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Neuro-Degenerative Diseases
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May 31, 2017
SLC25A46 Mutations Associated with Autosomal Recessive Cerebellar Ataxia in North African Families
Monia B Hammer, Jinhui Ding, Fanny Mochel, et al.
Neuro-Degenerative Diseases
|
July 12, 2007
Comprehensive screening of a North American Parkinson's disease cohort for LRRK2 mutation
Janel Johnson, Coro Paisán-Ruíz, Grisel Lopez, et al.
Neurobiology of Disease
|
June 18, 2016
Next-generation sequencing reveals substantial genetic contribution to dementia with Lewy bodies
Joshua T Geiger, Jinhui Ding, Barbara Crain, et al.
American Journal of Human Genetics
|
January 22, 2013
Mutations in GBA2 cause autosomal-recessive cerebellar ataxia with spasticity
Monia B Hammer, Ghada Eleuch-Fayache, Lucia V Schottlaender, et al.
Human Molecular Genetics
|
September 24, 2013
Genetic comorbidities in Parkinson's disease
Mike A Nalls, Mohamad Saad, Alastair J Noyce, et al.
Nature Genetics
|
December 28, 2023
Multi-ancestry genome-wide association meta-analysis of Parkinson's disease
Jonggeol Jeffrey Kim, Dan Vitale, Diego Véliz Otani, et al.
Medrxiv : the Preprint Server for Health Sciences
|
November 21, 2023
Investigation of the genetic aetiology of Lewy body diseases with and without dementia
Lesley Wu, Raquel Real, Alejandro Martinez, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 27, 2016
Menopause accelerates biological aging
Morgan E Levine, Ake T Lu, Brian H Chen, et al.
Nature Neuroscience
|
August 11, 2022
A CRISPRi/a platform in human iPSC-derived microglia uncovers regulators of disease states
Nina M Dräger, Sydney M Sattler, Cindy Tzu-Ling Huang, et al.
NPJ Parkinson'S Disease
|
December 16, 2022
Identification and prediction of Parkinson's disease subtypes and progression using machine learning in two cohorts
Anant Dadu, Vipul Satone, Rachneet Kaur, et al.
Page
of 40
Search research articles
Search
Showing results (201-210 of 397) with videos related to
Sort By:
Page
of 40
Neuro-Degenerative Diseases
|
May 31, 2017
SLC25A46 Mutations Associated with Autosomal Recessive Cerebellar Ataxia in North African Families
Monia B Hammer, Jinhui Ding, Fanny Mochel, et al.
Neuro-Degenerative Diseases
|
July 12, 2007
Comprehensive screening of a North American Parkinson's disease cohort for LRRK2 mutation
Janel Johnson, Coro Paisán-Ruíz, Grisel Lopez, et al.
Neurobiology of Disease
|
June 18, 2016
Next-generation sequencing reveals substantial genetic contribution to dementia with Lewy bodies
Joshua T Geiger, Jinhui Ding, Barbara Crain, et al.
American Journal of Human Genetics
|
January 22, 2013
Mutations in GBA2 cause autosomal-recessive cerebellar ataxia with spasticity
Monia B Hammer, Ghada Eleuch-Fayache, Lucia V Schottlaender, et al.
Human Molecular Genetics
|
September 24, 2013
Genetic comorbidities in Parkinson's disease
Mike A Nalls, Mohamad Saad, Alastair J Noyce, et al.
Nature Genetics
|
December 28, 2023
Multi-ancestry genome-wide association meta-analysis of Parkinson's disease
Jonggeol Jeffrey Kim, Dan Vitale, Diego Véliz Otani, et al.
Medrxiv : the Preprint Server for Health Sciences
|
November 21, 2023
Investigation of the genetic aetiology of Lewy body diseases with and without dementia
Lesley Wu, Raquel Real, Alejandro Martinez, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 27, 2016
Menopause accelerates biological aging
Morgan E Levine, Ake T Lu, Brian H Chen, et al.
Nature Neuroscience
|
August 11, 2022
A CRISPRi/a platform in human iPSC-derived microglia uncovers regulators of disease states
Nina M Dräger, Sydney M Sattler, Cindy Tzu-Ling Huang, et al.
NPJ Parkinson'S Disease
|
December 16, 2022
Identification and prediction of Parkinson's disease subtypes and progression using machine learning in two cohorts
Anant Dadu, Vipul Satone, Rachneet Kaur, et al.
Page
of 40