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Movement Disorders : Official Journal of the Movement Disorder Society
|
October 20, 2020
Plasma Neurofilament Light as a Biomarker of Neurological Involvement in Wilson's Disease
Samuel Shribman, Carolin Heller, Maggie Burrows, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
May 29, 2023
A Double-Blind, Randomized, Placebo-Controlled Trial of Ursodeoxycholic Acid (UDCA) in Parkinson's Disease
Thomas Payne, Matthew Appleby, Ellen Buckley, et al.
Annals of Neurology
|
September 13, 2013
TigarB causes mitochondrial dysfunction and neuronal loss in PINK1 deficiency
Laura J Flinn, Marcus Keatinge, Sandrine Bretaud, et al.
Annals of Neurology
|
May 20, 2024
Polygenic Risk Scores Validated in Patient-Derived Cells Stratify for Mitochondrial Subtypes of Parkinson's Disease
Giuseppe Arena, Zied Landoulsi, Dajana Grossmann, et al.
Progress in Neurobiology
|
February 15, 2020
Deep phenotyping of peripheral tissue facilitates mechanistic disease stratification in sporadic Parkinson's disease
Phillippa J Carling, Heather Mortiboys, Claire Green, et al.
Human Molecular Genetics
|
September 18, 2015
Glucocerebrosidase 1 deficient Danio rerio mirror key pathological aspects of human Gaucher disease and provide evidence of early microglial activation preceding alpha-synuclein-independent neuronal cell death
Marcus Keatinge, Hai Bui, Aswin Menke, et al.
Brain : a Journal of Neurology
|
March 23, 2013
A genetic study of Wilson's disease in the United Kingdom
Alison J Coffey, Miranda Durkie, Stephen Hague, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
April 18, 2025
Treatment Selection and Prioritization for the EJS ACT-PD MAMS Trial Platform
Cristina Gonzalez-Robles, Dilan Athauda, Thomas R Barber, et al.
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of 9
Search research articles
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Showing results (81-90 of 88) with videos related to
Sort By:
Page
of 9
You have reached the last page of results.
This site can display upto 88 results.
Movement Disorders : Official Journal of the Movement Disorder Society
|
October 20, 2020
Plasma Neurofilament Light as a Biomarker of Neurological Involvement in Wilson's Disease
Samuel Shribman, Carolin Heller, Maggie Burrows, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
May 29, 2023
A Double-Blind, Randomized, Placebo-Controlled Trial of Ursodeoxycholic Acid (UDCA) in Parkinson's Disease
Thomas Payne, Matthew Appleby, Ellen Buckley, et al.
Annals of Neurology
|
September 13, 2013
TigarB causes mitochondrial dysfunction and neuronal loss in PINK1 deficiency
Laura J Flinn, Marcus Keatinge, Sandrine Bretaud, et al.
Annals of Neurology
|
May 20, 2024
Polygenic Risk Scores Validated in Patient-Derived Cells Stratify for Mitochondrial Subtypes of Parkinson's Disease
Giuseppe Arena, Zied Landoulsi, Dajana Grossmann, et al.
Progress in Neurobiology
|
February 15, 2020
Deep phenotyping of peripheral tissue facilitates mechanistic disease stratification in sporadic Parkinson's disease
Phillippa J Carling, Heather Mortiboys, Claire Green, et al.
Human Molecular Genetics
|
September 18, 2015
Glucocerebrosidase 1 deficient Danio rerio mirror key pathological aspects of human Gaucher disease and provide evidence of early microglial activation preceding alpha-synuclein-independent neuronal cell death
Marcus Keatinge, Hai Bui, Aswin Menke, et al.
Brain : a Journal of Neurology
|
March 23, 2013
A genetic study of Wilson's disease in the United Kingdom
Alison J Coffey, Miranda Durkie, Stephen Hague, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
April 18, 2025
Treatment Selection and Prioritization for the EJS ACT-PD MAMS Trial Platform
Cristina Gonzalez-Robles, Dilan Athauda, Thomas R Barber, et al.
Page
of 9