Infection, ISSN 0300-8126, 10/2018, Volume 46, Issue 5, pp. 607 - 615
To analyse safety and efficacy of treatment based on ombitasvir/paritaprevir/ritonavir/dasabuvir plus ribavirin in the sub-group of GT1 patients older than...
Cirrhosis | Ombitasvir | Medicine & Public Health | General Practice / Family Medicine | Infectious Diseases | Internal Medicine | Paritaprevir | Elderly | Dasabuvir | Humans | Hepacivirus - genetics | Hepatitis C, Chronic - virology | Male | Carbamates - administration & dosage | Hepatitis C, Chronic - complications | Uracil - administration & dosage | Ribavirin - administration & dosage | Aged, 80 and over | Female | Drug Therapy, Combination | Liver Cirrhosis - etiology | Liver Cirrhosis - diagnosis | Ritonavir - administration & dosage | Antiviral Agents - therapeutic use | Genotype | Treatment Outcome | Hepatitis C, Chronic - diagnosis | Hepatitis C, Chronic - drug therapy | Antiviral Agents - administration & dosage | Anilides - administration & dosage | Antiviral Agents - adverse effects | Biomarkers | Aged | Macrocyclic Compounds - administration & dosage | Sulfonamides - administration & dosage | Uracil - analogs & derivatives | Complications and side effects | Research | Hepatitis C | Drug therapy | Liver cirrhosis | Risk factors | Hypertension | Effectiveness | Liver diseases | Ritonavir | Health risks | Viruses | Pharmacology | Bilirubin | Multivariate analysis | Ribonucleic acid--RNA | Patients | Ribavirin | Hepatitis | Patient safety | Safety | Hepatitis C virus | Genotypes
Cirrhosis | Ombitasvir | Medicine & Public Health | General Practice / Family Medicine | Infectious Diseases | Internal Medicine | Paritaprevir | Elderly | Dasabuvir | Humans | Hepacivirus - genetics | Hepatitis C, Chronic - virology | Male | Carbamates - administration & dosage | Hepatitis C, Chronic - complications | Uracil - administration & dosage | Ribavirin - administration & dosage | Aged, 80 and over | Female | Drug Therapy, Combination | Liver Cirrhosis - etiology | Liver Cirrhosis - diagnosis | Ritonavir - administration & dosage | Antiviral Agents - therapeutic use | Genotype | Treatment Outcome | Hepatitis C, Chronic - diagnosis | Hepatitis C, Chronic - drug therapy | Antiviral Agents - administration & dosage | Anilides - administration & dosage | Antiviral Agents - adverse effects | Biomarkers | Aged | Macrocyclic Compounds - administration & dosage | Sulfonamides - administration & dosage | Uracil - analogs & derivatives | Complications and side effects | Research | Hepatitis C | Drug therapy | Liver cirrhosis | Risk factors | Hypertension | Effectiveness | Liver diseases | Ritonavir | Health risks | Viruses | Pharmacology | Bilirubin | Multivariate analysis | Ribonucleic acid--RNA | Patients | Ribavirin | Hepatitis | Patient safety | Safety | Hepatitis C virus | Genotypes
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Genome-wide meta-analyses identify three loci associated with primary biliary cirrhosis
Nature Genetics, ISSN 1061-4036, 08/2010, Volume 42, Issue 8, pp. 658 - 660
A genome-wide association screen for primary biliary cirrhosis risk alleles was performed in an Italian cohort. The results from the Italian cohort replicated...
SYSTEMIC-LUPUS-ERYTHEMATOSUS | VARIANTS | SPI-B | TRANSCRIPTION | GENETICS & HEREDITY | RISK | ASTHMA | CELL | EXPRESSION | Canada | Interferon Regulatory Factors | European Continental Ancestry Group - genetics | Genome-Wide Association Study | Meta-Analysis as Topic | Humans | Alleles | Liver Cirrhosis, Biliary | Genome | Odds Ratio | Autoimmunity | Chromosome mapping | Autoantibodies | Genomics | Development and progression | Genetic aspects | Biliary cirrhosis | Research | Properties | Methods | Celiac disease | Medical research | Disease | Autoimmune diseases
SYSTEMIC-LUPUS-ERYTHEMATOSUS | VARIANTS | SPI-B | TRANSCRIPTION | GENETICS & HEREDITY | RISK | ASTHMA | CELL | EXPRESSION | Canada | Interferon Regulatory Factors | European Continental Ancestry Group - genetics | Genome-Wide Association Study | Meta-Analysis as Topic | Humans | Alleles | Liver Cirrhosis, Biliary | Genome | Odds Ratio | Autoimmunity | Chromosome mapping | Autoantibodies | Genomics | Development and progression | Genetic aspects | Biliary cirrhosis | Research | Properties | Methods | Celiac disease | Medical research | Disease | Autoimmune diseases
Journal Article
JAMA, ISSN 0098-7484, 11/2013, Volume 310, Issue 20, pp. 2164 - 2173
IMPORTANCE Pediatric-onset Crohn disease is more aggressive than adult-onset disease, has high rates of resistance to existing drugs, and can lead to permanent...
YOUNG-ADULTS | MEDICINE, GENERAL & INTERNAL | INFLAMMATORY-BOWEL-DISEASE | THERAPY | EFFICACY | SAFETY | PEDIATRIC-PATIENTS | THROMBOEMBOLIC EVENTS | OPEN-LABEL | ACTIVITY INDEX | INFLIXIMAB | Severity of Illness Index | Thalidomide - adverse effects | Double-Blind Method | Humans | Immunosuppressive Agents - therapeutic use | Male | Treatment Outcome | Remission Induction | Crohn Disease - pathology | Crohn Disease - drug therapy | Adolescent | Age of Onset | Female | Immunosuppressive Agents - adverse effects | Thalidomide - therapeutic use | Child | Crohn's disease | Dosage and administration | Research | Drug therapy | Thalidomide | Clinical trials | Prescription drugs | Pediatrics | Childrens health | Crohns disease
YOUNG-ADULTS | MEDICINE, GENERAL & INTERNAL | INFLAMMATORY-BOWEL-DISEASE | THERAPY | EFFICACY | SAFETY | PEDIATRIC-PATIENTS | THROMBOEMBOLIC EVENTS | OPEN-LABEL | ACTIVITY INDEX | INFLIXIMAB | Severity of Illness Index | Thalidomide - adverse effects | Double-Blind Method | Humans | Immunosuppressive Agents - therapeutic use | Male | Treatment Outcome | Remission Induction | Crohn Disease - pathology | Crohn Disease - drug therapy | Adolescent | Age of Onset | Female | Immunosuppressive Agents - adverse effects | Thalidomide - therapeutic use | Child | Crohn's disease | Dosage and administration | Research | Drug therapy | Thalidomide | Clinical trials | Prescription drugs | Pediatrics | Childrens health | Crohns disease
Journal Article
Hepatology, ISSN 0270-9139, 12/2017, Volume 66, Issue 6, pp. 1814 - 1825
We evaluated the cost‐effectiveness of two alternative direct‐acting antiviral (DAA) treatment policies in a real‐life cohort of hepatitis C virus–infected...
Hepatitis | Population studies | Liver diseases | Hepatitis C | Cost analysis | Fibrosis | Original
Hepatitis | Population studies | Liver diseases | Hepatitis C | Cost analysis | Fibrosis | Original
Journal Article
Liver International, ISSN 1478-3223, 12/2018, Volume 38, Issue 12, pp. 2190 - 2198
Background & Aims Advances in direct‐acting antiviral treatment of HCV have reinvigorated public health initiatives aimed at identifying affected individuals....
HCV | chronic infection | linkage to care | WHO | VIRUS-INFECTION | RISK-FACTORS | NATIONAL PROGRESS | UNIVERSAL | PREVALENCE | GENERAL-POPULATION | INJECT DRUGS | PEOPLE | GASTROENTEROLOGY & HEPATOLOGY | EPIDEMIOLOGY | HCV-INFECTION | Antiviral agents | Evaluation | Hepatitis C virus | Hepatitis C | Analysis | Hepatitis | Screening | Liver diseases | Liver | Strategy | Birth | Icebergs | Patients | Public health | Viral Hepatitis
HCV | chronic infection | linkage to care | WHO | VIRUS-INFECTION | RISK-FACTORS | NATIONAL PROGRESS | UNIVERSAL | PREVALENCE | GENERAL-POPULATION | INJECT DRUGS | PEOPLE | GASTROENTEROLOGY & HEPATOLOGY | EPIDEMIOLOGY | HCV-INFECTION | Antiviral agents | Evaluation | Hepatitis C virus | Hepatitis C | Analysis | Hepatitis | Screening | Liver diseases | Liver | Strategy | Birth | Icebergs | Patients | Public health | Viral Hepatitis
Journal Article
Digestive and Liver Disease, ISSN 1590-8658, 2016, Volume 48, Issue 5, pp. 455 - 467
Abstract Patients with cirrhosis present with hemostatic alterations secondary to reduced availability of pro-coagulant and anti-coagulant factors. The net...
Gastroenterology and Hepatology | Cirrhosis | Hemostasis | Thrombosis | Bleeding | PORTAL-VEIN THROMBOSIS | ACUTE VARICEAL HEMORRHAGE | RECOMBINANT FACTOR VIIA | RANDOMIZED CONTROLLED-TRIAL | VON-WILLEBRAND-FACTOR | ACTIVATED FACTOR-VII | DEEP VENOUS THROMBOSIS | MOLECULAR-WEIGHT HEPARIN | INTERNATIONAL NORMALIZED RATIO | GASTROENTEROLOGY & HEPATOLOGY | FRESH-FROZEN PLASMA | Coagulants - therapeutic use | Gastrointestinal Hemorrhage - prevention & control | Liver Cirrhosis - complications | Postoperative Hemorrhage - prevention & control | Humans | Blood Coagulation Tests | Anticoagulants - therapeutic use | Esophageal and Gastric Varices - etiology | Liver Cirrhosis - physiopathology | Thrombosis - prevention & control | Drug Monitoring | Care and treatment | Conferences, meetings and seminars | Conferences and conventions | Liver cirrhosis
Gastroenterology and Hepatology | Cirrhosis | Hemostasis | Thrombosis | Bleeding | PORTAL-VEIN THROMBOSIS | ACUTE VARICEAL HEMORRHAGE | RECOMBINANT FACTOR VIIA | RANDOMIZED CONTROLLED-TRIAL | VON-WILLEBRAND-FACTOR | ACTIVATED FACTOR-VII | DEEP VENOUS THROMBOSIS | MOLECULAR-WEIGHT HEPARIN | INTERNATIONAL NORMALIZED RATIO | GASTROENTEROLOGY & HEPATOLOGY | FRESH-FROZEN PLASMA | Coagulants - therapeutic use | Gastrointestinal Hemorrhage - prevention & control | Liver Cirrhosis - complications | Postoperative Hemorrhage - prevention & control | Humans | Blood Coagulation Tests | Anticoagulants - therapeutic use | Esophageal and Gastric Varices - etiology | Liver Cirrhosis - physiopathology | Thrombosis - prevention & control | Drug Monitoring | Care and treatment | Conferences, meetings and seminars | Conferences and conventions | Liver cirrhosis
Journal Article
PLoS ONE, ISSN 1932-6203, 10/2014, Volume 9, Issue 10, p. e110284
Background: Triple therapy including Telaprevir or Boceprevir still represents in many European countries the standard of care for patients with Hepatitis C...
TELAPREVIR TVR | TRIAL | IL28B POLYMORPHISM | PLUS RIBAVIRIN | VIRUS-INFECTION | MULTIDISCIPLINARY SCIENCES | CHRONIC HEPATITIS-C | TRIPLE-THERAPY | BOCEPREVIR | INTERIM ANALYSIS | Decision Making | Genetic Association Studies | Proline - analogs & derivatives | Humans | Middle Aged | Hepacivirus - genetics | Hepatitis C, Chronic - virology | Genotype | Male | Treatment Outcome | Hepatitis C, Chronic - drug therapy | Oligopeptides - therapeutic use | Interleukins - genetics | Proline - therapeutic use | Female | Italy | Drug Therapy, Combination | Hepatitis C, Chronic - genetics | Precision Medicine | Therapy | Liver diseases | Internal medicine | Anemia | Liver | Medical services | Viruses | Infections | Patients | Medicine | Hepatitis | Body mass index | Genotype & phenotype | Infectious diseases | Hospitals | Body mass | Hepatology | Body size | Gastroenterology | Interferon | Hepatitis C virus | Hepatitis C | Genotypes
TELAPREVIR TVR | TRIAL | IL28B POLYMORPHISM | PLUS RIBAVIRIN | VIRUS-INFECTION | MULTIDISCIPLINARY SCIENCES | CHRONIC HEPATITIS-C | TRIPLE-THERAPY | BOCEPREVIR | INTERIM ANALYSIS | Decision Making | Genetic Association Studies | Proline - analogs & derivatives | Humans | Middle Aged | Hepacivirus - genetics | Hepatitis C, Chronic - virology | Genotype | Male | Treatment Outcome | Hepatitis C, Chronic - drug therapy | Oligopeptides - therapeutic use | Interleukins - genetics | Proline - therapeutic use | Female | Italy | Drug Therapy, Combination | Hepatitis C, Chronic - genetics | Precision Medicine | Therapy | Liver diseases | Internal medicine | Anemia | Liver | Medical services | Viruses | Infections | Patients | Medicine | Hepatitis | Body mass index | Genotype & phenotype | Infectious diseases | Hospitals | Body mass | Hepatology | Body size | Gastroenterology | Interferon | Hepatitis C virus | Hepatitis C | Genotypes
Journal Article
Genes and Immunity, ISSN 1466-4879, 05/2013, Volume 14, Issue 3, pp. 179 - 186
Genome-wide association studies (GWAS) have successfully identified several loci associated with primary biliary cirrhosis (PBC) risk. Pathway analysis...
autoimmune disease | hedgehog signaling | linear combination test | phosphatidylinositol signaling | CELLS | ACTIVATION | VARIANTS | IMMUNOLOGY | IDENTIFICATION | SENSORS | EPITHELIAL-MESENCHYMAL TRANSITION | RESPONSES | DISEASES | GENE | GENETICS & HEREDITY | TRAITS | Genetic Predisposition to Disease - genetics | Meta-Analysis as Topic | Gene Frequency | Humans | Middle Aged | Databases, Genetic | Genotype | Male | Signal Transduction - genetics | Liver Cirrhosis, Biliary - genetics | Linkage Disequilibrium | Canada | Algorithms | Female | Italy | Polymorphism, Single Nucleotide | Genome-Wide Association Study - methods | Cohort Studies | Quantitative trait loci | Physiological aspects | Development and progression | Genetic aspects | Biliary cirrhosis | Research | Hedgehog proteins
autoimmune disease | hedgehog signaling | linear combination test | phosphatidylinositol signaling | CELLS | ACTIVATION | VARIANTS | IMMUNOLOGY | IDENTIFICATION | SENSORS | EPITHELIAL-MESENCHYMAL TRANSITION | RESPONSES | DISEASES | GENE | GENETICS & HEREDITY | TRAITS | Genetic Predisposition to Disease - genetics | Meta-Analysis as Topic | Gene Frequency | Humans | Middle Aged | Databases, Genetic | Genotype | Male | Signal Transduction - genetics | Liver Cirrhosis, Biliary - genetics | Linkage Disequilibrium | Canada | Algorithms | Female | Italy | Polymorphism, Single Nucleotide | Genome-Wide Association Study - methods | Cohort Studies | Quantitative trait loci | Physiological aspects | Development and progression | Genetic aspects | Biliary cirrhosis | Research | Hedgehog proteins
Journal Article
Journal of Gastroenterology, ISSN 0944-1174, 3/2016, Volume 51, Issue 3, pp. 271 - 280
The ABCB4 gene encodes the MDR3 protein. Mutations of this gene cause progressive familial intrahepatic cholestasis type 3 (PFIC3) in children, but their...
Primary biliary cirrhosis | Medicine & Public Health | Colorectal Surgery | Hepatology | ABCB4 | Gastroenterology | Abdominal Surgery | Primary sclerosing cholangitis | MDR3 protein | Idiopathic chronic cholestasis | Surgical Oncology | Cholangiocarcinoma | GENE-MUTATIONS | TYPE-3 | CLINICAL-FEATURES | CHOLELITHIASIS | VARIANT | SCLEROSING CHOLANGITIS | PRIMARY BILIARY-CIRRHOSIS | SPECTRUM | GASTROENTEROLOGY & HEPATOLOGY | BILE | Amino Acid Sequence | Cholestasis - genetics | Cholestasis, Intrahepatic - genetics | ATP Binding Cassette Transporter, Sub-Family B - deficiency | Humans | Middle Aged | Cholangitis, Sclerosing - genetics | Male | Liver Cirrhosis, Biliary - genetics | Case-Control Studies | Young Adult | Phenotype | Sequence Alignment | Adolescent | Age of Onset | Pregnancy Complications - genetics | Adult | Female | Aged | Mutation | ATP Binding Cassette Transporter, Sub-Family B - genetics | Child | Chronic Disease | Proteins | Genetic research | Genetic aspects | Adults | Liver cirrhosis
Primary biliary cirrhosis | Medicine & Public Health | Colorectal Surgery | Hepatology | ABCB4 | Gastroenterology | Abdominal Surgery | Primary sclerosing cholangitis | MDR3 protein | Idiopathic chronic cholestasis | Surgical Oncology | Cholangiocarcinoma | GENE-MUTATIONS | TYPE-3 | CLINICAL-FEATURES | CHOLELITHIASIS | VARIANT | SCLEROSING CHOLANGITIS | PRIMARY BILIARY-CIRRHOSIS | SPECTRUM | GASTROENTEROLOGY & HEPATOLOGY | BILE | Amino Acid Sequence | Cholestasis - genetics | Cholestasis, Intrahepatic - genetics | ATP Binding Cassette Transporter, Sub-Family B - deficiency | Humans | Middle Aged | Cholangitis, Sclerosing - genetics | Male | Liver Cirrhosis, Biliary - genetics | Case-Control Studies | Young Adult | Phenotype | Sequence Alignment | Adolescent | Age of Onset | Pregnancy Complications - genetics | Adult | Female | Aged | Mutation | ATP Binding Cassette Transporter, Sub-Family B - genetics | Child | Chronic Disease | Proteins | Genetic research | Genetic aspects | Adults | Liver cirrhosis
Journal Article