7 Inherited forms of rickets and osteomalacia-Reference-Cited by-同舟云学术

7 Inherited forms of rickets and osteomalacia

Published:1988-02 Issue:1 Volume:2 Page:157-191
ISSN:0950-351X
Container-title:Baillière's Clinical Endocrinology and Metabolism
language:en
Short-container-title:Baillière's Clinical Endocrinology and Metabolism

Author:

Thakker R.V.,O'Riordan J.L.H.

Publisher

Elsevier BV

Subject

Endocrinology,Biochemistry

Reference159 articles.

1. Oculo-cerebro-renal syndrome;Abbassi;American Journal of Diseases of Children,1968

2. Intraspinal new bone formation and spinal cord compression in familial hypophosphataemic vitamin D resistant osteomalacia;Adams;Quarterly Journal of Medicine,1986

3. The parathyroid Glands and Metabolic Bone Disease;Albright,1948

4. Rickets resistant to vitamin D therapy;Albright;American Journal of Diseases of Children,1937

5. Familial Fanconi Syndrome with malabsorption and galactose intolerance, norman kinase and transferase activity: a report on two siblings;Aperia;Acta Paediatrica Scandinavica,1981

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2. Genetic Testing Confirmed the Early Diagnosis of X-Linked Hypophosphatemic Rickets in a 7-Month-Old Infant;Journal of Investigative Medicine High Impact Case Reports;2015-07-01

3. A NovelPHEXMutation in Japanese Patients with X-Linked Hypophosphatemic Rickets;Case Reports in Genetics;2015

4. Hypophosphatemic rickets is associated with disruption of mineral orientation at the nanoscale in the flat scapula bones of rachitic mice with development;Bone;2012-09

5. Novel PHEX Gene Mutation Associated with X Linked Hypophosphatemic Rickets;Nephron Physiology;2010