L Marmorstein - Ophthalmic Genetics, 2004 - Informa Pharma Science Abstract Malattia leventinese (ML) or Doyne honeycomb retinal dystrophy (DHRD)
was the first clinically and histopathologically described Mendelian
maculopathy. The gene responsible for ML/ DHRD, EFEMP1 (fibulin-3/S1-5/FBNL ... Cited by 15 - Related articles - BL Direct - All 5 versions
MA Dantas, JS Slakter, S Negrao, RA Fonseca … - Ophthalmology, 2002 - Elsevier To describe a case of a patient with documented genetic mallatia leventinese who
developed a classic choroidal neovascular membrane and underwent photodynamic
therapy (PDT) with verteporfin (Visudyne; CIBA Vision Corp., Duluth, GA). Cited by 11 - Related articles - BL Direct - All 9 versions
- ►iovs.org DM Gerber, FL Munier, G Niemeyer - Investigative ophthalmology & visual science, 2003 - ARVO RESULTS. Both inherited macular degenerations caused a marked decrease in visual
acuity, the latest after age 65. Most patients with ML retained good visual
function (0.8–1.0) until the fifth decade, followed by a rapid decrease ... Cited by 7 - Related articles - BL Direct - All 4 versions
- ►iovs.org M Michaelides, SA Jenkins, MA Brantley Jr, … - Investigative ophthalmology & visual science, 2006 - ARVO RESULTS. Twenty-nine subjects from 19 families were ascertained with inherited
or early-onset drusen. Twenty-four (83%) subjects from 15 families were found to
harbor the R345W fibulin-3 mutation. Peripapillary deposition and a radial ... Cited by 3 - Related articles - BL Direct - All 4 versions
- ►nih.gov EH Souied, N Leveziel, G Querques, J … - British Journal of Ophthalmology, 2006 - bjo.bmj.com Background/aim: Malattia leventinese (ML) is an inherited macular degeneration
characterised by the presence of small radial drusen. Despite extensive
descriptions of this study of the fundus, angiographic features of ML have ... Cited by 1 - Related articles - BL Direct - All 7 versions
T Takeuchi, T Hayashi, M Bedell, K Zhang, … - Investigative Ophthalmology & Visual Science, 2009 - ARVO Page 1. 1 A novel haplotype with the R345W mutation in the EFEMP1 gene
associated with autosomal dominant drusen in a Japanese family ... Related articles