{"id":47194,"date":"2020-03-12T05:10:24","date_gmt":"2020-03-12T05:10:24","guid":{"rendered":"https:\/\/www.deberes.net\/tesis\/sin-categoria\/contribucion-al-estudio-de-la-histogenesis-de-los-tumores-experimentales-inducidos-por-fibras-de-asbestiforme-y-similares\/"},"modified":"2020-03-12T05:10:24","modified_gmt":"2020-03-12T05:10:24","slug":"contribucion-al-estudio-de-la-histogenesis-de-los-tumores-experimentales-inducidos-por-fibras-de-asbestiforme-y-similares","status":"publish","type":"post","link":"https:\/\/www.deberes.net\/tesis\/ciencias-medicas\/contribucion-al-estudio-de-la-histogenesis-de-los-tumores-experimentales-inducidos-por-fibras-de-asbestiforme-y-similares\/","title":{"rendered":"Contribucion al estudio de la histogenesis de los tumores experimentales inducidos por fibras de asbestiforme y similares"},"content":{"rendered":"<h2>Tesis doctoral de <strong> Tomas Alvarez Gago <\/strong><\/h2>\n<p>Se inyectaron intraperitonealmente a 330 ratas ivan wistar divididas en 8 grupos de 40 animales excepto el ultimo que estaba constituido por 50  fibras de vidrio finas y gruesas  crocidolita y nemalita. Las fracciones de vidrio fina y grosera se obtuvieron tras trituracion y sedimentacion de 2 10 y 50 mgrs. Esta ultima dosis se fracciono en dos de 25 mgrs. Inyectandose con un intervalo de una semana. La dosis de crocidolita fue unica y de 2 mgrs. Y la nemalita doble y de 40 mgrs. En total 174 animales presentaron tumor de ellos  163 eran mesoteliomas. Tambien se estudian las lesiones precoces y se concluye con la posibilidad de un origen submesotelial de los mesoteliomas.<\/p>\n<p>&nbsp;<\/p>\n<h3>Datos acad\u00e9micos de la tesis doctoral \u00ab<strong>Contribucion al estudio de la histogenesis de los tumores experimentales inducidos por fibras de asbestiforme y similares<\/strong>\u00ab<\/h3>\n<ul>\n<li><strong>T\u00edtulo de la tesis:<\/strong>\u00a0 Contribucion al estudio de la histogenesis de los tumores experimentales inducidos por fibras de asbestiforme y similares <\/li>\n<li><strong>Autor:<\/strong>\u00a0 Tomas Alvarez Gago <\/li>\n<li><strong>Universidad:<\/strong>\u00a0 Valladolid<\/li>\n<li><strong>Fecha de lectura de la tesis:<\/strong>\u00a0 01\/01\/1980<\/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>Antonio Cardesa Garc\u00eda<\/li>\n<\/ul>\n<\/li>\n<li><strong>Tribunal<\/strong>\n<ul>\n<li>Presidente del tribunal: Ramon Velasco Alonso <\/li>\n<li>Antonio Cardesa Garc\u00eda (vocal)<\/li>\n<li>Cesar Aguirre Viani (vocal)<\/li>\n<li>Juliana Fari\u00f1a Gonzalez (vocal)<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Tesis doctoral de Tomas Alvarez Gago Se inyectaron intraperitonealmente a 330 ratas ivan wistar divididas en 8 grupos de 40 [&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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