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T Cavallaro

Showing results (51-60 of 65) with videos related to

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Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|January 7, 2004
Inter-nerves and intra-nerve conduction heterogeneity in CMTX with Arg(15)Gln mutationM Capasso, A Di Muzio, M Ferrarini, et al.
Neurology|November 17, 2010
Four novel cases of periaxin-related neuropathy and review of the literatureC Marchesi, M Milani, M Morbin, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 6, 2007
Variables influencing quality of life and disability in Charcot Marie Tooth (CMT) patients: Italian multicentre studyL Padua, I Aprile, T Cavallaro, et al.
Brain Pathology (Zurich, Switzerland)|April 17, 2001
Increased expression of the normal cellular isoform of prion protein in inclusion-body myositis, inflammatory myopathies and denervation atrophyG Zanusso, G Vattemi, S Ferrari, et al.
Neurology|October 15, 2003
Charcot-Marie-Tooth disease with giant axons: a clinicopathological and genetic entityG Lus, E Nelis, A Jordanova, et al.
Neurology|June 10, 2010
Severe CMT type 2 with fatal encephalopathy associated with a novel MFN2 splicing mutationF Boaretto, A Vettori, A Casarin, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|December 3, 2003
Atypical familial motor neuropathy in patients with mutant TTR Ile68LeuF Salvi, C Scaglione, R Michelucci, et al.
European Journal of Neurology|May 11, 2016
Novel outcome measures for Charcot-Marie-Tooth disease: validation and reliability of the 6-min walk test and StepWatch(™) Activity Monitor and identification of the walking features related to higher quality of lifeL Padua, C Pazzaglia, D Pareyson, et al.
Acta Neuropathologica|August 1, 1996
Clinicopathological and genetic studies of two further Italian families with cerebral autosomal dominant arteriopathyA Malandrini, P Carrera, S Palmeri, et al.
Neurology|April 2, 1999
Mitochondrial G8363A mutation presenting as cerebellar ataxia and lipomas in an Italian familyC Casali, G M Fabrizi, F M Santorelli, et al.
Pageof 7

Showing results (51-60 of 65) with videos related to

Sort By:
Pageof 7
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|January 7, 2004
Inter-nerves and intra-nerve conduction heterogeneity in CMTX with Arg(15)Gln mutationM Capasso, A Di Muzio, M Ferrarini, et al.
Neurology|November 17, 2010
Four novel cases of periaxin-related neuropathy and review of the literatureC Marchesi, M Milani, M Morbin, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 6, 2007
Variables influencing quality of life and disability in Charcot Marie Tooth (CMT) patients: Italian multicentre studyL Padua, I Aprile, T Cavallaro, et al.
Brain Pathology (Zurich, Switzerland)|April 17, 2001
Increased expression of the normal cellular isoform of prion protein in inclusion-body myositis, inflammatory myopathies and denervation atrophyG Zanusso, G Vattemi, S Ferrari, et al.
Neurology|October 15, 2003
Charcot-Marie-Tooth disease with giant axons: a clinicopathological and genetic entityG Lus, E Nelis, A Jordanova, et al.
Neurology|June 10, 2010
Severe CMT type 2 with fatal encephalopathy associated with a novel MFN2 splicing mutationF Boaretto, A Vettori, A Casarin, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|December 3, 2003
Atypical familial motor neuropathy in patients with mutant TTR Ile68LeuF Salvi, C Scaglione, R Michelucci, et al.
European Journal of Neurology|May 11, 2016
Novel outcome measures for Charcot-Marie-Tooth disease: validation and reliability of the 6-min walk test and StepWatch(™) Activity Monitor and identification of the walking features related to higher quality of lifeL Padua, C Pazzaglia, D Pareyson, et al.
Acta Neuropathologica|August 1, 1996
Clinicopathological and genetic studies of two further Italian families with cerebral autosomal dominant arteriopathyA Malandrini, P Carrera, S Palmeri, et al.
Neurology|April 2, 1999
Mitochondrial G8363A mutation presenting as cerebellar ataxia and lipomas in an Italian familyC Casali, G M Fabrizi, F M Santorelli, et al.
Pageof 7