- ►bmj.com [PDF] JC ZECH, S ZAOUCHE, F MOURIER, H … - British Medical Journal, 1999 - bjo.bmj.com PLAUCHU, JEAN-DANIEL GRANGE and CHRISTIANE TREPSAT JEAN-CHRISTOPHE ZECH, SANDRA
ZAOUCHE, FRANÇOIS MOURIER, HENRI ... References http://bjo.bmj.com/cgi/content
/full/83/10/1194b#BIBL This article cites 2 articles, 1 of which can be ... Cited by 6 - Related articles - All 6 versions
CK Pager, LK Sarin, JL Federman, R Eagle, … - American journal of ophthalmology, 2001 - Elsevier RESULTS: Two weeks after initial presentation, the visual acuity of this
34-year-old man decreased to LE: 20/100. Funduscopic evaluation revealed a
subretinal hemorrhage involving the center of the foveal in the left eye ... Cited by 8 - Related articles - BL Direct - All 7 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 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
M Matsumoto, EI Traboulsi - American journal of ophthalmology, 2001 - Elsevier PURPOSE: To report a new North American family with dominant radial drusen and
Arg345Trp mutation in the EFEMP1 gene. ... METHODS: Clinical and molecular
genetic family study. ... RESULTS: Four family members had macular ... Cited by 8 - Related articles - BL Direct - All 8 versions
MC Gaillard, TJ Wolfensberger, S Uffer, I … - Klinische Monatsblätter für Augenheilkunde, 2005 - ncbi.nlm.nih.gov BACKGROUND: Malattia Leventinese (ML) is a genetically homogeneous macular
dystrophy with an autosomal dominant mode of inheritance. Ophthalmoscopically it
is recognisable by a radial pattern of drusen-like deposits in the macula ... Cited by 4 - Related articles
N Narendran, RH Guymer, M Cain, PN Baird - Eye, 2004 - nature.com Age-related macular degeneration (AMD) is considered a complex genetic disease,
although the genetic influences are not yet fully understood. Genetic analysis
is hampered by the late onset of disease and the difficulty in obtaining ... Cited by 5 - Related articles - All 4 versions
[CITATION] Rod and cone-function in Malattia Leventinese and in retinitis pigmentosa
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
