Linda Beneforti
Overview
Explore the profile of Linda Beneforti including associated specialties, affiliations and a list of published articles.
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Articles
5
Citations
45
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Recent Articles
1.
Beneforti L, Chinnici A, Coniglio M, Papa M, Punzi L, Sieni E, et al.
Br J Haematol
. 2024 Jul;
205(3):1234-1237.
PMID: 38986479
No abstract available.
2.
Pegoraro F, Chinnici A, Beneforti L, Tanturli M, Trambusti I, De Fusco C, et al.
Haematologica
. 2024 Feb;
109(8):2515-2524.
PMID: 38385274
Primary hemophagocytic lymphohistiocytosis (pHLH) is a severe, life-threatening hyperinflammatory syndrome caused by defects in genes of the granule-dependent cytotoxic pathway. Here we investigated the clinical presentation and outcome in a...
3.
Chinnici A, Beneforti L, Pegoraro F, Trambusti I, Tondo A, Favre C, et al.
Front Immunol
. 2023 Jul;
14:1210041.
PMID: 37426667
Hemophagocytic Lymphohistiocytosis (HLH) is a rare clinical condition characterized by sustained but ineffective immune system activation, leading to severe and systemic hyperinflammation. It may occur as a genetic or sporadic...
4.
Beneforti L, Dander E, Bresolin S, Bueno C, Acunzo D, Bertagna M, et al.
Br J Haematol
. 2020 Mar;
190(2):262-273.
PMID: 32118299
ETV6-RUNX1 (E/R) fusion gene, arising in utero from translocation t(12;21)(p13:q22), is the most frequent alteration in childhood acute lymphoblastic leukemia (ALL). However, E/R is insufficient to cause overt leukemia since...
5.
Portale F, Beneforti L, Fallati A, Biondi A, Palmi C, Cazzaniga G, et al.
Exp Hematol
. 2019 Mar;
73:7-12.e4.
PMID: 30825516
The TEL-AML1 fusion gene, generated by the t(12;21) chromosome translocation, arises in a progenitor/stem cell and could induce clonal expansion of a persistent preleukemic B-cell clone which, on acquisition of...