Zobrazeno 1 - 10 of 17 pro vyhledávání: '"Marcus Vinicius Cristino de Albuquerque"'
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Akademický článek
Phenotype variability and early onset ataxia symptoms in spinocerebellar ataxia type 7: comparison and correlation with other spinocerebellar ataxias
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
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2
Akademický článek
Adult onset sporadic ataxias: a diagnostic challenge
Autor: Orlando Graziani Povoas Barsottini, Marcus Vinicius Cristino de Albuquerque, Pedro Braga Neto, José Luiz Pedroso
Publikováno v: Arquivos de Neuro-Psiquiatria, Vol 72, Iss 3, Pp 232-240 (2014)
Patients with adult onset non-familial progressive ataxia are classified in sporadic ataxia group. There are several disease categories that may manifest with sporadic ataxia: toxic causes, immune-mediated ataxias, vitamin deficiency, infectious dise
Externí odkaz: https://doaj.org/article/02061ae5c4bb49e381afc4ee4732b3d9
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5
SCA1 patients may present as hereditary spastic paraplegia and must be included in spastic-ataxias group
Autor: Wladimir Bocca Vieira de Rezende Pinto, Laura Bannach Jardim, Pedro Braga-Neto, Orlando Graziani Povoas Barsottini, Maria Luiza Saraiva-Pereira, Paulo Victor Sgobbi de Souza, José Luiz Pedroso, Marcus Vinicius Cristino de Albuquerque
Publikováno v: Parkinsonism & Related Disorders. 21:1243-1246
Introduction The combination of cerebellar ataxia and spasticity is common. However, autosomal dominant genetic diseases presenting with spastic-ataxia are a smaller group. Pyramidal signs have been frequently observed in several SCA subtypes, partic
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f4811b6c422e1e4781f2302fb77b17d
https://doi.org/10.1016/j.parkreldis.2015.07.015
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6
Adult onset sporadic ataxias: a diagnostic challenge
Autor: Marcus Vinicius Cristino de Albuquerque, Orlando Graziani Povoas Barsottini, José Luiz Pedroso, Pedro Braga Neto
Publikováno v: Arquivos de Neuro-Psiquiatria, Vol 72, Iss 3, Pp 232-240 (2014)
Arquivos de Neuro-Psiquiatria v.72 n.3 2014
Arquivos de neuro-psiquiatria
Academia Brasileira de Neurologia
instacron:ABNEURO
Patients with adult onset non-familial progressive ataxia are classified in sporadic ataxia group. There are several disease categories that may manifest with sporadic ataxia: toxic causes, immune-mediated ataxias, vitamin deficiency, infectious dise
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::995cb50ad199d499404a5ac923cacfca
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2014000300232&lng=en&tlng=en
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8
Clinical and epidemiological profiles of non-traumatic myelopathies
Autor: Marcus Vinicius Cristino de Albuquerque, Lívia Almeida Dutra, Orlando Graziani Povoas Barsottini, Wladimir Bocca Vieira de Rezende Pinto, José Luiz Pedroso, Paulo Victor Sgobbi de Souza
Publikováno v: Arquivos de Neuro-Psiquiatria, Volume: 74, Issue: 2, Pages: 161-165, Published: FEB 2016
Arquivos de Neuro-Psiquiatria v.74 n.2 2016
Arquivos de neuro-psiquiatria
Academia Brasileira de Neurologia
instacron:ABNEURO
Arquivos de Neuro-Psiquiatria, Vol 74, Iss 2, Pp 161-165 (2016)
Non-traumatic myelopathies represent a heterogeneous group of neurological conditions. Few studies report clinical and epidemiological profiles regarding the experience of referral services. Objective To describe clinical characteristics of a non-tra
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3721475cba70bd7646ed5a6a790fd7bd
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2016000200015&lng=en&tlng=en
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9
Should spinocerebellar ataxias be included in the differential diagnosis for Huntington's diseases-like syndromes?
Autor: Marcus Vinicius Cristino de Albuquerque, Laura Bannach Jardim, Orlando Graziani Povoas Barsottini, José Luiz Pedroso, Maria Eliza Thomaz de Freitas, Maria Luiza Saraiva-Pereira
Publikováno v: Journal of the Neurological Sciences. 347:356-358
In this article, we describe three patients with different spinocerebellar ataxia (SCA) subtypes presenting with unusual movement disorders predominantly characterized by choreoathetosis, which, together with their autosomal dominant pattern of inher
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4805431060a0f56e41d35b05638c19f
https://doi.org/10.1016/j.jns.2014.09.050
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10
Clinical spectrum of early onset cerebellar ataxia with retained tendon reflexes: an autosomal recessive ataxia not to be missed
Autor: Pedro Braga-Neto, Marcus Vinicius Cristino de Albuquerque, Irapuá Ferreira Ricarte, Orlando Graziani Povoas Barsottini, José Luiz Pedroso
Publikováno v: Arquivos de Neuro-Psiquiatria v.71 n.6 2013
Arquivos de neuro-psiquiatria
Academia Brasileira de Neurologia
instacron:ABNEURO
Arquivos de Neuro-Psiquiatria, Vol 71, Iss 6, Pp 345-348 (2013)
Autosomal recessive cerebellar ataxias are a heterogeneous group of neurological disorders. In 1981, a neurological entity comprised by early onset progressive cerebellar ataxia, dysarthria, pyramidal weakness of the limbs and retained or increased u
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f20f4d4bbfc375b3f144b12a1d645b8
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2013000600345
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