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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.British Journal of Cancer|May 1, 1995
p53 oncoprotein overexpression correlates with mutagen-induced chromosome fragility in head and neck cancer patients with multiple malignanciesO Gallo, S Bianchi, M L Giovannucci-Uzzielli, et al.Microbial Drug Resistance (Larchmont, N.Y.)|January 1, 1995
Molecular epidemiology of enterococci with high-level resistance to aminoglycosidesO Privitera, A Agodi, M Puntorieri, 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.Muscle & Nerve|April 24, 2001
Insulin treatment enhances expression of IGF-I in sural nerves of diabetic patientsM Grandis, L Nobbio, M Abbruzzese, 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.Annals of Neurology|July 18, 2001
PMP22 transgenic dorsal root ganglia cultures show myelin abnormalities similar to those of human CMT1AL Nobbio, G Mancardi, M Grandis, et al.International Journal of Immunopathology and Pharmacology|June 12, 2003
Simple renal cysts in hypertensive patients: relation between cyst growing and anti-hypertensive therapyC Schiavone, L Salvatore, A Primavera, 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.Pageof 12