Zobrazeno 1 - 10
of 1 593
pro vyhledávání: '"Malandrini A"'
Autor:
Anna Amela Valsecchi, Filippo Giovanardi, Francesco Malandrini, Michela Meregaglia, Alberto Servetto, Chiara Bennati, Carmine Pinto, Massimo Di Maio, Oriana Ciani
Publikováno v:
Breast, Vol 78, Iss , Pp 103817- (2024)
Background: Inclusion of patient-reported outcomes (PROs) in oncology clinical trials is strongly recommended. However, selecting the most appropriate patient-reported outcome measures (PROMs) is not easy. This study aimed to develop a breast cancer
Externí odkaz:
https://doaj.org/article/37033068ba08440294db2b5dd2fcb9b0
Autor:
Valsecchi, Anna Amela, Giovanardi, Filippo, Malandrini, Francesco, Meregaglia, Michela, Servetto, Alberto, Bennati, Chiara, Pinto, Carmine, Di Maio, Massimo, Ciani, Oriana
Publikováno v:
In The Breast December 2024 78
Autor:
Malandrini, Francesco, Meregaglia, Michela, Di Maio, Massimo, Pinto, Carmine, De Lorenzo, Francesco, Ciani, Oriana
Publikováno v:
In European Journal of Cancer August 2024 207
Autor:
Diego Lopergolo, Gian Nicola Gallus, Giuseppe Pieraccini, Francesca Boscaro, Gianna Berti, Giovanni Serni, Nila Volpi, Patrizia Formichi, Silvia Bianchi, Denise Cassandrini, Vincenzo Sorrentino, Daniela Rossi, Filippo Maria Santorelli, Nicola De Stefano, Alessandro Malandrini
Publikováno v:
Cells, Vol 13, Iss 17, p 1504 (2024)
CCDC78 was identified as a novel candidate gene for autosomal dominant centronuclear myopathy-4 (CNM4) approximately ten years ago. However, to date, only one family has been described, and the function of CCDC78 remains unclear. Here, we analyze for
Externí odkaz:
https://doaj.org/article/2fc80b87022e401688a1c19ab88409c3
Autor:
Fernanda Fortunato, Francesca Bianchi, Giulia Ricci, Francesca Torri, Francesca Gualandi, Marcella Neri, Marianna Farnè, Fabio Giannini, Alessandro Malandrini, Nila Volpi, Diego Lopergolo, Vincenzo Silani, Nicola Ticozzi, Federico Verde, Davide Pareyson, Silvia Fenu, Silvia Bonanno, Vincenzo Nigro, Cristina Peduto, Paola D’Ambrosio, Roberta Zeuli, Mariateresa Zanobio, Esther Picillo, Serenella Servidei, Guido Primiano, Cristina Sancricca, Monica Sciacco, Roberta Brusa, Massimiliano Filosto, Stefano Cotti Piccinelli, Elena Pegoraro, Tiziana Mongini, Luca Solero, Giulio Gadaleta, Chiara Brusa, Carlo Minetti, Claudio Bruno, Chiara Panicucci, Valeria A. Sansone, Christian Lunetta, Alice Zanolini, Antonio Toscano, Alessia Pugliese, Giulia Nicocia, Enrico Bertini, Michela Catteruccia, Daria Diodato, Antonio Atalaia, Teresinha Evangelista, Gabriele Siciliano, Alessandra Ferlini
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-7 (2023)
Abstract Background The development of e-health technologies for teleconsultation and exchange of knowledge is one of the core purposes of European Reference Networks (ERNs), including the ERN EURO-NMD for rare neuromuscular diseases. Within ERNs, th
Externí odkaz:
https://doaj.org/article/a63c0e0266e34366b30660e184a94201
Autor:
Alice Tarantola, Monica Hildegard Otto, Patrizio Armeni, Francesco Costa, Francesco Malandrini, Claudio Jommi
Publikováno v:
Journal of Pharmaceutical Policy and Practice, Vol 16, Iss 1, Pp 1-13 (2023)
Abstract Early access programs (EAPs) generally refer to patient access to medicines/indications before marketing authorization, possibly extended to price and reimbursement approval. These programs include compassionate use, which is usually covered
Externí odkaz:
https://doaj.org/article/8d6401fd725a4f5fb756bbf97b1bb5c0
Autor:
Leccese, Deborah, Rodolico, Gabriele Rosario, Sperti, Martina, Cassandrini, Denise, Bartolini, Marco, Ingannato, Assunta, Nacmias, Benedetta, Bracco, Laura, Malandrini, Alessandro, Santorelli, Filippo Maria, Bessi, Valentina, Matà, Sabrina
Publikováno v:
In Clinical Neurology and Neurosurgery September 2023 232
Akademický článek
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Akademický článek
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Autor:
Sara Aguti, Gian Nicola Gallus, Silvia Bianchi, Simona Salvatore, Anna Rubegni, Gianna Berti, Patrizia Formichi, Nicola De Stefano, Alessandro Malandrini, Diego Lopergolo
Publikováno v:
Cells, Vol 13, Iss 4, p 329 (2024)
Objective: To identify novel biomarkers as an alternative diagnostic tool for limb girdle muscular dystrophy (LGMD). Background: LGMD encompasses a group of muscular dystrophies characterized by proximal muscles weakness, elevated CK levels and dystr
Externí odkaz:
https://doaj.org/article/2885ad79e6d1491eb0ea11c7ce31409b