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Neurology|February 1, 1997
Underexpression of messenger RNA for peripheral myelin protein 22 in hereditary neuropathy with liability to pressure palsiesA Schenone, L Nobbio, P Mandich, et al.
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.
American Journal of Medical Genetics|April 1, 1990
Autosomal dominant polycystic kidney disease: a linkage evaluation of heterogeneity in Italy. Italian Collaborative Group on Polycystic Kidney DiseaseP Mandich, G Restagno, G Novelli, 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 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.
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.
Human Heredity|January 1, 1991
Forensic applications of molecular genetic analysis: an Italian collaborative study on paternity testing by the determination of variable number of tandem repeat DNA polymorphismsP Gasparini, P Mandich, G Novelli, et al.
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