共 16 条
[1]
Armitage G.C., Development of a Classification System for Periodontal Diseases and Conditions, Ann Periodontol, 4, pp. 1-6, (1999)
[2]
Assadi F., Hypophosphatemia An Evidence-based Problem-Solving Approach to Clinical Cases, Iranian Journal of Kidney Diseases, 4, (2010)
[3]
Farach-Carson M.C., Nemere I., Membrane receptors for vitamin D steroid hormones: potential new drug targets, Curr Drug Targets, 4, pp. 67-76, (2003)
[4]
Feng J.Q., Huang H., Lu Y., Et al., The Dentin matrix protein 1 (Dmp1) is specifically expressed in mineralized, but not soft, tissues during development, J Dent Res, 82, pp. 776-780, (2003)
[5]
Feng J.Q., Ward L.M., Liu S., Et al., Loss of DMP1 causes rickets and osteomalacia and identifies a role for osteocytes in mineral metabolism, Nat Genet, 38, pp. 1310-1315, (2006)
[6]
Goodman J.R., Gelbier M.J., Bennett J.H., Winter G.B., Dental problems associated with hypophosphataemic vitamin D resistant rickets, Int J Pediatr Dent, 8, pp. 19-28, (1998)
[7]
Ji-Mei S.U., Yun L.I., Xiao-Wei Y.E., Zhi-Fang W.U., Oral findings of hypophosphatemic vitamin D-resistant rickets: report of two cases Chin Med J, 120, pp. 1468-1470, (2007)
[8]
Lorenz-Depiereux B., Bastepe M., Benet-Pages A., Et al., DMP1 mutations in autosomal recessive hypophosphatemia implicate a bone matrix protein in the regulation of Phosphate homeostasis, Nat Genet, 38, pp. 1248-1250, (2006)
[9]
Lorenz-Depiereux B., Schnabel D., Tiosano D., Hausler G., Strom T., Loss-of-Function ENPP1 Mutations Cause Both Generalized Arterial Calcification of Infancy and Autosomal-Recessive Hypophosphatemic Rickets, Am J Hum Genet., 86, 2, pp. 267-272, (2010)
[10]
Negri A.L., Hereditary hypophosphatemias: New genes in the bone-kidney axis, Journal Asian Pacific Society of Nephrology, 12, pp. 317-320, (2007)