da Silva LCS - Search Results

1

Mucopolysaccharidosis VII in Brazil: natural history and clinical findings.

Giugliani R, Barth AL, Dumas MRC, da Silva Franco JF, de Rosso Giuliani L, Grangeiro CHP, Horovitz DDG, Kim CA, de Araújo Leão EKE, de Medeiros PFV, Miguel DSCG, Moreira MESA, Dos Santos HMGP, da Silva LCS, da Silva LR, de Souza IN, Nalin T, Garcia D. Giugliani R, et al. Among authors: da silva lcs. Orphanet J Rare Dis. 2021 May 22;16(1):238. doi: 10.1186/s13023-021-01870-w. Orphanet J Rare Dis. 2021. PMID: 34022924 Free PMC article. Review.

2

Epidemiology of rare diseases in Brazil: protocol of the Brazilian Rare Diseases Network (RARAS-BRDN).

Félix TM, de Oliveira BM, Artifon M, Carvalho I, Bernardi FA, Schwartz IVD, Saute JA, Ferraz VEF, Acosta AX, Sorte NB, Alves D; RARAS Network group. Félix TM, et al. Orphanet J Rare Dis. 2022 Feb 24;17(1):84. doi: 10.1186/s13023-022-02254-4. Orphanet J Rare Dis. 2022. PMID: 35209917 Free PMC article.

3

Mucopolysaccharidosis VI and effects on growth of the apical bases: a case report.

Ferreira Dos Reis M, Pinheiro LR, Pinheiro MDGR, de Almeida HA, Feio PDSQ, de Almeida SC, de Souza ICN, Giugliani R, Schwartz IVD, Cavaleiro RMDS, Pinheiro JJV, da Silva LCS. Ferreira Dos Reis M, et al. Among authors: da silva lcs. Spec Care Dentist. 2018 May;38(3):176-184. doi: 10.1111/scd.12290. Epub 2018 May 3. Spec Care Dentist. 2018. PMID: 29722897

4

Mucopolysaccharidosis I, II, and VI: Brief review and guidelines for treatment.

Giugliani R, Federhen A, Rojas MV, Vieira T, Artigalás O, Pinto LL, Azevedo AC, Acosta A, Bonfim C, Lourenço CM, Kim CA, Horovitz D, Bonfim D, Norato D, Marinho D, Palhares D, Santos ES, Ribeiro E, Valadares E, Guarany F, de Lucca GR, Pimentel H, de Souza IN, Correa J Sr, Fraga JC, Goes JE, Cabral JM, Simionato J, Llerena J Jr, Jardim L, Giuliani L, da Silva LC, Santos ML, Moreira MA, Kerstenetzky M, Ribeiro M, Ruas N, Barrios P, Aranda P, Honjo R, Boy R, Costa R, Souza C, Alcantara FF, Avilla SG, Fagondes S, Martins AM. Giugliani R, et al. Genet Mol Biol. 2010 Oct;33(4):589-604. doi: 10.1590/S1415-47572010005000093. Epub 2010 Dec 1. Genet Mol Biol. 2010. PMID: 21637564 Free PMC article.

5

Visual Dysfunction of Type I and VI Mucopolysaccharidosis Patients Evaluated with Visual Evoked Cortical Potential.

Gomes BD, Souza Gda S, Viana GM, de Souza IC, Feio Pdo S, Schwartz IV, Marinho DR, Filho Mda S, Giugliani R, Silveira LC, da Silva LC. Gomes BD, et al. Case Rep Ophthalmol. 2012 Jan;3(1):104-12. doi: 10.1159/000337492. Epub 2012 Mar 26. Case Rep Ophthalmol. 2012. PMID: 22548043 Free PMC article.

6

Phenylketonuria Diagnosis by Massive Parallel Sequencing and Genotype-Phenotype Association in Brazilian Patients.

Tresbach RH, Sperb-Ludwig F, Ligabue-Braun R, Tonon T, de Oliveira Cardoso MT, Heredia RS, da Silva Rosa MTA, Martins BC, Poubel MO, da Silva LCS, Maillot F, Schwartz IVD. Tresbach RH, et al. Among authors: da silva lcs. Genes (Basel). 2020 Dec 25;12(1):20. doi: 10.3390/genes12010020. Genes (Basel). 2020. PMID: 33375644 Free PMC article.

7

Poly(L-co-D,L lactic acid-co-Trimethylene Carbonate) 3D printed scaffold cultivated with mesenchymal stem cells directed to bone reconstruction: In vitro and in vivo studies.

Asami J, Hausen MA, Komatsu D, Ferreira LM, Silva GBG, da Silva LCSC, Baldo DA, Oliveira Junior JM, Motta AC, Duek EAR. Asami J, et al. Among authors: da silva lcsc. J Biomater Appl. 2022 Apr;36(9):1550-1566. doi: 10.1177/08853282211066246. Epub 2022 Feb 7. J Biomater Appl. 2022. PMID: 35130780

8

Inhibition of reductase systems by 2-AAPA modulates peroxiredoxin oxidation and mitochondrial function in A172 glioblastoma cells.

de Souza LF, Schmitz AE, da Silva LCS, de Oliveira KA, Nedel CB, Tasca CI, de Bem AF, Farina M, Dafre AL. de Souza LF, et al. Among authors: da silva lcs. Toxicol In Vitro. 2017 Aug;42:273-280. doi: 10.1016/j.tiv.2017.04.028. Epub 2017 Apr 29. Toxicol In Vitro. 2017. PMID: 28461233

9

Evaluation of the tshr gene reveals polymorphisms associated with typical symptoms in primary congenital hypothyroidism.

Cortinhas Alves EA, Andrade RC, de Melo Amaral CE, Fernandes Caldato MC, Rocha Bastos AM, da Silva LC. Cortinhas Alves EA, et al. J Pediatr Endocrinol Metab. 2016 Jan;29(1):71-6. doi: 10.1515/jpem-2015-0130. J Pediatr Endocrinol Metab. 2016. PMID: 26356361

10

Mucopolysaccharidoses in northern Brazil: Targeted mutation screening and urinary glycosaminoglycan excretion in patients undergoing enzyme replacement therapy.

Viana GM, de Lima NO, Cavaleiro R, Alves E, Souza IC, Feio R, Leistner-Segal S, Schwartz I, Giugliani R, da Silva LC. Viana GM, et al. Genet Mol Biol. 2011 Jul;34(3):410-5. doi: 10.1590/S1415-47572011005000025. Epub 2011 Jul 1. Genet Mol Biol. 2011. PMID: 21931511 Free PMC article.

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