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The Netherlands Journal of Medicine|May 24, 2007
Heterozygous alpha-I antitrypsin deficiency as a co-factor in the development of chronic liver disease: a reviewK F Kok, P J Wahab, R H J Houwen, et al.Current Problems in Diagnostic Radiology|July 13, 2024
Evaluation of Hepatocellular Carcinoma Surveillance with Contrast-enhanced MRI in a High-Risk Western European CohortFederico I F Fiduzi, François E J A Willemssen, Céline van de Braak, et al.Journal of Hepatology|July 14, 2001
Randomized trial of lamivudine versus hepatitis B immunoglobulin for long-term prophylaxis of hepatitis B recurrence after liver transplantationN V Naoumov, A R Lopes, P Burra, et al.Journal of Medical Virology|January 20, 2009
An improved approach to identify epidemiological and phylogenetic transmission pairs of source and contact tracing of hepatitis BIrene K Veldhuijzen, Ted H M Mes, Maria C Mostert, et al.Alimentary Pharmacology & Therapeutics|November 25, 2011
The long-term outcome of patients with polycystic liver disease treated with lanreotideM Chrispijn, F Nevens, T J G Gevers, et al.The Journal of Infectious Diseases|May 22, 2022
Levels of Antibodies to Hepatitis B Core Antigen Are Associated With Liver Inflammation and Response to Peginterferon in Patients With Chronic Hepatitis BSylvia M Brakenhoff, Robert J de Knegt, Jeffrey Oliveira, et al.The American Journal of Gastroenterology|October 13, 2006
Successful treatment with peginterferon alfa-2b of HBeAg-positive HBV non-responders to standard interferon or lamivudineHajo J Flink, Bettina E Hansen, E Jenny Heathcote, et al.Antiviral Therapy|February 5, 2008
Modelling of early viral kinetics and pegylated interferon-alpha2b pharmacokinetics in patients with HBeag-positive chronic hepatitis BMartijn J ter Borg, Bettina E Hansen, Eva Herrmann, et al.Prenatal Diagnosis|September 17, 2003
Prenatal detection of complex chromosomal aberrations using advanced molecular cytogenetic techniquesJ M de Pater, L C P Govaerts, S A de Man, et al.Journal of Human Genetics|March 27, 2018
Correction: Broadening the phenotypic spectrum of pathogenic LARP7 variants: two cases with intellectual disability, variable growth retardation and distinct facial featuresIris H I M Hollink, Majid Alfadhel, Anwar S Al-Wakeel, et al.Pageof 49