Alves SM - Search Results

1

Challenges in Lung Cancer Approaches: from the Clinical Issues to the Novel Therapies.

Coelho SP, Capelas ML, Alves SM, Sá L, de Mello RA. Coelho SP, et al. Among authors: alves sm. Recent Adv DNA Gene Seq. 2015;9(1):45-50. doi: 10.2174/2352092210666151214110725. Recent Adv DNA Gene Seq. 2015. PMID: 26655954 Review.

2

From bedside to cell biology: a century of history on lysosomal dysfunction.

Coutinho MF, Matos L, Alves S. Coutinho MF, et al. Gene. 2015 Jan 15;555(1):50-8. doi: 10.1016/j.gene.2014.09.054. Epub 2014 Sep 29. Gene. 2015. PMID: 25275857 Review.

3

Molecular analysis of mucopolysaccharidosis type IIIB in Portugal: evidence of a single origin for a common mutation (R234C) in the Iberian Peninsula.

Mangas M, Nogueira C, Prata MJ, Lacerda L, Coll MJ, Soares G, Ribeiro G, Amaral O, Ferreira C, Alves C, Coutinho MF, Alves S. Mangas M, et al. Clin Genet. 2008 Mar;73(3):251-6. doi: 10.1111/j.1399-0004.2007.00951.x. Epub 2008 Jan 23. Clin Genet. 2008. PMID: 18218046

4

Molecular characterization of Portuguese patients with mucopolysaccharidosis IIIC: two novel mutations in the HGSNAT gene.

Coutinho MF, Lacerda L, Prata MJ, Ribeiro H, Lopes L, Ferreira C, Alves S. Coutinho MF, et al. Clin Genet. 2008 Aug;74(2):194-5. doi: 10.1111/j.1399-0004.2008.01040.x. Epub 2008 Jun 2. Clin Genet. 2008. PMID: 18518886 No abstract available.

5

Molecular analysis of the GNPTAB and GNPTG genes in 13 patients with mucolipidosis type II or type III - identification of eight novel mutations.

Encarnação M, Lacerda L, Costa R, Prata MJ, Coutinho MF, Ribeiro H, Lopes L, Pineda M, Ignatius J, Galvez H, Mustonen A, Vieira P, Lima MR, Alves S. Encarnação M, et al. Clin Genet. 2009 Jul;76(1):76-84. doi: 10.1111/j.1399-0004.2009.01185.x. Clin Genet. 2009. PMID: 19659762

6

Origin and spread of a common deletion causing mucolipidosis type II: insights from patterns of haplotypic diversity.

Coutinho MF, Encarnação M, Gomes R, da Silva Santos L, Martins S, Sirois-Gagnon D, Bargal R, Filocamo M, Raas-Rothschild A, Tappino B, Laprise C, Cury GK, Schwartz IV, Artigalás O, Prata MJ, Alves S. Coutinho MF, et al. Clin Genet. 2011 Sep;80(3):273-80. doi: 10.1111/j.1399-0004.2010.01539.x. Epub 2010 Sep 29. Clin Genet. 2011. PMID: 20880125

7

Lysosomal multienzymatic complex-related diseases: a genetic study among Portuguese patients.

Coutinho MF, Lacerda L, Macedo-Ribeiro S, Baptista E, Ribeiro H, Prata MJ, Alves S. Coutinho MF, et al. Clin Genet. 2012 Apr;81(4):379-93. doi: 10.1111/j.1399-0004.2011.01625.x. Epub 2011 Mar 1. Clin Genet. 2012. PMID: 21214877

8

Glycosaminoglycan storage disorders: a review.

Coutinho MF, Lacerda L, Alves S. Coutinho MF, et al. Biochem Res Int. 2012;2012:471325. doi: 10.1155/2012/471325. Epub 2011 Oct 5. Biochem Res Int. 2012. PMID: 22013531 Free PMC article.

9

Mannose-6-phosphate pathway: a review on its role in lysosomal function and dysfunction.

Coutinho MF, Prata MJ, Alves S. Coutinho MF, et al. Mol Genet Metab. 2012 Apr;105(4):542-50. doi: 10.1016/j.ymgme.2011.12.012. Epub 2011 Dec 23. Mol Genet Metab. 2012. PMID: 22266136 Review.

10

Mucolipidosis type II α/β with a homozygous missense mutation in the GNPTAB gene.

Coutinho MF, Santos Lda S, Girisha KM, Satyamoorthy K, Lacerda L, Prata MJ, Alves S. Coutinho MF, et al. Am J Med Genet A. 2012 May;158A(5):1225-8. doi: 10.1002/ajmg.a.35295. Epub 2012 Apr 11. Am J Med Genet A. 2012. PMID: 22495880 No abstract available.

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