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遗传性球形红细胞增多症一例报告 被引量:1

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出处 《第二军医大学学报》 CAS CSCD 北大核心 2002年第3期253-253,共1页 Academic Journal of Second Military Medical University
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同被引文献14

  • 1古健,朱康儿.造血干细胞移植治疗重型地中海贫血[J].国外医学(输血及血液学分册),2005,28(2):162-165. 被引量:2
  • 2Peker S,Akar N,Demiralp D O.Proteomic identification of erythrocyte membrane protein deficiency in hereditary spherocytosis[J].Mol Bio Rep,2012,39(3):3161-3167.
  • 3Bolton Maggs P H,Langer J C,Iolascon A,et al.Guidelines for the diagnosis and management of hereditary spherocytosis:2011 update[J].Br J Haematol,2012,156(1):37-49.
  • 4Bader Meunier B,Gauthier F,Archambaud F,et al.Long-term evaluation of the beneficial effect of subtotal splenectomy for management of hereditary spherocytosis.[J].Blood,2001,97(2):399-403.
  • 5Kimura F,Ito H,Shimizu H,et al.Partial splenic embolization for the treatment of hereditary spherocytosis[J].AJRAmJ Roentgenol,2003,181(4):1021-1024.
  • 6Chen W,Zhang X,Shang X,et al.The molecular basis of beta-thalassemia intermedia in southern China:genotypic heterogeneity and phenotypic diversity[J]BMC Med Genet,2010,11:31.
  • 7Puthenveetil G,Scholes J,Carbonell D,et al.Successful correction of the human beta-thalassemia major phenotype using a lentiviral vector[J].Blood,2004,104(12):3445-3453.
  • 8Akar N,Gokce H.Red blood cell indexes in patients in patients with hereditary spherocytosis and beta-thalassemia combination[J].Pediatr Hematol Oncol,2002,19(8):569-573.
  • 9黄,高兴华,郭柳薇,李颖莉,李雪兰,陈萍.MCV、EOFT及Hb电泳联合检测在地中海贫血筛查中的价值[J].山东医药,2009,49(35):89-90. 被引量:6
  • 10卢新天.遗传性球形红细胞增多症发病机制、诊断及治疗进展[J].中国小儿血液与肿瘤杂志,2009,14(6):243-245. 被引量:7

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