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<dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:invenio="http://invenio-software.org/elements/1.0" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"><dc:identifier>doi:10.1007/s12094-017-1807-y</dc:identifier><dc:language>eng</dc:language><dc:creator>Losa, F.</dc:creator><dc:creator>Soler, G.</dc:creator><dc:creator>Casado, A.</dc:creator><dc:creator>Estival, A.</dc:creator><dc:creator>Fernández, I.</dc:creator><dc:creator>Giménez, S.</dc:creator><dc:creator>Longo, F.</dc:creator><dc:creator>Pazo-Cid, R.</dc:creator><dc:creator>Salgado, J.</dc:creator><dc:creator>Seguí, M.Á.</dc:creator><dc:title>SEOM clinical guideline on unknown primary cancer (2017)</dc:title><dc:identifier>ART-2017-104275</dc:identifier><dc:description>Cancer of unknown primary site is a histologically confirmed cancer that manifests in advanced stage, with no identifiable primary site following standard diagnostic procedures. Patients are initially categorized based on the findings of the initial biopsy: adenocarcinoma, squamous-cell carcinoma, neuroendocrine carcinoma, and poorly differentiated carcinoma. Appropriate patient management requires understanding several clinical and pathological features that aid in identifying several subsets of patients with more responsive tumors.</dc:description><dc:date>2017</dc:date><dc:source>http://zaguan.unizar.es/record/65289</dc:source><dc:doi>10.1007/s12094-017-1807-y</dc:doi><dc:identifier>http://zaguan.unizar.es/record/65289</dc:identifier><dc:identifier>oai:zaguan.unizar.es:65289</dc:identifier><dc:identifier.citation>Clinical and Translational Oncology 20 (2017), 89 – 96</dc:identifier.citation><dc:rights>by</dc:rights><dc:rights>http://creativecommons.org/licenses/by/3.0/es/</dc:rights><dc:rights>info:eu-repo/semantics/openAccess</dc:rights></dc:dc>

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