1Rauch F, Travers R, Norman M E, et al. Deficient bone formation in idiopathic juvenile osteoporosis: a histomorphometric study of cancellousbone[J].J Bone Miner Res,2000,15:957 -963.
2Cassidy J T. Osteopenia and osteoporosis in children[J].Clin Exp Rheumatol,1999,17:245 -250.
3Villaverde V, Inocencio J D, Menrino R, et al. Difficulty walking. A presentation of idiopathic juvenile osteoporosis[J].J Rheumat,1998,25:173- 176.
4Rauch F, Travers R, Norman M E, et al.The bone formation defect in idiopathic juvenile osteoporosis is surface specific[J].Bone,2002,31:85 -89.
5Dawson P A, Kelly T E, Marini J C. Extension of pheno type associated with structural mutations in type I collagen: siblings with juvenile osteoporosis have an alpha2(I)Gly436→Arg substitution[J].J Bone Miner Res,1999,14:449 -455.
6Lornc R S. Idiopathic juvenile osteoporosis[J].Calcif Tissue Int,2002,70:395- 397.
7Boot A M, Ridder M, Pols H, et al. Bone mineral density in children and adolescents: Relation to puberty, calcium intake and physical activity[J].J Clin Endocrinol Metab,1997,82:57 -62.
8Allgrove J. Biphosphonates[J].Arch Dis Child,1997,76:73 -75.
9Shaw N J, Boivin C M, Crabtree N J. Intravenous pamidronate in juvenile osteoporosis[J].Arch Dis Child,2000,83:143 -145.
10Bianco P, Robey P G. Disease of bone and the stromal cell lineage[J].J Bone Miner Res,1999,14:336 -341.
4CHEUNG M S,GLORIEUX F H.Osteogenesis Imperfecta:update on presentation and management[J].Rev Endocr Metab Disord,2008,9(2):153-160.
5SILLENCE D O,RIMOIN D L.Classification of osteogenesis imperfect[J].Lancet,1978,1(8072):1041-1042.
6RAUCH F,GLORIEUX F H.Osteogenesis imperfecta[J].Lancet,2004,363(9418):1377-1385.
7CABRAL W A,CHANG W,BARNES A M,et al.Prolyl 3-hydroxylase1deficiency causes a recessive metabolic bone disorder resembling lethal/severe osteogenesis imperfecta[J].Nat Genet,2007,39(3):359-365.
8CHEUNG M S,GLORIEUX F H.Osteogenesis Imperfecta:update on presentation and management[J].Rev Endocr Metab Disord,2008.9(2):153-160.
9KIM H J,RICE D P,KETTUNEN P J,et al.FGF-,BMPand Shh-mediated signalling pathways in the regulation of cranial suture morphogenesis and calvarial bone development[J].Development,1998,125(7):1241-1251.
10MARINI J C,FORLINO A,CABRAL W A,et al.Consortium for osteogenesis imperfecta mutations in the helical domain of type I collagen:regions rich in lethal mutations align with collagen binding sites for integrins and proteoglycans[J].Hum Mutat,2007,28(3):209-221.