SY Cohen, L Dubois, R Tadayoni, C Delahaye … - British Journal of Ophthalmology, 2007 - bjo.bmj.com Results: Patients with newly diagnosed CNV in series 1 comprised 67 women and 33
men, aged 57–96 years (mean 79.5). CNV was “classic” (32 eyes),
“occult” (41) or exhibited vascularised pigment epithelial detachment ... Cited by 4 - Related articles - BL Direct - All 4 versions
[CITATION] Retinal Angiomatous Proliferation: Diagnosis and Treatment Options
Y Rutishauser-Arnold, AM Thölen - Klinische Monatsblätter für Augenheilkunde, 2007 - ncbi.nlm.nih.gov BACKGROUND: Intravitreal triamcinolone injections are used for the treatment of
occult choroidal neovascularisations (CNV) combined with photodynamic therapy
(PDT). However, this therapy is not without considerable risks. The ... Cited by 4 - Related articles - BL Direct
GR Kuerzinger, GK Lang, GE Lang - Klinische MonatsblÃĪtter fÞr Augenheilkunde, 2006 - ncbi.nlm.nih.gov BACKGROUND: Angiomatous proliferation in ARMD originates from the retina and
extends into the subretinal space. Retinal angiomatous proliferation (RAP) is
diagnosed with angiography. This study investigates the characteristics of ... Cited by 5 - Related articles - BL Direct
A Polito, MC Napolitano, F Bandello, RG … - ANNALS-ACADEMY OF MEDICINE SINGAPORE, 2006 - annals.edu.sg Introduction Retinal angiomatous proliferation (RAP), initially described as
deep retinal vascular anomalous complex in 1992 by Hartnett et al,1,2 has been
recently defined as a new, distinct form of exudative age-related macular ... Cited by 6 - Related articles - View as HTML - BL Direct - All 4 versions
JL Prenner, BJ Rosenblatt, MJ Tolentino, GS … - Retina, 2003 - journals.lww.com Dr. Prenner's research is supported by the Ronald G. Michels Foundation and the
Heed Foundation. Support has been provided by an unrestricted gift from Research
to Prevent Blindness, Inc. to the University of Pennsylvania; gifts to the ... Cited by 6 - Related articles - BL Direct - All 3 versions
S Borooah, C Collins, A Wright, B Dhillon - British Journal of Ophthalmology, 2009 - bjo.bmj.com Aim: This study describes, in detail, the phenotype of late-onset retinal
macular degeneration (L-ORMD) an inherited condition affecting both the retina
and anterior segment. A staging based on clinical characteristics is ... Cited by 1 - Related articles - All 5 versions
