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A Novel pattern of uridine diphosphate glucuronosyltransferase polymorphisms associated with hyperbilirubinemia during nilotinib treatment

Fozza, Claudio and Pardini, Simonetta and Coiana, Alessandra and Rosatelli, Maria Cristina and Longinotti, Maurizio Roberto (2013) A Novel pattern of uridine diphosphate glucuronosyltransferase polymorphisms associated with hyperbilirubinemia during nilotinib treatment. Blood Cells, Molecules, and Diseases, Vol. 51 (3), p. 162. eISSN 1096-0961. Article.

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DOI: 10.1016/j.bcmd.2013.05.007

Abstract

[Letter to the Editor] Here we report on a patient who developed hyperbilirubinemia during nilotinib treatment, showing a pattern of UGT1A1 polymorphisms so far undescribed in this clinical setting.

Item Type:Article
ID Code:9209
Status:Published
Refereed:Yes
Uncontrolled Keywords:Bilirubin, uridine, UGT1A1 polymorphisms
Subjects:Area 06 - Scienze mediche > MED/15 Malattie del sangue
Divisions:001 Università di Sassari > 01-a Nuovi Dipartimenti dal 2012 > Scienze Biomediche
Publisher:Academic Press / Elsevier
eISSN:1096-0961
Deposited On:27 Sep 2013 10:52

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