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dc.contributor.author Bánusz, Rita
dc.contributor.author Varadi Z
dc.contributor.author Varga, Edit
dc.contributor.author Jakab, Zsuzsanna
dc.contributor.author Garami, Miklós
dc.contributor.author Csóka, Monika
dc.date.accessioned 2016-01-15T08:02:08Z
dc.date.available 2016-01-15T08:02:08Z
dc.date.issued 2014
dc.identifier 84904045202
dc.identifier.citation pagination=59-64; journalVolume=58; journalIssueNumber=1; journalTitle=MAGYAR ONKOLÓGIA;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/2281
dc.description.abstract Malignant tumors of mesenchymal origin are called sarcomas. Mesenchymal cells normally mature into skeletal muscle, smooth muscle, fat, fibrous tissue, bone and cartilage. Rhabdomyosarcoma (RMS) arises from immature mesenchymal cells that are committed to skeletal muscle lineage. However, it can also arise in tissues in which striated muscle is normally not found (such as the urinary tract). Undifferentiated sarcomas cannot be ascribed to any specific lineage. Treatment results improved significantly in the last decade by combined treatment (chemotherapy, surgery, irradiation, in some cases targeted therapy). Good treatment results can be achieved in pediatric oncology centers by early diagnosis and adequate treatment according to international treatment protocols.
dc.relation.ispartof urn:issn:0025-0244
dc.title Gyermekkori lágyrészsarcomak diagnosztikája es kezelése.
dc.type Journal Article
dc.date.updated 2015-11-06T12:54:13Z
dc.language.rfc3066 hu
dc.identifier.mtmt 2573482
dc.identifier.pubmed 24712008
dc.contributor.department SE/AOK/K/II. Sz. Gyermekgyógyászati Klinika
dc.contributor.institution Semmelweis Egyetem


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