Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Marcondes França Jr"'
Autor:
Alberto R. M. Martinez, Marcelo B. Nunes, Nayara D. Immich, Luiza Piovesana, Marcondes França Jr, Lidiane S. Campos, Anelyssa D?Abreu
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 72, Iss 2, Pp 119-122 (2014)
Primary hemifacial spasm (HFS) is characterized by irregular and involuntary contraction of the muscles innervated by the ipsilateral facial nerve. Treatment controls symptoms and improves quality of life (QoL). Objective : Evaluate the initial diagn
Externí odkaz:
https://doaj.org/article/518a0ed7de794cf395d6af92a7d072c1
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 71, Iss 1, Pp 35-39 (2013)
Pleomorphic xanthoastrocytoma (PXA) is a rare glioma. This paper aimed to analyze magnetic resonance imaging (MRI) characteristics in a series of patients diagnosed with PXA. We analyzed MRI findings in 9 patients with histopathologic diagnosis of PX
Externí odkaz:
https://doaj.org/article/1f4af55a5538425991024323d26980b1
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 69, Iss 3, Pp 566-567 (2011)
Externí odkaz:
https://doaj.org/article/09f931be9cbc4418b0637b930c43b0f0
Publikováno v:
Arquivos de Neuro-Psiquiatria, Iss ahead, p 0 (2012)
Pleomorphic xanthoastrocytoma (PXA) is a rare glioma. This paper aimed to analyze magnetic resonance imaging (MRI) characteristics in a series of patients diagnosed with PXA. We analyzed MRI findings in 9 patients with histopathologic diagnosis of PX
Externí odkaz:
https://doaj.org/article/516c4f8fa7c14025b20febe066b274dc
Autor:
Ingrid Faber, Eduardo Rafael Pereira, Alberto R. M. Martinez, Marcondes França Jr, Hélio Afonso Ghizoni Teive
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 75, Iss 11, Pp 813-818
ABSTRACT The authors have constructed a brief timeline of major clinical research related to hereditary spastic paraplegia (HSP). This timeline summarizes the evolution of HSP research, from the first clinical descriptions by Adolf von Strümpell in
Externí odkaz:
https://doaj.org/article/dee68d99f40c40d48e27bdf39ea610d3
Publikováno v:
Neuropediatrics. 53:358-360
Spinocerebellar ataxia type 5 (SCA5) is a rare subtype of SCA that usually affects adults. It has been recently reported in children in Europe, North America, and China. This study aims to describe clinical, radiological, and genetic data of a child
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b5ce735c94d9944b744e1e3044041bd
https://doi.org/10.1055/a-1849-8128
https://doi.org/10.1055/a-1849-8128