Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Michael P Whyte

Showing results (21-30 of 165) with videos related to

Pageof 17
Sort By:
Bone|August 31, 2016
Hypophosphatasia: Natural history study of 101 affected children investigated at one research centerMichael P Whyte, Deborah Wenkert, Fan Zhang
Journal of Clinical Densitometry : the Official Journal of the International Society for Clinical Densitometry|March 20, 2012
Dual-energy X-ray absorptiometry interpretation: a simple equation for height correction in preteenage childrenFan Zhang, Michael P Whyte, Deborah Wenkert
The Journal of Clinical Endocrinology and Metabolism|January 11, 2007
Adult hypophosphatasia treated with teriparatideMichael P Whyte, Steven Mumm, Chad Deal
The New England Journal of Medicine|May 14, 2004
High-bone-mass disease and LRP5Michael P Whyte, William H Reinus, Steven Mumm
Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists|January 19, 2007
Low serum alkaline phosphatase activity and pathologic fracture: case report and brief review of hypophosphatasia diagnosed in adulthoodHasnain M Khandwala, Steven Mumm, Michael P Whyte
The Journal of Hand Surgery|July 6, 2012
Idiopathic multicentric osteolysis: upper extremity manifestations and surgical considerations during childhoodCharles A Goldfarb, Jennifer A Steffen, Michael P Whyte
Cancer Letters|June 6, 2020
The two faces of giant cell tumor of boneFederica Scotto di Carlo, Michael P Whyte, Fernando Gianfrancesco
The Journal of Pediatrics|June 14, 2006
Homozygosity for TNSALP mutation 1348c>T (Arg433Cys) causes infantile hypophosphatasia manifesting transient disease correction and variably lethal outcome in a kindred of black ancestryMichael P Whyte, Kevan Essmyer, Michael Geimer, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|September 10, 2013
Pregnancy-associated osteoporosis with a heterozygous deactivating LDL receptor-related protein 5 (LRP5) mutation and a homozygous methylenetetrahydrofolate reductase (MTHFR) polymorphismFiona J Cook, Steven Mumm, Michael P Whyte, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|April 13, 2005
Oropharyngeal skeletal disease accompanying high bone mass and novel LRP5 mutationMichael R Rickels, Xiafang Zhang, Steven Mumm, et al.
Pageof 17

Showing results (21-30 of 165) with videos related to

Sort By:
Pageof 17
Bone|August 31, 2016
Hypophosphatasia: Natural history study of 101 affected children investigated at one research centerMichael P Whyte, Deborah Wenkert, Fan Zhang
Journal of Clinical Densitometry : the Official Journal of the International Society for Clinical Densitometry|March 20, 2012
Dual-energy X-ray absorptiometry interpretation: a simple equation for height correction in preteenage childrenFan Zhang, Michael P Whyte, Deborah Wenkert
The Journal of Clinical Endocrinology and Metabolism|January 11, 2007
Adult hypophosphatasia treated with teriparatideMichael P Whyte, Steven Mumm, Chad Deal
The New England Journal of Medicine|May 14, 2004
High-bone-mass disease and LRP5Michael P Whyte, William H Reinus, Steven Mumm
Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists|January 19, 2007
Low serum alkaline phosphatase activity and pathologic fracture: case report and brief review of hypophosphatasia diagnosed in adulthoodHasnain M Khandwala, Steven Mumm, Michael P Whyte
The Journal of Hand Surgery|July 6, 2012
Idiopathic multicentric osteolysis: upper extremity manifestations and surgical considerations during childhoodCharles A Goldfarb, Jennifer A Steffen, Michael P Whyte
Cancer Letters|June 6, 2020
The two faces of giant cell tumor of boneFederica Scotto di Carlo, Michael P Whyte, Fernando Gianfrancesco
The Journal of Pediatrics|June 14, 2006
Homozygosity for TNSALP mutation 1348c>T (Arg433Cys) causes infantile hypophosphatasia manifesting transient disease correction and variably lethal outcome in a kindred of black ancestryMichael P Whyte, Kevan Essmyer, Michael Geimer, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|September 10, 2013
Pregnancy-associated osteoporosis with a heterozygous deactivating LDL receptor-related protein 5 (LRP5) mutation and a homozygous methylenetetrahydrofolate reductase (MTHFR) polymorphismFiona J Cook, Steven Mumm, Michael P Whyte, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|April 13, 2005
Oropharyngeal skeletal disease accompanying high bone mass and novel LRP5 mutationMichael R Rickels, Xiafang Zhang, Steven Mumm, et al.
Pageof 17