de Vasconcellos JP - Search Results

1

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: de vasconcellos jp. 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.

2

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: de melo mb. J Glaucoma. 2003 Apr;12(2):104-7. doi: 10.1097/00061198-200304000-00003. J Glaucoma. 2003. PMID: 12671463

3

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: de melo mb, de vasconcellos jp. Invest Ophthalmol Vis Sci. 2006 May;47(5):1803-9. doi: 10.1167/iovs.05-0979. Invest Ophthalmol Vis Sci. 2006. PMID: 16638984

4

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: de melo mb, de almeida gv, de vasconcellos jp. Ophthalmic Genet. 2009 Mar;30(1):13-8. doi: 10.1080/13816810802502970. Ophthalmic Genet. 2009. PMID: 19172505

5

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: de melo mb, de vasconcellos jp. J Glaucoma. 2010 Mar;19(3):176-82. doi: 10.1097/IJG.0b013e3181a98bae. J Glaucoma. 2010. PMID: 19528825

6

New mutation in the myocilin gene segregates with juvenile-onset open-angle glaucoma in a Brazilian family.

Braghini CA, Neshich IA, Neshich G, Soardi FC, de Mello MP, Costa VP, de Vasconcellos JP, de Melo MB. Braghini CA, et al. Among authors: de melo mb, de mello mp, de vasconcellos jp. Gene. 2013 Jul 1;523(1):50-7. doi: 10.1016/j.gene.2013.02.054. Epub 2013 Apr 5. Gene. 2013. PMID: 23566828 Free article.

7

Genotype-Phenotype Correlations in CYP1B1-Associated Primary Congenital Glaucoma Patients Representing Two Large Cohorts from India and Brazil.

de Melo MB, Mandal AK, Tavares IM, Ali MH, Kabra M, de Vasconcellos JP, Senthil S, Sallum JM, Kaur I, Betinjane AJ, Moura CR, Paula JS, Costa KA, Sarfarazi M, Paolera MD, Finzi S, Ferraz VE, Costa VP, Belfort R Jr, Chakrabarti S. de Melo MB, et al. Among authors: de vasconcellos jp. PLoS One. 2015 May 15;10(5):e0127147. doi: 10.1371/journal.pone.0127147. eCollection 2015. PLoS One. 2015. PMID: 25978063 Free PMC article.

8

Investigation of CAV1/CAV2 rs4236601 and CDKN2B-AS1 rs2157719 in primary open-angle glaucoma patients from Brazil.

Nunes HF, Ananina G, Costa VP, Zanchin NIT, de Vasconcellos JPC, de Melo MB. Nunes HF, et al. Ophthalmic Genet. 2018 Apr;39(2):194-199. doi: 10.1080/13816810.2017.1393830. Epub 2017 Nov 7. Ophthalmic Genet. 2018. PMID: 29111846

9

Estimating the age of the p.Cys433Arg variant in the MYOC gene in patients with primary open-angle glaucoma.

Marques AM, Ananina G, Costa VP, de Vasconcellos JPC, de Melo MB. Marques AM, et al. PLoS One. 2018 Nov 16;13(11):e0207409. doi: 10.1371/journal.pone.0207409. eCollection 2018. PLoS One. 2018. PMID: 30444892 Free PMC article. Clinical Trial.

10

Occurrence of MYOC and CYP1B1 variants in juvenile open angle glaucoma Brazilian patients.

Svidnicki PV, Braghini CA, Costa VP, Schimiti RB, de Vasconcellos JPC, de Melo MB. Svidnicki PV, et al. Ophthalmic Genet. 2018 Dec;39(6):717-724. doi: 10.1080/13816810.2018.1546405. Ophthalmic Genet. 2018. PMID: 30484747

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