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Showing results (161-170 of 190) with videos related to

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Lancet (London, England)|November 3, 1998
Simultaneous occurrence of spongiform encephalopathy in a man and his cat in ItalyG Zanusso, E Nardelli, A Rosati, et al.
Acta Neuropathologica|January 1, 1995
Role of HIV in the pathogenesis of distal symmetrical peripheral neuropathyN Rizzuto, T Cavallaro, S Monaco, et al.
Neurology|May 26, 2004
Expression of protein kinase C isoforms and interleukin-1beta in myofibrillar myopathyG Vattemi, P Tonin, M Mora, et al.
European Neurology|October 25, 2008
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy and right-to-left shunt: lack of evidence for an association in a prevalence studyS Mazzucco, G P Anzola, M Ferrarini, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|December 18, 2009
Natural history of Charcot-Marie-Tooth 2: 2-year follow-up of muscle strength, walking ability and quality of lifeLuca Padua, D Pareyson, I Aprile, et al.
Archives of Internal Medicine|March 11, 1996
Stereotactic brain biopsy in human immunodeficiency virus-infected patientsR Luzzati, S Ferrari, A Nicolato, 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.
Journal of Neurology, Neurosurgery, and Psychiatry|November 5, 1997
Multiple sclerosis associated with duplicated CMT1A: a report of two casesE Frasson, A Polo, A Di Summa, et al.
Human Mutation|September 12, 2000
Detection of mutations in the ALD gene (ABCD1) in seven Italian families: description of four novel mutationsM G Lira, M Mottes, P F Pignatti, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|December 16, 2000
PMP22 related congenital hypomyelination neuropathyG M Fabrizi, A Simonati, F Taioli, et al.
Pageof 19

Showing results (161-170 of 190) with videos related to

Sort By:
Pageof 19
Lancet (London, England)|November 3, 1998
Simultaneous occurrence of spongiform encephalopathy in a man and his cat in ItalyG Zanusso, E Nardelli, A Rosati, et al.
Acta Neuropathologica|January 1, 1995
Role of HIV in the pathogenesis of distal symmetrical peripheral neuropathyN Rizzuto, T Cavallaro, S Monaco, et al.
Neurology|May 26, 2004
Expression of protein kinase C isoforms and interleukin-1beta in myofibrillar myopathyG Vattemi, P Tonin, M Mora, et al.
European Neurology|October 25, 2008
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy and right-to-left shunt: lack of evidence for an association in a prevalence studyS Mazzucco, G P Anzola, M Ferrarini, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|December 18, 2009
Natural history of Charcot-Marie-Tooth 2: 2-year follow-up of muscle strength, walking ability and quality of lifeLuca Padua, D Pareyson, I Aprile, et al.
Archives of Internal Medicine|March 11, 1996
Stereotactic brain biopsy in human immunodeficiency virus-infected patientsR Luzzati, S Ferrari, A Nicolato, 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.
Journal of Neurology, Neurosurgery, and Psychiatry|November 5, 1997
Multiple sclerosis associated with duplicated CMT1A: a report of two casesE Frasson, A Polo, A Di Summa, et al.
Human Mutation|September 12, 2000
Detection of mutations in the ALD gene (ABCD1) in seven Italian families: description of four novel mutationsM G Lira, M Mottes, P F Pignatti, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|December 16, 2000
PMP22 related congenital hypomyelination neuropathyG M Fabrizi, A Simonati, F Taioli, et al.
Pageof 19