Detalhe da pesquisa
1.
Homozygous mutations in PXDN cause congenital cataract, corneal opacity, and developmental glaucoma.
Am J Hum Genet
; 89(3): 464-73, 2011 Sep 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-21907015
2.
Ophthalmic findings in Apert's syndrome after craniofacial surgery: twenty-nine years' experience.
Ophthalmology
; 113(2): 347-52, 2006 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-16458095
3.
Ophthalmic findings in apert syndrome prior to craniofacial surgery.
Am J Ophthalmol
; 142(2): 328-30, 2006 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-16876521
4.
The ophthalmic sequelae of Pfeiffer syndrome and the long-term visual outcomes after craniofacial surgery.
J AAPOS
; 20(4): 315-9, 2016 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-27418250
5.
Juvenile arthritis-associated uveitis: visual outcomes and prognosis.
Can J Ophthalmol
; 39(6): 614-20, 2004 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-15559647
6.
A survey of severe visual impairment and blindness in children attending thirteen schools for the blind in sri lanka.
Ophthalmic Epidemiol
; 18(1): 36-43, 2011 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-21275594
7.
A survey of visual impairment and blindness in children attending four schools for the blind in Cambodia.
Ophthalmic Epidemiol
; 17(4): 225-33, 2010 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-20642345
8.
A survey of visual impairment and blindness in children attending seven schools for the blind in Myanmar.
Ophthalmic Epidemiol
; 16(6): 370-7, 2009.
Artigo
em Inglês
| MEDLINE | ID: mdl-19995202
9.
Differential effects of FGFR2 mutation in ophthalmic findings in Apert syndrome.
J Craniofac Surg
; 18(1): 39-42, 2007 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-17251833