Zobrazeno 1 - 10
of 46
pro vyhledávání: '"Ataxia espinocerebelar"'
Autor:
Marcus Vinicius Cristino de Albuquerque, José Luiz Pedroso, Pedro Braga Neto, Orlando Graziani Povoas Barsottini
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 73, Iss 1, Pp 18-21 (2015)
The spinocerebellar ataxias (SCA) are a group of neurodegenerative disorders characterized by heterogeneous clinical presentation. Spinocerebellar ataxia type 7 (SCA7) is caused by an abnormal CAG repeat expansion and includes cerebellar signs associ
Externí odkaz:
https://doaj.org/article/0724f57d7856466293ce62b9213b83a8
Autor:
Adriana Moro, Renato P. Munhoz, Walter O. Arruda, Salmo Raskin, Mariana Moscovich, Hélio A.G. Teive
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 72, Iss 9, Pp 659-662 (2014)
Spinocerebellar ataxia type 3 (SCA3) involves cerebellar, pyramidal, extrapyramidal, motor neuron and oculomotor systems with strong phenotypic heterogeneity, that lead us to classify the disorder into different clinical subtypes according to the pre
Externí odkaz:
https://doaj.org/article/14fce1d8b73d4321b216e62f57484cd6
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 65, Iss 4a, Pp 965-968 (2007)
The authors report the history of spinocerebellar ataxia 10 (SCA10), since its first report in a large Portuguese-ancestry Family with autosomal dominant pure cerebellar ataxia, till the final identification of further families without Mexican ancest
Externí odkaz:
https://doaj.org/article/092924775ac645089aab6db1a538c127
Autor:
Bianca Simone Zeigelboim, Hélio A.G. Teive, Rosane Sampaio, Ari Leon Jurkiewicz, Paulo B.N. Liberalesso
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 69, Iss 5, Pp 760-765 (2011)
OBJECTIVE: To describe the alterations observed in electronystagmography (ENG) of patients with spinocerebellar ataxia (SCA) types 2 and 3. METHOD: Sixteen patients were studied and the following procedures were carried out: anamnesis, otorhinolaryng
Externí odkaz:
https://doaj.org/article/bf2a1f1a2a804bd0b3f8b263cbf7be96
Autor:
Aline Andrade Freund, Rosana Hermínia Scola, Hélio A.G. Teive, Raquel Cristina Arndt, Magda Clara Vieira da Costa-Ribeiro, Lupe Furtado Alle, Lineu Cesar Werneck
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 67, Iss 4, Pp 1124-1132 (2009)
The diagnosis and incidence of spinocerebelar ataxias (SCA) is sometimes difficult to analyze due the overlap of phenotypes subtypes and are disorders of mutations caused by CAG trinucleotide repeat expansion. To investigate the incidence of the SCA
Externí odkaz:
https://doaj.org/article/fe14ad9987ec434197c717b3d0caf617
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 66, Iss 3b, Pp 691-694 (2008)
Spinocerebellar ataxia type 6 (SCA 6) is an autosomal dominant cerebellar ataxia caused by CAG repeat expansion in the SCA6 gene, a alpha 1A voltage-dependent calcium channel subunit gene on chromosome 19p13. SCA-6 is characterized predominantly by s
Externí odkaz:
https://doaj.org/article/9cd399cf065d4a01b34b0c895317cadf
Autor:
Iscia Lopes-Cendesi, Hélio G.A. Teive, Maria E Calcagnotto, Jaderson C. da Costa, Francisco Cardoso, Erika Viana, Jaime A. Maciel, João Radvany, Walter O. Arruda, Paulo C. Trevisol-Bittencourt, Pedro Rosa Neto, Isabel Silveira, Carlos E. Steiner, Walter Pinto-Júnior, André S. Santos, Ylmar Correa Neto, Lineu C. Werneck, Abelardo Q.C. Araújo, Gerson Carakushansky, Luiz R. Mello, Laura B. Jardim, Guy A. Rouleau
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 55, Iss 3B, Pp 519-529 (1997)
Spinocerebellar ataxia type 1 (SCA1), spinocerebellar ataxia type 2 (SCA2) and Machado-Joseph disease or spinocerebellar ataxia type 3 (MJD/SCA3) are three distinctive forms of autosomal dominant spinocerebellar ataxia (SCA) caused by expansions of a
Externí odkaz:
https://doaj.org/article/02bdfc208fe340e890a607549bd42d95
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 64, Iss 2a, Pp 222-227 (2006)
We conducted a 320 year retrospective survey of the history and genealogy of a large Brazilian family with SCA7. The ancestral couple was from the State of Ceará, Brazil, and the genealogical tree was composed of 577 individuals, including 217 males
Externí odkaz:
https://doaj.org/article/69e36aa28a0d4efaa78ef0395313a3fd
Autor:
APPELT, Pablo Andrei
Publikováno v:
Biblioteca Digital de Teses e Dissertações da UFTM
Universidade Federal do Triangulo Mineiro (UFTM)
instacron:UFTM
Universidade Federal do Triangulo Mineiro (UFTM)
instacron:UFTM
Introdução: A ataxia espinocerebelar é uma doença neurodegenerativa hereditária caracterizada por alterações na marcha, equilíbrio e coordenação motora. Terapias com células tronco têm sido utilizadas como alternativa para retardar a evol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3056::eaeefc5153c4e4b14b0dfc9db1d00c8e
http://bdtd.uftm.edu.br/handle/123456789/1170
http://bdtd.uftm.edu.br/handle/123456789/1170
Autor:
Leda M. N. Keim, Yuri Rodrigues Luz de Araujo, Fernanda Baseggio Lopes Figueiredo, Mariana da Silva Salvino Klem Galvez, Camilla Polonini Martins, Laura Alice Santos de Oliveira
Publikováno v:
Fisioterapia em Movimento v.34 2021
Fisioterapia em Movimento
Pontifícia Universidade Católica do Paraná (PUC-PR)
instacron:PUC_PR
Fisioterapia em Movimento, Volume: 34, Article number: e34123, Published: 13 DEC 2021
Fisioterapia em Movimento
Pontifícia Universidade Católica do Paraná (PUC-PR)
instacron:PUC_PR
Fisioterapia em Movimento, Volume: 34, Article number: e34123, Published: 13 DEC 2021
Introduction: Spinocerebellar ataxia 3 (SCA3) is a hereditary disease associated with progressive cerebellar and extracerebellar degeneration. Although there is no effective therapy for SCA3, some of its symptoms can be relieved with symptomatic trea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d452c38384ff74b9add5ad66a044288f
https://doi.org/10.1590/fm.2021.34123
https://doi.org/10.1590/fm.2021.34123