Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Jose Luiz, Pedroso"'
Autor:
Jose Luiz Pedroso, Thiago Cardoso Vale, Julian Letícia de Freitas, Filipe Miranda Milagres Araújo, Alex Tiburtino Meira, Pedro Braga Neto, Marcondes C. França, Vitor Tumas, Hélio A. G. Teive, Orlando G. P. Barsottini
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 81, Iss 11, Pp 1000-1007 (2023)
Background Hereditary or familial spastic paraplegias (SPG) comprise a group of genetically and phenotypically heterogeneous diseases characterized by progressive degeneration of the corticospinal tracts. The complicated forms evolve with other vario
Externí odkaz:
https://doaj.org/article/c01cdf9fe5124b339a883b1b9be69b80
Autor:
Ingrid Faber, Alberto Rolim Muro Martinez, Thiago Junqueira Ribeiro de Rezende, Carlos Roberto Martins, Jr., Melina Pazian Martins, Charles Marques Lourenço, Wilson Marques, Jr., Celeste Montecchiani, Antonio Orlacchio, Jose Luiz Pedroso, Orlando Graziani Povoas Barsottini, Íscia Lopes-Cendes, Marcondes Cavalcante França, Jr.
Publikováno v:
NeuroImage: Clinical, Vol 19, Iss , Pp 848-857 (2018)
SPG11 mutations are the major cause of autosomal recessive Hereditary Spastic Paraplegia. The disease has a wide phenotypic variability indicating many regions of the nervous system besides the corticospinal tract are affected. Despite this, anatomic
Externí odkaz:
https://doaj.org/article/59ff3845fca940aca030b09a701cc5e8
Autor:
Carolina Yuri P. Aizawa, Jose Luiz Pedroso, Pedro Braga-Neto, Marilia Rezende Callegari, Orlando Graziani Povoas Barsottini
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 71, Iss 8, Pp 508-511 (2013)
OBJECTIVES: To assess balance and ability to function in patients with spinocerebellar ataxia. METHODS: A total of 44 patients with different spinocerebellar ataxia types 1, 2, 3, and 6 were evaluated using the Tinetti balance and gait assessment and
Externí odkaz:
https://doaj.org/article/c067d399a51642fd86958eac5083d925
Autor:
Jose Luiz Pedroso, Pedro Braga-Neto, Irapua Ferreira Ricarte, Marcus Vinicius Cristino Albuquerque, Orlando Graziani Povoas Barsottini
Publikováno v:
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://doaj.org/article/ea68893828ca4b4789cdb720d96113fe
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 71, Iss 12, Pp 973-975 (2013)
Several assumptions about the function of the cerebellum and semiotic signs have been described over the centuries. Among the long list of famous researchers who have provided a strong contribution and who have left their names on the highway of cere
Externí odkaz:
https://doaj.org/article/f26f02d487fb49a38170a1644b4c917b
Autor:
Ricardo Mendes Rogerio, Jose Luiz Pedroso, Acary Souza Bulle Oliveira, Lazaro Luis Faria do Amaral
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 71, Iss 11, Pp 907-908 (2013)
Externí odkaz:
https://doaj.org/article/3df7e65faa7c4f11971dbe9d69fb299e
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 71, Iss 12, Pp 977-977 (2013)
Externí odkaz:
https://doaj.org/article/225d3ae8ac354aa19e4558d86f645079
Autor:
Wladimir Bocca Vieira de Rezende Pinto, Paulo Victor Sgobbi de Souza, Jose Luiz Pedroso, Orlando Graziani Povoas Barsottini
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 71, Iss 11, Pp 911-911 (2013)
Externí odkaz:
https://doaj.org/article/5dc1df3dc0634c138f3a20a5d0f0f8b9
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 71, Iss 10, Pp 824-824 (2013)
Externí odkaz:
https://doaj.org/article/25a075f5801a4f1e8d139f9f37644f0c
Autor:
Ingrid, Faber, Alberto Rolim Muro, Martinez, Carlos Roberto, Martins, Maidane Luise, Maia, Juliana Pasquotto, Souza, Charles Marques, Lourenço, Wilson, Marques, Celeste, Montecchiani, Antonio, Orlacchio, Jose Luiz, Pedroso, Orlando Graziani Povoas, Barsottini, Celso Darío, Ramos, Íscia, Lopes-Cendes, Joseph H, Friedman, Bárbara Juarez, Amorim, Marcondes Cavalcante, França
Publikováno v:
Movement disorders : official journal of the Movement Disorder Society. 33(10)
Molecular imaging has proven to be a powerful tool to elucidate degenerated paths in a wide variety of neurological diseases and has not been systematically studied in hereditary spastic paraplegias.To investigate dopaminergic degeneration in a cohor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::635761be059b0e6902e7411a20783089
https://pubmed.ncbi.nlm.nih.gov/30306626
https://pubmed.ncbi.nlm.nih.gov/30306626