Bianca Maria Ricerca
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Explore the profile of Bianca Maria Ricerca including associated specialties, affiliations and a list of published articles.
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12
Citations
133
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Recent Articles
1.
Silvestrini A, Meucci E, Ricerca B, Mancini A
Int J Mol Sci
. 2023 Jul;
24(13).
PMID: 37446156
Despite the physiological role of oxidant molecules, oxidative stress (OS) could underlie several human diseases. When the levels of antioxidants are too low or too high, OS occurs, leading to...
2.
Roland B, Richards K, Hrizo S, Eicher S, Barile Z, Chang T, et al.
Biochim Biophys Acta Mol Basis Dis
. 2019 May;
1865(9):2257-2266.
PMID: 31075491
Mutations in the gene triosephosphate isomerase (TPI) lead to a severe multisystem condition that is characterized by hemolytic anemia, a weakened immune system, and significant neurologic symptoms such as seizures,...
3.
Putzulu R, Piccirillo N, Orlando N, Massini G, Maresca M, Scavone F, et al.
Transfus Apher Sci
. 2017 Feb;
56(2):234-237.
PMID: 28185828
Chronic red blood cell transfusions remain an essential part of supportive treatment in patients with thalassaemia and sickle cell disease (SCD). Red blood cell (RBC) transfusions expose patients to the...
4.
Radio F, Majore S, Binni F, Valiante M, Ricerca B, De Bernardo C, et al.
Blood Cells Mol Dis
. 2013 Sep;
52(2-3):83-7.
PMID: 24055163
Objective: Hereditary hemochromatosis (HH) is a common Mendelian disorder of iron metabolism. Eighty percent of northern Europeans descendant HH patients carry the same mutation (p.C282Y) in the HFE gene. Simultaneously,...
5.
Tisi M, Bozzoli V, Giachelia M, Massini G, Ricerca B, Maiolo E, et al.
Leuk Lymphoma
. 2013 May;
55(2):270-5.
PMID: 23647063
Anemia is a frequent sign in patients with diffuse large B-cell lymphoma (DLBCL) at diagnosis. We determined erythropoietin, hepcidin and interleukin-6 (IL-6) in plasma samples of 53 patients with DLBCL....
6.
Majore S, Ricerca B, Radio F, Binni F, Cosentino I, Gallusi G, et al.
Blood Cells Mol Dis
. 2012 Sep;
50(1):31-2.
PMID: 22981443
No abstract available.
7.
Minucci A, Ricerca B, Tripodi D, Matarazzo L, De Michele T, Giardina B, et al.
Clin Biochem
. 2011 Aug;
44(14-15):1261-3.
PMID: 21821016
We report a case of a patient affected by compound heterozygosis for two PK-LR gene mutations: p.R486W (c.1456C>T) and p.M403I (c.1209G>A). Our patient suffered from an initial moderate hemolytic anemia...
8.
Pinnetti C, Baroncelli S, Molinari A, Nardini G, Genovese O, Ricerca B, et al.
J Infect
. 2011 Jun;
63(2):144-50.
PMID: 21683094
Objective: Although zidovudine-free regimens are increasingly used in pregnancy, their haematological effects in mothers and newborns are incompletely defined. Methods: The haematological profiles of 119 HIV-infected women and their neonates...
9.
Ricerca B, di Girolamo A, Rund D
Mediterr J Hematol Infect Dis
. 2011 Mar;
1(1):e2009028.
PMID: 21415996
The clinical approach to thalassemia and hemoglobinopathies, specifically Sickle Cell Disease (SCD), based on transfusions, iron chelation and bone marrow transplantation has ameliorated their prognosis. Nevertheless, infections still may cause...
10.
Teofili L, Giona F, Torti L, Cenci T, Ricerca B, Rumi C, et al.
Haematologica
. 2009 Aug;
95(1):65-70.
PMID: 19713221
Unlabelled: Background The MPL(Ser505Asn) mutation has been reported to be a cause of hereditary thrombocythemia. Recently, we detected this mutation in a large proportion of children with familial thrombocythemia, suggesting...