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Movement Disorders : Official Journal of the Movement Disorder Society
|
July 22, 2022
Underrepresented Populations in Parkinson's Genetics Research: Current Landscape and Future Directions
Artur Francisco Schumacher-Schuh, Andrei Bieger, Olaitan Okunoye, et al.
Parkinsonism & Related Disorders
|
December 10, 2021
WARS2 mutations cause dopa-responsive early-onset parkinsonism and progressive myoclonus ataxia
Matej Skorvanek, Irena Rektorova, Wim Mandemakers, et al.
Nature Medicine
|
August 7, 2025
Strengthening Africa's brain health and economic resilience
Mie Rizig, Connor McLaughlin, Vaibhav A Narayan, et al.
Research Square
|
June 10, 2024
p.L1795F LRRK2 variant is a common cause of Parkinson's disease in Central Europe
Miriam Ostrozovicova, Gertrud Tamas, Petr Dušek, et al.
Ebiomedicine
|
September 26, 2025
Broadening dementia risk models: building on the 2024 Lancet Commission report for a more inclusive global framework
Cyprian M Mostert, Chinedu Udeh-Momoh, Andrea Sylvia Winkler, et al.
Movement Disorders Clinical Practice
|
March 22, 2025
Prevalence and Clinical Characteristics of the LRRK2 p.L1795F Variant in Central Europeans with Early-Onset and Familial Parkinson's Disease
Miriam Ostrozovicova, Gertrud Tamas, Agsha Atputhavadivel, et al.
NPJ Parkinson'S Disease
|
September 25, 2025
Genome-wide association study of REM sleep behavior disorder in Parkinson's disease
Yuri L Sosero, Karl Heilbron, Pierre Fontanillas, et al.
Medrxiv : the Preprint Server for Health Sciences
|
December 11, 2023
Insights into Ancestral Diversity in Parkinsons Disease Risk: A Comparative Assessment of Polygenic Risk Scores
Paula Saffie Awad, Mary B Makarious, Inas Elsayed, et al.
NPJ Parkinson'S Disease
|
July 3, 2025
Insights into ancestral diversity in Parkinson's disease risk: a comparative assessment of polygenic risk scores
Paula Saffie-Awad, Spencer M Grant, Mary B Makarious, et al.
NPJ Parkinson'S Disease
|
November 6, 2024
The p.Gly2019Ser is a common LRRK2 pathogenic variant among Egyptians with familial and sporadic Parkinson's disease
Martina B William, Sharifa Hamed, Ali Shalash, et al.
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Search research articles
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Showing results (21-30 of 43) with videos related to
Sort By:
Page
of 5
Movement Disorders : Official Journal of the Movement Disorder Society
|
July 22, 2022
Underrepresented Populations in Parkinson's Genetics Research: Current Landscape and Future Directions
Artur Francisco Schumacher-Schuh, Andrei Bieger, Olaitan Okunoye, et al.
Parkinsonism & Related Disorders
|
December 10, 2021
WARS2 mutations cause dopa-responsive early-onset parkinsonism and progressive myoclonus ataxia
Matej Skorvanek, Irena Rektorova, Wim Mandemakers, et al.
Nature Medicine
|
August 7, 2025
Strengthening Africa's brain health and economic resilience
Mie Rizig, Connor McLaughlin, Vaibhav A Narayan, et al.
Research Square
|
June 10, 2024
p.L1795F LRRK2 variant is a common cause of Parkinson's disease in Central Europe
Miriam Ostrozovicova, Gertrud Tamas, Petr Dušek, et al.
Ebiomedicine
|
September 26, 2025
Broadening dementia risk models: building on the 2024 Lancet Commission report for a more inclusive global framework
Cyprian M Mostert, Chinedu Udeh-Momoh, Andrea Sylvia Winkler, et al.
Movement Disorders Clinical Practice
|
March 22, 2025
Prevalence and Clinical Characteristics of the LRRK2 p.L1795F Variant in Central Europeans with Early-Onset and Familial Parkinson's Disease
Miriam Ostrozovicova, Gertrud Tamas, Agsha Atputhavadivel, et al.
NPJ Parkinson'S Disease
|
September 25, 2025
Genome-wide association study of REM sleep behavior disorder in Parkinson's disease
Yuri L Sosero, Karl Heilbron, Pierre Fontanillas, et al.
Medrxiv : the Preprint Server for Health Sciences
|
December 11, 2023
Insights into Ancestral Diversity in Parkinsons Disease Risk: A Comparative Assessment of Polygenic Risk Scores
Paula Saffie Awad, Mary B Makarious, Inas Elsayed, et al.
NPJ Parkinson'S Disease
|
July 3, 2025
Insights into ancestral diversity in Parkinson's disease risk: a comparative assessment of polygenic risk scores
Paula Saffie-Awad, Spencer M Grant, Mary B Makarious, et al.
NPJ Parkinson'S Disease
|
November 6, 2024
The p.Gly2019Ser is a common LRRK2 pathogenic variant among Egyptians with familial and sporadic Parkinson's disease
Martina B William, Sharifa Hamed, Ali Shalash, et al.
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of 5