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European Journal of Neurology|May 20, 2008
DRD3 Ser9Gly variant is not associated with essential tremor in a series of Italian patientsC Vitale, R Gulli, P Ciotti, et al.Neuroscience Letters|April 18, 1998
mRNA distribution in adult human brain of GRIN2B, a N-methyl-D-aspartate (NMDA) receptor subunitA M Schito, A Pizzuti, E Di Maria, et al.European Journal of Physical and Rehabilitation Medicine|December 11, 2014
Tinetti and Berg balance scales correlate with disability in hereditary peripheral neuropathies: a preliminary studyM Monti Bragadin, L Francini, E Bellone, et al.Human Molecular Genetics|January 1, 1994
Analysis of the trinucleotide repeat expansion in Italian families affected with Huntington diseaseA Novelletto, F Persichetti, G Sabbadini, et al.Journal of Neurology, Neurosurgery, and Psychiatry|September 21, 2004
A novel mutation of GDAP1 associated with Charcot-Marie-Tooth disease in three Italian families: evidence for a founder effectE Di Maria, R Gulli, P Balestra, et al.European Journal of Neurology|April 15, 2014
Contribution of copy number variations in CMT1X: a retrospective studyS Capponi, A Geroldi, I Pezzini, et al.Journal of the Neurological Sciences|March 1, 1994
Hereditary motor and sensory neuropathy with myelin outfolding: clinical, genetic and neuropathological study of three casesA Schenone, M Abbruzzese, A Uccelli, et al.Molecular Genetics and Metabolism|June 25, 1999
Isolation and characterization of a novel transcript embedded within HIRA, a gene deleted in DiGeorge syndromeA Pizzuti, G Novelli, A Ratti, et al.American Journal of Medical Genetics|February 24, 2001
Family and molecular data for a fine analysis of age at onset in Huntington diseaseF Squitieri, G Sabbadini, P Mandich, et al.Annals of Neurology|May 13, 1999
Congenital hypomyelination due to myelin protein zero Q215X mutationP Mandich, G L Mancardi, A Varese, et al.Pageof 5