Pardini VC - Search Results

1

Epidemic Spread of SARS-CoV-2 Lineage B.1.1.7 in Brazil.

Moreira FRR, Bonfim DM, Zauli DAG, Silva JP, Lima AB, Malta FSV, Ferreira ACS, Pardini VC, Magalhães WCS, Queiroz DC, Souza RM, Geddes VEV, Costa WC, Moreira RG, Faria NR, Voloch CM, Souza RP, Aguiar RS. Moreira FRR, et al. Among authors: pardini vc. Viruses. 2021 May 26;13(6):984. doi: 10.3390/v13060984. Viruses. 2021. PMID: 34073177 Free PMC article.

2

Founder effect of the 669insA mutation in BSCL2 gene causing Berardinelli-Seip congenital lipodystrophy in a cluster from Brazil.

Gomes KB, Pardini VC, Ferreira AC, Fonseca CG, Fernandes AP. Gomes KB, et al. Among authors: pardini vc. Ann Hum Genet. 2007 Nov;71(Pt 6):729-34. doi: 10.1111/j.1469-1809.2007.00369.x. Epub 2007 May 29. Ann Hum Genet. 2007. PMID: 17535271

3

Frequency of the S65C mutation in the hemochromatosis gene in Brazil.

Oliveira VC, Caxito FA, Gomes KB, Castro AM, Pardini VC, Ferreira AC. Oliveira VC, et al. Among authors: pardini vc. Genet Mol Res. 2009 Jul 14;8(3):794-8. doi: 10.4238/vol8-3gmr562. Genet Mol Res. 2009. PMID: 19681031 Free article.

4

Assessment of microsatellite instability in colorectal cancer patients from Brazil.

Leite SM, Gomes KB, Pardini VC, Ferreira AC, Oliveira VC, Cruz GM. Leite SM, et al. Among authors: pardini vc. Mol Biol Rep. 2010 Jan;37(1):375-80. doi: 10.1007/s11033-009-9807-9. Mol Biol Rep. 2010. PMID: 19784864

5

Cryopreservation does not alter karyotype, multipotency, or NANOG/SOX2 gene expression of amniotic fluid mesenchymal stem cells.

Angelo PC, Ferreira AC, Fonseca VD, Frade SP, Ferreira CS, Malta FS, Pereira AK, Leite HV, Brum AP, Pardini VC, Gomes KB, Cabral AC. Angelo PC, et al. Among authors: pardini vc. Genet Mol Res. 2012 Apr 19;11(2):1002-12. doi: 10.4238/2012.April.19.5. Genet Mol Res. 2012. PMID: 22576926 Free article.

6

Frequency of FMR1 premutation in individuals with ataxia and/or tremor and/or parkinsonism.

Reis AH, Ferreira AC, Gomes KB, Aguiar MJ, Fonseca CG, Cardoso FE, Pardini VC, Carvalho MR. Reis AH, et al. Among authors: pardini vc. Genet Mol Res. 2008 Jan 29;7(1):74-84. doi: 10.4238/vol7-1gmr357. Genet Mol Res. 2008. PMID: 18273822 Free article.

7

Mutations in the seipin and AGPAT2 genes clustering in consanguineous families with Berardinelli-Seip congenital lipodystrophy from two separate geographical regions of Brazil.

Gomes KB, Fernandes AP, Ferreira AC, Pardini H, Garg A, Magré J, Pardini VC. Gomes KB, et al. Among authors: pardini h, pardini vc. J Clin Endocrinol Metab. 2004 Jan;89(1):357-61. doi: 10.1210/jc.2003-030415. J Clin Endocrinol Metab. 2004. PMID: 14715872

8

Phenotypic heterogeneity in biochemical parameters correlates with mutations in AGPAT2 or Seipin genes among Berardinelli-Seip congenital lipodystrophy patients.

Gomes KB, Pardini VC, Ferreira AC, Fernandes AP. Gomes KB, et al. Among authors: pardini vc. J Inherit Metab Dis. 2005;28(6):1123-31. doi: 10.1007/s10545-005-0038-5. J Inherit Metab Dis. 2005. PMID: 16435205

9

[Isolation, differentiation and biochemical aspects of amniotic fluid stem cell].

Cabral AC, Angelo PC, Leite HV, Pereira AK, Lopes AP, Oliveira MB, Borges KB, Pardini VC, Ferreira AC. Cabral AC, et al. Among authors: pardini vc. Rev Assoc Med Bras (1992). 2008 Nov-Dec;54(6):489-93. doi: 10.1590/s0104-42302008000600011. Rev Assoc Med Bras (1992). 2008. PMID: 19197524 Free article. Portuguese.

10

Type 1 diabetes susceptibility determined by HLA alleles and CTLA-4 and insulin genes polymorphisms in Brazilians.

Ferreira AC, Gomes KB, Sampaio IB, Oliveira VC, Pardini VC, Godard AL. Ferreira AC, et al. Among authors: pardini vc. Arq Bras Endocrinol Metabol. 2009 Apr;53(3):368-73. doi: 10.1590/s0004-27302009000300012. Arq Bras Endocrinol Metabol. 2009. PMID: 19578600

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