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Relevant bibliographies by topics / Foot and mouth

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Academic literature on the topic 'Foot and mouth'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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Journal articles on the topic "Foot and mouth"

1

Bates, Jane. "Foot in mouth." Nursing Standard 21, no. 6 (October 18, 2006): 26. http://dx.doi.org/10.7748/ns.21.6.26.s33.

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Shaila, M. S. "Eradication of foot-and-mouth disease: a foot in mouth proposition." Journal of Biosciences 26, no. 2 (June 2001): 125–26. http://dx.doi.org/10.1007/bf02703634.

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Davies, Gareth. "Foot and mouth disease." Research in Veterinary Science 73, no. 3 (December 2002): 195–99. http://dx.doi.org/10.1016/s0034-5288(02)00105-4.

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SHORT, PATRICIA. "FOOT-AND-MOUTH OUTBREAK." Chemical & Engineering News 85, no. 33 (August 13, 2007): 11. http://dx.doi.org/10.1021/cen-v085n033.p011.

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Kerr, Cathel. "Foot and mouth latest." Trends in Microbiology 9, no. 6 (June 2001): 257. http://dx.doi.org/10.1016/s0966-842x(01)02092-3.

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Woolhouse, Mark, and Alex Donaldson. "Managing foot-and-mouth." Nature 410, no. 6828 (March 2001): 515–16. http://dx.doi.org/10.1038/35069250.

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Lubroth, Juan. "Foot-and-mouth disease." Veterinary Clinics of North America: Food Animal Practice 18, no. 3 (November 2002): 475–99. http://dx.doi.org/10.1016/s0749-0720(02)00036-1.

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Elsayed Elmeligy, Elsayed Ebrahime. "Foot and Mouth Disease." SOJ Veterinary Sciences 3, no. 4 (August 4, 2017): 1–2. http://dx.doi.org/10.15226/2381-2907/3/4/00138.

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Grubman, Marvin J., and Barry Baxt. "Foot-and-Mouth Disease." Clinical Microbiology Reviews 17, no. 2 (April 2004): 465–93. http://dx.doi.org/10.1128/cmr.17.2.465-493.2004.

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SUMMARY Foot-and-mouth disease (FMD) is a highly contagious disease of cloven-hoofed animals. The disease was initially described in the 16th century and was the first animal pathogen identified as a virus. Recent FMD outbreaks in developed countries and their significant economic impact have increased the concern of governments worldwide. This review describes the reemergence of FMD in developed countries that had been disease free for many years and the effect that this has had on disease control strategies. The etiologic agent, FMD virus (FMDV), a member of the Picornaviridae family, is examined in detail at the genetic, structural, and biochemical levels and in terms of its antigenic diversity. The virus replication cycle, including virus-receptor interactions as well as unique aspects of virus translation and shutoff of host macromolecular synthesis, is discussed. This information has been the basis for the development of improved protocols to rapidly identify disease outbreaks, to differentiate vaccinated from infected animals, and to begin to identify and test novel vaccine candidates. Furthermore, this knowledge, coupled with the ability to manipulate FMDV genomes at the molecular level, has provided the framework for examination of disease pathogenesis and the development of a more complete understanding of the virus and host factors involved.

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Bell, Elaine. "Foot-and-mouth vaccine." Nature Reviews Immunology 2, no. 8 (August 2002): 540. http://dx.doi.org/10.1038/nri879.

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Dissertations / Theses on the topic "Foot and mouth"

1

Foster-Cuevas, Mildred. "Immunodeterminants of foot-and-mouth disease virus." Thesis, University of Hertfordshire, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.338562.

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Puig, Arturo. "Lipopeptide vaccines against foot and mouth disease." Thesis, University College London (University of London), 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.428103.

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Nayak, Arabinda. "Foot and mouth disease virus RNA replication." Thesis, University of Surrey, 2005. http://epubs.surrey.ac.uk/842873/.

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Infection of susceptible cells with foot and mouth disease virus (FMDV) results in multiplication of the RNA genome and assembly of mature virions. The entire process of genome replication is completed in a few hours and encompasses many intracellular events. Like other picornaviruses, FMDV uses a peptide primed RNA replication mechanism. The factors that are required to uridylylate each of the three FMDV VPg peptides and the role of the FMDV cis-acting replication element (cre) or 3B Uridylylation Site (bus) in VPg uridylylation have been determined. The native N-terminus of the FMDV 3Dpol enzyme is a pre-requisite for VPg uridylylation in vitro and the effects of mutations in the RNA template are consistent with a slide-back mechanism. The role of the poly(A) tail in uridylylating VPg was insignificant using full-length FMDV RNA transcripts suggesting the possibility of an alternative mechanism of VPg incorporation into negative strand RNA. The optimal RNA sequences required for VPg uridylylation were found to be within the 5' non-coding region (NCR). Furthermore, the results also showed evidence for RNA-RNA interactions between distinct structures from within the 5' NCR that influence VPg uridylylation. The polymerase precursor 3CDpro is also a prerequisite for uridylylation of each of the FMDV VPg peptides. However BCpro alone can substitute for 3 CD, but is much less efficient. It also appeared that the overall charge of the VPg peptides determines their recognition by the FMDV 3Dpol. The RNA binding activity of the 3C was found to be required for its stimulatory effects on VPg uridylylation. Unlike the poliovirus cloverleaf, the FMDV S-fragment (at the 5' end of the genome) does not interact with the FMDV 3CD precursor protein; however it binds specifically to a cellular factor p48. The crude replication complexes (CRCs) isolated from FMDV-infected cells were found to synthesize viral RNA very efficiently and an in vitro RNA replication system developed using these CRCs can be used to study the complete RNA replication events of FMDV.

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Cottam, Eleanor Myfanwy. "Micro-evolution of foot-and-mouth disease virus." Thesis, Connect to e-thesis. Move to record for print version, 2008. http://theses.gla.ac.uk/92/.

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Thesis (Ph.D.) - University of Glasgow, 2008.
Ph.D. thesis submitted to the Division of Biochemistry and Molecular Biology, Institute of Biomedical and Life Sciences, University of Glasgow, 2008. Includes bibliographical references. Print version also available.

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Lea, Susan Mary. "Structural studies on foot-and-mouth disease virus." Thesis, University of Oxford, 1993. http://ora.ox.ac.uk/objects/uuid:438dc0ae-b899-40fd-84dc-03d3fc1a537f.

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Foot-and-mouth disease viruses (FMDVs) constitute the aphthovirus genus of the Picornaviridae. The structures of Oi subtype viruses OiK and G67 have been solved and comparisons reveal the structural basis of monoclonal antibody escape mutations in G67. Escape mutations are seen to occur at surface-exposed residues and to provoke structural changes limited to the altered side chains. Comparisons of the structures of O₁ and O₁BFS (Acharya et al., Nature 337, 709-716 (1989)) suggest that changes occurring 'in-the-field' in response to polyclonal antibody pressure may be subtly different from mutations produced by monoclonal antibody pressure in vitro. Field mutations are seen to alter less exposed residues and to have more far-reaching structural effects than the in vitro, monoclonal provoked mutations. Crystals of G67 are seen to be 'intimately twinned', the data possessing extra symmetry due to a mis-packing of the crystals. A protocol, based on current real-space averaging procedures with a novel constraint imposed, has been used successfully to deconvolute these data. This method might be more generally applied to deconvolute the wavelength overlaps that occur when using the Laue method. The structures of C-S8cl and mutant SD6-6 have been solved at a resolution of 3.5Å. These structures enable comparisons between members of different FMDV serotypes to be made for the first time, namely: serotype 0 (O₁BFS) and serotype C (C-S8cl). Flexibility of the Arg-Gly-Asp containing G-H loop of VP1 is seen to be amongst the most conserved structural features. This loop is implicated in receptor binding and possible roles for the observed flexibility are discussed. The CS8cl structure also reveals more detail in previously disordered regions of the capsid, namely: the N-terminal residues of VP2 and potential myristate density under the 5-fold axis of the virion. Analysis of structures from the Protein Data Bank reveals different patterns of amino acid use in proteins involved in the two halves of the immune recognition event i.e. immunoglobulins and viruses. These patterns seem to be based not only on the characteristics of the most used amino acids but also on characteristics of the nucleotide codons used to code for them.

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Edacheril, Mathew. "Assessment of herd immunity to foot-and-mouth disease." Thesis, University of Reading, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.314315.

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Howes, Emma Louise. "Investigating the foot-and-mouth disease virus 3A protein." Thesis, University of St Andrews, 2018. http://hdl.handle.net/10023/15521.

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Foot-and-Mouth Disease Virus (FMDV) is a globally important pathogen responsible for causing Foot-and-Mouth Disease (FMD) in wildlife and domestic livestock species and has significant economic impacts. FMD is difficult to control due to its highly infectious nature, wide diversity of host species and the existence of multiple serotypes; therefore, understanding the processes of FMDV infection and viral RNA replication are key to the development of improved diagnostics and vaccines. This thesis investigates the potential roles of the FMDV 3A non-structural protein using a combination of sub-genomic replicons, recombinant viruses and proteomics techniques. The picornavirus 3A protein has previously been linked with roles in replication complex formation, virulence and determining viral host range. This thesis presents findings showing that a naturally occurring deletion in 3A had differing effects on replication in cells lines derived from different natural hosts thereby supporting the conclusion that 3A has an important role in viral host range. Proteomic (immunoprecipitation and mass spectroscopy) investigations were carried out to identify potential cellular interaction partners of FMDV 3A, and the impact on infection and replication of reducing expression of two selected cellular proteins Rab7L1 and TBC1D20 was investigated. The 3A protein of FMDV was shown to include a conserved FFAT motif (which bind the ER resident protein VAP) in its N terminal domain. A role for this motif was also investigated with the results suggesting that the 3A FFAT motif is important for efficient viral replication. Finally, the potential role of 3A to act as the donor of 3B during replication was investigated. Key findings from experiments using FMDV replicons and recombinant viruses showed that full-length P3 and the processing intermediate 3ABBB are not required for viral RNA replication suggesting that the preferred donor of 3B for uridylation is likely a 3BC containing precursor protein.

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Mahdi, Ali Jafar. "Foot and mouth disease in Iraq: strategy and control." Kansas State University, 2010. http://hdl.handle.net/2097/4620.

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Master of Science
Department of Diagnostic Medicine/Pathobiology
Gary A. Anderson
Foot-and-mouth disease (FMD) is a highly infectious viral disease of cattle, pigs, sheep, goats, buffalo, and artiodactyl wildlife species. Foot-and-mouth disease virus is endemic and periodic devastating epidemics have occurred and caused heavy economic losses in Iraq for a long time. The first official cases of FMD were recorded in 1937, while the first record of a specific FMD serotype in Iraq was serotype A in 1952. Other serotypes have been reported since then; serotypes O, SAT-1 and Asia1 were recorded in 1957, 1962, and 1975, respectively. Veterinary Services in Iraq has been severely weakened over the past two decades, and its infrastructure has been devastated as a consequence of previous political conflicts, wars and international sanctions. The breakdown of Veterinary Services led to the disruption of disease control strategies, collapse of disease surveillance and monitoring, and weakening of response systems. The destruction of the Al-Dora FMD laboratories for diagnosis and vaccine production by the United Nation in 1996, and the restrictions placed on the importation of vaccines have strongly affected the FMD control program. A severe epidemic of FMD occurred in Iraq in 1998, affecting 2.5 million ruminants and causing heavy losses in newly born animals. It is estimated to have killed about 550,000 animals. The outbreak was due to the serotype O1 Middle East strain which has affected large and small ruminants. In 2009, Iraq was severely affected by new serotype A (subtype A Iran 05). The major efforts of Veterinary Services in Iraq have been directed towards control of FMD by vaccination strategies. Two types of vaccine have been used, trivalent vaccine (O, A 22, and Asia 1) for cattle and buffalo and monovalent vaccine (O Manisa) for sheep and goats. Vaccination has been implemented once yearly on a voluntary basis. Sometimes other limited control measures have accompanied vaccination, which include quarantine, movement control, focused vaccination, disinfection, and public awareness programs. The FMD control program in Iraq has been confronted by many challenges: deficits in FMD surveillance and emergency preparedness, limited diagnostic capabilities, difficulties in restricting animal movement, and lack and irregular supply of appropriate vaccines.

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Sahle, Mesfin. "An epidemiological study on the genetic relationships of foot and mouth disease viruses in East Africa." Pretoria : [s.n.], 2010. http://upetd.up.ac.za/thesis/available/etd-08132008-095346/.

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O'Connor, Steven Patrick. "The production of foot-and-mouth disease virus-like particles in the plant Nicotiana benthamiana: a potential candidate vaccine for foot-and-mouth disease." Master's thesis, University of Cape Town, 2018. http://hdl.handle.net/11427/29378.

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Foot and mouth disease virus (FMDV) infects cloven-hoofed animals causing the highly contagious foot and mouth disease. It is spread by contact or through aerosol. The disease is often debilitating for infected animals and can be fatal. Severe measures are taken to contain outbreaks; quarantine and trade restrictions are imposed and herds with infected individuals are culled to prevent the spread of the disease. Consequently, outbreaks of the disease have drastic implications for agriculture and social economies which can be devastating for affected countries. There are seven serotypes of the virus; of which SAT1, SAT2, and SAT3 are endemic to Africa. South African buffalo populations such as those in the Kruger National Park, are natural carriers of FMDV (Thomson 1995). Careful monitoring and regular vaccination are necessary to detect and prevent outbreaks and the spread of the disease to livestock of neighbouring areas and farms. The vaccines currently used are inactivated FMDV virions. These are produced in cell culture, an expensive process that requires high levels of biosafety. Furthermore, inactivated virions present non-structural proteins (NSPs) and thus cannot be distinguished from the infectious virus by imported ELISA kits that utilise the NSPs as coating antigens and conventionally produced detecting antibodies. We aimed to use recombinant constructs encoding the FMDV capsid and protease genes, cloned into the different vectors; pRIC, pEAQ and pTRAc, for transient expression in Nicotiana benthamiana to generate virus-like particles as an alternative vaccine candidate. Using a plant based expression system presents numerous advantages over the traditional cell culture production of the vaccine currently used. After having synthesised the FMDV genes P12A and 3C, the fusion gene P1-2A-3C (required for the vaccine) was cloned into these different plant expression vectors available in our laboratory. With Agrobacteria mediated infiltration of N. benthamiana, we demonstrated expression of recombinant protein by western blotting; and Coomassie stain, for each of the different constructs. Analytical ultra-centrifugation through a sucrose gradient was used to purify protein extracts. Comparison against a dilution series of bovine serum albumin was used to quantify the yield for each respective vector construct by densitometry. Transmission Electron Microscopy (TEM) imaging was used to qualitatively determine virus-like particle (VLP) assembly. In conclusion, we demonstrate proof of concept for a viable alternative approach for the production of a candidate vaccine for FMDV.

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Books on the topic "Foot and mouth"

1

[Kirby, E. ]. Foot and mouth. [s.l.]: [Impact Press], 2000.

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International Office of Epizootics. Foot and Mouth Disease Commission Conference. Foot and mouth disease. Paris: Office Intrernational des Epizooties, 1987.

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Barclay, Christopher. Foot and mouth disease. London: House of Commons Library, 2001.

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van der Zijpp, A. J., M. J. E. Braker, C. H. A. M. Eilers, H. Kieft, T. A. Vogelzang, and S. J. Oosting. Foot and Mouth Disease. The Netherlands: Wageningen Academic Publishers, 2004. http://dx.doi.org/10.3920/978-90-8686-530-7.

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Barclay, Christopher. Farming after foot and mouth. london: House of CommonsLibrary, 2001.

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Trades Union Congress. Economic and Social Affairs Department. Foot and mouth and benefits. [London]: TUC ESAD, 2001.

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Mahy, Brian W. J., ed. Foot-and-Mouth Disease Virus. Berlin, Heidelberg: Springer Berlin Heidelberg, 2005. http://dx.doi.org/10.1007/b138628.

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Trades Union Congress. Economic and Social Affairs Department. Economic impact of foot and mouth. [London]: TUC ESAD, 2001.

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Fintan, Taite, ed. Foot in mouth: Famous Irish political gaffes. Dublin: Mentor Books, 2006.

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Saul, Bellow. Him with his foot in his mouth. London: Penguin, 2011.

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Book chapters on the topic "Foot and mouth"

1

Sebhatu, Tesfaalem Tekleghiorghis. "Foot-and-Mouth Disease." In Transboundary Animal Diseases in Sahelian Africa and Connected Regions, 207–31. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-25385-1_11.

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Grubman, Marvin J., Luis L. Rodriguez, and Teresa de los Santos. "Foot-and-Mouth Disease." In The Picornaviruses, 397–410. Washington, DC, USA: ASM Press, 2014. http://dx.doi.org/10.1128/9781555816698.ch25.

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Lu, Puxuan, and BoPing Zhou. "Hand-Foot-Mouth Disease." In Radiology of Infectious Diseases: Volume 1, 127–55. Dordrecht: Springer Netherlands, 2015. http://dx.doi.org/10.1007/978-94-017-9882-2_17.

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Ruiz, Vanesa, and Andrés Wigdorovitz. "Foot-and-mouth Disease." In Prospects of Plant-Based Vaccines in Veterinary Medicine, 311–43. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-90137-4_15.

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Gilbert, Patricia. "Hand, foot and mouth syndrome." In The A-Z Reference Book of Childhood Conditions, 87–88. Boston, MA: Springer US, 1995. http://dx.doi.org/10.1007/978-1-4899-7098-5_20.

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Reich, Danya, Corinna Eleni Psomadakis, and Bobby Buka. "Hand, Foot, and Mouth Disease." In Top 50 Dermatology Case Studies for Primary Care, 321–29. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-18627-6_48.

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van der Wal, Jacqueline E. "Hand-Foot-and-Mouth Disease." In Encyclopedia of Soil Science, 208–9. Dordrecht: Springer Netherlands, 2016. http://dx.doi.org/10.1007/978-3-319-28085-1_727.

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Metze, Dieter, Vanessa F. Cury, Ricardo S. Gomez, Luiz Marco, Dror Robinson, Eitan Melamed, Alexander K. C. Leung, et al. "Hand-Foot-and-Mouth Disease." In Encyclopedia of Molecular Mechanisms of Disease, 771. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-29676-8_3375.

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Jing, Yuan, Huang Wen-Xian, Zeng Hong-Wu, Li Jian-Ming, Ou Shan-Xing, Gou Ji-zhou, Yang Guang, Zheng Guang-Ping, Shan Wan-Shui, and Lou Ming-Wu. "Hand-Foot-and-Mouth Disease." In Diagnostic Imaging of Emerging Infectious Diseases, 153–68. Dordrecht: Springer Netherlands, 2016. http://dx.doi.org/10.1007/978-94-017-7363-8_7.

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van der Wal, Jacqueline E. "Hand-Foot-and-Mouth Disease." In Encyclopedia of Pathology, 1–2. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-28845-1_727-1.

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Conference papers on the topic "Foot and mouth"

1

J Oates, Briony. "Foot and Mouth Disease: Informing the Community?" In 2002 Informing Science + IT Education Conference. Informing Science Institute, 2002. http://dx.doi.org/10.28945/2550.

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The 2001 foot and mouth disease (FMD) outbreak in the UK had a significant impact on the economic and social wellbeing of rural communities. This paper examines the FMD pages of four local government websites in Northern England: Cumbria, Durham, Northumberland and North Yorkshire County Councils. Each county was badly affected by FMD. The contents of the FMD webpages are analysed and compared: which audiences were addressed, what information was provided or omitted, and how well the audiences’ needs were met. The study shows the breadth of audience types and information that could have been included, but no site covered all the necessary angles. Furthermore, the websites did little to address the psychological problems arising from FMD or to enhance participation and democracy in their local communities. By examining how the councils informed those affected, lessons can be learnt which are relevant to any future disruption to a community.

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Khammadov, N. I., A. I. Khamidullina, K. V. Usoltsev, and T. Kh Faizov. "GENETIC POLYMORPHISMS OF FOOT AND MOUTH DISEASE VIRUS." In Molecular Diagnostics and Biosafety. Federal Budget Institute of Science 'Central Research Institute for Epidemiology', 2020. http://dx.doi.org/10.36233/978-5-9900432-9-9-247.

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Aryan, Mohammad Farhad, Worarat Krathu, Chonlameth Arpnikanondt, and Boonrat Tassaneetrithep. "Image Recognition for Detecting Hand Foot and Mouth Disease." In IAIT2020: The 11th International Conference on Advances in Information Technology. New York, NY, USA: ACM, 2020. http://dx.doi.org/10.1145/3406601.3406640.

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Longinotti, G., G. Ybarra, P. Lloret, C. Moina, A. Ciochinni, D. R. Serantes, L. Malatto, M. Roberti, S. Tropea, and L. Fraigi. "Diagnosis of foot-and-mouth disease by electrochemical enzyme-linked immunoassay." In 2010 32nd Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC 2010). IEEE, 2010. http://dx.doi.org/10.1109/iembs.2010.5626230.

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Pongsumpun, Puntani, and Napasool Wongvanich. "Age Structural Model of the Hand Foot Mouth Disease in Thailand." In 2018 2nd European Conference on Electrical Engineering and Computer Science (EECS). IEEE, 2018. http://dx.doi.org/10.1109/eecs.2018.00033.

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Abe, Maiku. "Risk-Sharing Model Of Foot-and-Mouth Disease Outbreak in Japan." In 2019 IEEE 8th Global Conference on Consumer Electronics (GCCE). IEEE, 2019. http://dx.doi.org/10.1109/gcce46687.2019.9015512.

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Wang, Jiaojiao, Jinglu Chen, Quannan Zu, Zhidong Cao, Saike He, and Daniel Dajun Zeng. "Healthcare-seeking behavior study on Beijing Hand-Foot-Mouth Disease Patients." In 2019 IEEE International Conference on Intelligence and Security Informatics (ISI). IEEE, 2019. http://dx.doi.org/10.1109/isi.2019.8823283.

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Исупова, М., and M. Isupova. "ROLE OF MOUTH PROCESSES IN THE DYNAMICS OF ACCUMULATIVE FORMS IN COASTAL ZONE OF BLACK SEA (WITHIN THE RUSSIAN SECTOR)." In Sea Coasts – Evolution ecology, economy. Academus Publishing, 2018. http://dx.doi.org/10.31519/conferencearticle_5b5ce3cbeb5b90.32745131.

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The processes in the river mouth areas play a special role in the formation and dynamics of coastal accumulative forms. The experience of Russian and foreign specialists on investigations of river mouths shows a modern intensification of sea impact on the river deltas in the world and enhance the abrasion of their delta coastlines. These processes show a trend of transformation of different mouths from the fluvial-dominated objects to the marine-dominated objects. A striking example of this process is the variability of the mouth fan, which has a complicated structure, and the mouth bars. In most cases, the structure of the mouth fan presents several successive layers. There are the following 1) abovewater and submarine sand layers; 2) layer of silty sediments of the sea slope of the mouth fan; 3) gently sloping layers of clay, component the foot of the mouth fan; 4) layer of shelf sand, not related to the formation of mouth fan. Each of these layers is characterized by a specific size and composition of sediments. Under intensification of abrasion of the mouth accumulative forms (accordance with the stage of this abrasion), the sediments significantly differed by composition, can be penetrate in the lithodynamic coastal system. A rather complex topography of the underwater slope rugged canyons is typical for the Russian coast of the Black Sea. Through these canyons, sediments, entering the river mouth area and playing an important role in the dynamics of coastal accumulative forms, can be delivered to the depths. These depths exclude of their return.

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Carvalho, Luiz Max F., Leonardo Bacelar Lima Santos, Paulo E. P. Burke, Marcos Quiles, and Waldemir de Castro Silveira. "A geographically-aware complex network approach for foot-and-mouth disease phylodynamics." In 6th International Conference on Nonlinear Science and Complexity. São José dos Campos, Brazil: INPE Instituto Nacional de Pesquisas Espaciais, 2016. http://dx.doi.org/10.20906/cps/nsc2016-0047.

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Matsushima, Masatomo, and Hironori Matsushima. "Infectious pattern of foot-and-mouth disease and the modified SIR model." In CENTRAL EUROPEAN SYMPOSIUM ON THERMOPHYSICS 2019 (CEST). AIP Publishing, 2019. http://dx.doi.org/10.1063/1.5114538.

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Reports on the topic "Foot and mouth"

1

Hullinger, P. New England Foot and Mouth Disease Tabletop Exercise. Office of Scientific and Technical Information (OSTI), September 2008. http://dx.doi.org/10.2172/945849.

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M., BLAKE. Reflections on the Foot-and-Mouth Disease Epidemic of 2001: an Irish Perspective. O.I.E (World Organisation for Animal Health), April 2021. http://dx.doi.org/10.20506/bull.2021.nf.3165.

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This year marks the 20-year anniversary of the foot-and-mouth disease (FMD) epidemic, which originated in the United Kingdom (UK) in February 2001, and subsequently spread to Ireland, the Netherlands and France.

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Kostova-Vassilevska, T. On The Use Of Models To Assess Foot-And-Mouth Disease Transmission And Control. Office of Scientific and Technical Information (OSTI), July 2004. http://dx.doi.org/10.2172/15014467.

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C., MIDDLEMISS. Reflections on the Foot-and-Mouth Disease Epidemic of 2001: a United Kingdom Perspective. O.I.E (World Organisation for Animal Health), April 2021. http://dx.doi.org/10.20506/bull.2021.nf.3166.

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Thanda Kyaw, Ai. Socio-Economic Impacts of Foot and Mouth Disease Among Cattle Farmers in Sagaing and Mandalay Areas, Myanmar. O.I.E (World Organisation for Animal Health), May 2014. http://dx.doi.org/10.20506/standz.2784.

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The World Organisation for Animal Health (OIE) Sub-Regional Representation for South East Asia (OIE SRR-SEA) implemented the Stop Transboundary Animal Diseases and Zoonoses (STANDZ) Programme funded by AusAID to strengthen the veterinary services and effectively manage the control and eradication of foot and mouth disease (FMD) in Cambodia, Lao PDR and Myanmar. The purpose of the study is to understand how FMD outbreaks impact smallholder farmers, both men and women, at the household and village level and how control and eradication of FMD would benefit them. Specific aims are to estimate the direct and indirect socio-economic costs associated with the outbreaks of FMD as well as of the measures taken by farmers to deal with such outbreaks and to identify issues that contributed to the socio-economic impacts of FMD outbreaks and opportunities to reduce them.

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McLeod, Ross. Costs of FMD in SE Asia and economic benefits of the Southeast Asia Foot and Mouth Disease Campaign. O.I.E (World Organisation for Animal Health), July 2013. http://dx.doi.org/10.20506/standz.2780.

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Qiu, Yu, Ronello Abila, Pranee Rodtian, Donald P. King, Nick J. Knowles, Thanh Long Ngo, Tri Vu Le, et al. Emergence of Exotic O/ME-SA/Ind-2001d Foot-and-Mouth Disease Viruses in South-East Asia in 2015. O.I.E (World Organisation for Animal Health), January 2015. http://dx.doi.org/10.20506/standz.2781.

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Frieson, Kate Grace. A Gender Assessment of SEACFMD 2020: A Roadmap to Prevent, Control and Eradicate foot and mouth disease (by 2020) in Southeast Asia and China. O.I.E (World Organisation for Animal Health), December 2013. http://dx.doi.org/10.20506/standz.2785.

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This gender assessment of SEACFMD 2020: A Roadmap to Prevent, Control and Eradicate foot and mouth disease (by 2020) in Southeast Asia and China, responds to the requirement of AusAID that all strategies affecting human health, food security and poverty alleviation incorporate a gender perspective as women are not often included in the technical and community based aspects of programs relating to animal health and disease control. Gender roles and responsibilities affect women’s and men’s ability and incentive to participate in FMD roadmap activities, and can potentially lead to different project impacts for men and women.

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Nampanya, Sonevilay, Syseng Khounsy, and Peter Windsor. Assessment of socio-economic impacts of Foot and Mouth Disease vaccination programmes in Northern and Central provinces Lao PDR (STANDZ Programme). O.I.E (World Organisation for Animal Health), January 2014. http://dx.doi.org/10.20506/standz.2777.

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Hindson, B., B. Baker, L. Bentley Tammero, R. Lenhoff, P. Naraghi-Arani, E. Vitalis, T. Slezak, et al. Diagnostic evaluation of a multiplexed RT-PCR microsphere array assay for the detection of foot-and-mouth and look-alike disease viruses. Office of Scientific and Technical Information (OSTI), September 2007. http://dx.doi.org/10.2172/922093.

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