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Thomas O Carpenter

Showing results (51-60 of 122) with videos related to

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Frontiers in Endocrinology|April 22, 2025
Advancing patient evidence in XLH (APEX): rationale and design of a real-world XLH global data unification programMaria Luisa Brandi, Thomas O Carpenter, Seiji Fukumoto, et al.
American Journal of Medical Genetics. Part A|November 10, 2004
Multisystem study of 20 older adults with Williams syndromeElizabeth M Cherniske, Thomas O Carpenter, Cheryl Klaiman, et al.
Kidney International Reports|August 24, 2019
Description of 5 Novel <i>SLC34A3/</i>NPT2c Mutations Causing Hereditary Hypophosphatemic Rickets With HypercalciuriaAlyssa Chen, Hannah Ro, Venkat Ram Rakesh Mundra, et al.
Annals of Allergy, Asthma & Immunology : Official Publication of the American College of Allergy, Asthma, & Immunology|April 22, 2014
Effect of vitamin D-binding protein genotype on the development of asthma in childrenAledie Navas-Nazario, Fang Yong Li, Veronika Shabanova, et al.
Journal of the Endocrine Society|February 2, 2026
Bone Age Delay in X-linked HypophosphatemiaJulio Soto, Rucha Anant Patki, Lauren J Ehrlich, et al.
The Journal of Clinical Endocrinology and Metabolism|September 8, 2022
Long-term Burosumab Administration Is Safe and Effective in Adults With X-linked HypophosphatemiaThomas J Weber, Erik A Imel, Thomas O Carpenter, et al.
The Journal of Steroid Biochemistry and Molecular Biology|March 1, 2016
Characterization of additional vitamin D binding protein variantsLei Fu, Chad R Borges, Douglas S Rehder, et al.
Bone|November 7, 2022
The efficacy and safety of burosumab in two patients with cutaneous skeletal hypophosphatemia syndromeJeffrey Sugarman, Ann Maruri, Dale J Hamilton, et al.
The Journal of Clinical Endocrinology and Metabolism|November 28, 2019
Relationship of Total and Free 25-Hydroxyvitamin D to Biomarkers and Metabolic Indices in Healthy ChildrenChristine A Simpson, Jane H Zhang, Dirk Vanderschueren, et al.
The Journal of Clinical Endocrinology and Metabolism|November 25, 2011
Genetic defect in CYP24A1, the vitamin D 24-hydroxylase gene, in a patient with severe infantile hypercalcemiaAndrew Dauber, Thutrang T Nguyen, Etienne Sochett, et al.
Pageof 13

Showing results (51-60 of 122) with videos related to

Sort By:
Pageof 13
Frontiers in Endocrinology|April 22, 2025
Advancing patient evidence in XLH (APEX): rationale and design of a real-world XLH global data unification programMaria Luisa Brandi, Thomas O Carpenter, Seiji Fukumoto, et al.
American Journal of Medical Genetics. Part A|November 10, 2004
Multisystem study of 20 older adults with Williams syndromeElizabeth M Cherniske, Thomas O Carpenter, Cheryl Klaiman, et al.
Kidney International Reports|August 24, 2019
Description of 5 Novel <i>SLC34A3/</i>NPT2c Mutations Causing Hereditary Hypophosphatemic Rickets With HypercalciuriaAlyssa Chen, Hannah Ro, Venkat Ram Rakesh Mundra, et al.
Annals of Allergy, Asthma & Immunology : Official Publication of the American College of Allergy, Asthma, & Immunology|April 22, 2014
Effect of vitamin D-binding protein genotype on the development of asthma in childrenAledie Navas-Nazario, Fang Yong Li, Veronika Shabanova, et al.
Journal of the Endocrine Society|February 2, 2026
Bone Age Delay in X-linked HypophosphatemiaJulio Soto, Rucha Anant Patki, Lauren J Ehrlich, et al.
The Journal of Clinical Endocrinology and Metabolism|September 8, 2022
Long-term Burosumab Administration Is Safe and Effective in Adults With X-linked HypophosphatemiaThomas J Weber, Erik A Imel, Thomas O Carpenter, et al.
The Journal of Steroid Biochemistry and Molecular Biology|March 1, 2016
Characterization of additional vitamin D binding protein variantsLei Fu, Chad R Borges, Douglas S Rehder, et al.
Bone|November 7, 2022
The efficacy and safety of burosumab in two patients with cutaneous skeletal hypophosphatemia syndromeJeffrey Sugarman, Ann Maruri, Dale J Hamilton, et al.
The Journal of Clinical Endocrinology and Metabolism|November 28, 2019
Relationship of Total and Free 25-Hydroxyvitamin D to Biomarkers and Metabolic Indices in Healthy ChildrenChristine A Simpson, Jane H Zhang, Dirk Vanderschueren, et al.
The Journal of Clinical Endocrinology and Metabolism|November 25, 2011
Genetic defect in CYP24A1, the vitamin D 24-hydroxylase gene, in a patient with severe infantile hypercalcemiaAndrew Dauber, Thutrang T Nguyen, Etienne Sochett, et al.
Pageof 13