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[vc_row][vc_column][vc_column_text]<\/p>\n

Contribucions a ORPHANET \/ Contribuciones a ORPHANET \/\u00a0Contributions to ORPHANET<\/h3>\n

La Dra. Mayka Sanchez forma parte de la comisi\u00f3n Europea y Espa\u00f1ola de Orphanet y ha redactado en ingl\u00e9s los abstracts de <\/span><\/span>8 enfermedades raras<\/b><\/span><\/span>:<\/span><\/span><\/p>\n

1. IRIDA: <\/span><\/span>http:\/\/www.orpha.net\/consor\/cgi-bin\/OC_Exp.php?lng=EN&Expert=209981<\/span><\/span><\/span><\/a><\/u><\/span><\/span><\/p>\n

2. Anemias diseritropoyeticas cong\u00e9nitas (CDA), incluido CDA 1, 2, 3, 4 y CDA con trombocitosis)<\/span><\/p>\n

http:\/\/www.orpha.net\/consor\/cgi-bin\/OC_Exp.php?lng=EN&Expert=85<\/span><\/span><\/a><\/u><\/span><\/span>
\n<\/span>http:\/\/www.orpha.net\/consor\/cgi-bin\/OC_Exp.php?lng=EN&Expert=293825<\/span><\/span><\/a><\/u><\/span><\/span>
\n<\/span>http:\/\/www.orpha.net\/consor\/cgi-bin\/OC_Exp.php?lng=EN&Expert=98869<\/span><\/span><\/a><\/u><\/span><\/span>
\n<\/span>http:\/\/www.orpha.net\/consor\/cgi-bin\/OC_Exp.php?lng=EN&Expert=98873<\/span><\/span><\/a><\/u><\/span><\/span>
\n<\/span>http:\/\/www.orpha.net\/consor\/cgi-bin\/OC_Exp.php?lng=EN&Expert=98870<\/span><\/span><\/a><\/u><\/span><\/span>
\n<\/span>http:\/\/www.orpha.net\/consor\/cgi-bin\/OC_Exp.php?lng=EN&Expert=67044<\/span><\/span><\/a><\/u><\/span><\/span><\/p>\n

3. Atransferrinemia:<\/span><\/p>\n

http:\/\/www.orpha.net\/consor\/cgi-bin\/OC_Exp.php?lng=EN&Expert=1195<\/span><\/span><\/span><\/a><\/u><\/span><\/span><\/p>\n

Adem\u00e1s ha contribuido en la validaci\u00f3n de m\u00faltiples traducciones del ingl\u00e9s al castellano para este portal. <\/span><\/p>\n

Marca Registrada Europea \/ European Trade Mark<\/h3>\n

Marca Registrada Europea<\/b><\/span><\/span> HIGHFERRITIN: Con ayuda de la Asociaci\u00f3n de pacientes de Hemocromatosis AEH <\/span><\/span>www.hemocromatosis.es<\/span><\/span><\/span><\/a><\/u><\/span><\/span> se ha procedido a registrar en fecha 18\/05\/2015 HIGHFERRITIN y su dise\u00f1o como marca Registrada Europea (referencia TM1480EU00, marca comunitaria numero 1409369) en las clases 5,9,42 y 44.<\/span><\/span><\/p>\n

Eines de Telemedicina \/ Herramientas de Telemedicina \/ Telemedicine Tools<\/h3>\n

We have created the\u00a0telemedicine web tool<\/strong>\u00a0for the diagnosis and management of patients with hyperferritinemia HIGHFERRITIN,\u00a0http:\/\/highferritin.imppc.org<\/a>. We are collecting patient data for a future study on the causes of hyperferritinemia. We are proceeding to make an app app for mobile phones and tablets to make this\u00a0telemedicine tool\u00a0<\/strong>more accessible to medical\u00a0doctors.\u00a0<\/span><\/p>\n

CoDysAn<\/strong>,\u00a0http:\/\/codysan.eu, has been developed with the aim of efficiently diagnose and manage patients with CDA. It also offers the option to get in contact with patient organisations.<\/span><\/p>\n

[\/vc_column_text][\/vc_column][\/vc_row]<\/p>\n","protected":false},"excerpt":{"rendered":"

[vc_row][vc_column][vc_column_text] Contribucions a ORPHANET \/ Contribuciones a ORPHANET \/\u00a0Contributions to ORPHANET La Dra. Mayka Sanchez forma parte de la comisi\u00f3n Europea y Espa\u00f1ola de Orphanet y ha redactado en ingl\u00e9s los abstracts de 8 enfermedades raras: 1. IRIDA: http:\/\/www.orpha.net\/consor\/cgi-bin\/OC_Exp.php?lng=EN&Expert=209981 2. Anemias diseritropoyeticas cong\u00e9nitas (CDA), incluido CDA 1, 2, 3, 4 y CDA con trombocitosis) http:\/\/www.orpha.net\/consor\/cgi-bin\/OC_Exp.php?lng=EN&Expert=85…<\/p>\n","protected":false},"author":5,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_oct_exclude_from_cache":false,"om_disable_all_campaigns":false,"_monsterinsights_skip_tracking":false,"_monsterinsights_sitenote_active":false,"_monsterinsights_sitenote_note":"","_monsterinsights_sitenote_category":0,"_uf_show_specific_survey":0,"_uf_disable_surveys":false,"footnotes":""},"class_list":["post-600","page","type-page","status-publish","hentry","description-off"],"jetpack_sharing_enabled":true,"_links":{"self":[{"href":"https:\/\/bloodgenetics.com\/wp-json\/wp\/v2\/pages\/600","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/bloodgenetics.com\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/bloodgenetics.com\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/bloodgenetics.com\/wp-json\/wp\/v2\/users\/5"}],"replies":[{"embeddable":true,"href":"https:\/\/bloodgenetics.com\/wp-json\/wp\/v2\/comments?post=600"}],"version-history":[{"count":8,"href":"https:\/\/bloodgenetics.com\/wp-json\/wp\/v2\/pages\/600\/revisions"}],"predecessor-version":[{"id":2090,"href":"https:\/\/bloodgenetics.com\/wp-json\/wp\/v2\/pages\/600\/revisions\/2090"}],"wp:attachment":[{"href":"https:\/\/bloodgenetics.com\/wp-json\/wp\/v2\/media?parent=600"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}