{"id":5509,"date":"2015-11-20T11:19:38","date_gmt":"2015-11-20T09:19:38","guid":{"rendered":"http:\/\/www.toscanalifesciences.org\/it\/?p=5509"},"modified":"2023-02-07T23:19:59","modified_gmt":"2023-02-07T22:19:59","slug":"a-ma-me-mi-onlus-dona-a-tls-10mila-euro-per-la-ricerca-aciduria-metilmalonica","status":"publish","type":"post","link":"https:\/\/www.toscanalifesciences.org\/it\/news-e-eventi\/a-ma-me-mi-onlus-dona-a-tls-10mila-euro-per-la-ricerca-aciduria-metilmalonica\/","title":{"rendered":"A.Ma.Me.mi Onlus dona a TLS 10mila euro per la ricerca sull&#8217;aciduria metilmalonica"},"content":{"rendered":"<div>Insieme per la ricerca sulle malattie rare. Sono Toscana Life Sciences e l\u2019Associazione Malattie Metaboliche Memi, che ieri, gioved\u00ec 19 novembre, ha scelto di donare alla Fondazione senese un contributo concreto in occasione dell\u2019evento <strong>\u201cInsieme per la ricerca\u201d<\/strong>, svoltosi a Cambiasca, nella provincia di Verbano Cusio Ossola. Lara Righes, presidente dell\u2019<strong>A.Ma.Me.mi Onlus<\/strong>, ha consegnato ad Andrea Paolini, direttore generale della Fondazione TLS, 10mila euro per sostenere il <strong>progetto MMACHC<\/strong>, di cui \u00e8 titolare la ricercatrice Laura Tinti attraverso un finanziamento Telethon, all\u2019interno dell\u2019incubatore senese.\u00a0<\/div>\n<div>\u00a0<\/div>\n<div>Lo studio ha l\u2019obiettivo di trovare possibili terapie contro l\u2019<strong>aciduria metilmalonica<\/strong>, il pi\u00f9 frequente difetto congenito del metabolismo della vitamina B12. Una malattia rara che provoca, soprattutto tra i bambini fino a un anno e tra gli adolescenti, gravi manifestazioni a livello neurologico, oculari, ematologiche, renali, gastrointestinali, cardiache e polmonari.<\/div>\n<div>\u00a0<\/div>\n<div>Lara Righes, fondatrice di A.Ma.Me.mi Onlus, \u00e8 la mamma di una bimba affetta da aciduria metilmalonico con omocistinuria; da qui nasce la volont\u00e0 di impegnarsi nella <strong>raccolta fondi da destinare alla ricerca<\/strong> per una malattia ancora poco conosciuta, che ha trovato pieno sostegno in tutta la comunit\u00e0 di Cambiasca. All\u2019incontro erano presenti anche Claudio Liera, sindaco della cittadina piemontese e Cristina Tinti, coordinatrice dei progetti Orphan e incubation manager di Fondazione Tls.\u00a0<\/div>\n<div>\u00a0<\/div>\n<div>\u201cRingraziamo l\u2019Associazione Malattie Metaboliche Memi \u2013 sottolinea Andrea Paolini \u00a0\u2013 per il contributo che ha deciso di devolvere alla Fondazione TLS. Un aiuto prezioso soprattutto perch\u00e9 si inserisce in un ambito di ricerca, quello della malattie rare, in cui \u00a0\u00e8 fondamentale il networking tra finanziamenti pubblici e privati, know how dei centri di ricerca, l\u2019expertise di sviluppo della piccola e media impresa biotech. Se a questa sinergia si aggiunge la solidariet\u00e0 e l\u2019impegno di associazioni come l\u2019A.Ma.Me.mi le possibilit\u00e0 di trovare soluzioni concrete anche per le malattie rare aumentano\u201d.<\/div>\n<div>\u00a0<\/div>\n<div>\u201cL\u2019obiettivo del progetto \u2013 aggiunge Cristina Tinti \u2013 \u00e8 capire come si possa sostituire la proteina difettosa in questi pazienti, MMACHC, con una versione correttamente funzionante. Il lavoro svolto fino ad oggi offre prospettive interessanti per il futuro. Un impegno che oggi \u00e8 pi\u00f9 forte anche grazie alla solidariet\u00e0 dell\u2019 A.Ma.Me.mi\u201d. Per maggiori informazioni \u00e8 possibile visitare il sito <a href=\"http:\/\/www.toscanalifesciences.org\/\" target=\"_blank\" rel=\"noopener\">www.toscanalifesciences.org<\/a>, nella pagina dedicata al progetto MMACHC, e il portale dell\u2019 A.Ma.Me.mi Onlus.<\/div>\n<div>\u00a0<\/div>\n<div>\u00a0<\/div>\n","protected":false},"excerpt":{"rendered":"<p>Insieme per la ricerca sulle malattie rare. Sono Toscana Life Sciences e l\u2019Associazione Malattie Metaboliche Memi, che ieri, gioved\u00ec 19&#8230;<\/p>\n","protected":false},"author":6,"featured_media":14333,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[10,9],"tags":[],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v23.2 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>A.Ma.Me.mi Onlus dona a TLS 10mila euro per la ricerca sull&#039;aciduria metilmalonica - Toscana Life Sciences<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.toscanalifesciences.org\/it\/news-e-eventi\/a-ma-me-mi-onlus-dona-a-tls-10mila-euro-per-la-ricerca-aciduria-metilmalonica\/\" \/>\n<meta property=\"og:locale\" content=\"it_IT\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"A.Ma.Me.mi Onlus dona a TLS 10mila euro per la ricerca sull&#039;aciduria metilmalonica - Toscana Life Sciences\" \/>\n<meta property=\"og:description\" content=\"Insieme per la ricerca sulle malattie rare. 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