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Journal of Neurology
|
July 6, 2026
Movement disorders in GLUT1 deficiency syndrome: a systematic review of the literature
Zeno Bercini, Annalisa Gessani, Jessica Rossi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
June 23, 2021
Potential PINK1 Founder Effect in Polynesia Causing Early-Onset Parkinson's Disease
Shilpan G Patel, Christina M Buchanan, Eoin Mulroy, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
September 6, 2025
Phenotypical Differentiation of Tremor Using Time Series Feature Extraction and Machine Learning
Verena Häring, Veronika Selzam, Juan Francisco Martin-Rodriguez, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
May 12, 2023
Longitudinal Synaptic Loss in Primary Tauopathies: An In Vivo [<sup>11</sup> C]UCB-J Positron Emission Tomography Study
Negin Holland, P Simon Jones, George Savulich, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
April 26, 2024
Differential Synaptic Loss in β-Amyloid Positive Versus β-Amyloid Negative Corticobasal Syndrome
Negin Holland, George Savulich, P Simon Jones, et al.
Nature Communications
|
December 19, 2023
Synaptic density affects clinical severity via network dysfunction in syndromes associated with frontotemporal lobar degeneration
David J Whiteside, Negin Holland, Kamen A Tsvetanov, et al.
Brain : a Journal of Neurology
|
August 28, 2020
A Māori specific RFC1 pathogenic repeat configuration in CANVAS, likely due to a founder allele
Sarah J Beecroft, Andrea Cortese, Roisin Sullivan, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
January 31, 2026
Psychiatric Disorders and Apathy in Mixed Movement Disorders Linked to ADCY5 (MxMD-ADCY5)
Aurélie Méneret, Clément Tarrano, Asya Ekmen, et al.
European Journal of Nuclear Medicine and Molecular Imaging
|
January 28, 2026
Loss of serotonergic function in carriers of PRKN mutations: a [<sup>11</sup>C]DASB PET study
Edoardo Rosario de Natale, Heather Wilson, Joji P Verghese, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
October 8, 2021
Dissecting the Phenotype and Genotype of PLA2G6-Related Parkinsonism
Francesca Magrinelli, Sahil Mehta, Giulia Di Lazzaro, et al.
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of 11
Search research articles
Search
Showing results (91-100 of 102) with videos related to
Sort By:
Page
of 11
Journal of Neurology
|
July 6, 2026
Movement disorders in GLUT1 deficiency syndrome: a systematic review of the literature
Zeno Bercini, Annalisa Gessani, Jessica Rossi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
June 23, 2021
Potential PINK1 Founder Effect in Polynesia Causing Early-Onset Parkinson's Disease
Shilpan G Patel, Christina M Buchanan, Eoin Mulroy, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
September 6, 2025
Phenotypical Differentiation of Tremor Using Time Series Feature Extraction and Machine Learning
Verena Häring, Veronika Selzam, Juan Francisco Martin-Rodriguez, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
May 12, 2023
Longitudinal Synaptic Loss in Primary Tauopathies: An In Vivo [<sup>11</sup> C]UCB-J Positron Emission Tomography Study
Negin Holland, P Simon Jones, George Savulich, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
April 26, 2024
Differential Synaptic Loss in β-Amyloid Positive Versus β-Amyloid Negative Corticobasal Syndrome
Negin Holland, George Savulich, P Simon Jones, et al.
Nature Communications
|
December 19, 2023
Synaptic density affects clinical severity via network dysfunction in syndromes associated with frontotemporal lobar degeneration
David J Whiteside, Negin Holland, Kamen A Tsvetanov, et al.
Brain : a Journal of Neurology
|
August 28, 2020
A Māori specific RFC1 pathogenic repeat configuration in CANVAS, likely due to a founder allele
Sarah J Beecroft, Andrea Cortese, Roisin Sullivan, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
January 31, 2026
Psychiatric Disorders and Apathy in Mixed Movement Disorders Linked to ADCY5 (MxMD-ADCY5)
Aurélie Méneret, Clément Tarrano, Asya Ekmen, et al.
European Journal of Nuclear Medicine and Molecular Imaging
|
January 28, 2026
Loss of serotonergic function in carriers of PRKN mutations: a [<sup>11</sup>C]DASB PET study
Edoardo Rosario de Natale, Heather Wilson, Joji P Verghese, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
October 8, 2021
Dissecting the Phenotype and Genotype of PLA2G6-Related Parkinsonism
Francesca Magrinelli, Sahil Mehta, Giulia Di Lazzaro, et al.
Page
of 11