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Annals of Neurology
|
May 29, 2009
SNCA variants are associated with increased risk for multiple system atrophy
Sonja W Scholz, Henry Houlden, Claudia Schulte, et al.
The Journal of Clinical Investigation
|
April 21, 2026
Pathogenic variants in BORCS5 Cause a Spectrum of Neurodevelopmental and Neurodegenerative Disorders with Lysosomal Dysfunction
Niccolò E Mencacci, Georgia Minakaki, Reza Maroofian, et al.
Hepatology International
|
September 1, 2017
Liver failure determines the outcome in patients of acute-on-chronic liver failure (ACLF): comparison of APASL ACLF research consortium (AARC) and CLIF-SOFA models
A Choudhury, A Jindal, R Maiwall, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
May 14, 2017
Which ante mortem clinical features predict progressive supranuclear palsy pathology?
Gesine Respondek, Carolin Kurz, Thomas Arzberger, et al.
Neurology
|
September 16, 2016
A genome-wide association study in multiple system atrophy
Anna Sailer, Sonja W Scholz, Michael A Nalls, et al.
Brain : a Journal of Neurology
|
July 5, 2014
Parkinson's disease in GTP cyclohydrolase 1 mutation carriers
Niccolò E Mencacci, Ioannis U Isaias, Martin M Reich, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
May 4, 2017
Clinical diagnosis of progressive supranuclear palsy: The movement disorder society criteria
Günter U Höglinger, Gesine Respondek, Maria Stamelou, et al.
NPJ Parkinson'S Disease
|
March 30, 2024
Genotype-phenotype correlation in PRKN-associated Parkinson's disease
Poornima Jayadev Menon, Sara Sambin, Baptiste Criniere-Boizet, et al.
Mechanisms of Ageing and Development
|
January 1, 2021
A geroscience approach for Parkinson's disease: Conceptual framework and design of PROPAG-AGEING project
Chiara Pirazzini, Tiago Azevedo, Luca Baldelli, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
January 19, 2026
International Registry of NKX2-1-Related Disorders: Clinical, Genetic, and Imaging Perspectives
Laia Nou-Fontanet, Claudia Ravelli, Lydie Burglen, et al.
Page
of 80
Search research articles
Search
Showing results (781-790 of 797) with videos related to
Sort By:
Page
of 80
Annals of Neurology
|
May 29, 2009
SNCA variants are associated with increased risk for multiple system atrophy
Sonja W Scholz, Henry Houlden, Claudia Schulte, et al.
The Journal of Clinical Investigation
|
April 21, 2026
Pathogenic variants in BORCS5 Cause a Spectrum of Neurodevelopmental and Neurodegenerative Disorders with Lysosomal Dysfunction
Niccolò E Mencacci, Georgia Minakaki, Reza Maroofian, et al.
Hepatology International
|
September 1, 2017
Liver failure determines the outcome in patients of acute-on-chronic liver failure (ACLF): comparison of APASL ACLF research consortium (AARC) and CLIF-SOFA models
A Choudhury, A Jindal, R Maiwall, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
May 14, 2017
Which ante mortem clinical features predict progressive supranuclear palsy pathology?
Gesine Respondek, Carolin Kurz, Thomas Arzberger, et al.
Neurology
|
September 16, 2016
A genome-wide association study in multiple system atrophy
Anna Sailer, Sonja W Scholz, Michael A Nalls, et al.
Brain : a Journal of Neurology
|
July 5, 2014
Parkinson's disease in GTP cyclohydrolase 1 mutation carriers
Niccolò E Mencacci, Ioannis U Isaias, Martin M Reich, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
May 4, 2017
Clinical diagnosis of progressive supranuclear palsy: The movement disorder society criteria
Günter U Höglinger, Gesine Respondek, Maria Stamelou, et al.
NPJ Parkinson'S Disease
|
March 30, 2024
Genotype-phenotype correlation in PRKN-associated Parkinson's disease
Poornima Jayadev Menon, Sara Sambin, Baptiste Criniere-Boizet, et al.
Mechanisms of Ageing and Development
|
January 1, 2021
A geroscience approach for Parkinson's disease: Conceptual framework and design of PROPAG-AGEING project
Chiara Pirazzini, Tiago Azevedo, Luca Baldelli, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
January 19, 2026
International Registry of NKX2-1-Related Disorders: Clinical, Genetic, and Imaging Perspectives
Laia Nou-Fontanet, Claudia Ravelli, Lydie Burglen, et al.
Page
of 80