Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Basilia Piraino"'
Autor:
Carmela Mento, Basilia Piraino, Amelia Rizzo, Roberta Vento, Luciana Rigoli, Emanuela Moschella, Carmelo Salpietro, Salvatore Settineri
Publikováno v:
International Journal of Psychological Research, Vol 8, Iss 1, Pp 90-97 (2015)
Background. Thalassemia is a chronic disease that can lead to an impact on psychological functioning and social behavior of patients. However, still little is known about the specific psychological aspects of the disease, such as the degree of tensi
Externí odkaz:
https://doaj.org/article/b7ad0b5114eb459196aafdd1d872f363
Autor:
Giuseppa Visalli, Angela Di Pietro, Elisa Ferro, Carmelo Salpietro, Basilia Piraino, Maria Angela La Rosa
Publikováno v:
European Journal of Haematology. 98:67-74
Objective The hemojuvelin-bone morphogenetic protein axis is the principal iron-dependent mechanism of hepcidin regulation. The determination of sHJV levels could allow for a better understanding of the pathophysiological mechanisms of hepcidin regul
Autor:
Giuseppa Visalli, Elisa Ferro, Gaetano Randazzo Papa, Basilia Piraino, Angela Di Pietro, Domenico Giuseppe D'Ascola, Gaetano Roccamo, Maria Angela La Rosa, Rosa Civa, Carmelo Salpietro
Redox imbalance and genotoxic damage are commonly observed in β thalassaemic patients. The aim of this study was to assess the role of anaemia in oxidative and genotoxic damage in regularly transfused thalassaemic patients, undergoing iron chelation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::254b52f1057ea7b0f5490d21a226f85d
http://hdl.handle.net/11570/3107355
http://hdl.handle.net/11570/3107355
Autor:
Basilia Piraino, Giuseppa Visalli, Gaetano Randazzo Papa, Maria Angela La Rosa, Elisa Ferro, Angela Di Pietro, Rosa Civa
Publikováno v:
Mutagenesis. 32(2)
In previously reported studies, we observed significantly high genotoxicity biomarkers in regularly transfused thalassaemic patients, thus, in this study, we better investigated the genotoxic effect of iron overload and of thalassaemia complications,
Autor:
Giuseppa Visalli, Carmelo Salpietro, Maria Angela La Rosa, Angela Di Pietro, Monica Currò, Elisa Ferro, Basilia Piraino
Publikováno v:
British Journal of Haematology. 174:824-826
Keywords: hypoxia inducible factor 1; glucose transporter 1; hypoxia; transfusion; erythropoiesis
Autor:
Bijoy K. Khandheria, Scipione Carerj, Luciana Rigoli, Basilia Piraino, Gianluca Di Bella, Concetta Zito, Maurizio Cusmà Piccione, Lilia Oreto, Carmelo Salpietro, Cesare de Gregorio, Valeria Ferraù
Publikováno v:
The American Journal of Cardiology. 112:1246-1251
The aim of the present study was to evaluate left ventricular myocardial deformation and carotid arterial stiffness using 2-dimensional strain and echo-tracking in patients with asymptomatic β-thalassemia major (β-TM) without significant myocardial
Autor:
Elisabetta Chiodi, Saveria Campisi, Liana Cuccia, Domenico Giuseppe D'Ascola, Claudio Ascioti, Maria E. Lai, Alessia Pepe, Giuseppe Rossi, Vincenzo Positano, Angelo Zuccarelli, Calogera Gerardi, Salvatore Grimaldi, Maria Rita Gamberini, Michele Santodirocco, Massimo Lombardi, L. Gulino, Antonella Meloni, Basilia Piraino, Anna Spasiano, Vincenzo Caruso
Publikováno v:
British Journal of Haematology. 163:520-527
Summary The relationship between diabetes mellitus (DM) and cardiac complications has never been systematically studied in thalassaemia major (TM). We evaluated a large retrospective historical cohort of TM to determine whether DM is associated with
Autor:
Lucia Maria Bruno, Federica Bellone, Nunziata Morabito, Rita Maria Agostino, Eleni Tsiantouli, Giorgio Basile, Carmelo Salpietro, Elisabetta Morini, Agostino Gaudio, Antonino Lasco, Basilia Piraino, Antonino Catalano, Maria Angela La Rosa
Publikováno v:
Journal of bone and mineral metabolism. 34(5)
Subjects affected by thalassemia major (TM) often have reduced bone mass and increased fracture risk. Strontium ranelate (SrR) is an effective treatment for postmenopausal and male osteoporosis. To date, no data exist on the use of SrR in the treatme
Autor:
Teresa Arrigo, Caterina Cuppari, Valeria Chirico, Antonio David, Antonio Lacquaniti, L. Grasso, Carmelo Salpietro, Luciana Rigoli, Basilia Piraino, M C Cutrupi
Summary High mobility group box -1 (HMGB1) represents a common causal agent for various types of diseases, including infective pathologies. This study aimed to investigate the role of HMGB1 in β-thalassemia major (TM) by evaluating its diagnostic an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8d5cd6b38a220d54ac460bd0e2effdf
http://hdl.handle.net/11570/3091974
http://hdl.handle.net/11570/3091974
Autor:
Carmelo Salpietro, Valeria Chirico, Antonio Lacquaniti, Luciana Rigoli, Teresa Arrigo, Vincenzo Salpietro, Maria Amorini, Basilia Piraino
Publikováno v:
European journal of haematology. 94(5)
Introduction Endocrinopathies and metabolic disorders-characterized β thalassemic (βT) patients and the prevention and treatment of these comorbidities are important targets to be achieved. The aim of the study was to analyze the diagnostic and pro