Web Images Videos Maps News Shopping Gmail more »
Sign in
Scholar Home  
  Advanced Scholar Search
Scholar Preferences
Scholar Results 1 - 10 of about 40 citing Michaelides: The cone dysfunction syndromes. (0.07 sec) 

Progressive cone and cone-rod dystrophies: phenotypes and underlying molecular genetic …


M Michaelides, AJ Hardcastle, DM Hunt, AT … - Survey of ophthalmology, 2006 - Elsevier
The cone and cone–rod dystrophies form part of a heterogeneous group of
retinal disorders that are an important cause of visual impairment in children
and adults. There have been considerable advances made in recent years in ...
Cited by 21 - Related articles - All 15 versions

A detailed phenotypic study of “cone dystrophy with supernormal rod ERG”

- nih.gov - Free from Publisher
M Michaelides, GE Holder, AR Webster, DM … - British Journal of Ophthalmology, 2005 - bjo.bmj.com
Results: The onset of symptoms was in the first and second decades of life.
Subjects presented with reduced central vision and marked photophobia. All
individuals were myopic and colour vision testing revealed severely reduced ...
Cited by 13 - Related articles - All 9 versions

The zebrafish pob gene encodes a novel protein required for survival of red cone …

- genetics.org
MR Taylor, S Kikkawa, A Diez-Juan, V … - Genetics, 2005 - Genetics Soc America
The zebrafish mutant, partial optokinetic response b (pob), was isolated using
an N-ethyl N-nitrosourea (ENU)-based screening strategy designed to identify
larvae with defective optokinetic responses in red but not white light. ...
Cited by 9 - Related articles - All 10 versions

Function and dysfunction of CNG channels: insights from channelopathies and mouse …


M Biel, S Michalakis - Molecular Neurobiology, 2007 - Springer
Abstract Channels directly gated by cyclic nucleotides (CNG channels) are
important cellular switches that mediate influx of Na + and Ca 2+ in response to
increases in the intracellular concentration of cAMP and cGMP. In ...
Cited by 8 - Related articles - BL Direct - All 3 versions

X-linked cone dysfunction syndrome with myopia and protanopia

- cam.ac.uk [PDF] 
M Michaelides, S Johnson, K Bradshaw, GE … - Ophthalmology, 2005 - Elsevier
Subjects underwent both detailed clinical examination and psychophysical
testing. After informed consent was obtained, blood samples were taken for DNA
extraction, and molecular genetic analysis was performed. The strategy for ...
Cited by 7 - Related articles - All 16 versions

Differential optical densities of intraretinal spaces

- iovs.org
D Barthelmes, FKP Sutter, MC Gillies - Investigative Ophthalmology & Visual Science, 2008 - ARVO
METHODS. Retrospective analysis of eyes with idiopathic perifoveal
telangiectasia (IPT), diabetic macular edema (DME), idiopathic central serous
chorioretinopathy (CSC), retinitis pigmentosa (RP), or cone dystrophy (CD) ...
Cited by 4 - Related articles - All 4 versions

Ocular gene therapy: current progress and future prospects

- cell.com
P Colella, G Cotugno, A Auricchio - Trends in Molecular Medicine, 2009 - Elsevier
As gene therapy begins to produce its first clinical successes, interest in
ocular gene transfer has grown owing to the favorable safety and efficacy
characteristics of the eye as a target organ for drug delivery. Important ...
Cited by 3 - Related articles - All 4 versions

Tinted contact lenses as an alternative management for photophobia in stationary cone …


SN Rajak, ADM Currie, VJP Dubois, M Morris, … - Journal of AAPOS, 2006 - Elsevier
Stationary cone dystrophies are a spectrum of disorders characterized by
bilateral reduced visual acuities, reduced or absent color vision, central
scotomata, nystagmus, and photophobia. 1 They present during infancy and do ...
Cited by 4 - Related articles - All 9 versions

[CITATION] A case of idiopathic perifoveal telangiectasia preceded by features of cone dystrophy


D Barthelmes, MC Gillies, JC Fleischhauer, …, 2007 - nature.com
Jump to main content; Jump to navigation; nature.com homepage; Publications AZ index;
Browse by subject. My account; Submit manuscript; Register; Subscribe; RCOphth ...
Cited by 2 - Related articles - BL Direct - All 3 versions

Genetic etiology and clinical consequences of complete and incomplete achromatopsia


AAHJ Thiadens, NWR Slingerland, S Roosing, … - Ophthalmology, 2009 - Elsevier
To investigate the genetic causes of complete and incomplete achromatopsia
(ACHM) and assess the association between disease-causing mutations, phenotype
at diagnosis, and visual prognosis. ... Probands with complete ACHM (n = ...
Cited by 2 - Related articles - All 7 versions


Result Page: 

1

2

3

4

Next


 


Go to Google Home - About Google - About Google Scholar

©2009 Google