{"id":31719,"date":"2026-05-22T14:33:26","date_gmt":"2026-05-22T12:33:26","guid":{"rendered":"https:\/\/alan.lu\/?page_id=31719"},"modified":"2026-05-22T14:38:10","modified_gmt":"2026-05-22T12:38:10","slug":"centre-de-ressources-plateformes","status":"publish","type":"page","link":"https:\/\/alan.lu\/fr\/centre-de-ressources-plateformes\/","title":{"rendered":"Centre de ressources : organisations et plateformes"},"content":{"rendered":"<div class=\"wpb-content-wrapper\"><p>[vc_row][vc_column][vc_column_text css=&#8221;&#8221;]<\/p>\n<h2 style=\"text-align: center;\">Organisations &amp; Plateformes<\/h2>\n<p>[\/vc_column_text]<div class=\"edgtf-separator-holder clearfix  edgtf-separator-center\">\n\t<div class=\"edgtf-separator\" style=\"border-color: #00bcdf;width: 50px;border-bottom-width: 3px;margin-top: 25px;margin-bottom: 25px\"><\/div>\n<\/div>\n[vc_empty_space height=&#8221;50px&#8221;][\/vc_column][\/vc_row][vc_row content_width=&#8221;grid&#8221;][vc_column][vc_empty_space height=&#8221;50px&#8221;][\/vc_column][\/vc_row][vc_row content_width=&#8221;grid&#8221;][vc_column width=&#8221;1\/3&#8243;][vc_column_text css=&#8221;&#8221;]<\/p>\n<h3 style=\"text-align: left;\">AFM-TELETHON<\/h3>\n<p>[\/vc_column_text][vc_empty_space height=&#8221;35px&#8221;][vc_column_text]<a href=\"http:\/\/www.afm-telethon.com\/\" target=\"_blank\" rel=\"noopener noreferrer\">www.afm-telethon.com<\/a><\/p>\n<p>L&#8217;Association Fran\u00e7aise contre les Myopathies (AFM-T\u00e9l\u00e9thon) est une association de parents et de malades qui m\u00e8ne un combat sans rel\u00e2che contre des maladies g\u00e9n\u00e9tiques, rares et lourdement invalidantes.[\/vc_column_text][vc_empty_space height=&#8221;50px&#8221;][\/vc_column][vc_column width=&#8221;1\/3&#8243;][vc_column_text]<\/p>\n<h3 style=\"text-align: left;\">EUPATI<\/h3>\n<p>[\/vc_column_text][vc_empty_space height=&#8221;35px&#8221;][vc_column_text]<a href=\"https:\/\/eupati.eu\/\" target=\"_blank\" rel=\"noopener noreferrer\">www.eupati.eu<\/a><\/p>\n<p>EUPATI (European Patients\u2019 Academy on Therapeutic Innovation) est un partenariat public-priv\u00e9 multipartite. EUPATI propose des formations pour renforcer les capacit\u00e9s des patients et des repr\u00e9sentants des patients \u00e0 comprendre et \u00e0 contribuer de mani\u00e8re significative \u00e0 la recherche et au d\u00e9veloppement de m\u00e9dicaments, et pour am\u00e9liorer la disponibilit\u00e9 des informations m\u00e9dicales pour les patients et autres parties prenantes.[\/vc_column_text][vc_empty_space height=&#8221;50px&#8221;][\/vc_column][vc_column width=&#8221;1\/3&#8243;][vc_column_text]<\/p>\n<h3 style=\"text-align: left;\">EURORDIS<\/h3>\n<p>[\/vc_column_text][vc_empty_space height=&#8221;35px&#8221;][vc_column_text]<a href=\"http:\/\/www.eurordis.org\/\" target=\"_blank\" rel=\"noopener noreferrer\">www.eurordis.org<\/a><\/p>\n<p>Alliance \u00e0 but non lucratif, EURORDIS-Rare Diseases Europe regroupe 944 associations de patients atteints de maladie rare, repr\u00e9sentant 73 pays. EURORDIS vise \u00e0 am\u00e9liorer la qualit\u00e9 de vie des personnes vivant avec des maladies rares en Europe \u00e0 travers un plaidoyer pour des changements politiques au niveau europ\u00e9en, un soutien pour la recherche et le d\u00e9veloppement de m\u00e9dicaments, des actions de sensibilisation et en facilitant la mise en r\u00e9seau entre les groupes de patients.[\/vc_column_text][vc_empty_space height=&#8221;50px&#8221;][\/vc_column][\/vc_row][vc_row content_width=&#8221;grid&#8221;][vc_column width=&#8221;1\/3&#8243;][vc_column_text]<\/p>\n<h3 style=\"text-align: left;\">MYOBASE<\/h3>\n<p>[\/vc_column_text][vc_empty_space height=&#8221;35px&#8221;][vc_column_text]<a href=\"http:\/\/www.myobase.org\/\" target=\"_blank\" rel=\"noopener noreferrer\">www.myobase.org<\/a><\/p>\n<p><span style=\"font-weight: 400;\">Myobase est un portail documentaire sur les maladies neuromusculaires, cr\u00e9e par AFM-T\u00e9l\u00e9thon.<\/span>[\/vc_column_text][vc_empty_space height=&#8221;50px&#8221;][\/vc_column][vc_column width=&#8221;1\/3&#8243;][vc_column_text]<\/p>\n<h3 style=\"text-align: left;\">ORPHANET<\/h3>\n<p>[\/vc_column_text][vc_empty_space height=&#8221;35px&#8221;][vc_column_text]<a href=\"http:\/\/www.orpha.net\/\" target=\"_blank\" rel=\"noopener noreferrer\">www.orpha.net<\/a><\/p>\n<p><span style=\"font-weight: 400;\">Le portail europ\u00e9en des maladies rares et des m\u00e9dicaments orphelins. Orphanet est une ressource unique, rassemblant et am\u00e9liorant la connaissance sur les maladies rares, afin de faciliter et de perfectionner le diagnostic, le soin et le traitement des patients atteints de maladies rares. La plateforme Orphanet contient des r\u00e9pertoires des maladies rares, des centres experts, des essais cliniques, des registres, des m\u00e9dicaments orphelins et beaucoup plus<\/span>.[\/vc_column_text][vc_empty_space height=&#8221;50px&#8221;][\/vc_column][vc_column width=&#8221;1\/3&#8243;][vc_column_text]<\/p>\n<h3 style=\"text-align: left;\">INFO-HANDICAP LUXEMBOURG<\/h3>\n<p>[\/vc_column_text][vc_empty_space height=&#8221;35px&#8221;][vc_column_text]<a href=\"https:\/\/info-handicap.lu\/\" target=\"_blank\" rel=\"noopener noreferrer\">info-handicap.lu<\/a><\/p>\n<p><span style=\"font-weight: 400;\">Depuis 1993, le Centre National d\u2019Information et de Rencontre du Handicap est \u00e0 l\u2019\u00e9coute des personnes handicap\u00e9es, de leurs familles, des professionnels et, d\u2019une fa\u00e7on g\u00e9n\u00e9rale, de toute personne \u00e0 la recherche de renseignements sp\u00e9cifiques.<\/span>[\/vc_column_text][vc_empty_space height=&#8221;50px&#8221;][\/vc_column][\/vc_row][vc_row content_width=&#8221;grid&#8221;][vc_column width=&#8221;1\/3&#8243;][vc_column_text css=&#8221;&#8221;]<\/p>\n<h3 style=\"text-align: left;\">Fili\u00e8res de Sant\u00e9 Maladies Rares in France<\/h3>\n<p>[\/vc_column_text][vc_empty_space height=&#8221;35px&#8221;][vc_column_text css=&#8221;&#8221;]<a href=\"https:\/\/www.filieresmaladiesrares.fr\/les-23-filieres\/\" target=\"_blank\" rel=\"noopener noreferrer\">https:\/\/www.filieresmaladiesrares.fr<\/a><\/p>\n<p>En France, il existe 23 FSMR chacune couvrant un champ large et coh\u00e9rent de maladies, soit proches dans leurs manifestations, leurs cons\u00e9quences ou leur prise en charge, soit responsables d\u2019une atteinte d\u2019un m\u00eame organe ou d\u2019un syst\u00e8me.[\/vc_column_text][vc_empty_space height=&#8221;50px&#8221;][\/vc_column][\/vc_row][vc_row][vc_column][vc_empty_space height=&#8221;50px&#8221;][\/vc_column][\/vc_row][vc_row content_width=&#8221;grid&#8221; css=&#8221;.vc_custom_1596118384380{padding-top: 36px !important;padding-bottom: 41px !important;background-color: #ee3f75 !important;}&#8221;][vc_column css=&#8221;.vc_custom_1492609383973{padding-top: 2px !important;}&#8221;]\t<div class=\"edgtf-call-to-action normal\" style=\"background-color: #ee3f75;\">\n\n\t\t\t\t<div class=\"edgtf-container-inner\">\n\t\t\t\t\t<div class=\"edgtf-call-to-action-row-75-25 clearfix\" style=\"padding: 20px;\">\n\t\t\t\t\t\t<div class=\"edgtf-text-wrapper edgtf-call-to-action-column1 edgtf-call-to-action-cell left\">\n\t\t\t\t\t<div class=\"edgtf-call-to-action-text\" style=\"text-align: left\">\n<h2><span style=\"color: #ffffff;\">Contactez-nous en cas de questions ou besoin d\u2019assistance<\/span><\/h2>\n\t\t\t\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\n\t\t\t\t\t\t\t\t\t<div class=\"edgtf-button-wrapper edgtf-call-to-action-column2 edgtf-call-to-action-cell\" style =\"text-align: right ;\">\n\t\t\t\t\t\t<a itemprop=\"url\" href=\"\/contact-us\/\" target=\"_self\" style=\"color: #ee3f75;background-color: #ffffff;border-color: #ffffff\" class=\"edgtf-btn edgtf-btn-large edgtf-btn-solid edgtf-btn-custom-hover-bg edgtf-btn-custom-border-hover edgtf-btn-custom-hover-color\" data-hover-bg-color=\"#ee3f75\" data-hover-color=\"#ffffff\" data-hover-border-color=\"#ffffff\" >\t<span class=\"edgtf-btn-text\">Contact us<\/span>    <\/a>\t\t\t\t\t<\/div>\n\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t<\/div>\n[\/vc_column][\/vc_row]<\/p>\n<\/div>","protected":false},"excerpt":{"rendered":"<p>[vc_row][vc_column][vc_column_text css=&#8221;&#8221;] Organisations &amp; Plateformes [\/vc_column_text][vc_empty_space height=&#8221;50px&#8221;][\/vc_column][\/vc_row][vc_row content_width=&#8221;grid&#8221;][vc_column][vc_empty_space height=&#8221;50px&#8221;][\/vc_column][\/vc_row][vc_row content_width=&#8221;grid&#8221;][vc_column width=&#8221;1\/3&#8243;][vc_column_text css=&#8221;&#8221;] AFM-TELETHON [\/vc_column_text][vc_empty_space height=&#8221;35px&#8221;][vc_column_text]www.afm-telethon.com L&#8217;Association Fran\u00e7aise contre les Myopathies (AFM-T\u00e9l\u00e9thon) est une association de parents et de malades qui&#8230;<\/p>\n","protected":false},"author":2,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"give_campaign_id":0,"inline_featured_image":false,"footnotes":""},"class_list":["post-31719","page","type-page","status-publish","hentry"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.4 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Centre de ressources : organisations et plateformes, - ALAN<\/title>\n<meta name=\"robots\" content=\"noindex, follow\" \/>\n<meta property=\"og:locale\" content=\"fr_FR\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Centre de ressources : organisations et plateformes, - ALAN\" \/>\n<meta property=\"og:description\" content=\"[vc_row][vc_column][vc_column_text css=&#8221;&#8221;] Organisations &amp; 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