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Katie Sidle

Showing results (1-10 of 22) with videos related to

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Brain : a Journal of Neurology|March 10, 2022
The role of astrocytes in prion-like mechanisms of neurodegenerationPhillip Smethurst, Hannah Franklin, Benjamin E Clarke, et al.
Muscle & Nerve|July 23, 2013
An unusual presentation for SOD1-ALS: isolated facial diplegiaPietro Fratta, Michael G Hanna, Elizabeth M C Fisher, et al.
Practical Neurology|November 21, 2022
Globular glial tauopathy type IIPatrick W Cullinane, Katie Sidle, Kailash P Bhatia, et al.
Frontiers in Neurology|July 26, 2021
Administration of Riluzole Oral Suspension During the Different Stages of Amyotrophic Lateral SclerosisMónica Povedano Panades, Philippe Couratier, Katie Sidle, et al.
Neurobiology of Disease|September 4, 2016
In vitro prion-like behaviour of TDP-43 in ALSPhillip Smethurst, Jia Newcombe, Claire Troakes, et al.
The Cochrane Database of Systematic Reviews|February 22, 2023
Methods for informing people with amyotrophic lateral sclerosis/motor neuron disease of their diagnosisPaolo Bongioanni, Gian Domenico Borasio, David J Oliver, et al.
Brain : a Journal of Neurology|February 11, 2020
Distinct responses of neurons and astrocytes to TDP-43 proteinopathy in amyotrophic lateral sclerosisPhillip Smethurst, Emmanuel Risse, Giulia E Tyzack, et al.
Neurobiology of Aging|January 16, 2015
Investigation of next-generation sequencing technologies as a diagnostic tool for amyotrophic lateral sclerosisSarah Morgan, Maryam Shoai, Pietro Fratta, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|December 7, 2013
Profilin1 E117G is a moderate risk factor for amyotrophic lateral sclerosisPietro Fratta, James Charnock, Toby Collins, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|June 17, 2016
Systemic inflammatory response and neuromuscular involvement in amyotrophic lateral sclerosisChing-Hua Lu, Kezia Allen, Felicia Oei, et al.
Pageof 3

Showing results (1-10 of 22) with videos related to

Sort By:
Pageof 3
Brain : a Journal of Neurology|March 10, 2022
The role of astrocytes in prion-like mechanisms of neurodegenerationPhillip Smethurst, Hannah Franklin, Benjamin E Clarke, et al.
Muscle & Nerve|July 23, 2013
An unusual presentation for SOD1-ALS: isolated facial diplegiaPietro Fratta, Michael G Hanna, Elizabeth M C Fisher, et al.
Practical Neurology|November 21, 2022
Globular glial tauopathy type IIPatrick W Cullinane, Katie Sidle, Kailash P Bhatia, et al.
Frontiers in Neurology|July 26, 2021
Administration of Riluzole Oral Suspension During the Different Stages of Amyotrophic Lateral SclerosisMónica Povedano Panades, Philippe Couratier, Katie Sidle, et al.
Neurobiology of Disease|September 4, 2016
In vitro prion-like behaviour of TDP-43 in ALSPhillip Smethurst, Jia Newcombe, Claire Troakes, et al.
The Cochrane Database of Systematic Reviews|February 22, 2023
Methods for informing people with amyotrophic lateral sclerosis/motor neuron disease of their diagnosisPaolo Bongioanni, Gian Domenico Borasio, David J Oliver, et al.
Brain : a Journal of Neurology|February 11, 2020
Distinct responses of neurons and astrocytes to TDP-43 proteinopathy in amyotrophic lateral sclerosisPhillip Smethurst, Emmanuel Risse, Giulia E Tyzack, et al.
Neurobiology of Aging|January 16, 2015
Investigation of next-generation sequencing technologies as a diagnostic tool for amyotrophic lateral sclerosisSarah Morgan, Maryam Shoai, Pietro Fratta, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|December 7, 2013
Profilin1 E117G is a moderate risk factor for amyotrophic lateral sclerosisPietro Fratta, James Charnock, Toby Collins, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|June 17, 2016
Systemic inflammatory response and neuromuscular involvement in amyotrophic lateral sclerosisChing-Hua Lu, Kezia Allen, Felicia Oei, et al.
Pageof 3