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Brain : a Journal of Neurology
|
March 15, 2022
Diagnostic accuracy of cerebrospinal fluid biomarkers in genetic prion diseases
Matthias Schmitz, Anna Villar-Piqué, Peter Hermann, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
March 4, 2025
Spinocerebellar Ataxia Progression Measured with the Patient-Reported Outcome Measure of Ataxia
Anna L Burt, Gilbert L'Italien, Susan L Perlman, et al.
Nature Genetics
|
August 16, 2011
Exome sequencing identifies ACSF3 as a cause of combined malonic and methylmalonic aciduria
Jennifer L Sloan, Jennifer J Johnston, Irini Manoli, et al.
Cerebellum (London, England)
|
January 2, 2024
The Cerebellar Cognitive Affective/Schmahmann Syndrome Scale in Spinocerebellar Ataxias
Louisa P Selvadurai, Susan L Perlman, Tetsuo Ashizawa, et al.
Human Mutation
|
November 7, 2019
A diagnostic ceiling for exome sequencing in cerebellar ataxia and related neurological disorders
Kathie J Ngo, Jessica E Rexach, Hane Lee, et al.
Journal of Neurology
|
June 1, 2024
SARA captures disparate progression and responsiveness in spinocerebellar ataxias
Emilien Petit, Tanja Schmitz-Hübsch, Giulia Coarelli, et al.
Quality of Life Research : an International Journal of Quality of Life Aspects of Treatment, Care and Rehabilitation
|
August 15, 2016
HDQLIFE: development and assessment of health-related quality of life in Huntington disease (HD)
N E Carlozzi, S G Schilling, J-S Lai, et al.
Annals of Neurology
|
August 26, 2023
Detection of High-Risk Paraneoplastic Antibodies against TRIM9 and TRIM67 Proteins
Christopher M Bartley, Thomas T Ngo, Le Duy Do, et al.
Cerebellum (London, England)
|
August 12, 2022
The S-Factor, a New Measure of Disease Severity in Spinocerebellar Ataxia: Findings and Implications
Louisa P Selvadurai, Susan L Perlman, George R Wilmot, et al.
Neurology
|
June 8, 2019
Age at onset in genetic prion disease and the design of preventive clinical trials
Eric Vallabh Minikel, Sonia M Vallabh, Margaret C Orseth, et al.
Page
of 17
Search research articles
Search
Showing results (151-160 of 170) with videos related to
Sort By:
Page
of 17
Brain : a Journal of Neurology
|
March 15, 2022
Diagnostic accuracy of cerebrospinal fluid biomarkers in genetic prion diseases
Matthias Schmitz, Anna Villar-Piqué, Peter Hermann, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
March 4, 2025
Spinocerebellar Ataxia Progression Measured with the Patient-Reported Outcome Measure of Ataxia
Anna L Burt, Gilbert L'Italien, Susan L Perlman, et al.
Nature Genetics
|
August 16, 2011
Exome sequencing identifies ACSF3 as a cause of combined malonic and methylmalonic aciduria
Jennifer L Sloan, Jennifer J Johnston, Irini Manoli, et al.
Cerebellum (London, England)
|
January 2, 2024
The Cerebellar Cognitive Affective/Schmahmann Syndrome Scale in Spinocerebellar Ataxias
Louisa P Selvadurai, Susan L Perlman, Tetsuo Ashizawa, et al.
Human Mutation
|
November 7, 2019
A diagnostic ceiling for exome sequencing in cerebellar ataxia and related neurological disorders
Kathie J Ngo, Jessica E Rexach, Hane Lee, et al.
Journal of Neurology
|
June 1, 2024
SARA captures disparate progression and responsiveness in spinocerebellar ataxias
Emilien Petit, Tanja Schmitz-Hübsch, Giulia Coarelli, et al.
Quality of Life Research : an International Journal of Quality of Life Aspects of Treatment, Care and Rehabilitation
|
August 15, 2016
HDQLIFE: development and assessment of health-related quality of life in Huntington disease (HD)
N E Carlozzi, S G Schilling, J-S Lai, et al.
Annals of Neurology
|
August 26, 2023
Detection of High-Risk Paraneoplastic Antibodies against TRIM9 and TRIM67 Proteins
Christopher M Bartley, Thomas T Ngo, Le Duy Do, et al.
Cerebellum (London, England)
|
August 12, 2022
The S-Factor, a New Measure of Disease Severity in Spinocerebellar Ataxia: Findings and Implications
Louisa P Selvadurai, Susan L Perlman, George R Wilmot, et al.
Neurology
|
June 8, 2019
Age at onset in genetic prion disease and the design of preventive clinical trials
Eric Vallabh Minikel, Sonia M Vallabh, Margaret C Orseth, et al.
Page
of 17