Aniridiesyndrom-Reference-Cited by-同舟云学术

Aniridiesyndrom

Published:2014-12 Issue:12 Volume:111 Page:1145-1156
ISSN:0941-293X
Container-title:Der Ophthalmologe
language:de
Short-container-title:Ophthalmologe

Author:

Käsmann-Kellner B.,Seitz B.

Publisher

Springer Science and Business Media LLC

Subject

Ophthalmology

Link

http://link.springer.com/content/pdf/10.1007/s00347-014-3060-x.pdf

Reference30 articles.

1. Almousa R, Lake DB (2014) Intraocular pressure control with Ahmed glaucoma drainage device in patients with cicatricial ocular surface disease-associated or aniridia-related glaucoma. Int Ophthalmol 34(4):753–760

2. Bamiou DE, Campbell NG, Musiek FE et al (2007) Auditory and verbal working memory deficits in a child with congenital aniridia due to a PAX6 mutation. Int J Audiol 46(4):196–202

3. Bamiou DE, Free SL, Sisodiya SM et al (2007) Auditory interhemispheric transfer deficits, hearing difficulties, and brain magnetic resonance imaging abnormalities in children with congenital aniridia due to PAX6 mutations. Arch Pediatr Adolesc Med 161(5):463–469

4. Beby F, Dieterich K, Calvas P (2011) A [c.566-2A>G] heterozygous mutation in the PAX6 gene causes aniridia with mild visual impairment. Eye (Lond) 25(5):657–658

5. Brémond-Gignac D, Bitoun P, Reis LM et al (2010) Identification of dominant FOXE3 and PAX6 mutations in patients with congenital cataract and aniridia. Mol Vis 16:1705–1711

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