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Journal of Cataract and Refractive Surgery|September 18, 2017
Visual quality and performance comparison between 2 refractive rotationally asymmetric multifocal intraocular lensesRichard N McNeely, Eric Pazo, Andrew Spence, et al.
Journal of Cataract and Refractive Surgery|June 13, 2017
Visual outcomes and patient satisfaction 3 and 12 months after implantation of a refractive rotationally asymmetric multifocal intraocular lensRichard N McNeely, Eric Pazo, Andrew Spence, et al.
Ophthalmology Science|October 17, 2022
Successful Proof-of-Concept for Topical Delivery of Novel Peptide ALM201 with Potential Usefulness for Treating Neovascular Eye DisordersGideon Obasanmi, M Andrew Nesbit, Diego Cobice, et al.
The Journal of Clinical Endocrinology and Metabolism|February 6, 2010
Identification of a second kindred with familial hypocalciuric hypercalcemia type 3 (FHH3) narrows localization to a <3.5 megabase pair region on chromosome 19q13.3M Andrew Nesbit, Fadil M Hannan, Una Graham, et al.
The Journal of Clinical Endocrinology and Metabolism|May 14, 2010
A missense glial cells missing homolog B (GCMB) mutation, Asn502His, causes autosomal dominant hypoparathyroidismSamantha M Mirczuk, Michael R Bowl, M Andrew Nesbit, et al.
Nature Clinical Practice. Endocrinology & Metabolism|December 18, 2007
Familial isolated primary hyperparathyroidism caused by mutations of the MEN1 geneFadil M Hannan, M Andrew Nesbit, Paul T Christie, et al.
The Journal of Clinical Endocrinology and Metabolism|February 12, 2005
Functional analysis of a novel GATA3 mutation in a family with the hypoparathyroidism, deafness, and renal dysplasia syndromeAlireza Zahirieh, M Andrew Nesbit, Asif Ali, et al.
Scientific Reports|January 22, 2022
User experience of home-based AbC-19 SARS-CoV-2 antibody rapid lateral flow immunoassay testMin Jing, Raymond Bond, Louise J Robertson, et al.
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