DAIDONE, VIVIANA

DAIDONE, VIVIANA  

Dipartimento di Salute della Donna e del Bambino - SDB  

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Risultati 1 - 20 di 42 (tempo di esecuzione: 0.014 secondi).
Titolo Data di pubblicazione Autori Rivista Serie Titolo libro
The Lesson Learned from the New c.2547-1G>T Mutation Combined with p.R854Q: When a Type 2N Mutation Reveals a Quantitative von Willebrand Factor Defect 2022 Casonato, AlessandraFerrari, SilviaRubin, BeatriceGianesello, LisaDaidone, Viviana + THROMBOSIS AND HAEMOSTASIS - -
The lesson learned from the new c.2547-1G>T mutation combined with p.R854Q:when a type 2N mutation reveals a quantitative von Willebrand factor defect. 2022 Casonato ARubin BGianesello LDaidone V. + THROMBOSIS AND HAEMOSTASIS - -
Von Willebrand disease type Vicenza: In search of a classification for the archetype of reduced von Willebrand factor survival 2021 Casonato SGalletta EGalvanin FDaidone V EJHAEM - -
Acquired von Willebrand Syndrome Hiding Inherited von Willebrand Disease Can Explain Severe Bleeding in Patients With Aortic Stenosis. 2020 Casonato AGalletta EDaidone V. + ARTERIOSCLEROSIS, THROMBOSIS, AND VASCULAR BIOLOGY - -
Cryptic noncanonical splice site activation is part of the mechanism that abolishes multimer organization in the c.2269_2270del von Willebrand factor 2019 Daidone, VivianaGalletta, EvaCasonato, Alessandra + HAEMATOLOGICA - -
A Mechanistic Model to Quantify von Willebrand Factor Release, Survival and Proteolysis in Patients with von Willebrand Disease 2018 Ferrari, MyriamBarolo, MassimilianoDaidone, VivianaPadrini, RobertoBezzo, FabrizioCasonato, Alessandra + THROMBOSIS AND HAEMOSTASIS - -
The elusive and heterogeneous pattern of type 2M von Willebrand disease: A diagnostic challenge 2018 Casonato, AlessandraGalletta, EvaDaidone, Viviana EUROPEAN JOURNAL OF HAEMATOLOGY - -
Type 1 von Willebrand disease due to a vicinal cysteine loss (p.C524Y) disclosed after a thrombotic episode 2018 Daidone, VivianaGalletta, EvaCasonato, Alessandra THROMBOSIS RESEARCH - -
Type 2N von Willebrand disease: Characterization and diagnostic difficulties 2018 Casonato, A.Galletta, E.Sarolo, L.Daidone, V. HAEMOPHILIA - -
Type 3 von Willebrand disease mistaken for moderate haemophilia A: a lesson still to be learned 2018 Galletta, EDaidone, VCasonato, S + HAEMOPHILIA - -
Haemostatic patterns and bleeding scores of a genetically characterised Italian family with combined haemophilia A and type 1 von Willebrand disease 2017 DAIDONE, VIVIANAPONTARA, ELENABOSCARO, FRANCESCAPELOSO CATTINI, MARIA GRAZIAMILAN, MARTACASONATO, SANDRA BLOOD COAGULATION & FIBRINOLYSIS - -
Two novel ITGA2B mutations in a Glanzmann thrombasthaenia family associated with different platelet phenotypic expression 2017 DAIDONE, VIVIANAMILAN, MARTAGALLETTA, EVAGRESELE, PAOLOCASONATO, SANDRA + BLOOD TRANSFUSION - -
Type 2B von Willebrand disease with or without large multimers: A distinction of the two sides of the disorder is long overdue 2017 Casonato, AlessandraDaidone, VivianaGalletta, EvaBertomoro, Antonella PLOS ONE - -
Diagnostic Value of Measuring Platelet Von Willebrand Factor in Von Willebrand Disease. 2016 CASONATO, SANDRAPELOSO CATTINI, MARIA GRAZIADAIDONE, VIVIANAPONTARA, ELENABERTOMORO, ANTONELLAPRANDONI, PAOLO PLOS ONE - -
The Bleeding Assessment Tool and laboratory data in the characterisation of a female with inherited haemophilia A 2016 DAIDONE, VIVIANAGALLETTA, EVABERTOMORO, ANTONELLACASONATO, SANDRA BLOOD TRANSFUSION - -
Usefulness of the Total Thrombus-Formation Analysis System (T-TAS) in the diagnosis and characterization of von Willebrand disease 2016 DAIDONE, VIVIANABARBON, GIOVANNIPELOSO CATTINI, MARIA GRAZIAPONTARA, ELENAROMUALDI, CHIARADI PASQUALE, IRENECASONATO, SANDRA + HAEMOPHILIA - -
A venous thromboembolism risk assessment model for patients with Cushing’s syndrome 2015 ZILIO, MARIALUISAMAZZAI, LINDABARBOT, MATTIACECCATO, FILIPPODAIDONE, VIVIANACASONATO, SANDRANOVENTA, FRANCOPRANDONI, PAOLOBOSCARO, MARCOSCARONI, CARLA + ENDOCRINE - -
Higher and lower active circulating VWF levels: different facets of von Willebrand disease 2015 CASONATO, SANDRAPONTARA, ELENAMORPURGO, MARGHERITASARTORELLO, FRANCESCADAIDONE, VIVIANA + BRITISH JOURNAL OF HAEMATOLOGY - -
Severe, recessive type 1 is a discrete form of von Willebrand disease: The lesson learned from the c.1534-3C>A von Willebrand factor mutation 2015 CASONATO, SANDRAPELOSO CATTINI, MARIA GRAZIABARBON, GIOVANNIDAIDONE, VIVIANAPONTARA, ELENA THROMBOSIS RESEARCH - -
The p.R1819_C1948delinsS mutation makes von Willebrand factor ADAMTS13-resistant and reduces its collagen-binding capacity 2015 DAIDONE, VIVIANASAGA, GIORGIABARBON, GIOVANNIPONTARA, ELENAPELOSO CATTINI, MARIA GRAZIAMORPURGO, MARGHERITAZANOTTI, GIUSEPPECASONATO, SANDRA BRITISH JOURNAL OF HAEMATOLOGY - -