FGF23 concentrations vary with disease status in autosomal dominant hypophosphatemic rickets

Journal of Bone and Mineral Research

Volumn 22, Issue 4, 2007, Pages 520-526

  Imel, Erik A ^a   Hui, Siu L ^a   Econs, Michael J ^a,b  

^a INDIANA UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b Clinical Building 459 ^*  (United States)

Author keywords

Autosomal dominant hypophosphatemic rickets; Fibroblast growth factor 23; Osteomalacia; Phosphate; Rickets

Indexed keywords

CALCITRIOL; FIBROBLAST GROWTH FACTOR 23; PHOSPHATE; FIBROBLAST GROWTH FACTOR;

ADOLESCENT; ADULT; AGED; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CONTROLLED STUDY; DISEASE SEVERITY; ENZYME LINKED IMMUNOSORBENT ASSAY; FEMALE; HUMAN; HYPOPHOSPHATEMIA; MAJOR CLINICAL STUDY; MALE; OBSERVATIONAL STUDY; PHOSPHATE BLOOD LEVEL; PHOSPHATURIA; RARE DISEASE; RICKETS; BLOOD; CASE CONTROL STUDY; CASE REPORT; DOMINANT GENE; GENETICS; MIDDLE AGED; MUTATION; VITAMIN D RESISTANT RICKETS;

ADOLESCENT; ADULT; AGED; AGED, 80 AND OVER; CASE-CONTROL STUDIES; FEMALE; FIBROBLAST GROWTH FACTORS; GENES, DOMINANT; HUMANS; HYPOPHOSPHATEMIC RICKETS, X-LINKED DOMINANT; MALE; MIDDLE AGED; MUTATION; PHOSPHATES;

EID: 34249664523     PISSN: 08840431     EISSN: None     Source Type: Journal    
DOI: 10.1359/jbmr.070107     Document Type: Article

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