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Anthony T Moore

Showing results (41-50 of 304) with videos related to

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The British Journal of Ophthalmology|August 30, 2017
Bullous X linked retinoschisis: clinical features and prognosisAnne-Marie Hinds, Abigail Fahim, Anthony T Moore, et al.
The British Journal of Ophthalmology|August 28, 2017
Active surveillance of choroidal neovascularisation in children: incidence, aetiology and management findings from a national study in the UKMariya Moosajee, Alessandro Abbouda, Barnaby Foot, et al.
Molecular Vision|June 17, 2016
The clinical features of retinal disease due to a dominant mutation in RPE65Sarah Hull, Rajarshi Mukherjee, Graham E Holder, 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.
Survey of Ophthalmology|April 28, 2004
Molecular genetic basis of inherited cataract and associated phenotypesM Ashwin Reddy, Peter J Francis, Vanita Berry, et al.
Journal of Cataract and Refractive Surgery|October 3, 2006
Increased crystalline lens thickness and phacomorphic glaucoma in patients with Fanconi anemiaMostafa A Elgohary, K Sheng Lim, Dilani Siriwardena, et al.
Experimental Eye Research|May 25, 2010
Focus on molecules: centrosomal protein 290 (CEP290)Phillip Moradi, Wayne L Davies, Donna S Mackay, et al.
Eye (London, England)|August 4, 2021
Variants in PAX6, PITX3 and HSF4 causing autosomal dominant congenital cataractsVanita Berry, Alex Ionides, Nikolas Pontikos, et al.
American Journal of Ophthalmology Case Reports|March 6, 2018
Ocular findings in a patient with fucosidosisLucía Rivera Sánchez, Julius T Oatts, Jacque L Duncan, et al.
European Journal of Human Genetics : EJHG|June 18, 2015
Ocular and neurodevelopmental features of Duchenne muscular dystrophy: a signature of dystrophin function in the central nervous systemValeria Ricotti, Herbert Jägle, Maria Theodorou, et al.
Pageof 31

Showing results (41-50 of 304) with videos related to

Sort By:
Pageof 31
The British Journal of Ophthalmology|August 30, 2017
Bullous X linked retinoschisis: clinical features and prognosisAnne-Marie Hinds, Abigail Fahim, Anthony T Moore, et al.
The British Journal of Ophthalmology|August 28, 2017
Active surveillance of choroidal neovascularisation in children: incidence, aetiology and management findings from a national study in the UKMariya Moosajee, Alessandro Abbouda, Barnaby Foot, et al.
Molecular Vision|June 17, 2016
The clinical features of retinal disease due to a dominant mutation in RPE65Sarah Hull, Rajarshi Mukherjee, Graham E Holder, 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.
Survey of Ophthalmology|April 28, 2004
Molecular genetic basis of inherited cataract and associated phenotypesM Ashwin Reddy, Peter J Francis, Vanita Berry, et al.
Journal of Cataract and Refractive Surgery|October 3, 2006
Increased crystalline lens thickness and phacomorphic glaucoma in patients with Fanconi anemiaMostafa A Elgohary, K Sheng Lim, Dilani Siriwardena, et al.
Experimental Eye Research|May 25, 2010
Focus on molecules: centrosomal protein 290 (CEP290)Phillip Moradi, Wayne L Davies, Donna S Mackay, et al.
Eye (London, England)|August 4, 2021
Variants in PAX6, PITX3 and HSF4 causing autosomal dominant congenital cataractsVanita Berry, Alex Ionides, Nikolas Pontikos, et al.
American Journal of Ophthalmology Case Reports|March 6, 2018
Ocular findings in a patient with fucosidosisLucía Rivera Sánchez, Julius T Oatts, Jacque L Duncan, et al.
European Journal of Human Genetics : EJHG|June 18, 2015
Ocular and neurodevelopmental features of Duchenne muscular dystrophy: a signature of dystrophin function in the central nervous systemValeria Ricotti, Herbert Jägle, Maria Theodorou, et al.
Pageof 31