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1دورية أكاديمية
المؤلفون: Martinez-Gutierrez, Marlen, Arcila-Quiceno, Victor, Trejos-Suarez, Juanita, Ruiz-Saenz, Julian
المصدر: Revista do Instituto de Medicina Tropical de São Paulo; Vol. 61 (2019); e34 ; Revista do Instituto de Medicina Tropical de São Paulo; v. 61 (2019); e34 ; 1678-9946 ; 0036-4665
مصطلحات موضوعية: Acute diarrhoea, Colombia, Molecular characterization, Post-vaccination, Rotavirus
وصف الملف: application/pdf; application/xml
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2دورية أكاديمية
المؤلفون: Martínez Gutiérrez, Marlen, Arcila Quiceno, Victor, Trejos Suárez, Juanita, Ruiz Saenz, Julian
المساهمون: CLINIUDES
مصطلحات موضوعية: Acute diarrhoea, Colombia, Molecular characterization, Post-vaccination, Rotavirus
وصف الملف: 1 p; application/pdf
العلاقة: 10; 34, julio 2019.; 61; Martinez-Gutierrez M, Arcila-Quiceno V, Trejos-Suarez J, Ruiz-Saenz J. Prevalence and molecular typing of rotavirus in children with acute diarrhoea in Northeastern Colombia. Rev Inst Med Trop Sao Paulo. 2019 Jul 1;61:e34. doi:10.1590/S1678-9946201961034. PMID: 31269110; PMCID: PMC6609135.; Rev Inst Med Trop Sao Paulo . 2019 Jul 1;61:e34. doi:10.1590/S1678-9946201961034.; Revista do Instituto de Medicina Tropical de Sao Paulo; https://repositorio.udes.edu.co/handle/001/5659Test
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3دورية أكاديمية
المؤلفون: Ruiz Saenz, Julian, Martinez Gutierrez, Marlen, Arcila Quiceno, Victor, Trejos Suarez, Juanita
المصدر: 1. Nguyen TV, Le Van P, Le Huy C, Weintraub A. Diarrhea caused by rotavirus in children less than 5 years of age in Hanoi, Vietnam. J Clin Microbiol. 2004;42:5745-50. ; 2. Mokomane M, Kasvosve I, Melo E, Pernica JM, Goldfarb DM. The global problem of childhood diarrhoeal diseases: emerging strategies in prevention and management. Ther Adv Infect Dis. 2018;5:29-43. ; 3. GBD Diarrhoeal Diseases Collaborators. Estimates of global, regional, and national morbidity, mortality, and aetiologies of diarrhoeal diseases: a systematic analysis for the Global Burden of Disease Study 2015. Lancet Infect Dis. 2017;17:909-48. ; 4. Crawford SE, Ramani ....
مصطلحات موضوعية: Acute diarrhoea, Colombia, Molecular characterization, Post-vaccination, Rotavirus
وصف الملف: application/pdf
العلاقة: Rev Inst Med Trop Sao Paulo; https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/31269110Test/; http://hdl.handle.net/20.500.12494/15181Test; Martinez-Gutierrez M, Arcila-Quiceno V, Trejos-Suarez J, Ruiz-Saenz J. (2019) Prevalence and molecular typing of rotavirus in children with acute diarrhoea in Northeastern Colombia. Rev Inst Med Trop Sao Paulo. 2019 Jul 1;61:e34. doi:10.1590/S1678-9946201961034.
الإتاحة: https://doi.org/20.500.12494/15181Test
https://doi.org/10.1590/S1678-9946201961034Test
https://hdl.handle.net/20.500.12494/15181Test -
4دورية أكاديمية
مصطلحات موضوعية: ACUTE DIARRHEA, ACUTE DISEASE, ACUTE GASTROENTERITIS, AGE DISTRIBUTION, ARTICLE, CLASSIFICATION, COLOMBIA, COMPLEMENTARY DNA, CROSS-SECTIONAL STUDIES, CROSS-SECTIONAL STUDY, CHILD, PRESCHOOL, DEHYDRATION, DIARRHEA, DNA SYNTHESIS, ENZYME LINKED IMMUNOSORBENT ASSAY, ENZYME-LINKED IMMUNOSORBENT ASSAY, FECES, FECES ANALYSIS, FEMALE, GENETICS, GENOTYPE, GENOTYPING TECHNIQUE, HOSPITALIZATION, HUMAN, HUMANS, IMMUNOAFFINITY CHROMATOGRAPHY, IMMUNOLOGICAL PROCEDURES, INFANT, NEWBORN
وصف الملف: e34
العلاقة: REV INST MED TROP SP; https://doi.org/10.1590/S1678-9946201961034Test; https://www.scopus.com/inward/record.uri?eid=2-s2.0-85069267283&doi=10.1590%2fs1678-9946201961034&partnerID=40&md5=a563f1492b962917eec683e3cbc5324fTest; https://hdl.handle.net/20.500.12494/50900Test; Martinez Gutierrez Marlen,Arcila Quiceno Victor,Trejos-Suarez J,Ruiz Saenz Julian.Prevalence and molecular typing of rotavirus in children with acute diarrhoea in Northeastern Colombia.REV INST MED TROP SP. 2019. 61.: e34
الإتاحة: https://doi.org/20.500.12494/50900Test
https://doi.org/10.1590/S1678-9946201961034Test
https://hdl.handle.net/20.500.12494/50900Test -
5دورية أكاديمية
المؤلفون: Ruiz Saenz, Julian, Martínez Gutiérrez, Marlén, Arcila Quiceno, Victor, Trejos Suarez, Juanita
مصطلحات موضوعية: Acute diarrhoea, Colombia, Molecular characterization, Post-vaccination, Rotavirus
وصف الملف: application/pdf
العلاقة: https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/31269110Test/; Rev Inst Med Trop Sao Paulo; 1. Nguyen TV, Le Van P, Le Huy C, Weintraub A. Diarrhea caused by rotavirus in children less than 5 years of age in Hanoi, Vietnam. J Clin Microbiol. 2004;42:5745-50.; 2. Mokomane M, Kasvosve I, Melo E, Pernica JM, Goldfarb DM. The global problem of childhood diarrhoeal diseases: emerging strategies in prevention and management. Ther Adv Infect Dis. 2018;5:29-43.; 3. GBD Diarrhoeal Diseases Collaborators. Estimates of global, regional, and national morbidity, mortality, and aetiologies of diarrhoeal diseases: a systematic analysis for the Global Burden of Disease Study 2015. Lancet Infect Dis. 2017;17:909-48.; 4. Crawford SE, Ramani S, Tate JE, Parashar UD, Svensson L, Hagbom M, et al. Rotavirus infection. Nat Rev Dis Primers. 2017;3:17083.; 5. Parashar UD, Gibson CJ, Bresse J, Glass RI. Rotavirus and severe childhood diarrhea. Emerg Infect Dis. 2006;12:304-6.; 6. World Health Organization. Meeting of the immunization Strategic Advisory Group of Experts, April 2009: conclusions and recommendations. Wkly Epidemiol Rec. 2009;84:220-36.; 7. Tate JE, Burton AH, Boschi-Pinto C, Parashar UD, World Health Organization-Coordinated Global Rotavirus Surveillance Network. Global, regional, and national estimates of rotavirus mortality in children; 8. Troeger C, Khalil IA, Rao PC, Cao S, Blacker BF, Ahmed T, et al. Rotavirus vaccination and the global burden of rotavirus diarrhea among children younger than 5 years. JAMA Pediatr. 2018;172:958-65.; 9. Bucardo F, Nordgren J. Impact of vaccination on the molecular epidemiology and evolution of group A rotaviruses in Latin America and factors affecting vaccine efficacy. Infect Genet Evol. 2015;34:106-13.; 11. Cáceres DC, Peláez D, Sierra N, Estrada E, Sánchez L. La carga de la enfermedad por rotavirus en niños menores de cinco años, Colombia, 2004. Rev Panam Salud Publica. 2006;20:9-21.; 12. Uribe Yepes MA, Rodríguez Villamizar LA, Gómez González YA, Olaya Gamboa LE, Rodríguez Santamaría SM. Aislamientos de patógenos comunes asociados con enfermedad diarreica aguda en menores de cinco años, Bucaramanga, Colombia. MedUNAB. 2009;12:72-9.; 13. World Health Organization. Manual of rotavirus detection and characterization methods. Geneva: WHO; 2009.; 14. Gouvea V, Glass RI, Woods P, Taniguchi K, Clark HF, Forrester B, et al. Polymerase chain reaction amplification and typing of rotavirus nucleic acid from stool specimens. J Clin Microbiol. 1990;28:276-82.; https://hdl.handle.net/20.500.12494/15181Test; Martinez-Gutierrez M, Arcila-Quiceno V, Trejos-Suarez J, Ruiz-Saenz J. (2019) Prevalence and molecular typing of rotavirus in children with acute diarrhoea in Northeastern Colombia. Rev Inst Med Trop Sao Paulo. 2019 Jul 1;61:e34. doi:10.1590/S1678-9946201961034.
الإتاحة: https://doi.org/20.500.12494/15181Test
https://doi.org/10.1590/S1678-9946201961034Test
https://hdl.handle.net/20.500.12494/15181Test -
6دورية أكاديمية
المؤلفون: Martínez Gutiérrez, Marlén, Ruiz Saenz, Julian
مصطلحات موضوعية: Immune response, Vaccination, Colombia, Santander, Sheltered animals, Cats, Dogs, Rabies virus
جغرافية الموضوع: 38(11)
وصف الملف: application/pdf
العلاقة: http://www.scielo.br/scielo.php?script=sci_abstract&pid=S0100-736X2018001102109&lng=en&nrm=isoTest; Pesquisa Veterinária Brasileira; https://hdl.handle.net/20.500.12494/15091Test; Trujillo-Rojas LM, Martínez-Gutiérrez M, Ruiz-Saenz J. Low level of the immune response against rabies virus in dogs and cats - a cross-sectional study in sheltered animals, Santander, Colombia. Pesq. Vet. Bras. 2018. 38(11): 2109-2116.
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7دورية أكاديمية
مصطلحات موضوعية: CATS, COLOMBIA, DOGS, IMMUNE RESPONSE, RABIES VIRUS, SANTANDER, SHELTERED ANIMALS, VACCINATION
وصف الملف: 2109-2116
العلاقة: PESQUISA VET BRASIL; https://doi.org/10.1590/1678-5150-PVB-5997Test; https://www.scopus.com/inward/record.uri?eid=2-s2.0-85058189922&doi=10.1590%2f1678-5150-PVB-5997&partnerID=40&md5=ae6157c810fc834139b3adf6089ece47Test; https://hdl.handle.net/20.500.12494/50454Test; Trujillo-Rojas L.M.,Martinez Gutierrez Marlen,Ruiz Saenz Julian.Low level of the immune response against rabies virus in dogs and cats, a cross-sectional study in sheltered animals, Santander, Colombia.PESQUISA VET BRASIL. 2018. 38. (11):p. 2109-2116
الإتاحة: https://doi.org/20.500.12494/50454Test
https://doi.org/10.1590/1678-5150-PVB-5997Test
https://hdl.handle.net/20.500.12494/50454Test -
8دورية أكاديمية
المؤلفون: Martínez Gutierrez, Marlen, Quintero-Gil, Diana, Uribe-Yepes, Alexander, Ospina, Martha, Diaz, Francisco Javier
المصدر: N.E.A. Murray, M.B. Quam, A. Wilder-Smith Epidemiology of dengue: past, present and future prospects Clin Epidemiol, 5 (2013), pp. 299-309 ; S. Bhatt, P.W. Gething, O.J. Brady, J.P. Messina, A.W. Farlow, C.L. Moyes, et al. The global distribution and burden of dengue Nature, 496 (2013), pp. 504-507 ; H.A. Rothan, H. Bahrani, Z. Mohamed, N. Abd Rahman, R. Yusof Fusion of protegrin-1 and plectasin to MAP30 shows significant inhibition activity against Dengue virus replication PLoS One, 9 (2014), p. e94561 ; M.Q. Benedict, R.S. Levine, W.A. Hawley, L.P. Lounibos Spread of the tiger: global risk of invasion by the ....
مصطلحات موضوعية: Aedes aegypti, C6/36 cells, Colombia, Dengue, Vector competence, Viral replication
جغرافية الموضوع: 22(4)
وصف الملف: 257-272; application/pdf
العلاقة: Braz J Infect Dis; https://www.sciencedirect.com/science/article/pii/S1413867018300540?via%3DihubTest; http://hdl.handle.net/20.500.12494/15303Test; Quintero-Gil D. C., Uribe-Yepes A., Ospina M., Díaz FJ y Martinez-Gutierrez M. (2018). Differences in the replicative capacities of clinical isolates of dengue virus in C6/36 cells and in urban populations of Aedes aegypti from Colombia, South America. Braz J Infect Dis. 2018 Jul - Aug;22(4):257-272. Recuperado de
الإتاحة: https://doi.org/20.500.12494/15303Test
https://doi.org/10.1016/j.bjid.2018.07.010Test
https://hdl.handle.net/20.500.12494/15303Test -
9دورية أكاديمية
المؤلفون: Martínez Gutiérrez, Marlen, Ruiz Sáenz, Julian
مصطلحات موضوعية: Immune response, Vaccination, Colombia, Santander, Sheltered animals, Cats, Dogs, Rabies virus
جغرافية الموضوع: 38(11)
وصف الملف: application/pdf
العلاقة: Pesquisa Veterinária Brasileira; http://www.scielo.br/scielo.php?script=sci_abstract&pid=S0100-736X2018001102109&lng=en&nrm=isoTest; http://hdl.handle.net/20.500.12494/15091Test; Trujillo-Rojas LM, Martínez-Gutiérrez M, Ruiz-Saenz J. Low level of the immune response against rabies virus in dogs and cats - a cross-sectional study in sheltered animals, Santander, Colombia. Pesq. Vet. Bras. 2018. 38(11): 2109-2116.
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10دورية أكاديمية
المؤلفون: Martínez Gutiérrez, Marlén, Quintero-Gil, Diana, Uribe-Yepes, Alexander, Ospina, Martha, Diaz, Francisco Javier
مصطلحات موضوعية: Aedes aegypti, C6/36 cells, Colombia, Dengue, Vector competence, Viral replication
جغرافية الموضوع: 22(4)
وصف الملف: 257-272; application/pdf
العلاقة: https://www.sciencedirect.com/science/article/pii/S1413867018300540?via%3DihubTest; Braz J Infect Dis; N.E.A. Murray, M.B. Quam, A. Wilder-Smith Epidemiology of dengue: past, present and future prospects Clin Epidemiol, 5 (2013), pp. 299-309; S. Bhatt, P.W. Gething, O.J. Brady, J.P. Messina, A.W. Farlow, C.L. Moyes, et al. The global distribution and burden of dengue Nature, 496 (2013), pp. 504-507; H.A. Rothan, H. Bahrani, Z. Mohamed, N. Abd Rahman, R. Yusof Fusion of protegrin-1 and plectasin to MAP30 shows significant inhibition activity against Dengue virus replication PLoS One, 9 (2014), p. e94561; M.Q. Benedict, R.S. Levine, W.A. Hawley, L.P. Lounibos Spread of the tiger: global risk of invasion by the mosquito Aedes albopictus Vector Borne Zoo Dis (Larchmont, NY), 7 (2007), pp. 76-85; E. Holmes, S. Twiddy The origin, emergence and evolutionary genetics of dengue virus Infect Genet Evol, 3 (2003), pp. 19-28; R. Bartenschlager, S. Miller Molecular aspects of Dengue virus replication Future Microbiol, 3 (2008), pp. 155-165; J.A. Usme-Ciro, J.A. Mendez, K.D. Laiton, A. Páez The relevance of dengue virus genotypes surveillance at country level before vaccine approval Hum Vac Immunotherapeut, 10 (2014), pp. 2674-2678; L.A. Villar, D.P. Rojas, S. Besada-Lombana, E. Sarti Epidemiological Trends of Dengue Disease in Colombia (2000-2011): A Systematic Review PLoS Negl Trop Dis, 9 (2015), pp. 1-16; H. Rodríguez, F. de la Hoz Dengue and dengue and vector behaviour in Cáqueza, Colombia Rev Sal Púb (Bogotá, Colombia), 7 (2004), pp. 1-15; J. Nicholson, S.A. Ritchie, A.F. Van Den Hurk Aedes albopictus (Diptera: Culicidae) as a potential vector of endemic and exotic arboviruses in Australia J Med Entomol, 51 (2014), pp. 661-669; J. Jaimes-Dueñez, S. Arboleda, O. Triana-Chávez, A. Gómez-Palacio Spatio-temporal distribution of Aedes aegypti (Diptera: Culicidae) mitochondrial lineages in cities with distinct dengue incidence rates suggests complex population dynamics of the dengue vector in Colombia PLoS Negl Trop Dis, 9 (2015), pp. 1-21; L.D. Kramer, G.D. Ebel Dynamics of flavivirus infection in mosquitoes Adv Virus Res, 60 (2003), pp. 187-232; C.C. Liu, S.C. Wu Mosquito and mammalian cells grown on microcarriers for four‐serotype dengue virus production: variations in virus titer, plaque morphology, and replication rate Biotechnol Bioeng, 85 (2004), pp. 482-488; M.L. Muñoz, A. Cisneros, J. Cruz, P. Das, R. Tovar, A. Ortega Putative dengue virus receptors from mosquito cells FEMS Microbiol Lett, 168 (1998), pp. 251-258; J. Salas-Benito, J. Reyes-Del Valle, M. Salas-Benito, I. Ceballos-Olvera, C. Mosso, R.M. del Angel Evidence that the 45-kD glycoprotein, part of a putative dengue virus receptor complex in the mosquito cell line C6/36, is a Heat-Shock-related protein Am J Trop Med Hyg, 77 (2007), pp. 283-290; P. Sakoonwatanyoo, V. Boonsanay, D.R. Smith Growth and production of the dengue virus in C6/36 cells and identification of a laminin-binding protein as a candidate serotype 3 and 4 receptor protein Intervirology, 49 (2006), pp. 161-172; G. Kuno Early history of laboratory breeding of Aedes aegypti (Diptera: Culicidae) focusing on the origins and use of selected strains J Med Entomol, 47 (2014), pp. 957-971; J.L. Hardy, E.J. Houk, L.D. Kramer, W.C. Reeves Intrinsic factors affecting vector competence of mosquitoes for arboviruses Ann Rev Entomol, 28 (1983), pp. 229-262; J.R. Anderson, R. Rico-Hesse Aedes aegypti vectorial capacity is determined by the infecting genotype of dengue virus Am J Trop Med Hyg, 75 (2006), pp. 886-892; D.J. Gubler, S. Nalim, R. Tan, H. Saipan, J. Sulianti Saroso Variation in susceptibility to oral infection with dengue viruses among geographic strains of Aedes aegypti Am J Trop Med Hyg, 28 (1979), pp. 1045-1052; C. Gomez-Machorro, K.E. Bennett, M. del Lourdes Munoz, W.C. Black 4th Quantitative trait loci affecting dengue midgut infection barriers in an advanced intercross line of Aedes aegypti Insect Mol Biol, 13 (2004), pp. 637-648; L.B. Dickson, I. Sanchez-Vargas, M. Sylla, K. Fleming, W.C. Black 4th Vector competence in West African Aedes aegypti Is Flavivirus species and genotype dependent PLoS Negl Trop Dis, 8 (2014), p. e3153; J.M. Cadavid, G. Rúa, O. Campo, G. Bedoya, W. Rojas Microgeographic and temporal genetic changes of Aedes aegypti from Medellín, Colombia Biomédica, 35 (2014), pp. 53-61; M.C. Ospina, F.J. Diaz, J.E. Osorio Prolonged co-circulation of two distinct Dengue virus Type 3 lineages in the hyperendemic area of Medellin, Colombia Am J Trop Med Hyg, 83 (2010), pp. 72-78; O.P. Forattini Culicidologia Médica: Identificação, Biologia, Epidemiologia, vol. 2 (1996), p. 549; L.J. Chien, T.L. Liao, P.Y. Shu, J.H. Huang, D.J. Gubler, G.J. Chang Development of real-time reverse transcriptase PCR assays to detect and serotype dengue viruses J Clin Microbiol, 44 (2006), pp. 1295-1304; S. Kumar, G. Stecher, K. Tamura MEGA7: molecular evolutionary genetics analysis version 7.0 for bigger datasets Mol Biol Evol (2016) msw054; L. Gutiérrez-Ruiz, D.C. Quintero-Gil, M. Martínez-Gutiérrez Actualización en diagnóstico del dengue: evolución de las técnicas y su aplicación real en la clínica Medicina y laboratorio, 18 (2012), pp. 411-441; M. Hussain, S. Asgari MicroRNA-like viral small RNA from Dengue virus 2 autoregulates its replication in mosquito cells Proc Natl Acad Sci U S A, 111 (2014), pp. 2746-2751; M.I. Salazar, J.H. Richardson, I. Sánchez-Vargas, K.E. Olson, B.J. Beaty Dengue virus type 2: replication and tropisms in orally infected Aedes aegypti mosquitoes BMC Microbiol, 7 (2007), p. 9; I. Sánchez-Vargas, J.C. Scott, B.K. Poole-Smith, A.W. Franz, V. Barbosa-Solomieu, J. Wilusz, et al. Dengue virus type 2 infections of Aedes aegypti are modulated by the mosquito’s RNA interference pathway PLoS Pathog, 5 (2009), p. e1000299; X.X. Guo, X.J. Zhu, C.X. Li, Y.D. Dong, Y.M. Zhang, D. Xing, et al. Vector competence of Aedes albopictus and Aedes aegypti (Diptera: Culicidae) for DEN2-43 and New Guinea C virus strains of dengue 2 virus Acta Trop, 128 (2013), pp. 566-570; J. Junjhon, J.G. Pennington, T.J. Edwards, R. Perera, J. Lanman, R.J. Kuhn Ultrastructural characterization and three-dimensional architecture of replication sites in dengue virus-infected mosquito cells J Virol, 88 (2014), pp. 4687-4697; https://hdl.handle.net/20.500.12494/15303Test; Quintero-Gil D. C., Uribe-Yepes A., Ospina M., Díaz FJ y Martinez-Gutierrez M. (2018). Differences in the replicative capacities of clinical isolates of dengue virus in C6/36 cells and in urban populations of Aedes aegypti from Colombia, South America. Braz J Infect Dis. 2018 Jul - Aug;22(4):257-272. Recuperado de
الإتاحة: https://doi.org/20.500.12494/15303Test
https://doi.org/10.1016/j.bjid.2018.07.010Test
https://hdl.handle.net/20.500.12494/15303Test
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