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C Ciano

Showing results (21-30 of 32) with videos related to

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Neurology|April 13, 2000
Cranial nerve involvement in CMT disease type 1 due to early growth response 2 gene mutationD Pareyson, F Taroni, S Botti, et al.
Neurology|April 1, 1996
Phenotypic heterogeneity in hereditary neuropathy with liability to pressure palsies associated with chromosome 17p11.2-12 deletionD Pareyson, V Scaioli, F Taroni, et al.
Neuroimage|August 15, 2006
Movement-related desynchronization-synchronization (ERD/ERS) in patients with Unverricht-Lundborg diseaseE Visani, P Agazzi, L Canafoglia, et al.
Muscle & Nerve|December 8, 1998
Detection of hereditary neuropathy with liability to pressure palsies among patients with acute painless mononeuropathy or plexopathyD Pareyson, A Solari, F Taroni, et al.
Neurology|November 1, 1992
HMSN III phenotype due to homozygous expression of a dominant HMSN II geneA Sghirlanzoni, D Pareyson, M R Balestrini, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|January 2, 2013
Giant SEPs and SEP-recovery function in Unverricht-Lundborg diseaseE Visani, L Canafoglia, D Rossi Sebastiano, et al.
Neurology|December 30, 2004
Sensorimotor cortex excitability in Unverricht-Lundborg disease and Lafora body diseaseL Canafoglia, C Ciano, F Panzica, et al.
European Journal of Neurology|January 26, 2016
Amyotrophic lateral sclerosis causes small fiber pathologyE Dalla Bella, R Lombardi, C Porretta-Serapiglia, et al.
Neurology|May 5, 1999
Infantile neuroaxonal dystrophy: clinical spectrum and diagnostic criteriaN Nardocci, G Zorzi, L Farina, et al.
Neurology|April 13, 2005
Sequential antibodies to potassium channels and glutamic acid decarboxylase in neuromyotoniaC Antozzi, C Frassoni, A Vincent, et al.
Pageof 4

Showing results (21-30 of 32) with videos related to

Sort By:
Pageof 4
Neurology|April 13, 2000
Cranial nerve involvement in CMT disease type 1 due to early growth response 2 gene mutationD Pareyson, F Taroni, S Botti, et al.
Neurology|April 1, 1996
Phenotypic heterogeneity in hereditary neuropathy with liability to pressure palsies associated with chromosome 17p11.2-12 deletionD Pareyson, V Scaioli, F Taroni, et al.
Neuroimage|August 15, 2006
Movement-related desynchronization-synchronization (ERD/ERS) in patients with Unverricht-Lundborg diseaseE Visani, P Agazzi, L Canafoglia, et al.
Muscle & Nerve|December 8, 1998
Detection of hereditary neuropathy with liability to pressure palsies among patients with acute painless mononeuropathy or plexopathyD Pareyson, A Solari, F Taroni, et al.
Neurology|November 1, 1992
HMSN III phenotype due to homozygous expression of a dominant HMSN II geneA Sghirlanzoni, D Pareyson, M R Balestrini, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|January 2, 2013
Giant SEPs and SEP-recovery function in Unverricht-Lundborg diseaseE Visani, L Canafoglia, D Rossi Sebastiano, et al.
Neurology|December 30, 2004
Sensorimotor cortex excitability in Unverricht-Lundborg disease and Lafora body diseaseL Canafoglia, C Ciano, F Panzica, et al.
European Journal of Neurology|January 26, 2016
Amyotrophic lateral sclerosis causes small fiber pathologyE Dalla Bella, R Lombardi, C Porretta-Serapiglia, et al.
Neurology|May 5, 1999
Infantile neuroaxonal dystrophy: clinical spectrum and diagnostic criteriaN Nardocci, G Zorzi, L Farina, et al.
Neurology|April 13, 2005
Sequential antibodies to potassium channels and glutamic acid decarboxylase in neuromyotoniaC Antozzi, C Frassoni, A Vincent, et al.
Pageof 4