Maternal and infantile hypercalcemia caused by vitamin-D-hydroxylase mutations and vitamin D intake

References

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Mutations in<i>CYP24A1</i>and Idiopathic Infantile Hypercalcemia Karl P. Schlingmann, Martin Kaufmann, Stefanie Weber, New England Journal of Medicine	2011	663
Deficient Mineralization of Intramembranous Bone in Vitamin D-24-Hydroxylase-Ablated Mice Is Due to Elevated 1,25-Dihydroxyvitamin D and Not to the Absence of 24,25-Dihydroxyvitamin D* René St‐Arnaud, Alice Arabian, Rose Travers, Endocrinology	2000	329
Calcium and Bone Metabolism Disorders During Pregnancy and Lactation Christopher S. Kovács Endocrinology and Metabolism Clinics of North America NutritionLactationPhysiologyClinical NutritionMaternal Health	2011	230
Hypercalcemia, Hypercalciuria, and Elevated Calcitriol Concentrations with Autosomal Dominant Transmission Due to<i>CYP24A1</i>Mutations: Effects of Ketoconazole Therapy Peter J. Tebben, Dawn S. Milliner, Ronald L. Horst, The Journal of Clinical Endocrinology & Metabolism	2012	185
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Altered Pharmacokinetics of 1α,25-Dihydroxyvitamin D<sub>3</sub>and 25-Hydroxyvitamin D<sub>3</sub>in the Blood and Tissues of the 25-Hydroxyvitamin D-24-Hydroxylase (<i>Cyp24a1</i>) Null Mouse Sonoko Masuda, Valarie Byford, Alice Arabian, Endocrinology Vitamin D HomeostasisAltered PharmacokineticsBiochemistry25-Hydroxyvitamin D-24-hydroxylaseMedicine	2004	180
Loss-of-Function Mutations of <i>CYP24A1</i> , the Vitamin D 24-Hydroxylase Gene, Cause Long-standing Hypercalciuric Nephrolithiasis and Nephrocalcinosis Dganit Dinour, Pazit Beckerman, Liat Ganon, The Journal of Urology	2013	137
Genetic Defect in<i>CYP24A1</i>, the Vitamin D 24-Hydroxylase Gene, in a Patient with Severe Infantile Hypercalcemia Andrew Dauber, Thutrang Nguyen, Etienne Sochett, The Journal of Clinical Endocrinology & Metabolism	2011	127
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