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American Journal of Ophthalmology
|
March 24, 2024
IQCB1 (NPHP5)-Retinopathy: Clinical and Genetic Characterization and Natural History
Sagnik Sen, Lorenzo Fabozzi, Kaoru Fujinami, et al.
Ophthalmology
|
October 11, 2020
Autosomal Recessive Bestrophinopathy: Clinical Features, Natural History, and Genetic Findings in Preparation for Clinical Trials
Giuseppe Casalino, Kamron N Khan, Monica Armengol, et al.
Ophthalmology
|
February 6, 2018
Leber Congenital Amaurosis Associated with Mutations in CEP290, Clinical Phenotype, and Natural History in Preparation for Trials of Novel Therapies
Leo Sheck, Wayne I L Davies, Phillip Moradi, et al.
Ophthalmology
|
October 15, 2018
Retinopathy Associated with Biallelic Mutations in PYGM (McArdle Disease)
Omar A Mahroo, Kamron N Khan, Genevieve Wright, et al.
Molecular Vision
|
March 16, 2012
Functional characterization of a novel c.614-622del rhodopsin mutation in a French pedigree with retinitis pigmentosa
Cécilia Maubaret, Maria Kosmaoglou, Sancy Low, et al.
Perception
|
September 24, 2005
Comparison of fundus autofluorescence and minimum-motion measurements of macular pigment distribution profiles derived from identical retinal areas
Anthony G Robson, Glen Harding, Frederik J G M van Kuijk, et al.
Vision Research
|
June 24, 2003
Macular pigment density and distribution: comparison of fundus autofluorescence with minimum motion photometry
Anthony G Robson, Jack D Moreland, Daniel Pauleikhoff, et al.
Archives of Biochemistry and Biophysics
|
November 7, 2006
Xanthophyll accumulation in the human retina during supplementation with lutein or zeaxanthin - the LUXEA (LUtein Xanthophyll Eye Accumulation) study
Wolfgang Schalch, William Cohn, Felix M Barker, et al.
Investigative Ophthalmology & Visual Science
|
July 1, 2025
A Phenotypic Study of CRB1 Retinopathy Secondary to the Variant p.(Pro836Thr) Prevalent in Those of Black African Ancestry
Wendy M Wong, Anthony G Robson, Rebecca A Baker, et al.
Ophthalmology
|
May 3, 2011
Phenotypic variability in RDH5 retinopathy (Fundus Albipunctatus)
Panagiotis I Sergouniotis, Elliott H Sohn, Zheng Li, et al.
Page
of 19
Search research articles
Search
Showing results (91-100 of 188) with videos related to
Sort By:
Page
of 19
American Journal of Ophthalmology
|
March 24, 2024
IQCB1 (NPHP5)-Retinopathy: Clinical and Genetic Characterization and Natural History
Sagnik Sen, Lorenzo Fabozzi, Kaoru Fujinami, et al.
Ophthalmology
|
October 11, 2020
Autosomal Recessive Bestrophinopathy: Clinical Features, Natural History, and Genetic Findings in Preparation for Clinical Trials
Giuseppe Casalino, Kamron N Khan, Monica Armengol, et al.
Ophthalmology
|
February 6, 2018
Leber Congenital Amaurosis Associated with Mutations in CEP290, Clinical Phenotype, and Natural History in Preparation for Trials of Novel Therapies
Leo Sheck, Wayne I L Davies, Phillip Moradi, et al.
Ophthalmology
|
October 15, 2018
Retinopathy Associated with Biallelic Mutations in PYGM (McArdle Disease)
Omar A Mahroo, Kamron N Khan, Genevieve Wright, et al.
Molecular Vision
|
March 16, 2012
Functional characterization of a novel c.614-622del rhodopsin mutation in a French pedigree with retinitis pigmentosa
Cécilia Maubaret, Maria Kosmaoglou, Sancy Low, et al.
Perception
|
September 24, 2005
Comparison of fundus autofluorescence and minimum-motion measurements of macular pigment distribution profiles derived from identical retinal areas
Anthony G Robson, Glen Harding, Frederik J G M van Kuijk, et al.
Vision Research
|
June 24, 2003
Macular pigment density and distribution: comparison of fundus autofluorescence with minimum motion photometry
Anthony G Robson, Jack D Moreland, Daniel Pauleikhoff, et al.
Archives of Biochemistry and Biophysics
|
November 7, 2006
Xanthophyll accumulation in the human retina during supplementation with lutein or zeaxanthin - the LUXEA (LUtein Xanthophyll Eye Accumulation) study
Wolfgang Schalch, William Cohn, Felix M Barker, et al.
Investigative Ophthalmology & Visual Science
|
July 1, 2025
A Phenotypic Study of CRB1 Retinopathy Secondary to the Variant p.(Pro836Thr) Prevalent in Those of Black African Ancestry
Wendy M Wong, Anthony G Robson, Rebecca A Baker, et al.
Ophthalmology
|
May 3, 2011
Phenotypic variability in RDH5 retinopathy (Fundus Albipunctatus)
Panagiotis I Sergouniotis, Elliott H Sohn, Zheng Li, et al.
Page
of 19