Molecular pathogenesis of hypophosphatemic rickets
SM Jan De Beur, MA Levine - The Journal of Clinical …, 2002 - academic.oup.com
The past several years have brought dramatic advances in our understanding of the
molecular and biochemical bases of inherited and acquired hypophosphatemic disorders. In …
molecular and biochemical bases of inherited and acquired hypophosphatemic disorders. In …
Overexpression of Phex in osteoblasts fails to rescue the Hyp mouse phenotype
S Liu, R Guo, Q Tu, LD Quarles - Journal of Biological Chemistry, 2002 - ASBMB
Inactivating mutations of Phex, a phosphate-regulating endopeptidase, cause
hypophosphatemia and impaired mineralization in X-linked hypophosphatemia (XLH) and …
hypophosphatemia and impaired mineralization in X-linked hypophosphatemia (XLH) and …
Heritable forms of rickets and osteomalacia
MP Whyte - Connective Tissue and Its Heritable Disorders …, 2002 - Wiley Online Library
Rickets and osteomalacia are generic terms for the clinical consequences of impaired
mineralization of skeletal matrix in the pediatric and adult populations, respectively. In this …
mineralization of skeletal matrix in the pediatric and adult populations, respectively. In this …
Nutritional support and management of musculoskeletal diseases
MJ Favus, TO Utset, C Lee - Nutritional Aspects and Clinical …, 2002 - taylorfrancis.com
Musculoskeletal diseases are common chronic disorders that affect children and adults in
North America. This chapter reviews the common metabolic bone and joint disorders with …
North America. This chapter reviews the common metabolic bone and joint disorders with …
A rare rickets case: hypophosphatemic rickets
GÖK Faysal, S KALMAN - Gülhane Tip Dergisi, 2002 - search.proquest.com
Rickets, though a metabolic disorder seen especially as a result of exogenous vitamin D
deficiency, is a childhood disease whose frequency of occurrence has gradually diminished …
deficiency, is a childhood disease whose frequency of occurrence has gradually diminished …