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A T Moore

Showing results (121-130 of 148) with videos related to

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The British Journal of Ophthalmology|December 20, 2005
Smoking and age related macular degeneration: the number of pack years of cigarette smoking is a major determinant of risk for both geographic atrophy and choroidal neovascularisationJ C Khan, D A Thurlby, H Shahid, et al.
Journal of Medical Genetics|September 22, 2001
Clustering and frequency of mutations in the retinal guanylate cyclase (GUCY2D) gene in patients with dominant cone-rod dystrophiesA M Payne, A G Morris, S M Downes, et al.
The British Journal of Ophthalmology|October 27, 2007
Functional correlates of fundus autofluorescence abnormalities in patients with RPGR or RIMS1 mutations causing cone or cone rod dystrophyA G Robson, M Michaelides, V A Luong, et al.
The British Journal of Ophthalmology|August 1, 1992
Abnormal dark adaptation kinetics in autosomal dominant sector retinitis pigmentosa due to rod opsin mutationA T Moore, F W Fitzke, C M Kemp, et al.
Journal of Medical Genetics|September 3, 2002
Mapping of a novel locus for achromatopsia (ACHM4) to 1p and identification of a germline mutation in the alpha subunit of cone transducin (GNAT2)I A Aligianis, T Forshew, S Johnson, et al.
The British Journal of Ophthalmology|January 25, 2003
A clinical and molecular genetic study of a rare dominantly inherited syndrome (MRCS) comprising of microcornea, rod-cone dystrophy, cataract, and posterior staphylomaM A Reddy, P J Francis, V Berry, et al.
Neurology|April 14, 2004
Cognitive functioning in humans with mutations of the PAX6 geneP J Thompson, T N Mitchell, S L Free, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 16, 2001
Autosomal dominant cone-rod dystrophy with mutations in the guanylate cyclase 2D gene encoding retinal guanylate cyclase-1S M Downes, A M Payne, R E Kelsell, et al.
American Journal of Human Genetics|April 1, 1994
Further refinement of the location for autosomal dominant retinitis pigmentosa on chromosome 7p (RP9)C F Inglehearn, T J Keen, M al-Maghtheh, et al.
Mitochondrion|July 22, 2017
The pattern of retinal ganglion cell dysfunction in Leber hereditary optic neuropathyA Majander, A G Robson, C João, et al.
Pageof 15

Showing results (121-130 of 148) with videos related to

Sort By:
Pageof 15
The British Journal of Ophthalmology|December 20, 2005
Smoking and age related macular degeneration: the number of pack years of cigarette smoking is a major determinant of risk for both geographic atrophy and choroidal neovascularisationJ C Khan, D A Thurlby, H Shahid, et al.
Journal of Medical Genetics|September 22, 2001
Clustering and frequency of mutations in the retinal guanylate cyclase (GUCY2D) gene in patients with dominant cone-rod dystrophiesA M Payne, A G Morris, S M Downes, et al.
The British Journal of Ophthalmology|October 27, 2007
Functional correlates of fundus autofluorescence abnormalities in patients with RPGR or RIMS1 mutations causing cone or cone rod dystrophyA G Robson, M Michaelides, V A Luong, et al.
The British Journal of Ophthalmology|August 1, 1992
Abnormal dark adaptation kinetics in autosomal dominant sector retinitis pigmentosa due to rod opsin mutationA T Moore, F W Fitzke, C M Kemp, et al.
Journal of Medical Genetics|September 3, 2002
Mapping of a novel locus for achromatopsia (ACHM4) to 1p and identification of a germline mutation in the alpha subunit of cone transducin (GNAT2)I A Aligianis, T Forshew, S Johnson, et al.
The British Journal of Ophthalmology|January 25, 2003
A clinical and molecular genetic study of a rare dominantly inherited syndrome (MRCS) comprising of microcornea, rod-cone dystrophy, cataract, and posterior staphylomaM A Reddy, P J Francis, V Berry, et al.
Neurology|April 14, 2004
Cognitive functioning in humans with mutations of the PAX6 geneP J Thompson, T N Mitchell, S L Free, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 16, 2001
Autosomal dominant cone-rod dystrophy with mutations in the guanylate cyclase 2D gene encoding retinal guanylate cyclase-1S M Downes, A M Payne, R E Kelsell, et al.
American Journal of Human Genetics|April 1, 1994
Further refinement of the location for autosomal dominant retinitis pigmentosa on chromosome 7p (RP9)C F Inglehearn, T J Keen, M al-Maghtheh, et al.
Mitochondrion|July 22, 2017
The pattern of retinal ganglion cell dysfunction in Leber hereditary optic neuropathyA Majander, A G Robson, C João, et al.
Pageof 15