ABBRUZZESE, MICHELE
ABBRUZZESE, MICHELE
100009 - Dipartimento di Neuroscienze, Riabilitazione, Oftalmologia, Genetica e Scienze Materno-Infantili
17p11.2 duplication is a common finding in sporadic cases of charcot-marie-tooth type 1
1994-01-01 Mancardi, G. L.; Uccelli, A.; Bellone, E.; Sghirlanzoni, A.; Mandich, P.; Pareyson, D.; Schenone, A.; Abbruzzese, M.; Ajmar, F.
A reassessment of sensory evoked potential parameters in multiple sclerosis: a discriminant analysis approach.
1981-01-01 Abbruzzese, Giovanni; Cocito, Leonardo; Ratto, S; Abbruzzese, Michele; Leandri, Massimo; Favale, Emilio
A restricted T cell response to myelin basic protein (MBP) is stable in multiple sclerosis (MS) patients.
1998-01-01 Uccelli, Antonio; Giunti, Debora; Salvetti, M; Ristori, G; Fenoglio, Daniela; Abbruzzese, Michele; Mancardi, GIOVANNI LUIGI
A study of lactoferrin and antibodies against lactoferrin in neurological diseases.
1998-01-01 S., Penco; B., Villaggio; Mancardi, GIOVANNI LUIGI; Abbruzzese, Michele; C., Garre
Acute axonal form of Guillain-Barre syndrome in a multiple sclerosis patient: chance association or linked disorders?
2000-01-01 Capello, E.; Roccatagliata, Luca; Schenone, Angelo; Gazzola, P.; Inglese, MARIA MATILDE; Abbruzzese, Michele; Mancardi, GIOVANNI LUIGI
Axonal damage and demyelination in long-term dorsal root ganglia cultures from a rat model of Charcot-Marie-Tooth type 1A disease
2006-01-01 Nobbio, Lucilla; Gherardi, Gianfranco; Vigo, Tiziana; Passalacqua, Mario; Melloni, Edon; Abbruzzese, Michele; Mancardi, GIOVANNI LUIGI; Nave, K. A.; Schenone, Angelo
Case 11-1997: critical-illness myopathy.
1997-01-01 Primavera, Alberto; Abbruzzese, Michele
Charcot-Marie-Tooth (CMT) 1a duplication at 17p11.2 in Italian families.
1992-01-01 Bellone, Emilia; Mandich, Paola; Mancardi, GIOVANNI LUIGI; Schenone, Angelo; Uccelli, Antonio; Abbruzzese, Michele; Sghirlanzoni, A; Pareyson, D; Ajmar, F.
Conduction time of the lemniscal pathway in males and females.
1980-01-01 Abbruzzese, Giovanni; Abbruzzese, Michele; Cocito, Leonardo; Favale, Emilio; Leandri, Massimo; Ratto, S.
Correlation between PMP-22 messenger RNA expression and phenotype in hereditary neuropathy with liability to pressure palsies
1997-01-01 Schenone, Angelo; Nobbio, L.; Caponetto, C.; Abbruzzese, Michele; Mandich, Paola; Bellone, Emilia; Ajmar, Franco; Gherardi, G.; Windebank, A. J.; Mancardi, GIOVANNI LUIGI
De novo duplication in Charcot-Marie Tooth type 1A.
1996-01-01 Mandich, Paola; Bellone, Emilia; Schenone, Angelo; Mancardi, GIOVANNI LUIGI; Abbruzzese, Michele; Ajmar, Franco
Different movement disorders responsive to carbamazepine in patients with brainstem focal lesions
2001-01-01 L., Benedetti; C., Finocchi; Grandis, Marina; A., Murialdo; Marinelli, Lucio; Abbruzzese, Michele; Marchese, Roberta; Schenone, Angelo; Abbruzzese, Giovanni
Due nuove componenti del potenziale evocato corticale somestesico. Osservazioni preliminari nel soggetto normale.
1979-01-01 Abbruzzese, Michele; Favale, Emilio; Leandri, Massimo; Ratto, S.
Early abnormalities in sciatic nerve function and structure in a rat model of Charcot-Marie-Tooth type 1A disease.
2004-01-01 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
Electrophysio-logical assessment of the central lemniscal pathway in man.
1979-01-01 Abbruzzese, Michele; Favale, Emilio; Leandri, Massimo; Ratto, S.
Experimental Charcot-Marie-Tooth type 1A: A cDNA microarrays analysis
2005-01-01 Vigo, Tiziana; Nobbio, Lucilla; Hummelen, Pv; Abbruzzese, Michele; Mancardi, GIOVANNI LUIGI; Verpoorten, N; Verhoeven, K; Sereda, Mw; Nave, Ka; Timmerman, V; Schenone, Angelo
Granulocyte-macrophage colony-stimulating factor activity in cerebrospinal fluid
1999-01-01 Leonardi, A.; Penco, S.; Gramigni, C.; Bason, C.; Ribizzi, G.; Gazzola, P.; Mancardi, GIOVANNI LUIGI; Bianchi, Giovanna; Abbruzzese, Michele; Garre', Cecilia
Guillain barré syndrome of axonal type in a multple sclerosis patient: Fortuitous association or linked disorders?
1997-01-01 Roccatagliata, L.; Capello, E.; Schenone, A.; Inglese, M.; Nobbio, L.; Grandis, M.; Maritato, F.; Abbruzzese, M.; Mancardi, G. L.
Hereditary motor and sensory neuropathy with myelin outfolding: clinical, genetic and neuropathological study of three cases
1994-01-01 Schenone, Angelo; Abbruzzese, Michele; Uccelli, Antonio; Mandich, Paola; James, R.; Bellone, Emilia; Giunchedi, M.; Rolando, S.; Capello, E.; Mancardi, GIOVANNI LUIGI
Hereditary motor and sensory neuropathy with deafness, mental retardation and absence of large myelinated fibers.
1992-01-01 Mancardi, GIOVANNI LUIGI; M. D., Rocco; Schenone, Angelo; Veneselli, EDVIGE MARIA; M., Doria; Abbruzzese, Michele; Tabaton, Massimo; C., Borrone
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| 17p11.2 duplication is a common finding in sporadic cases of charcot-marie-tooth type 1 | 1-gen-1994 | Mancardi, G. L.; Uccelli, A.; Bellone, E.; Sghirlanzoni, A.; Mandich, P.; Pareyson, D.; Schenone, A.; Abbruzzese, M.; Ajmar, F. | |
| A reassessment of sensory evoked potential parameters in multiple sclerosis: a discriminant analysis approach. | 1-gen-1981 | Abbruzzese, Giovanni; Cocito, Leonardo; Ratto, S; Abbruzzese, Michele; Leandri, Massimo; Favale, Emilio | |
| 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 | |
| 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 | |
| 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 | |
| Axonal damage and demyelination in long-term dorsal root ganglia cultures from a rat model of Charcot-Marie-Tooth type 1A disease | 1-gen-2006 | Nobbio, Lucilla; Gherardi, Gianfranco; Vigo, Tiziana; Passalacqua, Mario; Melloni, Edon; Abbruzzese, Michele; Mancardi, GIOVANNI LUIGI; Nave, K. A.; Schenone, Angelo | |
| Case 11-1997: critical-illness myopathy. | 1-gen-1997 | Primavera, Alberto; Abbruzzese, Michele | |
| Charcot-Marie-Tooth (CMT) 1a duplication at 17p11.2 in Italian families. | 1-gen-1992 | Bellone, Emilia; Mandich, Paola; Mancardi, GIOVANNI LUIGI; Schenone, Angelo; Uccelli, Antonio; Abbruzzese, Michele; Sghirlanzoni, A; Pareyson, D; Ajmar, F. | |
| Conduction time of the lemniscal pathway in males and females. | 1-gen-1980 | Abbruzzese, Giovanni; Abbruzzese, Michele; Cocito, Leonardo; Favale, Emilio; Leandri, Massimo; Ratto, S. | |
| 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 | |
| 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 | |
| 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 | |
| Due nuove componenti del potenziale evocato corticale somestesico. Osservazioni preliminari nel soggetto normale. | 1-gen-1979 | Abbruzzese, Michele; Favale, Emilio; Leandri, Massimo; Ratto, S. | |
| 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 | |
| Electrophysio-logical assessment of the central lemniscal pathway in man. | 1-gen-1979 | Abbruzzese, Michele; Favale, Emilio; Leandri, Massimo; Ratto, S. | |
| 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 | |
| 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 | |
| Guillain barré syndrome of axonal type in a multple sclerosis patient: Fortuitous association or linked disorders? | 1-gen-1997 | Roccatagliata, L.; Capello, E.; Schenone, A.; Inglese, M.; Nobbio, L.; Grandis, M.; Maritato, F.; Abbruzzese, M.; Mancardi, G. L. | |
| Hereditary motor and sensory neuropathy with myelin outfolding: clinical, genetic and neuropathological study of three cases | 1-gen-1994 | Schenone, Angelo; Abbruzzese, Michele; Uccelli, Antonio; Mandich, Paola; James, R.; Bellone, Emilia; Giunchedi, M.; Rolando, S.; Capello, E.; Mancardi, GIOVANNI LUIGI | |
| Hereditary motor and sensory neuropathy with deafness, mental retardation and absence of large myelinated fibers. | 1-gen-1992 | Mancardi, GIOVANNI LUIGI; M. D., Rocco; Schenone, Angelo; Veneselli, EDVIGE MARIA; M., Doria; Abbruzzese, Michele; Tabaton, Massimo; C., Borrone |