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Items: 1 to 20 of 77

1.

The culture of limbal stromal cells and corneal endothelial cells.

Polisetti N, Joyce NC.

Methods Mol Biol. 2013;1014:131-9. doi: 10.1007/978-1-62703-432-6_8.

PMID:
23690009
2.

Stem cell-based therapy for corneal epithelial reconstruction: present and future.

Menzel-Severing J, Kruse FE, Schlötzer-Schrehardt U.

Can J Ophthalmol. 2013 Feb;48(1):13-21. doi: 10.1016/j.jcjo.2012.11.009. Review.

PMID:
23419294
3.

Anterior segment optical coherence tomography in congenital corneal opacities.

Majander AS, Lindahl PM, Vasara LK, Krootila K.

Ophthalmology. 2012 Dec;119(12):2450-7. doi: 10.1016/j.ophtha.2012.06.050. Epub 2012 Sep 5.

PMID:
22959105
4.

PAX6 mutations identified in 4 of 35 families with microcornea.

Wang P, Sun W, Li S, Xiao X, Guo X, Zhang Q.

Invest Ophthalmol Vis Sci. 2012 Sep 19;53(10):6338-42.

PMID:
22893676
5.

Aniridia.

Hingorani M, Hanson I, van Heyningen V.

Eur J Hum Genet. 2012 Oct;20(10):1011-7. doi: 10.1038/ejhg.2012.100. Epub 2012 Jun 13. Review.

6.

Bilateral Wilms' tumor: Mansoura multi-centers 15 years experience.

Halim A, Elashry R, Soliman O, Sarhan O.

J Oncol Pharm Pract. 2012 Mar;18(1):115-21. doi: 10.1177/1078155210396575. Epub 2012 Jan 10. Erratum in: J Oncol Pharm Pract. 2012 Sep;18(3):383. Halim, Amal [added]; Soliman, Othman [added]; Sarhan, Osama [added].

PMID:
22235062
7.

Glaucoma and frequency of ocular and general diseases in 30 patients with aniridia: a clinical study.

Gramer E, Reiter C, Gramer G.

Eur J Ophthalmol. 2012 Jan-Feb;22(1):104-10. doi: 10.5301/EJO.2011.8318.

PMID:
22167549
8.

Concurrent presentation of aniridia and megalocornea without glaucoma.

Lipsky SN, Salim S.

J AAPOS. 2011 Jun;15(3):297-8. doi: 10.1016/j.jaapos.2011.02.007. Epub 2011 Jun 12.

PMID:
21665500
9.

Run-on mutation in the PAX6 gene and chorioretinal degeneration in autosomal dominant aniridia.

Aggarwal S, Jinda W, Limwongse C, Atchaneeyasakul LO, Phadke SR.

Mol Vis. 2011;17:1305-9. Epub 2011 May 7.

10.

Clinical utility gene card for: WAGR syndrome.

Clericuzio C, Hingorani M, Crolla JA, van Heyningen V, Verloes A.

Eur J Hum Genet. 2011 Apr;19(4). doi: 10.1038/ejhg.2010.220. Epub 2011 Jan 12. No abstract available.

11.

Using protein design algorithms to understand the molecular basis of disease caused by protein-DNA interactions: the Pax6 example.

Alibés A, Nadra AD, De Masi F, Bulyk ML, Serrano L, Stricher F.

Nucleic Acids Res. 2010 Nov;38(21):7422-31. doi: 10.1093/nar/gkq683. Epub 2010 Aug 4.

12.

Complications and visual prognosis in children with aniridia.

Lee H, Meyers K, Lanigan B, O'Keefe M.

J Pediatr Ophthalmol Strabismus. 2010 Jul-Aug;47(4):205-10; quiz 211-2. doi: 10.3928/01913913-20090818-07. Epub 2009 Aug 21.

PMID:
20635810
13.

Corneal involvement in congenital aniridia.

Edén U, Riise R, Tornqvist K.

Cornea. 2010 Oct;29(10):1096-102. doi: 10.1097/ICO.0b013e3181d20493.

PMID:
20567200
14.

Midterm results of cultivated autologous and allogeneic limbal epithelial transplantation in limbal stem cell deficiency.

Pauklin M, Fuchsluger TA, Westekemper H, Steuhl KP, Meller D.

Dev Ophthalmol. 2010;45:57-70. doi: 10.1159/000315020. Epub 2010 May 18. Review.

PMID:
20502027
15.

Malformations of the brain in two fetuses with a compound heterozygosity for two PAX6 mutations.

Schmidt-Sidor B, Szymańska K, Williamson K, van Heyningen V, Roszkowski T, Wierzba-Bobrowicz T, Zaremba J.

Folia Neuropathol. 2009;47(4):372-82.

16.

PAX6 aniridia and interhemispheric brain anomalies.

Abouzeid H, Youssef MA, ElShakankiri N, Hauser P, Munier FL, Schorderet DF.

Mol Vis. 2009 Oct 17;15:2074-83.

17.

Detailed ophthalmologic evaluation of 43 individuals with PAX6 mutations.

Hingorani M, Williamson KA, Moore AT, van Heyningen V.

Invest Ophthalmol Vis Sci. 2009 Jun;50(6):2581-90. doi: 10.1167/iovs.08-2827. Epub 2009 Feb 14.

PMID:
19218613
18.

Characterization of 11p14-p12 deletion in WAGR syndrome by array CGH for identifying genes contributing to mental retardation and autism.

Xu S, Han JC, Morales A, Menzie CM, Williams K, Fan YS.

Cytogenet Genome Res. 2008;122(2):181-7. doi: 10.1159/000172086. Epub 2008 Dec 18. Erratum in: Cytogenet Genome Res. 2009;124(1):112.

PMID:
19096215
19.

Aniridia: current pathology and management.

Lee H, Khan R, O'Keefe M.

Acta Ophthalmol. 2008 Nov;86(7):708-15. doi: 10.1111/j.1755-3768.2008.01427.x. Epub 2008 Oct 6. Review.

20.

Genetic analysis of chromosome 11p13 and the PAX6 gene in a series of 125 cases referred with aniridia.

Robinson DO, Howarth RJ, Williamson KA, van Heyningen V, Beal SJ, Crolla JA.

Am J Med Genet A. 2008 Mar 1;146A(5):558-69. doi: 10.1002/ajmg.a.32209.

PMID:
18241071

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