A novel pattern of uridine diphosphate glucuronosyltranferase polymorphisms associated with hyperbilirubinemia during nilotinib treatment

COIANA, ALESSANDRA;ROSATELLI, MARIA CRISTINA;
2013-01-01

Abstract

We report on a patient with chronic phase CML who developed hyperbilirubinemia during nilotinib treatment, showing a pattern of UGT1A1 polymorphisms so far undescribed in this clinical setting.
2013
Inglese
BLOOD CELLS, MOLECULES, & DISEASES
51
3
162
162
1
WOS:000322942800007
2-s2.0-84881022017
23769327
Esperti anonimi
internazionale
scientifica
Adult; Genotype; Glucuronosyltransferase; Humans; Hyperbilirubinemia; Leukemia, myelogenous, chronic, BCR-ABL positive; Male; Polymorphism, genetic; Pyrimidinec
no
Fozza, C.; Pardini, S.; Coiana, Alessandra; Rosatelli, MARIA CRISTINA; Longinotti, M.
1.1 Articolo in rivista
info:eu-repo/semantics/article
1 Contributo su Rivista::1.1 Articolo in rivista
262
5
reserved
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