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Brain : a Journal of Neurology
|
October 28, 2025
Predictive models for ataxia progression and conversion in spinocerebellar ataxia type 1 and 3
Emilien Petit, Giulia Coarelli, David Morgan, 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.
Annals of Neurology
|
September 12, 2024
Clinical, Radiological and Pathological Features of a Large American Cohort of Spinocerebellar Ataxia (SCA27B)
Widad Abou Chaar, Anirudh N Eranki, Hannah A Stevens, 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.
Alzheimer'S Research & Therapy
|
March 15, 2019
Lewy Body Dementia Association's Research Centers of Excellence Program: Inaugural Meeting Proceedings
Bethany Peterson, Melissa Armstrong, Douglas Galasko, et al.
Nature Genetics
|
May 5, 2015
Mutations in XPR1 cause primary familial brain calcification associated with altered phosphate export
Andrea Legati, Donatella Giovannini, Gaël Nicolas, 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.
Movement Disorders : Official Journal of the Movement Disorder Society
|
May 11, 2026
A Severity-Agnostic Atrophy Pattern in Spinocerebellar Ataxia Type 3: Volumetrics from ENIGMA-Ataxia
Jason W Robertson, Isaac Adanyeguh, David J Arpin, 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.
Neurogenetics
|
January 22, 2013
Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification
Sandy Chan Hsu, Renee L Sears, Roberta R Lemos, et al.
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of 7
Search research articles
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Showing results (51-60 of 64) with videos related to
Sort By:
Page
of 7
Brain : a Journal of Neurology
|
October 28, 2025
Predictive models for ataxia progression and conversion in spinocerebellar ataxia type 1 and 3
Emilien Petit, Giulia Coarelli, David Morgan, 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.
Annals of Neurology
|
September 12, 2024
Clinical, Radiological and Pathological Features of a Large American Cohort of Spinocerebellar Ataxia (SCA27B)
Widad Abou Chaar, Anirudh N Eranki, Hannah A Stevens, 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.
Alzheimer'S Research & Therapy
|
March 15, 2019
Lewy Body Dementia Association's Research Centers of Excellence Program: Inaugural Meeting Proceedings
Bethany Peterson, Melissa Armstrong, Douglas Galasko, et al.
Nature Genetics
|
May 5, 2015
Mutations in XPR1 cause primary familial brain calcification associated with altered phosphate export
Andrea Legati, Donatella Giovannini, Gaël Nicolas, 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.
Movement Disorders : Official Journal of the Movement Disorder Society
|
May 11, 2026
A Severity-Agnostic Atrophy Pattern in Spinocerebellar Ataxia Type 3: Volumetrics from ENIGMA-Ataxia
Jason W Robertson, Isaac Adanyeguh, David J Arpin, 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.
Neurogenetics
|
January 22, 2013
Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification
Sandy Chan Hsu, Renee L Sears, Roberta R Lemos, et al.
Page
of 7