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Michael P Whyte

Showing results (61-70 of 165) with videos related to

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Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|November 4, 2014
Lenz-Majewski hyperostotic dwarfism with hyperphosphoserinuria from a novel mutation in PTDSS1 encoding phosphatidylserine synthase 1Michael P Whyte, Amanda Blythe, William H McAlister, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|March 14, 2007
Juvenile Paget's disease: the second reported, oldest patient is homozygous for the TNFRSF11B "Balkan" mutation (966_969delTGACinsCTT), which elevates circulating immunoreactive osteoprotegerin levelsMichael P Whyte, Panagiotis N Singhellakis, Michael B Petersen, et al.
The Journal of Clinical Endocrinology and Metabolism|February 8, 2007
Sporadic hyperphosphatasia syndrome featuring periostitis and accelerated skeletal turnover without receptor activator of nuclear factor-kappaB, osteoprotegerin, or sequestosome-1 gene defectsSuat Simsek, Natalja M Basoski, Nathalie Bravenboer, et al.
Bone|May 23, 2025
Markedly discordant hypophosphatasia in a young girlVikram Prakash, Samer Elbabaa, Richard Banks, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|October 15, 2013
Calcific periarthritis as the only clinical manifestation of hypophosphatasia in middle-aged sistersNúria Guañabens, Steven Mumm, Ingrid Möller, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|May 29, 2008
Bisphosphonate-induced osteopetrosis: novel bone modeling defects, metaphyseal osteopenia, and osteosclerosis fractures after drug exposure ceasesMichael P Whyte, William H McAlister, Deborah V Novack, et al.
JIMD Reports|April 13, 2013
Outcome of perinatal hypophosphatasia in manitoba mennonites: a retrospective cohort analysisEdward C W Leung, Aizeddin A Mhanni, Martin Reed, et al.
Bone|January 10, 2016
Congenital insensitivity to pain: Fracturing without apparent skeletal pathobiology caused by an autosomal dominant, second mutation in SCN11A encoding voltage-gated sodium channel 1.9Voraluck Phatarakijnirund, Steven Mumm, William H McAlister, et al.
Bone|September 28, 2020
Pharmacodynamics of asfotase alfa in adults with pediatric-onset hypophosphatasiaLothar Seefried, Priya S Kishnani, Scott Moseley, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|October 4, 2006
Recovery from skeletal fluorosis (an enigmatic, American case)Etah S Kurland, Rifka C Schulman, Joseph E Zerwekh, et al.
Pageof 17

Showing results (61-70 of 165) with videos related to

Sort By:
Pageof 17
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|November 4, 2014
Lenz-Majewski hyperostotic dwarfism with hyperphosphoserinuria from a novel mutation in PTDSS1 encoding phosphatidylserine synthase 1Michael P Whyte, Amanda Blythe, William H McAlister, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|March 14, 2007
Juvenile Paget's disease: the second reported, oldest patient is homozygous for the TNFRSF11B "Balkan" mutation (966_969delTGACinsCTT), which elevates circulating immunoreactive osteoprotegerin levelsMichael P Whyte, Panagiotis N Singhellakis, Michael B Petersen, et al.
The Journal of Clinical Endocrinology and Metabolism|February 8, 2007
Sporadic hyperphosphatasia syndrome featuring periostitis and accelerated skeletal turnover without receptor activator of nuclear factor-kappaB, osteoprotegerin, or sequestosome-1 gene defectsSuat Simsek, Natalja M Basoski, Nathalie Bravenboer, et al.
Bone|May 23, 2025
Markedly discordant hypophosphatasia in a young girlVikram Prakash, Samer Elbabaa, Richard Banks, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|October 15, 2013
Calcific periarthritis as the only clinical manifestation of hypophosphatasia in middle-aged sistersNúria Guañabens, Steven Mumm, Ingrid Möller, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|May 29, 2008
Bisphosphonate-induced osteopetrosis: novel bone modeling defects, metaphyseal osteopenia, and osteosclerosis fractures after drug exposure ceasesMichael P Whyte, William H McAlister, Deborah V Novack, et al.
JIMD Reports|April 13, 2013
Outcome of perinatal hypophosphatasia in manitoba mennonites: a retrospective cohort analysisEdward C W Leung, Aizeddin A Mhanni, Martin Reed, et al.
Bone|January 10, 2016
Congenital insensitivity to pain: Fracturing without apparent skeletal pathobiology caused by an autosomal dominant, second mutation in SCN11A encoding voltage-gated sodium channel 1.9Voraluck Phatarakijnirund, Steven Mumm, William H McAlister, et al.
Bone|September 28, 2020
Pharmacodynamics of asfotase alfa in adults with pediatric-onset hypophosphatasiaLothar Seefried, Priya S Kishnani, Scott Moseley, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|October 4, 2006
Recovery from skeletal fluorosis (an enigmatic, American case)Etah S Kurland, Rifka C Schulman, Joseph E Zerwekh, et al.
Pageof 17