GALLETTA, EVA

GALLETTA, EVA  

Dipartimento di Biologia - DiBio  

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Risultati 1 - 16 di 16 (tempo di esecuzione: 0.017 secondi).
Titolo Data di pubblicazione Autori Rivista Serie Titolo libro
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 - -
Browning Effects of a Chronic Pterostilbene Supplementation in Mice Fed a High-Fat Diet 2019 La Spina, MartinaGalletta, EvaAzzolini, MicheleGomez Zorita, SaioaParrasia, SofiaSalvalaio, MarikaBiasutto, Lucia + INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES - -
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 - -
Long-Term Pterostilbene Supplementation of a High-Fat Diet Increases Adiponectin Expression in the Subcutaneous White Adipose Tissue 2022 Sofia ParrasiaEva GallettaMartina La Spina 1 + NUTRACEUTICALS - -
Multiple Mechanisms Converging on Transcription Factor EB Activation by the Natural Phenol Pterostilbene 2021 La Spina, MartinaAzzolini, MicheleParrasia, SofiaGalletta, EvaChrisam, MartinaMattarei, AndreaTiso, Natascia + OXIDATIVE MEDICINE AND CELLULAR LONGEVITY - -
No von Willebrand factor domains other than A1 are involved in type 2B von Willebrand disease: what the p.R924Q and p.A2178S variants teach us 2023 Alessandra, CasonatoLisa, GianeselloDaniela, RegazzoEva, Galletta + RESEARCH AND PRACTICE IN THROMBOSIS AND HAEMOSTASIS - -
SPP1 genotype and glucocorticoid treatment modify osteopontin expression in Duchenne muscular dystrophy cells 2017 VIANELLO, SARAPANTIC, BORISFUSTO, AURORABELLO, LUCAGALLETTA, EVABORGIA, DORIANAGAVASSINI, BRUNO FRANCESCOSEMPLICINI, CLAUDIOSORARU', GIANNIVITIELLO, LIBEROPEGORARO, ELENA HUMAN MOLECULAR GENETICS - -
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 - -
The elusive and heterogeneous pattern of type 2M von Willebrand disease: A diagnostic challenge 2018 Casonato, AlessandraGalletta, EvaDaidone, Viviana EUROPEAN JOURNAL OF HAEMATOLOGY - -
The GIP/GIPR axis in medullary thyroid cancer: clinical and molecular findings 2022 Regazzo, DanielaBertazza, LorisGalletta, EvaBarollo, SusiMondin, AlbertoIacobone, MaurizioZilio, EleonoraScaroni, CarlaRadu, Claudia Mariadi Benedetto, GiuliettaMian, CaterinaOcchi, Gianluca + ENDOCRINE-RELATED CANCER - -
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 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 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 - -
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 - -
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 - -