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European Journal of Haematology|August 8, 2018
The elusive and heterogeneous pattern of type 2M von Willebrand disease: A diagnostic challengeAlessandra Casonato, Eva Galletta, Viviana Daidone
Blood Transfusion = Trasfusione Del Sangue|October 25, 2021
Acquired von Willebrand syndrome in patients with monoclonal gammopathy of undetermined significance investigated using a mechanistic approachEva Galletta, Federico Galvanin, Antonella Bertomoro, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|July 10, 2020
Acquired von Willebrand Syndrome Hiding Inherited von Willebrand Disease Can Explain Severe Bleeding in Patients With Aortic StenosisAlessandra Casonato, Eva Galletta, Giuseppe Cella, et al.
International Journal of Molecular Sciences|November 2, 2019
Browning Effects of a Chronic Pterostilbene Supplementation in Mice Fed a High-Fat DietMartina La Spina, Eva Galletta, Michele Azzolini, et al.
Plos One|September 10, 2013
Revertant fibers in the mdx murine model of Duchenne muscular dystrophy: an age- and muscle-related reappraisalSarah R Pigozzo, Lorena Da Re, Chiara Romualdi, et al.
Human Molecular Genetics|June 9, 2017
SPP1 genotype and glucocorticoid treatment modify osteopontin expression in Duchenne muscular dystrophy cellsSara Vianello, Boris Pantic, Aurora Fusto, et al.
Endocrine-Related Cancer|October 9, 2025
GIPR in GH-PitNETs: molecular and functional insightsMattia Dalle Nogare, Serena Avallone, Eva Galletta, et al.
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