{"id":34640,"date":"1998-01-01T00:00:00","date_gmt":"1998-01-01T00:00:00","guid":{"rendered":"https:\/\/www.deberes.net\/tesis\/sin-categoria\/heterogeneidad-molecular-de-la-beta-talasemia-en-espana\/"},"modified":"1998-01-01T00:00:00","modified_gmt":"1998-01-01T00:00:00","slug":"heterogeneidad-molecular-de-la-beta-talasemia-en-espana","status":"publish","type":"post","link":"https:\/\/www.deberes.net\/tesis\/quimica\/heterogeneidad-molecular-de-la-beta-talasemia-en-espana\/","title":{"rendered":"Heterogeneidad molecular de la beta-talasemia en espa\u00f1a."},"content":{"rendered":"<h2>Tesis doctoral de <strong> Paloma Ropero Gradilla <\/strong><\/h2>\n<p>Las talasemias son un grupo de anemias hereditarias que se caracterizan por la ausencia total o parcial de s\u00edntesis de las cadenas de globina que constituyen la hemoglobina. Cuando la cadena afecta es la alfa se denomina alfa talasemia y beta talasemia, cuando es beta.  hasta la d\u00e9cada de los 80, se sab\u00eda que la alteraci\u00f3n responsable se localizaba en los genes siendo por lo tanto hereditaria, pero es a partir de esta fecha cuando se empieza a conocer el tipo de mutaciones y donde se localiza. Con este trabajo se ha intentado poner de manifiesto la gran heterogeneidad de la beta talasemia en espa\u00f1a, ya que esta enfermedad est\u00e1 relacionada con zonas donde existi\u00f3 la malaria. Por ello hemos pensado que ser\u00eda interesante conocerla.<\/p>\n<p>&nbsp;<\/p>\n<h3>Datos acad\u00e9micos de la tesis doctoral \u00ab<strong>Heterogeneidad molecular de la beta-talasemia en espa\u00f1a.<\/strong>\u00ab<\/h3>\n<ul>\n<li><strong>T\u00edtulo de la tesis:<\/strong>\u00a0 Heterogeneidad molecular de la beta-talasemia en espa\u00f1a. <\/li>\n<li><strong>Autor:<\/strong>\u00a0 Paloma Ropero Gradilla <\/li>\n<li><strong>Universidad:<\/strong>\u00a0 Complutense de Madrid<\/li>\n<li><strong>Fecha de lectura de la tesis:<\/strong>\u00a0 01\/01\/1998<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n<h3>Direcci\u00f3n y tribunal<\/h3>\n<ul>\n<li><strong>Director de la tesis<\/strong>\n<ul>\n<li>Ana Villegas Martinez<\/li>\n<\/ul>\n<\/li>\n<li><strong>Tribunal<\/strong>\n<ul>\n<li>Presidente del tribunal: Benito Del Castillo Garcia <\/li>\n<li> R\u00f3denas De La Rocha Sof\u00eda (vocal)<\/li>\n<li>Domingo Espinos Perez (vocal)<\/li>\n<li>Felix Carbonell Ramon (vocal)<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Tesis doctoral de Paloma Ropero Gradilla Las talasemias son un grupo de anemias hereditarias que se caracterizan por la ausencia [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"site-sidebar-layout":"default","site-content-layout":"","ast-site-content-layout":"","site-content-style":"default","site-sidebar-style":"default","ast-global-header-display":"","ast-banner-title-visibility":"","ast-main-header-display":"","ast-hfb-above-header-display":"","ast-hfb-below-header-display":"","ast-hfb-mobile-header-display":"","site-post-title":"","ast-breadcrumbs-content":"","ast-featured-img":"","footer-sml-layout":"","theme-transparent-header-meta":"","adv-header-id-meta":"","stick-header-meta":"","header-above-stick-meta":"","header-main-stick-meta":"","header-below-stick-meta":"","astra-migrate-meta-layouts":"default","ast-page-background-enabled":"default","ast-page-background-meta":{"desktop":{"background-color":"var(--ast-global-color-4)","background-image":"","background-repeat":"repeat","background-position":"center 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