Resultats globals: 1 registres trobats en 0.05 segons.
Articles, 1 registres trobats
Articles 1 registres trobats  
1.
11 p, 793.9 KB The international X-linked hypophosphataemia (XLH) registry (NCT03193476) : rationale for and description of an international, observational study / Padidela, Raja (University of Manchester) ; Nilsson, Ola (Örebro University) ; Makitie, Outi (Helsinki University Hospital (Finlàndia)) ; Beck-Nielsen, Signe (Aarhus University Hospital (Aarhus, Dinamarca)) ; Ariceta Iraola, Gema (Hospital Universitari Vall d'Hebron) ; Schnabel, Dirk (University Medicine Berlin) ; Brandi, Maria Luisa (University of Florence) ; Boot, Annemieke (University of Groningen) ; Levtchenko, Elena (University Hospitals Leuven (Bèlgica)) ; Smyth, Michael (Kyowa Kirin International) ; Jandhyala, Ravi (Medialis Ltd (Regne Unit)) ; Mughal, Zulf (University of Manchester)
X-linked hypophosphataemia (XLH) is a rare, hereditary, progressive and lifelong phosphate wasting disorder characterised by pathological elevations in fibroblast growth factor (FGF) 23 concentration and activity; XLH has an incidence of approximately 1 in 20-25,000 individuals. [...]
2020 - 10.1186/s13023-020-01434-4
Orphanet Journal of Rare Diseases, Vol. 15 (june 2020)  

Us interessa rebre alertes sobre nous resultats d'aquesta cerca?
Definiu una alerta personal via correu electrònic o subscribiu-vos al canal RSS.