{"id":14422,"date":"2020-02-05T18:29:41","date_gmt":"2020-02-05T17:29:41","guid":{"rendered":"https:\/\/eufortrisomy21.eu\/?page_id=14422"},"modified":"2022-02-01T23:58:37","modified_gmt":"2022-02-01T22:58:37","slug":"21march20","status":"publish","type":"page","link":"https:\/\/eufortrisomy21.eu\/lt\/21march20\/","title":{"rendered":"2020 m. Kovo 21 d"},"content":{"rendered":"<h1>\n\t\t\n\t<\/h1>\n<h2>\n\t\tKovo 21 d., Net ir kriz\u0117s viduryje, mes galime pamin\u0117ti Pasaulin\u0119 Dauno sindromo dien\u0105 su Europos Parlamento nariais ir tyr\u0117jais\n\t<\/h2>\n\t<p>Pasaulin\u0117s Dauno sindromo dienos proga, kovo 21 d<sup>\u0161v<\/sup>, Europos Parlamente buvo suplanuota daugyb\u0117 rengini\u0173, kurie buvo at\u0161aukti d\u0117l sveikatos kriz\u0117s Covid-19.<\/p>\n<p>Nepaisant to, <strong>daugiau nei 100 Europos Parlamento nari\u0173<\/strong> (MEPs) &#8211; willing to honour persons with Down syndrome on this special day &#8211; <strong>pasira\u0161\u0117 deklaracij\u0105<\/strong> patvirtindami Dauno sindrom\u0105 turin\u010di\u0173 artim\u0173j\u0173 orum\u0105 ir neatimamas teises. Atstovaujamos visos politin\u0117s grup\u0117s (GUE, S&amp;D, Verts \/ ALE, Renew, PPE, ECR, ID ir NA).<\/p>\n<p><strong>Europos tyrin\u0117tojai<\/strong>, who were invited by MEPs to publicly present their works in the European Parliament, have written &#8211; alongside with other experts &#8211; <strong>op<\/strong>:<\/p>\n<strong>&#8220;Looking for Down syndrome treatment:<br \/>\nan inspiring scientific project which deserves EU&#8217;s political will&#8221;<\/strong>\n<p>Pasaulin\u0117s Dauno sindromo dienos proga jis bus paskelbtas Europos laikra\u0161\u010diuose. \u0160iame straipsnyje apibendrinami terapini\u0173 tyrim\u0173 tikslai ir prover\u017eiai: suma\u017einti negali\u0105 ir pagerinti Dauno sindrom\u0105 turin\u010di\u0173 asmen\u0173 gyvenimo kokyb\u0119 ir savaranki\u0161kum\u0105. Nor\u0117dami gauti daugiau informacijos apie mokslo laim\u0117jimus, pridedamos trys santraukos.<\/p>\n<p>Let&#8217;s follow <em>Trisomijos Europa 21<\/em> socialiniuose tinkluose.<\/p>\n\t\t\t<a href=\"https:\/\/eufortrisomy21.eu\/lt\/21march20\/declaration\/\" target=\"_self\" role=\"button\" rel=\"noopener\">\n\t\t\t\t\t\t\tDEKLARACIJA ir pasira\u0161iusi\u0173 EP nari\u0173\n\t\t\t\t\t<\/a>\n\t\t\t<a href=\"https:\/\/eufortrisomy21.eu\/lt\/21march20\/challenge\/\" target=\"_self\" role=\"button\" rel=\"noopener\">\n\t\t\t\t\t\t\tNeatitinkan\u010di\u0173 kojini\u0173 i\u0161\u0161\u016bkis\n\t\t\t\t\t<\/a>\n\t\t\t<a href=\"https:\/\/eufortrisomy21.eu\/lt\/21march20\/research\/\" target=\"_self\" role=\"button\" rel=\"noopener\">\n\t\t\t\t\t\t\tTyrimai\n\t\t\t\t\t<\/a>","protected":false},"excerpt":{"rendered":"<p>On March 21, even in the midst of the health crisis, we can honour World Down Syndrome Day with Members&hellip;<\/p>","protected":false},"author":2,"featured_media":0,"parent":0,"menu_order":10,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_acf_changed":false,"footnotes":""},"class_list":["post-14422","page","type-page","status-publish","hentry"],"acf":[],"_links":{"self":[{"href":"https:\/\/eufortrisomy21.eu\/lt\/wp-json\/wp\/v2\/pages\/14422"}],"collection":[{"href":"https:\/\/eufortrisomy21.eu\/lt\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/eufortrisomy21.eu\/lt\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/eufortrisomy21.eu\/lt\/wp-json\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/eufortrisomy21.eu\/lt\/wp-json\/wp\/v2\/comments?post=14422"}],"version-history":[{"count":0,"href":"https:\/\/eufortrisomy21.eu\/lt\/wp-json\/wp\/v2\/pages\/14422\/revisions"}],"wp:attachment":[{"href":"https:\/\/eufortrisomy21.eu\/lt\/wp-json\/wp\/v2\/media?parent=14422"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}