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Clinical Infectious Diseases, ISSN 1058-4838, 7/2012, Volume 55, Issue 1, pp. 126 - 136
Journal Article
JAIDS Journal of Acquired Immune Deficiency Syndromes, ISSN 1525-4135, 06/2016, Volume 72, Issue 2, pp. 206 - 213
Journal Article
The Journal of Infectious Diseases, ISSN 0022-1899, 6/2013, Volume 207, Issue 12, pp. 1909 - 1921
Crimean-Congo hemorrhagic fever (CCHF) is a widely distributed viral hemorrhagic fever characterized by rapid onset of flu-like symptoms often followed by... 
Pathology | Disease models | Interleukins | Tissue samples | Crimean Congo hemorrhagic fever virus | Viral diseases | Viruses | Infections | Platelets | Dosage | pathology | coagulopathy | proinflammatory response | thrombocytopenia | CCHFV | interferon α/β receptor knockout mice | CELLS | INFECTIOUS DISEASES | PREDICTOR | MICROBIOLOGY | MODEL | IMMUNOLOGY | PATHOGENESIS | TRANSMISSION | REPLICATION | DISSEMINATED INTRAVASCULAR COAGULATION | beta receptor knockout mice | CCHF VIRUS | AFRICAN | interferon alpha | Liver - virology | Spleen - virology | Liver - pathology | Viremia | Hemorrhagic Fever, Crimean - complications | Humans | Liver Failure, Acute - virology | Viral Load | Blood Coagulation Disorders - virology | Hemorrhagic Fever, Crimean - immunology | Receptor, Interferon alpha-beta - genetics | Spleen - pathology | Disease Models, Animal | Hemorrhagic Fever Virus, Crimean-Congo - physiology | Cytokines - metabolism | Lymphoid Tissue - virology | Mice, Inbred C57BL | Thrombocytopenia - immunology | Hemorrhagic Fever Virus, Crimean-Congo - immunology | Thrombocytopenia - pathology | Thrombocytopenia - virology | Disease Progression | Mice, Knockout | Lymphoid Tissue - pathology | Animals | Hemorrhagic Fever, Crimean - pathology | Blood Coagulation Disorders - pathology | Receptor, Interferon alpha-beta - immunology | Blood Coagulation Disorders - immunology | Liver Failure, Acute - immunology | Liver Failure, Acute - pathology | Chemokines - metabolism | Mice | Major and Brief Reports | β receptor knockout mice | interferon α
Journal Article
PLoS ONE, ISSN 1932-6203, 09/2016, Volume 11, Issue 9, p. e0162492
The high rate of hepatitis C virus (HCV) infection among transfusion related risk groups such as patients with inherited bleeding disorders highlighting the... 
DRUG-USERS | PRISONERS | RISK-FACTORS | PHYLOGENIES | INJECTION | MULTIDISCIPLINARY SCIENCES | GENETIC HISTORY | JMODELTEST | MOLECULAR EPIDEMIOLOGY | INFECTION | PREVALENCE | Blood Coagulation Disorders - epidemiology | Humans | Middle Aged | Phylogeography | Viral Nonstructural Proteins - genetics | Genotype | Hepacivirus - pathogenicity | Male | Phylogeny | Young Adult | Blood Coagulation Disorders - virology | RNA, Viral - genetics | Hepatitis C - classification | Hepatitis C - epidemiology | Adolescent | Hepatitis C - virology | Adult | Female | Aged | Iran - epidemiology | Antiviral agents | Medical research | Biological products | Analysis | Hemophilia | Medicine, Experimental | Genetic aspects | Hepatitis C virus | Health aspects | Blood transfusion | Blood donors | Diseases | Developed countries | Blood transfusions | Epidemics | Drug abuse | Substance abuse treatment | Transfusion | Disorders | Science | Alcohol | Viruses | Systematic review | Infections | Epidemiology | Blood | Bleeding | Hepatitis | Acquired immune deficiency syndrome--AIDS | Human immunodeficiency virus--HIV | Phylogenetics | Expansion | Public health | Blood products | Blood & organ donations | Risk groups | Health risks | Patients | RNA-directed RNA polymerase | Virology | Studies | Screening | Disease transmission | Genetic engineering | Hepatitis C | Acquired immune deficiency syndrome | AIDS | HIV | Human immunodeficiency virus
Journal Article
Pediatric Critical Care Medicine, ISSN 1529-7535, 05/2013, Volume 14, Issue 4, pp. e176 - e181
Journal Article
The Southeast Asian journal of tropical medicine and public health, ISSN 0125-1562, 2015, Volume 46, pp. 43 - 45
The pathogenesis of hematologic changes in dengue patients is not clearly understood. Consistent hematological findings include vasculopathy, thrombocytopenia,... 
Severe Dengue - physiopathology | Blood Coagulation Disorders - virology | Hemostasis | Humans | Severe Dengue - virology | Thrombocytopenia - physiopathology | Dengue - physiopathology | Dengue - virology | Thrombocytopenia - virology | Blood Coagulation Disorders - physiopathology
Journal Article
Journal Article
Journal Article
Journal Article
Thrombosis and Haemostasis, ISSN 0340-6245, 06/2000, Volume 83, Issue 6, pp. 807 - 810
Summary Background Hepatitis C virus (HCV) infected hemophiliacs respond at low rate to interferon (IFN) monotherapy. Aims To assess efficacy of IFN and RBV in... 
Commentary | HCV | Interferon | Clotting disorders | Ribavirin | PLACEBO | ribavirin | RAPID CLEARANCE | FACTOR-VIII | clotting disorders | HEMOPHILIC PATIENTS | PREVALENCE | interferon | COMBINATION | ALPHA-INTERFERON | RANDOMIZED TRIAL | VIRUS-RNA | PERIPHERAL VASCULAR DISEASE | INFECTION | HEMATOLOGY | HIV Antibodies - blood | Neutrophils - cytology | Predictive Value of Tests | Hemophilia A - virology | Prognosis | Age Factors | Hepatitis C - drug therapy | Humans | Middle Aged | Interferons - adverse effects | Hepacivirus - genetics | Male | RNA, Viral - blood | Alanine Transaminase - blood | Blood Coagulation Disorders - virology | Ribavirin - administration & dosage | Sensitivity and Specificity | Factor VII Deficiency - virology | von Willebrand Diseases - drug therapy | Adult | Female | Drug Therapy, Combination | Child | Hemophilia B - virology | HIV Seronegativity - drug effects | Blood Coagulation Disorders - congenital | Hemoglobins - metabolism | Treatment Outcome | Reverse Transcriptase Polymerase Chain Reaction | Antiviral Agents - administration & dosage | Hemophilia B - drug therapy | Blood Coagulation Disorders - drug therapy | Hepatitis C - diagnosis | Interferons - administration & dosage | Platelet Count | Ribavirin - adverse effects | von Willebrand Diseases - virology | Antiviral Agents - adverse effects | Factor VII Deficiency - drug therapy | Adolescent | Age of Onset | Hemophilia A - drug therapy | Chronic Disease | Hepatitis C - etiology
Journal Article
Journal Article