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P Whyte

Showing results (421-430 of 454) 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|July 17, 2015
Neonatal High Bone Mass With First Mutation of the NF-κB Complex: Heterozygous De Novo Missense (p.Asp512Ser) RELA (Rela/p65)Anja L Frederiksen, Martin J Larsen, Klaus Brusgaard, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
First-stage autosomal genome screen in extended pedigrees suggests genes predisposing to low bone mineral density on chromosomes 1p, 2p and 4qM Devoto, K Shimoya, J Caminis, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|September 10, 2013
Panostotic expansile bone disease with massive jaw tumor formation and a novel mutation in the signal peptide of RANKAnne L Schafer, Steven Mumm, Ivan El-Sayed, et al.
The Journal of Clinical Endocrinology and Metabolism|October 13, 1998
Mutational analysis of PHEX gene in X-linked hypophosphatemiaP H Dixon, P T Christie, C Wooding, et al.
Medicine|May 1, 1997
Paget bone disease involving young adults in 3 generations of a Korean familyG S Kim, S H Kim, J K Cho, et al.
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.
Pageof 46

Showing results (421-430 of 454) with videos related to

Sort By:
Pageof 46
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|July 17, 2015
Neonatal High Bone Mass With First Mutation of the NF-κB Complex: Heterozygous De Novo Missense (p.Asp512Ser) RELA (Rela/p65)Anja L Frederiksen, Martin J Larsen, Klaus Brusgaard, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
First-stage autosomal genome screen in extended pedigrees suggests genes predisposing to low bone mineral density on chromosomes 1p, 2p and 4qM Devoto, K Shimoya, J Caminis, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|September 10, 2013
Panostotic expansile bone disease with massive jaw tumor formation and a novel mutation in the signal peptide of RANKAnne L Schafer, Steven Mumm, Ivan El-Sayed, et al.
The Journal of Clinical Endocrinology and Metabolism|October 13, 1998
Mutational analysis of PHEX gene in X-linked hypophosphatemiaP H Dixon, P T Christie, C Wooding, et al.
Medicine|May 1, 1997
Paget bone disease involving young adults in 3 generations of a Korean familyG S Kim, S H Kim, J K Cho, et al.
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.
Pageof 46