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Neuroscience Letters|July 14, 1995
Molecular analysis of three cases with hereditary motor and sensory neuropathy with myelin outfoldingR James, E Bellone, E Nelis, et al.
European Neurology|January 1, 1994
17p11.2 duplication is a common finding in sporadic cases of Charcot-Marie-Tooth type 1G L Mancardi, A Uccelli, E Bellone, et al.
Journal of the American Chemical Society|September 23, 2015
Mechanistic Investigations of Water Oxidation by a Molecular Cobalt Oxide Analogue: Evidence for a Highly Oxidized Intermediate and Exclusive Terminal Oxo ParticipationAndy I Nguyen, Micah S Ziegler, Pascual Oña-Burgos, 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.
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.
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.
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