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镰状细胞病的研究进展 被引量:8

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作者 杨方源 孟文
机构地区 桂林医学院附院
出处 《中国小儿血液》 2004年第5期235-238,共4页 China Child Blood
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  • 1应小燕.妊娠合并镰状细胞贫血疼痛型危象17例分析[J].中华妇产科杂志,1999,34(7):429-430. 被引量:4
  • 2Missenecek, Memanus C, Fuggle P, et al. Psychological adjustment and family functioning in a group of British children with Sickle Cell disease; Preliminary empirical findings and a meta analysis. Br J Clin Psychol, 1996;35(3) :439.
  • 3Chang, J.C. Xnei Wei Kam. Diagnosis of the Sickle Cell anemia. By direct analysis of sickle mutation. Lancet, 1987:21:1127.
  • 4Plaatt OS, Thorington BD, Brambilla DJ. Pain in Sickle Cell diseade. N EnglJ Med, 1997:350.
  • 5Ballas SK. The Sickle Cell painfull crisis in adults. Hemoglobin, 1995; 19(6) :323.
  • 6Hebbel RP, Vercellotti GM. The endothelial biology of sickle cell disease. J Lab Med, 1979;129:288.
  • 7Ohene Frempong K, Steven J, Lyma W. Cerebrovascular accidents in Sickle Cell disease Rate and risk factor. Blood,1998;91(1) :288.
  • 8Van den Berg M, Boers GHj, Frankem. DG, et al. Hypenrhomocystinanemia and endothelial dysfunction in young patiens with peripheral arterial occlusive disease. Eur J Clin Invest Blood,1996;87:77.
  • 9Sprinkle R H. The American joural of pediatrie Hematology.1986;8(2) :337.
  • 10Wocters HJ, Ten cate H, Thomas LLM, et al. Low- intensity oral anticoagulation in sickle cell disease rever ses the prethrombotic state: promise for treatment. Br J Haematol Blood, 1996;87:771.

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