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Showing results (261-270 of 320) with videos related to

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Neurology|August 26, 1998
Giant dystrophin deletion associated with congenital cataract and mild muscular dystrophyM Mirabella, G Galluzzi, G Manfredi, et al.
Experimental Brain Research|August 11, 2001
Inhibition of biceps brachii muscle motor area by painful heat stimulation of the skinM Valeriani, D Restuccia, V Di Lazzaro, et al.
Neuromuscular Disorders : NMD|June 14, 2002
Hypermyelinating neuropathy, mental retardation and epilepsy in a case of merosin deficiencyF Deodato, M Sabatelli, E Ricci, et al.
Journal of the Neurological Sciences|March 1, 1993
Manifesting heterozygotes in McArdle's disease: clinical, morphological and biochemical studies in a familyG Manfredi, G Silvestri, S Servidei, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|December 1, 1996
Changes in spinal cord excitability in a patient with rhythmic segmental myoclonusV Di Lazzaro, D Restuccia, R Nardone, et al.
Neuromuscular Disorders : NMD|February 5, 2008
Natural history of CMT1A including QoL: a 2-year prospective studyL Padua, D Pareyson, I Aprile, et al.
Journal of Neurology|December 24, 1997
Ocular palsies in the absence of other neurological or ocular symptoms: analysis of 105 casesA P Batocchi, A Evoli, L Majolini, et al.
European Journal of Neurology|August 28, 2003
Incidence of first-ever ischemic and hemorrhagic stroke in a well-defined community of southern Italy, 1993-1995D Intiso, P Stampatore, M M Zarrelli, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|August 7, 2001
Neurophysiological classification of ulnar entrapment across the elbowL Padua, I Aprile, O Mazza, et al.
Neurology|April 13, 2000
A new mtDNA mutation associated with a progressive encephalopathy and cytochrome c oxidase deficiencyG Silvestri, T Mongini, F Odoardi, et al.
Pageof 32

Showing results (261-270 of 320) with videos related to

Sort By:
Pageof 32
Neurology|August 26, 1998
Giant dystrophin deletion associated with congenital cataract and mild muscular dystrophyM Mirabella, G Galluzzi, G Manfredi, et al.
Experimental Brain Research|August 11, 2001
Inhibition of biceps brachii muscle motor area by painful heat stimulation of the skinM Valeriani, D Restuccia, V Di Lazzaro, et al.
Neuromuscular Disorders : NMD|June 14, 2002
Hypermyelinating neuropathy, mental retardation and epilepsy in a case of merosin deficiencyF Deodato, M Sabatelli, E Ricci, et al.
Journal of the Neurological Sciences|March 1, 1993
Manifesting heterozygotes in McArdle's disease: clinical, morphological and biochemical studies in a familyG Manfredi, G Silvestri, S Servidei, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|December 1, 1996
Changes in spinal cord excitability in a patient with rhythmic segmental myoclonusV Di Lazzaro, D Restuccia, R Nardone, et al.
Neuromuscular Disorders : NMD|February 5, 2008
Natural history of CMT1A including QoL: a 2-year prospective studyL Padua, D Pareyson, I Aprile, et al.
Journal of Neurology|December 24, 1997
Ocular palsies in the absence of other neurological or ocular symptoms: analysis of 105 casesA P Batocchi, A Evoli, L Majolini, et al.
European Journal of Neurology|August 28, 2003
Incidence of first-ever ischemic and hemorrhagic stroke in a well-defined community of southern Italy, 1993-1995D Intiso, P Stampatore, M M Zarrelli, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|August 7, 2001
Neurophysiological classification of ulnar entrapment across the elbowL Padua, I Aprile, O Mazza, et al.
Neurology|April 13, 2000
A new mtDNA mutation associated with a progressive encephalopathy and cytochrome c oxidase deficiencyG Silvestri, T Mongini, F Odoardi, et al.
Pageof 32