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Michael P Whyte

Showing results (141-150 of 165) with videos related to

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Bone|December 28, 2020
Coalescing expansile skeletal disease: Delineation of an extraordinary osteopathy involving the IFITM5 mutation of osteogenesis imperfecta type VMichael P Whyte, James Aronson, William H McAlister, et al.
The New England Journal of Medicine|May 24, 2018
Burosumab Therapy in Children with X-Linked HypophosphatemiaThomas O Carpenter, Michael P Whyte, Erik A Imel, et al.
JCI Insight|October 5, 2016
Asfotase alfa therapy for children with hypophosphatasiaMichael P Whyte, Katherine L Madson, Dawn Phillips, et al.
Bone|September 1, 2019
Bruck syndrome 2 variant lacking congenital contractures and involving a novel compound heterozygous PLOD2 mutationSteven Mumm, Gary S Gottesman, Deborah Wenkert, et al.
Bone|May 17, 2021
Vitamin B<sub>6</sub> deficiency with normal plasma levels of pyridoxal 5'-phosphate in perinatal hypophosphatasiaMichael P Whyte, Jennifer D May, William H McAlister, et al.
Nature Reviews. Endocrinology|October 17, 2022
Author Correction: Skeletal and extraskeletal disorders of biomineralizationMichael T Collins, Gemma Marcucci, Hans-Joachim Anders, et al.
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.
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.
Pageof 17

Showing results (141-150 of 165) with videos related to

Sort By:
Pageof 17
Bone|December 28, 2020
Coalescing expansile skeletal disease: Delineation of an extraordinary osteopathy involving the IFITM5 mutation of osteogenesis imperfecta type VMichael P Whyte, James Aronson, William H McAlister, et al.
The New England Journal of Medicine|May 24, 2018
Burosumab Therapy in Children with X-Linked HypophosphatemiaThomas O Carpenter, Michael P Whyte, Erik A Imel, et al.
JCI Insight|October 5, 2016
Asfotase alfa therapy for children with hypophosphatasiaMichael P Whyte, Katherine L Madson, Dawn Phillips, et al.
Bone|September 1, 2019
Bruck syndrome 2 variant lacking congenital contractures and involving a novel compound heterozygous PLOD2 mutationSteven Mumm, Gary S Gottesman, Deborah Wenkert, et al.
Bone|May 17, 2021
Vitamin B<sub>6</sub> deficiency with normal plasma levels of pyridoxal 5'-phosphate in perinatal hypophosphatasiaMichael P Whyte, Jennifer D May, William H McAlister, et al.
Nature Reviews. Endocrinology|October 17, 2022
Author Correction: Skeletal and extraskeletal disorders of biomineralizationMichael T Collins, Gemma Marcucci, Hans-Joachim Anders, et al.
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.
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.
Pageof 17