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O Edwards

Showing results (111-120 of 137) with videos related to

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Molecular Vision|March 16, 2007
Retinal pathology and skin barrier defect in mice carrying a Stargardt disease-3 mutation in elongase of very long chain fatty acids-4Anne McMahon, Igor A Butovich, Nathan L Mata, et al.
Ophthalmology|September 15, 1999
Visual acuity impairment in patients with retinitis pigmentosa at age 45 years or olderS Grover, G A Fishman, R J Anderson, et al.
Investigative Ophthalmology & Visual Science|June 26, 2009
Contribution of copy number variation in the regulation of complement activation locus to development of age-related macular degenerationKatharina E Schmid-Kubista, Nirubol Tosakulwong, Yanhong Wu, et al.
American Journal of Human Genetics|January 9, 2008
Mutations in KCNJ13 cause autosomal-dominant snowflake vitreoretinal degenerationJ Fielding Hejtmancik, Xiaodong Jiao, Anren Li, et al.
Ocular Immunology and Inflammation|February 17, 2021
Drug-induced Sarcoid Uveitis with BiologicsBianka Sobolewska, Edoardo Baglivo, Albert O Edwards, et al.
American Journal of Ophthalmology|September 23, 1998
Malattia leventinese: refinement of the genetic locus and phenotypic variability in autosomal dominant macular drusenA O Edwards, M L Klein, C B Berselli, et al.
Clinical Genetics|September 1, 1994
Unilateral renal aplasia in X-linked Kallmann's syndromeJ M Kirk, D B Grant, G M Besser, et al.
Annals of Gastroenterology|September 4, 2020
The use of 5-aminosalicylates in Crohn's disease: a retrospective study using the UK Clinical Practice Research DatalinkAilsa Hart, Siew C Ng, John Watkins, et al.
Molecular Vision|August 19, 2011
Copy number variation in the complement factor H-related genes and age-related macular degenerationKatharina E Kubista, Nirubol Tosakulwong, Yanhong Wu, et al.
Ophthalmology|July 1, 2014
No clinically significant association between CFH and ARMS2 genotypes and response to nutritional supplements: AREDS report number 38Emily Y Chew, Michael L Klein, Traci E Clemons, et al.
Pageof 14

Showing results (111-120 of 137) with videos related to

Sort By:
Pageof 14
Molecular Vision|March 16, 2007
Retinal pathology and skin barrier defect in mice carrying a Stargardt disease-3 mutation in elongase of very long chain fatty acids-4Anne McMahon, Igor A Butovich, Nathan L Mata, et al.
Ophthalmology|September 15, 1999
Visual acuity impairment in patients with retinitis pigmentosa at age 45 years or olderS Grover, G A Fishman, R J Anderson, et al.
Investigative Ophthalmology & Visual Science|June 26, 2009
Contribution of copy number variation in the regulation of complement activation locus to development of age-related macular degenerationKatharina E Schmid-Kubista, Nirubol Tosakulwong, Yanhong Wu, et al.
American Journal of Human Genetics|January 9, 2008
Mutations in KCNJ13 cause autosomal-dominant snowflake vitreoretinal degenerationJ Fielding Hejtmancik, Xiaodong Jiao, Anren Li, et al.
Ocular Immunology and Inflammation|February 17, 2021
Drug-induced Sarcoid Uveitis with BiologicsBianka Sobolewska, Edoardo Baglivo, Albert O Edwards, et al.
American Journal of Ophthalmology|September 23, 1998
Malattia leventinese: refinement of the genetic locus and phenotypic variability in autosomal dominant macular drusenA O Edwards, M L Klein, C B Berselli, et al.
Clinical Genetics|September 1, 1994
Unilateral renal aplasia in X-linked Kallmann's syndromeJ M Kirk, D B Grant, G M Besser, et al.
Annals of Gastroenterology|September 4, 2020
The use of 5-aminosalicylates in Crohn's disease: a retrospective study using the UK Clinical Practice Research DatalinkAilsa Hart, Siew C Ng, John Watkins, et al.
Molecular Vision|August 19, 2011
Copy number variation in the complement factor H-related genes and age-related macular degenerationKatharina E Kubista, Nirubol Tosakulwong, Yanhong Wu, et al.
Ophthalmology|July 1, 2014
No clinically significant association between CFH and ARMS2 genotypes and response to nutritional supplements: AREDS report number 38Emily Y Chew, Michael L Klein, Traci E Clemons, et al.
Pageof 14