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Journal of Neurology
|
October 15, 2013
Marked phenotypic variability in two siblings with congenital myasthenic syndrome due to mutations in MUSK
Lorenzo Maggi, R Brugnoni, V Scaioli, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
November 19, 2004
Subcortical nodular heterotopia: a functional MRI and somatosensory evoked potentials study
F Villani, P Vitali, V Scaioli, et al.
Neurology
|
December 30, 2004
Sensorimotor cortex excitability in Unverricht-Lundborg disease and Lafora body disease
L Canafoglia, C Ciano, F Panzica, et al.
Brain Research Bulletin
|
July 6, 2010
Event-related potential (ERP) markers of melodic processing: The N2 component is modulated by structural complexity, not by melodic 'meaningfulness'
L Minati, L Salvatoni, C Rosazza, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology
|
March 29, 2005
FVEPs in Creutzfeldt-Jacob disease: waveforms and interaction with the periodic EEG pattern assessed by single sweep analysis
E Visani, P Agazzi, V Scaioli, et al.
Neurology
|
November 17, 2010
Four novel cases of periaxin-related neuropathy and review of the literature
C Marchesi, M Milani, M Morbin, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology
|
August 2, 2014
Significance of multiple neurophysiological measures in patients with chronic disorders of consciousness
Davide Rossi Sebastiano, F Panzica, E Visani, et al.
Neurology
|
March 3, 2010
Vitamin E neuroprotection for cisplatin neuropathy: a randomized, placebo-controlled trial
A Pace, D Giannarelli, E Galiè, et al.
Neurology
|
March 15, 2006
Novel mutations in the HSN2 gene causing hereditary sensory and autonomic neuropathy type II
K Coen, D Pareyson, M Auer-Grumbach, et al.
Page
of 5
Search research articles
Search
Showing results (41-50 of 49) with videos related to
Sort By:
Page
of 5
You have reached the last page of results.
This site can display upto 49 results.
Journal of Neurology
|
October 15, 2013
Marked phenotypic variability in two siblings with congenital myasthenic syndrome due to mutations in MUSK
Lorenzo Maggi, R Brugnoni, V Scaioli, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
November 19, 2004
Subcortical nodular heterotopia: a functional MRI and somatosensory evoked potentials study
F Villani, P Vitali, V Scaioli, et al.
Neurology
|
December 30, 2004
Sensorimotor cortex excitability in Unverricht-Lundborg disease and Lafora body disease
L Canafoglia, C Ciano, F Panzica, et al.
Brain Research Bulletin
|
July 6, 2010
Event-related potential (ERP) markers of melodic processing: The N2 component is modulated by structural complexity, not by melodic 'meaningfulness'
L Minati, L Salvatoni, C Rosazza, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology
|
March 29, 2005
FVEPs in Creutzfeldt-Jacob disease: waveforms and interaction with the periodic EEG pattern assessed by single sweep analysis
E Visani, P Agazzi, V Scaioli, et al.
Neurology
|
November 17, 2010
Four novel cases of periaxin-related neuropathy and review of the literature
C Marchesi, M Milani, M Morbin, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology
|
August 2, 2014
Significance of multiple neurophysiological measures in patients with chronic disorders of consciousness
Davide Rossi Sebastiano, F Panzica, E Visani, et al.
Neurology
|
March 3, 2010
Vitamin E neuroprotection for cisplatin neuropathy: a randomized, placebo-controlled trial
A Pace, D Giannarelli, E Galiè, et al.
Neurology
|
March 15, 2006
Novel mutations in the HSN2 gene causing hereditary sensory and autonomic neuropathy type II
K Coen, D Pareyson, M Auer-Grumbach, et al.
Page
of 5