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Journal of Neurology|May 1, 1995
Molecular diagnosis of hereditary neuropathy with liability to pressure palsies (HNPP) by detection of 17p11.2 deletion in Italian patientsP Mandich, R James, S Nassani, et al.Annals of Neurology|December 24, 1997
Correlation between PMP-22 messenger RNA expression and phenotype in hereditary neuropathy with liability to pressure palsiesA Schenone, L Nobbio, C Caponnetto, et al.Journal of the Neurological Sciences|July 1, 1995
Progressive sensory-motor polyneuropathy with tomaculous changes is associated to 17p11.2 deletionG L Mancardi, P Mandich, S Nassani, et al.Clinical Genetics|June 1, 1995
Screening of neurofibromatosis type 1 gene: identification of a large deletion and of an intronic variantA Grifa, M R Piemontese, S Melchionda, et al.Italian Journal of Neurological Sciences|August 10, 2000
Predictive testing for Huntington's disease: ten years' experience in two Italian centresP Mandich, G Jacopini, E Di Maria, et al.Human Molecular Genetics|July 1, 1994
Polymorphism analysis of the huntingtin gene in Italian families affected with Huntington diseaseA Novelletto, F Persichetti, G Sabbadini, et al.American Journal of Medical Genetics|May 8, 1999
Exclusion of the ninjurin gene as a candidate for hereditary sensory neuropathies type I and type IIP Mandich, E Bellone, E Di Maria, 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.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.Pageof 8