Detalhe da pesquisa
1.
Mutation spectrum and clinical investigation of achromatopsia patients with mutations in the GNAT2 gene.
Hum Mutat
; 40(8): 1145-1155, 2019 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-31058429
2.
Cardiovascular Risk Factors in Central Retinal Artery Occlusion: Results of a Prospective and Standardized Medical Examination.
Ophthalmology
; 122(9): 1881-8, 2015 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-26231133
3.
Decreased catalytic activity and altered activation properties of PDE6C mutants associated with autosomal recessive achromatopsia.
Hum Mol Genet
; 20(4): 719-30, 2011 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-21127010
4.
A homologous genetic basis of the murine cpfl1 mutant and human achromatopsia linked to mutations in the PDE6C gene.
Proc Natl Acad Sci U S A
; 106(46): 19581-6, 2009 Nov 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-19887631
5.
Central retinal artery occlusion: local intra-arterial fibrinolysis versus conservative treatment, a multicenter randomized trial.
Ophthalmology
; 117(7): 1367-75.e1, 2010 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-20609991
6.
CNGB3 mutations account for 50% of all cases with autosomal recessive achromatopsia.
Eur J Hum Genet
; 13(3): 302-8, 2005 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-15657609
7.
Novel insights into the molecular pathogenesis of CYP4V2-associated Bietti's retinal dystrophy.
Mol Genet Genomic Med
; 3(1): 14-29, 2015 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-25629076
8.
Ten novel ORF15 mutations confirm mutational hot spot in the RPGR gene in European patients with X-linked retinitis pigmentosa.
Hum Mutat
; 20(5): 405, 2002 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-12402343
9.
Mutation analysis of NR2E3 and NRL genes in Enhanced S Cone Syndrome.
Hum Mutat
; 24(5): 439, 2004 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-15459973
10.
Intraocular biopsy using special forceps: a new instrument and refined surgical technique.
Br J Ophthalmol
; 95(1): 79-82, 2011 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-21163820
11.
Multifocal electroretinography in patients with exudative amd and intravitreal treatment with pegaptanib sodium.
Retina
; 27(7): 864-72, 2007 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-17891010
12.
A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss.
Hum Genet
; 121(2): 203-11, 2007 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-17171570
13.
Photodynamic therapy using verteporfin for choroidal neovascularization associated with angioid streaks--long-term effects.
Ophthalmic Res
; 38(4): 209-17, 2006.
Artigo
em Inglês
| MEDLINE | ID: mdl-16679809
14.
Long-term effect of acetazolamide treatment of patients with uveitic chronic cystoid macular edema is limited by persisting inflammation.
Retina
; 25(2): 182-8, 2005.
Artigo
em Inglês
| MEDLINE | ID: mdl-15689809
15.
Photodynamic therapy for symptomatic choroidal hemangioma: visual and anatomic results.
Ophthalmology
; 109(12): 2284-94, 2002 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-12466172
16.
The role of photodynamic therapy in the treatment of symptomatic choroidal hemangioma.
Graefes Arch Clin Exp Ophthalmol
; 243(5): 393-6, 2005 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-15700182