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P Whyte

Showing results (431-440 of 454) with videos related to

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Nature Reviews. Endocrinology|May 16, 2022
Skeletal and extraskeletal disorders of biomineralizationMichael T Collins, Gemma Marcucci, Hans-Joachim Anders, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|April 4, 2003
Marrow cell transplantation for infantile hypophosphatasiaMichael P Whyte, Joanne Kurtzberg, William H McAlister, et al.
BMJ Open Sport & Exercise Medicine|October 11, 2021
Charter to establish clinical exercise physiology as a recognised allied health profession in the UK: a call to actionHelen Jones, Keith P George, Andrew Scott, et al.
American Journal of Medical Genetics. Part A|February 9, 2008
Clinical studies in familial VCP myopathy associated with Paget disease of bone and frontotemporal dementiaVirginia E Kimonis, Sarju G Mehta, Erin C Fulchiero, et al.
Endocrine Connections|January 22, 2020
Studies of mice deleted for Sox3 and uc482: relevance to X-linked hypoparathyroidismKatie U Gaynor, Irina V Grigorieva, Samantha M Mirczuk, et al.
British Journal of Sports Medicine|February 2, 2022
Exercise prehabilitation during neoadjuvant chemotherapy may enhance tumour regression in oesophageal cancer: results from a prospective non-randomised trialJanine Zylstra, Greg P Whyte, Kerri Beckmann, et al.
Bone|November 28, 2017
Gnathodiaphyseal dysplasia: Severe atypical presentation with novel heterozygous mutation of the anoctamin gene (ANO5)Ghada A Otaify, Michael P Whyte, Gary S Gottesman, et al.
The American Journal of Clinical Nutrition|January 5, 2002
Elevated plasma 4-pyridoxic acid in renal insufficiencyStephen P Coburn, Robert D Reynolds, J Dennis Mahuren, et al.
The Journal of Clinical Investigation|September 17, 2005
MMP13 mutation causes spondyloepimetaphyseal dysplasia, Missouri type (SEMD(MO)Ann M Kennedy, Masaki Inada, Stephen M Krane, et al.
Nature Genetics|December 11, 2012
Mutations in AP2S1 cause familial hypocalciuric hypercalcemia type 3M Andrew Nesbit, Fadil M Hannan, Sarah A Howles, et al.
Pageof 46

Showing results (431-440 of 454) with videos related to

Sort By:
Pageof 46
Nature Reviews. Endocrinology|May 16, 2022
Skeletal and extraskeletal disorders of biomineralizationMichael T Collins, Gemma Marcucci, Hans-Joachim Anders, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|April 4, 2003
Marrow cell transplantation for infantile hypophosphatasiaMichael P Whyte, Joanne Kurtzberg, William H McAlister, et al.
BMJ Open Sport & Exercise Medicine|October 11, 2021
Charter to establish clinical exercise physiology as a recognised allied health profession in the UK: a call to actionHelen Jones, Keith P George, Andrew Scott, et al.
American Journal of Medical Genetics. Part A|February 9, 2008
Clinical studies in familial VCP myopathy associated with Paget disease of bone and frontotemporal dementiaVirginia E Kimonis, Sarju G Mehta, Erin C Fulchiero, et al.
Endocrine Connections|January 22, 2020
Studies of mice deleted for Sox3 and uc482: relevance to X-linked hypoparathyroidismKatie U Gaynor, Irina V Grigorieva, Samantha M Mirczuk, et al.
British Journal of Sports Medicine|February 2, 2022
Exercise prehabilitation during neoadjuvant chemotherapy may enhance tumour regression in oesophageal cancer: results from a prospective non-randomised trialJanine Zylstra, Greg P Whyte, Kerri Beckmann, et al.
Bone|November 28, 2017
Gnathodiaphyseal dysplasia: Severe atypical presentation with novel heterozygous mutation of the anoctamin gene (ANO5)Ghada A Otaify, Michael P Whyte, Gary S Gottesman, et al.
The American Journal of Clinical Nutrition|January 5, 2002
Elevated plasma 4-pyridoxic acid in renal insufficiencyStephen P Coburn, Robert D Reynolds, J Dennis Mahuren, et al.
The Journal of Clinical Investigation|September 17, 2005
MMP13 mutation causes spondyloepimetaphyseal dysplasia, Missouri type (SEMD(MO)Ann M Kennedy, Masaki Inada, Stephen M Krane, et al.
Nature Genetics|December 11, 2012
Mutations in AP2S1 cause familial hypocalciuric hypercalcemia type 3M Andrew Nesbit, Fadil M Hannan, Sarah A Howles, et al.
Pageof 46