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Pierre Toulon et al.
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Romy M. W. Kremers et al.
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Julien Perrin et al.
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Tami Livnat et al.
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Ida Martinelli et al.
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M. E. de la Morena-Barrio et al.
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Genetic sequence analysis of inherited bleeding diseases
Flora Peyvandi et al.
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Ala Nozari et al.
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L. Rugeri et al.
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Eva Richard et al.
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Nobutsune Ishikawa et al.
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Ophira Salomon et al.
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Armando Tripodi et al.
HAEMATOLOGICA-THE HEMATOLOGY JOURNAL (2008)
Risk assessment of acute vascular events in congenital disorder of glycosylation type Ia
J. B. Arnoux et al.
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R. Y. J. Tamminga et al.
PEDIATRIC HEMATOLOGY AND ONCOLOGY (2008)
Radiologic and neurophysiologic aspects of stroke-like episodes in children with congenital disorder of glycosylation type Ia
Argirios Dinopoulos et al.
PEDIATRICS (2007)
Thrombin generation, a function test of the haemostatic-thrombotic system
H. Coenraad Hemker et al.
THROMBOSIS AND HAEMOSTASIS (2006)
Use of calibrated automated thrombinography ± thrombo-modulin to recognise the prothrombotic phenotype
Yesim Dargaud et al.
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Mimics of childhood stroke: Characteristics of a prospective cohort
Renee A. Shellhaas et al.
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K Hansson et al.
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Anesthesia considerations in carbohydrate-deficient glycoprotein syndrome type I
E Meaudre et al.
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JH McVey et al.
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Dose-response study of recombinant human soluble thrombomodulin (ART-123) in the prevention of venous thromboernbolism after total hip replacement
C Kearon et al.
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Evidence of normal thrombin generation in cirrhosis despite abnormal conventional coagulation tests
A Tripodi et al.
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Phase I of a novel recombinant human soluble thrombomodulin, ART-123
S Moll et al.
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Detection of conformational transformation of antithrombin in blood with crossed immunoelectrophoresis: New application for a classical method
J Corral et al.
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KG Mann et al.
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CJ Davidson et al.
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Structure of β-antithrombin and the effect of glycosylation on antithrombin's heparin affinity and activity
AJ McCoy et al.
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Calibrated automated thrombin generation measurement in clotting plasma
HC Hemker et al.
PATHOPHYSIOLOGY OF HAEMOSTASIS AND THROMBOSIS (2003)
Medical progress - Gastroesophageal variceal hemorrhage
AI Sharara et al.
NEW ENGLAND JOURNAL OF MEDICINE (2001)
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C Van Geet et al.
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The role of factor XI in thrombin generation induced by low concentrations of tissue factor
IMLW Keularts et al.
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