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Showing results (171-180 of 190) with videos related to

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Annals of Neurology|October 1, 1982
Locked-in syndrome in multiple sclerosis with sparing of the ventral portion of the ponsA Forti, G Ambrosetto, M Amore, et al.
Cancer|May 15, 1985
A distinctive cutaneous malignant neoplasm expressing the Langerhans cell phenotype. Synchronous occurrence with B-chronic lymphocytic leukemiaF Bonetti, D M Knowles, M Chilosi, 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.
Human Mutation|January 1, 1995
A 48-bp insertion between exon 13 and 14 of the HEXB gene causes infantile-onset Sandhoff diseaseM Gomez-Lira, C Perusi, N Brutti, et al.
Lancet (London, England)|June 8, 1996
Critical illness myopathy and neuropathyN Latronico, F Fenzi, D Recupero, et al.
Journal of Neuropathology and Experimental Neurology|January 1, 1995
Experimental induction of myelin changes by anti-MAG antibodies and terminal complement complexS Monaco, S Ferrari, B Bonetti, 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.
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.
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.
Molecular and Cellular Probes|June 17, 1999
Two novel missense mutations causing adrenoleukodystrophy in Italian patientsC Perusi, M Gomez-Lira, M Mottes, et al.
Pageof 19

Showing results (171-180 of 190) with videos related to

Sort By:
Pageof 19
Annals of Neurology|October 1, 1982
Locked-in syndrome in multiple sclerosis with sparing of the ventral portion of the ponsA Forti, G Ambrosetto, M Amore, et al.
Cancer|May 15, 1985
A distinctive cutaneous malignant neoplasm expressing the Langerhans cell phenotype. Synchronous occurrence with B-chronic lymphocytic leukemiaF Bonetti, D M Knowles, M Chilosi, 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.
Human Mutation|January 1, 1995
A 48-bp insertion between exon 13 and 14 of the HEXB gene causes infantile-onset Sandhoff diseaseM Gomez-Lira, C Perusi, N Brutti, et al.
Lancet (London, England)|June 8, 1996
Critical illness myopathy and neuropathyN Latronico, F Fenzi, D Recupero, et al.
Journal of Neuropathology and Experimental Neurology|January 1, 1995
Experimental induction of myelin changes by anti-MAG antibodies and terminal complement complexS Monaco, S Ferrari, B Bonetti, 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.
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.
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.
Molecular and Cellular Probes|June 17, 1999
Two novel missense mutations causing adrenoleukodystrophy in Italian patientsC Perusi, M Gomez-Lira, M Mottes, et al.
Pageof 19