Gastroenterology, ISSN 0016-5085, 05/2019, Volume 156, Issue 6, pp. S-1336 - S-1336
Journal Article
Gastroenterology, ISSN 0016-5085, 2012, Volume 142, Issue 5, pp. S-954 - S-955
Journal Article
Journal of Viral Hepatitis, ISSN 1352-0504, 12/2019, Volume 26, Issue 12, pp. 1481 - 1488
Serum hepatitis B virus (HBV) RNA has emerged as a novel biomarker of treatment response. This study aimed to investigate the role of this marker in predicting...
chronic hepatitis B | stopping rule | virological response | cccDNA | entecavir | HBsAg | pegylated interferon | HBV RNA
chronic hepatitis B | stopping rule | virological response | cccDNA | entecavir | HBsAg | pegylated interferon | HBV RNA
Journal Article
Hepatology, ISSN 0270-9139, 11/2014, Volume 60, Issue 5, pp. 1697 - 1707
Transarterial chemoembolization (TACE) is the current standard of treatment for unresectable intermediate‐stage hepatocellular carcinoma (HCC). Brivanib, a...
ANGIOGENESIS | ALANINATE | TRANSCATHETER ARTERIAL CHEMOEMBOLIZATION | DUAL INHIBITOR | FACTOR RECEPTOR-2 | SORAFENIB | GASTROENTEROLOGY & HEPATOLOGY | EXPRESSION | CONFIDENCE | ENDOTHELIAL GROWTH-FACTOR | KINASES | Triazines - pharmacology | Alanine - therapeutic use | Alanine - adverse effects | Double-Blind Method | Triazines - therapeutic use | Chemoembolization, Therapeutic | Humans | Middle Aged | Liver Neoplasms - drug therapy | Receptors, Fibroblast Growth Factor - antagonists & inhibitors | Male | Vascular Endothelial Growth Factor A - antagonists & inhibitors | Young Adult | Alanine - analogs & derivatives | Carcinoma, Hepatocellular - drug therapy | Treatment Failure | Aged, 80 and over | Adult | Female | Triazines - adverse effects | Aged | Chemotherapy, Adjuvant | Alanine - pharmacology | Confidence intervals | Liver cancer | Chemotherapy | Drug therapy | Ovarian cancer
ANGIOGENESIS | ALANINATE | TRANSCATHETER ARTERIAL CHEMOEMBOLIZATION | DUAL INHIBITOR | FACTOR RECEPTOR-2 | SORAFENIB | GASTROENTEROLOGY & HEPATOLOGY | EXPRESSION | CONFIDENCE | ENDOTHELIAL GROWTH-FACTOR | KINASES | Triazines - pharmacology | Alanine - therapeutic use | Alanine - adverse effects | Double-Blind Method | Triazines - therapeutic use | Chemoembolization, Therapeutic | Humans | Middle Aged | Liver Neoplasms - drug therapy | Receptors, Fibroblast Growth Factor - antagonists & inhibitors | Male | Vascular Endothelial Growth Factor A - antagonists & inhibitors | Young Adult | Alanine - analogs & derivatives | Carcinoma, Hepatocellular - drug therapy | Treatment Failure | Aged, 80 and over | Adult | Female | Triazines - adverse effects | Aged | Chemotherapy, Adjuvant | Alanine - pharmacology | Confidence intervals | Liver cancer | Chemotherapy | Drug therapy | Ovarian cancer
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 10/2004, Volume 351, Issue 15, pp. 1521 - 1531
In this placebo-controlled trial of patients with chronic hepatitis B and advanced fibrosis or cirrhosis, lamivudine reduced the rate of disease progression....
PROGNOSTIC FACTORS | UNITED-STATES | SURVIVAL | MEDICINE, GENERAL & INTERNAL | HEPATOCELLULAR-CARCINOMA | VIRUS | CIRRHOSIS | TERM FOLLOW-UP | E-ANTIGEN SEROCONVERSION | NATURAL COURSE | INTERFERON THERAPY | Carcinoma, Hepatocellular - mortality | Prospective Studies | Carcinoma, Hepatocellular - prevention & control | Humans | Middle Aged | Male | Liver Neoplasms - mortality | Lamivudine - adverse effects | Lamivudine - therapeutic use | Adult | Female | Liver Neoplasms - prevention & control | Severity of Illness Index | Liver Cirrhosis - drug therapy | Liver Cirrhosis - etiology | Double-Blind Method | Antiviral Agents - therapeutic use | Disease Progression | Drug Resistance - genetics | Hepatitis B, Chronic - complications | Hepatitis B, Chronic - drug therapy | Antiviral Agents - adverse effects | Adolescent | Hepatitis B virus - genetics | Liver Cirrhosis - pathology | Aged | Mutation | Lamivudine | Care and treatment | Dosage and administration | Liver diseases | Hepatitis B | Hepatitis | Liver cancer | Liver cirrhosis | Mortality
PROGNOSTIC FACTORS | UNITED-STATES | SURVIVAL | MEDICINE, GENERAL & INTERNAL | HEPATOCELLULAR-CARCINOMA | VIRUS | CIRRHOSIS | TERM FOLLOW-UP | E-ANTIGEN SEROCONVERSION | NATURAL COURSE | INTERFERON THERAPY | Carcinoma, Hepatocellular - mortality | Prospective Studies | Carcinoma, Hepatocellular - prevention & control | Humans | Middle Aged | Male | Liver Neoplasms - mortality | Lamivudine - adverse effects | Lamivudine - therapeutic use | Adult | Female | Liver Neoplasms - prevention & control | Severity of Illness Index | Liver Cirrhosis - drug therapy | Liver Cirrhosis - etiology | Double-Blind Method | Antiviral Agents - therapeutic use | Disease Progression | Drug Resistance - genetics | Hepatitis B, Chronic - complications | Hepatitis B, Chronic - drug therapy | Antiviral Agents - adverse effects | Adolescent | Hepatitis B virus - genetics | Liver Cirrhosis - pathology | Aged | Mutation | Lamivudine | Care and treatment | Dosage and administration | Liver diseases | Hepatitis B | Hepatitis | Liver cancer | Liver cirrhosis | Mortality
Journal Article
Hepatology, ISSN 0270-9139, 07/2011, Volume 54, Issue 1, pp. 91 - 100
A randomized, open‐label comparative study of entecavir versus adefovir therapy was performed in subjects with chronic hepatitis B who had hepatic...
LAMIVUDINE TREATMENT | MANAGEMENT | THERAPY | NAIVE PATIENTS | CIRRHOSIS | RESISTANCE | DIPIVOXIL | GASTROENTEROLOGY & HEPATOLOGY | Adenine - analogs & derivatives | Liver Failure - mortality | Organophosphonates - therapeutic use | Antiviral Agents - therapeutic use | Guanine - analogs & derivatives | Humans | Middle Aged | Drug Resistance, Viral | Organophosphonates - adverse effects | Male | Survival Rate | Treatment Outcome | DNA, Viral - blood | Dose-Response Relationship, Drug | Liver Failure - virology | Adenine - adverse effects | Hepatitis B, Chronic - drug therapy | Adenine - therapeutic use | Antiviral Agents - adverse effects | Hepatitis B virus - genetics | Lamivudine - therapeutic use | Female | Guanine - adverse effects | Guanine - therapeutic use | Hepatitis | Interferon | Liver cirrhosis | Mortality
LAMIVUDINE TREATMENT | MANAGEMENT | THERAPY | NAIVE PATIENTS | CIRRHOSIS | RESISTANCE | DIPIVOXIL | GASTROENTEROLOGY & HEPATOLOGY | Adenine - analogs & derivatives | Liver Failure - mortality | Organophosphonates - therapeutic use | Antiviral Agents - therapeutic use | Guanine - analogs & derivatives | Humans | Middle Aged | Drug Resistance, Viral | Organophosphonates - adverse effects | Male | Survival Rate | Treatment Outcome | DNA, Viral - blood | Dose-Response Relationship, Drug | Liver Failure - virology | Adenine - adverse effects | Hepatitis B, Chronic - drug therapy | Adenine - therapeutic use | Antiviral Agents - adverse effects | Hepatitis B virus - genetics | Lamivudine - therapeutic use | Female | Guanine - adverse effects | Guanine - therapeutic use | Hepatitis | Interferon | Liver cirrhosis | Mortality
Journal Article
Gastroenterology Clinics of North America, ISSN 0889-8553, 12/2015, Volume 44, Issue 4, pp. 883 - 900
The management of hepatitis C virus (HCV) infection in special populations is challenging. The efficacy and safety data of the currently approved all-oral...
Decompensated cirrhosis | Chronic kidney disease | Treatment | HIV coinfection | Hepatitis C virus | Liver transplantation | LIVER-TRANSPLANTATION | HUMAN-IMMUNODEFICIENCY-VIRUS | HCV INFECTION | SUSTAINED VIROLOGICAL RESPONSE | TREATMENT-NAIVE | TREATMENT-EXPERIENCED PATIENTS | GENOTYPE 1 INFECTION | GASTROENTEROLOGY & HEPATOLOGY | VIRAL-HEPATITIS | DRUG-DRUG INTERACTIONS | SEVERE RENAL IMPAIRMENT | Liver Transplantation | Antiviral Agents - therapeutic use | Coinfection - drug therapy | Liver Cirrhosis - complications | Humans | Hepatitis C, Chronic - surgery | Combined Modality Therapy | Hepatitis C, Chronic - complications | Hepatitis C, Chronic - drug therapy | Liver Cirrhosis - virology | Kidney Failure, Chronic - virology | HIV Infections - complications | Kidney Failure, Chronic - complications | Drug Therapy, Combination
Decompensated cirrhosis | Chronic kidney disease | Treatment | HIV coinfection | Hepatitis C virus | Liver transplantation | LIVER-TRANSPLANTATION | HUMAN-IMMUNODEFICIENCY-VIRUS | HCV INFECTION | SUSTAINED VIROLOGICAL RESPONSE | TREATMENT-NAIVE | TREATMENT-EXPERIENCED PATIENTS | GENOTYPE 1 INFECTION | GASTROENTEROLOGY & HEPATOLOGY | VIRAL-HEPATITIS | DRUG-DRUG INTERACTIONS | SEVERE RENAL IMPAIRMENT | Liver Transplantation | Antiviral Agents - therapeutic use | Coinfection - drug therapy | Liver Cirrhosis - complications | Humans | Hepatitis C, Chronic - surgery | Combined Modality Therapy | Hepatitis C, Chronic - complications | Hepatitis C, Chronic - drug therapy | Liver Cirrhosis - virology | Kidney Failure, Chronic - virology | HIV Infections - complications | Kidney Failure, Chronic - complications | Drug Therapy, Combination
Journal Article
Journal of Gastroenterology and Hepatology, ISSN 0815-9319, 11/2018, Volume 33, Issue 11, pp. 1822 - 1828
Background and Aim Eradication rates of Helicobacter pylori following standard triple therapy are declining worldwide, but high‐dose proton pump...
Helicobacter pylori | proton pump inhibitors | dyspepsia | CONCOMITANT THERAPY | METAANALYSIS | MANAGEMENT | EFFICACY | CLARITHROMYCIN RESISTANCE | CYP2C19 | AMOXICILLIN | CONSENSUS REPORT | TRIAL | INFECTION | GASTROENTEROLOGY & HEPATOLOGY | Prospective Studies | Nausea - chemically induced | Humans | Middle Aged | Male | Helicobacter Infections | Nausea - epidemiology | Proton Pump Inhibitors - administration & dosage | Time Factors | Clarithromycin - administration & dosage | Gastritis - microbiology | Adult | Female | Amoxicillin - administration & dosage | Anti-Bacterial Agents - adverse effects | Drug Therapy, Combination | Dizziness - epidemiology | Lansoprazole - administration & dosage | Gastritis - drug therapy | Proton Pump Inhibitors - adverse effects | Clarithromycin - adverse effects | Dizziness - chemically induced | Treatment Outcome | Lansoprazole - adverse effects | Amoxicillin - adverse effects | Aged | Patient Compliance | Anti-Bacterial Agents - administration & dosage | Drug resistance in microorganisms | Urea | Care and treatment | Amoxicillin | Dosage and administration | Patient compliance | Side effects | Clarithromycin | Motivation | Compliance | Dyspepsia | Antibiotic resistance | Nausea | Metronidazole | Patients
Helicobacter pylori | proton pump inhibitors | dyspepsia | CONCOMITANT THERAPY | METAANALYSIS | MANAGEMENT | EFFICACY | CLARITHROMYCIN RESISTANCE | CYP2C19 | AMOXICILLIN | CONSENSUS REPORT | TRIAL | INFECTION | GASTROENTEROLOGY & HEPATOLOGY | Prospective Studies | Nausea - chemically induced | Humans | Middle Aged | Male | Helicobacter Infections | Nausea - epidemiology | Proton Pump Inhibitors - administration & dosage | Time Factors | Clarithromycin - administration & dosage | Gastritis - microbiology | Adult | Female | Amoxicillin - administration & dosage | Anti-Bacterial Agents - adverse effects | Drug Therapy, Combination | Dizziness - epidemiology | Lansoprazole - administration & dosage | Gastritis - drug therapy | Proton Pump Inhibitors - adverse effects | Clarithromycin - adverse effects | Dizziness - chemically induced | Treatment Outcome | Lansoprazole - adverse effects | Amoxicillin - adverse effects | Aged | Patient Compliance | Anti-Bacterial Agents - administration & dosage | Drug resistance in microorganisms | Urea | Care and treatment | Amoxicillin | Dosage and administration | Patient compliance | Side effects | Clarithromycin | Motivation | Compliance | Dyspepsia | Antibiotic resistance | Nausea | Metronidazole | Patients
Journal Article
PLOS ONE, ISSN 1932-6203, 07/2019, Volume 14, Issue 7, p. e0219516
Background Patients with acute-on-chronic liver failure (ACLF) precipitated by hepatic injury and extrahepatic insults had distinct clinical phenotypes, and...
MORTALITY | SURVIVAL | CLIF-SOFA | SCORE | PACIFIC ASSOCIATION | INDICATORS | MULTIDISCIPLINARY SCIENCES | DISTINCT | CIRRHOTIC-PATIENTS | CRITICALLY-ILL PATIENTS | Liver failure | Care and treatment | Phenotype | Prognosis | Diagnosis | Research | Risk factors | Phenotypes | Liver diseases | Laboratories | Syngeneic grafts | Liver | Mortality | Infections | Transplantation | Patients | Bleeding | Consortia | Medicine | Survival analysis | Hepatitis | Allografts | Sodium | Etiology | Hepatology | Medical prognosis | Gastroenterology | Models | Risk management | Failure | Liver transplantation
MORTALITY | SURVIVAL | CLIF-SOFA | SCORE | PACIFIC ASSOCIATION | INDICATORS | MULTIDISCIPLINARY SCIENCES | DISTINCT | CIRRHOTIC-PATIENTS | CRITICALLY-ILL PATIENTS | Liver failure | Care and treatment | Phenotype | Prognosis | Diagnosis | Research | Risk factors | Phenotypes | Liver diseases | Laboratories | Syngeneic grafts | Liver | Mortality | Infections | Transplantation | Patients | Bleeding | Consortia | Medicine | Survival analysis | Hepatitis | Allografts | Sodium | Etiology | Hepatology | Medical prognosis | Gastroenterology | Models | Risk management | Failure | Liver transplantation
Journal Article
Hepatology Research, ISSN 1386-6346, 03/2017, Volume 47, Issue 3, pp. E161 - E168
Aim Entecavir (ETV) and tenofovir disoproxil fumarate (TDF) are considered among the most potent antiviral agents for the treatment of chronic hepatitis B...
hepatitis B | safety profile | antiviral therapy | HBeAg seroconversion, efficacy | KIDNEY-DISEASE | HBEAG | FOLLOW-UP | efficacy | THERAPY | HBeAg seroconversion | NAIVE PATIENTS | ALAFENAMIDE | PHARMACOKINETICS | DISOPROXIL FUMARATE | RESISTANCE | INFECTION | GASTROENTEROLOGY & HEPATOLOGY | Tenofovir | Antigens | Control | Clinical trials | Hepatitis C virus | Hepatitis C | Drug therapy | Health aspects | Liver cirrhosis | Hepatitis B | Antiviral agents | Alanine | Hepatitis B surface antigen | Liver | Chronic infection | Malignancy | Seroconversion | Patients | Hepatitis B e antigen | Cirrhosis | Hepatitis | Antiviral activity | Alanine transaminase | Interferon | Deoxyribonucleic acid--DNA
hepatitis B | safety profile | antiviral therapy | HBeAg seroconversion, efficacy | KIDNEY-DISEASE | HBEAG | FOLLOW-UP | efficacy | THERAPY | HBeAg seroconversion | NAIVE PATIENTS | ALAFENAMIDE | PHARMACOKINETICS | DISOPROXIL FUMARATE | RESISTANCE | INFECTION | GASTROENTEROLOGY & HEPATOLOGY | Tenofovir | Antigens | Control | Clinical trials | Hepatitis C virus | Hepatitis C | Drug therapy | Health aspects | Liver cirrhosis | Hepatitis B | Antiviral agents | Alanine | Hepatitis B surface antigen | Liver | Chronic infection | Malignancy | Seroconversion | Patients | Hepatitis B e antigen | Cirrhosis | Hepatitis | Antiviral activity | Alanine transaminase | Interferon | Deoxyribonucleic acid--DNA
Journal Article
Journal of the Medical Association of Thailand, ISSN 0125-2208, 04/2018, Volume 101, Issue 4, pp. S135 - S142
Journal Article
Journal of Gastroenterology and Hepatology, ISSN 0815-9319, 02/2018, Volume 33, Issue 2, pp. 411 - 417
Background and Aim Current treatments of functional dyspepsia (FD) are unsatisfied. Tricyclic antidepressants alter visceral hypersensitivity and brain–gut...
nortriptyline | tricyclic antidepressant | functional dyspepsia | safety | efficacy | AMITRIPTYLINE | GUIDELINES | ANTIDEPRESSANT MEDICATIONS | TRICYCLIC ANTIDEPRESSANTS | ESCITALOPRAM | LEEDS DYSPEPSIA | GASTROINTESTINAL DISORDERS | QUESTIONNAIRE | GASTROENTEROLOGY & HEPATOLOGY | BOWEL DISORDERS | POSTPRANDIAL SYMPTOMS | Dyspepsia - drug therapy | Humans | Middle Aged | Male | Treatment Outcome | Young Adult | Asian Continental Ancestry Group | Nortriptyline - administration & dosage | Nortriptyline - adverse effects | Antidepressive Agents, Tricyclic - adverse effects | Adult | Female | Aged | Antidepressive Agents, Tricyclic - administration & dosage | Nortriptyline | Medical research | Gastrointestinal agents | Dyspepsia | Analysis | Clinical trials | Medicine, Experimental | Motivation | Antidepressants | Hypersensitivity | Tricyclic antidepressants | Safety | Quality of life
nortriptyline | tricyclic antidepressant | functional dyspepsia | safety | efficacy | AMITRIPTYLINE | GUIDELINES | ANTIDEPRESSANT MEDICATIONS | TRICYCLIC ANTIDEPRESSANTS | ESCITALOPRAM | LEEDS DYSPEPSIA | GASTROINTESTINAL DISORDERS | QUESTIONNAIRE | GASTROENTEROLOGY & HEPATOLOGY | BOWEL DISORDERS | POSTPRANDIAL SYMPTOMS | Dyspepsia - drug therapy | Humans | Middle Aged | Male | Treatment Outcome | Young Adult | Asian Continental Ancestry Group | Nortriptyline - administration & dosage | Nortriptyline - adverse effects | Antidepressive Agents, Tricyclic - adverse effects | Adult | Female | Aged | Antidepressive Agents, Tricyclic - administration & dosage | Nortriptyline | Medical research | Gastrointestinal agents | Dyspepsia | Analysis | Clinical trials | Medicine, Experimental | Motivation | Antidepressants | Hypersensitivity | Tricyclic antidepressants | Safety | Quality of life
Journal Article
Gastroenterology, ISSN 0016-5085, 05/2019, Volume 156, Issue 6, pp. S-1343 - S-1344
Journal Article
Gastroenterology, ISSN 0016-5085, 05/2018, Volume 154, Issue 6, pp. S-1132 - S-1132
Journal Article
世界肝病学杂志:英文版(电子版), ISSN 1948-5182, 2013, Volume 5, Issue 9, pp. 496 - 504
Hepatitis C genotype 6 is endemic in Southeast Asia[prevalence varies between 10%-60% among all hepatitis C virus(HCV) infection], as well as also sporadically...
Pegylated | C | therapy | Genotype | Southeast | interferon | Epidemiology | Ribavirin | Hepatitis | Treatment | Response-guided | Asia | 6 | Southeast asia | Pegylated interferon | Hepatitis c | Response-guided therapy | Genotype 6 | Southeast Asia | Minireviews | Hepatitis C
Pegylated | C | therapy | Genotype | Southeast | interferon | Epidemiology | Ribavirin | Hepatitis | Treatment | Response-guided | Asia | 6 | Southeast asia | Pegylated interferon | Hepatitis c | Response-guided therapy | Genotype 6 | Southeast Asia | Minireviews | Hepatitis C
Journal Article
Journal of Hepatology, ISSN 0168-8278, 2012, Volume 56, Issue 6, pp. 1247 - 1253
Background & Aims TMC435 is an investigational, once-daily, oral NS3/4A protease inhibitor currently in phase III development for the treatment of hepatitis C...
Gastroenterology and Hepatology | Genotype | Antiviral | HCV | Monotherapy | TMC435 | Simeprevir | Hepatitis C - drug therapy | Antiviral Agents - therapeutic use | Humans | Middle Aged | Hepacivirus - genetics | Male | Sulfonamides - pharmacokinetics | Sulfonamides - therapeutic use | Heterocyclic Compounds, 3-Ring - adverse effects | Heterocyclic Compounds, 3-Ring - therapeutic use | Adolescent | Hepatitis C - virology | Sulfonamides - adverse effects | Adult | Female | Aged | Hepacivirus - classification | Heterocyclic Compounds, 3-Ring - pharmacokinetics | Medical research | Antiviral agents | Aspartate | Hepatitis | Protease inhibitors | Proteases | Electrocardiogram | Electrocardiography | Medicine, Experimental | Genetic aspects | Dosage and administration | Hepatitis C virus | Hepatitis C | Health aspects
Gastroenterology and Hepatology | Genotype | Antiviral | HCV | Monotherapy | TMC435 | Simeprevir | Hepatitis C - drug therapy | Antiviral Agents - therapeutic use | Humans | Middle Aged | Hepacivirus - genetics | Male | Sulfonamides - pharmacokinetics | Sulfonamides - therapeutic use | Heterocyclic Compounds, 3-Ring - adverse effects | Heterocyclic Compounds, 3-Ring - therapeutic use | Adolescent | Hepatitis C - virology | Sulfonamides - adverse effects | Adult | Female | Aged | Hepacivirus - classification | Heterocyclic Compounds, 3-Ring - pharmacokinetics | Medical research | Antiviral agents | Aspartate | Hepatitis | Protease inhibitors | Proteases | Electrocardiogram | Electrocardiography | Medicine, Experimental | Genetic aspects | Dosage and administration | Hepatitis C virus | Hepatitis C | Health aspects
Journal Article
Hepatology International, ISSN 1936-0533, 4/2015, Volume 9, Issue 2, pp. 202 - 208
Hepatitis B virus (HBV) infection is still prevalent in Asia, including Thailand. HBV can archive in hepatocytes for life and can reactivate after...
Medicine & Public Health | Colorectal Surgery | Hepatology | Surgery | Rheumatoid arthritis | HBV reactivation | Chronic HBV | Methotrexate | Thailand | Hepatitis B | FULMINANT-HEPATITIS | VIRUS-INFECTION | NATURAL-HISTORY | ARTHRITIS | DISCONTINUATION | THERAPY | DISEASE | C VIRUS | GASTROENTEROLOGY & HEPATOLOGY | WITHDRAWAL | ANTIGEN | Spondylarthropathies - drug therapy | Cross-Sectional Studies | Humans | Middle Aged | Male | Methotrexate - therapeutic use | Hepatitis B virus - physiology | Hepatitis B Surface Antigens - blood | DNA, Viral - blood | Hepatitis B Antibodies - blood | Virus Activation - drug effects | Time Factors | Arthritis, Rheumatoid - drug therapy | Hepatitis B virus - genetics | Lupus Erythematosus, Systemic - drug therapy | Adult | Female | Hepatitis B, Chronic - blood | Aged | Viral Load - drug effects | Hepatitis B virus - immunology | Antirheumatic Agents - therapeutic use | Relapse | Dosage and administration | Drug therapy | Risk factors | Diseases
Medicine & Public Health | Colorectal Surgery | Hepatology | Surgery | Rheumatoid arthritis | HBV reactivation | Chronic HBV | Methotrexate | Thailand | Hepatitis B | FULMINANT-HEPATITIS | VIRUS-INFECTION | NATURAL-HISTORY | ARTHRITIS | DISCONTINUATION | THERAPY | DISEASE | C VIRUS | GASTROENTEROLOGY & HEPATOLOGY | WITHDRAWAL | ANTIGEN | Spondylarthropathies - drug therapy | Cross-Sectional Studies | Humans | Middle Aged | Male | Methotrexate - therapeutic use | Hepatitis B virus - physiology | Hepatitis B Surface Antigens - blood | DNA, Viral - blood | Hepatitis B Antibodies - blood | Virus Activation - drug effects | Time Factors | Arthritis, Rheumatoid - drug therapy | Hepatitis B virus - genetics | Lupus Erythematosus, Systemic - drug therapy | Adult | Female | Hepatitis B, Chronic - blood | Aged | Viral Load - drug effects | Hepatitis B virus - immunology | Antirheumatic Agents - therapeutic use | Relapse | Dosage and administration | Drug therapy | Risk factors | Diseases
Journal Article
PLoS ONE, ISSN 1932-6203, 03/2017, Volume 12, Issue 3, p. e0173263
Evidence of a role of vitamin D in the immune system is increasing. Low serum vitamin D is associated with increased hepatitis B virus replication. Genome-wide...
LAMIVUDINE | THERAPY | POLYMORPHISMS | PEGINTERFERON ALPHA-2A | VIRUS INFECTION | ANALOGS | MULTIDISCIPLINARY SCIENCES | RIBAVIRIN | T-CELLS | GENOME-WIDE ASSOCIATION | Hepatitis B e Antigens - immunology | Recombinant Proteins - therapeutic use | Hepatitis B, Chronic - drug therapy | Cholestanetriol 26-Monooxygenase - genetics | Humans | Interferon-alpha - therapeutic use | Cytochrome P450 Family 2 - genetics | Polyethylene Glycols - therapeutic use | Hepatitis B Core Antigens - immunology | Care and treatment | Peginterferon alfa-2a | Vitamin D | Genetic variation | Analysis | Calcifediol | Dosage and administration | Alfacalcidol | Research | Hepatitis B | Therapy | Genes | 7-Dehydrocholesterol reductase | Chronic infection | Viruses | Infections | Genomes | Single-nucleotide polymorphism | Multivariate analysis | D gene | Hepatitis | α-Interferon | Hepatology | Gastroenterology | Pretreatment | Hepatitis B virus | Deoxyribonucleic acid--DNA | Genotypes | Immune system | Antigens | Immune response | Internal medicine | Vitamin deficiency | Genetic diversity | Patients | Seroconversion | Medicine | Hepatitis B e antigen | Hospitals | Interferon | Vitamin D receptors | Polymorphism | Deoxyribonucleic acid | DNA
LAMIVUDINE | THERAPY | POLYMORPHISMS | PEGINTERFERON ALPHA-2A | VIRUS INFECTION | ANALOGS | MULTIDISCIPLINARY SCIENCES | RIBAVIRIN | T-CELLS | GENOME-WIDE ASSOCIATION | Hepatitis B e Antigens - immunology | Recombinant Proteins - therapeutic use | Hepatitis B, Chronic - drug therapy | Cholestanetriol 26-Monooxygenase - genetics | Humans | Interferon-alpha - therapeutic use | Cytochrome P450 Family 2 - genetics | Polyethylene Glycols - therapeutic use | Hepatitis B Core Antigens - immunology | Care and treatment | Peginterferon alfa-2a | Vitamin D | Genetic variation | Analysis | Calcifediol | Dosage and administration | Alfacalcidol | Research | Hepatitis B | Therapy | Genes | 7-Dehydrocholesterol reductase | Chronic infection | Viruses | Infections | Genomes | Single-nucleotide polymorphism | Multivariate analysis | D gene | Hepatitis | α-Interferon | Hepatology | Gastroenterology | Pretreatment | Hepatitis B virus | Deoxyribonucleic acid--DNA | Genotypes | Immune system | Antigens | Immune response | Internal medicine | Vitamin deficiency | Genetic diversity | Patients | Seroconversion | Medicine | Hepatitis B e antigen | Hospitals | Interferon | Vitamin D receptors | Polymorphism | Deoxyribonucleic acid | DNA
Journal Article