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Showing results (151-160 of 190) with videos related to

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The Journal of Biological Chemistry|October 30, 2001
pH-dependent prion protein conformation in classical Creutzfeldt-Jakob diseaseG Zanusso, A Farinazzo, M Fiorini, et al.
Clinical Genetics|April 3, 1999
Mutations associated with very late-onset metachromatic leukodystrophyC Perusi, M G Lira, R F Duyff, et al.
Neuromuscular Disorders : NMD|August 26, 1998
Charcot-Marie-Tooth disease: an intermediate formM Villanova, V Timmerman, P De Jonghe, et al.
Muscle & Nerve|June 17, 1998
Clinical and pathological correlations in Charcot-Marie-Tooth neuropathy type 1A with the 17p11.2p12 duplication: a cross-sectional morphometric and immunohistochemical study in twenty casesG M Fabrizi, A Simonati, M Morbin, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|September 23, 2008
Evaluating endothelial function of the common carotid artery: an in vivo human modelS Mazzucco, F Bifari, M Trombetta, et al.
Neuromuscular Disorders : NMD|February 5, 2008
Natural history of CMT1A including QoL: a 2-year prospective studyL Padua, D Pareyson, I Aprile, et al.
Neuropediatrics|May 1, 1988
Cerebro-ocular dysplasia and muscular dystrophy: report of two casesA Federico, M T Dotti, A Malandrini, et al.
Annals of Neurology|February 1, 1997
Botulinum toxin treatment of muscle cramps: a clinical and neurophysiological studyL Bertolasi, A Priori, G Tomelleri, et al.
Neuropediatrics|November 9, 2000
A CLN2 gene nonsense mutation is associated with severe caudate atrophy and dystonia in LINCLA Simonati, E Santorum, A Tessa, et al.
Neuromuscular Disorders : NMD|July 10, 1999
Congenital hypomyelination neuropathy with Ser72Leu substitution in PMP22A Simonati, G M Fabrizi, A Pasquinelli, et al.
Pageof 19

Showing results (151-160 of 190) with videos related to

Sort By:
Pageof 19
The Journal of Biological Chemistry|October 30, 2001
pH-dependent prion protein conformation in classical Creutzfeldt-Jakob diseaseG Zanusso, A Farinazzo, M Fiorini, et al.
Clinical Genetics|April 3, 1999
Mutations associated with very late-onset metachromatic leukodystrophyC Perusi, M G Lira, R F Duyff, et al.
Neuromuscular Disorders : NMD|August 26, 1998
Charcot-Marie-Tooth disease: an intermediate formM Villanova, V Timmerman, P De Jonghe, et al.
Muscle & Nerve|June 17, 1998
Clinical and pathological correlations in Charcot-Marie-Tooth neuropathy type 1A with the 17p11.2p12 duplication: a cross-sectional morphometric and immunohistochemical study in twenty casesG M Fabrizi, A Simonati, M Morbin, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|September 23, 2008
Evaluating endothelial function of the common carotid artery: an in vivo human modelS Mazzucco, F Bifari, M Trombetta, et al.
Neuromuscular Disorders : NMD|February 5, 2008
Natural history of CMT1A including QoL: a 2-year prospective studyL Padua, D Pareyson, I Aprile, et al.
Neuropediatrics|May 1, 1988
Cerebro-ocular dysplasia and muscular dystrophy: report of two casesA Federico, M T Dotti, A Malandrini, et al.
Annals of Neurology|February 1, 1997
Botulinum toxin treatment of muscle cramps: a clinical and neurophysiological studyL Bertolasi, A Priori, G Tomelleri, et al.
Neuropediatrics|November 9, 2000
A CLN2 gene nonsense mutation is associated with severe caudate atrophy and dystonia in LINCLA Simonati, E Santorum, A Tessa, et al.
Neuromuscular Disorders : NMD|July 10, 1999
Congenital hypomyelination neuropathy with Ser72Leu substitution in PMP22A Simonati, G M Fabrizi, A Pasquinelli, et al.
Pageof 19