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Scholar Results 1 - 7 of 7 citing Jacobson: Evidence for retinal remodelling in retinitis pigmentosa caused by PDE6B mutation. (0.07 sec) 

Retinal laminar architecture in human retinitis pigmentosa caused by rhodopsin gene …

- iovs.org
TS Aleman, AV Cideciyan, A Sumaroka, EAM … - Investigative Ophthalmology & Visual Science, 2008 - ARVO
RESULTS. Class A patients had only cone-mediated vision. The outer nuclear layer
(ONL) thinned with eccentricity and was not detectable within 3 to 4 mm of the
fovea. Scotomatous extracentral retina showed loss of ONL, thickening of ...
Cited by 14 - Related articles - BL Direct - All 2 versions

Retinal disease in Usher syndrome III caused by mutations in the clarin-1 gene

- iovs.org
W Herrera, TS Aleman, AV Cideciyan, AJ … - Investigative Ophthalmology & Visual Science, 2008 - ARVO
1 From the Scheie Eye Institute, Department of Ophthalmology, University of
Pennsylvania, Philadelphia, Pennsylvania; the 2 Department of Ophthalmology,
Hadassah-Hebrew University Medical Center, Jerusalem, Israel; the 3 ...
Cited by 12 - Related articles - BL Direct - All 3 versions

Thickness of Receptor and Post-receptor Retinal Layers in Patients with Retinitis …


DC Hood, CE Lin, MA Lazow, KG Locke, X … - Investigative Ophthalmology & Visual Science, 2009 - ARVO
METHODS. FdOCT scans were obtained from the horizontal midline in 30 patients
with RP and 23 control subjects of comparable age. Raw images were exported and
the thicknesses of photoreceptor/RPE, inner nuclear, RGC plus inner ...
Cited by 2 - Related articles - All 3 versions

rd1 Mouse Retina Shows an Imbalance in the Activity of Cysteine Protease Cathepsins and …

- iovs.org
S Ahuja, P Ahuja-Jensen, LE Johnson, AR … - Investigative Ophthalmology & Visual Science, 2008 - ARVO
RESULTS. The pigment epithelium, photoreceptors, and inner retinal and ganglion
cell layers of both wt and rd1 retinas showed cysC and cathepsin-B labeling.
CysC immunostaining was extensive in the optic nerve head fibers. The rd1 ...
Cited by 1 - Related articles - BL Direct - All 2 versions

A novel mutation and phenotypes in phosphodiesterase 6 deficiency


SH Tsang, I Tsui, CL Chou, J Zernant, E … - American Journal of Ophthalmology, 2008 - Elsevier
A disease-associated allele was identified in 32% of patients. Two probands (5%)
had PDE6 mutations. The first proband was a compound heterozygote for known
R102C and N216S alleles in PDE6A (MIM#180071). Pedigree analysis determined ...
Cited by 2 - Related articles - All 9 versions

Electrical activity and neuronal survival


RG Corredor, JL Goldberg - Journal of Neural Engineering, 2009 - iop.org
Abstract The failure of regeneration in the central nervous system (CNS) remains
an enormous scientific and clinical challenge. After injury or in degenerative
diseases, neurons in the adult mammalian CNS fail to regrow their axons and ...
Related articles

Normal Central Retinal Function and Structure Preserved in Retinitis Pigmentosa


S Jacobson, A Roman, T Aleman, A Sumaroka, … - Investigative Ophthalmology & Visual Science, 2009 - ARVO
Page 1. Normal Central Retinal Function and Structure Preserved in Retinitis Pigmentosa
Samuel G. Jacobson1*, Alejandro J. Roman1, Tomas S. Aleman1, Alexander ...
Related articles - All 2 versions


 


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