Factor X deficiency and intracranial bleeding: Who is at risk?

Haemophilia

Volumn 17, Issue 5, 2011, Pages 759-763

  Rauch, R ^a,b   Girisch, M ^b   Wiegand, G ^b   Schroeder, W ^c   Hofbeck, M ^b   Welisch, E ^a   Wulff, K ^c  

^a UNIVERSITY OF WESTERN ONTARIO   (Canada)

^b University Hospital for Children and Adolescents   (Germany)

^c UNIVERSITY OF GREIFSWALD   (Germany)

Author keywords

Children; Factor X deficiency; Gene analysis; Intracranial bleeding

Indexed keywords

BLOOD CLOTTING FACTOR 10; FRESH FROZEN PLASMA; FX P BEHRING; UNCLASSIFIED DRUG;

ARTICLE; BLEEDING; BLOOD CLOTTING FACTOR 10 DEFICIENCY; BLOOD TRANSFUSION; BRAIN HEMORRHAGE; BRAIN HERNIA; CASE REPORT; CONSANGUINEOUS MARRIAGE; CRANIOTOMY; DISEASE SEVERITY; EXON; FAMILY HISTORY; FOLLOW UP; GASTROINTESTINAL HEMORRHAGE; GENE MUTATION; GENE SEQUENCE; GENOTYPE; HETEROZYGOSITY; HIGH RISK PATIENT; HOMOZYGOSITY; HUMAN; INFANT; INTERNATIONAL NORMALIZED RATIO; IRAN; MALE; MISSENSE MUTATION; NUCLEOTIDE SEQUENCE; PARTIAL THROMBOPLASTIN TIME; POSTNATAL CARE; PRIORITY JOURNAL; SUBSTITUTION THERAPY;

CONSANGUINITY; DNA MUTATIONAL ANALYSIS; EXONS; FACTOR X; FACTOR X DEFICIENCY; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HUMANS; INFANT; INTRACRANIAL HEMORRHAGES; IRAN; MALE; MUTATION;

EID: 80052029200     PISSN: 13518216     EISSN: 13652516     Source Type: Journal    
DOI: 10.1111/j.1365-2516.2011.02591.x     Document Type: Article

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