|1.||Tamm, Ernst R: 3 articles (06/2008 - 10/2002)|
|2.||Semina, Elena V: 2 articles (03/2015 - 01/2012)|
|3.||Reis, Linda M: 2 articles (03/2015 - 01/2012)|
|4.||Glaser, Tom: 2 articles (01/2012 - 01/2006)|
|5.||Caputo, Georges: 2 articles (11/2011 - 01/2010)|
|6.||Dureau, Pascal: 2 articles (11/2011 - 01/2010)|
|7.||Azuma, Noriyuki: 2 articles (02/2011 - 06/2003)|
|8.||Inatani, Masaru: 2 articles (03/2010 - 07/2009)|
|9.||Cvekl, Ales: 2 articles (04/2004 - 10/2002)|
|10.||Cortina, Maria S: 1 article (11/2015)|
10/01/1999 - "Steroid-induced glaucoma and anterior segment dysgenesis, excluding Peters anomaly, had uniformly good outcomes. "
03/01/2010 - "The anomalies are comparable to Peters anomaly, a type of developmental glaucoma in humans. "
10/01/2009 - "Patients with Peters' anomaly had similar graft survival rates to patients with other congenital opacities (67% vs 48% survival at 1 year, P = 0.78) Patients with pretransplant and/or posttransplant glaucoma had worse 1-year graft survival compared with patients without preoperative glaucoma (glaucoma 32% vs no glaucoma 70%, P = 0.02) Pretransplant and/or posttransplant glaucoma was the only independent predictor of worse graft survival in a multivariate analysis (P = 0.02). "
07/01/2009 - "These dysfunctions are phenotypes of the human developmental glaucoma, Peters anomaly. "
06/01/2009 - "Most eyes had primary congenital glaucoma (28/42, 66.7%), aphakic glaucoma (5/42, 11.9%) or Peters anomaly (5/42, 11.9%). "
01/01/2015 - "This study involved 19 eyes of 10 consecutive infants with congenital corneal opacity, 13 eyes with Peters anomaly (PA, 7 cases) and 6 eye with sclerocornea (SC, 3 cases), recruited at the Kyoto Prefectural University of Medicine, Kyoto, Japan between September 2001 and January 2009. "
08/01/2014 - "The aim of this study was to determine the incidence of Peters anomaly (PA) and congenital corneal opacities (CCO) interfering with vision in the United States. "
01/01/2015 - "Typically, histopathology of Peters anomaly shows immature or absent Descemet's membrane and attenuated endothelial cells in the area of the corneal opacity, in addition to thinning or absence of Bowman's membrane and defects in the posterior stroma. "
01/01/2015 - "Peters anomaly is a rare developmental abnormality of the anterior segment of the eye and is one of the main causes of congenital corneal opacities. "
08/01/2014 - "Incidence of Peters anomaly and congenital corneal opacities interfering with vision in the United States."
12/01/2006 - "Ten patients affected with Peters anomaly, 8 with Rieger anomaly, and 3 with aniridia were included in this study. "
01/01/2015 - "Human PAX6 mutations are associated with severe ocular disorders such as aniridia, Peters anomaly and chronic limbal stem cell insufficiency. "
08/01/2013 - "Case 2 was diagnosed as congenital aniridia combined with Peters anomaly in both eyes. "
01/01/2012 - "Four of these changes, c.47C>T (p.Thr16Met), c.359C>T (p.Pro120Leu), c.517A>C (p.Asn173His), and c.818_829dup (p.Arg273_Gly276dup), affected conserved regions and were observed primarily in probands with aniridia or Peters anomaly; out of these four variants, one, p.Arg273_Gly276dup, was not detected in control populations and two, p.Pro120Leu and p.Asn173His, were statistically enriched in cases with aniridia or Peters anomaly. "
02/01/2011 - "We report a child with aniridia and Peters anomaly associated with a PAX6 gene mutation."
06/01/2012 - "Our present study observed the morphologic changes in conventional Msx2 knockout (KO) mice and found phenotypes consistent with Peters anomaly and microphthalmia seen in humans. "
11/01/2014 - "Ophthalmopathologic examination of the eyes revealed microphthalmia with anterior segment developmental anomalies, in particular sclerocornea and Peters' anomaly, respectively. "
11/01/2014 - "Analysis of 24 unrelated A/M exomes identified a novel c.2122G>A, p.(Gly708Arg) mutation in an additional patient with unilateral microphthalmia, bilateral microcornea and Peters anomaly; the mutation was absent in the unaffected mother and the unaffected father was not available. "
06/01/2008 - "Sox11-deficient mice show a persistent lens stalk, a delay in lens formation, and the phenotypes of Peters' anomaly and microphthalmia at birth. "
02/01/2003 - "Malformed fetuses displayed a range of ocular defects that included microphthalmia and keratolenticular dysgenesis (Peters anomaly). "
10/01/1997 - "The clinical picture and pathology study indicated this case as a Peters' anomaly presenting congenital aphakia."
01/01/2005 - "To describe two cases of secondary congenital aphakia in association with Peters anomaly. "
10/01/1997 - "Congenital aphakia in Peters' anomaly syndrome. "
01/01/1972 - "A typical case of Peters' anomaly with primary aphakia."
01/01/2005 - "Secondary congenital aphakia from corneal perforation should be considered in the presentation of severe Peters anomaly."
|2.||cytochrome P-450 CYP1B1 (CYP1B1)
|3.||DNA (Deoxyribonucleic Acid)
|5.||Vascular Endothelial Growth Factor A (Vascular Endothelial Growth Factor)
|6.||Nonsense Codon (Nonsense Mutation)
|9.||Proteins (Proteins, Gene)
|5.||Corneal Transplantation (Keratoplasty)