Silveira I - Search Results

1

Motor and cognitive deficits in the heterozygous leaner mouse, a Cav2.1 voltage-gated Ca2+ channel mutant.

Alonso I, Marques JM, Sousa N, Sequeiros J, Olsson IA, Silveira I. Alonso I, et al. Among authors: silveira i. Neurobiol Aging. 2008 Nov;29(11):1733-43. doi: 10.1016/j.neurobiolaging.2007.04.005. Epub 2007 May 21. Neurobiol Aging. 2008. PMID: 17513018

2

Genetic linkage studies of Machado-Joseph disease with chromosome 14q STRPs in 16 Portuguese-Azorean kindreds.

Sequeiros J, Silveira I, Maciel P, Coutinho P, Manaia A, Gaspar C, Burlet P, Loureiro L, Guimarães J, Tanaka H, et al. Sequeiros J, et al. Among authors: silveira i. Genomics. 1994 Jun;21(3):645-8. doi: 10.1006/geno.1994.1327. Genomics. 1994. PMID: 7959745

3

High germinal instability of the (CTG)n at the SCA8 locus of both expanded and normal alleles.

Silveira I, Alonso I, Guimarães L, Mendonça P, Santos C, Maciel P, Fidalgo De Matos JM, Costa M, Barbot C, Tuna A, Barros J, Jardim L, Coutinho P, Sequeiros J. Silveira I, et al. Am J Hum Genet. 2000 Mar;66(3):830-40. doi: 10.1086/302827. Am J Hum Genet. 2000. PMID: 10712199 Free PMC article.

4

Neurologic findings in Machado-Joseph disease: relation with disease duration, subtypes, and (CAG)n.

Jardim LB, Pereira ML, Silveira I, Ferro A, Sequeiros J, Giugliani R. Jardim LB, et al. Among authors: silveira i. Arch Neurol. 2001 Jun;58(6):899-904. doi: 10.1001/archneur.58.6.899. Arch Neurol. 2001. PMID: 11405804

5

Machado-Joseph disease in South Brazil: clinical and molecular characterization of kindreds.

Jardim LB, Pereira ML, Silveira I, Ferro A, Sequeiros J, Giugliani R. Jardim LB, et al. Among authors: silveira i. Acta Neurol Scand. 2001 Oct;104(4):224-31. doi: 10.1034/j.1600-0404.2001.00020.x. Acta Neurol Scand. 2001. PMID: 11589651

6

A survey of spinocerebellar ataxia in South Brazil - 66 new cases with Machado-Joseph disease, SCA7, SCA8, or unidentified disease-causing mutations.

Jardim LB, Silveira I, Pereira ML, Ferro A, Alonso I, do Céu Moreira M, Mendonça P, Ferreirinha F, Sequeiros J, Giugliani R. Jardim LB, et al. Among authors: silveira i. J Neurol. 2001 Oct;248(10):870-6. doi: 10.1007/s004150170072. J Neurol. 2001. PMID: 11697524

7

Trinucleotide repeats in 202 families with ataxia: a small expanded (CAG)n allele at the SCA17 locus.

Silveira I, Miranda C, Guimarães L, Moreira MC, Alonso I, Mendonça P, Ferro A, Pinto-Basto J, Coelho J, Ferreirinha F, Poirier J, Parreira E, Vale J, Januário C, Barbot C, Tuna A, Barros J, Koide R, Tsuji S, Holmes SE, Margolis RL, Jardim L, Pandolfo M, Coutinho P, Sequeiros J. Silveira I, et al. Arch Neurol. 2002 Apr;59(4):623-9. doi: 10.1001/archneur.59.4.623. Arch Neurol. 2002. PMID: 11939898

8

Use of fluoxetine for treatment of Machado-Joseph disease: an open-label study.

Monte TL, Rieder CR, Tort AB, Rockenback I, Pereira ML, Silveira I, Ferro A, Sequeiros J, Jardim LB. Monte TL, et al. Among authors: silveira i. Acta Neurol Scand. 2003 Mar;107(3):207-10. doi: 10.1034/j.1600-0404.2003.02132.x. Acta Neurol Scand. 2003. PMID: 12614314 Clinical Trial.

9

Searching for modulating effects of SCA2, SCA6 and DRPLA CAG tracts on the Machado-Joseph disease (SCA3) phenotype.

Jardim L, Silveira I, Pereira ML, do Céu Moreira M, Mendonça P, Sequeiros J, Giugliani R. Jardim L, et al. Among authors: silveira i. Acta Neurol Scand. 2003 Mar;107(3):211-4. doi: 10.1034/j.1600-0404.2003.00046.x. Acta Neurol Scand. 2003. PMID: 12614315

10

Phenotypes of spinocerebellar ataxia type 6 and familial hemiplegic migraine caused by a unique CACNA1A missense mutation in patients from a large family.

Alonso I, Barros J, Tuna A, Coelho J, Sequeiros J, Silveira I, Coutinho P. Alonso I, et al. Among authors: silveira i. Arch Neurol. 2003 Apr;60(4):610-4. doi: 10.1001/archneur.60.4.610. Arch Neurol. 2003. PMID: 12707077 Free article.

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