Detalhe da pesquisa
1.
Long-term clinical outcome and phenotypic variability in hyperphosphatemic familial tumoral calcinosis and hyperphosphatemic hyperostosis syndrome caused by a novel GALNT3 mutation; case report and review of the literature.
BMC Genet
; 15: 98, 2014 Sep 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-25249269
2.
Hereditary hypophosphatemia in Norway: a retrospective population-based study of genotypes, phenotypes, and treatment complications.
Eur J Endocrinol
; 174(2): 125-36, 2016 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-26543054
3.
Association between novel indices of malnutrition-inflammation complex syndrome and cardiovascular disease in hemodialysis patients.
Hemodial Int
; 9(2): 159-68, 2005 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-16191065
4.
Exome sequencing reveals FAM20c mutations associated with fibroblast growth factor 23-related hypophosphatemia, dental anomalies, and ectopic calcification.
J Bone Miner Res
; 28(6): 1378-85, 2013 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-23325605