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Scholar Results 1 - 7 of 7 citing Klevering: Central areolar choroidal dystrophy associated with dominantly inherited drusen. (0.10 sec) 

Update on the genetics of macular dystrophies


I Voo, KW Small - Retina, 2004 - journals.lww.com
Although 1it was once argued that hereditary mac- ular dystrophies represent a
single dystrophic process,1 it has become clear through advances in molecular
genetics that this is not the case. Each year brings exponentially more ...
Cited by 3 - Related articles - BL Direct - All 2 versions

Clinical findings in a multigeneration family with autosomal dominant central areolar …


CN Keilhauer, T Meigen, BHF Weber - Archives of Ophthalmology, 2006 - archopht.highwire.org
Methods Sixteen members from 2 generations underwent ophthalmologic examination,
including best-corrected visual acuity, examination of the anterior segments,
and inspection of the ocular fundus after pharmacologic mydriasis. All ...
Cited by 3 - Related articles - All 5 versions

Macular Dystrophies


BJ Klevering, JJC van Lith-Verhoeven, CB … - Essentials in ophthalmology: Medical retina. Berlin: …, 1999 - Springer
A variety of dystrophies, principally locat- ed at the macula, can be
distinguished ac- cording to fundus appearance, inheritance pattern and, in some
cases, molecular ge- netic analysis.Although these disorders are all ...
Cited by 1 - Related articles - All 2 versions

Extensive Macular Atrophy with Pseudodrusen-like Appearance: A New Clinical Entity


CJF Boon, T Theelen, CB Hoyng - American journal of ophthalmology, 2009 - Elsevier
In their interesting paper, Hamel and associates describe a group of relatively
young patients with extensive macular atrophy and pseudodrusen-like lesions, and
they state that this is a new clinical entity. 1 The phenotyping of these ...
Related articles - All 42 versions

Indocyanine Green Angiography Features of Central Areolar Choroidal Dystrophy


B Guigui, O Semoun, G Querques, G Coscas, … - Retinal Cases and Brief Reports, 2009 - journals.lww.com
Central areolar choroidal dystrophy (CACD) is an inherited autosomal dominant
macular disease. Diagnosis of CACD is clinical, based on fundus ex- amination
and fluorescein angiography (FA) features1 and described in 1977 by Noble.2 ...
Related articles

MACULAR DYSTROPHY ASSOCIATED WITH THE ARG172TRP SUBSTITUTION IN …


S ANAND, E SHERIDAN, F CASSIDY, C … - Retina, 2009 - journals.lww.com
The peripherin/RDS gene encodes a photoreceptor- specific glycoprotein that is
localized in the outer segment disk membranes of both rods and cones. It is
believed to play an important role in the assembly, orientation, and ...
Related articles - All 3 versions

Central Areolar Choroidal Dystrophy


CJF Boon, BJ Klevering, FPM Cremers, MN … - Ophthalmology, 2009 - Elsevier
Ophthalmologic examination, including color vision testing, fundus photography,
fluorescein angiography, fundus autofluorescence (FAF) imaging, optical
coherence tomography, full-field electroretinography (ERG), multifocal ERG, ...
Related articles - All 22 versions


 


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