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Haemophilia : the Official Journal of the World Federation of Hemophilia|August 17, 2019
Real-life experience in switching to new extended half-life products at European haemophilia centresFlora Peyvandi, Isabella Garagiola, Marco Boscarino, et al.American Journal of Hematology|July 27, 2005
Mutations in the MCFD2 gene and a novel mutation in the LMAN1 gene in Indian families with combined deficiency of factor V and VIIIDipika Mohanty, Kanjaksha Ghosh, Shrimati Shetty, et al.Haematologica|October 7, 2008
Nonsense-mediated mRNA decay in the ADAMTS13 gene caused by a 29-nucleotide deletionIsabella Garagiola, Carla Valsecchi, Silvia Lavoretano, et al.Frontiers in Medicine|April 22, 2024
Gender equity in hemophilia: need for healthcare, familial, and societal advocacyRoberta Gualtierotti, Isabella Garagiola, Mimosa Mortarino, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|July 8, 2026
Preimplantation Genetic Testing for Families at Risk of Haemophilia: Ten-Year Single-Centre ExperienceMimosa Mortarino, Isabella Garagiola, Valeria Nicotra, 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.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.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.International Journal of Molecular Sciences|September 28, 2023
Genetic Variants Identified by Whole Exome Sequencing in a Large Italian Family with High Plasma Levels of Factor VIII and Von Willebrand FactorSilvia Spena, Andrea Cairo, Francesca Gianniello, et al.Molecular Genetics & Genomic Medicine|April 12, 2016
A recurrent F8 mutation (c.6046C>T) causing hemophilia A in 8% of northern Italian patients: evidence for a founder effectIsabella Garagiola, Sabrina Seregni, Mimosa Mortarino, et al.Pageof 5