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<article xlink="http://www.w3.org/1999/xlink" dtd-version="1.0" article-type="healthcare" lang="en"><front><journal-meta><journal-id journal-id-type="publisher">IJCRR</journal-id><journal-id journal-id-type="nlm-ta">I Journ Cur Res Re</journal-id><journal-title-group><journal-title>International Journal of Current Research and Review</journal-title><abbrev-journal-title abbrev-type="pubmed">I Journ Cur Res Re</abbrev-journal-title></journal-title-group><issn pub-type="ppub">2231-2196</issn><issn pub-type="opub">0975-5241</issn><publisher><publisher-name>Radiance Research Academy</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">1341</article-id><article-id pub-id-type="doi"/><article-id pub-id-type="doi-url"/><article-categories><subj-group subj-group-type="heading"><subject>Healthcare</subject></subj-group></article-categories><title-group><article-title>CHROMOSOMAL ABNORMALITIES IN PHILADELPHIA CHROMOSOME- NEGATIVE CELLS IN PATIENT WITH CHRONIC MYELOGENOUS LEUKEMIA TREATED WITH FIRST GENERATION TYROSINE KINASE INHIBITOR- SINGLE CENTER EXPERIENCE&#13;
</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>S.</surname><given-names>Trajkova</given-names></name></contrib><contrib contrib-type="author"><name><surname>L.</surname><given-names>Cevreska</given-names></name></contrib><contrib contrib-type="author"><name><surname>M.</surname><given-names>Pavkovic</given-names></name></contrib><contrib contrib-type="author"><name><surname>.</surname><given-names>Panovska Stavridis I</given-names></name></contrib><contrib contrib-type="author"><name><surname>D.</surname><given-names>Dukovski</given-names></name></contrib><contrib contrib-type="author"><name><surname>M.</surname><given-names>Popova-Simjanovska</given-names></name></contrib><contrib contrib-type="author"><name><surname>L.</surname><given-names>Cadievski</given-names></name></contrib><contrib contrib-type="author"><name><surname>A.</surname><given-names>Stojanovic</given-names></name></contrib></contrib-group><pub-date pub-type="ppub"><day>25</day><month>05</month><year>2013</year></pub-date><volume>)</volume><issue/><fpage>57</fpage><lpage>61</lpage><permissions><copyright-statement>This article is copyright of Popeye Publishing, 2009</copyright-statement><copyright-year>2009</copyright-year><license license-type="open-access" href="http://creativecommons.org/licenses/by/4.0/"><license-p>This is an open-access article distributed under the terms of the Creative Commons Attribution (CC BY 4.0) Licence. You may share and adapt the material, but must give appropriate credit to the source, provide a link to the licence, and indicate if changes were made.</license-p></license></permissions><abstract><p>Chronic myelogenous leukemia (CML) is characterized by the presence of a Bcr-Abl fusion protein with deregulated tyrosine kinase activity that is required for maintaining the malignant phenotype. Imatinib as a selective inhibitor of Bcr-Abl induces complete cytogenetic remission in the majority of patients with CML in chronic phase. Targeted therapy of CML with imatinib favors the manifestation of Ph-(negative) clone disorders in some patients. Facts indicate that patients on imatinib should be followed with conventional cytogenetics, even after induction of complete remission. We report a case of a patient with CML, in chronic phase treated with imatinib which induces the most common abnormality trisomy 8.&#13;
</p></abstract><kwd-group><kwd>Chronic myelogenous leukemia</kwd><kwd> imatinib</kwd><kwd> Philadelphia chromosome</kwd><kwd> clone evolution</kwd></kwd-group></article-meta></front></article>
