The spectrum of von Willebrand's disease revisited

E. J. Bowie, D. N. Fass, J. D. Olson, C. A. Owen

Resultado de la investigación: Review articlerevisión exhaustiva

Resumen

The authors examined nine patients with presumed von Willebrand's disease who present the spectrum of that disorder. Two had findings that would be accepted generally as diagnostic of von Willebrand's disease, and seven had variations of the usual pattern. The commonest variation was the combination of borderline and variable levels of coagulant Factor VIII, commensurate levels of Factor VIII related antigen, and low levels of ristocetin Willebrand factor.

Idioma originalEnglish (US)
Páginas (desde-hasta)35-41
Número de páginas7
PublicaciónMayo Clinic Proceedings
Volumen51
N.º1
EstadoPublished - dic 1 1976

ASJC Scopus subject areas

  • Medicine(all)

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