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Scholar Results 1 - 10 of about 16 citing Kabanarou: Congenital stationary night blindness and a “Schubert-Bornschein” type electrophys.... (0.07 sec) 

ON-and OFF-response of the photopic electroretinogram in relation to stimulus …


M Sustar, M Hawlina, J Brecelj - Documenta Ophthalmologica, 2006 - Springer
The photopic electroretinogram, evoked with long duration stimuli (eg 150 ms),
forms three prominent waves—a, b and d. The a-wave is a negative wave, which
appears immediately after the onset of the stimulus. The b-wave (ON- ...
Cited by 8 - Related articles - BL Direct - All 4 versions

The negative ERG: clinical phenotypes and disease mechanisms of inner retinal dysfunction


I Audo, AG Robson, GE Holder, AT Moore - Survey of Ophthalmology, 2008 - Elsevier
Inner retinal dysfunction is encountered in a number of retinal disorders,
either inherited or acquired, as a primary or predominant defect. Fundus
examination is rarely diagnostic in these disorders, although some show ...
Cited by 3 - Related articles - All 9 versions

Identification and functional characterization of a novel rhodopsin mutation associated …

- iovs.org
C Zeitz, AK Gross, D Leifert, B Kloeckener- … - Investigative Ophthalmology & Visual Science, 2008 - ARVO
1 From the Division of Medical Molecular Genetics and Gene Diagnostics,
Institute of Medical Genetics, University of Zurich, Zurich, Switzerland; the 2
Institut de la Vision, INSERM (Institut National de la Santé et de la ...
Cited by 2 - Related articles - All 2 versions

Clinical and electroretinographic characteristics of congenital stationary night blindness in …


LS Sandmeyer, CB Breaux, S Archer, BH … - Veterinary Ophthalmology, 2007 - interscience.wiley.com
It is also possible that your web browser is not configured or not able to
display style sheets. In this case, although the visual presentation will be
degraded, the site should continue to be functional. We recommend using the ...
Cited by 3 - Related articles - BL Direct - All 3 versions

A novel constitutively active rhodopsin mutation (p. Ala295Val) causes autosomal …

- iovs.org [PDF] 
C Zeitz, AK Gross, D Leifert, B Kloeckener- … - Investigative Ophthalmology & Visual Science, 2008 - ARVO
Page 1. A novel constitutively active rhodopsin mutation (p.Ala295Val) causes
autosomal dominant CSNB Christina Zeitz 1,2*‡ , Alecia ...
Cited by 2 - Related articles

The genetics of hereditary retinopathies and optic neuropathies


A Iannaccone, RC Dystrophies, C Dystrophies … - Compr Ophthalmol Update, 2005 - medscape.com
In recent years, advances in molecular genetics have impacted the understanding
and the classification of hereditary retinal and optic nerve disease perhaps
more than any other group of eye diseases. This new molecular knowledge now ...
Cited by 1 - Related articles

Sequence variations of GRM6 in patients with high myopia


X Xu, S Li, X Xiao, P Wang, X Guo, Q Zhang, 2009 - molvis.org
Methods: DNA was prepared from the venous leukocytes of 96 Chinese patients with
high myopia (refraction of spherical equivalent of at least −6.00 diopters
[D]) and 96 controls (refraction of spherical equivalent between −0.50 D ...
Related articles - Cached - All 2 versions

[PDF] MAJOR REVIEW


I Audo, AG Robson, GE Holder, AT Moore, F … - SURVEY OF OPHTHALMOLOGY, 2008 - assets0.pubget.com
Abstract. Inner retinal dysfunction is encountered in a number of retinal
disorders, either inherited or acquired, as a primary or predominant defect.
Fundus examination is rarely diagnostic in these disorders, although some ...
Related articles - View as HTML

Clinical disorders affecting mesopic vision.


A Petzold, GT Plant - Ophthalmic & Physiological Optics, 2006 - prsjournal.net
The visual system allows us to see over a remarkable range of illumination. In
fact, the visual system covers approximately 11 log units change in illumination
(Stockman and Sharpe, 2006). We can adapt to see in bright sunlight relying ...
Related articles - Cached - BL Direct - All 5 versions

The Genetics of Hereditary Retinopathies and Optic Neuropathies: Cone Dystrophies and …


C Dystrophies - orthopedics.medscape.com
Cone dystrophies and cone-rod dystrophies are a group of progressive diseases in
which, opposite to rod-cone dystrophies, cone dysfunction (hence, light
aversion, central scotomas, and loss of central vision) prevails compared ...
Related articles


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