Prophylaxis in rare coagulation disorders-factor X deficiency

Thrombosis Research

Volumn 118, Issue SUPPL. 1, 2006, Pages

  Auerswald, G ^a  

^a KLINIKUM BREMEN MITTE   (Germany)

Author keywords

Coagulation; Factor X deficiency; Haemorrhage; Prophylaxis

Indexed keywords

BLOOD CLOTTING FACTOR 10; BLOOD CLOTTING FACTOR 9 CONCENTRATE; FIX HS; PROTEINASE; PROTHROMBIN COMPLEX; VITAMIN K GROUP;

ARTICLE; BLEEDING DISORDER; BLOOD CLOTTING; BLOOD CLOTTING DISORDER; BLOOD CLOTTING FACTOR 10 DEFICIENCY; DISEASE SEVERITY; DNA POLYMORPHISM; ERYTHROCYTE TRANSFUSION; GENE MUTATION; HUMAN; MENORRHAGIA; PHENOTYPE; POSTOPERATIVE HEMORRHAGE; PRIORITY JOURNAL; PROPHYLAXIS; REGISTER; SURGICAL TECHNIQUE; THROMBOEMBOLISM;

ADOLESCENT; ADULT; BLOOD COAGULATION DISORDERS; CHILD; CHILD, PRESCHOOL; FACTOR X DEFICIENCY; FEMALE; HEMORRHAGE; HUMANS; MALE; PREMEDICATION; REGISTRIES;

EID: 33646032774     PISSN: 00493848     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.thromres.2006.01.015     Document Type: Article

References (3)

1. Uprichard J., and Perry D.J. Factor X deficiency. Blood Rev 16 (2002) 97-110
2. Herrmann F.H., Wulff K., Lopaciuk S., and Pollmann H. Two novel Factor X gene mutations in severe Factor X deficiency-Greifswald Registry of Factor X deficiency. Thromb Haemost 1 S1 (2001) [Abstract P1126]
3. Wulff K., and Herrmann F.H. Molecular genetic analysis in the Factor X gene in patients with congenital FX deficiency. J Thromb Haemost 1 S1 (2003) [Abstract P1201]