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Kamron N Khan

Showing results (1-10 of 31) with videos related to

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The British Journal of Ophthalmology|August 23, 2013
A cautious approach to interpreting retrospective dataKamron N Khan, Rubina Rahman
Retina (Philadelphia, Pa.)|November 26, 2013
CorrespondenceKamron N Khan, Rubina Rahman
The British Journal of Ophthalmology|November 10, 2019
Macular dystrophies: clinical and imaging features, molecular genetics and therapeutic optionsNajiha Rahman, Michalis Georgiou, Kamron N Khan, et al.
Retina (Philadelphia, Pa.)|February 23, 2017
THE FUNDUS PHENOTYPE ASSOCIATED WITH THE p.Ala243Val BEST1 MUTATIONKamron N Khan, Farrah Islam, Anthony T Moore, et al.
Ophthalmology|August 11, 2016
Clinical and Genetic Features of Choroideremia in ChildhoodKamron 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 studyChiara Pizzamiglio, Omar A Mahroo, Kamron N Khan, et al.
The British Journal of Ophthalmology|January 19, 2011
Changing the status quo biasKamron N Khan, Manir Ali, Carmel Toomes, et al.
BMJ (Clinical Research Ed.)|November 8, 2013
Patterns of inheritance, not always easily visibleKamron 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 NeovascularizationUgo Introini, Giuseppe Casalino, Kamron N Khan, et al.
Retina (Philadelphia, Pa.)|October 21, 2016
FUNCTIONAL AND ANATOMICAL OUTCOMES OF CHOROIDAL NEOVASCULARIZATION COMPLICATING BEST1-RELATED RETINOPATHYKamron N Khan, Omar A Mahroo, Farrah Islam, et al.
Pageof 4

Showing results (1-10 of 31) with videos related to

Sort By:
Pageof 4
The British Journal of Ophthalmology|August 23, 2013
A cautious approach to interpreting retrospective dataKamron N Khan, Rubina Rahman
Retina (Philadelphia, Pa.)|November 26, 2013
CorrespondenceKamron N Khan, Rubina Rahman
The British Journal of Ophthalmology|November 10, 2019
Macular dystrophies: clinical and imaging features, molecular genetics and therapeutic optionsNajiha Rahman, Michalis Georgiou, Kamron N Khan, et al.
Retina (Philadelphia, Pa.)|February 23, 2017
THE FUNDUS PHENOTYPE ASSOCIATED WITH THE p.Ala243Val BEST1 MUTATIONKamron N Khan, Farrah Islam, Anthony T Moore, et al.
Ophthalmology|August 11, 2016
Clinical and Genetic Features of Choroideremia in ChildhoodKamron 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 studyChiara Pizzamiglio, Omar A Mahroo, Kamron N Khan, et al.
The British Journal of Ophthalmology|January 19, 2011
Changing the status quo biasKamron N Khan, Manir Ali, Carmel Toomes, et al.
BMJ (Clinical Research Ed.)|November 8, 2013
Patterns of inheritance, not always easily visibleKamron 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 NeovascularizationUgo Introini, Giuseppe Casalino, Kamron N Khan, et al.
Retina (Philadelphia, Pa.)|October 21, 2016
FUNCTIONAL AND ANATOMICAL OUTCOMES OF CHOROIDAL NEOVASCULARIZATION COMPLICATING BEST1-RELATED RETINOPATHYKamron N Khan, Omar A Mahroo, Farrah Islam, et al.
Pageof 4