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D Pareyson

Showing results (51-60 of 113) with videos related to

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Neurology|December 31, 1997
Gene dosage effects in hereditary peripheral neuropathy. Expression of peripheral myelin protein 22 in Charcot-Marie-Tooth disease type 1A and hereditary neuropathy with liability to pressure palsies nerve biopsiesJ M Gabriel, B Erne, D Pareyson, et al.
Journal of Neurology|March 26, 2011
Pendular nystagmus in progressive ataxia and palatal tremorR Bassani, C Mariotti, L Nanetti, et al.
Italian Journal of Neurological Sciences|April 1, 1988
Anti AChR antibody: relevance to diagnosis and clinical aspects of myasthenia gravisR Mantegazza, D Pareyson, F Baggi, et al.
Neurology|September 10, 2003
Axonal swellings predict the degeneration of epidermal nerve fibers in painful neuropathiesG Lauria, M Morbin, R Lombardi, et al.
Neuromuscular Disorders : NMD|July 6, 2007
POEMS syndrome: relapse after successful autologous peripheral blood stem cell transplantationF Giglia, L Chiapparini, L Fariselli, et al.
Neurology|October 27, 1997
Very late onset Friedreich's ataxia without cardiomyopathy is associated with limited GAA expansion in the X25 geneC Gellera, D Pareyson, B Castellotti, et al.
Italian Journal of Neurological Sciences|October 1, 1995
Kennedy's disease: clinical and molecular study of two Italian familiesD Pareyson, B Castellotti, S Botti, et al.
Neuromuscular Disorders : NMD|June 1, 2016
Laryngeal and phrenic nerve involvement in a patient with hereditary neuropathy with liability to pressure palsies (HNPP)A Cortese, G Piccolo, A Lozza, et al.
Annals of Neurology|February 5, 1998
A novel mutation in the mitochondrial tRNA(Val) gene associated with a complex neurological presentationV Tiranti, L D'Agruma, D Pareyson, et al.
Muscle & Nerve|December 8, 1998
Detection of hereditary neuropathy with liability to pressure palsies among patients with acute painless mononeuropathy or plexopathyD Pareyson, A Solari, F Taroni, et al.
Pageof 12

Showing results (51-60 of 113) with videos related to

Sort By:
Pageof 12
Neurology|December 31, 1997
Gene dosage effects in hereditary peripheral neuropathy. Expression of peripheral myelin protein 22 in Charcot-Marie-Tooth disease type 1A and hereditary neuropathy with liability to pressure palsies nerve biopsiesJ M Gabriel, B Erne, D Pareyson, et al.
Journal of Neurology|March 26, 2011
Pendular nystagmus in progressive ataxia and palatal tremorR Bassani, C Mariotti, L Nanetti, et al.
Italian Journal of Neurological Sciences|April 1, 1988
Anti AChR antibody: relevance to diagnosis and clinical aspects of myasthenia gravisR Mantegazza, D Pareyson, F Baggi, et al.
Neurology|September 10, 2003
Axonal swellings predict the degeneration of epidermal nerve fibers in painful neuropathiesG Lauria, M Morbin, R Lombardi, et al.
Neuromuscular Disorders : NMD|July 6, 2007
POEMS syndrome: relapse after successful autologous peripheral blood stem cell transplantationF Giglia, L Chiapparini, L Fariselli, et al.
Neurology|October 27, 1997
Very late onset Friedreich's ataxia without cardiomyopathy is associated with limited GAA expansion in the X25 geneC Gellera, D Pareyson, B Castellotti, et al.
Italian Journal of Neurological Sciences|October 1, 1995
Kennedy's disease: clinical and molecular study of two Italian familiesD Pareyson, B Castellotti, S Botti, et al.
Neuromuscular Disorders : NMD|June 1, 2016
Laryngeal and phrenic nerve involvement in a patient with hereditary neuropathy with liability to pressure palsies (HNPP)A Cortese, G Piccolo, A Lozza, et al.
Annals of Neurology|February 5, 1998
A novel mutation in the mitochondrial tRNA(Val) gene associated with a complex neurological presentationV Tiranti, L D'Agruma, D Pareyson, et al.
Muscle & Nerve|December 8, 1998
Detection of hereditary neuropathy with liability to pressure palsies among patients with acute painless mononeuropathy or plexopathyD Pareyson, A Solari, F Taroni, et al.
Pageof 12