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Gaucher disease demonstrated by bone scintigraphy: report of one case |
The Third Hospital, Hebei Medical University, Shijiazhuang 050051, China |
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Received: 08 February 2018
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[1]中华医学会儿科学分会遗传代谢内分泌学组,中华医学会儿科学分会血液学组,中华医学会血液学分会红细胞疾病(贫血)学组. 中国戈谢病诊治专家共识(2015)[J]. 中华儿科杂志,2015,53(4):256-261.
[2]Msrtins AM, Valadares ER, Porta G, et al. Recommendations on diagnosis, treatment, and monitoring for Garcher disease[J]. J Pediatr, 2009, 155(4 Suppl): S10-S18.
[3]刘婕,李小松. 高雪氏病[J]. 实用儿科临床杂志,1998,13(2):174.
[4]Kaplan P, Andersson HC, Kacena KA, et al. The clinical and demographic acteristics of nonneuronopathic Gaucher disease in 887 children at diagnosis[J]. Arch Pediatr Adolesc Med, 2006, 160(6): 603-608.
[5]Israel O, Jerushalmi J. Scintigraphic findings in Gaucher’s disease[J]. J Nucl Med, 1986, 27(6): 1557-1563.
[6]Mass M, Van Kuijk C, Stoker J, et al. Quantification of bone involvement in Gaucher disease; MR imaging bone marrow burden score as an alternative to Dixon quantitative chemical shift MR imaging-initial experience[J]. Radiology, 2003, 229(2): 554-561. |
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