Hereditary vitamin D resistant rickets: Identification of a novel splice site mutation in the vitamin D receptor gene and successful treatment with oral calcium therapy-Reference-Cited by-同舟云学术

Hereditary vitamin D resistant rickets: Identification of a novel splice site mutation in the vitamin D receptor gene and successful treatment with oral calcium therapy

Published:2009-10 Issue:4 Volume:45 Page:743-746
ISSN:8756-3282
Container-title:Bone
language:en
Short-container-title:Bone

Author:

Ma Nina S.,Malloy Peter J.,Pitukcheewanont Pisit,Dreimane Daina,Geffner Mitchell E.,Feldman David

Publisher

Elsevier BV

Subject

Histology,Physiology,Endocrinology, Diabetes and Metabolism

Reference16 articles.

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2. Hereditary 1,25-dihydroxyvitamin D resistant rickets;Malloy,2005

3. Rickets and alopecia with resistance to 1,25-dihydroxyvitamin D: two different clinical courses with two different cellular defects;Balsan;J. Clin. Endocrinol. Metab.,1983

4. Absent intestinal response to calciferols in hereditary resistance to 1,25-dihydroxyvitamin D: documentation and effective therapy with high dose intravenous calcium infusions;Bliziotes;J. Clin. Endocrinol. Metab.,1988

5. Long-term nocturnal calcium infusions can cure rickets and promote normal mineralization in hereditary resistance to 1,25-dihydroxyvitamin D;Balsan;J. Clin. Invest.,1986

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