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Carmela De Fusco

Explore the profile of Carmela De Fusco including associated specialties, affiliations and a list of published articles. Areas
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Articles 9
Citations 71
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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.
Giardino G, Lanni V, Mascolo M, Russo D, Cirillo E, Romano R, et al.
Front Immunol . 2024 Apr; 15:1370991. PMID: 38633254
Background And Aims: X lymphoproliferative syndrome type 1 (XLP1) is a rare inborn error of immunity due to mutations of , encoding for slam-associated protein (SAP). The clinical phenotype includes...
3.
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...
4.
Civino A, Alighieri G, Prete E, Caroleo A, Magni-Manzoni S, Vinti L, et al.
Lancet Rheumatol . 2024 Jan; 3(7):e507-e516. PMID: 38279403
Background: Presenting symptoms of childhood cancers might mimic those of rheumatic diseases. However, the evidence available to guide differential diagnosis remains scarce. Preventing wrong or delayed diagnosis is therefore important...
5.
Pegoraro F, Mazzariol M, Trambusti I, Bakhshi S, Mallick S, Dunkel I, et al.
Blood . 2023 Jul; 142(13):1167-1171. PMID: 37490651
No abstract available.
6.
Cariello V, Lombardo P, Castelli L, Brillantino C, De Fusco C, Rossi A, et al.
Radiol Case Rep . 2022 Aug; 17(8):2747-2753. PMID: 35990570
Langerhans cell histiocytosis (LCH) is a myeloid neoplasm characterized by a clonal proliferation of CD1a+/CD207+ dendritic cells. Although individuals of any age can be affected, the disease is most common...
7.
Giardino G, Veropalumbo C, Ruggiero G, Naddei R, Rubino V, Udhayachandran A, et al.
Br J Haematol . 2013 Jul; 162(5):713-7. PMID: 23808825
No abstract available.
8.
Trambas C, Gallo F, Pende D, Marcenaro S, Moretta L, De Fusco C, et al.
Blood . 2005 Mar; 106(3):932-7. PMID: 15741215
Mutations in the perforin gene have been found in patients with hemophagocytic lymphohistiocytosis (HLH), a rare autosomal recessive disease. We describe a patient expressing perforin with amino acid changes A91V...
9.
Spada E, Sagliocca L, Sourdis J, Garbuglia A, Poggi V, De Fusco C, et al.
J Clin Microbiol . 2004 Sep; 42(9):4230-6. PMID: 15365016
The minimum spanning tree (MST) model was applied to identify the history of transmission of hepatitis C virus (HCV) infection in an outbreak involving five children attending a pediatric oncology-hematology...