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Article

Oncogenic osteomalacia: is there a new phosphate regulating hormone?

Clinical endocrinology - 1 Dec 1997

Nelson A E, Robinson B G, Mason R S

Abstract excerpt

Oncogenic osteomalacia is a syndrome associated with rare, usually mesenchymal tumours, which is characterized by hypophosphataemia, phosphaturia and low concentrations of 1,25-dihydroxyvitamin D. The reversal of clinical and biochemical abnormalities following removal of the tumour, indicates it is the source of a humoral factor that is responsible for these abnormalities. It has been demonstrated that the...

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Identifiers

PMID: 9497867
DOI: 10.1046/j.1365-2265.1997.3591138.x

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Oncogenic osteomalacia: is there a new phosphate regulating hormone?PMID 9497867Read ↗

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Cloning and sequencing of human PEX from a bone cDNA library: evidence for its developmental stage-specific regulation in osteoblasts.Semantic proximity Read ↗

Coordinated maturational regulation of PHEX and renal phosphate transport inhibitory activity: evidence for the pathophysiological role of PHEX in X-linked hypophosphatemia.Semantic proximity Read ↗

The Autosomal Dominant Hypophosphatemic Rickets (ADHR) Gene Is a Secreted Polypeptide Overexpressed by Tumors that Cause Phosphate WastingSemantic proximity Read ↗

Fibroblast growth factor 23 in oncogenic osteomalacia and X-linked hypophosphatemia.Semantic proximity Read ↗

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