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Mechanisms of fibrin polymerization and clinical implicationsLoss of fibrinogen in zebrafish results in symptoms consistent with human hypofibrinogenemiaDiagnosis and Treatment of von Willebrand Disease and Rare Bleeding DisordersThrombosis in Inherited Fibrinogen Disorders.Severe bleeding in a woman heterozygous for the fibrinogen gammaR275C mutation.Zebrafish as a model system for the study of hemostasis and thrombosis.Natural history of patients with congenital dysfibrinogenemia.Modeling Disorders of Blood Coagulation in the Zebrafish.Design and application of a 23-gene panel by next-generation sequencing for inherited coagulation bleeding disorders.Treatment of congenital fibrinogen deficiency: overview and recent findings.Inherited disorders of blood coagulation.Fibrinogen replacement therapy for congenital fibrinogen deficiency.Paradoxical thrombosis part 1: factor replacement therapy, inherited clotting factor deficiencies and prolonged APTT.Genomic approaches to bleeding disorders.Thromboembolic events in patients with severe inherited fibrinogen deficiency.What Is the Biological and Clinical Relevance of Fibrin?Congenital afibrinogenemia: from etiopathogenesis to challenging clinical management.Fibrin Formation, Structure and Properties.Use of purified fibrinogen concentrate for dysfibrinogenemia and importance of laboratory fibrinogen activity measurement.Fibrinogen facilitates atherosclerotic formation in Sprague-Dawley rats: A rodent model of atherosclerosis.Coagulation factor activity and clinical bleeding severity in rare bleeding disorders: results from the European Network of Rare Bleeding Disorders.Clinical Consequences and Molecular Bases of Low Fibrinogen Levels.Identification of Two Novel Fibrinogen Bβ Chain Mutations in Two Slovak Families with Quantitative Fibrinogen Disorders.Congenital hypofibrinogenemia in pregnancy: a report of 11 cases.The fibrous form of intracellular inclusion bodies in recombinant variant fibrinogen-producing cells is specific to the hepatic fibrinogen storage disease-inducible variant fibrinogen.Molecular analysis of afibrinogenemic mutations caused by a homozygous FGA1238 bp deletion, and a compound heterozygous FGA1238 bp deletion and novel FGA c.54+3A>C substitution.Identification and characterization of novel mutations implicated in congenital fibrinogen 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 fibrinogen disorders.
@en
Congenital fibrinogen disorders.
@nl
type
label
Congenital fibrinogen disorders.
@en
Congenital fibrinogen disorders.
@nl
prefLabel
Congenital fibrinogen disorders.
@en
Congenital fibrinogen disorders.
@nl
P356
P1476
Congenital fibrinogen disorders.
@en
P2093
Marguerite Neerman-Arbez
Philippe de Moerloose
P304
P356
10.1055/S-0029-1225758
P577
2009-06-01T00:00:00Z