von Willebrand disease type 2N: Uncovering a congenital bleeding disorder in a patient with hepatitis C, cirrhosis, and coagulopathy†

Andrew A. Lane; Elizabeth M. Van Cott; Bimalangshu R. Dey

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von Willebrand disease type 2N: Uncovering a congenital bleeding disorder in a patient with hepatitis C, cirrhosis, and coagulopathy†

机译：von Willebrand 2N型疾病：发现患有丙型肝炎，肝硬化和凝血病的先天性出血疾病†

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《AMERICAN JOURNAL OF HEMATOLOGY》 |2010年第2期|p.134-135|共2页
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Andrew A. Lane; Elizabeth M. Van Cott; Bimalangshu R. Dey;
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Department of Medicine, Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, Massachusetts;

Department of Pathology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts;

Department of Medicine, Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, Massachusetts;

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1. von Willebrand disease type 2N: uncovering a congenital bleeding disorder in a patient with hepatitis C, cirrhosis, and coagulopathy. [J] . Lane AA, Van Cott EM, Dey BR American Journal of Hematology . 2010,第2期

机译：von Willebrand 2N型疾病：发现丙型肝炎，肝硬化和凝血病患者先天性出血性疾病。
2. Similarity in joint and mucous bleeding syndromes in type 2N von Willebrand disease and severe hemophilia A coexisting with type 1 von Willebrand disease in two Chinese pedigrees. [J] . H H Qin, Z F Xing, X F Wang, Blood cells, molecules and diseases . 2014,第4期

机译：在两个中国谱系中，2N型von Willebrand病和严重血友病A与1型von Willebrand病并存的关节和粘液出血综合征相似。
3. Life-threatening bleeding in a patient with mild hemophilia A and heterozygosity for von Willebrand disease Type 2N [J] . Allan John N., Friedman Kenneth D., DeSancho Maria T. International journal of hematology . 2014,第6期

机译：A型轻度血友病和2N型von Willebrand病杂合性患者的危及生命的出血
4. Preoperative DDAVP-Testing in Patients with von Willebrand Disease [C] . H.-H. Wolf, K.Jordan, A.Fruhauf Hemophilia Symposium . 2008

机译：von Willebrand疾病患者的术前DDAVP测试
5. Are hemophilia and von Willebrands patients being adequately protected from hepatitis A and B? [D] . Wood, Jerri L. 2006

机译：血友病患者和von Willebrands患者是否得到充分的甲型和乙型肝炎保护？
6. Effect of Genetic Variation in STXBP5 and STX2 on von Willebrand Factor and Bleeding Phenotype in Type 1 von Willebrand Disease Patients [O] . Janine E. van Loon, Yvonne V. Sanders, Eva M. de Wee, 2009

机译：STXBP5和STX2遗传变异对1型von Willebrand病患者von Willebrand因子和出血表型的影响
7. Recombinant von Willebrand factor for severe gastrointestinal bleeding unresponsive to other treatments in a patient with type 2A von Willebrand disease [O] . Racquel Brown 2017

机译：重组von Willebrand因子对患者2A von Willebrand疾病的患者的其他治疗无响应胃肠道

von Willebrand disease type 2N: Uncovering a congenital bleeding disorder in a patient with hepatitis C, cirrhosis, and coagulopathy†

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