期刊文献+

Calvarial defects and Dandy-Walker malformation in association withneurofibromatosis type 1

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摘要 Neurofibromatosis type 1(NF1)is an autosomal dominant disorder in which the nerve tissue grows tumors that may be benign and may cause serious damage by compressing nerves and other tissues.The NF1 gene
出处 《Chinese Medical Journal》 SCIE CAS CSCD 2014年第6期1187-1188,共2页 中华医学杂志(英文版)
基金 This study was supported by grants from National Natural Science Foundation of China (No. 81071215), Natural Science Foundation of Heilongjiang Province of China (No. D201062), Foreign Collaboration Project of Heilongjiang Province (No. WB10B104), and Science Foundation of the First Affiliated Hospital of Harbin Medical University (No. 2011BS13 ).
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  • 1Arrington DK, Danehy AR, Peleggi A, Proctor MR, Irons MB, Ullrich NJ. Calvarial detects and skeletal dysplasia in patients with neurofibromatosis type 1. J Neurosurg Pediatr 2013; 11: 410-416.
  • 2Mislow JM, Proctor MR, Mcneely PD, Greene AK, Rogers GE Calvarial del;ects associated with neurofibromatosis type I. Report of two cases. J Neurosurg 2007; 106 (6 Suppl): 484-489.
  • 3Brunetti-Pierri N, Doty SB, Hicks J, Phan K, Mendoza-Londono R, Blazo M, et al. Generalized metabolic bone disease in neurofibromatosis type I. Mol Genet Metab 2008, 94: 105-111.
  • 4Heerva E, Alanne MH, Peltonen S, Kuorilehto T, Hentnnen T, Vaananen K, et al. Osteoclasts in neurofibromatosis type 1 display enhanced resorption capacity, aberrant morphology, and resistance to serum deprivation. Bone 2010; 47: 583-590.

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