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Journal of Clinical Densitometry : the Official Journal of the International Society for Clinical Densitometry|May 30, 2006
Effect of calcium tablets on interpretation of lumbar spine DXA scansDavid L Kendler, Gary M Kiebzak, Catherine G Ambrose, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|June 5, 2004
Novel UBA domain mutations of SQSTM1 in Paget's disease of bone: genotype phenotype correlation, functional analysis, and structural consequencesLynne J Hocking, Gavin J A Lucas, Anna Daroszewska, et al.Ophthalmology. Retina|February 13, 2022
North Carolina Macular Dystrophy: Long-term Follow-up of the Original FamilyKent W Small, Robert Wiggins, Nitin Udar, et al.Human Molecular Genetics|August 22, 2002
A mutation in the gene TNFRSF11B encoding osteoprotegerin causes an idiopathic hyperphosphatasia phenotypeTim Cundy, Madhuri Hegde, Dorit Naot, et al.Molecular Vision|June 1, 2006
Further support of the role of CYP1B1 in patients with Peters anomalyAndrea Vincent, Gail Billingsley, Megan Priston, et al.The Clinical Neuropsychologist|February 2, 2013
Efficacy of the ANAM General Neuropsychological Screening Battery (ANAM GNS) for detecting neurocognitive impairment in a mixed clinical sampleJonathan Woodhouse, Daniel J Heyanka, Jim Scott, et al.Kidney International Reports|January 16, 2023
Kidney-Function Trajectories From Young Adulthood to Midlife: Identifying Risk Strata and Opportunities for InterventionHayley Guiney, Robert Walker, Jonathan Broadbent, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|April 19, 2018
Mutations That Alter the Carboxy-Terminal-Propeptide Cleavage Site of the Chains of Type I Procollagen Are Associated With a Unique Osteogenesis Imperfecta PhenotypeTim Cundy, Michael Dray, John Delahunt, et al.Frontiers in Molecular Biosciences|September 2, 2022
Less is more: Enterobactin concentration dependency in copper tolerance and toxicityDaiana Romina Peralta, Juan Vicente Farizano, Natalia Bulacio Gil, et al.Ophthalmic Genetics|December 13, 2021
Best Vitelliform Macular Dystrophy (BVMD) is a phenocopy of North Carolina Macular Dystrophy (NCMD/MCDR1)Kent W Small, Lee M Jampol, Benjamin Bakall, et al.Pageof 15