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A T Moore

Showing results (61-70 of 148) with videos related to

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The British Journal of Ophthalmology|October 19, 2004
Norrie disease and peripheral venous insufficiencyM Michaelides, P J Luthert, R Cooling, et al.
The British Journal of Ophthalmology|July 1, 1995
Ischaemic retinopathy occurring in patients receiving bone marrow allografts and campath-1G: a clinicopathological studyA R Webster, J R Anderson, E M Richards, et al.
Eye (London, England)|January 1, 1992
Genetic counselling in X-linked ocular albinism: clinical features of the carrier stateS J Charles, A T Moore, J W Grant, et al.
Journal of Medical Genetics|September 1, 1990
Alstrom's syndrome: further evidence of autosomal recessive inheritance and endocrinological dysfunctionS J Charles, A T Moore, J R Yates, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 1, 1989
Lisch nodules in neurofibromatosis type 2. Case reportS J Charles, A T Moore, J R Yates, et al.
The British Journal of Ophthalmology|December 1, 1996
Preschool vision screening: outcome of children referred to the hospital eye serviceD K Newman, A Hitchcock, H McCarthy, et al.
Eye (London, England)|January 1, 1991
Ophthalmological screening for von Hippel-Lindau diseaseA T Moore, E R Maher, P Rosen, et al.
Eye (London, England)|January 1, 1997
Lipaemia retinalis in a premature infant with type I hyperlipoproteinaemiaA P Rotchford, D K Newman, A T Moore, et al.
Journal of Medical Genetics|June 3, 2004
An autosomal recessive cone-rod dystrophy associated with amelogenesis imperfectaM Michaelides, A Bloch-Zupan, G E Holder, et al.
The British Journal of Ophthalmology|April 20, 2006
Congenital stationary night blindness associated with mutations in GRM6 encoding glutamate receptor MGluR6E O'Connor, L E Allen, K Bradshaw, et al.
Pageof 15

Showing results (61-70 of 148) with videos related to

Sort By:
Pageof 15
The British Journal of Ophthalmology|October 19, 2004
Norrie disease and peripheral venous insufficiencyM Michaelides, P J Luthert, R Cooling, et al.
The British Journal of Ophthalmology|July 1, 1995
Ischaemic retinopathy occurring in patients receiving bone marrow allografts and campath-1G: a clinicopathological studyA R Webster, J R Anderson, E M Richards, et al.
Eye (London, England)|January 1, 1992
Genetic counselling in X-linked ocular albinism: clinical features of the carrier stateS J Charles, A T Moore, J W Grant, et al.
Journal of Medical Genetics|September 1, 1990
Alstrom's syndrome: further evidence of autosomal recessive inheritance and endocrinological dysfunctionS J Charles, A T Moore, J R Yates, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 1, 1989
Lisch nodules in neurofibromatosis type 2. Case reportS J Charles, A T Moore, J R Yates, et al.
The British Journal of Ophthalmology|December 1, 1996
Preschool vision screening: outcome of children referred to the hospital eye serviceD K Newman, A Hitchcock, H McCarthy, et al.
Eye (London, England)|January 1, 1991
Ophthalmological screening for von Hippel-Lindau diseaseA T Moore, E R Maher, P Rosen, et al.
Eye (London, England)|January 1, 1997
Lipaemia retinalis in a premature infant with type I hyperlipoproteinaemiaA P Rotchford, D K Newman, A T Moore, et al.
Journal of Medical Genetics|June 3, 2004
An autosomal recessive cone-rod dystrophy associated with amelogenesis imperfectaM Michaelides, A Bloch-Zupan, G E Holder, et al.
The British Journal of Ophthalmology|April 20, 2006
Congenital stationary night blindness associated with mutations in GRM6 encoding glutamate receptor MGluR6E O'Connor, L E Allen, K Bradshaw, et al.
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