Zobrazeno 1 - 10
of 198
pro vyhledávání: '"Rita, Gamberini"'
Publikováno v:
Smart Cities, Vol 7, Iss 2, Pp 735-757 (2024)
A surging demand for sustainable energy and the urgency to lower greenhouse gas emissions is driving industrial systems towards more eco-friendly and cost-effective models. Biogas from agricultural and municipal organic waste is gaining momentum as a
Externí odkaz:
https://doaj.org/article/4381fbf2561d443ebe61359211f3aba6
Autor:
Antonella Meloni, Laura Pistoia, Amalia Lupi, Riccardo Righi, Antonino Vallone, Massimiliano Missere, Stefania Renne, Priscilla Fina, Ada Riva, Maria Rita Gamberini, Valerio Cecinati, Francesco Sorrentino, Rosamaria Rosso, Giuseppe Messina, Paolo Ricchi, Vincenzo Positano, Sophie Mavrogeni, Emilio Quaia, Filippo Cademartiri, Alessia Pepe
Publikováno v:
Tomography, Vol 9, Iss 5, Pp 1711-1722 (2023)
Background. The E-MIOT (Extension-Myocardial Iron Overload in Thalassemia) project is an Italian Network assuring high-quality quantification of tissue iron overload by magnetic resonance imaging (MRI). We evaluated the impact of the COVID-19 pandemi
Externí odkaz:
https://doaj.org/article/dd9d9df5616243f494c090aa67e6d38b
Autor:
Maria Rita Gamberini, Cristina Zuccato, Matteo Zurlo, Lucia Carmela Cosenza, Alessia Finotti, Roberto Gambari
Publikováno v:
Hematology Reports, Vol 15, Iss 3, Pp 432-439 (2023)
The β-thalassemias are a group of monogenic hereditary hematological disorders caused by deletions and/or mutations of the β-globin gene, leading to low or absent production of adult hemoglobin (HbA). For β-thalassemia, sirolimus has been under cl
Externí odkaz:
https://doaj.org/article/cb0e102625de42d687cf73b2b04b12dd
Autor:
Veronica Bordoni, Maddalena Casale, Valeria Maria Pinto, Rita Carsetti, Barbara Gianesin, Maria Rita Gamberini, Leila Mazdai, Susanna Barella, Anna Rita Denotti, Francesca Colavita, Silverio Perrotta, Aurelio Maggio, Lorella Pitrolo, Sabrina Quintino, Marco Caminati, Filippo Mazzi, Jacopo Ceolan, Lucia De Franceschi, Gian Luca Forni, Franco Locatelli, Chiara Agrati
Publikováno v:
HemaSphere, Vol 7, p e98163b7 (2023)
Externí odkaz:
https://doaj.org/article/61f3b3097b73470598f72a91beb56bfe
Autor:
Matteo Zurlo, Cristina Zuccato, Lucia Carmela Cosenza, Jessica Gasparello, Maria Rita Gamberini, Alice Stievano, Monica Fortini, Marco Prosdocimi, Alessia Finotti, Roberto Gambari
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 20, p 15049 (2023)
The β-thalassemias are hereditary monogenic diseases characterized by a low or absent production of adult hemoglobin and excess in the content of α-globin. This excess is cytotoxic for the erythroid cells and responsible for the β-thalassemia-asso
Externí odkaz:
https://doaj.org/article/c0382c4011cb481eba8fab3644c2458e
Autor:
Roberto Gambari, Cristina Zuccato, Lucia Carmela Cosenza, Matteo Zurlo, Jessica Gasparello, Alessia Finotti, Maria Rita Gamberini, Marco Prosdocimi
Publikováno v:
Biology, Vol 12, Iss 9, p 1202 (2023)
In this review article, we present the fascinating story of rapamycin (sirolimus), a drug able to induce γ-globin gene expression and increased production of fetal hemoglobin (HbF) in erythroid cells, including primary erythroid precursor cells (ErP
Externí odkaz:
https://doaj.org/article/9b516fe69a7b4406aa1fd7419ea2538d
Autor:
Antonio Piga, Filomena Longo, Maria Rita Gamberini, Ersi Voskaridou, Paolo Ricchi, Vincenzo Caruso, Antonello Pietrangelo, Xiaosha Zhang, Jeevan K. Shetty, Kenneth M. Attie, Immacolata Tartaglione
Publikováno v:
Therapeutic Advances in Hematology, Vol 13 (2022)
Background: β-thalassemia is a hereditary blood disorder resulting in ineffective erythropoiesis and anemia. Management of anemia with regular blood transfusions is associated with complications including iron overload. Here, we report long-term saf
Externí odkaz:
https://doaj.org/article/bdfb531090f0420bb0ab5e73c2a170fd
Autor:
Cristina Zuccato, Lucia Carmela Cosenza, Matteo Zurlo, Jessica Gasparello, Chiara Papi, Elisabetta D’Aversa, Giulia Breveglieri, Ilaria Lampronti, Alessia Finotti, Monica Borgatti, Chiara Scapoli, Alice Stievano, Monica Fortini, Eric Ramazzotti, Nicola Marchetti, Marco Prosdocimi, Maria Rita Gamberini, Roberto Gambari
Publikováno v:
Therapeutic Advances in Hematology, Vol 13 (2022)
Introduction: β-thalassemia is caused by autosomal mutations in the β-globin gene, which induce the absence or low-level synthesis of β-globin in erythroid cells. It is widely accepted that a high production of fetal hemoglobin (HbF) is beneficial
Externí odkaz:
https://doaj.org/article/3a428c6ac29340b587bac650085e82e1
Autor:
Antonella Meloni, Laura Pistoia, Maria Rita Gamberini, Liana Cuccia, Roberto Lisi, Valerio Cecinati, Paolo Ricchi, Calogera Gerardi, Gennaro Restaino, Riccardo Righi, Vincenzo Positano, Filippo Cademartiri
Publikováno v:
Diagnostics, Vol 13, Iss 5, p 890 (2023)
We assessed the prognostic value of multiparametric cardiovascular magnetic resonance (CMR) in predicting death from heart failure (HF) in thalassemia major (TM). We considered 1398 white TM patients (30.8 ± 8.9 years, 725 women) without a history o
Externí odkaz:
https://doaj.org/article/f5adc1cfe7354b75ae2b18485b5db24d
Publikováno v:
Applied Sciences, Vol 12, Iss 21, p 11071 (2022)
In this paper, we present the re-engineering process of an assembly line that features speed reducers and multipliers for agricultural applications. The “as-is” line was highly inefficient due to several issues, including the age of the machines,
Externí odkaz:
https://doaj.org/article/827bfd9c0d2a4390b0431b52ce59cb6a