Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Lorena, Casareto"'
Autor:
Chiara Baldo, Lorena Casareto, Alessandra Renieri, Giuseppe Merla, Barbara Garavaglia, Stefano Goldwurm, Elena Pegoraro, Maurizio Moggio, Marina Mora, Luisa Politano, Luca Sangiorgi, Raffaella Mazzotti, Valeria Viotti, Ilaria Meloni, Maria Teresa Pellico, Chiara Barzaghi, Chiuhui Mary Wang, Lucia Monaco, Mirella Filocamo
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 11, Iss 1, Pp 1-8 (2016)
Abstract Background Rare diseases (RDs) are often neglected because they affect a small percentage of the population (6–8 %), which makes research and development of new therapies challenging processes. Easy access to high-quality samples and assoc
Externí odkaz:
https://doaj.org/article/006e79c58f444a9789a5afc43fab50c6
Publikováno v:
eLS
Biobanks are bioresources of human samples linked to relevant personal and health data of the participants, which are collected, processed and stored in an organised system. Their primary purpose is to provide biospecimens for researchers to help imp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::868a56a765cc64633bd09dbd5736431a
https://doi.org/10.1002/9780470015902.a0022486
https://doi.org/10.1002/9780470015902.a0022486
Autor:
Maria Teresa Pellico, Luca Sangiorgi, Marina Mora, Stefano Goldwurm, Raffaella Mazzotti, Mirella Filocamo, Chiuhui Mary Wang, Chiara Barzaghi, Elena Pegoraro, Luisa Politano, Valeria Viotti, Maurizio Moggio, Alessandra Renieri, Lucia Monaco, Giuseppe Merla, C. Baldo, Ilaria Meloni, Lorena Casareto, Barbara Garavaglia
Publikováno v:
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, Vol 11, Iss 1, Pp 1-8 (2016)
Orphanet Journal of Rare Diseases, Vol 11, Iss 1, Pp 1-8 (2016)
Background Rare diseases (RDs) are often neglected because they affect a small percentage of the population (6–8 %), which makes research and development of new therapies challenging processes. Easy access to high-quality samples and associated cli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a8334171a474b129de984a102ed0846
http://hdl.handle.net/11577/3232604
http://hdl.handle.net/11577/3232604
Autor:
Mirella, Filocamo, Chiara, Baldo, Stefano, Goldwurm, Renieri, Alessandra, Corrado, Angelini, Maurizio, Moggio, Marina, Mora, Giuseppe, Merla, Luisa, Politano, Barbara, Garavaglia, Lorena, Casareto, Francesca, Bricarelli, Telethon Network of Genetic Biobanks Staff, Corsolini, F, Galotto, S, Mazzotti, R, Stroppiana, G, Castagnetta, M, Mogni, M, Viotti, V, Bonetti, A, Felici, F, Natuzzi, F, Amabile, S, Frullanti, E, Meloni, I, Fanin, M, Nascimbeni, A, Pegoraro, E, Peterle, E, Napoli, L, Ripolone, M, Sciacco, M, Violano, R, Canioni, E, Gibertini, S, Saredi, S, Zanotti, S, Fusco, C, Micale, L, Pellico, Mt, Zelante, L, D'Ambrosio, P, Picillo, E, Taglia, A, Barzaghi, C, Panteghini, C, Valletta, L.
Publikováno v:
Orphanet Journal of Rare Diseases
Several examples have always illustrated how access to large numbers of biospecimens and associated data plays a pivotal role in the identification of disease genes and the development of pharmaceuticals. Hence, allowing researchers to access to sign
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e22aaff59f6ff5d95ee3086e46d5264