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Progressive sensory-motor polyneuropathy with tomaculous changes is associated to 17p11.2 deletion. 1-gen-1995 Mancardi, GIOVANNI LUIGI; Mandich, Paola; Nassani, S.; Schenone, Angelo; James, R.; Defferrari, R.; Bellone, Emilia; Giunchedi, M.; Ajmar, Franco; Abbruzzese, Michele
Molecular diagnosis of hereditary neuropathy with liability to pressure palsies (HNPP) by detection of 17p11.2 deletion in Italian patients. 1-gen-1995 Mandich, Paola; R., James; S., Nassani; R., Defferrari; Bellone, Emilia; Mancardi, GIOVANNI LUIGI; Schenone, Angelo; Abbruzzese, Michele; M., Rocchi; Ajmar, Franco
De novo duplication in Charcot-Marie Tooth type 1A. 1-gen-1996 Mandich, Paola; Bellone, Emilia; Schenone, Angelo; Mancardi, GIOVANNI LUIGI; Abbruzzese, Michele; Ajmar, Franco
Use of cosH1 probe in hereditary neuropathy with liability to pressure palsies: a reliable genetic test for demonstration of identical size of 17p11.2 deletion in unrelated patients. 1-gen-1996 Bellone, Emilia; Schenone, Angelo; Mancardi, GIOVANNI LUIGI; G. A., Nicholson; Abbruzzese, Michele; F., Ajmar; Mandich, Paola
Correlation between PMP-22 messenger RNA expression and phenotype in hereditary neuropathy with liability to pressure palsies 1-gen-1997 Schenone, Angelo; Nobbio, L.; Caponetto, C.; Abbruzzese, Michele; Mandich, Paola; Bellone, Emilia; Ajmar, Franco; Gherardi, G.; Windebank, A. J.; Mancardi, GIOVANNI LUIGI
Underexpression of messenger RNA for peripheral myelin protein 22 in hereditary neuropathy with liability to pressure palsies 1-gen-1997 Schenone, Angelo; Nobbio, Lucilla; Mandich, Paola; Bellone, Emilia; Abbruzzese, Michele; Ajmar, Franco; Mancardi, GIOVANNI LUIGI; Windebank, Aj
Case 11-1997: critical-illness myopathy. 1-gen-1997 Primavera, Alberto; Abbruzzese, Michele
Multifocal motor neuropathy with conduction block after Campylobacter jejuni enteritis. 1-gen-1997 Abbruzzese, Michele; L., Reni; Schenone, Angelo; Mancardi, GIOVANNI LUIGI; Primavera, Alberto
A study of lactoferrin and antibodies against lactoferrin in neurological diseases. 1-gen-1998 S., Penco; B., Villaggio; Mancardi, GIOVANNI LUIGI; Abbruzzese, Michele; C., Garre
A restricted T cell response to myelin basic protein (MBP) is stable in multiple sclerosis (MS) patients. 1-gen-1998 Uccelli, Antonio; Giunti, Debora; Salvetti, M; Ristori, G; Fenoglio, Daniela; Abbruzzese, Michele; Mancardi, GIOVANNI LUIGI
Granulocyte-macrophage colony-stimulating factor activity in cerebrospinal fluid 1-gen-1999 Leonardi, A.; Penco, S.; Gramigni, C.; Bason, C.; Ribizzi, G.; Gazzola, P.; Mancardi, GIOVANNI LUIGI; Bianchi, Giovanna; Abbruzzese, Michele; Garre', Cecilia
Acute axonal form of Guillain-Barre syndrome in a multiple sclerosis patient: chance association or linked disorders? 1-gen-2000 Capello, E.; Roccatagliata, Luca; Schenone, Angelo; Gazzola, P.; Inglese, MARIA MATILDE; Abbruzzese, Michele; Mancardi, GIOVANNI LUIGI
Early electophysiological changes in transgenic rat model of charcot-marie-tooth. 1-gen-2001 Grandis, Marina; Abbruzzese, Michele; Lunardi, Gianluigi; Nobbio, L.; Mancardi, GIOVANNI LUIGI; Leandri, Massimo; Schenone, Angelo
Different movement disorders responsive to carbamazepine in patients with brainstem focal lesions 1-gen-2001 L., Benedetti; C., Finocchi; Grandis, Marina; A., Murialdo; Marinelli, Lucio; Abbruzzese, Michele; Marchese, Roberta; Schenone, Angelo; Abbruzzese, Giovanni
PMP22 transgenic dorsal root ganglia cultures show myelin abnormalities similar to those of human CMT1A. 1-gen-2001 Nobbio, Lucilla; Mancardi, GIOVANNI LUIGI; Grandis, Marina; G., Levi; U., Suter; K. A., Nave; A. J., Windebank; Abbruzzese, Michele; Schenone, Angelo
Insulin treatment enhances expression of IGF-I in sural nerves of diabetic patients. 1-gen-2001 Grandis, Marina; Nobbio, Lucilla; Abbruzzese, Michele; L., Banchi; Minuto, Francesco; A., Barreca; S., Garrone; Mancardi, GIOVANNI LUIGI; Schenone, Angelo
Sonography of the median nerve in Charcot-Marie-Tooth disease 1-gen-2002 Martinoli, Carlo; Schenone, Angelo; Bianchi, S.; Mandich, Paola; Caponetto, C.; Abbruzzese, Michele; Derchi, Lorenzo
Impairment of PMP22 transgenic Schwann cells differentiation in culture: implications for Charcot-Marie-Tooth type 1A disease. 1-gen-2004 Nobbio, Lucilla; Vigo, T; Abbruzzese, Michele; Levi, G; Brancolini, C; Mantero, S; Grandis, Marina; Benedetti, L; Mancardi, GIOVANNI LUIGI; Schenone, Angelo
Early abnormalities in sciatic nerve function and structure in a rat model of Charcot-Marie-Tooth type 1A disease. 1-gen-2004 Grandis, Marina; Leandri, Massimo; Vigo, Tiziana; Cilli, M; Sereda, Mw; Gherardi, G; Benedetti, L; Mancardi, GIOVANNI LUIGI; Abbruzzese, Michele; Nave, Ka; Nobbio, Lucilla; Schenone, Angelo
Experimental Charcot-Marie-Tooth type 1A: A cDNA microarrays analysis 1-gen-2005 Vigo, Tiziana; Nobbio, Lucilla; Hummelen, Pv; Abbruzzese, Michele; Mancardi, GIOVANNI LUIGI; Verpoorten, N; Verhoeven, K; Sereda, Mw; Nave, Ka; Timmerman, V; Schenone, Angelo
Mostrati risultati da 21 a 40 di 42
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