about
Inherited ADAMTS13 deficiency (Upshaw-Schulman syndrome): a short review.Autosomal dominant C1149R von Willebrand disease: phenotypic findings and their implications.Von Willebrand factor/factor VIII concentrates in the treatment of von Willebrand disease.Diagnosis of inherited von Willebrand disease: comparison of two methodologies and analysis of the discrepancies.A novel mutation in ADAMTS13 of a child with Upshaw-Schulman SyndromeType 2M von Willebrand disease: a variant of type 2A?Diagnosis and management of von Willebrand disease in SpainAcquired von Willebrand syndrome and mitral valve prosthesis leakage. A pilot study
P50
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P50
description
investigador
@es
researcher
@en
wetenschapper
@nl
name
A Pérez-Rodríguez
@en
A Pérez-Rodríguez
@nl
type
label
A Pérez-Rodríguez
@en
A Pérez-Rodríguez
@nl
prefLabel
A Pérez-Rodríguez
@en
A Pérez-Rodríguez
@nl
P31
P496
0000-0001-5856-005X