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JAMA
|
March 20, 2024
Skin Biopsy Detection of Phosphorylated α-Synuclein in Patients With Synucleinopathies
Christopher H Gibbons, Todd Levine, Charles Adler, et al.
The Journal of Neuropsychiatry and Clinical Neurosciences
|
May 12, 2025
Suicidal Ideation in Spinocerebellar Ataxia
Levi Peppel, Ruo-Yah Lai, Christian Rummey, et al.
Cognitive and Behavioral Neurology : Official Journal of the Society for Behavioral and Cognitive Neurology
|
May 8, 2024
Promoting Growth in Behavioral Neurology: A Path Forward
James R Bateman, Sylvia Josephy-Hernandez, Liana G Apostolova, et al.
Movement Disorders Clinical Practice
|
February 29, 2024
Fatigue Impacts Quality of Life in People with Spinocerebellar Ataxias
Ruo-Yah Lai, Christian Rummey, Christian J Amlang, et al.
Brain : a Journal of Neurology
|
January 27, 2025
Multiomic analyses direct hypotheses for Creutzfeldt-Jakob disease risk genes
Fahri Küçükali, Elizabeth Hill, Tijs Watzeels, et al.
Plos One
|
July 30, 2024
Genome wide association study of clinical duration and age at onset of sporadic CJD
Holger Hummerich, Helen Speedy, Tracy Campbell, et al.
Cerebellum (London, England)
|
November 11, 2025
Correction: The Natural History Study and Biomarker Collection of the Clinical Research Consortium for the Study of Cerebellar Ataxia (CRC-SCA)
Yicheng Lin, Nadia Amokrane, Sandie Worley, et al.
Cerebellum (London, England)
|
July 18, 2025
The Natural History Study and Biomarker Collection of the Clinical Research Consortium for the Study of Cerebellar Ataxia (CRC-SCA)
Yicheng Lin, Nadia Amokrane, Sandie Worley, et al.
The Lancet. Neurology
|
September 19, 2020
Identification of novel risk loci and causal insights for sporadic Creutzfeldt-Jakob disease: a genome-wide association study
Emma Jones, Holger Hummerich, Emmanuelle Viré, et al.
Human Molecular Genetics
|
May 5, 2012
Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases
Giovanni Coppola, Subashchandrabose Chinnathambi, Jason JiYong Lee, et al.
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Showing results (161-170 of 170) with videos related to
Sort By:
Page
of 17
You have reached the last page of results.
This site can display upto 170 results.
JAMA
|
March 20, 2024
Skin Biopsy Detection of Phosphorylated α-Synuclein in Patients With Synucleinopathies
Christopher H Gibbons, Todd Levine, Charles Adler, et al.
The Journal of Neuropsychiatry and Clinical Neurosciences
|
May 12, 2025
Suicidal Ideation in Spinocerebellar Ataxia
Levi Peppel, Ruo-Yah Lai, Christian Rummey, et al.
Cognitive and Behavioral Neurology : Official Journal of the Society for Behavioral and Cognitive Neurology
|
May 8, 2024
Promoting Growth in Behavioral Neurology: A Path Forward
James R Bateman, Sylvia Josephy-Hernandez, Liana G Apostolova, et al.
Movement Disorders Clinical Practice
|
February 29, 2024
Fatigue Impacts Quality of Life in People with Spinocerebellar Ataxias
Ruo-Yah Lai, Christian Rummey, Christian J Amlang, et al.
Brain : a Journal of Neurology
|
January 27, 2025
Multiomic analyses direct hypotheses for Creutzfeldt-Jakob disease risk genes
Fahri Küçükali, Elizabeth Hill, Tijs Watzeels, et al.
Plos One
|
July 30, 2024
Genome wide association study of clinical duration and age at onset of sporadic CJD
Holger Hummerich, Helen Speedy, Tracy Campbell, et al.
Cerebellum (London, England)
|
November 11, 2025
Correction: The Natural History Study and Biomarker Collection of the Clinical Research Consortium for the Study of Cerebellar Ataxia (CRC-SCA)
Yicheng Lin, Nadia Amokrane, Sandie Worley, et al.
Cerebellum (London, England)
|
July 18, 2025
The Natural History Study and Biomarker Collection of the Clinical Research Consortium for the Study of Cerebellar Ataxia (CRC-SCA)
Yicheng Lin, Nadia Amokrane, Sandie Worley, et al.
The Lancet. Neurology
|
September 19, 2020
Identification of novel risk loci and causal insights for sporadic Creutzfeldt-Jakob disease: a genome-wide association study
Emma Jones, Holger Hummerich, Emmanuelle Viré, et al.
Human Molecular Genetics
|
May 5, 2012
Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases
Giovanni Coppola, Subashchandrabose Chinnathambi, Jason JiYong Lee, et al.
Page
of 17