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Sonja W Scholz

Showing results (1-10 of 142) with videos related to

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The Lancet. Neurology|October 15, 2017
Restless legs syndrome: is it all in the genes?Sonja W Scholz
Human Mutation|October 29, 2009
PINK1 mutations: does the dosage make the poison?Sonja W Scholz
Neurology|March 29, 2017
Author response: A genome-wide association study in multiple system atrophySonja W Scholz, Henry Houlden
Movement Disorders : Official Journal of the Movement Disorder Society|January 12, 2018
Identification of new α-synuclein regulator by nontraditional drug development pipelineXi Chen, Sonja W Scholz
International Journal of Molecular Sciences|October 27, 2015
Genetics Underlying Atypical Parkinsonism and Related Neurodegenerative DisordersSonja W Scholz, Jose Bras
Continuum (Minneapolis, Minn.)|December 2, 2024
Genetics and Neuropathology of Neurodegenerative DementiasSonja W Scholz, Inma Cobos
Neurology|February 6, 2015
GBA mutations and Parkinson disease: when genotype meets phenotypeSonja W Scholz, Beom S Jeon
Movement Disorders : Official Journal of the Movement Disorder Society|January 25, 2019
DNA typos spell trouble: Somatic mutations as a cause of idiopathic neurodegenerative diseases?Marya S Sabir, Sonja W Scholz
Movement Disorders : Official Journal of the Movement Disorder Society|November 27, 2020
Hot Topic: Epigenetics in Parkinson's Disease: A New Frontier for Disease-Modifying TherapiesMakayla K Portley, Sonja W Scholz
Brain : a Journal of Neurology|May 24, 2023
Precision diagnosis and staging of TDP-43 proteinopathies: harnessing the power of artificial intelligenceRichard A Hickman, Sonja W Scholz
Pageof 15

Showing results (1-10 of 142) with videos related to

Sort By:
Pageof 15
The Lancet. Neurology|October 15, 2017
Restless legs syndrome: is it all in the genes?Sonja W Scholz
Human Mutation|October 29, 2009
PINK1 mutations: does the dosage make the poison?Sonja W Scholz
Neurology|March 29, 2017
Author response: A genome-wide association study in multiple system atrophySonja W Scholz, Henry Houlden
Movement Disorders : Official Journal of the Movement Disorder Society|January 12, 2018
Identification of new α-synuclein regulator by nontraditional drug development pipelineXi Chen, Sonja W Scholz
International Journal of Molecular Sciences|October 27, 2015
Genetics Underlying Atypical Parkinsonism and Related Neurodegenerative DisordersSonja W Scholz, Jose Bras
Continuum (Minneapolis, Minn.)|December 2, 2024
Genetics and Neuropathology of Neurodegenerative DementiasSonja W Scholz, Inma Cobos
Neurology|February 6, 2015
GBA mutations and Parkinson disease: when genotype meets phenotypeSonja W Scholz, Beom S Jeon
Movement Disorders : Official Journal of the Movement Disorder Society|January 25, 2019
DNA typos spell trouble: Somatic mutations as a cause of idiopathic neurodegenerative diseases?Marya S Sabir, Sonja W Scholz
Movement Disorders : Official Journal of the Movement Disorder Society|November 27, 2020
Hot Topic: Epigenetics in Parkinson's Disease: A New Frontier for Disease-Modifying TherapiesMakayla K Portley, Sonja W Scholz
Brain : a Journal of Neurology|May 24, 2023
Precision diagnosis and staging of TDP-43 proteinopathies: harnessing the power of artificial intelligenceRichard A Hickman, Sonja W Scholz
Pageof 15