Growth in X-linked hypophosphatemic rickets

G Ariceta, CB Langman - European journal of pediatrics, 2007 - Springer
Growth failure appears frequently in children with X-linked hypophosphatemic rickets
(XLHR) due to hypophosphatemia, disease severity, body disproportion, and primary bone …

[PDF][PDF] PHEX gene mutations and genotype-phenotype analysis of Korean patients with hypophosphatemic rickets

HR Song, JW Park, DY Cho, JH Yang… - Journal of Korean …, 2007 - synapse.koreamed.org
Familial hypophosphatemic rickets (FHR) is defined as a group of disorders caused by a
defect in renal phosphate transport, leading to phosphate wasting and hypophosphatemia …

Three Novel Mutations of the PHEX Gene in Three Chinese Families with X-linked Dominant Hypophosphatemic Rickets

W Xia, X Meng, Y Jiang, M Li, X Xing, L Pang… - Calcified Tissue …, 2007 - Springer
X-linked dominant hypophosphatemia (XLH, OMIM307800), the most prevalent form of
inherited rickets in humans, is a dominant disorder of phosphate homeostasis characterized …

Novel PHEX mutation associated with hypophosphatemic rickets

KM Roetzer, F Varga, E Zwettler… - Nephron …, 2007 - karger.com
Background: X-linked hypophosphatemia (XLH) is the most prevalent heritable form of
rickets. It is a dominantly inherited disorder, characterized by renal phosphate wasting …

[PDF][PDF] Growth failure associated with skeletal disorders

MG Vogiatzi, K Lin-Su - 2007 - endotext.org
Skeletal disorders are a heterogeneous group of disorders, which result in disproportionate
short stature. In an attempt to develop uniformity, an international nomenclature and …

[引用][C] 细胞外基质磷酸化糖蛋白的研究现状

韦曦, 刘路, 凌均棨 - 国际口腔医学杂志, 2007