Costa VP - Search Results

1

Association of variants in the ATXN2 (rs7137828), FOXC1 (rs2745572) and TXNRD2 (rs35934224) genes as risk factors for primary open-angle glaucoma development in a Brazilian cohort.

Rodrigues TAR, de Souza BB, Bertozzo VHE, de Castro JNP, Camargo ACL, Costa FF, Schimiti RB, Costa VP, de Vasconcellos JPC, de Melo MB. Rodrigues TAR, et al. Among authors: costa vp, costa ff. Ophthalmic Genet. 2023 Jun;44(3):246-252. doi: 10.1080/13816810.2023.2191704. Epub 2023 Mar 30. Ophthalmic Genet. 2023. PMID: 36994723

2

Full-threshold versus Swedish Interactive Threshold Algorithm (SITA) in normal individuals undergoing automated perimetry for the first time.

Schimiti RB, Avelino RR, Kara-José N, Costa VP. Schimiti RB, et al. Among authors: costa vp. Ophthalmology. 2002 Nov;109(11):2084-92; discussion 2092. doi: 10.1016/s0161-6420(02)01253-8. Ophthalmology. 2002. PMID: 12414419 Clinical Trial.

3

Penetrance and phenotype of the Cys433Arg myocilin mutation in a family pedigree with primary open-angle glaucoma.

de Vasconcellos JP, de Melo MB, Schimiti R, Costa FF, Costa VP. de Vasconcellos JP, et al. Among authors: costa vp, costa ff. J Glaucoma. 2003 Apr;12(2):104-7. doi: 10.1097/00061198-200304000-00003. J Glaucoma. 2003. PMID: 12671463

4

A novel mutation in the GJA1 gene in a family with oculodentodigital dysplasia.

Vasconcellos JP, Melo MB, Schimiti RB, Bressanim NC, Costa FF, Costa VP. Vasconcellos JP, et al. Among authors: costa vp, costa ff. Arch Ophthalmol. 2005 Oct;123(10):1422-6. doi: 10.1001/archopht.123.10.1422. Arch Ophthalmol. 2005. PMID: 16219735

5

Structural assessment of PITX2, FOXC1, CYP1B1, and GJA1 genes in patients with Axenfeld-Rieger syndrome with developmental glaucoma.

Cella W, de Vasconcellos JP, de Melo MB, Kneipp B, Costa FF, Longui CA, Costa VP. Cella W, et al. Among authors: costa vp, costa ff. Invest Ophthalmol Vis Sci. 2006 May;47(5):1803-9. doi: 10.1167/iovs.05-0979. Invest Ophthalmol Vis Sci. 2006. PMID: 16638984

6

[Full Threshold vs. SITA in glaucomatous patients undergoing automated perimetry for the first time].

Schimiti RB, Arcieri ES, Avelino RR, Matsuo T, Costa VP. Schimiti RB, et al. Among authors: costa vp. Arq Bras Oftalmol. 2006 Mar-Apr;69(2):145-50. doi: 10.1590/s0004-27492006000200002. Epub 2006 May 8. Arq Bras Oftalmol. 2006. PMID: 16699660 Free article. Clinical Trial. Portuguese.

7

Sensitivity and specificity of frequency-doubling technology, tendency-oriented perimetry, SITA Standard and SITA Fast perimetry in perimetrically inexperienced individuals.

Pierre-Filho Pde T, Schimiti RB, de Vasconcellos JP, Costa VP. Pierre-Filho Pde T, et al. Among authors: costa vp. Acta Ophthalmol Scand. 2006 Jun;84(3):345-50. doi: 10.1111/j.1600-0420.2006.00639.x. Acta Ophthalmol Scand. 2006. PMID: 16704696 Free article.

8

Lack of association between optineurin gene variants T34T, E50K, M98K, 691_692insAG and R545Q and primary open angle glaucoma in Brazilian patients.

Caixeta-Umbelino C, de Vasconcellos JP, Costa VP, Kasahara N, Della Paolera M, de Almeida GV, Cohen R, Mandia C Jr, Rocha MN, Richeti F, Longui CA, de Melo MB. Caixeta-Umbelino C, et al. Among authors: costa vp. Ophthalmic Genet. 2009 Mar;30(1):13-8. doi: 10.1080/13816810802502970. Ophthalmic Genet. 2009. PMID: 19172505

9

CYP1B1 gene analysis in primary congenital glaucoma Brazilian patients: novel mutations and association with poor prognosis.

Della Paolera M, de Vasconcellos JP, Umbelino CC, Kasahara N, Rocha MN, Richeti F, Costa VP, Tavares A, de Melo MB. Della Paolera M, et al. Among authors: costa vp. J Glaucoma. 2010 Mar;19(3):176-82. doi: 10.1097/IJG.0b013e3181a98bae. J Glaucoma. 2010. PMID: 19528825

10

Myocilin mt.1 gene promoter single nucleotide polymorphism (-1000C>G) in Brazilian patients with primary open angle glaucoma.

Kasahara N, Caixeta-Umbelino C, Paolera MD, Rocha MN, Richeti F, Vasconcellos JP, Cohen R, Costa VP, Longui CA, Melo MR, Melo MB. Kasahara N, et al. Among authors: costa vp. Ophthalmic Genet. 2011 Mar;32(1):18-23. doi: 10.3109/13816810.2010.535887. Epub 2010 Dec 21. Ophthalmic Genet. 2011. PMID: 21174523

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