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Annals of Neurology|January 10, 2002
Novel heteroplasmic mtDNA mutation in a family with heterogeneous clinical presentationsP Corona, E Lamantea, M Greco, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 20, 2012
Updating on Italian stroke units: the "CCM study"D Guidetti, M Spallazzi, D Toni, et al.
Neuroepidemiology|January 1, 1993
Incidence of stroke in young adults in the Reggio Emilia area, northern ItalyD Guidetti, M Baratti, R G Zucco, et al.
American Journal of Medical Genetics|January 2, 1995
Androgen receptor gene (CAG)n repeat analysis in the differential diagnosis between Kennedy disease and other motoneuron disordersA Ferlini, M C Patrosso, D Guidetti, et al.
Giornale Italiano Di Nefrologia : Organo Ufficiale Della Societa Italiana Di Nefrologia|April 22, 2009
[Prevention and therapy of critical ischemia in hemodialyzed patients]M Andreoli, G Galli, A Arienzo, et al.
European Journal of Epidemiology|May 8, 2003
Risk of sporadic amyotrophic lateral sclerosis associated with seropositivity for herpesviruses and echovirus-7C Cermelli, M Vinceti, F Beretti, et al.
European Journal of Physical and Rehabilitation Medicine|February 15, 2014
Post-stroke rehabilitation in Italy: inconsistencies across regional strategiesD Guidetti, M Spallazzi, M Baldereschi, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|February 10, 2004
An Italian case of CADASIL with mutation CGC-TCG in codon 1006, exon 19 Notch3 geneD Guidetti, B Casali, R L Mazzei, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 19, 2005
The spectrum of Notch3 mutations in 28 Italian CADASIL familiesM T Dotti, A Federico, R Mazzei, et al.
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