Saraiva-Pereira ML - Search Results

1

A randomized, phase 2 clinical trial of lithium carbonate in Machado-Joseph disease.

Saute JA, de Castilhos RM, Monte TL, Schumacher-Schuh AF, Donis KC, D'Ávila R, Souza GN, Russo AD, Furtado GV, Gheno TC, de Souza DO, Portela LV, Saraiva-Pereira ML, Camey SA, Torman VB, de Mello Rieder CR, Jardim LB. Saute JA, et al. Mov Disord. 2014 Apr;29(4):568-73. doi: 10.1002/mds.25803. Epub 2014 Jan 7. Mov Disord. 2014. PMID: 24399647 Clinical Trial.

2

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

3

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

4

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

5

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

6

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.

7

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

8

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

9

Occupational therapy in spinocerebellar ataxia type 3: an open-label trial.

Silva RC, Saute JA, Silva AC, Coutinho AC, Saraiva-Pereira ML, Jardim LB. Silva RC, et al. Braz J Med Biol Res. 2010 Jun;43(6):537-42. doi: 10.1590/s0100-879x2010005000009. Epub 2010 Apr 16. Braz J Med Biol Res. 2010. PMID: 20414586 Free article. Clinical Trial.

10

Clinical and biochemical study of 29 Brazilian patients with metachromatic leukodystrophy.

Artigalás O, Lagranha VL, Saraiva-Pereira ML, Burin MG, Lourenço CM, van der Linden H Jr, Santos ML, Rosemberg S, Steiner CE, Kok F, de Souza CF, Jardim LB, Giugliani R, Schwartz IV. Artigalás O, et al. J Inherit Metab Dis. 2010 Dec;33 Suppl 3:S257-62. doi: 10.1007/s10545-010-9140-4. Epub 2010 Jul 2. J Inherit Metab Dis. 2010. PMID: 20596894

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