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The British Journal of Ophthalmology
|
August 23, 2013
A cautious approach to interpreting retrospective data
Kamron N Khan, Rubina Rahman
Retina (Philadelphia, Pa.)
|
November 26, 2013
Correspondence
Kamron N Khan, Rubina Rahman
The British Journal of Ophthalmology
|
November 10, 2019
Macular dystrophies: clinical and imaging features, molecular genetics and therapeutic options
Najiha Rahman, Michalis Georgiou, Kamron N Khan, et al.
Retina (Philadelphia, Pa.)
|
February 23, 2017
THE FUNDUS PHENOTYPE ASSOCIATED WITH THE p.Ala243Val BEST1 MUTATION
Kamron N Khan, Farrah Islam, Anthony T Moore, et al.
Ophthalmology
|
August 11, 2016
Clinical and Genetic Features of Choroideremia in Childhood
Kamron N Khan, Farrah Islam, Anthony T Moore, et al.
Journal of Inherited Metabolic Disease
|
September 17, 2021
Phenotype and genotype of 197 British patients with McArdle disease: An observational single-centre study
Chiara Pizzamiglio, Omar A Mahroo, Kamron N Khan, et al.
The British Journal of Ophthalmology
|
January 19, 2011
Changing the status quo bias
Kamron N Khan, Manir Ali, Carmel Toomes, et al.
BMJ (Clinical Research Ed.)
|
November 8, 2013
Patterns of inheritance, not always easily visible
Kamron N Khan, Manir Ali, James A Poulter, et al.
Ophthalmic Surgery, Lasers & Imaging Retina
|
November 21, 2018
Clinical Course of Autosomal Recessive Bestrophinopathy Complicated by Choroidal Neovascularization
Ugo Introini, Giuseppe Casalino, Kamron N Khan, et al.
Retina (Philadelphia, Pa.)
|
October 21, 2016
FUNCTIONAL AND ANATOMICAL OUTCOMES OF CHOROIDAL NEOVASCULARIZATION COMPLICATING BEST1-RELATED RETINOPATHY
Kamron N Khan, Omar A Mahroo, Farrah Islam, et al.
Page
of 4
Search research articles
Search
Showing results (1-10 of 31) with videos related to
Sort By:
Page
of 4
The British Journal of Ophthalmology
|
August 23, 2013
A cautious approach to interpreting retrospective data
Kamron N Khan, Rubina Rahman
Retina (Philadelphia, Pa.)
|
November 26, 2013
Correspondence
Kamron N Khan, Rubina Rahman
The British Journal of Ophthalmology
|
November 10, 2019
Macular dystrophies: clinical and imaging features, molecular genetics and therapeutic options
Najiha Rahman, Michalis Georgiou, Kamron N Khan, et al.
Retina (Philadelphia, Pa.)
|
February 23, 2017
THE FUNDUS PHENOTYPE ASSOCIATED WITH THE p.Ala243Val BEST1 MUTATION
Kamron N Khan, Farrah Islam, Anthony T Moore, et al.
Ophthalmology
|
August 11, 2016
Clinical and Genetic Features of Choroideremia in Childhood
Kamron N Khan, Farrah Islam, Anthony T Moore, et al.
Journal of Inherited Metabolic Disease
|
September 17, 2021
Phenotype and genotype of 197 British patients with McArdle disease: An observational single-centre study
Chiara Pizzamiglio, Omar A Mahroo, Kamron N Khan, et al.
The British Journal of Ophthalmology
|
January 19, 2011
Changing the status quo bias
Kamron N Khan, Manir Ali, Carmel Toomes, et al.
BMJ (Clinical Research Ed.)
|
November 8, 2013
Patterns of inheritance, not always easily visible
Kamron N Khan, Manir Ali, James A Poulter, et al.
Ophthalmic Surgery, Lasers & Imaging Retina
|
November 21, 2018
Clinical Course of Autosomal Recessive Bestrophinopathy Complicated by Choroidal Neovascularization
Ugo Introini, Giuseppe Casalino, Kamron N Khan, et al.
Retina (Philadelphia, Pa.)
|
October 21, 2016
FUNCTIONAL AND ANATOMICAL OUTCOMES OF CHOROIDAL NEOVASCULARIZATION COMPLICATING BEST1-RELATED RETINOPATHY
Kamron N Khan, Omar A Mahroo, Farrah Islam, et al.
Page
of 4