Showing results (131-140 of 163) with videos related to
Sort By:
Pageof 17
Psychosomatic Medicine|December 17, 2008
Changes in cortical potential associated with modulation of peripheral sympathetic activity in patients with epilepsyYoko Nagai, Hugo D Critchley, John C Rothwell, et al.Muscle & Nerve|July 23, 2013
Vascular endothelial growth factor and amyotrophic lateral sclerosis: the interplay with exercise and noninvasive ventilationRita Carilho, Mamede de Carvalho, Michael Swash, et al.Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|May 5, 2022
Respiratory onset in amyotrophic lateral sclerosis: clinical features and spreading patternSusana Pinto, Marta Gromicho, Miguel Oliveira Oliveira Santos, et al.Annals of Translational Medicine|May 9, 2024
A brief physiology and pathophysiology of the anorectum based on the Integral Theory paradigmDarren M Gold, Michael Swash, Ahmed Farag, et al.Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|December 24, 2023
A neurophysiological approach to mirror movements in amyotrophic lateral sclerosisJosé Castro, Tomás Pedrosa, Inês Alves, et al.Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders : Official Publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases|July 23, 2005
Neurophysiological measures in amyotrophic lateral sclerosis: markers of progression in clinical trialsMamede de Carvalho, Adriano Chio, Reinhard Dengler, et al.Journal of Neurology|April 8, 2020
Diaphragmatic CMAP amplitude from phrenic nerve stimulation predicts functional decline in ALSBruno Miranda, Marta Gromicho, Mariana Pereira, et al.Epilepsy & Behavior : E&B|August 30, 2008
On the prevalence of bipolar disorder in epilepsyMarco Mula, Bettina Schmitz, Regina Jauch, et al.Clinical Neurophysiology Practice|May 29, 2024
Revisiting the compound muscle action potential (CMAP)Paul E Barkhaus, Sanjeev D Nandedkar, Mamede de Carvalho, et al.Neuromuscular Disorders : NMD|March 24, 2009
Late-onset axial myopathy with cores due to a novel heterozygous dominant mutation in the skeletal muscle ryanodine receptor (RYR1) geneHeinz Jungbluth, Suzanne Lillis, Haiyan Zhou, et al.Pageof 17