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Mayo Clinic Proceedings|February 14, 2006
Human immunodeficiency virus-associated peripheral neuropathiesSergio Ferrari, Sandro Vento, Salvatore Monaco, et al.
Bioscience Reports|June 2, 2007
Neuropathology of mitochondrial diseasesMassimiliano Filosto, Giuliano Tomelleri, Paola Tonin, et al.
Brain : a Journal of Neurology|May 23, 2006
SERCA1 and calsequestrin storage myopathy: a new surplus protein myopathyGiuliano Tomelleri, Laura Palmucci, Paola Tonin, et al.
Neuromuscular Disorders : NMD|February 21, 2006
Gene dosage sensitivity of a novel mutation in the intracellular domain of P0 associated with Charcot-Marie-Tooth disease type 1BGian Maria Fabrizi, Maria Pellegrini, Chiara Angiari, et al.
Muscle & Nerve|November 25, 2005
Overexpression of ErbB2 and ErbB3 receptors in Schwann cells of patients with Charcot-Marie-tooth disease type 1ARoberto Massa, Camilla Palumbo, Tiziana Cavallaro, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|October 14, 2004
An unusual transthyretin gene missense mutation (TTR Phe33Val) linked to familial amyloidotic polyneuropathyRoberta Frigerio, Gian Maria Fabrizi, Moreno Ferrarini, et al.
The Journal of Biological Chemistry|July 13, 2004
Identification of distinct N-terminal truncated forms of prion protein in different Creutzfeldt-Jakob disease subtypesGianluigi Zanusso, Alessia Farinazzo, Frances Prelli, et al.
Neuromuscular Disorders : NMD|March 18, 2008
Novel mitochondrial tRNA Leu(CUN) transition and D4Z4 partial deletion in a patient with a facioscapulohumeral phenotypeMassimiliano Filosto, Paola Tonin, Mauro Scarpelli, et al.
Journal of Neuro-Oncology|February 3, 2009
Epilepsy in glioblastoma multiforme: correlation with glutamine synthetase levelsAnna Rosati, Silvia Marconi, Bianca Pollo, et al.
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