Literature DB >> 18427259

Anterior segment dysgenesis: Peters anomaly and sclerocornea.

Mona Harissi-Dagher1, Kathryn Colby.   

Abstract

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Year:  2008        PMID： 18427259     DOI： 10.1097/IIO.0b013e318169526c

Source DB:  PubMed          Journal:  Int Ophthalmol Clin        ISSN： 0020-8167


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  15 in total

1.  Boston Keratoprosthesis: expanding the boundaries.

Authors:  Mona Harissi-Dagher
Journal:  Digit J Ophthalmol       Date:  2011-11-03

2.  Loss of Msx2 function down-regulates the FoxE3 expression and results in anterior segment dysgenesis resembling Peters anomaly.

Authors:  Jiangyue Zhao; Kirio Kawai; Hongyan Wang; Di Wu; Mingwu Wang; Zhicao Yue; Jinsong Zhang; Yi-Hsin Liu
Journal:  Am J Pathol       Date:  2012-04-13       Impact factor: 4.307

3.  Newborn with an absent red reflex.

Authors:  Sanjeev Y Tuli; Beverly P Giordano; Maria Kelly; Donald Fillipps; Sonal S Tuli
Journal:  J Pediatr Health Care       Date:  2011-12-22       Impact factor: 1.812

4.  Two novel mutations of the PAX6 gene causing different phenotype in a cohort of Chinese patients.

Authors:  X Zhang; Y Tong; W Xu; B Dong; H Yang; L Xu; Y Li
Journal:  Eye (Lond)       Date:  2011-09-09       Impact factor: 3.775

5.  A novel, non-stop mutation in FOXE3 causes an autosomal dominant form of variable anterior segment dysgenesis including Peters anomaly.

Authors:  Lance Doucette; Jane Green; Bridget Fernandez; Gordon J Johnson; Patrick Parfrey; Terry-Lynn Young
Journal:  Eur J Hum Genet       Date:  2010-12-08       Impact factor: 4.246

6.  A novel mutation of PAX6 in Chinese patients with new clinical features of Peters' anomaly.

Authors:  Xiuhua Jia; Xiangming Guo; Xiaoyun Jia; Xueshan Xiao; Shiqiang Li; Qingjiong Zhang
Journal:  Mol Vis       Date:  2010-04-15       Impact factor: 2.367

7.  Anterior segment dysgenesis correlation with epithelial-mesenchymal transition in Smad4 knockout mice.

Authors:  Jing Li; Yu Qin; Fang-Kun Zhao; Di Wu; Xue-Fei He; Jia Liu; Jiang-Yue Zhao; Jin-Song Zhang
Journal:  Int J Ophthalmol       Date:  2016-07-18       Impact factor: 1.779

8.  Peters anomaly with post axial polydactyly, bilateral camptodactyly and club foot in a Kenyan neonate: a case report.

Authors:  Aruyaru Stanley Mwenda
Journal:  J Med Case Rep       Date:  2012-01-17

9.  Epithelial phenotype in total sclerocornea.

Authors:  David Hui-Kang Ma; Lung-Kung Yeh; Hung-Chi Chen; Anna Marie Chang; Yi-Ju Ho; Shirley H L Chang; Unique Yang
Journal:  Mol Vis       Date:  2014-04-11       Impact factor: 2.367

10.  FOXE3 contributes to Peters anomaly through transcriptional regulation of an autophagy-associated protein termed DNAJB1.

Authors:  Shahid Y Khan; Shivakumar Vasanth; Firoz Kabir; John D Gottsch; Arif O Khan; Raghothama Chaerkady; Mei-Chong W Lee; Carmen C Leitch; Zhiwei Ma; Julie Laux; Rafael Villasmil; Shaheen N Khan; Sheikh Riazuddin; Javed Akram; Robert N Cole; C Conover Talbot; Nader Pourmand; Norann A Zaghloul; J Fielding Hejtmancik; S Amer Riazuddin
Journal:  Nat Commun       Date:  2016-04-06       Impact factor: 14.919
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