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Defining the boundaries of normal thrombin generation: investigations into hemostasisInherited disorders of blood coagulation.Congenital factor II deficiency: moroccan cases.Prophylactic administration of prothrombin complex concentrates for congenital prothrombin deficiency with a novel frameshift mutation, prothrombin saitama.Coagulation factor activity and clinical bleeding severity in rare bleeding disorders: results from the European Network of Rare Bleeding Disorders.Phenotypic and genetic analysis of dysprothrombinemia due to a novel homozygous mutation.Bleeding manifestations in heterozygotes with congenital FVII deficiency: a comparison with unaffected family members during a long observation period.Congenital prothrombin defects: they are not only associated with bleeding but also with thrombosis: a new classification is needed.Molecular assessment of some cardiovascular genetic risk factors among Iraqi patients with ischemic heart diseases.Rare congenital bleeding disorders
P2860
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P2860
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on June 2009
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Congenital prothrombin deficiency.
@en
Congenital prothrombin deficiency.
@nl
type
label
Congenital prothrombin deficiency.
@en
Congenital prothrombin deficiency.
@nl
prefLabel
Congenital prothrombin deficiency.
@en
Congenital prothrombin deficiency.
@nl
P356
P1476
Congenital prothrombin deficiency.
@en
P2093
Raimondo De Cristofaro
Stefano Lancellotti
P304
P356
10.1055/S-0029-1225759
P577
2009-06-01T00:00:00Z