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T Cavallaro

Showing results (41-50 of 65) with videos related to

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Neuromuscular Disorders : NMD|July 10, 1999
Congenital hypomyelination neuropathy with Ser72Leu substitution in PMP22A Simonati, G M Fabrizi, A Pasquinelli, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 10, 2008
Relationship between clinical examination, quality of life, disability and depression in CMT patients: Italian multicenter studyL Padua, I Aprile, T Cavallaro, et al.
Archives of Gerontology and Geriatrics|May 26, 2004
Dementia with Lewy bodies: a reviewL Rampello, S Cerasa, A Alvano, et al.
Neurology|December 15, 2004
Segmental conduction abnormalities and myelin thickenings in Val102/fs null mutation of MPZ geneM V De Angelis, A Di Muzio, M Capasso, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|December 16, 2000
PMP22 related congenital hypomyelination neuropathyG M Fabrizi, A Simonati, F Taioli, et al.
Acta Neuropathologica|January 1, 1996
Neuronal intranuclear inclusion disease: polymerase chain reaction and ultrastructural study of rectal biopsy specimen in a new caseA Malandrini, G M Fabrizi, T Cavallaro, et al.
European Journal of Neurology|January 16, 2007
Quality of life is not impaired in patients with hereditary neuropathy with liability to pressure palsiesL Padua, C Pazzaglia, T Cavallaro, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 1, 1996
The A to G transition at nt 3243 of the mitochondrial tRNALeu(UUR) may cause an MERRF syndromeG M Fabrizi, E Cardaioli, G S Grieco, et al.
Acta Neurologica|February 1, 1990
AIDS--associated predominantly sensory neuropathy. The role of herpes virusesS Ferrari, B Bonetti, S Monaco, et al.
Neurology|April 1, 2009
Further evidence that mutations in FGD4/frabin cause Charcot-Marie-Tooth disease type 4HG M Fabrizi, F Taioli, T Cavallaro, et al.
Pageof 7

Showing results (41-50 of 65) with videos related to

Sort By:
Pageof 7
Neuromuscular Disorders : NMD|July 10, 1999
Congenital hypomyelination neuropathy with Ser72Leu substitution in PMP22A Simonati, G M Fabrizi, A Pasquinelli, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 10, 2008
Relationship between clinical examination, quality of life, disability and depression in CMT patients: Italian multicenter studyL Padua, I Aprile, T Cavallaro, et al.
Archives of Gerontology and Geriatrics|May 26, 2004
Dementia with Lewy bodies: a reviewL Rampello, S Cerasa, A Alvano, et al.
Neurology|December 15, 2004
Segmental conduction abnormalities and myelin thickenings in Val102/fs null mutation of MPZ geneM V De Angelis, A Di Muzio, M Capasso, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|December 16, 2000
PMP22 related congenital hypomyelination neuropathyG M Fabrizi, A Simonati, F Taioli, et al.
Acta Neuropathologica|January 1, 1996
Neuronal intranuclear inclusion disease: polymerase chain reaction and ultrastructural study of rectal biopsy specimen in a new caseA Malandrini, G M Fabrizi, T Cavallaro, et al.
European Journal of Neurology|January 16, 2007
Quality of life is not impaired in patients with hereditary neuropathy with liability to pressure palsiesL Padua, C Pazzaglia, T Cavallaro, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 1, 1996
The A to G transition at nt 3243 of the mitochondrial tRNALeu(UUR) may cause an MERRF syndromeG M Fabrizi, E Cardaioli, G S Grieco, et al.
Acta Neurologica|February 1, 1990
AIDS--associated predominantly sensory neuropathy. The role of herpes virusesS Ferrari, B Bonetti, S Monaco, et al.
Neurology|April 1, 2009
Further evidence that mutations in FGD4/frabin cause Charcot-Marie-Tooth disease type 4HG M Fabrizi, F Taioli, T Cavallaro, et al.
Pageof 7