Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/131352
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dc.contributor.authorPablo Oppezzo
dc.date.accessioned2017-04-30T13:33:01Z-
dc.date.available2017-04-30T13:33:01Z-
dc.date.issued2012
dc.identifier.isbn978-953-307-881-6
dc.identifier.urihttp://hdl.handle.net/123456789/131352-
dc.description.abstractB-cell chronic lymphocytic leukemia (CLL) is considered a single disease with extremely variable course, and survival rates ranging from months to decades. It is clear that clinical heterogeneity reflects biologic diversity with at least two major subtypes in terms of cellular proliferation, clinical aggressiveness and prognosis. As CLL progresses, abnormal hematopoiesis results in pancitopenia and decreased immunoglobulin production, followed by nonspecific symptoms such as fatigue or malaise. A cure is usually not possible, and delayed treatment (until symptoms develop) is aimed at lengthening life and decreasing symptoms. Researchers are playing a lead role in investigating CLL's cause and the role of genetics in the pathogenesis of this disorder. Research programs are dedicated towards understanding the basic mechanisms underlying CLL with the hope of improving treatment options.
dc.language.isoeng
dc.publisherInTech
dc.relation.isbasedon10.5772/1156
dc.relation.urihttp://www.intechopen.com/books/chronic-lymphocytic-leukemia
dc.rights.uriCC by (姓名標示)
dc.sourceInTech
dc.subject.classificationMedicine
dc.subject.classification Oncology
dc.titleChronic Lymphocytic Leukemia
dc.type電子教課書
dc.classification醫學類
Theme:教科書-醫學類

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