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Showing results (121-130 of 190) with videos related to

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Neurology|January 17, 2007
The role of muscle biopsy in investigating isolated muscle painM Filosto, P Tonin, G Vattemi, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 1, 1978
Stiff-man syndrome associated with nocturnal myoclonus and epilepsyP Martinelli, P Pazzaglia, P Montagna, et al.
Neurology|July 20, 2007
Two novel mutations in dynamin-2 cause axonal Charcot-Marie-Tooth diseaseG M Fabrizi, M Ferrarini, T Cavallaro, et al.
Neuroscience Research|May 1, 1995
Tau protein immunolocalization in fetal and adult human spinal cordP Liberini, A Valerio, G Moretto, et al.
Neuromuscular Disorders : NMD|December 7, 2002
Hepatitis C virus infection and myositis: a virus localization studyA Di Muzio, B Bonetti, M Capasso, et al.
The Journal of Bone and Joint Surgery. British Volume|December 11, 1997
Lower-limb lengthening in short stature. An electrophysiological and clinical assessment of peripheral nerve functionA Polo, R Aldegheri, A Zambito, et al.
Rivista Di Patologia Nervosa E Mentale|March 1, 1982
[Histopathologic and ultrastructural study of various amputation neuromas]A Maleci, G Moretto, F Fenzi, et al.
Neurology|April 28, 2004
Giant axon and neurofilament accumulation in Charcot-Marie-Tooth disease type 2EG M Fabrizi, T Cavallaro, C Angiari, et al.
Rivista Di Neurobiologia : Organo Ufficiale Della Societa Dei Neurologi, Neuroradiologi E Neurochirurghi Ospedalieri|July 1, 1982
[Hereditary sensory neuropathies with acrodystrophic lesions. Nosographic considerations]B Lucci, A Marbini, F Gemignani, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 4, 2006
A novel missense mutation in the L1CAM gene in a boy with L1 diseaseA Simonati, F Boaretto, A Vettori, et al.
Pageof 19

Showing results (121-130 of 190) with videos related to

Sort By:
Pageof 19
Neurology|January 17, 2007
The role of muscle biopsy in investigating isolated muscle painM Filosto, P Tonin, G Vattemi, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 1, 1978
Stiff-man syndrome associated with nocturnal myoclonus and epilepsyP Martinelli, P Pazzaglia, P Montagna, et al.
Neurology|July 20, 2007
Two novel mutations in dynamin-2 cause axonal Charcot-Marie-Tooth diseaseG M Fabrizi, M Ferrarini, T Cavallaro, et al.
Neuroscience Research|May 1, 1995
Tau protein immunolocalization in fetal and adult human spinal cordP Liberini, A Valerio, G Moretto, et al.
Neuromuscular Disorders : NMD|December 7, 2002
Hepatitis C virus infection and myositis: a virus localization studyA Di Muzio, B Bonetti, M Capasso, et al.
The Journal of Bone and Joint Surgery. British Volume|December 11, 1997
Lower-limb lengthening in short stature. An electrophysiological and clinical assessment of peripheral nerve functionA Polo, R Aldegheri, A Zambito, et al.
Rivista Di Patologia Nervosa E Mentale|March 1, 1982
[Histopathologic and ultrastructural study of various amputation neuromas]A Maleci, G Moretto, F Fenzi, et al.
Neurology|April 28, 2004
Giant axon and neurofilament accumulation in Charcot-Marie-Tooth disease type 2EG M Fabrizi, T Cavallaro, C Angiari, et al.
Rivista Di Neurobiologia : Organo Ufficiale Della Societa Dei Neurologi, Neuroradiologi E Neurochirurghi Ospedalieri|July 1, 1982
[Hereditary sensory neuropathies with acrodystrophic lesions. Nosographic considerations]B Lucci, A Marbini, F Gemignani, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 4, 2006
A novel missense mutation in the L1CAM gene in a boy with L1 diseaseA Simonati, F Boaretto, A Vettori, et al.
Pageof 19