about
X-linked megalocornea caused by mutations in CHRDL1 identifies an essential role for ventroptin in anterior segment developmentLmx1b is required for murine trabecular meshwork formation and for maintenance of corneal transparencyMutations in CPAMD8 Cause a Unique Form of Autosomal-Recessive Anterior Segment DysgenesisA method to preserve limbus during penetrating keratoplasty for a case of presumed PHACES syndrome with sclerocornea: A case reportA novel mutation of PAX6 in Chinese patients with new clinical features of Peters' anomalyType II Peter's anomaly with histopathological proof: a case reportPediatric glaucoma suspects.A Chinese family with Axenfeld-Rieger syndrome: report of the clinical and genetic findingsAxenfeld-Rieger syndrome and spectrum of PITX2 and FOXC1 mutationsHomozygous mutations in PXDN cause congenital cataract, corneal opacity, and developmental glaucomaTwo novel mutations of the PAX6 gene causing different phenotype in a cohort of Chinese patients.Loss of Msx2 function down-regulates the FoxE3 expression and results in anterior segment dysgenesis resembling Peters anomaly.A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma.Analysis of FOXD3 sequence variation in human ocular disease.Unusual Surprises in Glaucoma Filtering Surgeries: Lessons Learned and Review of Literature.Identification of an Alu-repeat-mediated deletion of OPTN upstream region in a patient with a complex ocular phenotype.Whole exome sequencing identifies a heterozygous missense variant in the PRDM5 gene in a family with Axenfeld-Rieger syndrome.Absence of NR2E1 mutations in patients with aniridia.Molecular and developmental mechanisms of anterior segment dysgenesis.Congenital corneal opacities - a surgical approach to nomenclature and classification.Pharmacogenetics of ophthalmic topical beta-blockers.An epidemiological investigation of a Forkhead box protein E3 founder mutation underlying the high frequency of sclerocornea, aphakia, and microphthalmia in a Mexican village.Recent perspectives in ocular drug delivery.Identification of a novel frameshift mutation in PITX2 gene in a Chinese family with Axenfeld-Rieger syndrome.Novel and recurrent PITX3 mutations in Belgian families with autosomal dominant congenital cataract and anterior segment dysgenesis have similar phenotypic and functional characteristics.Epithelial phenotype in total sclerocornea.Conditions that can be mistaken as early childhood glaucoma.Genomics and anterior segment dysgenesis: a review.Novel Genetic Findings in a Chinese Family with Axenfeld-Rieger SyndromeA novel mouse model of anterior segment dysgenesis (ASD): conditional deletion of Tsc1 disrupts ciliary body and iris developmentThe 6p25 deletion syndrome: An update on a rare neurocristopathy.Minimally invasive microneedles for ocular drug delivery.Unclassified Axenfeld-Rieger Syndrome: A CASE SERIES and Review of Literature.Anterior segment dysgenesis (Peters' anomaly) in two snow leopard (Panthera uncia) cubs.A Surgical Approach to Pediatric Glaucoma.Glaucoma spectrum and age-related prevalence of individuals with FOXC1 and PITX2 variants.Magnetic resonance imaging findings in Axenfeld-Rieger syndrome.The rare Axenfeld-Rieger syndrome with systemic anomalies: A case report and brief review of literatureLate-onset endophthalmitis secondary to exposed glaucoma tube implant in a rare case of paediatric glaucoma.Identification of genes expressed preferentially in the developing peripheral margin of the optic cup.
P2860
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P2860
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年学术文章
@wuu
2006年学术文章
@zh-cn
2006年学术文章
@zh-hans
2006年学术文章
@zh-my
2006年学术文章
@zh-sg
2006年學術文章
@yue
2006年學術文章
@zh
2006年學術文章
@zh-hant
name
A review of anterior segment dysgeneses.
@ast
A review of anterior segment dysgeneses.
@en
type
label
A review of anterior segment dysgeneses.
@ast
A review of anterior segment dysgeneses.
@en
prefLabel
A review of anterior segment dysgeneses.
@ast
A review of anterior segment dysgeneses.
@en
P2093
P1476
A review of anterior segment dysgeneses
@en
P2093
Daniela Vaideanu
Faisal Idrees
Peng T Khaw
Scott G Fraser
P304
P356
10.1016/J.SURVOPHTHAL.2006.02.006
P577
2006-05-01T00:00:00Z