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Alex Rajput

Showing results (81-90 of 101) with videos related to

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Movement Disorders : Official Journal of the Movement Disorder Society|January 13, 2009
FGF20 and Parkinson's disease: no evidence of association or pathogenicity via alpha-synuclein expressionChristian Wider, Justus C Dachsel, Alexandra I Soto, et al.
Biorxiv : the Preprint Server for Biology|April 17, 2026
WDR44 drives de novo α-synuclein aggregation at the lysosomal membrane and promotes neuronal dysfunction in Parkinson's DiseaseMaxime Teixeira, Razan Sheta, Morgan Bérard, et al.
Brain : a Journal of Neurology|December 8, 2022
Mitochondrial DNA heteroplasmy distinguishes disease manifestation in PINK1/PRKN-linked Parkinson's diseaseJoanne Trinh, Andrew A Hicks, Inke R König, et al.
Iscience|September 20, 2019
Rewiring of the Human Mitochondrial Interactome during Neuronal Reprogramming Reveals Regulators of the Respirasome and NeurogenesisMohamed Taha Moutaoufik, Ramy Malty, Shahreen Amin, et al.
Tremor and Other Hyperkinetic Movements (New York, N.Y.)|February 16, 2026
Copy Number Variant Duplications Associated with Essential TremorMiranda Medeiros, Calwing Liao, Allison A Dilliott, et al.
Parkinsonism & Related Disorders|December 6, 2020
Exome-wide rare variant analysis in familial essential tremorMonica Diez-Fairen, Gabrielle Houle, Sara Ortega-Cubero, et al.
American Journal of Human Genetics|July 19, 2011
VPS35 mutations in Parkinson diseaseCarles Vilariño-Güell, Christian Wider, Owen A Ross, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 19, 2019
How to apply the movement disorder society criteria for diagnosis of progressive supranuclear palsyMax-Joseph Grimm, Gesine Respondek, Maria Stamelou, et al.
Medrxiv : the Preprint Server for Health Sciences|January 31, 2024
A pathogenic variant in RAB32 causes autosomal dominant Parkinson's disease and activates LRRK2 kinaseEmil K Gustavsson, Jordan Follett, Joanne Trinh, et al.
The Lancet. Neurology|April 13, 2024
RAB32 Ser71Arg in autosomal dominant Parkinson's disease: linkage, association, and functional analysesEmil K Gustavsson, Jordan Follett, Joanne Trinh, et al.
Pageof 11

Showing results (81-90 of 101) with videos related to

Sort By:
Pageof 11
Movement Disorders : Official Journal of the Movement Disorder Society|January 13, 2009
FGF20 and Parkinson's disease: no evidence of association or pathogenicity via alpha-synuclein expressionChristian Wider, Justus C Dachsel, Alexandra I Soto, et al.
Biorxiv : the Preprint Server for Biology|April 17, 2026
WDR44 drives de novo α-synuclein aggregation at the lysosomal membrane and promotes neuronal dysfunction in Parkinson's DiseaseMaxime Teixeira, Razan Sheta, Morgan Bérard, et al.
Brain : a Journal of Neurology|December 8, 2022
Mitochondrial DNA heteroplasmy distinguishes disease manifestation in PINK1/PRKN-linked Parkinson's diseaseJoanne Trinh, Andrew A Hicks, Inke R König, et al.
Iscience|September 20, 2019
Rewiring of the Human Mitochondrial Interactome during Neuronal Reprogramming Reveals Regulators of the Respirasome and NeurogenesisMohamed Taha Moutaoufik, Ramy Malty, Shahreen Amin, et al.
Tremor and Other Hyperkinetic Movements (New York, N.Y.)|February 16, 2026
Copy Number Variant Duplications Associated with Essential TremorMiranda Medeiros, Calwing Liao, Allison A Dilliott, et al.
Parkinsonism & Related Disorders|December 6, 2020
Exome-wide rare variant analysis in familial essential tremorMonica Diez-Fairen, Gabrielle Houle, Sara Ortega-Cubero, et al.
American Journal of Human Genetics|July 19, 2011
VPS35 mutations in Parkinson diseaseCarles Vilariño-Güell, Christian Wider, Owen A Ross, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 19, 2019
How to apply the movement disorder society criteria for diagnosis of progressive supranuclear palsyMax-Joseph Grimm, Gesine Respondek, Maria Stamelou, et al.
Medrxiv : the Preprint Server for Health Sciences|January 31, 2024
A pathogenic variant in RAB32 causes autosomal dominant Parkinson's disease and activates LRRK2 kinaseEmil K Gustavsson, Jordan Follett, Joanne Trinh, et al.
The Lancet. Neurology|April 13, 2024
RAB32 Ser71Arg in autosomal dominant Parkinson's disease: linkage, association, and functional analysesEmil K Gustavsson, Jordan Follett, Joanne Trinh, et al.
Pageof 11