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Michael P Whyte

Showing results (71-80 of 165) with videos related to

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American Journal of Medical Genetics. Part A|January 15, 2016
Auricular ossification: A newly recognized feature of osteoprotegerin-deficiency juvenile Paget diseaseGary S Gottesman, Katherine L Madson, William H McAlister, et al.
Archives of Dermatology|January 20, 2010
Buschke-Ollendorff syndrome: absence of LEMD3 mutation in an affected familyMichelle Yadegari, Michael P Whyte, Steven Mumm, et al.
Bone|July 31, 2020
High bone mass from mutation of low-density lipoprotein receptor-related protein 6 (LRP6)María Lorena Brance, Lucas R Brun, Nicolás M Cóccaro, et al.
The Lancet. Diabetes & Endocrinology|January 15, 2019
Efficacy and safety of burosumab in children aged 1-4 years with X-linked hypophosphataemia: a multicentre, open-label, phase 2 trialMichael P Whyte, Thomas O Carpenter, Gary S Gottesman, et al.
Bone|September 21, 2021
Hypophosphatasia: Vitamin B<sub>6</sub> status of affected children and adultsMichael P Whyte, Fan Zhang, Deborah Wenkert, et al.
Bone|February 5, 2023
Early identification of a 12-bp tandem duplication in TNFRSF11A encoding receptor activator of nuclear factor-kappa B (RANK): Clinical characterization and response to bisphosphonate therapyMeghan Craven, Mary Ellen Vajravelu, Karuna V Shekdar, et al.
The Journal of Clinical Endocrinology and Metabolism|July 29, 2020
Growth Curves for Children with X-linked HypophosphatemiaMeng Mao, Thomas O Carpenter, Michael P Whyte, et al.
JBMR Plus|December 19, 2022
X-Linked Hypophosphatemia Caused by the Prevailing North American <i>PHEX</i> Variant c.*231A>G; Exon 13-15 Duplication Is Often Misdiagnosed as Ankylosing Spondylitis and Manifests in Both Men and WomenKathryn McCrystal Dahir, Margo Black, Gary S Gottesman, et al.
The New England Journal of Medicine|July 19, 2002
Osteoprotegerin deficiency and juvenile Paget's diseaseMichael P Whyte, Sara E Obrecht, Patrick M Finnegan, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|July 18, 2015
Reply: Response to: Rapid Skeletal Turnover in a Radiographic Mimic of Osteopetrosis Might Be Secondary to Systemic MastocytosisMichael P Whyte, Katherine L Madson, William H McAlister, et al.
Pageof 17

Showing results (71-80 of 165) with videos related to

Sort By:
Pageof 17
American Journal of Medical Genetics. Part A|January 15, 2016
Auricular ossification: A newly recognized feature of osteoprotegerin-deficiency juvenile Paget diseaseGary S Gottesman, Katherine L Madson, William H McAlister, et al.
Archives of Dermatology|January 20, 2010
Buschke-Ollendorff syndrome: absence of LEMD3 mutation in an affected familyMichelle Yadegari, Michael P Whyte, Steven Mumm, et al.
Bone|July 31, 2020
High bone mass from mutation of low-density lipoprotein receptor-related protein 6 (LRP6)María Lorena Brance, Lucas R Brun, Nicolás M Cóccaro, et al.
The Lancet. Diabetes & Endocrinology|January 15, 2019
Efficacy and safety of burosumab in children aged 1-4 years with X-linked hypophosphataemia: a multicentre, open-label, phase 2 trialMichael P Whyte, Thomas O Carpenter, Gary S Gottesman, et al.
Bone|September 21, 2021
Hypophosphatasia: Vitamin B<sub>6</sub> status of affected children and adultsMichael P Whyte, Fan Zhang, Deborah Wenkert, et al.
Bone|February 5, 2023
Early identification of a 12-bp tandem duplication in TNFRSF11A encoding receptor activator of nuclear factor-kappa B (RANK): Clinical characterization and response to bisphosphonate therapyMeghan Craven, Mary Ellen Vajravelu, Karuna V Shekdar, et al.
The Journal of Clinical Endocrinology and Metabolism|July 29, 2020
Growth Curves for Children with X-linked HypophosphatemiaMeng Mao, Thomas O Carpenter, Michael P Whyte, et al.
JBMR Plus|December 19, 2022
X-Linked Hypophosphatemia Caused by the Prevailing North American <i>PHEX</i> Variant c.*231A>G; Exon 13-15 Duplication Is Often Misdiagnosed as Ankylosing Spondylitis and Manifests in Both Men and WomenKathryn McCrystal Dahir, Margo Black, Gary S Gottesman, et al.
The New England Journal of Medicine|July 19, 2002
Osteoprotegerin deficiency and juvenile Paget's diseaseMichael P Whyte, Sara E Obrecht, Patrick M Finnegan, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|July 18, 2015
Reply: Response to: Rapid Skeletal Turnover in a Radiographic Mimic of Osteopetrosis Might Be Secondary to Systemic MastocytosisMichael P Whyte, Katherine L Madson, William H McAlister, et al.
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