Qualitative Research to Explore the Patient Experience of X-Linked Hypophosphatemia and Evaluate the Suitability of the BPI-SF and WOMAC® as Clinical Trial End Points.
Theodore-Oklota, Christina; Bonner, Nicola; Spencer, Holly; Arbuckle, Rob; Chen, Chao-Yin; Skrinar, Alison.
; 21(8): 973-983, 2018 08.
Artigo em Inglês | MEDLINE | ID: mdl-30098676
CRISPR/Cas9-mediated mutation of PHEX in rabbit recapitulates human X-linked hypophosphatemia (XLH).
A radiological study on intra- and extra-cranial calcifications in adults with X-linked hypophosphatemia and associations with other mineralizing enthesopathies and childhood medical treatment.
Contemporary Medical and Surgical Management of X-linked Hypophosphatemic Rickets.
Results of deformity correction in children with X-linked hereditary hypophosphatemic rickets by external fixation or combined technique.
[Vitamin D dependency and its treatment].
Hypophosphatemic rickets and osteomalacia.
[Novel PHEX gene mutations in patients with X-linked hypophosphatemic rickets: an analysis of 2 cases].
The expanding family of hypophosphatemic syndromes.
Evaluation of bone mineral density and microarchitectural parameters by DXA and HR-pQCT in 37 children and adults with X-linked hypophosphatemic rickets.
Hypophosphatemic rickets: unraveling the role of FGF23.