Pregnancy and delivery in patients with homozygous or heterozygous R854Q type 2N von Willebrand disease [4]

Journal of Thrombosis and Haemostasis

Volumn 3, Issue 2, 2005, Pages 391-392

  Castaman, Giancarlo ^a   Bertoncello, K ^a   Bernardi, M ^a   Rodeghiero, F ^a  

^a SAN BORTOLO HOSPITAL   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

VON WILLEBRAND FACTOR; BLOOD CLOTTING FACTOR 8;

DELIVERY; GENE MUTATION; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; LETTER; PREGNANCY; PRIORITY JOURNAL; VON WILLEBRAND DISEASE; BLOOD; CASE REPORT; FEMALE; GENETICS; HETEROZYGOTE; HOMOZYGOTE; MISSENSE MUTATION; PREGNANCY COMPLICATION;

DELIVERY, OBSTETRIC; FACTOR VIII; FEMALE; HETEROZYGOTE; HOMOZYGOTE; HUMANS; MUTATION, MISSENSE; PREGNANCY; PREGNANCY COMPLICATIONS, HEMATOLOGIC; VON WILLEBRAND DISEASE; VON WILLEBRAND FACTOR;

EID: 20844452746     PISSN: 15387933     EISSN: 15387836     Source Type: Journal    
DOI: 10.1111/j.1538-7836.2005.01162.x     Document Type: Letter

References (8)

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3. Castaman G, Novella E, Contino L, Demicheli M, Rodeghiero F. First Italian families with homozygous R854Q type 2N von Willebrand disease. Thromb Haemost 2002; 88: 534-5.
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7. Lopez-Fernandez MF, Blanco-Lopez MJ, Castineira MP, Batlle J. Further evidence for recessive inheritance of von Willebrand disease with abnormal binding of von Willebrand factor to factor VIII. Am J Hematol 1992; 40: 20-7.
8. Federici AB, Mazurier C, Berntorp E, Lee CA, Scharrer I, Goudemand J, Lethagen S, Nitu I, Ludwig G, Hilbert L, Mannucci PM. Biologic response to desmopressin in patients with severe type 1 and type 2 von Willebrand disease: results of a multicenter European study. Blood 2004; 103: 2032-8.