Galletta E - Search Results

1

Two novel ITGA2B mutations in a Glanzmann thrombasthaenia family associated with different platelet phenotypic expression.

Daidone V, Bury L, Milan M, Galletta E, Gresele P, Casonato A. Daidone V, et al. Among authors: galletta e. Blood Transfus. 2017 Sep;15(5):487-488. doi: 10.2450/2016.0055-16. Epub 2016 Jul 12. Blood Transfus. 2017. PMID: 27416581 Free PMC article. No abstract available.

2

The Bleeding Assessment Tool and laboratory data in the characterisation of a female with inherited haemophilia A.

Daidone V, Galletta E, Bertomoro A, Casonato A. Daidone V, et al. Among authors: galletta e. Blood Transfus. 2018 Jan;16(1):114-117. doi: 10.2450/2016.0132-16. Epub 2016 Nov 15. Blood Transfus. 2018. PMID: 27893350 Free PMC article. No abstract available.

3

Acquired von Willebrand Syndrome Hiding Inherited von Willebrand Disease Can Explain Severe Bleeding in Patients With Aortic Stenosis.

Casonato A, Galletta E, Cella G, Barbon G, Daidone V. Casonato A, et al. Among authors: galletta e. Arterioscler Thromb Vasc Biol. 2020 Sep;40(9):2187-2194. doi: 10.1161/ATVBAHA.120.314656. Epub 2020 Jul 9. Arterioscler Thromb Vasc Biol. 2020. PMID: 32640909 Free article.

4

Acquired von Willebrand syndrome in patients with monoclonal gammopathy of undetermined significance investigated using a mechanistic approach.

Galletta E, Galvanin F, Bertomoro A, Daidone V, Casonato A. Galletta E, et al. Blood Transfus. 2023 Jan;21(1):74-82. doi: 10.2450/2021.0121-21. Epub 2021 Sep 3. Blood Transfus. 2023. PMID: 34694218 Free PMC article.

5

Type 2B von Willebrand disease with or without large multimers: A distinction of the two sides of the disorder is long overdue.

Casonato A, Daidone V, Galletta E, Bertomoro A. Casonato A, et al. Among authors: galletta e. PLoS One. 2017 Jun 22;12(6):e0179566. doi: 10.1371/journal.pone.0179566. eCollection 2017. PLoS One. 2017. PMID: 28640903 Free PMC article.

6

Type 1 von Willebrand disease due to a vicinal cysteine loss (p.C524Y) disclosed after a thrombotic episode.

Daidone V, Galletta E, Casonato A. Daidone V, et al. Among authors: galletta e. Thromb Res. 2018 Jan;161:91-93. doi: 10.1016/j.thromres.2017.11.021. Epub 2017 Nov 26. Thromb Res. 2018. PMID: 29220693 No abstract available.

7

The elusive and heterogeneous pattern of type 2M von Willebrand disease: A diagnostic challenge.

Casonato A, Galletta E, Daidone V. Casonato A, et al. Among authors: galletta e. Eur J Haematol. 2018 Aug 6. doi: 10.1111/ejh.13159. Online ahead of print. Eur J Haematol. 2018. PMID: 30084138

8

Von Willebrand disease type Vicenza: In search of a classification for the archetype of reduced von Willebrand factor survival.

Casonato A, Galletta E, Galvanin F, Daidone V. Casonato A, et al. Among authors: galletta e. EJHaem. 2021 May 5;2(3):340-348. doi: 10.1002/jha2.196. eCollection 2021 Aug. EJHaem. 2021. PMID: 35844701 Free PMC article.

9

Type 2N von Willebrand disease: Characterization and diagnostic difficulties.

Casonato A, Galletta E, Sarolo L, Daidone V. Casonato A, et al. Among authors: galletta e. Haemophilia. 2018 Jan;24(1):134-140. doi: 10.1111/hae.13366. Epub 2017 Nov 8. Haemophilia. 2018. PMID: 29115006

10

Cryptic non-canonical splice site activation is part of the mechanism that abolishes multimer organization in the c.2269_2270del von Willebrand factor.

Daidone V, Galletta E, De Marco L, Casonato A. Daidone V, et al. Among authors: galletta e. Haematologica. 2020 Apr;105(4):1120-1128. doi: 10.3324/haematol.2019.222679. Epub 2019 Jul 18. Haematologica. 2020. PMID: 31320553 Free PMC article.

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