Clinicovirologic analysis of hepatitis C infection in transfusion-dependent β-thalassemia major children
Author:
Publisher
Wiley
Subject
Biochemistry, medical,Clinical Biochemistry,Hematology,General Medicine
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1. A high frequency of Gilbert syndrome (UGT1A1*28/*28) and associated hyperbilirubinemia but not cholelithiasis in adolescent and adult north Indian patients with transfusion-dependent β-thalassemia;Annals of Hematology;2020-07-16
2. THE COURSE OF HEPATITIS C INFECTION AND RESPONSE TO ANTI-VIRAL THERAPY IN PATIENTS WITH THALASSEMIA MAJOR AND HEPATITIS C INFECTION: A LONGITUDINAL, PROSPECTIVE STUDY.;Mediterranean Journal of Hematology and Infectious Diseases;2019-10-30
3. Cognitive dysfunction in β-thalassemia major and intermedia patients and its clinical correlates;Middle East Current Psychiatry;2016-07
4. Characteristics of Seropositive Hepatitis B and C Thalassemia Major Patients in South-East of Iran;Biotechnology and Health Sciences;2016-03-30
5. ADAMTS13 Levels in Young Patients With β-Thalassemia Major;Clinical and Applied Thrombosis/Hemostasis;2014-11-26
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