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Brain : a Journal of Neurology
|
May 25, 2016
Genetic and phenotypic characterization of complex hereditary spastic paraplegia
Eleanna Kara, Arianna Tucci, Claudia Manzoni, et al.
Current Opinion in Microbiology
|
February 18, 2024
Multi-layered genome defences in bacteria
Aleksei Agapov, Kate S Baker, Paritosh Bedekar, et al.
Parkinsonism & Related Disorders
|
May 27, 2026
Essential genetic testing in movement disorders - results from a Delphi study
Vanessa Carvalho, Leonor Correia Guedes, Emilia Gatto, et al.
Movement Disorders Clinical Practice
|
February 10, 2022
Biallelic Loss-of-Function <i>NDUFA12</i> Variants Cause a Wide Phenotypic Spectrum from Leigh/Leigh-Like Syndrome to Isolated Optic Atrophy
Francesca Magrinelli, Elisa Cali, Vinícius Lopes Braga, et al.
Brain : a Journal of Neurology
|
November 8, 2005
Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic data
Naheed L Khan, Shushant Jain, John M Lynch, et al.
Neurology
|
October 2, 2019
Stridor in multiple system atrophy: Consensus statement on diagnosis, prognosis, and treatment
Pietro Cortelli, Giovanna Calandra-Buonaura, Eduardo E Benarroch, et al.
The Journal of Clinical Investigation
|
May 3, 2008
GLUT1 mutations are a cause of paroxysmal exertion-induced dyskinesias and induce hemolytic anemia by a cation leak
Yvonne G Weber, Alexander Storch, Thomas V Wuttke, et al.
Parkinsonism & Related Disorders
|
April 11, 2021
Dysphagia in multiple system atrophy consensus statement on diagnosis, prognosis and treatment
Giovanna Calandra-Buonaura, Enrico Alfonsi, Luca Vignatelli, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
May 1, 2026
Distinct Brain Drivers and Shared Cerebello-Cortical Input in ADCY5 and SGCE Hyperkinetic Movements
Clément Tarrano, Cécile Galléa, Asya Ekmen, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
September 2, 2017
Treatable inherited rare movement disorders
H A Jinnah, Alberto Albanese, Kailash P Bhatia, et al.
Page
of 80
Search research articles
Search
Showing results (761-770 of 797) with videos related to
Sort By:
Page
of 80
Brain : a Journal of Neurology
|
May 25, 2016
Genetic and phenotypic characterization of complex hereditary spastic paraplegia
Eleanna Kara, Arianna Tucci, Claudia Manzoni, et al.
Current Opinion in Microbiology
|
February 18, 2024
Multi-layered genome defences in bacteria
Aleksei Agapov, Kate S Baker, Paritosh Bedekar, et al.
Parkinsonism & Related Disorders
|
May 27, 2026
Essential genetic testing in movement disorders - results from a Delphi study
Vanessa Carvalho, Leonor Correia Guedes, Emilia Gatto, et al.
Movement Disorders Clinical Practice
|
February 10, 2022
Biallelic Loss-of-Function <i>NDUFA12</i> Variants Cause a Wide Phenotypic Spectrum from Leigh/Leigh-Like Syndrome to Isolated Optic Atrophy
Francesca Magrinelli, Elisa Cali, Vinícius Lopes Braga, et al.
Brain : a Journal of Neurology
|
November 8, 2005
Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic data
Naheed L Khan, Shushant Jain, John M Lynch, et al.
Neurology
|
October 2, 2019
Stridor in multiple system atrophy: Consensus statement on diagnosis, prognosis, and treatment
Pietro Cortelli, Giovanna Calandra-Buonaura, Eduardo E Benarroch, et al.
The Journal of Clinical Investigation
|
May 3, 2008
GLUT1 mutations are a cause of paroxysmal exertion-induced dyskinesias and induce hemolytic anemia by a cation leak
Yvonne G Weber, Alexander Storch, Thomas V Wuttke, et al.
Parkinsonism & Related Disorders
|
April 11, 2021
Dysphagia in multiple system atrophy consensus statement on diagnosis, prognosis and treatment
Giovanna Calandra-Buonaura, Enrico Alfonsi, Luca Vignatelli, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
May 1, 2026
Distinct Brain Drivers and Shared Cerebello-Cortical Input in ADCY5 and SGCE Hyperkinetic Movements
Clément Tarrano, Cécile Galléa, Asya Ekmen, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
September 2, 2017
Treatable inherited rare movement disorders
H A Jinnah, Alberto Albanese, Kailash P Bhatia, et al.
Page
of 80