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Movement Disorders : Official Journal of the Movement Disorder Society
|
September 9, 2005
G2019S dardarin substitution is a common cause of Parkinson's disease in a Portuguese cohort
Jose Miguel Bras, Rita Joao Guerreiro, Maria Helena Ribeiro, et al.
BMC Neurology
|
January 24, 2008
Analysis of Parkinson disease patients from Portugal for mutations in SNCA, PRKN, PINK1 and LRRK2
Jose Bras, Rita Guerreiro, Maria Ribeiro, et al.
Journal of Comparative Effectiveness Research
|
June 6, 2025
Expert perspectives on the use of safinamide for Parkinson's disease in Portugal: insights from a Portuguese Delphi Consensus
Ana Margarida Rodrigues, Cristina Costa, Miguel Gago, et al.
Parkinsonism & Related Disorders
|
March 17, 2024
SQSTM1 Pro392Leu presenting as a corticobasal syndrome with progressive nonfluent aphasia
Miguel Tábuas-Pereira, Marisa Lima, Catarina Bernardes, et al.
Clinical Neuropharmacology
|
February 28, 2008
Effects of nebicapone on levodopa pharmacokinetics, catechol-O-methyltransferase activity, and motor fluctuations in patients with Parkinson disease
Joaquim J Ferreira, Luis Almeida, Luis Cunha, et al.
Molecular Neurodegeneration
|
October 25, 2024
Gut-first Parkinson's disease is encoded by gut dysbiome
Mário F Munoz-Pinto, Emanuel Candeias, Inês Melo-Marques, et al.
Parkinsonism & Related Disorders
|
January 23, 2025
Validation of the Portuguese version of the Movement Disorder Society non-motor rating scale (MDS-NMS) in Parkinson's disease
Thiago Cardoso Vale, Daniela Pereira Santos, Daniel Sabino de Oliveira, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
January 24, 2023
Embracing Monogenic Parkinson's Disease: The MJFF Global Genetic PD Cohort
Eva-Juliane Vollstedt, Susen Schaake, Katja Lohmann, et al.
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of 2
Search research articles
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Showing results (11-20 of 18) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 18 results.
Movement Disorders : Official Journal of the Movement Disorder Society
|
September 9, 2005
G2019S dardarin substitution is a common cause of Parkinson's disease in a Portuguese cohort
Jose Miguel Bras, Rita Joao Guerreiro, Maria Helena Ribeiro, et al.
BMC Neurology
|
January 24, 2008
Analysis of Parkinson disease patients from Portugal for mutations in SNCA, PRKN, PINK1 and LRRK2
Jose Bras, Rita Guerreiro, Maria Ribeiro, et al.
Journal of Comparative Effectiveness Research
|
June 6, 2025
Expert perspectives on the use of safinamide for Parkinson's disease in Portugal: insights from a Portuguese Delphi Consensus
Ana Margarida Rodrigues, Cristina Costa, Miguel Gago, et al.
Parkinsonism & Related Disorders
|
March 17, 2024
SQSTM1 Pro392Leu presenting as a corticobasal syndrome with progressive nonfluent aphasia
Miguel Tábuas-Pereira, Marisa Lima, Catarina Bernardes, et al.
Clinical Neuropharmacology
|
February 28, 2008
Effects of nebicapone on levodopa pharmacokinetics, catechol-O-methyltransferase activity, and motor fluctuations in patients with Parkinson disease
Joaquim J Ferreira, Luis Almeida, Luis Cunha, et al.
Molecular Neurodegeneration
|
October 25, 2024
Gut-first Parkinson's disease is encoded by gut dysbiome
Mário F Munoz-Pinto, Emanuel Candeias, Inês Melo-Marques, et al.
Parkinsonism & Related Disorders
|
January 23, 2025
Validation of the Portuguese version of the Movement Disorder Society non-motor rating scale (MDS-NMS) in Parkinson's disease
Thiago Cardoso Vale, Daniela Pereira Santos, Daniel Sabino de Oliveira, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
January 24, 2023
Embracing Monogenic Parkinson's Disease: The MJFF Global Genetic PD Cohort
Eva-Juliane Vollstedt, Susen Schaake, Katja Lohmann, et al.
Page
of 2