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Medrxiv : the Preprint Server for Health Sciences
|
September 15, 2025
The <i>LRRK2</i> p.A419V variant associates with risk of Parkinson's disease in the East Asian population and an evaluation on age of onset
Kai Shi Lim, Maria Teresa Periñan, Elaine Guo Yan Chew, et al.
JAMA Neurology
|
July 11, 2022
Six Action Steps to Address Global Disparities in Parkinson Disease: A World Health Organization Priority
Nicoline Schiess, Rodrigo Cataldi, Michael S Okun, et al.
Medrxiv : the Preprint Server for Health Sciences
|
July 17, 2025
Rare but Relevant: Assessing Variants in Dystonia-linked Genes in Parkinson's Disease
Lara M Lange, Zih-Hua Fang, Laurel Screven, et al.
NPJ Parkinson'S Disease
|
November 18, 2025
LRRK2 p.G2385R and p.R1628P variants in a multi-ethnic Asian Parkinson's Cohort: epidemiology and clinical insights
Jun Wen Goh, Jia Lun Lim, Tzi Shin Toh, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
October 11, 2025
Rare but Relevant? Assessing Variants in Dystonia-Linked Genes in Parkinson's Disease
Lara M Lange, Zih-Hua Fang, Laurel Screven, et al.
Medrxiv : the Preprint Server for Health Sciences
|
July 3, 2026
<i>GCH1</i> p.Ser80Asn Confers Risk for Parkinson's Disease in East Asian Populations
Yi Wen Tay, Andrew Leslie Lee, Jie Ping Schee, et al.
Medrxiv : the Preprint Server for Health Sciences
|
July 3, 2026
Repeat expansions in Parkinson's disease and parkinsonism across ancestries: insights from a global genetic cohort
Lara M Lange, Catalina Cerquera-Cleves, Ai Huey Tan, et al.
Nature Genetics
|
July 24, 2019
Noncoding CGG repeat expansions in neuronal intranuclear inclusion disease, oculopharyngodistal myopathy and an overlapping disease
Hiroyuki Ishiura, Shota Shibata, Jun Yoshimura, et al.
Medrxiv : the Preprint Server for Health Sciences
|
December 16, 2024
Genetic Diversity and Expanded Phenotypes in Dystonia: Insights from Large-Scale Exome Sequencing
Mirja Thomsen, Fabian Ott, Sebastian Loens, et al.
Human Molecular Genetics
|
December 25, 2016
Genome-wide association study of Parkinson's disease in East Asians
Jia Nee Foo, Louis C Tan, Ishak D Irwan, et al.
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Showing results (101-110 of 117) with videos related to
Sort By:
Page
of 12
Medrxiv : the Preprint Server for Health Sciences
|
September 15, 2025
The <i>LRRK2</i> p.A419V variant associates with risk of Parkinson's disease in the East Asian population and an evaluation on age of onset
Kai Shi Lim, Maria Teresa Periñan, Elaine Guo Yan Chew, et al.
JAMA Neurology
|
July 11, 2022
Six Action Steps to Address Global Disparities in Parkinson Disease: A World Health Organization Priority
Nicoline Schiess, Rodrigo Cataldi, Michael S Okun, et al.
Medrxiv : the Preprint Server for Health Sciences
|
July 17, 2025
Rare but Relevant: Assessing Variants in Dystonia-linked Genes in Parkinson's Disease
Lara M Lange, Zih-Hua Fang, Laurel Screven, et al.
NPJ Parkinson'S Disease
|
November 18, 2025
LRRK2 p.G2385R and p.R1628P variants in a multi-ethnic Asian Parkinson's Cohort: epidemiology and clinical insights
Jun Wen Goh, Jia Lun Lim, Tzi Shin Toh, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
October 11, 2025
Rare but Relevant? Assessing Variants in Dystonia-Linked Genes in Parkinson's Disease
Lara M Lange, Zih-Hua Fang, Laurel Screven, et al.
Medrxiv : the Preprint Server for Health Sciences
|
July 3, 2026
<i>GCH1</i> p.Ser80Asn Confers Risk for Parkinson's Disease in East Asian Populations
Yi Wen Tay, Andrew Leslie Lee, Jie Ping Schee, et al.
Medrxiv : the Preprint Server for Health Sciences
|
July 3, 2026
Repeat expansions in Parkinson's disease and parkinsonism across ancestries: insights from a global genetic cohort
Lara M Lange, Catalina Cerquera-Cleves, Ai Huey Tan, et al.
Nature Genetics
|
July 24, 2019
Noncoding CGG repeat expansions in neuronal intranuclear inclusion disease, oculopharyngodistal myopathy and an overlapping disease
Hiroyuki Ishiura, Shota Shibata, Jun Yoshimura, et al.
Medrxiv : the Preprint Server for Health Sciences
|
December 16, 2024
Genetic Diversity and Expanded Phenotypes in Dystonia: Insights from Large-Scale Exome Sequencing
Mirja Thomsen, Fabian Ott, Sebastian Loens, et al.
Human Molecular Genetics
|
December 25, 2016
Genome-wide association study of Parkinson's disease in East Asians
Jia Nee Foo, Louis C Tan, Ishak D Irwan, et al.
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of 12