Frontiers in Microbiology, ISSN 1664-302X, 11/2017, Volume 8, p. 2163
HCV represents a global health problem with similar to 200 million individuals currently infected, worldwide. With the high cost of antiviral therapies, the...
Virus like particles | Hepatitis C | Hepatitis C vaccines | Neutralizing antibody | HEPATITIS-C-VIRUS | neutralizing antibody | MICROBIOLOGY | INJECTING DRUG-USERS | B SURFACE-ANTIGEN | SUSTAINED VIROLOGICAL RESPONSE | T-CELL RESPONSES | ENVELOPE GLYCOPROTEIN 2 | BROADLY NEUTRALIZING ANTIBODIES | IMMUNE-RESPONSES | virus like particles | E2 GLYCOPROTEIN | HUMAN MONOCLONAL-ANTIBODIES
Virus like particles | Hepatitis C | Hepatitis C vaccines | Neutralizing antibody | HEPATITIS-C-VIRUS | neutralizing antibody | MICROBIOLOGY | INJECTING DRUG-USERS | B SURFACE-ANTIGEN | SUSTAINED VIROLOGICAL RESPONSE | T-CELL RESPONSES | ENVELOPE GLYCOPROTEIN 2 | BROADLY NEUTRALIZING ANTIBODIES | IMMUNE-RESPONSES | virus like particles | E2 GLYCOPROTEIN | HUMAN MONOCLONAL-ANTIBODIES
Journal Article
Journal of Travel Medicine, ISSN 1195-1982, 01/2016, Volume 23, Issue 1, pp. 1 - 1
Journal Article
Journal of Travel Medicine, ISSN 1195-1982, 11/2017, Volume 24, Issue 6
Abstract Our knowledge of the health problems and infections encountered by international travellers has evolved considerably in the past decades. The growth...
GRADE | Malaria | Travel vaccines | Vaccinomics | Network studies | Travel medicine research | RETURNED TRAVELERS | INFECTIOUS DISEASES | network studies | HEPATITIS-A | RABIES POSTEXPOSURE PROPHYLAXIS | SENTINEL SURVEILLANCE DATA | GEOSENTINEL SURVEILLANCE | CLINICAL-FEATURES | malaria | TETRAVALENT DENGUE VACCINE | SYSTEMS BIOLOGY APPROACH | HUMAN GUT MICROBIOME | MEDICINE, GENERAL & INTERNAL | PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH | travel vaccines | vaccinomics | travel medicine research | ZIKA VIRUS | Travel-Related Illness | Disease Transmission, Infectious | Global Health | Health Priorities | Research Design | Humans | Medicine | Travel | Traveltime | Infectious diseases | Travellers | Health problems | Research | Epidemiology | Travel medicine
GRADE | Malaria | Travel vaccines | Vaccinomics | Network studies | Travel medicine research | RETURNED TRAVELERS | INFECTIOUS DISEASES | network studies | HEPATITIS-A | RABIES POSTEXPOSURE PROPHYLAXIS | SENTINEL SURVEILLANCE DATA | GEOSENTINEL SURVEILLANCE | CLINICAL-FEATURES | malaria | TETRAVALENT DENGUE VACCINE | SYSTEMS BIOLOGY APPROACH | HUMAN GUT MICROBIOME | MEDICINE, GENERAL & INTERNAL | PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH | travel vaccines | vaccinomics | travel medicine research | ZIKA VIRUS | Travel-Related Illness | Disease Transmission, Infectious | Global Health | Health Priorities | Research Design | Humans | Medicine | Travel | Traveltime | Infectious diseases | Travellers | Health problems | Research | Epidemiology | Travel medicine
Journal Article
Clinical Infectious Diseases, ISSN 1058-4838, 11/2006, Volume 43, Issue 9, pp. 1185 - 1193
Travelers returning to their country of origin to visit friends and relatives (VFRs) have increased risk of travel-related health problems. We examined...
Travel | Demography | Tuberculosis | Malaria | Travelers | Diarrhea | Infections | Preventive medicine | Travel medicine | Diseases | UNITED-STATES | INFECTIOUS DISEASES | COUNTRIES | INTERNATIONAL-TRAVEL | RISK | MICROBIOLOGY | IMMUNOLOGY | ATTITUDES | SEXUALLY-TRANSMITTED-DISEASES | INFECTIOUS-DISEASES | MALARIA | HEALTH KNOWLEDGE | HIV TRANSMISSION | Communicable Diseases - classification | Friends | Humans | Middle Aged | Child, Preschool | Infant | Male | Communicable Disease Control | Adolescent | Aged, 80 and over | Adult | Family | Female | Aged | Child | Emigration and Immigration | Evaluation | Demographic aspects | Research | Health aspects | Risk factors
Travel | Demography | Tuberculosis | Malaria | Travelers | Diarrhea | Infections | Preventive medicine | Travel medicine | Diseases | UNITED-STATES | INFECTIOUS DISEASES | COUNTRIES | INTERNATIONAL-TRAVEL | RISK | MICROBIOLOGY | IMMUNOLOGY | ATTITUDES | SEXUALLY-TRANSMITTED-DISEASES | INFECTIOUS-DISEASES | MALARIA | HEALTH KNOWLEDGE | HIV TRANSMISSION | Communicable Diseases - classification | Friends | Humans | Middle Aged | Child, Preschool | Infant | Male | Communicable Disease Control | Adolescent | Aged, 80 and over | Adult | Family | Female | Aged | Child | Emigration and Immigration | Evaluation | Demographic aspects | Research | Health aspects | Risk factors
Journal Article
Journal of travel medicine, 01/2016, Volume 23, Issue 1
Journal Article
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Full Text
Progress in the development of preventive and therapeutic vaccines for hepatitis C virus
Journal of Hepatology, ISSN 0168-8278, 2011, Volume 54, Issue 6, pp. 1273 - 1285
Hepatitis C virus (HCV) is a blood borne disease estimated to chronically infect 3% of the worlds’ population causing significant morbidity and mortality....
Gastroenterology and Hepatology | Preventative vaccines | Therapeutic vaccines | Antivirals | Cellular immunity | Vaccines | Hepatitis C | Neutralising antibody | NEUTRALIZING ANTIBODIES | DENDRITIC CELLS | HYPERVARIABLE REGION 1 | GENETIC-VARIATION | T-CELL RESPONSES | PEGINTERFERON ALPHA-2B | IMMUNE-RESPONSES | IN-VIVO | NONSTRUCTURAL PROTEIN-3 | GASTROENTEROLOGY & HEPATOLOGY | PHASE-I | Antibodies, Viral - biosynthesis | Hepatitis C - therapy | Hepacivirus - immunology | Humans | Clinical Trials as Topic | Viral Hepatitis Vaccines - therapeutic use | Virus Internalization | Host-Pathogen Interactions - immunology | Epitopes - immunology | Hepatitis C - immunology | Models, Immunological | Animals | Antibodies, Neutralizing - biosynthesis | Viral Hepatitis Vaccines - isolation & purification | Hepatitis C - prevention & control | Immunity, Cellular | Virus diseases | Peptides | Dendritic cells | Cross infection | Nosocomial infections | Biological response modifiers | Hepatitis C virus | T cells | Health aspects | Recombinant proteins | Antigenic determinants
Gastroenterology and Hepatology | Preventative vaccines | Therapeutic vaccines | Antivirals | Cellular immunity | Vaccines | Hepatitis C | Neutralising antibody | NEUTRALIZING ANTIBODIES | DENDRITIC CELLS | HYPERVARIABLE REGION 1 | GENETIC-VARIATION | T-CELL RESPONSES | PEGINTERFERON ALPHA-2B | IMMUNE-RESPONSES | IN-VIVO | NONSTRUCTURAL PROTEIN-3 | GASTROENTEROLOGY & HEPATOLOGY | PHASE-I | Antibodies, Viral - biosynthesis | Hepatitis C - therapy | Hepacivirus - immunology | Humans | Clinical Trials as Topic | Viral Hepatitis Vaccines - therapeutic use | Virus Internalization | Host-Pathogen Interactions - immunology | Epitopes - immunology | Hepatitis C - immunology | Models, Immunological | Animals | Antibodies, Neutralizing - biosynthesis | Viral Hepatitis Vaccines - isolation & purification | Hepatitis C - prevention & control | Immunity, Cellular | Virus diseases | Peptides | Dendritic cells | Cross infection | Nosocomial infections | Biological response modifiers | Hepatitis C virus | T cells | Health aspects | Recombinant proteins | Antigenic determinants
Journal Article
JOURNAL OF TRAVEL MEDICINE, ISSN 1195-1982, 03/2018, Volume 25, Issue 1
Background: Biologic therapy has revolutionized the management of refractory chronic autoimmune and auto-inflammatory disease, as well as several malignancies,...
RHEUMATOID-ARTHRITIS | INFECTIOUS DISEASES | ANTI-TNF | INTERLEUKIN-1 RECEPTOR ANTAGONIST | JUVENILE IDIOPATHIC ARTHRITIS | B-CELL DEPLETION | MONOCLONAL-ANTIBODY | infection risk | Travel | PNEUMOCOCCAL VACCINE | MEDICINE, GENERAL & INTERNAL | PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH | INFLAMMATORY-BOWEL-DISEASE | biologic agent | INFLUENZA VACCINATION | vaccine response | NECROSIS FACTOR THERAPY | Biological Factors - therapeutic use | Immunocompromised Host - immunology | Travel-Related Illness | Humans | Vaccination | Quality of Life | Risk | Communicable Disease Control - methods | Health care | Therapy | Infections | Vaccines | Immunity | Risks | Literature reviews | Biological effects | Immunology | Defence mechanisms | Remission | Yellow fever | Immune system | Vector-borne diseases | Immune response | Risk groups | Immunomodulation | Health risks | Agents | Disease control | Patients | Fever | Quality of life | Medicine | Immunosuppression | Risk management | Best practice
RHEUMATOID-ARTHRITIS | INFECTIOUS DISEASES | ANTI-TNF | INTERLEUKIN-1 RECEPTOR ANTAGONIST | JUVENILE IDIOPATHIC ARTHRITIS | B-CELL DEPLETION | MONOCLONAL-ANTIBODY | infection risk | Travel | PNEUMOCOCCAL VACCINE | MEDICINE, GENERAL & INTERNAL | PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH | INFLAMMATORY-BOWEL-DISEASE | biologic agent | INFLUENZA VACCINATION | vaccine response | NECROSIS FACTOR THERAPY | Biological Factors - therapeutic use | Immunocompromised Host - immunology | Travel-Related Illness | Humans | Vaccination | Quality of Life | Risk | Communicable Disease Control - methods | Health care | Therapy | Infections | Vaccines | Immunity | Risks | Literature reviews | Biological effects | Immunology | Defence mechanisms | Remission | Yellow fever | Immune system | Vector-borne diseases | Immune response | Risk groups | Immunomodulation | Health risks | Agents | Disease control | Patients | Fever | Quality of life | Medicine | Immunosuppression | Risk management | Best practice
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 5/2015, Volume 112, Issue 18, pp. 5803 - 5808
We have shown that cellular inhibitor of apoptosis proteins (cIAPs) impair clearance of hepatitis B virus (HBV) infection by preventing TNF-mediated...
Smac mimetic | Cellular inhibitor of apoptosis proteins | Hepatitis B virus | Birinapant | TNF | CANCER-CELLS | IMMUNITY | ACTIVATION | VIRUS-INFECTION | hepatitis B virus | MULTIDISCIPLINARY SCIENCES | PERSISTENT LCMV INFECTION | birinapant | RESPONSES | THERAPY | REACTIVATION | MOUSE MODEL | cellular inhibitor of apoptosis proteins | Hepatitis B - metabolism | Guanine - analogs & derivatives | Hepatocytes - metabolism | Hepatitis B Surface Antigens - blood | Hepatocytes - cytology | Guanine - pharmacology | Inhibitor of Apoptosis Proteins - antagonists & inhibitors | Indoles - pharmacology | Inhibitor of Apoptosis Proteins - metabolism | Disease Models, Animal | Antiviral Agents - pharmacology | Microscopy, Electron, Scanning | CD4-Positive T-Lymphocytes - cytology | Dipeptides - pharmacology | Liver - metabolism | Mice, Inbred C57BL | Immunophenotyping | Plasmids - metabolism | Mice, Inbred C3H | DNA, Viral - blood | Animals | Hepatitis B - drug therapy | Hepatocytes - virology | Mice | Prevention | Viral proteins | Host-virus relationships | Observations | Health aspects | Hepatitis B | Apoptosis | Biological Sciences
Smac mimetic | Cellular inhibitor of apoptosis proteins | Hepatitis B virus | Birinapant | TNF | CANCER-CELLS | IMMUNITY | ACTIVATION | VIRUS-INFECTION | hepatitis B virus | MULTIDISCIPLINARY SCIENCES | PERSISTENT LCMV INFECTION | birinapant | RESPONSES | THERAPY | REACTIVATION | MOUSE MODEL | cellular inhibitor of apoptosis proteins | Hepatitis B - metabolism | Guanine - analogs & derivatives | Hepatocytes - metabolism | Hepatitis B Surface Antigens - blood | Hepatocytes - cytology | Guanine - pharmacology | Inhibitor of Apoptosis Proteins - antagonists & inhibitors | Indoles - pharmacology | Inhibitor of Apoptosis Proteins - metabolism | Disease Models, Animal | Antiviral Agents - pharmacology | Microscopy, Electron, Scanning | CD4-Positive T-Lymphocytes - cytology | Dipeptides - pharmacology | Liver - metabolism | Mice, Inbred C57BL | Immunophenotyping | Plasmids - metabolism | Mice, Inbred C3H | DNA, Viral - blood | Animals | Hepatitis B - drug therapy | Hepatocytes - virology | Mice | Prevention | Viral proteins | Host-virus relationships | Observations | Health aspects | Hepatitis B | Apoptosis | Biological Sciences
Journal Article
International Journal of Dermatology, ISSN 0011-9059, 02/2019, Volume 58, Issue 2, pp. 221 - 227
Background Melioidosis is mainly observed in South‐East Asia, where Burkholderia pseudomallei is endemic. Cutaneous melioidosis (CM) has rarely been described...
PSEUDOMALLEI | DERMATOLOGY | Abscess - microbiology | Humans | Skin Diseases, Bacterial - drug therapy | Trimethoprim, Sulfamethoxazole Drug Combination - therapeutic use | Melioidosis - surgery | Skin Diseases, Bacterial - diagnosis | Meropenem - therapeutic use | Skin Diseases, Bacterial - surgery | Anti-Bacterial Agents - therapeutic use | Amoxicillin-Potassium Clavulanate Combination - therapeutic use | Melioidosis - drug therapy | Skin Diseases, Bacterial - complications | Melioidosis - complications | Melioidosis - diagnosis | Drug Therapy, Combination | Infectious Disease Incubation Period | Ceftazidime - therapeutic use | Therapy | Incubation | Clavulanic acid | Chronic infection | Infections | Cellulitis | Patients | Literature reviews | Melioidosis | Surgery | Abscesses | Amoxicillin | Cotrimoxazole | Skin | Meropenem | Diagnostic systems | Burkholderia | Localization | Ceftazidime
PSEUDOMALLEI | DERMATOLOGY | Abscess - microbiology | Humans | Skin Diseases, Bacterial - drug therapy | Trimethoprim, Sulfamethoxazole Drug Combination - therapeutic use | Melioidosis - surgery | Skin Diseases, Bacterial - diagnosis | Meropenem - therapeutic use | Skin Diseases, Bacterial - surgery | Anti-Bacterial Agents - therapeutic use | Amoxicillin-Potassium Clavulanate Combination - therapeutic use | Melioidosis - drug therapy | Skin Diseases, Bacterial - complications | Melioidosis - complications | Melioidosis - diagnosis | Drug Therapy, Combination | Infectious Disease Incubation Period | Ceftazidime - therapeutic use | Therapy | Incubation | Clavulanic acid | Chronic infection | Infections | Cellulitis | Patients | Literature reviews | Melioidosis | Surgery | Abscesses | Amoxicillin | Cotrimoxazole | Skin | Meropenem | Diagnostic systems | Burkholderia | Localization | Ceftazidime
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 5/2015, Volume 112, Issue 18, pp. 5797 - 5802
Hepatitis B virus (HBV) infection can result in a spectrum of outcomes from immune-mediated control to disease progression, cirrhosis, and liver cancer. The...
cIAP2 | cIAP1 | Cellular inhibitor of apoptosis proteins | Hepatitis B virus | TNF | hepatitis B virus | MULTIDISCIPLINARY SCIENCES | DISEASE | ALPHA | MICE | INFECTION | BLOCKADE | cellular inhibitor of apoptosis proteins | T-CELLS | Tumor Necrosis Factor-alpha - metabolism | Hepatitis B - metabolism | Baculoviral IAP Repeat-Containing 3 Protein | Hepatocytes - metabolism | Interferon-gamma - metabolism | Inhibitor of Apoptosis Proteins - metabolism | Disease Models, Animal | Liver Neoplasms - virology | Cytokines - metabolism | Signal Transduction | Liver - metabolism | Mice, Inbred C57BL | Ubiquitin-Protein Ligases - metabolism | Genotype | Immunophenotyping | CD8 Antigens - metabolism | Immunosuppression | Phenotype | Animals | Liver Neoplasms - metabolism | Hepatocytes - virology | Mice | DNA, Viral - genetics | CD4 Antigens - metabolism | Host-virus relationships | Viral proteins | Observations | Health aspects | Apoptosis | Biological Sciences
cIAP2 | cIAP1 | Cellular inhibitor of apoptosis proteins | Hepatitis B virus | TNF | hepatitis B virus | MULTIDISCIPLINARY SCIENCES | DISEASE | ALPHA | MICE | INFECTION | BLOCKADE | cellular inhibitor of apoptosis proteins | T-CELLS | Tumor Necrosis Factor-alpha - metabolism | Hepatitis B - metabolism | Baculoviral IAP Repeat-Containing 3 Protein | Hepatocytes - metabolism | Interferon-gamma - metabolism | Inhibitor of Apoptosis Proteins - metabolism | Disease Models, Animal | Liver Neoplasms - virology | Cytokines - metabolism | Signal Transduction | Liver - metabolism | Mice, Inbred C57BL | Ubiquitin-Protein Ligases - metabolism | Genotype | Immunophenotyping | CD8 Antigens - metabolism | Immunosuppression | Phenotype | Animals | Liver Neoplasms - metabolism | Hepatocytes - virology | Mice | DNA, Viral - genetics | CD4 Antigens - metabolism | Host-virus relationships | Viral proteins | Observations | Health aspects | Apoptosis | Biological Sciences
Journal Article
Clinical Infectious Diseases, ISSN 1058-4838, 2/2008, Volume 46, Issue 3, pp. 443 - 446
Among African immigrants in Melbourne, Victoria, Australia, we demonstrated lower geometric mean vitamin D levels in immigrants with latent tuberculosis...
Vitamin D deficiency | Brief Reports | Infectious diseases | Tuberculosis | Mycobacterium tuberculosis | Vitamin D | Geometric mean | Pulmonary tuberculosis | Latent tuberculosis | Infections | Refugees | MYCOBACTERIUM-TUBERCULOSIS | INFECTIOUS DISEASES | UNIT | LONDON | PULMONARY TUBERCULOSIS | MICROBIOLOGY | PREVALENCE | IMMUNOLOGY | REFUGEES | Tuberculosis - epidemiology | Humans | Middle Aged | Risk Factors | Male | Tuberculosis - microbiology | Vitamin D Deficiency - microbiology | Australia - epidemiology | Mycobacterium tuberculosis - isolation & purification | Vitamin D Deficiency - epidemiology | Adolescent | Adult | Africa South of the Sahara - ethnology | Female | Aged | Retrospective Studies | Emigrants and Immigrants | Tuberculosis - metabolism | Physiological aspects | Immigrants | Health aspects | Risk factors
Vitamin D deficiency | Brief Reports | Infectious diseases | Tuberculosis | Mycobacterium tuberculosis | Vitamin D | Geometric mean | Pulmonary tuberculosis | Latent tuberculosis | Infections | Refugees | MYCOBACTERIUM-TUBERCULOSIS | INFECTIOUS DISEASES | UNIT | LONDON | PULMONARY TUBERCULOSIS | MICROBIOLOGY | PREVALENCE | IMMUNOLOGY | REFUGEES | Tuberculosis - epidemiology | Humans | Middle Aged | Risk Factors | Male | Tuberculosis - microbiology | Vitamin D Deficiency - microbiology | Australia - epidemiology | Mycobacterium tuberculosis - isolation & purification | Vitamin D Deficiency - epidemiology | Adolescent | Adult | Africa South of the Sahara - ethnology | Female | Aged | Retrospective Studies | Emigrants and Immigrants | Tuberculosis - metabolism | Physiological aspects | Immigrants | Health aspects | Risk factors
Journal Article
Journal of Travel Medicine, ISSN 1195-1982, 11/2013, Volume 20, Issue 6, pp. 384 - 393
BackgroundDengue is a leading public health problem with an expanding global burden. Dengue virus is also a significant cause of illness in international...
RETURNED TRAVELERS | INFECTIOUS DISEASES | VIRUS-INFECTION | RISK-FACTORS | RAPID TEST | CLINICAL-FEATURES | NS1 ELISA | NORTH QUEENSLAND | G AVIDITY TEST | MEDICINE, GENERAL & INTERNAL | PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH | VACCINE CANDIDATE | HEMORRHAGIC-FEVER | Travel | Communicable Diseases - ethnology | Disease Outbreaks - statistics & numerical data | Dengue - ethnology | Global Health | Humans | Immunoglobulins | Health aspects | Dengue | Public health | Vaccines | Dengue fever | Travel medicine | Morbidity
RETURNED TRAVELERS | INFECTIOUS DISEASES | VIRUS-INFECTION | RISK-FACTORS | RAPID TEST | CLINICAL-FEATURES | NS1 ELISA | NORTH QUEENSLAND | G AVIDITY TEST | MEDICINE, GENERAL & INTERNAL | PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH | VACCINE CANDIDATE | HEMORRHAGIC-FEVER | Travel | Communicable Diseases - ethnology | Disease Outbreaks - statistics & numerical data | Dengue - ethnology | Global Health | Humans | Immunoglobulins | Health aspects | Dengue | Public health | Vaccines | Dengue fever | Travel medicine | Morbidity
Journal Article
Vaccine, ISSN 0264-410X, 2010, Volume 28, Issue 50, pp. 7993 - 8000
Abstract Japanese encephalitis chimeric virus vaccine (JE-CV) was developed to replace licensed mouse brain-derived vaccine (MBD-JE), the production of which...
Allergy and Immunology | Clinical trial, phase 3 | Attenuated vaccines | Japanese encephalitis vaccines | NONHUMAN-PRIMATES | STRAINS | MEDICINE, RESEARCH & EXPERIMENTAL | WILD-TYPE | VIRUS-VACCINE | PROTECTION | CANDIDATE | CHIMERIVAX-JE | IMMUNOLOGY | IMMUNIZATION | RECOMBINANT | SA14-14-2 | Japanese Encephalitis Vaccines - administration & dosage | Double-Blind Method | Humans | Japanese Encephalitis Vaccines - immunology | Middle Aged | Male | Neutralization Tests | Japanese Encephalitis Vaccines - adverse effects | Antibodies, Viral - blood | Young Adult | Vaccines, Attenuated - immunology | Encephalitis, Japanese - prevention & control | Vaccines, Attenuated - administration & dosage | Adolescent | Aged, 80 and over | Adult | Female | Aged | Vaccines, Attenuated - adverse effects | Antibodies, Neutralizing - blood | Clinical trials | Product development | Vaccines | Health aspects | Vaccination | Japanese encephalitis | Studies | Encephalitis | Licenses | Military personnel | Drug dosages | Tropical diseases
Allergy and Immunology | Clinical trial, phase 3 | Attenuated vaccines | Japanese encephalitis vaccines | NONHUMAN-PRIMATES | STRAINS | MEDICINE, RESEARCH & EXPERIMENTAL | WILD-TYPE | VIRUS-VACCINE | PROTECTION | CANDIDATE | CHIMERIVAX-JE | IMMUNOLOGY | IMMUNIZATION | RECOMBINANT | SA14-14-2 | Japanese Encephalitis Vaccines - administration & dosage | Double-Blind Method | Humans | Japanese Encephalitis Vaccines - immunology | Middle Aged | Male | Neutralization Tests | Japanese Encephalitis Vaccines - adverse effects | Antibodies, Viral - blood | Young Adult | Vaccines, Attenuated - immunology | Encephalitis, Japanese - prevention & control | Vaccines, Attenuated - administration & dosage | Adolescent | Aged, 80 and over | Adult | Female | Aged | Vaccines, Attenuated - adverse effects | Antibodies, Neutralizing - blood | Clinical trials | Product development | Vaccines | Health aspects | Vaccination | Japanese encephalitis | Studies | Encephalitis | Licenses | Military personnel | Drug dosages | Tropical diseases
Journal Article