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Scholar Results 1 - 4 of 4 citing Boon: Mutations in the peripherin/RDS gene are an important cause of multifocal pattern dystrophy.... (0.08 sec) 

Evidence of widespread retinal dysfunction in patients with Stargardt disease and …

- ►iovs.org
S Maia-Lopes, ED Silva, MF Silva, A Reis, P … - Investigative Ophthalmology & Visual Science, 2008 - ARVO
METHODS. Twenty-seven eyes from patients with STGD, 16 eyes from asymptomatic
relatives, and 44 age-matched control eyes were included. Chromatic CS function
was assessed by comparing protan, deutan, and tritan (Cambridge Color Test; ...
Cited by 4 - Related articles - BL Direct - All 2 versions

Hereditary retinal disease


P Goodwin - Current opinion in ophthalmology, 2008 - journals.lww.com
It is difficult to keep up with the rapid progress made in the world of ocular
genetics. Genotype-phenotype correlations are made, novel mutations are
discovered, and new treatments are attempted on a continual basis. This ...
Cited by 3 - Related articles - BL Direct - 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

Fundusautofluoreszenz bei erblichen Netzhauterkrankungen


T Theelen, CJF Boon, BJ Klevering, CB … - Der Ophthalmologe, 2008 - Springer
Seit den ersten Berichten über klinische Beobachtungen der Fundusautofluores-
zenz (FAF) im kurzwelligen Bereich [6] und nahen Infrarot [20] in der Mitte des
letzten Jahrzehnts ist das wissenschaft- liche und klinische Interesse an ...
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