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Peter Bede

Showing results (101-110 of 179) with videos related to

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Journal of the Neurological Sciences|December 7, 2021
Phenotypic categorisation of individual subjects with motor neuron disease based on radiological disease burden patterns: A machine-learning approachPeter Bede, Aizuri Murad, Jasmin Lope, et al.
BMJ Supportive & Palliative Care|March 22, 2014
Palliative care in amyotrophic lateral sclerosis: a review of current international guidelines and initiativesPeter Bede, David Oliver, James Stodart, et al.
Journal of Neurotrauma|November 13, 2018
Furosemide Unmasks Inhibitory Dysfunction after Spinal Cord Injury in Humans: Implications for SpasticityWanalee Klomjai, Nicolas Roche, Jean-Charles Lamy, et al.
European Journal of Neurology|May 10, 2025
Progressive Thalamo-Cortical Disconnection in Amyotrophic Lateral Sclerosis Genotypes: Structural Degeneration and Network Dysfunction of Thalamus-Relayed CircuitsMarlene Tahedl, Jana Kleinerova, Mark A Doherty, et al.
Biomedicines|March 28, 2025
Sensory Dysfunction in ALS and Other Motor Neuron Diseases: Clinical Relevance, Histopathology, Neurophysiology, and Insights from NeuroimagingJana Kleinerova, Rangariroyashe H Chipika, Ee Ling Tan, et al.
Journal of Integrative Neuroscience|May 28, 2022
Neurometabolic Alterations in Motor Neuron Disease: Insights from Magnetic Resonance SpectroscopyFoteini Christidi, Efstratios Karavasilis, Georgios D Argyropoulos, et al.
Annals of Neurology|July 10, 2013
Aggregation of neurologic and neuropsychiatric disease in amyotrophic lateral sclerosis kindreds: a population-based case-control cohort study of familial and sporadic amyotrophic lateral sclerosisSusan Byrne, Mark Heverin, Marwa Elamin, et al.
Cognitive and Behavioral Neurology : Official Journal of the Society for Behavioral and Cognitive Neurology|March 2, 2021
Neuropsychological Assessment Should Always be Considered in Myotonic Dystrophy Type 2Thomas Theodosiou, Foteini Christidi, Sofia Xirou, et al.
Neurology|April 5, 2013
Cognitive changes predict functional decline in ALS: a population-based longitudinal studyMarwa Elamin, Peter Bede, Susan Byrne, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|April 1, 2026
Impaired kinesthesia and cerebral integration during tendon vibration in amyotrophic lateral sclerosisArnaud Preuilh, Alexandra Lackmy-Vallée, Benoit Béranger, et al.
Pageof 18

Showing results (101-110 of 179) with videos related to

Sort By:
Pageof 18
Journal of the Neurological Sciences|December 7, 2021
Phenotypic categorisation of individual subjects with motor neuron disease based on radiological disease burden patterns: A machine-learning approachPeter Bede, Aizuri Murad, Jasmin Lope, et al.
BMJ Supportive & Palliative Care|March 22, 2014
Palliative care in amyotrophic lateral sclerosis: a review of current international guidelines and initiativesPeter Bede, David Oliver, James Stodart, et al.
Journal of Neurotrauma|November 13, 2018
Furosemide Unmasks Inhibitory Dysfunction after Spinal Cord Injury in Humans: Implications for SpasticityWanalee Klomjai, Nicolas Roche, Jean-Charles Lamy, et al.
European Journal of Neurology|May 10, 2025
Progressive Thalamo-Cortical Disconnection in Amyotrophic Lateral Sclerosis Genotypes: Structural Degeneration and Network Dysfunction of Thalamus-Relayed CircuitsMarlene Tahedl, Jana Kleinerova, Mark A Doherty, et al.
Biomedicines|March 28, 2025
Sensory Dysfunction in ALS and Other Motor Neuron Diseases: Clinical Relevance, Histopathology, Neurophysiology, and Insights from NeuroimagingJana Kleinerova, Rangariroyashe H Chipika, Ee Ling Tan, et al.
Journal of Integrative Neuroscience|May 28, 2022
Neurometabolic Alterations in Motor Neuron Disease: Insights from Magnetic Resonance SpectroscopyFoteini Christidi, Efstratios Karavasilis, Georgios D Argyropoulos, et al.
Annals of Neurology|July 10, 2013
Aggregation of neurologic and neuropsychiatric disease in amyotrophic lateral sclerosis kindreds: a population-based case-control cohort study of familial and sporadic amyotrophic lateral sclerosisSusan Byrne, Mark Heverin, Marwa Elamin, et al.
Cognitive and Behavioral Neurology : Official Journal of the Society for Behavioral and Cognitive Neurology|March 2, 2021
Neuropsychological Assessment Should Always be Considered in Myotonic Dystrophy Type 2Thomas Theodosiou, Foteini Christidi, Sofia Xirou, et al.
Neurology|April 5, 2013
Cognitive changes predict functional decline in ALS: a population-based longitudinal studyMarwa Elamin, Peter Bede, Susan Byrne, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|April 1, 2026
Impaired kinesthesia and cerebral integration during tendon vibration in amyotrophic lateral sclerosisArnaud Preuilh, Alexandra Lackmy-Vallée, Benoit Béranger, et al.
Pageof 18