Search research articles
Contact Us
Filters
Showing results (401-410 of 677) with videos related to
Page
of 68
Sort By:
Human Vaccines
|
April 3, 2008
Self-reported adverse health events following smallpox vaccination in a large prospective study of US military service members
Timothy S Wells, Cynthia A LeardMann, Tyler C Smith, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
November 16, 2001
Long-term protection of retinal structure but not function using RAAV.CNTF in animal models of retinitis pigmentosa
F Q Liang, T S Aleman, N S Dejneka, et al.
Human Mutation
|
July 20, 2001
Four novel mutations in the RPE65 gene in patients with Leber congenital amaurosis
M J Simovich, B Miller, H Ezzeldin, et al.
Noise & Health
|
January 21, 2015
Hearing loss associated with US military combat deployment
Timothy S Wells, Amber D Seelig, Margaret A K Ryan, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
June 17, 1998
Disease sequence from mutant rhodopsin allele to rod and cone photoreceptor degeneration in man
A V Cideciyan, D C Hood, Y Huang, et al.
Journal of the Optical Society of America. A, Optics, Image Science, and Vision
|
April 13, 2007
Reduced-illuminance autofluorescence imaging in ABCA4-associated retinal degenerations
Artur V Cideciyan, Malgorzata Swider, Tomas S Aleman, et al.
International Journal of Molecular Sciences
|
November 14, 2019
Autosomal Dominant Retinitis Pigmentosa Due to Class B <i>Rhodopsin</i> Mutations: An Objective Outcome for Future Treatment Trials
Alexander Sumaroka, Artur V Cideciyan, Jason Charng, et al.
Scientific Reports
|
August 3, 2017
CDHR1 mutations in retinal dystrophies
Katarina Stingl, Anja K Mayer, Pablo Llavona, et al.
Investigative Ophthalmology & Visual Science
|
April 14, 2017
Postretinal Structure and Function in Severe Congenital Photoreceptor Blindness Caused by Mutations in the GUCY2D Gene
Geoffrey K Aguirre, Omar H Butt, Ritobrato Datta, et al.
Investigative Ophthalmology & Visual Science
|
June 19, 2019
Treatment Potential for Macular Cone Vision in Leber Congenital Amaurosis Due to CEP290 or NPHP5 Mutations: Predictions From Artificial Intelligence
Alexander Sumaroka, Alexandra V Garafalo, Evelyn P Semenov, et al.
Page
of 68
Search research articles
Search
Showing results (401-410 of 677) with videos related to
Sort By:
Page
of 68
Human Vaccines
|
April 3, 2008
Self-reported adverse health events following smallpox vaccination in a large prospective study of US military service members
Timothy S Wells, Cynthia A LeardMann, Tyler C Smith, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
November 16, 2001
Long-term protection of retinal structure but not function using RAAV.CNTF in animal models of retinitis pigmentosa
F Q Liang, T S Aleman, N S Dejneka, et al.
Human Mutation
|
July 20, 2001
Four novel mutations in the RPE65 gene in patients with Leber congenital amaurosis
M J Simovich, B Miller, H Ezzeldin, et al.
Noise & Health
|
January 21, 2015
Hearing loss associated with US military combat deployment
Timothy S Wells, Amber D Seelig, Margaret A K Ryan, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
June 17, 1998
Disease sequence from mutant rhodopsin allele to rod and cone photoreceptor degeneration in man
A V Cideciyan, D C Hood, Y Huang, et al.
Journal of the Optical Society of America. A, Optics, Image Science, and Vision
|
April 13, 2007
Reduced-illuminance autofluorescence imaging in ABCA4-associated retinal degenerations
Artur V Cideciyan, Malgorzata Swider, Tomas S Aleman, et al.
International Journal of Molecular Sciences
|
November 14, 2019
Autosomal Dominant Retinitis Pigmentosa Due to Class B <i>Rhodopsin</i> Mutations: An Objective Outcome for Future Treatment Trials
Alexander Sumaroka, Artur V Cideciyan, Jason Charng, et al.
Scientific Reports
|
August 3, 2017
CDHR1 mutations in retinal dystrophies
Katarina Stingl, Anja K Mayer, Pablo Llavona, et al.
Investigative Ophthalmology & Visual Science
|
April 14, 2017
Postretinal Structure and Function in Severe Congenital Photoreceptor Blindness Caused by Mutations in the GUCY2D Gene
Geoffrey K Aguirre, Omar H Butt, Ritobrato Datta, et al.
Investigative Ophthalmology & Visual Science
|
June 19, 2019
Treatment Potential for Macular Cone Vision in Leber Congenital Amaurosis Due to CEP290 or NPHP5 Mutations: Predictions From Artificial Intelligence
Alexander Sumaroka, Alexandra V Garafalo, Evelyn P Semenov, et al.
Page
of 68