Zobrazeno 1 - 10
of 37
pro vyhledávání: '"síndrome de Creutzfeldt-Jakob"'
Autor:
Aureo do Carmo Filho, Karina Lebeis Pires, Isadora Gomes Mesquita, Luan Henrique Honório Rocha, Sergio Luis Schmidt
Publikováno v:
Revista Brasileira de Geriatria e Gerontologia, Vol 27 (2024)
Resumo A doença de Creutzfeldt-Jakob é uma condição rara causada por príons. Embora a forma mais notória da doença seja a infecciosa, a forma mais comum é a chamada esporádica, onde ocorre a transformação de proteínas citoplasmáticas das
Externí odkaz:
https://doaj.org/article/8cd2e45395044d40a8885d592f935e69
Autor:
Luiz Henrique Lélis Miranda, André Felipe Pastick de Holanda Oliveira, Davi Mariano de Carvalho, Gustavo Marques Figueredo Souza, João Guilherme Monteiro Magalhães, Joselmo Alberto Cabral Júnior, Pedro Thadeu Mertens Brainer de Queiroz Lima, Renato Melo Aguiar Júnior, Sérgio Pereira Lins Filho, Hugo Moura de Albuquerque Melo
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 80, Iss 08, Pp 837-844 (2022)
Background The Creutzfeldt-Jakob disease (CJD) is a spongiform encephalopathy that manifests as a rapidly progressive dementia syndrome. Currently, CJD has no cure, and many patients die within the first year, but some drugs are being studied as opti
Externí odkaz:
https://doaj.org/article/35d2b1d75691499ab6c201e28b4094ee
Autor:
Luiz Henrique Lélis Miranda, André Felipe Pastick de Holanda Oliveira, Davi Mariano de Carvalho, Gustavo Marques Figueredo Souza, João Guilherme Monteiro Magalhães, Joselmo Alberto Cabral Júnior, Pedro Thadeu Mertens Brainer de Queiroz Lima, Renato Melo Aguiar Júnior, Sérgio Pereira Lins Filho, Hugo Moura de Albuquerque Melo
Publikováno v:
Arquivos de Neuro-Psiquiatria, Volume: 80, Issue: 8, Pages: 837-844, Published: 21 NOV 2022
Arquivos de Neuro-Psiquiatria v.80 n.8 2022
Arquivos de neuro-psiquiatria
Academia Brasileira de Neurologia
instacron:ABNEURO
Arquivos de Neuro-Psiquiatria v.80 n.8 2022
Arquivos de neuro-psiquiatria
Academia Brasileira de Neurologia
instacron:ABNEURO
Background The Creutzfeldt-Jakob disease (CJD) is a spongiform encephalopathy that manifests as a rapidly progressive dementia syndrome. Currently, CJD has no cure, and many patients die within the first year, but some drugs are being studied as opti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d79b7a07987eae14a053765341a05bbc
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2022000900837&lng=en&tlng=en
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2022000900837&lng=en&tlng=en
Publikováno v:
PsiLogos, Vol 14, Iss 1 (2017)
Introdução: A catatonia é uma síndrome neuropsiquiátrica, classicamente associada à esquizofrenia, mas mais frequentemente relacionada com outras causas psiquiátricas, neurológicas e/ou metabólicas. Caso Clínico: Um homem de 61 anos foi in
Externí odkaz:
https://doaj.org/article/5d8128140ca542adb1462ffcaa752915
Publikováno v:
Arquivos de Neuro-Psiquiatria v.79 n.1 2021
Arquivos de neuro-psiquiatria
Academia Brasileira de Neurologia
instacron:ABNEURO
Arquivos de Neuro-Psiquiatria, Volume: 79, Issue: 1, Pages: 84-87, Published: 26 FEB 2021
Arquivos de Neuro-Psiquiatria, Vol 79, Iss 1, Pp 84-87 (2021)
Arquivos de neuro-psiquiatria
Academia Brasileira de Neurologia
instacron:ABNEURO
Arquivos de Neuro-Psiquiatria, Volume: 79, Issue: 1, Pages: 84-87, Published: 26 FEB 2021
Arquivos de Neuro-Psiquiatria, Vol 79, Iss 1, Pp 84-87 (2021)
Creutzfeldt-Jakob disease (CJD) is a transmissible spongiform encephalopathy whose initial description is associated with two German authors, Alfons Maria Jakob and Hans Gerhard Creutzfeldt. As polemic as the issue about the Creutzfeldt’s merit in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a35eba4307af111d5f95809e0f2e7d9
https://doi.org/10.1590/0004-282x-anp-2020-0274
https://doi.org/10.1590/0004-282x-anp-2020-0274
Autor:
Carneiro,Amandha Alencar Maia, Esmeraldo,Mateus Aragão, Silva,David Elison de Lima e, Ribeiro,Espártaco Moraes Lima
Publikováno v:
Dementia & Neuropsychologia, Issue: ahead, Published: 24 JUN 2022
Dementia & Neuropsychologia n.ahead 2022
Dementia & Neuropsychologia
Associação de Neurologia Cognitiva e do Comportamento (ANCC)
instacron:ANCC
Dementia & Neuropsychologia, Volume: 16, Issue: 4, Pages: 367-372, Published: 24 JUN 2022
Dementia & Neuropsychologia v.16 n.4 2022
Dementia & Neuropsychologia n.ahead 2022
Dementia & Neuropsychologia
Associação de Neurologia Cognitiva e do Comportamento (ANCC)
instacron:ANCC
Dementia & Neuropsychologia, Volume: 16, Issue: 4, Pages: 367-372, Published: 24 JUN 2022
Dementia & Neuropsychologia v.16 n.4 2022
Creutzfeldt-Jakob disease (CJD) is one of the transmissible spongiform encephalopathies that lead to rapidly progressive dementia. CJD has a low prevalence, and the average survival is only 1 year after the onset of symptoms. As the patients with CJD
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::a7b28c0b3c06e71e81d703377e421b66
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1980-57642022005008202&lng=en&tlng=en
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1980-57642022005008202&lng=en&tlng=en
Autor:
Tavares-Júnior,José Wagner Leonel, Carvalho,Renata de Oliveira, Feitosa,Raul Raposo Pereira, Rolim,Flávia de Paiva Santos, Rocha,Felipe Araújo, Pitombeira,Milena Sales, Malveira,George Linard Silva, Carvalho,João José Freitas de, Frota,Norberto Anizio Ferreira, Dias,Daniel Aguiar
Publikováno v:
Dementia & Neuropsychologia, Issue: ahead, Published: 23 MAY 2022
Dementia & Neuropsychologia, Volume: 16, Issue: 3, Pages: 361-364, Published: 23 MAY 2022
Dementia & Neuropsychologia v.16 n.3 2022
Dementia & Neuropsychologia
Associação de Neurologia Cognitiva e do Comportamento (ANCC)
instacron:ANCC
Dementia & Neuropsychologia, Volume: 16, Issue: 3, Pages: 361-364, Published: 23 MAY 2022
Dementia & Neuropsychologia v.16 n.3 2022
Dementia & Neuropsychologia
Associação de Neurologia Cognitiva e do Comportamento (ANCC)
instacron:ANCC
Prion diseases are an important cause of rapidly progressive dementias. Among them, the most common is sporadic Creutzfeldt-Jakob disease (CJD). It is a rare and incurable disease, with rapid progression to death. Objective: To describe the diagnosti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::025bc4ed4fe1c2d0b3b7516fc39a2669
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1980-57642022005004205&lng=en&tlng=en
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1980-57642022005004205&lng=en&tlng=en
Publikováno v:
Revista Médica del Uruguay, Vol 28, Iss 1, Pp 43-47 (2012)
Se presenta el caso clínico de una paciente de 66 años portadora de una encefalopatía espongiforme con criterios diagnósticos que configuran una enfermedad de Creutzfeldt-Jakob esporádica probable. Las abigarradas manifestaciones clínicas, junt
Externí odkaz:
https://doaj.org/article/f5505942938a41c29763fe17c19853a4
Autor:
Sara Lewin, Abayubá Perna, Ronald Salamano, Carlos Ketzoian, Daniel Salinas, María Mirta Rodríguez, Graciela Mañana
Publikováno v:
Revista Médica del Uruguay, Vol 28, Iss 1, Pp 35-42 (2012)
Introducción: las enfermedades priónicas son enfermedades de carácter degenerativo del sistema nervioso central de curso progresivo y desenlace fatal que presentan largos períodos de incubación antes de manifestarse clínicamente siendo hoy de g
Externí odkaz:
https://doaj.org/article/865dfb603b744cb3b1e74d702389a0cb
Autor:
VILLAMIL WILMER, JULIO GONZÁLES, JAIME ANDRÉS ARRIETA, CARLOS ÁLVAREZ, GUILLERMO BORJA, JUAN CARLOS VERGARA, DAVID BUELVAS
Publikováno v:
Infectio, Vol 11, Iss 3, Pp 124-128 (2007)
Se presenta el caso de una paciente de 65 años de edad con alucinaciones auditivas y visuales, rigidez en el hemicuerpo izquierdo que progresó al hemicuerpo derecho, con demostración por electroencefalograma de ondas trifásicas abundantes lentas,
Externí odkaz:
https://doaj.org/article/96a24df8c9b644a88479ad6402ce2df2