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JAMA Neurology
|
February 19, 2014
Mutations in GNAL: a novel cause of craniocervical dystonia
Kishore R Kumar, Katja Lohmann, Ikuo Masuho, et al.
Alzheimer'S Research & Therapy
|
August 21, 2016
A call for comparative effectiveness research to learn whether routine clinical care decisions can protect from dementia and cognitive decline
Penny A Dacks, Joshua J Armstrong, Stephen K Brannan, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
June 27, 2023
Genetic Testing in Parkinson's Disease
Gian Pal, Lola Cook, Jeanine Schulze, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
July 15, 2020
Nonsteroidal Anti-inflammatory Use and LRRK2 Parkinson's Disease Penetrance
Marta San Luciano, Caroline M Tanner, Cheryl Meng, et al.
Journal of Inherited Metabolic Disease
|
November 15, 2025
Liver Involvement in POLG Disease-a Multicentre Cohort Study of 202 Patients
Erle Kristensen, Karin Naess, Martin Engvall, et al.
ALTEX
|
January 18, 2025
Mapping out strategies to further develop human-relevant, new approach methodology (NAM)-based developmental neurotoxicity (DNT) testing
Eike Cöllen, Kristina Bartmann, Jonathan Blum, et al.
Cancers
|
April 23, 2022
Establishment of Novel Neuroendocrine Carcinoma Patient-Derived Xenograft Models for Receptor Peptide-Targeted Therapy
Catherine G Tran, Luis C Borbon, Jacqueline L Mudd, et al.
Annals of Neurology
|
November 9, 2024
Goal-Directed Rehabilitation Versus Standard Care for Individuals with Hereditary Cerebellar Ataxia: A Multicenter, Single-Blind, Randomized Controlled Superiority Trial
Sarah C Milne, Melissa Roberts, Shannon Williams, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
June 13, 2023
International Genetic Testing and Counseling Practices for Parkinson's Disease
Rachel Saunders-Pullman, Deborah Raymond, Roberto A Ortega, et al.
Annals of Neurology
|
April 19, 2013
Whispering dysphonia (DYT4 dystonia) is caused by a mutation in the TUBB4 gene
Katja Lohmann, Robert A Wilcox, Susen Winkler, et al.
Page
of 42
Search research articles
Search
Showing results (391-400 of 415) with videos related to
Sort By:
Page
of 42
JAMA Neurology
|
February 19, 2014
Mutations in GNAL: a novel cause of craniocervical dystonia
Kishore R Kumar, Katja Lohmann, Ikuo Masuho, et al.
Alzheimer'S Research & Therapy
|
August 21, 2016
A call for comparative effectiveness research to learn whether routine clinical care decisions can protect from dementia and cognitive decline
Penny A Dacks, Joshua J Armstrong, Stephen K Brannan, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
June 27, 2023
Genetic Testing in Parkinson's Disease
Gian Pal, Lola Cook, Jeanine Schulze, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
July 15, 2020
Nonsteroidal Anti-inflammatory Use and LRRK2 Parkinson's Disease Penetrance
Marta San Luciano, Caroline M Tanner, Cheryl Meng, et al.
Journal of Inherited Metabolic Disease
|
November 15, 2025
Liver Involvement in POLG Disease-a Multicentre Cohort Study of 202 Patients
Erle Kristensen, Karin Naess, Martin Engvall, et al.
ALTEX
|
January 18, 2025
Mapping out strategies to further develop human-relevant, new approach methodology (NAM)-based developmental neurotoxicity (DNT) testing
Eike Cöllen, Kristina Bartmann, Jonathan Blum, et al.
Cancers
|
April 23, 2022
Establishment of Novel Neuroendocrine Carcinoma Patient-Derived Xenograft Models for Receptor Peptide-Targeted Therapy
Catherine G Tran, Luis C Borbon, Jacqueline L Mudd, et al.
Annals of Neurology
|
November 9, 2024
Goal-Directed Rehabilitation Versus Standard Care for Individuals with Hereditary Cerebellar Ataxia: A Multicenter, Single-Blind, Randomized Controlled Superiority Trial
Sarah C Milne, Melissa Roberts, Shannon Williams, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
June 13, 2023
International Genetic Testing and Counseling Practices for Parkinson's Disease
Rachel Saunders-Pullman, Deborah Raymond, Roberto A Ortega, et al.
Annals of Neurology
|
April 19, 2013
Whispering dysphonia (DYT4 dystonia) is caused by a mutation in the TUBB4 gene
Katja Lohmann, Robert A Wilcox, Susen Winkler, et al.
Page
of 42