Relevant bibliographies by topics / Encefalopatia spongiforme

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Academic literature on the topic 'Encefalopatia spongiforme'

Author: Grafiati
Published: 11 March 2023

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Journal articles on the topic "Encefalopatia spongiforme"

1

Branović Čakanić, Karmen, Sanja Šeparović, Žaklin Acinger Rogić, et al. "Praćenje transmisivnih spongiformnih encefalopatija u Republici Hrvatskoj." Veterinarska stanica 53, no. 6 (2022): 709–21. http://dx.doi.org/10.46419/vs.53.6.6.

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Transmisivne spongiformne encefalopatije su grupa rijetkih, progresivnih neurodegenerativnih bolesti od kojih obolijevaju ljudi i veći broj životinjskih vrsta, a prouzroči ih prion. Infekcija je dugi vremenski period asimptomatska, a bolest je progresivna i neminovno letalnog ishoda. U skupinu transmisivnih spongiformnih encefalopatija spadaju: klasična i atipična goveđa spongiformna encefalopatija, klasični i atipični grebež u ovaca i koza, spongiformna encefalopatija jelena, transmisivna encefalopatija američke vidrice, mačja spongiformna encefalopatija, Creutzfeldt- Jakobova bolest, varijan
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Brandel, J. P., and S. Haïk. "Malattie da prioni o encefalopatie spongiformi trasmissibili." EMC - Neurologia 16, no. 2 (2016): 1–21. http://dx.doi.org/10.1016/s1634-7072(16)77562-3.

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KONINKLIJKE ACADEMIE VOOR GENE... "Advies over het risico op boviene spongiforme encefalopathie (BSE) bij mensen door transfusie van bloed van geïnfecteerde personen." Tijdschrift voor Geneeskunde 56, no. 12 (2000): 901–3. http://dx.doi.org/10.2143/tvg.56.12.5000780.

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Pocchiari, M. "LE ENCEFALOPATIE SPONGIFORMI TRASMISSIBILI." Microbiologia Medica 20, no. 3 (2005). http://dx.doi.org/10.4081/mm.2005.3440.

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Mulinelli, F. "STRATEGIE PER IL CONTROLLO DELLE ENCEFALOPATIE SPONGIFORMI TRASMISSIBILI ANIMALI IN ITALIA." Microbiologia Medica 19, no. 2 (2004). http://dx.doi.org/10.4081/mm.2004.3750.

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Dissertations / Theses on the topic "Encefalopatia spongiforme"

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FASOLI, Elisa. "Trasmissione intraspecie di encefalopatia spongiforme bovina e di encefalopatia spongiforme amiloidotica bovina. Caratterizzazione molecolare e ultrastrutturale di un nuovo ceppo di prione nel bovino." Doctoral thesis, Università degli Studi di Verona, 2008. http://hdl.handle.net/11562/337633.

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Le Encefalopatie Spongiformi Trasmissibili (TSE) o Malattie da Prioni, costituiscono un gruppo di malattie neurodegenerative fatali, ad eziologia sporadica, genetica o infettiva che colpiscono l’uomo e diverse specie animali. Il meccanismo patogenetico responsabile delle TSE consiste nella conversione conformazionale della normale proteina prionica cellulare (PrPC), con una struttura prevalentemente ad α-elica, in una forma aberrante, ricca in β-sheet, parzialmente insolubile in detergenti non ionici e resistente alla digestione con proteasi, denominata PrPSc, che rappresenta il marcato
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Pirisinu, Laura <1980&gt. "Agenti di encefalopatie spongiformi trasmissibili e zoonosi: tipizzazione molecolare." Doctoral thesis, Alma Mater Studiorum - Università di Bologna, 2011. http://amsdottorato.unibo.it/4145/1/Pirisinu_Laura_tesi.pdf.

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Transmissible spongiform encephalopathies (TSE) are neurodegenerative diseases caused by the conversion of the host-encoded cellular protein (PrPC) to a disease-associated isoform (PrPSc). The agent responsible for prion diseases may exist as different strains with specific biological and biochemical properties. According to the protein-only hypothesis, prion strain diversity is enciphered in PrPSc conformation. Molecular strain typing methods are based on the electrophoretic mobility of protease resistant core of PrPSc, on the susceptibility to protease digestion, on the glycosylation profile
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Pirisinu, Laura <1980&gt. "Agenti di encefalopatie spongiformi trasmissibili e zoonosi: tipizzazione molecolare." Doctoral thesis, Alma Mater Studiorum - Università di Bologna, 2011. http://amsdottorato.unibo.it/4145/.

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Transmissible spongiform encephalopathies (TSE) are neurodegenerative diseases caused by the conversion of the host-encoded cellular protein (PrPC) to a disease-associated isoform (PrPSc). The agent responsible for prion diseases may exist as different strains with specific biological and biochemical properties. According to the protein-only hypothesis, prion strain diversity is enciphered in PrPSc conformation. Molecular strain typing methods are based on the electrophoretic mobility of protease resistant core of PrPSc, on the susceptibility to protease digestion, on the glycosylation profile
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4

Sartori, Elena. "Drosophila melanogaster come modello per lo studio delle encefalopatie spongiformi trasmissibili umane di tipo ereditario." Doctoral thesis, Università degli studi di Padova, 2009. http://hdl.handle.net/11577/3427344.

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Prion diseases, or trasmissible spongiform encephalopathies (TSEs), are a group of fatal neurodegenerative diseases that affect humans and other mammalians. All these pathologies have long incubation periods followed by a crhonic neurological disease with fatal outcomes and have similar pathology limited to the central nervous system. TSEs are characterized hystopathologically by spongiosis and neural loss. The infectious agent in prion diseases is believed to be represented by a single protein, named prion protein (PrPC). The “Protein Only Hypothesis” [1] suggests that TSE are caused by a di
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DI, BARI MICHELE ANGELO. "Studio delle basi genetiche e molecolari nella trasmissione interspecifica delle malattie da prioni." Doctoral thesis, Università degli Studi di Roma "Tor Vergata", 2009. http://hdl.handle.net/2108/1026.

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Le encefalopatie spongiformi trasmissibili (EST), o malattie da prioni, sono malattie neurodegenerative che colpiscono l'uomo e gli animali. Le più note tra le EST animali sono l’encefalopatia spongiforme bovina (BSE) e la scrapie della pecora e della capra; le forme umane le più note sono la malattia di Creutzfeldt-Jakob (MCJ) e la variante della MCJ (vMCJ), legata all'epidemia di BSE. Le EST sono caratterizzate da tempi di incubazione estremamente lunghi ed esito invariabilmente fatale. Da un punto di vista patologico le lesioni, confinate al sistema nervoso centrale (SNC), consistono in s
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Ramalho, Maria Luísa Galvão. "BSE em Portugal no período 2002/2009 : evolução epidemiológica e considerações futuras." Master's thesis, Universidade Técnica de Lisboa. Faculdade de Medicina Veterinária, 2011. http://hdl.handle.net/10400.5/3060.

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Dissertação de Mestrado em Segurança Alimentar<br>A primeira grande crise alimentar da história contemporânea, ocorreu quando em 1986 se provou a relação entre o consumo de produtos alimentares com origem em bovinos infectados com a Encefalopatia Espongiforme Bovina (EEB) e uma nova variante da Doença de Creutzfeld-Jakob, uma doença neurodegenerativa e fatal que afecta o Homem. Na sequência desta descoberta, a União Europeia (U.E) impõe uma série de medidas: Planos de Vigilância, Controlo e Erradicação da EEB; retirada de certos produtos da cadeia alimentar humana e animal (MRE); restriç
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Borges, Álvarez Marta. "Establiment de metodologia analítica per a la purificació, separació i caracterització de biomarcadors proteics de malalties neurodegeneratives." Doctoral thesis, Universitat de Barcelona, 2012. http://hdl.handle.net/10803/119540.

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En aquesta tesi doctoral, s’ha desenvolupat metodologia analítica per a la purificació, separació i caracterització de prió cel•lular (PrPC) i superòxid dismutasa (SOD-1), dues proteïnes relacionades amb les Encefalopaties Espongiformes Transmissibles (TSEs) i l’Esclerosi Lateral Amiotròfica (ALS), respectivament. Les TSEs es caracteritzen per l’acumulació de la forma patològica del PrPC (PrPSc) al cervell dels animals afectats, mentre que a l’ALS s’observa la formació d’agregats de SOD-1. Avui dia, encara es desconeixen els factors que inicien i regulen les interaccions que condueixen a la fo
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Milius, Jonas. "Galvijų spongiforminės encefalopatijos ir virusinių ligų paplitimo, diagnostikos ir prevencijos retrospektyvi analizė Lietuvoje." Doctoral thesis, Lithuanian Academic Libraries Network (LABT), 2006. http://vddb.library.lt/obj/LT-eLABa-0001:E.02~2006~D_20061229_122358-22773.

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Assessment of occurrence and diagnostic methods of viral diseases in cattle – viral diarrhoea (BVD), infectious bovine rhinotracheitis (IBR), rabies, enzootic bovine leukosis (EBL), and spongiform encephalopathy (BSE) – was carried out for the first time in Lithuania. It was established that viruses of rabies, infectious rhinotraheitis and viral diarrhoea are most widespread in the country. It was determined that occurrence of rabies in cattle is parallel with the infection of wildlife with rabies virus. Analysis of eradication programme of enzootic bovine leucosis was done. It revealed that o
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Šobrová, Pavlína. "Diagnostické biosenzory pro encefalopatie způsobené priony." Doctoral thesis, 2013. http://www.nusl.cz/ntk/nusl-176905.

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Prion diseases are fatal transmisible neurodegenerative and infectious disorders (TSEs) of humans and animals, characterized by structural transition of the host-encoded cellular prion protein (PrPC) into the aberrantly folded pathologic isoform PrPSc. The main aim of this work is to summarize present information about prion diseases and their possibilities of determination pointed to electrochemical techniques. For this purpose cyclic voltammetry (CV), differential pulse voltammetry, differential pulse voltammetry Brdicka reaction and chronopotentiometric stripping analysis (CPSA) were used.
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Šafaříková, Eva. "Vlastnosti specifických protilátek prionových chorob a možnosti jejich využití." Doctoral thesis, 2015. http://www.nusl.cz/ntk/nusl-336165.

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Transmissive spongiform encephalopathies (TSEs) are neurodegenerative diseases characterized by depositions of abnormally folded prion protein (PrPTSE ) in brain. PrPTSE is at present the only specific biochemical marker of human and animal TSEs. Diagnostic tests are based on the detection of PrPres after proteinase K digestion of brain homogenate using Western blot or on the immunohistochemistry of fixed brain tissue, which are both difficult and time consuming. In this work we focused on development of a new type of tests based on PrP detection without need of proteinase K digestion. As depo
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Books on the topic "Encefalopatia spongiforme"

1

Morbo fatale. Rizzoli(IS), 1997.

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2

R, Bradley, Matthews D, and International Office of Epizootics, eds. Transmissible spongiform encephalopathies of animals =: Encéphalopathies spongiformes transmissibles des animaux = Encefalopatías espongiformes transmisibles de los animales. Office International des Épizooties, 1992.

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3

Food and Agriculture Organization of the United Nations. Regional Office for Latin America and the Caribbean. and Asociación Panamericana de Ciencias Veterinarias., eds. Novedades sobre la encefalopatia espongiforme de los bovinos =: News on the bovine spongiform encephalopaty. Oficina Regional de la FAO para América Latina y el Caribe, 1996.

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4

Novedades sobre la encefalopatia espongiforme de los bovinos y otras temas de interés =: News on the bovine spongiform encephalopaty and other interesting issues. Oficina Regional de la FAO para América Latina y el Caribe, 1996.

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5

World Health Organization (WHO). WHO Manual for Strengthening Diagnosis and Surveillance of Creutzfeldt-Jakob Disease. World Health Organization, 1999.

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