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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 metastasesEitan 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 geneGeoffrey 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 hypercalcemiaJosephine 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 variantsLei Fu, Chad R Borges, Douglas S Rehder, 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.
European Journal of Endocrinology|June 15, 2021
25-OHD response to vitamin D supplementation in children: effect of dose but not GC haplotypeChristine A Simpson, Jane H Zhang, Dirk Vanderschueren, 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 hormoneSteven D Mittelman, Geoffrey N Hendy, Richard A Fefferman, et al.
The Journal of Steroid Biochemistry and Molecular Biology|May 25, 2011
The ratio of serum 24,25-dihydroxyvitamin D(3) to 25-hydroxyvitamin D(3) is predictive of 25-hydroxyvitamin D(3) response to vitamin D(3) supplementationDennis Wagner, Heather E Hanwell, Kareena Schnabl, et al.
The Journal of Clinical Endocrinology and Metabolism|April 16, 2014
Codon Arg15 mutations of the AP2S1 gene: common occurrence in familial hypocalciuric hypercalcemia cases negative for calcium-sensing receptor (CASR) mutationsGeoffrey N Hendy, Lucie Canaff, Ron S Newfield, et al.
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