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Blood|December 31, 2016
Nonneutralizing antibodies against factor VIII and risk of inhibitor development in severe hemophilia AAntonino Cannavò, Carla Valsecchi, Isabella Garagiola, et al.
Pediatric Blood & Cancer|February 4, 2006
Spontaneous splenic rupture in a patient with factor XIII deficiency and a novel mutationHassan Khalife, Samar Muwakkit, Hayfa Al-Moussawi, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 25, 2021
Subclinical myopathic changes in COVID-19Davide Villa, Gianluca Ardolino, Linda Borellini, et al.
Journal of Thrombosis and Haemostasis : JTH|April 30, 2026
CORRELATION BETWEEN FACTOR VIII CHROMOGENIC ACTIVITY AND ANTIGEN LEVELS IN PATIENTS TREATED WITH AAV5-MEDIATED GENE THERAPY FOR HEMOPHILIA AFlora Peyvandi, Isabella Garagiola, Cristina Novembrino, et al.
Rheumatology and Therapy|June 15, 2022
Plasma Exchange in a Patient with Immune Thrombocytopenia Associated with Antiphospholipid Syndrome Hospitalized for COVID-19Federico Boggio, Alessandro Ciavarella, Sara Arcudi, et al.
Frontiers in Pediatrics|September 28, 2020
Thrombin Generation in Preterm Newborns With Intestinal Failure-Associated Liver DiseaseStefano Ghirardello, Genny Raffaeli, Erica Scalambrino, et al.
Thrombosis and Haemostasis|September 9, 2011
Common variants in the haemostatic gene pathway contribute to risk of early-onset myocardial infarction in the Italian populationIlaria Guella, Stefano Duga, Diego Ardissino, et al.
British Journal of Haematology|November 30, 2004
The P303T mutation in the human factor VII (FVII) gene alters the conformational state of the enzyme and causes a severe functional deficiencyFlora Peyvandi, Raimondo De Cristofaro, Isabella Garagiola, et al.
Thrombosis and Haemostasis|March 13, 2019
Clinical and Laboratory Features of Patients with Acquired Thrombotic Thrombocytopenic Purpura: Fourteen Years of the Milan TTP RegistryIlaria Mancini, Silvia Pontiggia, Roberta Palla, et al.
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