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Haemophilia : the Official Journal of the World Federation of Hemophilia
|
February 29, 2020
Evaluation of a fully automated von Willebrand factor assay panel for the diagnosis of von Willebrand disease
Francesca Stufano, Luciano Baronciani, Paolo Bucciarelli, et al.
Blood
|
June 16, 2017
Exploring the global landscape of genetic variation in coagulation factor XI deficiency
Rosanna Asselta, Elvezia Maria Paraboschi, Valeria Rimoldi, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
February 21, 2024
Safety and efficacy of combined dual antiplatelet therapy and factor VIII prophylaxis in patients with haemophilia A after acute coronary syndrome
Pasquale Agosti, Simona Maria Siboni, Alessandro Ciavarella, et al.
The Lancet. Haematology
|
November 5, 2025
Von Willebrand factor and von Willebrand disease in ageing: mechanisms, evolving phenotypes, and clinical implications
Omid Seidizadeh, Ferdows Atiq, Nathan T Connell, et al.
Haematologica
|
May 4, 2006
Fibrinogen Mumbai: intracellular retention due to a novel G434D mutation in the Bbeta-chain gene
Luca Monaldini, Rosanna Asselta, Stefano Duga, et al.
Plos One
|
April 9, 2013
Prevalence of disease and relationships between laboratory phenotype and bleeding severity in platelet primary secretion defects
Luca A Lotta, Alberto Maino, Giacomo Tuana, et al.
Haematologica
|
August 18, 2025
Genetic determinants of clinical variability in type 2 von Willebrand disease: bridging genotype and phenotype
Omid Seidizadeh, Alessandro Ciavarella, Luciano Baronciani, et al.
Hepatology (Baltimore, Md.)
|
January 12, 2024
Reappraisal of the conventional hemostasis tests as predictors of perioperative bleeding in the era of rebalanced hemostasis in cirrhosis
Armando Tripodi, Massimo Primignani, Roberta D'Ambrosio, et al.
Internal and Emergency Medicine
|
February 2, 2026
Prevalence of hospital readmission, related causes and determinants in older people from 2010 to 2022
Sara Mandelli, Ilaria Ardoino, Raffaella Rossio, et al.
European Journal of Human Genetics : EJHG
|
October 19, 2004
Congenital afibrinogenaemia caused by uniparental isodisomy of chromosome 4 containing a novel 15-kb deletion involving fibrinogen Aalpha-chain gene
Silvia Spena, Stefano Duga, Rosanna Asselta, et al.
Page
of 61
Search research articles
Search
Showing results (221-230 of 610) with videos related to
Sort By:
Page
of 61
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
February 29, 2020
Evaluation of a fully automated von Willebrand factor assay panel for the diagnosis of von Willebrand disease
Francesca Stufano, Luciano Baronciani, Paolo Bucciarelli, et al.
Blood
|
June 16, 2017
Exploring the global landscape of genetic variation in coagulation factor XI deficiency
Rosanna Asselta, Elvezia Maria Paraboschi, Valeria Rimoldi, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
February 21, 2024
Safety and efficacy of combined dual antiplatelet therapy and factor VIII prophylaxis in patients with haemophilia A after acute coronary syndrome
Pasquale Agosti, Simona Maria Siboni, Alessandro Ciavarella, et al.
The Lancet. Haematology
|
November 5, 2025
Von Willebrand factor and von Willebrand disease in ageing: mechanisms, evolving phenotypes, and clinical implications
Omid Seidizadeh, Ferdows Atiq, Nathan T Connell, et al.
Haematologica
|
May 4, 2006
Fibrinogen Mumbai: intracellular retention due to a novel G434D mutation in the Bbeta-chain gene
Luca Monaldini, Rosanna Asselta, Stefano Duga, et al.
Plos One
|
April 9, 2013
Prevalence of disease and relationships between laboratory phenotype and bleeding severity in platelet primary secretion defects
Luca A Lotta, Alberto Maino, Giacomo Tuana, et al.
Haematologica
|
August 18, 2025
Genetic determinants of clinical variability in type 2 von Willebrand disease: bridging genotype and phenotype
Omid Seidizadeh, Alessandro Ciavarella, Luciano Baronciani, et al.
Hepatology (Baltimore, Md.)
|
January 12, 2024
Reappraisal of the conventional hemostasis tests as predictors of perioperative bleeding in the era of rebalanced hemostasis in cirrhosis
Armando Tripodi, Massimo Primignani, Roberta D'Ambrosio, et al.
Internal and Emergency Medicine
|
February 2, 2026
Prevalence of hospital readmission, related causes and determinants in older people from 2010 to 2022
Sara Mandelli, Ilaria Ardoino, Raffaella Rossio, et al.
European Journal of Human Genetics : EJHG
|
October 19, 2004
Congenital afibrinogenaemia caused by uniparental isodisomy of chromosome 4 containing a novel 15-kb deletion involving fibrinogen Aalpha-chain gene
Silvia Spena, Stefano Duga, Rosanna Asselta, et al.
Page
of 61