All Stories

  1. Reply to: “DHEA and progesterone have a protective effect on ribavirin-induced hemolysis”
  2. Whom and how to screen for Wilson disease
  3. Phenotype–genotype correlations in patients with Wilson's disease
  4. A tool for selecting patients with a high probability of sustained virological response to peginterferon alfa‐2a (40kD)/ribavirin
  5. Breakthroughs in Treatment of Chronic Hepatitis C - Time for an Obituary for Peginterferon/Ribavirin?
  6. Predictive value of FIB-4 and APRI versus METAVIR on sustained virologic response in genotype 1 hepatitis C patients
  7. Treatment of Chronic Hepatitis C, Genotype 4
  8. Efficacy and Safety of Oral Chelators in Treatment of Patients With Wilson Disease
  9. Role of FDFT1 polymorphism for fibrosis progression in patients with chronic hepatitis C
  10. Silibinin: An old drug in the high tech era of liver transplantation
  11. Hepatoprotective and antiviral functions of silymarin components in hepatitis C virus infection
  12. Silymarin for HCV infection
  13. Treatment With Silymarin for Hepatitis C Virus
  14. Association between IL28B polymorphism and treatment response in patients with genotype 4 chronic hepatitis C
  15. Response guided therapy in patients with chronic hepatitis C – Yesterday, today and tomorrow
  16. Identification of a novel Wilson disease gene mutation frequent in Upper Austria: a genetic and clinical study
  17. The multiplicity of divergence mechanisms in a single evolving population
  18. Refined prediction of week 12 response and SVR based on week 4 response in HCV genotype 1 patients treated with peginterferon alfa-2a (40KD) and ribavirin
  19. Understanding silibinin’s modes of action against HCV using viral kinetic modeling
  20. Wilson disease
  21. Treatment options for anti-HCV treatment-experienced patients
  22. Defining Wilson Disease Phenotypes: From the Patient to the Bench and Back Again
  23. Treatment of Chronic Hepatitis C Genotype 1 Patients at An Academic Center in Europe Involved in Prospective, Controlled Trials
  24. Treatment of chronic hepatitis C – are interferons really necessary?
  25. Decreased serum antioxidant capacity in patients with Wilson disease is associated with neurological symptoms
  26. IL28B and interferon‐gamma inducible protein 10 for prediction of rapid virologic response and sustained virologic response in HIV‐HCV‐coinfected patients
  27. Polymorphism of methylenetetrahydrofolate reductase as disease modifier – A déjà-vu in Wilson disease?
  28. Hepatitis C: Personalisierte Therapie
  29. Management of hepatitis C virus genotype 4: Recommendations of An International Expert Panel
  30. Early virologic response and IL28B polymorphisms in patients with chronic hepatitis C genotype 3 treated with peginterferon alfa-2a and ribavirin
  31. Zinc Monotherapy Is Not as Effective as Chelating Agents in Treatment of Wilson Disease
  32. Silibinin monotherapy prevents graft infection after orthotopic liver transplantation in a patient with chronic hepatitis C
  33. Impact of HCV protease-inhibitor-based triple therapy for chronic HCV genotype 1 infection
  34. Intravenous silibinin as ‘rescue treatment’ for on-treatment non-responders to pegylated interferon/ribavirin combination therapy
  35. Dynamic Coinfection with Multiple Viral Subtypes in Acute Hepatitis C
  36. Hepatic Encephalopathy: Treatment
  37. Genetic analysis of BIRC4/XIAP as a putative modifier gene of Wilson disease
  38. Seminal fluid ribavirin level and functional semen parameters in patients with chronic hepatitis C on antiviral combination therapy
  39. Non-invasive assessment of hepatic fat accumulation in chronic hepatitis C by 1H magnetic resonance spectroscopy
  40. 4. Österreichischer Konsensusbericht zur Diagnose und Therapie der Hepatitis B 2009
  41. A double-blind, randomized, placebo-controlled trial of intravenous l-ornithine-l-aspartate on postural control in patients with cirrhosis
  42. Treatment of chronic hepatitis C—how much interferon is enough?
  43. Hepatocyte GP73 expression in Wilson disease
  44. Experimental models of hepatic encephalopathy: ISHEN guidelines
  45. Silibinin (Legalon-SIL) Inhibits HCV Replication In Vitro
  46. A crossing in therapy for hepatitis C virus genotype 2 or 3: Increasing ribavirin dose with shortened duration or reducing ribavirin dose with standard duration #
  47. The optimal ribavirin dose for patients infected with hepatitis C virus genotype 3: Should we utilize more? #
  48. Peter Ferenci, MD
  49. Percutaneous ethanol instillation therapy for hepatocellular carcinoma – a randomized controlled trial
  50. Reply
  51. W1002 Silibinin Is a Potent Antiviral Agent in Patients with Chronic HCV Infection Not Responding to Peginterferon/Ribavirin Therapy
  52. Depression in chronic hepatitis: the virus, the drug, or the ethnic background?
  53. Evolution of Crohn’s disease-associated Nod2 mutations
  54. Differentiation of nonalcoholic from alcoholic steatohepatitis: are routine laboratory markers useful?
  55. MARS and the failing liver—Any help from the outer space?
  56. Treatment Options for Hepatic Encephalopathy: A Review
  57. An Algorithm for the Management of Hepatic Encephalopathy
  58. Re-evaluation of the penicillamine challenge test in the diagnosis of Wilson’s disease in children
  59. Morbidity and mortality in paid Austrian plasma donors infected with hepatitis C at plasma donation in the 1970s
  60. Late-Onset Wilson’s Disease
  61. Common NOD2/CARD15 variants are not associated with susceptibility or the clinicopathologic characteristics of sporadic colorectal cancer in Hungarian patients
  62. Novel mutations of the ATP7B gene among 109 Hungarian patients with Wilson??s disease
  63. Standard interferon-alpha in combination with ribavirin for hepatitis C patients with advanced liver disease and thrombocytopenia
  64. The Host or the Virus? Impact of Genetic Factors on the Outcome of Hepatitis C Virus Infection
  65. Regional distribution of mutations of the ATP7B gene in patients with Wilson disease: impact on genetic testing
  66. Wilson Disease
  67. Efficacy of 24 weeks treatment with peginterferon alfa-2b plus ribavirin in patients with chronic hepatitis C infected with genotype 1 and low pretreatment viremia
  68. Wilson Disease
  69. Response to letter from Professor Peter Ferenci
  70. Prediction of Progression to Cirrhosis by a Glutathione S-Transferase P1 Polymorphism in Subjects With Hereditary Hemochromatosis
  71. Sonographic diagnosis of coeliac disease in a case with suspected acute liver failure
  72. Wilson’s Disease
  73. Diagnostic Value of Quantitative Hepatic Copper Determination in Patients With Wilson’s Disease
  74. Successful Treatment of Chronic Hepatitis D with a Short Course of Peginterferon alfa-2a
  75. Dysfunction of the liver affects the sense of smell
  76. Increased C282Y Heterozygosity in Gestational Diabetes
  77. Pathophysiology and Clinical Features of Wilson Disease
  78. Current Treatment for chronic hepatitis C
  79. Hepatic Encephalopathy
  80. Transjugular intrahepatic portosystemic shunt in Vienna – A decade later
  81. Retreatment of patients with chronic hepatitis C not responding to interferon/ribavirin combination therapy with daily interferon plus ribavirin plus amantadine
  82. Predictors of Response to Therapy for Chronic Hepatitis C
  83. Treatment of chronic viral hepatitis
  84. Protease inhibitors for treatment of chronic hepatitis C—a new target for the magic bullet identified
  85. Prediction of Spontaneous Viral Clearance in Acute Hepatitis C by Viral Load Measurements
  86. Diagnosis and phenotypic classification of Wilson disease1
  87. Early viral kinetics in chronic hepatitis C virus genotype 4 infection
  88. Suppression of hematopoiesis during therapy with different IFN-α mono- and combination therapy regimes
  89. Centrilobular necrosis in autoimmune hepatitis: A histological feature associated with an acute onset of disease
  90. Hepatitis C viral dynamics: basic concept and clinical significance
  91. Porphyria cutanea tarda during interferon/ribavirin therapy for chronic hepatitis C
  92. Hepatocellular fat accumulation and low serum cholesterol in patients infected with HCV-3a
  93. Liver pathology in compound heterozygous patients for hemochromatosis mutations
  94. Rapid suppression of hematopoiesis by standard or pegylated interferon-α
  95. Primary IFN-resistance in chronic hepatitis C virus genotype 4 infection
  96. Hematological changes during IFN/ribavirin combination therapy in patients with chronic hepatitis C
  97. Primary interferon resistance and treatment response in chronic hepatitis C infection
  98. Hepatic transport systems
  99. Common mutations of ATP7B in Wilson disease patients from Hungary
  100. Postcremation diagnosis from an electric shaver
  101. Wilson disease in two consecutive generations: an exceptional family
  102. Portal hypertension
  103. Effect of pegylated (PEG 40kd) interferon (IFN)α-2a on early virus elimination in patients infected with HCV subtype 1
  104. TWELVE MONTHS OF LAMIVUDINE TREATMENT FOR CHRONIC HEPATITIS B VIRUS INFECTION IN RENAL TRANSPLANT RECIPIENTS12
  105. His1069Gln mutation in Hungarian patients with Wilson's disease
  106. Genetic testing and pedigree analysis in an exceptional family with Wilson's disease. How far should we go by genetic analysis?
  107. Hepatocellular carcinoma in Austria: aetiological and clinical characteristics at presentation
  108. Letters to the Editor
  109. Wilson's disease in eastern germany: High frequency of the H1069Q mutation and correlation with the neurological manifestation
  110. Treatment with amantadine +ribavirin +interferon in patients with chronic hepatitis C not responding to interferon/ribavirin combination therapy
  111. Differential thrombopoietin response to treatment-induced thrombocytopenia: IFN VS. IFN-ribavirin VS. PEG-IFN
  112. Cognitive brain function is subclinically impaired in patients with chronic hepatitis C - does hepatitis C affect the brain?
  113. Combination of interferon (IFN) induction therapy and ribavirin in chronic hepatitis C
  114. Mutations of the Wilson's disease gene in Austria-genotype/phenotype correlations and feasibility of mutation analysis
  115. Genetic testing and pedigree analysis in an exceptional family with Wilson's disease. How far should we go by genetic analysis?
  116. Prevalence and Distribution of Hepatitis C Subtypes in Patients with Opioid Dependence
  117. Partial pressure of ammonia versus ammonia in hepatic encephalopathy
  118. Image of the month
  119. Prevalence and clinical importance of hypertransaminasaemia in coeliac disease
  120. CLINICAL ISSUES IN THE MANAGEMENT OF ALCOHOLIC LIVER DISEASE
  121. Effects of testosterone suppression on serum levels of hepatitis B surface antigen and HBV‐DNA in men
  122. WILSON'S DISEASE
  123. Screening for Wilson's disease in patients with liver diseases by serum ceruloplasmin
  124. Dose increase augments response rate to interferon-α in chronic hepatitis C
  125. Newer Approaches to Therapy of Hepatic Encephalopathy
  126. Treatment of Hepatic Encephalopathy in Patients with Cirrhosis of the Liver
  127. Diagnosis of Wilson's disease in an asymptomatic sibling by DNA linkage analysis
  128. Dental and periodontal disease in patients with cirrhosis - role of etiology of liver disease
  129. Vitamin D status in outpatients with Crohnʼs disease
  130. Folate Absorption in Crohn’s Disease
  131. Neuropharmacologic Modulation of Hepatic Encephalopathy: Experimental and Clinical Data
  132. Energy metabolism in acute hepatic failure
  133. Detailed evaluation of evoked potentials in Wilson's disease
  134. Beneficial effect of pharmacological modulation of the GABAA-benzodiazepine receptor on hepatic encephalopathy in the rat: Comparison with uremic encephalopathy
  135. The role of methanethiol in the pathogenesis of hepatic encephalopathy
  136. Increased serotoninergic and noradrenergic activity in hepatic encephalopathy in rats with thioacetamide—induced acute liver failure
  137. Energy Metabolism in Patients With Acute and Chronic Liver Disease
  138. Benzodiazepine Antagonist in the Treatment of Human Hepatic Encephalopathy
  139. Cerebral glutamine metabolism: Study of modulatory effects of glutamine on γ-aminobutyric acid-ergic neurotransmission
  140. Hepatologie
  141. Recurrence of hepatitis B in children with serologic evidence of past hepatitis B virus infection undergoing antileukemic chemotherapy
  142. Treatment Of Hepatic Encephalopathy With The Benzodiazepine Antagonist Flumazenil
  143. Overestimation of serum concentrations of γ-aminobutyric acid in patients with hepatic encephalopathy by the γ-aminobutyric acid-radioreceptor assay
  144. Long-term follow-up study of asymptomatic hbsag-positive voluntary blood donors in austria: A clinical and histologic evaluation of 242 cases
  145. The GABA Hypothesis of the Pathogenesis of Hepatic Encephalopathy: Current Status
  146. Lack of evidence for impaired dopamine receptor function in experimental hepatic coma in the rabbit
  147. A nonlinear kinetic model of γ-aminobutyric acid metabolism in a rabbit model of acute liver failure
  148. The Neurobiology of Hepatic Encephalopathy
  149. Impaired plasma amino‐acid clearance in patients with cirrhosis of the liver and portocaval shunt—its relation to insulin resistance
  150. Changes in the Status of Neurotransmitter Receptors in a Rabbit Model of Hepatic Encephalopathy
  151. Relative incidence of primary liver cancer in cirrhosis in Austria. Etiological considerations
  152. Changes in Glutamate Receptors on Synaptic Membranes Associated with Hepatic Encephalopathy or Hyperammonemia in the Rabbit
  153. bolism of the Inhibitory Neurotransmitter γ-Aminobutyric Acid in a Rabbit Model of Fulminant Hepatic Failure