Saraiva-Pereira ML - Search Results

1

Ancestral origin of the ATTCT repeat expansion in spinocerebellar ataxia type 10 (SCA10).

Almeida T, Alonso I, Martins S, Ramos EM, Azevedo L, Ohno K, Amorim A, Saraiva-Pereira ML, Jardim LB, Matsuura T, Sequeiros J, Silveira I. Almeida T, et al. PLoS One. 2009;4(2):e4553. doi: 10.1371/journal.pone.0004553. Epub 2009 Feb 23. PLoS One. 2009. PMID: 19234597 Free PMC article.

2

Reduced penetrance of intermediate size alleles in spinocerebellar ataxia type 10.

Alonso I, Jardim LB, Artigalas O, Saraiva-Pereira ML, Matsuura T, Ashizawa T, Sequeiros J, Silveira I. Alonso I, et al. Neurology. 2006 May 23;66(10):1602-4. doi: 10.1212/01.wnl.0000216266.30177.bb. Neurology. 2006. PMID: 16717236 No abstract available.

3

Spinocerebellar ataxias in 114 Brazilian families: clinical and molecular findings.

Trott A, Jardim LB, Ludwig HT, Saute JA, Artigalás O, Kieling C, Wanderley HY, Rieder CR, Monte TL, Socal M, Alonso I, Ferro A, Carvalho T, do Céu Moreira M, Mendonça P, Ferreirinha F, Silveira I, Sequeiros J, Giugliani R, Saraiva-Pereira ML. Trott A, et al. Clin Genet. 2006 Aug;70(2):173-6. doi: 10.1111/j.1399-0004.2006.00656.x. Clin Genet. 2006. PMID: 16879203 No abstract available.

4

Depressive symptoms in Machado-Joseph disease (SCA3) patients and their relatives.

Cecchin CR, Pires AP, Rieder CR, Monte TL, Silveira I, Carvalho T, Saraiva-Pereira ML, Sequeiros J, Jardim LB. Cecchin CR, et al. Community Genet. 2007;10(1):19-26. doi: 10.1159/000096276. Community Genet. 2007. PMID: 17167246

5

Machado-Joseph disease enhances genetic fitness: a comparison between affected and unaffected women and between MJD and the general population.

Prestes PR, Saraiva-Pereira ML, Silveira I, Sequeiros J, Jardim LB. Prestes PR, et al. Ann Hum Genet. 2008 Jan;72(Pt 1):57-64. doi: 10.1111/j.1469-1809.2007.00388.x. Epub 2007 Aug 7. Ann Hum Genet. 2008. PMID: 17683516

6

Survival estimates for patients with Machado-Joseph disease (SCA3).

Kieling C, Prestes PR, Saraiva-Pereira ML, Jardim LB. Kieling C, et al. Clin Genet. 2007 Dec;72(6):543-5. doi: 10.1111/j.1399-0004.2007.00910.x. Epub 2007 Sep 25. Clin Genet. 2007. PMID: 17894834

7

Pathogenic expansions of the SCA6 locus are associated with a common CACNA1A haplotype across the globe: founder effect or predisposing chromosome?

Craig K, Takiyama Y, Soong BW, Jardim LB, Saraiva-Pereira ML, Lythgow K, Morino H, Maruyama H, Kawakami H, Chinnery PF. Craig K, et al. Eur J Hum Genet. 2008 Jul;16(7):841-7. doi: 10.1038/ejhg.2008.20. Epub 2008 Feb 20. Eur J Hum Genet. 2008. PMID: 18285829

8

Intrafamilial variability of Parkinson phenotype in SCAs: novel cases due to SCA2 and SCA3 expansions.

Socal MP, Emmel VE, Rieder CR, Hilbig A, Saraiva-Pereira ML, Jardim LB. Socal MP, et al. Parkinsonism Relat Disord. 2009 Jun;15(5):374-8. doi: 10.1016/j.parkreldis.2008.09.005. Epub 2008 Nov 5. Parkinsonism Relat Disord. 2009. PMID: 18990604

9

Common origin of pure and interrupted repeat expansions in spinocerebellar ataxia type 2 (SCA2).

Ramos EM, Martins S, Alonso I, Emmel VE, Saraiva-Pereira ML, Jardim LB, Coutinho P, Sequeiros J, Silveira I. Ramos EM, et al. Am J Med Genet B Neuropsychiatr Genet. 2010 Mar 5;153B(2):524-531. doi: 10.1002/ajmg.b.31013. Am J Med Genet B Neuropsychiatr Genet. 2010. PMID: 19676102

10

No major clinical impact of Val66Met BDNF gene polymorphism on temporal lobe epilepsy.

Bragatti JA, Schenkel LC, Torres CM, Manfro GG, Blaya C, Souza AC, Souza DO, Saraiva-Pereira ML, Jardim LB, Leistner-Segal S, Bianchin MM. Bragatti JA, et al. Epilepsy Res. 2010 Feb;88(2-3):108-11. doi: 10.1016/j.eplepsyres.2009.10.003. Epub 2009 Nov 5. Epilepsy Res. 2010. PMID: 19896331

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