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The Neurologist
|
September 4, 2019
Dupuytren, Ledderhose, and Peyronie Diseases After Primidone Use For Essential Tremor
Luiz Felipe R Vasconcellos, Daniel Nassif, Mariana Spitz
Arquivos De Neuro-Psiquiatria
|
February 4, 2003
Organophosphate-induced delayed neuropathy: case report
Luiz Felipe R Vasconcellos, Ana Cláudia Leite, Osvaldo J M Nascimento
Geriatrics & Gerontology International
|
March 27, 2019
Mild cognitive impairment in Parkinson's disease: Characterization and impact on quality of life according to subtype
Luiz Felipe R Vasconcellos, João S Pereira, Helenice Charchat-Fichman, et al.
Parkinsonism & Related Disorders
|
March 31, 2015
Parkinson disease: α-synuclein mutational screening and new clinical insight into the p.E46K mutation
Márcia M G Pimentel, Fabíola C Rodrigues, Marco Antônio A Leite, et al.
Neuroscience Letters
|
October 30, 2016
Autosomal dominant Parkinson's disease: Incidence of mutations in LRRK2, SNCA, VPS35 and GBA genes in Brazil
Gabriella de M Abreu, Débora Cristina T Valença, Mário Campos, et al.
Neurobiology of Aging
|
October 22, 2018
CHCHD2 mutational screening in Brazilian patients with familial Parkinson's disease
Danielle D Voigt, Caroline M Nascimento, Ritiele B de Souza, et al.
Journal of the Neurological Sciences
|
October 10, 2017
Clinical profiles associated with LRRK2 and GBA mutations in Brazilians with Parkinson's disease
Camilla P da Silva, Gabriella de M Abreu, Pedro H Cabello Acero, et al.
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of 1
Search research articles
Search
Showing results (1-10 of 7) with videos related to
Sort By:
Page
of 1
The Neurologist
|
September 4, 2019
Dupuytren, Ledderhose, and Peyronie Diseases After Primidone Use For Essential Tremor
Luiz Felipe R Vasconcellos, Daniel Nassif, Mariana Spitz
Arquivos De Neuro-Psiquiatria
|
February 4, 2003
Organophosphate-induced delayed neuropathy: case report
Luiz Felipe R Vasconcellos, Ana Cláudia Leite, Osvaldo J M Nascimento
Geriatrics & Gerontology International
|
March 27, 2019
Mild cognitive impairment in Parkinson's disease: Characterization and impact on quality of life according to subtype
Luiz Felipe R Vasconcellos, João S Pereira, Helenice Charchat-Fichman, et al.
Parkinsonism & Related Disorders
|
March 31, 2015
Parkinson disease: α-synuclein mutational screening and new clinical insight into the p.E46K mutation
Márcia M G Pimentel, Fabíola C Rodrigues, Marco Antônio A Leite, et al.
Neuroscience Letters
|
October 30, 2016
Autosomal dominant Parkinson's disease: Incidence of mutations in LRRK2, SNCA, VPS35 and GBA genes in Brazil
Gabriella de M Abreu, Débora Cristina T Valença, Mário Campos, et al.
Neurobiology of Aging
|
October 22, 2018
CHCHD2 mutational screening in Brazilian patients with familial Parkinson's disease
Danielle D Voigt, Caroline M Nascimento, Ritiele B de Souza, et al.
Journal of the Neurological Sciences
|
October 10, 2017
Clinical profiles associated with LRRK2 and GBA mutations in Brazilians with Parkinson's disease
Camilla P da Silva, Gabriella de M Abreu, Pedro H Cabello Acero, et al.
Page
of 1