmidt B, Oliveira AS, Gabbai AA, Tengan CH. da Costa CK, et al. Among authors: oliveira as. J Neurol Sci. 2007 Dec 15;263(1-2):139-44. doi: 10.1016/j.jns.2007.07.006. Epub 2007 Aug 14. J Neurol Sci. 2007. PMID: 17698085

8

Progressive myopathy with a combined respiratory chain defect including Complex II.

Rodrigues Ade S, Kiyomoto BH, Oliveira AS, Gabbai AA, Schmidt B, Tengan CH. Rodrigues Ade S, et al. Among authors: oliveira as. J Neurol Sci. 2008 Jan 15;264(1-2):182-6. doi: 10.1016/j.jns.2007.08.002. Epub 2007 Sep 12. J Neurol Sci. 2008. PMID: 17850823

9

Conjugal amyotrophic lateral sclerosis in Brazil.

Godeiro C Jr, Oliveira AS, Felicio AC, Chieia MA, Gabbai AA. Godeiro C Jr, et al. Among authors: oliveira as. Arq Neuropsiquiatr. 2009 Dec;67(4):1045-8. doi: 10.1590/s0004-282x2009000600015. Arq Neuropsiquiatr. 2009. PMID: 20069216 Free article.

10

Conjugal amyotrophic lateral sclerosis.

Sica RE, Godeiro-Junior C, Oliveira AS, Felicio AC, Chieia MA, Gabbai AA. Sica RE, et al. Among authors: oliveira as. Arq Neuropsiquiatr. 2010 Apr;68(2):323; author reply 323-4. doi: 10.1590/s0004-282x2010000200036. Arq Neuropsiquiatr. 2010. PMID: 20464312 Free article. No abstract available.

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