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Ophthalmic Genetics|September 27, 2002
Familial unilateral Brown syndromeAlessandro Iannaccone, Nathalie McIntosh, Maria Laura Ciccarelli, et al.
Biomed Research International|March 4, 2014
Modulation of wolframin expression in human placenta during pregnancy: comparison among physiological and pathological statesAngela Lucariello, Angelica Perna, Carmine Sellitto, et al.
The Journal of Nutrition|August 31, 2004
Correlates of serum lutein + zeaxanthin: findings from the Third National Health and Nutrition Examination SurveyMichael Gruber, Richard Chappell, Amy Millen, et al.
Investigative Ophthalmology & Visual Science|February 27, 2004
Kinetics of visual field loss in Usher syndrome Type IIAlessandro Iannaccone, Stephen B Kritchevsky, Maria Laura Ciccarelli, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|August 3, 2002
Visual evoked potentials in children with neurofibromatosis type 1Alessandro Iannaccone, Richard A McCluney, Vickie R Brewer, et al.
Frontiers in Bioscience (Elite Edition)|December 29, 2011
Localization and distribution of wolframin in human tissuesMaria De Falco, Lucrezia Manente, Angela Lucariello, et al.
Clinical Ophthalmology (Auckland, N.Z.)|February 24, 2025
Impact of Dry Age-Related Macular Degeneration on Daily Activities and Quality of Life: Interview Findings From Patients and Caregivers Relative to a General PopulationChristina X Chamberlain, Antonia Morga, Yan Song, et al.
Vision Research|October 4, 2006
Retinitis pigmentosa associated with rhodopsin mutations: Correlation between phenotypic variability and molecular effectsAlessandro Iannaccone, David Man, Naushin Waseem, et al.
Vision Research|September 4, 2012
Phenotypic expression of Bardet-Biedl syndrome in patients homozygous for the common M390R mutation in the BBS1 geneKyle F Cox, Natalie C Kerr, Marina Kedrov, et al.
Vision Research|August 4, 2006
An unusual X-linked retinoschisis phenotype and biochemical characterization of the W112C RS1 mutationAlessandro Iannaccone, Marco Mura, Frank M Dyka, et al.
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