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脾切除治疗遗传性球形红细胞增多症17例 被引量:2

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作者 李磊 贾新建
机构地区 西安市儿童医院
出处 《陕西医学杂志》 CAS 2010年第10期1392-1393,共2页 Shaanxi Medical Journal
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参考文献3

  • 1瞿全.部分血液病脾切除指征及有关问题[J].实用外科杂志,1992,12(10):515-518. 被引量:10
  • 2赵新民.遗传性球形红细胞增多症50例脾切除术后的疗效观察[J].中华儿科杂志,1986,24(5):266-266.
  • 3夏惠生,主编.现代脾脏外科学[M].南京:江苏科技出版社,1990,263~264

共引文献12

同被引文献32

  • 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
  • 2张之南.血液病学[M].北京:人民卫生出版社,2003.1101-1106.
  • 3A Iolascon, RA Avvisati, C Piscopo. Hereditary spherocytosis [ J ]. Transfusion Clinique et Biologique, 2010, 17 (3) : 135-142.
  • 4Jean Delaunay. The molecular basis of hereditary red cell membrane disorders [J]. Blood Reviews, 2007, 21 ( 1 ) : 1-20.
  • 5Silverio Perrotta, Patrick G Gallagher, Narla Mohandas. Hereditary spherocytosis [ J]. Lancet, 2008, 372 (9647) : 1411- 1426.
  • 6Rosalind C Williamson, Ashley M Toye. Glycophorin A: Band 3aid [ J ]. Blood Cells, Molecules and Diseases, 2008, 41 (1) : 35- 43.
  • 7Vann Bennett, Jane Healy. Organizing the fluid membrane bilayer: diseases linked to spectrin and ankyrin [ J ]. Trends in Molecular Medicine, 2008, 14 ( 1 ) : 28-36.
  • 8Jose Sangerman, Yelena Maksimova, E Jennifer Edelman, et al. Ankyrin-linked hereditary spherocytosis in an African-American kindred [J]. American Journal of Hematology, 2008, 83 (10) : 789-794.
  • 9Edelmane J, Maksimova Y, Duru F, et al. A complex splicing defect associated with homozygous ankyrin-deficient hereditary spherocytosis [ J ~. Blood, 2007, 109 (12) : 5491-5493.
  • 10Garbarz M, Galand C, Bibas D, et al. A 5' splice region G→C mutation in exon 3 of the human beta-spectrin gene leads to decreased levels of beta-spectrin mRNA and is responsible for dominant hereditary spherocytosis (spectrin Guemene-Penfao ) [J]. Br J Haematol, 1998, 100(1) : 90-98.

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