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Auteur Farini A |
Documents disponibles écrits par cet auteur (29)
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Soussi S ; Savchenko L ; Rovina D ; Iacovoni JS ; Gottinger A ; Viallettes M ; Pioner JM ; Farini A ; Mallia S ; Rabino M ; Pompilio G ; Parini A ; Lairez O ; Gowran A ; Pizzinat N | 27/07/2023Article
Farini A ; Tripodi L ; Villa C ; Strati F ; Facoetti A ; Baselli G ; Troisi J ; Landolfi A ; Lonati C ; Molinaro D ; Wintzinger M ; Gatti S ; Cassani B ; Caprioli F ; Facciotti F ; Quattrocelli M ; Torrente Y | England | 19/12/2022Article
Tripodi L ; Molinaro D ; Fortunato F ; Mella C ; Cassani B ; Torrente Y ; Farini A | Switzerland | 24/11/2022Article
Farini A ; Sitzia C ; Villa C ; Cassani B ; Tripodi L ; Legato M ; Belicchi M ; Bella P ; Lonati C ; Gatti S ; Cerletti M ; Torrente Y | 08/04/2021Article
Farini A ; Villa C ; Di Silvestre D ; Bella P ; Tripodi L ; Rossi R ; Sitzia C ; Gatti S ; Mauri P ; Torrente Y | 05/2020Article
Sitzia C, Auteur ; Meregalli M ; Belicchi M ; Farini A ; Arosio M ; Bestetti D ; Villa C ; Valenti L ; Brambilla P ; Torrente Y | Switzerland | 07/2019Article
Sitzia C, Auteur ; Farini A ; Jardim L ; Razini P ; Belicchi M ; Cassinelli L ; Villa C ; Erratico S ; Parolini D ; Bella P ; da Silva Bizario JC ; Garcia L ; Dias-Baruffi M ; Meregalli M ; Torrente Y | 2016Article
Meregalli M, Auteur ; Farini A ; Sitzia C ; Beley C ; Razini P ; Cassinelli L ; Colleoni F ; Frattini P ; Santo N ; Galbiati E ; Prosperi D ; Tavelli A ; Belicchi M ; Garcia L ; Torrente Y | 2015Article
Meregalli M ; Navarro C ; Sitzia C ; Farini A ; Montani E ; Wein N ; Razini P ; Beley C ; Cassinelli L ; Parolini D ; Belicchi M ; Parazzoli D ; Garcia L ; Torrente Y | 2013Article
Meregalli M ; Farini A ; Colleoni F ; Cassinelli L ; Torrente Y | 2012Accès au résumé Pubmed/to pubmed abstractArticle
4th International Congress of Myology, 4ème colloque international de Myologie (9-13 mai 2011; Lille (France)) ; Sitzia C ; Farini A ; Navarro C ; D'Antona G ; Belicchi M ; Parolini D ; Bottinelli R ; Meregalli M ; Torrente Y | AFM-TELETHON | 2011Limb Girdle Muscular Dystrophies (LGMDs) are a group of muscular diseases characterized by predominant weakness and wasting of muscles of the pelvic and shoulder girdle. LGMD-2B and MM were found to arise from defects in the dysferlin gene. In L[...]Article
4th International Congress of Myology, 4ème colloque international de Myologie (9-13 mai 2011; Lille (France)) ; Erratico S ; Belicchi M ; Razini P ; Farini A ; Meregalli M ; Villa C ; Bresolin N ; Torrente Y | 2011Adult stem cells reside in all tissues, where they maintain homeostatic conditions and respond to injuries. These cells are regulated and supported by the surrounding microenvironment, called stem cell "niche", composed by cellular and molecular[...]Article
4th International Congress of Myology, 4ème colloque international de Myologie (9-13 mai 2011; Lille (France)) ; Villa C ; Farini A ; Erratico S ; Belicchi M ; Meregalli M ; Fiori F ; Rustichelli F ; Torrente Y | 2011Cell therapy is an emerging approach of regenerative medicine with significant efforts in clinical areas. Stem cells cannot be easily observed directly when injected systemically, and, therefore, their behaviors need to be visualized indirectly.[...]Article
4th International Congress of Myology, 4ème colloque international de Myologie (9-13 mai 2011; Lille (France)) ; Del Fraro G ; Meregalli M ; Farini A ; Belicchi M ; Parolini D ; Razini P ; Cassinelli L ; Angeloni V ; Maciotta S ; Bresolin N ; de Silva Bizario J ; Garcia L ; Torrente Y | 2011In DMD, skeletal and cardiac muscles are affected, leading to wheelchair dependency, respiratory failure and premature death. A combination of different strategies might enhance the possibility of successful therapy. We isolated CD133+ cells fro[...]Article
Farini A ; Belicchi M ; Parolini D ; Sitzia C ; Cassinelli L ; Del Fraro G ; Razini P ; Angeloni V ; Jardim L ; da Silva Bizario J ; Garcia L ; Torrente I | AFM-TELETHON | 2011In DMD, skeletal and cardiac muscles are affected, leading to wheelchair dependency, respiratory failure and premature death. Recent advances have pointed out a variety of possible therapeutic approaches. A combination of these strategies might [...]Article
Meregalli M ; Farini A ; Parolini D ; Maciotta S ; Torrente Y | 2010Accès au résumé PubMed / to PubMed abstractArticle
Marchesi C ; Belicchi M ; Meregalli M ; Farini A ; Cattaneo A ; Parolini D ; Gavina M ; Porretti L ; D'Angelo MG ; Bresolin N ; Torrente Y | 05/2008Article
Benchaouir R ; Meregalli M ; Farini A ; D'Antona G ; Belicchi M ; Goyenvalle A ; Battistelli M ; Bresolin N ; Bottinelli R ; Garcia L ; Torrente Y | 01/2008Accès au résumé PubMed / to PubMed abstractArticle
Meregalli M ; Farini A ; D'Antona G ; Belicchi M ; Goyenvalle A ; Parolini D ; Bresolin N ; Bottinelli R ; Garcia L ; Torrente Y | 2008Several recent advances have pointed out a variety of possible therapeutic approaches in muscular dystrophies, from pharmacological treatments to gene therapy and cell therapy with different types of newly identified stem cells. A combination of[...]Article
Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France) ; Belicchi M ; Meregalli M ; Razini P ; Cattaneo A ; Farini A ; Iacchetti E ; Porretti L ; Milani P ; Bresolin N ; Torrente Y | 2008The use of stem cells in regenerative medicine and cell-based therapies offers immense potential in diseases witch have currently no treatment such as Duchenne muscular dystrophy. A limitation to the use of CD133+ for a therapeutic application i[...]Article
Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France) ; Navarro C ; Farini A ; Meregalli M ; Belicchi M ; Parolini D ; Razini P ; Krahn M ; Wein N ; Bourg N ; Bartoli M ; Richard I ; Torrente Y | 2008Mutations in gene encoding Dysferlin are involved in Limb-gird Muscular Dystrophy type 2B (LGMD-2B) and and Miyoshi myopathy (MM), both diseases are characterized by progressive weakness and wasting of skeletal muscles. Dysferlin is abundantly e[...]Article
Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France) ; Maciotta S ; Meregalli M ; Farini A ; Belicchi M ; Parolini D ; Bresolin N ; Torrente Y | 2008DMD is caused by frameshift mutations in the gene encoding for dystrophin. These mutations are responsible for the loss of function of the dystrophin protein that leads to membrane destabilization and subsequent activation of pathophysiological [...]