Sfoglia per Autore
Correlation between clinical/neurophysiological findings and quality of life in Charcot-Marie-Tooth type 1A
2008-01-01 Padua, L.; Shy, M. E.; Aprile, I.; Cavallaro, Tiziana; Pareyson, D.; Quattrone, A.; Rizzuto, Nicolo'; Vita, G.; Tonali, P.; Schenone, A.
Axonal neuropathy due to myelin protein zero mutation misdiagnosed as amyloid neuropathy
2008-01-01 Briani, C.; Adami, F.; Cavallaro, Tiziana; Taioli, Federica; Ferrari, Sergio; Fabrizi, Gian Maria
Relationship between clinical examination, quality of life, disability and depression in CMT patients: Italian multicenter study.
2008-01-01 Padua, L; Aprile, I; Cavallaro, Tiziana; Commodari, I; Pareyson, D; Quattrone, A; Rizzuto, Nicolo'; Vita, G; Tonali, P; Schenone, A; Italian CMT QoL Study, Group; Fabrizi, Gian Maria; among study, Collaborators
Malattia di Charco-Marie-Tooth. Guida alla diagnosi molecolare.
2009-01-01 Fabrizi, Gian Maria; Taioli, Federica; Ferrarini, Moreno; Cabrini, Ilaria; Testi, Silvia; Cavallaro, Tiziana; Rizzuto, Nicolo'
Further evidence that mutations in FGD4/frabin cause Charcot-Marie-Tooth disease type 4H.
2009-01-01 Fabrizi, Gian Maria; Taioli, Federica; Cavallaro, Tiziana; Ferrari, Sergio; Bertolasi, Laura; Casarotto, M.; Rizzuto, Nicolo'; Deconinck, T.; Timmerman, V.; De Jonghe, P.
Multineuropathy in a patient with HBV infection, polyarteritis nodosa and celiac disease.
2009-01-01 Squintani, G.; Ferrari, Sergio; Caramaschi, P.; Cavallaro, Tiziana; Refatti, N.; Rizzuto, Nicolo'; Tonin, Paola
Clinico-pathological findings in a patient with progressive cerebellar ataxia, autoimmune polyendocrine syndrome, hepatocellular carcinoma and anti-GAD autoantibodies.
2010-01-01 Piccolo, G.; Tavazzi, E.; Cavallaro, Tiziana; Romani, A.; Scelsi, R.; Martino, G.
Severe CMT type 2 with fatal encephalopathy associated with a novel MFN2 splicing mutation.
2010-01-01 Boaretto, F.; Vettori, A.; Casarin, A.; Vazza, G.; Muglia, M.; Rossetto, M. G.; Cavallaro, Tiziana; Rizzuto, Nicolo'; Carelli, V.; Salviati, L.; Mostacciuolo, M. L.; Martinuzzi, A.
Four novel cases of periaxin-related neuropathy and review of the literature.
2010-01-01 Marchesi, C.; Milani, M.; Morbin, M.; Cesani, M.; Lauria, G.; Scaioli, V.; Piccolo, G.; Fabrizi, Gian Maria; Cavallaro, Tiziana; Taroni, F.; Pareyson, D.
Atypical Alzheimer's disease: a case report.
2010-01-01 Iemolo, F.; Cavallaro, Tiziana; Rizzuto, Nicolo'
Natural history of Charcot-Marie-Tooth 2: 2-year follow-up of muscle strength, walking ability and quality of life.
2010-01-01 Padua, L.; Pareyson, D.; Aprile, I.; Cavallaro, Tiziana; Quattrone, D. A.; Rizzuto, Nicolo'; Vita, G.; Tonali, P.; Schenone, A.
Déjerine-Sottas syndrome with a silent nucleotide change of myelin protein zero gene.
2011-01-01 Taioli, Federica; Cabrini, Ilaria; Cavallaro, Tiziana; Simonati, Alessandro; Testi, Silvia; Fabrizi, Gian Maria
Ascorbic acid in Charcot-Marie-Tooth disease type 1A (CMT-TRIAAL and CMT-TRAUK): a double-blind randomised trial.
2011-01-01 Pareyson, D.; Reilly, M. M.; Schenone, A.; Fabrizi, G. M.; Cavallaro, T.; Santoro, L.; Vita, G.; Quattrone, A.; Padua, L.; Gemignani, F.; Visioli, F.; Laurà, M.; Radice, D.; Calabrese, D.; Hughes, R. A.; Solari, A.
Inherited demyelinating neuropathies with micromutations of peripheral myelin protein 22 gene.
2011-01-01 Taioli, Federica; Cabrini, Ilaria; Cavallaro, Tiziana; Acler, M.; Fabrizi, Gian Maria
Vascular endothelial growth factor helps differentiate neuropathies in rare plasma cell dyscrasias.
2011-01-01 Briani, C.; Fabrizi, Gian Maria; Ruggero, S.; Torre, C. D.; Ferrarini, Moreno; Campagnolo, M.; Cavallaro, Tiziana; Ferrari, Sergio; Scarlato, M.; Taioli, Federica; Adami, F.
Variable presentations of TTR-related familial amyloid polyneuropathy in seventeen patients.
2011-01-01 Cappellari, M.; Cavallaro, Tiziana; Ferrarini, Moreno; Cabrini, Ilaria; Taioli, Federica; Ferrari, Sergio; Merlini, G.; Obici, L.; Briani, C.; Fabrizi, Gian Maria
Reply: Novel peripheral myelin protein 22 (PMP22) micromutations associated with variable phenotypes in Greek patients with Charcot–Marie–Tooth disease
2012-01-01 Fabrizi, Gian Maria; Taioli, Federica; Cavallaro, Tiziana
Sporadic transthyretin amyloidosis with a novel TTR gene mutation misdiagnosed as primary amyloidosis.
2012-01-01 Briani, C.; Cavallaro, Tiziana; Ferrari, Sergio; Taioli, Federica; Calamelli, S.; Verga, L.; Adami, F.; Fabrizi, Gian Maria
Neuropathy in eosinophilic granulomatosis with polyangiitis: a comparison study of 24 cases with or without prior leukotriene antagonist exposure.
2014-01-01 GIUSTI DEL GIARDINO, Luisa; Cavallaro, Tiziana; Anzola, Gp; Lombardi, C; Ferrari, Sergio
Pentraxin-3 and VEGF in POEMS syndrome: A 2-year longitudinal study.
2014-01-01 Briani, C.; Dalla Torre, C.; Lessi, F.; Cavallaro, Tiziana; Scarlato, M.; Ferrari, Sergio; Campagnolo, M.; Lucchetta, M.; Cabrini, Ilaria; Morbin, M.; Lauria, G.; Adami, F.; Manfredi, A. A.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Correlation between clinical/neurophysiological findings and quality of life in Charcot-Marie-Tooth type 1A | 1-gen-2008 | Padua, L.; Shy, M. E.; Aprile, I.; Cavallaro, Tiziana; Pareyson, D.; Quattrone, A.; Rizzuto, Nicolo'; Vita, G.; Tonali, P.; Schenone, A. | |
| Axonal neuropathy due to myelin protein zero mutation misdiagnosed as amyloid neuropathy | 1-gen-2008 | Briani, C.; Adami, F.; Cavallaro, Tiziana; Taioli, Federica; Ferrari, Sergio; Fabrizi, Gian Maria | |
| Relationship between clinical examination, quality of life, disability and depression in CMT patients: Italian multicenter study. | 1-gen-2008 | Padua, L; Aprile, I; Cavallaro, Tiziana; Commodari, I; Pareyson, D; Quattrone, A; Rizzuto, Nicolo'; Vita, G; Tonali, P; Schenone, A; Italian CMT QoL Study, Group; Fabrizi, Gian Maria; among study, Collaborators | |
| Malattia di Charco-Marie-Tooth. Guida alla diagnosi molecolare. | 1-gen-2009 | Fabrizi, Gian Maria; Taioli, Federica; Ferrarini, Moreno; Cabrini, Ilaria; Testi, Silvia; Cavallaro, Tiziana; Rizzuto, Nicolo' | |
| Further evidence that mutations in FGD4/frabin cause Charcot-Marie-Tooth disease type 4H. | 1-gen-2009 | Fabrizi, Gian Maria; Taioli, Federica; Cavallaro, Tiziana; Ferrari, Sergio; Bertolasi, Laura; Casarotto, M.; Rizzuto, Nicolo'; Deconinck, T.; Timmerman, V.; De Jonghe, P. | |
| Multineuropathy in a patient with HBV infection, polyarteritis nodosa and celiac disease. | 1-gen-2009 | Squintani, G.; Ferrari, Sergio; Caramaschi, P.; Cavallaro, Tiziana; Refatti, N.; Rizzuto, Nicolo'; Tonin, Paola | |
| Clinico-pathological findings in a patient with progressive cerebellar ataxia, autoimmune polyendocrine syndrome, hepatocellular carcinoma and anti-GAD autoantibodies. | 1-gen-2010 | Piccolo, G.; Tavazzi, E.; Cavallaro, Tiziana; Romani, A.; Scelsi, R.; Martino, G. | |
| Severe CMT type 2 with fatal encephalopathy associated with a novel MFN2 splicing mutation. | 1-gen-2010 | Boaretto, F.; Vettori, A.; Casarin, A.; Vazza, G.; Muglia, M.; Rossetto, M. G.; Cavallaro, Tiziana; Rizzuto, Nicolo'; Carelli, V.; Salviati, L.; Mostacciuolo, M. L.; Martinuzzi, A. | |
| Four novel cases of periaxin-related neuropathy and review of the literature. | 1-gen-2010 | Marchesi, C.; Milani, M.; Morbin, M.; Cesani, M.; Lauria, G.; Scaioli, V.; Piccolo, G.; Fabrizi, Gian Maria; Cavallaro, Tiziana; Taroni, F.; Pareyson, D. | |
| Atypical Alzheimer's disease: a case report. | 1-gen-2010 | Iemolo, F.; Cavallaro, Tiziana; Rizzuto, Nicolo' | |
| Natural history of Charcot-Marie-Tooth 2: 2-year follow-up of muscle strength, walking ability and quality of life. | 1-gen-2010 | Padua, L.; Pareyson, D.; Aprile, I.; Cavallaro, Tiziana; Quattrone, D. A.; Rizzuto, Nicolo'; Vita, G.; Tonali, P.; Schenone, A. | |
| Déjerine-Sottas syndrome with a silent nucleotide change of myelin protein zero gene. | 1-gen-2011 | Taioli, Federica; Cabrini, Ilaria; Cavallaro, Tiziana; Simonati, Alessandro; Testi, Silvia; Fabrizi, Gian Maria | |
| Ascorbic acid in Charcot-Marie-Tooth disease type 1A (CMT-TRIAAL and CMT-TRAUK): a double-blind randomised trial. | 1-gen-2011 | Pareyson, D.; Reilly, M. M.; Schenone, A.; Fabrizi, G. M.; Cavallaro, T.; Santoro, L.; Vita, G.; Quattrone, A.; Padua, L.; Gemignani, F.; Visioli, F.; Laurà, M.; Radice, D.; Calabrese, D.; Hughes, R. A.; Solari, A. | |
| Inherited demyelinating neuropathies with micromutations of peripheral myelin protein 22 gene. | 1-gen-2011 | Taioli, Federica; Cabrini, Ilaria; Cavallaro, Tiziana; Acler, M.; Fabrizi, Gian Maria | |
| Vascular endothelial growth factor helps differentiate neuropathies in rare plasma cell dyscrasias. | 1-gen-2011 | Briani, C.; Fabrizi, Gian Maria; Ruggero, S.; Torre, C. D.; Ferrarini, Moreno; Campagnolo, M.; Cavallaro, Tiziana; Ferrari, Sergio; Scarlato, M.; Taioli, Federica; Adami, F. | |
| Variable presentations of TTR-related familial amyloid polyneuropathy in seventeen patients. | 1-gen-2011 | Cappellari, M.; Cavallaro, Tiziana; Ferrarini, Moreno; Cabrini, Ilaria; Taioli, Federica; Ferrari, Sergio; Merlini, G.; Obici, L.; Briani, C.; Fabrizi, Gian Maria | |
| Reply: Novel peripheral myelin protein 22 (PMP22) micromutations associated with variable phenotypes in Greek patients with Charcot–Marie–Tooth disease | 1-gen-2012 | Fabrizi, Gian Maria; Taioli, Federica; Cavallaro, Tiziana | |
| Sporadic transthyretin amyloidosis with a novel TTR gene mutation misdiagnosed as primary amyloidosis. | 1-gen-2012 | Briani, C.; Cavallaro, Tiziana; Ferrari, Sergio; Taioli, Federica; Calamelli, S.; Verga, L.; Adami, F.; Fabrizi, Gian Maria | |
| Neuropathy in eosinophilic granulomatosis with polyangiitis: a comparison study of 24 cases with or without prior leukotriene antagonist exposure. | 1-gen-2014 | GIUSTI DEL GIARDINO, Luisa; Cavallaro, Tiziana; Anzola, Gp; Lombardi, C; Ferrari, Sergio | |
| Pentraxin-3 and VEGF in POEMS syndrome: A 2-year longitudinal study. | 1-gen-2014 | Briani, C.; Dalla Torre, C.; Lessi, F.; Cavallaro, Tiziana; Scarlato, M.; Ferrari, Sergio; Campagnolo, M.; Lucchetta, M.; Cabrini, Ilaria; Morbin, M.; Lauria, G.; Adami, F.; Manfredi, A. A. |
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