Article
A new variant of von Willebrand's disease (type I Padua): doublet-organized plasma von Willebrand factor oligomers in the presence of all size multimers.
Haematologia - 1 Jan 1994
Casonato A, Pontara E, Dannhäuser D, Bertomoro A, Sartori M T, Girolami A
Abstract excerpt
Type I von Willebrand's disease (vWd) is characterized by a concomitant decrease in plasma of von Willebrand factor antigen (vWf:Ag) and vWf ristocetin cofactor activity (vWf:RCoF), associated with the presence of all-size multimers. As a rule, there is no evidence of intrinsic abnormality in vWf...
Topics
- Adult
- Child, Preschool
- Deamino Arginine Vasopressin
- Electrophoresis, Polyacrylamide Gel
- Factor VIII
- Family Health
- Female
- Genetic Variation
- Hemostasis
- Humans
- Male
- Middle Aged
- Pedigree
- Peptide Fragments
- von Willebrand Diseases
- von Willebrand Factor