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Human Molecular Genetics|July 2, 2004
Nuclear receptor NR2E3 gene mutations distort human retinal laminar architecture and cause an unusual degenerationSamuel G Jacobson, Alexander Sumaroka, Tomas S Aleman, et al.
Developmental Medicine and Child Neurology|January 9, 1999
Visual, cognitive, and neurodevelopmental outcome at 51/2 years in children with perinatal haemorrhagic-ischaemic brain lesionsB M Van den Hout, P Eken, D Van der Linden, et al.
Alimentary Pharmacology & Therapeutics|January 29, 2015
Long-term follow-up of successful hepatitis C virus therapy: waning immune responses and disappearance of liver disease are consistent with cureM Hedenstierna, O Weiland, A Brass, et al.
Investigative Ophthalmology & Visual Science|March 24, 2004
Impairment of the transient pupillary light reflex in Rpe65(-/-) mice and humans with leber congenital amaurosisTomas S Aleman, Samuel G Jacobson, John D Chico, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 5, 2002
The nuclear receptor NR2E3 plays a role in human retinal photoreceptor differentiation and degenerationAnn H Milam, Linda Rose, Artur V Cideciyan, et al.
Retinal Cases & Brief Reports|July 16, 2019
ENHANCED S-CONE SYNDROME: VISUAL FUNCTION, CROSS-SECTIONAL IMAGING, AND CELLULAR STRUCTURE WITH ADAPTIVE OPTICS OPHTHALMOSCOPYMichael J Ammar, Kurt T Scavelli, Katherine E Uyhazi, et al.
Ophthalmic Genetics|December 5, 2022
Fleck-like lesions in <i>CEP290-associated</i> leber congenital amaurosis: a case seriesTomas S Aleman, Erin C O'Neil, Katherine E Uyhazi, et al.
JAMA Ophthalmology|September 8, 2017
Quantitative Assessment of Microstructural Changes of the Retina in Infants With Congenital Zika SyndromeTomas S Aleman, Camila V Ventura, Milena M Cavalcanti, et al.
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