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Keith Bradshaw

Showing results (1-10 of 11) with videos related to

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Vision Research|September 14, 2007
Contribution of post-receptoral cells to the a-wave of the human photopic electroretinogramKeith Bradshaw
Vision Research|August 31, 2010
Contribution of post-receporal cells to the cone a-wave of the human electroretinogram in congenital stationary night blindness and autoimmune-like retinopathyKeith Bradshaw, Renate Hanitzsch
Documenta Ophthalmologica. Advances in Ophthalmology|January 29, 2005
Comparison of ERGs recorded with skin and corneal-contact electrodes in normal children and adultsKeith Bradshaw, Ronald Hansen, Anne Fulton
Documenta Ophthalmologica. Advances in Ophthalmology|December 10, 2003
Abnormalities of the scotopic threshold response correlated with gene mutation in X-linked retinoschisis and congenital stationary night blindnessKeith Bradshaw, Douglas Newman, Louise Allen, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|October 1, 2004
A comparison of ERG abnormalities in XLRS and XLCSNBKeith Bradshaw, Louise Allen, Dorothy Trump, et al.
Ophthalmology|July 16, 2005
Cone-rod dystrophy, intrafamilial variability, and incomplete penetrance associated with the R172W mutation in the peripherin/RDS geneMichel Michaelides, Graham E Holder, Keith Bradshaw, et al.
Investigative Ophthalmology & Visual Science|March 27, 2003
An autosomal dominant bull's-eye macular dystrophy (MCDR2) that maps to the short arm of chromosome 4Michel Michaelides, Samantha Johnson, Arabella Poulson, et al.
Ophthalmology|June 15, 2005
X-linked cone dysfunction syndrome with myopia and protanopiaMichel Michaelides, Samantha Johnson, Keith Bradshaw, et al.
Human Mutation|January 29, 2003
Mutations in the CACNA1F and NYX genes in British CSNBX familiesIlaria Zito, Louise E Allen, Reshma J Patel, et al.
Investigative Ophthalmology & Visual Science|May 26, 2005
Identification of novel RPGR ORF15 mutations in X-linked progressive cone-rod dystrophy (XLCORD) familiesNeil D Ebenezer, Michel Michaelides, Sharon A Jenkins, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Vision Research|September 14, 2007
Contribution of post-receptoral cells to the a-wave of the human photopic electroretinogramKeith Bradshaw
Vision Research|August 31, 2010
Contribution of post-receporal cells to the cone a-wave of the human electroretinogram in congenital stationary night blindness and autoimmune-like retinopathyKeith Bradshaw, Renate Hanitzsch
Documenta Ophthalmologica. Advances in Ophthalmology|January 29, 2005
Comparison of ERGs recorded with skin and corneal-contact electrodes in normal children and adultsKeith Bradshaw, Ronald Hansen, Anne Fulton
Documenta Ophthalmologica. Advances in Ophthalmology|December 10, 2003
Abnormalities of the scotopic threshold response correlated with gene mutation in X-linked retinoschisis and congenital stationary night blindnessKeith Bradshaw, Douglas Newman, Louise Allen, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|October 1, 2004
A comparison of ERG abnormalities in XLRS and XLCSNBKeith Bradshaw, Louise Allen, Dorothy Trump, et al.
Ophthalmology|July 16, 2005
Cone-rod dystrophy, intrafamilial variability, and incomplete penetrance associated with the R172W mutation in the peripherin/RDS geneMichel Michaelides, Graham E Holder, Keith Bradshaw, et al.
Investigative Ophthalmology & Visual Science|March 27, 2003
An autosomal dominant bull's-eye macular dystrophy (MCDR2) that maps to the short arm of chromosome 4Michel Michaelides, Samantha Johnson, Arabella Poulson, et al.
Ophthalmology|June 15, 2005
X-linked cone dysfunction syndrome with myopia and protanopiaMichel Michaelides, Samantha Johnson, Keith Bradshaw, et al.
Human Mutation|January 29, 2003
Mutations in the CACNA1F and NYX genes in British CSNBX familiesIlaria Zito, Louise E Allen, Reshma J Patel, et al.
Investigative Ophthalmology & Visual Science|May 26, 2005
Identification of novel RPGR ORF15 mutations in X-linked progressive cone-rod dystrophy (XLCORD) familiesNeil D Ebenezer, Michel Michaelides, Sharon A Jenkins, et al.
Pageof 2