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JBMR Plus|April 17, 2023
LRP6 High Bone Mass Characterized in Two Generations Harboring a Unique Mutation of Low-Density Lipoprotein Receptor-Related Protein 6Michael P Whyte, Steven Mumm, Jonathan C Baker, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|July 28, 2006
Peak bone mass after exposure to antenatal betamethasone and prematurity: follow-up of a randomized controlled trialStuart R Dalziel, Sheryl Fenwick, Tim Cundy, et al.AACE Clinical Case Reports|June 12, 2020
HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA: A NOVEL HOMOZYGOUS MUTATION IN <i>SLC34A3</i> AND LITERATURE REVIEWSanjay K Bhadada, Subbiah Sridhar, Vandana Dhiman, et al.Archives of Ophthalmology (Chicago, Ill. : 1960)|June 16, 2010
Ocular manifestations of juvenile Paget diseaseNathan M Kerr, Hamilton R Cassinelli, Linda A DiMeglio, et al.The Journal of Steroid Biochemistry and Molecular Biology|July 1, 2004
Vitamin D antagonist, TEI-9647, inhibits osteoclast formation induced by 1alpha,25-dihydroxyvitamin D3 from pagetic bone marrow cellsSeiichi Ishizuka, Noriyoshi Kurihara, Daishiro Miura, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|December 22, 2006
Delayed development of Paget's disease in offspring inheriting SQSTM1 mutationsMark J Bolland, Pak Cheung Tong, Dorit Naot, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|January 5, 2002
Sequence analysis of measles virus nucleocapsid transcripts in patients with Paget's diseaseWilliam E Friedrichs, Sakamuri V Reddy, Jan M Bruder, et al.Diabetes Care|April 28, 2004
Insulin sensitivity in the offspring of women with type 1 and type 2 diabetesWendy A Hunter, Tim Cundy, Diana Rabone, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|January 29, 2019
Observations on the Natural History of Camurati-Engelmann DiseasePeter Hughes, Ibrahim Hassan, Lorna Que, et al.Bone|October 27, 2019
Juvenile Paget's disease with compound heterozygous mutations in TNFRSF11B presenting with recurrent clavicular fractures and a mild skeletal phenotypeDorit Naot, Louise C Wilson, Jeremy Allgrove, et al.Pageof 15