{"id":26357,"date":"2026-02-25T13:17:36","date_gmt":"2026-02-25T12:17:36","guid":{"rendered":"https:\/\/porib.com\/?p=26357"},"modified":"2026-02-25T13:18:18","modified_gmt":"2026-02-25T12:18:18","slug":"de-las-heras-j-cebolla-j-de-pedro-s-gomez-barrera-m-vitoria-i","status":"publish","type":"post","link":"https:\/\/porib.com\/en\/de-las-heras-j-cebolla-j-de-pedro-s-gomez-barrera-m-vitoria-i\/","title":{"rendered":"de las Heras J, Cebolla J, de Pedro S, Gomez-Barrera M, Vitoria I"},"content":{"rendered":"<div class=\"miniatura_foto\"><img loading=\"lazy\" decoding=\"async\" class=\"size-full wp-image-13999 alignleft\" src=\"https:\/\/porib.com\/wp-content\/uploads\/2021\/07\/Orphanet-Journal-of-Rare-Diseases-1.jpg\" alt=\"\" width=\"90\" height=\"120\" \/><\/div>\n<p style=\"text-align: justify;\"><strong>de las Heras J, Cebolla J, de Pedro S, Gomez-Barrera M, Vitoria I<\/strong><\/p>\n<p>&nbsp;<\/p>\n<p>&nbsp;<\/p>\n<h6 style=\"text-align: justify;\">Investigating the therapeutic profile of velaglucerase alfa in paediatric patients with Gaucher disease: A systematic review across all paediatric age groups<\/h6>\n<h6 style=\"text-align: justify;\"><strong>Orphanet J Rare Dis. 2026. doi: 10.1186\/s13023-026-04221-9<\/strong><\/h6>\n<div class=\"col80p\">\n<p style=\"text-align: justify;\"><a href=\"https:\/\/doi.org\/10.1186\/s13023-026-04221-9\" target=\"_blank\" rel=\"noopener\">M\u00c1S INFORMACI\u00d3N<\/a><\/p>\n<\/div>\n","protected":false},"excerpt":{"rendered":"<p>de las Heras J, Cebolla J, de Pedro S, Gomez-Barrera M, Vitoria I &nbsp; &nbsp; Investigating the therapeutic profile of velaglucerase alfa in paediatric patients with Gaucher disease: A systematic review across all paediatric age groups Orphanet J Rare Dis. 2026. doi: 10.1186\/s13023-026-04221-9 M\u00c1S INFORMACI\u00d3N<\/p>\n","protected":false},"author":4,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"quote","meta":{"footnotes":""},"categories":[921,941,971],"tags":[],"class_list":["post-26357","post","type-post","status-publish","format-quote","hentry","category-enfermedades-raras","category-revisiones-y-comparaciones-indirectas-tipo-de-proyecto","category-orphanet-journal-of-rare-diseases","post_format-post-format-quote"],"translation":{"provider":"WPGlobus","version":"2.10.3","language":"en","enabled_languages":["es","en"],"languages":{"es":{"title":true,"content":true,"excerpt":false},"en":{"title":false,"content":false,"excerpt":false}}},"_links":{"self":[{"href":"https:\/\/porib.com\/en\/wp-json\/wp\/v2\/posts\/26357"}],"collection":[{"href":"https:\/\/porib.com\/en\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/porib.com\/en\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/porib.com\/en\/wp-json\/wp\/v2\/users\/4"}],"replies":[{"embeddable":true,"href":"https:\/\/porib.com\/en\/wp-json\/wp\/v2\/comments?post=26357"}],"version-history":[{"count":3,"href":"https:\/\/porib.com\/en\/wp-json\/wp\/v2\/posts\/26357\/revisions"}],"predecessor-version":[{"id":26360,"href":"https:\/\/porib.com\/en\/wp-json\/wp\/v2\/posts\/26357\/revisions\/26360"}],"wp:attachment":[{"href":"https:\/\/porib.com\/en\/wp-json\/wp\/v2\/media?parent=26357"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/porib.com\/en\/wp-json\/wp\/v2\/categories?post=26357"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/porib.com\/en\/wp-json\/wp\/v2\/tags?post=26357"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}