A commercial elisa method for identifying type 2N von Willebrand disease patients and carriers

被引：0
|
作者：
Casonato, A. [1 ]
Pontara, E. [1 ]
Sartorello, F. [1 ]
Cattini, M. G. [1 ]
Daidone, V [1 ]
Casonato, A. [1 ]
机构：
[1] Univ Padua, Sch Med, Dept Cardiol Thorac & Vasc Sci, I-35100 Padua, Italy
来源：
JOURNAL OF THROMBOSIS AND HAEMOSTASIS | 2011年 / 9卷
关键词：
D O I：
暂无
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
P-TH-569
引用
收藏
页码：946 / 946
页数：1
相关论文
共 50 条
  • [41] Management of pregnancy complications in type 2N von Willebrand disease associated to a novel mutation
    Brennan, Y.
    Favaloro, E. J.
    Curtin, J.
    Curnow, J.
    HAEMOPHILIA, 2018, 24 (03) : E148 - E152
  • [42] Identifying type Vicenza von Willebrand disease
    Casonato, A
    Pontara, E
    Sartorello, F
    Cattini, MG
    Gallinaro, L
    Bertomoro, A
    Rosato, A
    Padrini, R
    Pagnan, A
    JOURNAL OF LABORATORY AND CLINICAL MEDICINE, 2006, 147 (02): : 96 - 102
  • [43] Compound heterozygosity for type 2N and type 1 von Willebrand disease (VWD) associated with a homozygous-like type 2N VWD phenotype
    Chan, J
    Mitchell, MJ
    Brown, DA
    Bromidge, ES
    Williams, C
    Smith, MP
    Savidge, GF
    THROMBOSIS AND HAEMOSTASIS, 1999, : 558 - 558
  • [44] Pregnancy and delivery in patients with homozygous or heterozygous R854Q type 2N von Willebrand disease
    Castaman, G
    Bertoncello, K
    Bernardi, M
    Rodeghiero, F
    JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2005, 3 (02) : 391 - 392
  • [45] Von Willebrand Disease Type1/Type 2N Compound Heterozygotes: Diagnostic and Management Challenges
    Botero, J. Perez
    Pruthi, R.
    Nichols, W.
    Patnaik, M.
    HAEMOPHILIA, 2015, 21 (03) : E271 - E271
  • [46] von Willebrand disease type1/type 2N compound heterozygotes: diagnostic and management challenges
    Botero, Juliana Perez
    Pruthi, Rajiv K.
    Nichols, William L.
    Ashrani, Aneel A.
    Patnaik, Mrinal M.
    BRITISH JOURNAL OF HAEMATOLOGY, 2017, 176 (06) : 994 - 997
  • [47] THE VON WILLEBRAND DISEASE TYPE 2A (IIH): A UNIQUE VARIANT OF VON WILLEBRAND FACTOR DUE TO COMBINED 2A(IIC)/2N DEFECTS
    Punzo, M.
    La Marca, S.
    Rubini, V
    Cozzi, G.
    Canciani, M. T.
    Baronciani, L.
    Mannucci, P. M.
    Federici, A. B.
    HAEMATOLOGICA, 2008, 93 : S115 - S115
  • [48] Segregation of type 1, type 3, and type 2N von Willebrand disease in three generations of an affected family
    Guilliatt, A. M.
    Theophilus, B. D. M.
    Enayat, M. S.
    Williams, M. D.
    JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2009, 7 : 528 - 528
  • [49] Segregation of type 1, type 3, and type 2N von Willebrand disease in three generations of an affected family
    Guilliatt, A. M.
    Theophilus, B. D. M.
    Enayat, M. S.
    Williams, M. D.
    BRITISH JOURNAL OF HAEMATOLOGY, 2009, 145 : 28 - 29
  • [50] 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
    Qin, H. H.
    Xing, Z. F.
    Wang, X. F.
    Ding, Q. L.
    Xi, X. D.
    Wang, H. L.
    BLOOD CELLS MOLECULES AND DISEASES, 2014, 52 (04) : 181 - 185
12345