Barbara Crescenzi
Overview
Explore the profile of Barbara Crescenzi including associated specialties, affiliations and a list of published articles.
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Articles
54
Citations
592
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Recent Articles
1.
Lema Fernandez A, Nardelli C, Pierini V, Crescenzi B, Pellanera F, Matteucci C, et al.
Genes Chromosomes Cancer
. 2024 Nov;
63(11):e70013.
PMID: 39604137
Jumping translocations (JT) are rare cytogenetic abnormalities associated with progression in myelodysplastic syndromes (MDS) and acute myeloid leukemia (AML). Typically, a tri-tetra-somic 1q chromosome is translocated to two or more...
2.
Mavridou E, Lema Fernandez A, Nardelli C, Pierini V, Quintini M, Arniani S, et al.
Genes Chromosomes Cancer
. 2024 Apr;
63(4):e23235.
PMID: 38656651
In myeloid neoplasms, both fusion genes and gene mutations are well-established events identifying clinicopathological entities. In this study, we present a thus far undescribed t(X;21)(p11.4;q22.12) in five cases with myelodysplastic...
3.
Zanelli M, Lugli A, Palicelli A, Sanguedolce F, Zizzo M, Cresta C, et al.
Curr Oncol
. 2023 Jan;
30(1):824-831.
PMID: 36661711
Mantle cell lymphoma is a B-cell malignancy, which, in its classic form, usually involves lymph nodes and extranodal sites, and, among the extranodal sites, the gastrointestinal tract and the Waldeyer's...
4.
Pierini V, Bardelli V, Giglio F, Arniani S, Matteucci C, Pellanera F, et al.
Hemasphere
. 2022 Oct;
6(11):e795.
PMID: 36285071
No abstract available.
5.
Arniani S, Pierini V, Pellanera F, Matteucci C, Di Giacomo D, Bardelli V, et al.
Leukemia
. 2022 Aug;
36(11):2577-2585.
PMID: 35974102
Chromothripsis is a mitotic catastrophe that arises from multiple double strand breaks and incorrect re-joining of one or a few chromosomes. We report on incidence, distribution, and features of chromothriptic...
6.
Ferrari A, Arniani S, Crescenzi B, Ascani S, Flenghi L, Pierini V, et al.
Leuk Lymphoma
. 2022 Jan;
63(6):1356-1362.
PMID: 35045798
High-grade B-cell lymphoma with and and/or rearrangements (DH/TH-HGBL) still miss an in-depth genomic characterization. To identify accompanying genetic events, we performed a pilot study on 7 cases by applying DNA...
7.
Di Giacomo D, Quintini M, Pierini V, Pellanera F, La Starza R, Gorello P, et al.
Ann Hematol
. 2021 Dec;
101(2):297-307.
PMID: 34859285
Platelet-derived growth factor receptor B (PDGFRB) gene rearrangements define a unique subgroup of myeloid and lymphoid neoplasms frequently associated with eosinophilia and characterized by high sensitivity to tyrosine kinase inhibition....
8.
Zanelli M, Stingeni L, Zizzo M, Martino G, Sanguedolce F, Marra A, et al.
Diagnostics (Basel)
. 2021 Jul;
11(7).
PMID: 34202434
A 73-year-old man presented with multiple lymphadenopathy. He had a 20-year history of palmoplantar psoriasis evolved to a diffuse erythrodermic picture in the last two years. Topic and systemic medications...
9.
Bottega R, Ravera S, Napolitano L, Chiappetta V, Zini N, Crescenzi B, et al.
J Cell Physiol
. 2021 Jan;
236(8):5664-5675.
PMID: 33432587
Warsaw breakage syndrome (WABS), is caused by biallelic mutations of DDX11, a gene coding a DNA helicase. We have recently reported two affected sisters, compound heterozygous for a missense (p.Leu836Pro)...
10.
Fontana D, Mauri M, Renso R, Docci M, Crespiatico I, Rost L, et al.
Nat Commun
. 2020 Nov;
11(1):5938.
PMID: 33230096
Recurrent somatic mutations in ETNK1 (Ethanolamine-Kinase-1) were identified in several myeloid malignancies and are responsible for a reduced enzymatic activity. Here, we demonstrate in primary leukemic cells and in cell...