Intermittent thrombocytopenia as a manifestation of Von Willebrand's disease;Intermitterende trombocytopenie als uiting van de ziekte van Von Willebrand

Nederlands Tijdschrift voor Geneeskunde

Volumn 146, Issue 25, 2002, Pages 1192-1195

  Gomez Garcia E B ^a   Brouwers, G J ^a   Kappers Klunne, M C ^a   Leebeek, F W G ^a   Van Vliet, H H D M ^a  

^a ERASMUS MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

DESMOPRESSIN; PREDNISONE; RISTOCETIN;

ADULT; ARTICLE; BLEEDING; CASE REPORT; CLINICAL FEATURE; DIAGNOSTIC ERROR; DIAGNOSTIC TEST; FEMALE; GENE MUTATION; GENETIC ANALYSIS; HUMAN; HUMAN CELL; IDIOPATHIC THROMBOCYTOPENIC PURPURA; MALE; SPLENECTOMY; THROMBOCYTE AGGLUTINATION; THROMBOCYTOPENIA; VON WILLEBRAND DISEASE;

ADULT; AGGLUTINATION TESTS; DIAGNOSIS, DIFFERENTIAL; FEMALE; HUMANS; MALE; MIDDLE AGED; THROMBOCYTOPENIA; VON WILLEBRAND DISEASE; VON WILLEBRAND FACTOR;

EID: 0037157527     PISSN: 00282162     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (8)

1. Impact, diagnosis and treatment of von Wille-brand disease
2. Heightened interaction between platelets and factor VIII/von Willebrand factor in a new subtype of von Willebrand's disease
3. Van gen naar ziekte; van mutaties in het Von Willebrand-factorgen naar hemorragische diathese en trombocytopenie
4. 578 of von Willebrand factor (vWF) differentially affects vWF interaction with platelets
5. A type 2b von Willebrand disease mutation (Ile546→Val) associated with an unusual phenotype
6. Von Willebrand's disease characterized by increased ristocetin sensitivity and the presence of all von Willebrand factor multimers in plasma
7. Von Willebrand factor mutation enhancing interaction with platelets in patients with normal multimeric structure
8. A new von Willebrand variant (type I, New York): Increased ristocetin-induced platelet aggregation and plasma von Willebrand factor containing the full range of multimers