000 01693 a2200481 4500
005 20250515173714.0
264 0 _c20090706
008 200907s 0 0 eng d
022 _a1421-9662
024 7 _a10.1159/000214856
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aMichiels, Jan Jacques
245 0 0 _aDominant von Willebrand disease type 2A groups I and II due to missense mutations in the A2 domain of the von Willebrand factor gene: diagnosis and management.
_h[electronic resource]
260 _bActa haematologica
_c2009
300 _a154-66 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article; Review
650 0 4 _aADAM Proteins
_xmetabolism
650 0 4 _aADAMTS13 Protein
650 0 4 _aAdult
650 0 4 _aAged
650 0 4 _aBleeding Time
650 0 4 _aBlood Protein Electrophoresis
650 0 4 _aCollagen
_xmetabolism
650 0 4 _aDeamino Arginine Vasopressin
_xtherapeutic use
650 0 4 _aExons
_xgenetics
650 0 4 _aFemale
650 0 4 _aHemorrhage
_xetiology
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMiddle Aged
650 0 4 _aMolecular Weight
650 0 4 _aMutation, Missense
650 0 4 _aPlatelet Aggregation
_xdrug effects
650 0 4 _aPregnancy
650 0 4 _aPregnancy Complications, Hematologic
_xblood
650 0 4 _aProtein Structure, Quaternary
650 0 4 _aProtein Structure, Tertiary
650 0 4 _avon Willebrand Diseases
_xclassification
650 0 4 _avon Willebrand Factor
_xanalysis
700 1 _avan Vliet, Huub H D M
773 0 _tActa haematologica
_gvol. 121
_gno. 2-3
_gp. 154-66
856 4 0 _uhttps://doi.org/10.1159/000214856
_zAvailable from publisher's website
999 _c18929823
_d18929823