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Methods in Molecular Biology (Clifton, N.J.)
|
August 25, 2014
Pharmacogenetics of the G protein-coupled receptors
Miles D Thompson, David E C Cole, Valerie Capra, et al.
Cancer
|
November 18, 2009
A phase 2 trial exploring the effects of high-dose (10,000 IU/day) vitamin D(3) in breast cancer patients with bone metastases
Eitan Amir, Christine E Simmons, Orit C Freedman, et al.
The Journal of Clinical Endocrinology and Metabolism
|
August 14, 2003
Recurrent familial hypocalcemia due to germline mosaicism for an activating mutation of the calcium-sensing receptor gene
Geoffrey N Hendy, Carla Minutti, Lucie Canaff, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
December 24, 2010
Kabuki syndrome and Crohn disease in a child with familial hypocalciuric hypercalcemia
Josephine Ho, Danya Fox, A Micheil Innes, et al.
The Journal of Steroid Biochemistry and Molecular Biology
|
March 1, 2016
Characterization of additional vitamin D binding protein variants
Lei Fu, Chad R Borges, Douglas S Rehder, et al.
Surgery
|
December 17, 2008
Re: Familial hyperparathyroidism: surgical outcome after 30 years of follow-up in three families with germline HRPT2 mutations
Vito Guarnieri, Michele Bisceglia, Nazzario Bonfitto, 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 Children
Christine A Simpson, Jane H Zhang, Dirk Vanderschueren, et al.
European Journal of Endocrinology
|
June 15, 2021
25-OHD response to vitamin D supplementation in children: effect of dose but not GC haplotype
Christine 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 hypercalcemia
Andrew Dauber, Thutrang T Nguyen, Etienne Sochett, et al.
The Journal of Clinical Endocrinology and Metabolism
|
April 13, 2006
A hypocalcemic child with a novel activating mutation of the calcium-sensing receptor gene: successful treatment with recombinant human parathyroid hormone
Steven D Mittelman, Geoffrey N Hendy, Richard A Fefferman, et al.
Page
of 16
Search research articles
Search
Showing results (101-110 of 160) with videos related to
Sort By:
Page
of 16
Methods in Molecular Biology (Clifton, N.J.)
|
August 25, 2014
Pharmacogenetics of the G protein-coupled receptors
Miles D Thompson, David E C Cole, Valerie Capra, et al.
Cancer
|
November 18, 2009
A phase 2 trial exploring the effects of high-dose (10,000 IU/day) vitamin D(3) in breast cancer patients with bone metastases
Eitan Amir, Christine E Simmons, Orit C Freedman, et al.
The Journal of Clinical Endocrinology and Metabolism
|
August 14, 2003
Recurrent familial hypocalcemia due to germline mosaicism for an activating mutation of the calcium-sensing receptor gene
Geoffrey N Hendy, Carla Minutti, Lucie Canaff, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
December 24, 2010
Kabuki syndrome and Crohn disease in a child with familial hypocalciuric hypercalcemia
Josephine Ho, Danya Fox, A Micheil Innes, et al.
The Journal of Steroid Biochemistry and Molecular Biology
|
March 1, 2016
Characterization of additional vitamin D binding protein variants
Lei Fu, Chad R Borges, Douglas S Rehder, et al.
Surgery
|
December 17, 2008
Re: Familial hyperparathyroidism: surgical outcome after 30 years of follow-up in three families with germline HRPT2 mutations
Vito Guarnieri, Michele Bisceglia, Nazzario Bonfitto, 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 Children
Christine A Simpson, Jane H Zhang, Dirk Vanderschueren, et al.
European Journal of Endocrinology
|
June 15, 2021
25-OHD response to vitamin D supplementation in children: effect of dose but not GC haplotype
Christine 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 hypercalcemia
Andrew Dauber, Thutrang T Nguyen, Etienne Sochett, et al.
The Journal of Clinical Endocrinology and Metabolism
|
April 13, 2006
A hypocalcemic child with a novel activating mutation of the calcium-sensing receptor gene: successful treatment with recombinant human parathyroid hormone
Steven D Mittelman, Geoffrey N Hendy, Richard A Fefferman, et al.
Page
of 16