Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Flora Peyvandi

Showing results (221-230 of 610) with videos related to

Pageof 61
Sort By:
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 diseaseFrancesca Stufano, Luciano Baronciani, Paolo Bucciarelli, et al.
Blood|June 16, 2017
Exploring the global landscape of genetic variation in coagulation factor XI deficiencyRosanna 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 syndromePasquale 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 implicationsOmid 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 geneLuca 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 defectsLuca 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 phenotypeOmid 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 cirrhosisArmando 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 2022Sara 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 geneSilvia Spena, Stefano Duga, Rosanna Asselta, et al.
Pageof 61

Showing results (221-230 of 610) with videos related to

Sort By:
Pageof 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 diseaseFrancesca Stufano, Luciano Baronciani, Paolo Bucciarelli, et al.
Blood|June 16, 2017
Exploring the global landscape of genetic variation in coagulation factor XI deficiencyRosanna 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 syndromePasquale 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 implicationsOmid 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 geneLuca 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 defectsLuca 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 phenotypeOmid 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 cirrhosisArmando 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 2022Sara 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 geneSilvia Spena, Stefano Duga, Rosanna Asselta, et al.
Pageof 61