5 Article(s)Download |
PMID | Title | Pub. Year | #Total Relationships |
1 | 31965220 | Congenital Hyperphosphatemic Conditions Caused by the Deficient Activity of FGF23. | 2021 Jan | 1 |
2 | 33685073 | The Successful Treatment of Deep Soft-tissue Calcifications with Topical Sodium Thiosulphate and Acetazolamide in a Boy with Hyperphosphatemic Familial Tumoral Calcinosis due to a Novel Mutation in FGF23 | 2021 Mar 9 | 1 |
3 | 24668887 | Hyperphosphatemic familial tumoral calcinosis: response to acetazolamide and postulated mechanisms. | 2014 Jun | 1 |
4 | 18982401 | A case of familial tumoral calcinosis/hyperostosis-hyperphosphatemia syndrome due to a compound heterozygous mutation in GALNT3 demonstrating new phenotypic features. | 2009 Jul | 1 |
5 | 19188744 | Familial tumoral calcinosis caused by a novel FGF23 mutation: response to induction of tubular renal acidosis with acetazolamide and the non-calcium phosphate binder sevelamer. | 2009 | 1 |