Zobrazeno 1 - 10
of 60
pro vyhledávání: '"Disma Renda"'
Autor:
Rita Barone, Bianca Magro, Angela Vitrano, Alessandro Inzerillo, Rossellina Rosso, Maria Grazia Bavetta, Giorgio Fusco, Mirko Olivo, Lorella Pitrolo, Antonino Giangreco, Rosario DI Maggio, Disma Renda, Angela Rao Camemi, Salvatore Gruttadauria, Aurelio Maggio
Publikováno v:
HemaSphere, Vol 7, p e4371393 (2023)
Externí odkaz:
https://doaj.org/article/ff3812ad92a743c793958e20e6bdd850
Autor:
Rosario Di Maggio, Alessandra Giuliano, Disma Renda, Giuseppina Calvaruso, Simona Raso, Lorella Pitrolo, Antonio Carroccio, Aurelio Maggio
Publikováno v:
Thalassemia Reports, Vol 12, Iss 3, Pp 85-89 (2022)
Venous thromboembolism (VTE) is a life-threatening complication, especially in case of recurrence. The appropriate duration of anticoagulant treatment following the first event is crucial. Risk factors that increase the risk of recurrence of VTE are
Externí odkaz:
https://doaj.org/article/3309d480ed2341b8b0c4ec40bc7230af
Autor:
Giuseppina Calvaruso, Marta Chiavetta, Disma Renda, Simona Raso, Francesco Dieli, Vincenzo Luca Lentini, Massimo Gentile, Antonio Carroccio, Aurelio Maggio
Publikováno v:
Thalassemia Reports, Vol 12, Iss 2, Pp 46-50 (2022)
Background: Haemophagocytic lymphohistiocytosis (HLH) is a rare and potentially life-threatening systemic hyperinflammatory disease, which can have several aetiologies. Clinical case: a 48-year-old woman affected by a transfusion-dependent β-thalass
Externí odkaz:
https://doaj.org/article/a378688d5d4c414f93f4ed945fac8c5a
Autor:
Rosario Di Maggio, Matthew M. Hsieh, Xiongce Zhao, Giuseppina Calvaruso, Paolo Rigano, Disma Renda, John F. Tisdale, Aurelio Maggio
Publikováno v:
International Journal of Molecular Sciences, Vol 19, Iss 3, p 681 (2018)
In sickle cell disease (SCD), hydroxyurea (HU) treatment decreases the number of vaso-occlusive crisis (VOC) and acute chest syndrome (ACS) by increasing fetal hemoglobin (HbF). Data are lacking regarding the frequency of HU dose modification or whet
Externí odkaz:
https://doaj.org/article/5851d9f3693749c187a2e69c3e197b49
Autor:
Gianfranca Damiani, Margherita Vinciguerra, Cristina Jakil, Monica Cannata, Filippo Cassarà, Francesco Picciotto, Giovanna Schillaci, Valentina Cigna, Disma Renda, Aldo Volpes, Francesca Sammartano, Samuela Milone, Adolfo Allegra, Cristina Passarello, Filippo Leto, Antonino Giambona
Publikováno v:
Thalassemia Reports, Vol 4, Iss 2 (2014)
Prenatal diagnosis of hemoglobinopathies involves the study of fetal material from blood, amniocytes, trophoblast coelomatic cells and fetal DNA in maternal circulation. Its first application dates back to the 70s and it involves globin chain synthes
Externí odkaz:
https://doaj.org/article/5368a77e1dfa40fab2029b9cfb1d1ab0
Autor:
Maria Concetta Renda, Disma Renda, Angela Piazza, Giuseppina Calvaruso, Emanuela Fecarotta, Antonino Giangreco, Aurelio Maggio
Publikováno v:
Thalassemia Reports, Vol 4, Iss 2 (2014)
In patients with β-thalassemia and sickle cell syndromes there is an important secondary iron overload due to regular blood transfusions and increased duodenal iron absorption. As in genetic hemochromatosis, also the secondary iron storage leads to
Externí odkaz:
https://doaj.org/article/7ba7f3025b264ca09ca6e54430ef1bce
Autor:
Maria Concetta Renda, Angela Vitrano, Massimo Attanasio, Emanuela Fecarotta, Angela Piazza, Antonino Giambona, Germana Fiorentino, Disma Renda, Paolo Rigano, Giuseppina Calvaruso, Filippo Cassarà, Aurelio Maggio
Publikováno v:
Thalassemia Reports, Vol 2, Iss 1, Pp e2-e2 (2012)
Nonsense-mediated mRNA decay (NMD) is a surveillance system to prevent the synthesis of non-functional proteins. In β-thalassemia, NMD may have a role in clinical outcome. An example of premature translation stop codons appearing for the first time
Externí odkaz:
https://doaj.org/article/253c4429dfb54491838a88d4ae90d0b7
Autor:
Cristina Passarello, Antonino Giambona, Monica Cannata, Margherita Vinciguerra, Disma Renda, Aurelio Maggio
Publikováno v:
Haematologica, Vol 97, Iss 3 (2012)
Externí odkaz:
https://doaj.org/article/9fa9c1002caa4ac6a55e6d82e96c01f3
Autor:
Antonino Giambona, Cristina Passarello, Margherita Vinciguerra, Rita Li Muli, Pietro Teresi, Maurizio Anzà, Gaetano Ruggeri, Disma Renda, Aurelio Maggio
Publikováno v:
Haematologica, Vol 93, Iss 9 (2008)
We report a retrospective analysis carried out on 23,485 subjects submitted to a screening program from 2000 to 2006. Of these subjects, 3,934 had borderline HbA2 values from 3.1 to 3.9%; 410 samples, analyzed previously using PCR methods and sequenc
Externí odkaz:
https://doaj.org/article/dac63fee170d4f5e9f686725398428de
Autor:
Filippo Cassarà, Monica Cannata, Giuseppina Calvaruso, Margherita Vinciguerra, Antonino Giambona, Filippo Leto, Disma Renda, Cristina Passarello, Aurelio Maggio
Publikováno v:
Hemoglobin. 41:234-238
We report two very rare changes in the second intron of the HBB gene, a substitution at nucleotide (nt) 726 [IVS-II-726 (A>G) (β+), NM_000518, HBB: c.316-125A>G] and a deletion of a cytosine at nt 809 [IVS-II-809 (-C) (β), NM_000518, HBB: c.316-42d