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Pesquisa : D12.776.124.486.485.114.573.601.849 [Categoria DeCS]
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  1 / 1361 MEDLINE  
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[PMID]:28535026
[Au] Autor:Hozgraefe B; Koria A; Sem V; Johansson J
[Ad] Endereço:AnOpIVA klinken, Sjukhuset i Arvika, Landstinget i Värmland - Arvika, Sweden AnOpIVA klinken, Sjukhuset i Arvika, Landstinget i Värmland - Arvika, Sweden.
[Ti] Título:Tetanus ­ nästan bortglömd men allvarlig sjukdom - Äldre kvinnor är en riskgrupp, diagnosen kan vara en utmaning..
[So] Source:Lakartidningen;114, 2017 May 22.
[Is] ISSN:1652-7518
[Cp] País de publicação:Sweden
[La] Idioma:swe
[Ab] Resumo:Tetanus, an almost forgotten but serious disease Tetanus is the systemic consequence of a local infection with Clostridium tetani, that produces toxin which spreads in the systemic circulation. In developed countries, it is extremely rare. Women born before 1950 are a group at risk due to lower prevalence of immunisation. This report describes a case of tetanus. The patient is a previously healthy 82-year-old woman. She presented to primary care with a complaint of stiffness in the neck and jaw. A physical exam and basic laboratory tests were normal apart from a slightly increased blood pressure. Later the same day she was admitted to the intensive care unit for suspected tetanus. During the night she deteriorated with marked stiffness in her thorax and, as a result of this, severe respiratory distress. After induction of anesthesia she was ventilated and intubated without problem. The treatment for tetanus, an antibody, was given 5 hours later after urgent delivery from the national supply. The patient was successfully weaned from the ventilator after 37 days. During intensive care she had fluctuating stiffness and autonomic instability, both commonly described in patients with tetanus.
[Mh] Termos MeSH primário: Tétano/diagnóstico
[Mh] Termos MeSH secundário: Idoso de 80 Anos ou mais
Feminino
Seres Humanos
Pneumonia/etiologia
Fatores de Risco
Tétano/complicações
Tétano/tratamento farmacológico
Tétano/imunologia
Antitoxina Tetânica/uso terapêutico
[Pt] Tipo de publicação:CASE REPORTS
[Nm] Nome de substância:
0 (Tetanus Antitoxin)
[Em] Mês de entrada:1711
[Cu] Atualização por classe:171109
[Lr] Data última revisão:
171109
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170524
[St] Status:MEDLINE


  2 / 1361 MEDLINE  
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[PMID]:28044038
[Au] Autor:Mitchell L; Adams W; Aspesberro F
[Ad] Endereço:Madigan Army Medical Center, Tacoma WA.
[Ti] Título:Case 6: Episodic Stiffness in a 30-month-old Girl.
[So] Source:Pediatr Rev;38(1):52-53, 2017 Jan.
[Is] ISSN:1526-3347
[Cp] País de publicação:United States
[La] Idioma:eng
[Mh] Termos MeSH primário: Rigidez Muscular/diagnóstico
Músculos do Pescoço/patologia
Tétano/diagnóstico
[Mh] Termos MeSH secundário: Anti-Infecciosos/uso terapêutico
Pré-Escolar
Diagnóstico Diferencial
Feminino
Seres Humanos
Metronidazol/uso terapêutico
Tétano/tratamento farmacológico
Antitoxina Tetânica/administração & dosagem
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Anti-Infective Agents); 0 (Tetanus Antitoxin); 140QMO216E (Metronidazole)
[Em] Mês de entrada:1705
[Cu] Atualização por classe:170504
[Lr] Data última revisão:
170504
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170104
[St] Status:MEDLINE
[do] DOI:10.1542/pir.2014-0142


  3 / 1361 MEDLINE  
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[PMID]:27806074
[Au] Autor:Li Y; Sun R; Wang Y; Li H; Zheng X
[Ad] Endereço:State Key Laboratory of Robotics, Shenyang Institute of Automation, Chinese Academy of Sciences, Shenyang, Liaoning, P. R. China.
[Ti] Título:A Novel Robot System Integrating Biological and Mechanical Intelligence Based on Dissociated Neural Network-Controlled Closed-Loop Environment.
[So] Source:PLoS One;11(11):e0165600, 2016.
[Is] ISSN:1932-6203
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:We propose the architecture of a novel robot system merging biological and artificial intelligence based on a neural controller connected to an external agent. We initially built a framework that connected the dissociated neural network to a mobile robot system to implement a realistic vehicle. The mobile robot system characterized by a camera and two-wheeled robot was designed to execute the target-searching task. We modified a software architecture and developed a home-made stimulation generator to build a bi-directional connection between the biological and the artificial components via simple binomial coding/decoding schemes. In this paper, we utilized a specific hierarchical dissociated neural network for the first time as the neural controller. Based on our work, neural cultures were successfully employed to control an artificial agent resulting in high performance. Surprisingly, under the tetanus stimulus training, the robot performed better and better with the increasement of training cycle because of the short-term plasticity of neural network (a kind of reinforced learning). Comparing to the work previously reported, we adopted an effective experimental proposal (i.e. increasing the training cycle) to make sure of the occurrence of the short-term plasticity, and preliminarily demonstrated that the improvement of the robot's performance could be caused independently by the plasticity development of dissociated neural network. This new framework may provide some possible solutions for the learning abilities of intelligent robots by the engineering application of the plasticity processing of neural networks, also for the development of theoretical inspiration for the next generation neuro-prostheses on the basis of the bi-directional exchange of information within the hierarchical neural networks.
[Mh] Termos MeSH primário: Neurônios/citologia
Robótica/instrumentação
Antitoxina Tetânica/farmacologia
[Mh] Termos MeSH secundário: Algoritmos
Fenômenos Biomecânicos
Técnicas de Cultura de Células
Seres Humanos
Redes Neurais (Computação)
Neurônios/efeitos dos fármacos
Software
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Tetanus Antitoxin)
[Em] Mês de entrada:1706
[Cu] Atualização por classe:170626
[Lr] Data última revisão:
170626
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:161103
[St] Status:MEDLINE
[do] DOI:10.1371/journal.pone.0165600


  4 / 1361 MEDLINE  
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[PMID]:27749688
[Au] Autor:Yan S; Chen SA; Zhang W; Yang F; Yang Y; Zhu Q; Zhu H; Sun X; Jiang M; Su Y; Zhang L; Xing Q; Luo X
[Ad] Endereço:aInstitutes of Biomedical Sciences bDepartment of Dermatology, Huashan Hospital cChildren's Hospital and Institutes of Biomedical Sciences, Fudan University, Shanghai dDepartment of Pharmacology, School of Medicine, Zhengzhou University, Zhengzhou, China.
[Ti] Título:HLA-A*02 alleles are associated with tetanus antitoxin-induced exanthematous drug eruptions in Chinese patients.
[So] Source:Pharmacogenet Genomics;26(12):538-546, 2016 Dec.
[Is] ISSN:1744-6880
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:OBJECTIVE: Tetanus antitoxin (TAT) is an effective antitetanus medicine, but may sometimes cause adverse drug reactions such as rapid-onset anaphylactic shock and late-onset cutaneous adverse drug reactions, including exanthematous drug eruptions (EDE). Human leukocyte antigen (HLA) class I alleles are strongly associated with different types of cutaneous adverse drug reactions. This study aimed to assess whether there is an association between TAT-induced EDE and HLA-A, HLA-B, and HLA-C alleles in the Chinese Han population. PATIENTS AND METHODS: We carried out an association study in 15 patients with TAT-induced EDE and two groups of general Han Chinese patients. Allele-level genotypes of the HLA-A, HLA-B, and HLA-C genes of each patient were determined using the PCR-sequence-specific oligonucleotides method. RESULTS: The carrier frequency of HLA serotype A2 was significantly higher in the TAT-induced EDE patients than in the general Han Chinese study participants from the human major histocompatibility complex database [n=283, odds ratio (OR)=6.93; P=0.0061]. Particularly, the carrier frequency of three A2 alleles, including HLA-A*02:01, HLA-A*02:06, and HLA-A*02:07, is significantly higher than that of the control group (OR=14.40; P=2.4×10). Furthermore, HLA-B*39:01 was in complete linkage disequilibrium with HLA-A*02:06 in the case patients. Consequently, the distribution of the HLA-A*02:06/-B*39:01 haplotype was also significantly different in the cases and the controls (OR=105.00; P=0.0024). CONCLUSION: The HLA-A*02:06/-B*39:01 haplotype is a potential genetic marker for the TAT-induced EDE. Furthermore, the HLA-A2 serotype, especially three alleles A*02:01, A*02:06, and A*02:07, was identified to be associated with the TAT-induced EDE in the Han Chinese population for the first time.
[Mh] Termos MeSH primário: Grupo com Ancestrais do Continente Asiático/genética
Exantema/genética
Antígenos HLA-A/genética
Antitoxina Tetânica/toxicidade
[Mh] Termos MeSH secundário: Adulto
Grupo com Ancestrais do Continente Asiático/etnologia
China/etnologia
Exantema/induzido quimicamente
Feminino
Estudos de Associação Genética
Seres Humanos
Masculino
Meia-Idade
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
0 (HLA-A Antigens); 0 (Tetanus Antitoxin)
[Em] Mês de entrada:1705
[Cu] Atualização por classe:170501
[Lr] Data última revisão:
170501
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:161028
[St] Status:MEDLINE


  5 / 1361 MEDLINE  
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[PMID]:27651411
[Au] Autor:Jarial KD; Sukumar S; Bhansali A
[Ad] Endereço:Department of Endocrinology, Post Graduate Institute of Medical Education and Research, Chandigarh, India.
[Ti] Título:Rat bite ulcer in an insensate foot.
[So] Source:BMJ Case Rep;2016, 2016 Sep 20.
[Is] ISSN:1757-790X
[Cp] País de publicação:England
[La] Idioma:eng
[Mh] Termos MeSH primário: Antídotos/administração & dosagem
Mordeduras e Picadas
Diabetes Mellitus Tipo 2/complicações
Pé Diabético/diagnóstico
Traumatismos do Pé/diagnóstico
/inervação
Antitoxina Tetânica/administração & dosagem
[Mh] Termos MeSH secundário: Combinação Amoxicilina e Clavulanato de Potássio/uso terapêutico
Animais
Diabetes Mellitus Tipo 2/fisiopatologia
Diagnóstico Diferencial
Traumatismos do Pé/patologia
Seres Humanos
Masculino
Meia-Idade
Ratos
Resultado do Tratamento
Inibidores de beta-Lactamases/uso terapêutico
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Antidotes); 0 (Tetanus Antitoxin); 0 (beta-Lactamase Inhibitors); 74469-00-4 (Amoxicillin-Potassium Clavulanate Combination)
[Em] Mês de entrada:1705
[Cu] Atualização por classe:170510
[Lr] Data última revisão:
170510
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:160922
[St] Status:MEDLINE


  6 / 1361 MEDLINE  
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[PMID]:27601113
[Au] Autor:Maharaj M; Dungwa N
[Ad] Endereço:Department of Paediatrics and Child Health, Witbank Hospital and School of Medicine, Faculty of Health Sciences, University of Pretoria, South Africa. nomdungwa@yahoo.com.
[Ti] Título:Neonatal tetanus associated with skin infection.
[So] Source:S Afr Med J;106(9):888-90, 2016 Aug 03.
[Is] ISSN:0256-9574
[Cp] País de publicação:South Africa
[La] Idioma:eng
[Ab] Resumo:A 1-week-old infant was brought to a regional hospital with a history of recurrent seizures following lower abdominal septic skin infection. She was found to have neonatal tetanus, and a spatula test was positive. The tetanus infection was associated with a superficial skin infection, common in neonates. Treatment included sedatives (diazepam, chlorpromazine, phenobarbitone and morphine), muscle relaxants, antibiotics and ventilation in the neonatal intensive care unit. Intrathecal and intramuscular immunoglobulin were given, and the wound was treated. The infant recovered, with no seizures by the 16th day from admission, and was off the ventilator by the 18th day. This was shorter than the usual 3 - 4 weeks for neonates with tetanus at the hospital. The question arises whether tetanus immunisation should be considered in infants with skin infections, which frequently occur in the neonatal period.
[Mh] Termos MeSH primário: Antibacterianos/administração & dosagem
Anticonvulsivantes/administração & dosagem
Diagnóstico Tardio
Hipnóticos e Sedativos/administração & dosagem
Dermatopatias Infecciosas/complicações
Pele/patologia
Antitoxina Tetânica/administração & dosagem
Tétano
[Mh] Termos MeSH secundário: Parede Abdominal
Desbridamento/métodos
Diagnóstico Tardio/efeitos adversos
Diagnóstico Tardio/prevenção & controle
Feminino
Seres Humanos
Fatores Imunológicos/administração & dosagem
Recém-Nascido
Necrose
Dermatopatias Infecciosas/diagnóstico
Dermatopatias Infecciosas/fisiopatologia
Dermatopatias Infecciosas/terapia
Tétano/diagnóstico
Tétano/etiologia
Tétano/fisiopatologia
Tétano/terapia
Resultado do Tratamento
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Anti-Bacterial Agents); 0 (Anticonvulsants); 0 (Hypnotics and Sedatives); 0 (Immunologic Factors); 0 (Tetanus Antitoxin)
[Em] Mês de entrada:1707
[Cu] Atualização por classe:170706
[Lr] Data última revisão:
170706
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:160908
[St] Status:MEDLINE
[do] DOI:10.7196/SAMJ.2016.v106i9.11139


  7 / 1361 MEDLINE  
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[PMID]:27552633
[Ti] Título:A Safe and Sane Fourth.
[So] Source:JAMA;316(8):885, 2016 Aug 23-30.
[Is] ISSN:1538-3598
[Cp] País de publicação:United States
[La] Idioma:eng
[Mh] Termos MeSH primário: Aniversários e Eventos Especiais
Traumatismos por Explosões/história
Tétano/história
[Mh] Termos MeSH secundário: Traumatismos por Explosões/complicações
Traumatismos por Explosões/epidemiologia
Cidades/epidemiologia
Cidades/história
História do Século XX
Seres Humanos
Tétano/etiologia
Tétano/mortalidade
Antitoxina Tetânica/administração & dosagem
Antitoxina Tetânica/história
Trismo/etiologia
Trismo/história
Trismo/mortalidade
Estados Unidos/epidemiologia
[Pt] Tipo de publicação:CLASSICAL ARTICLE; HISTORICAL ARTICLE; JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Tetanus Antitoxin)
[Em] Mês de entrada:1609
[Cu] Atualização por classe:161017
[Lr] Data última revisão:
161017
[Sb] Subgrupo de revista:AIM; IM
[Da] Data de entrada para processamento:160824
[St] Status:MEDLINE
[do] DOI:10.1001/jama.2015.17099


  8 / 1361 MEDLINE  
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[PMID]:27461125
[Au] Autor:Hirano F; Imamura S; Sasaki Y; Takikawa N; Sawata A; Yamamoto A; Uchiyama M; Shimazaki Y; Kojima A; Nagai H
[Ad] Endereço:National Veterinary Assay Laboratory, Ministry of Agriculture, Forestry and Fisheries, 1-15-1, Tokura, Kokubunji, Tokyo 185-8511, Japan. Electronic address: humiya_hirano@nval.maff.go.jp.
[Ti] Título:Establishment of an equine tetanus antitoxin reference standard for veterinary use in Japan.
[So] Source:Biologicals;44(5):374-7, 2016 Sep.
[Is] ISSN:1095-8320
[Cp] País de publicação:England
[La] Idioma:eng
[Ab] Resumo:To establish the first National Veterinary Assay Laboratory (NVAL) equine tetanus antitoxin reference standard for veterinary use, we manufactured vials of a candidate antitoxin. These were quality tested for moisture content, vacuum, colour, clarity, and the presence of foreign objects. Ultimately, 115 quality-controlled vials were prepared. To estimate the antitoxin potency of the candidate standard, three different laboratories conducted parallel line assays alongside the existing antitoxin standard. These potency estimates ranged from 38 to 42 IU. This activity was maintained for two years after manufacture, as compared with a fresh vial. No statistically significant non-linearity or non-parallelism of the regression lines was observed (p > 0.05). Statistical assessment of inter- and intra-laboratory variability revealed acceptable coefficients of variation of 3.2% and 2.4-3.1%, respectively. Based on these results, the potency of the potential reference standard was calculated at 40 units of antitoxin activity per 1-mL vial. Vials of this preparation were distributed for use as the first equine tetanus antitoxin reference standard for veterinary use in September 2015.
[Mh] Termos MeSH primário: Controle de Qualidade
Antitoxina Tetânica
Medicina Veterinária
[Mh] Termos MeSH secundário: Animais
Cavalos
Japão
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Tetanus Antitoxin)
[Em] Mês de entrada:1701
[Cu] Atualização por classe:170123
[Lr] Data última revisão:
170123
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:160728
[St] Status:MEDLINE


  9 / 1361 MEDLINE  
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[PMID]:26142434
[Au] Autor:van den Heuvel D; Jansen MA; Dik WA; Bouallouch-Charif H; Zhao D; van Kester KA; Smits-te Nijenhuis MA; Kolijn-Couwenberg MJ; Jaddoe VW; Arens R; van Dongen JJ; Moll HA; van Zelm MC
[Ad] Endereço:Department of Immunology.
[Ti] Título:Cytomegalovirus- and Epstein-Barr Virus-Induced T-Cell Expansions in Young Children Do Not Impair Naive T-cell Populations or Vaccination Responses: The Generation R Study.
[So] Source:J Infect Dis;213(2):233-42, 2016 Jan 15.
[Is] ISSN:1537-6613
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:BACKGROUND: Cytomegalovirus (CMV) and Epstein-Barr virus (EBV) induce effector memory T-cell expansions, which are variable and potentially depend on the age at primary exposure and coinfections. We evaluated the T-cell compartment and herpesvirus infections in 6-year-old children. METHODS: T-cell subsets and immunoglobulin G seropositivity for CMV, EBV, herpes-simplex virus 1, and varicella-zoster virus were studied in 1079 6-year-old children. A random subgroup of 225 children was evaluated for CMV and EBV seropositivity before 2 years of age and for vaccination responses against measles and tetanus. RESULTS: CMV and EBV infections were associated with significant expansions of CD27(-) and CD27(+) effector memory T cells, respectively. These expansions were enhanced in CMV-EBV-coinfected children and were independent of varicella-zoster virus or herpes-simplex virus 1 coinfection. Naive and central memory T-cell numbers were not affected, nor were anti-tetanus and anti-measles immunoglobulin G levels. Children infected before 2 years of age showed smaller effector memory T-cell expansions than those infected between 2 and 6 years of age. CONCLUSIONS: CMV- and EBV-related T-cell expansions do not impair naive T-cell numbers or maintenance of protective responses against nonrelated pathogens. Duration of infection was not directly related to larger expansions of effector memory T cells in children, suggesting that other mechanisms affect these expansions at later age.
[Mh] Termos MeSH primário: Citomegalovirus/fisiologia
Herpesvirus Humano 4/fisiologia
Vacina contra Sarampo/imunologia
Subpopulações de Linfócitos T/fisiologia
Antitoxina Tetânica/imunologia
[Mh] Termos MeSH secundário: Diferenciação Celular
Criança
Pré-Escolar
Herpesvirus Humano 1/imunologia
Herpesvirus Humano 3/imunologia
Seres Humanos
Sarampo/prevenção & controle
Tétano/prevenção & controle
Vacinação
[Pt] Tipo de publicação:CLINICAL STUDY; JOURNAL ARTICLE; RESEARCH SUPPORT, NON-U.S. GOV'T
[Nm] Nome de substância:
0 (Measles Vaccine); 0 (Tetanus Antitoxin)
[Em] Mês de entrada:1604
[Cu] Atualização por classe:151225
[Lr] Data última revisão:
151225
[Sb] Subgrupo de revista:AIM; IM
[Da] Data de entrada para processamento:150705
[St] Status:MEDLINE
[do] DOI:10.1093/infdis/jiv369


  10 / 1361 MEDLINE  
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[PMID]:26553691
[Au] Autor:Basta NE; Borrow R; Berthe A; Onwuchekwa U; Dembélé AT; Almond R; Frankland S; Patel S; Wood D; Nascimento M; Manigart O; Trotter CL; Greenwood B; Sow SO
[Ad] Endereço:Division of Epidemiology and Community Health, School of Public Health, University of Minnesota, Minneapolis Fogarty International Center, National Institutes of Health, Bethesda, Maryland.
[Ti] Título:Higher Tetanus Toxoid Immunity 2 Years After PsA-TT Introduction in Mali.
[So] Source:Clin Infect Dis;61 Suppl 5:S578-85, 2015 Nov 15.
[Is] ISSN:1537-6591
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:BACKGROUND: In 2010, mass vaccination with a then-new meningococcal A polysaccharide-tetanus toxoid protein conjugate vaccine (PsA-TT, or MenAfriVac) was undertaken in 1- to 29-year-olds in Bamako, Mali. Whether vaccination with PsA-TT effectively boosts tetanus immunity in a population with heterogeneous baseline tetanus immunity is not known. We assessed the impact of PsA-TT on tetanus toxoid (TT) immunity by quantifying age- and sex-specific immunity prior to and 2 years after introduction. METHODS: Using a household-based, age-stratified design, we randomly selected participants for a prevaccination serological survey in 2010 and a postvaccination survey in 2012. TT immunoglobulin G (IgG) antibodies were quantified and geometric mean concentrations (GMCs) pre- and postvaccination among all age groups targeted for vaccination were compared. The probability of TT IgG levels ≥0.1 IU/mL (indicating short-term protection) and ≥1.0 IU/mL (indicating long-term protection) by age and sex was determined using logistic regression models. RESULTS: Analysis of 793 prevaccination and 800 postvaccination sera indicated that while GMCs were low pre-PsA-TT, significantly higher GMCs in all age-sex strata were observed 2 years after PsA-TT introduction. The percentage with short-term immunity increased from 57.1% to 88.4% (31.3-point increase; 95% confidence interval [CI], 26.6-36.0;, P < .0001) and with long-term immunity increased from 20.0% to 58.5% (38.5-point increase; 95% CI, 33.7-43.3; P < .0001) pre- and postvaccination. CONCLUSIONS: Significantly higher TT immunity was observed among vaccine-targeted age groups up to 2 years after Mali's PsA-TT mass vaccination campaign. Our results, combined with evidence from clinical trials, strongly suggest that conjugate vaccines containing TT such as PsA-TT should be considered bivalent vaccines because of their ability to boost tetanus immunity.
[Mh] Termos MeSH primário: Anticorpos Antibacterianos/sangue
Vacinas Meningocócicas/administração & dosagem
Vacinas Meningocócicas/imunologia
Antitoxina Tetânica/sangue
Toxoide Tetânico/imunologia
[Mh] Termos MeSH secundário: Adolescente
Adulto
Criança
Pré-Escolar
Feminino
Seres Humanos
Imunoglobulina G/sangue
Lactente
Recém-Nascido
Masculino
Mali
Adulto Jovem
[Pt] Tipo de publicação:JOURNAL ARTICLE; RESEARCH SUPPORT, N.I.H., EXTRAMURAL; RESEARCH SUPPORT, NON-U.S. GOV'T; RESEARCH SUPPORT, U.S. GOV'T, NON-P.H.S.
[Nm] Nome de substância:
0 (Antibodies, Bacterial); 0 (Immunoglobulin G); 0 (MenAfriVac); 0 (Meningococcal Vaccines); 0 (Tetanus Antitoxin); 0 (Tetanus Toxoid)
[Em] Mês de entrada:1608
[Cu] Atualização por classe:170922
[Lr] Data última revisão:
170922
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:151111
[St] Status:MEDLINE
[do] DOI:10.1093/cid/civ513



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