Found: 7
Select item for more details and to access through your institution.
PRPH2 mutation c.582-1G>A causing adult-onset macular dystrophy with a benign concentric annular macular dystrophy phenotype in a family.
- Published in:
- 2024
- By:
- Publication type:
- Case Study
Long term evolution of combined hamartoma of the retina and retinal pigment epithelium.
- Published in:
- Vision Pan-America, 2014, v. 13, n. 2, p. 53
- By:
- Publication type:
- Article
Unilateral recurrent macular hole in a patient with retinitis pigmentosa: a case report.
- Published in:
- 2013
- By:
- Publication type:
- journal article
Vitreoretinal surgery for bilateral macular holes after laser-assisted in situ keratomileusis for the correction of myopia: a case report.
- Published in:
- 2012
- By:
- Publication type:
- journal article
Long-term evolution of Valsalva retinopathy: a case series.
- Published in:
- 2012
- By:
- Publication type:
- journal article
Spontaneous closure of stage IV idiopathic full-thickness macular hole and late reopening as a lamellar macular hole: a case report.
- Published in:
- 2012
- By:
- Publication type:
- journal article
Comprehensive SNP-chip for retinitis pigmentosa-Leber congenital amaurosis diagnosis: new mutations and detection of mutational founder effects.
- Published in:
- European Journal of Human Genetics, 2010, v. 18, n. 1, p. 118, doi. 10.1038/ejhg.2009.114
- By:
- Publication type:
- Article