MAZZEO, Anna

MAZZEO, Anna  

Dipartimento di Medicina Clinica e Sperimentale  

Mostra records
Risultati 1 - 20 di 299 (tempo di esecuzione: 0.064 secondi).
Titolo Data di pubblicazione Autore(i) File
2D Feature Strain Echocardiography in patients with transthyretin familial amyloid plyneuropathy and diffuse cardiac 99mTc-DPD accumulation 1-gen-2011 Minutoli, Fabio; DI BELLA, Gianluca; Restifo Pecorella, G; Crisafulli, C; Di Leo, R; Mazzeo, Anna; Carerj, Scipione; Baldari, Sergio
6MWT performance correlates with peripheral neuropathy but not with cardiac involvement in patients with hereditary transthyretin amyloidosis (hATTR) 1-gen-2019 Vita, Gian Luca; Stancanelli, Claudia; Gentile, Luca; Barcellona, Costanza; Russo, Massimo; Di Bella, Gianluca; Vita, Giuseppe; Mazzeo, Anna
A CMT1A PATIENT WITH PAINFUL AND DISABLING SYMPTOMS: FAST RECOVERY AFTER IVIG TREATMENT. 1-gen-2009 Mazzeo, Anna; Granata, Francesca; Longo, Marcello; Portaro, Simona; Messina, Corrado; Vita, G.; Toscano, Antonio
A multicenter, randomized, double-blind, placebo-controlled trial of long-term ascorbic acid treatment in Charcot-Marie-Tooth disease type 1A (CMT-TRIAAL): the study protocol 1-gen-2006 Pareyson, D; Schenone, A; Fabrizi, Gm; Santoro, L; Padua, L; Quattrone, A; Vita, Giuseppe; Gemignani, F; Visioli, F; Solari, A; E., Salsano; V., Scaioli; C., Ciano; M., Rimoldi; G., Lauria; E., Rizzetto; F., Camozzi; M., Grandis; E., Narciso; L., Nobbio; L., Benedetti; N., Rizzuto; T., Cavallaro; L., Bertolasi; A., Casano; F., Manganelli; M., Nolano; C., Pazzaglia; P., Valentino; R., Nistico’; D., Pirritano; A., Lucisano; M., Canino; Mazzeo, Anna; Aguennouz, M'Hammed; DI LEO, Rita; Girlanda, Paolo; G., Majorana; Ciranni, Annamaria; N., Lanzano; F., Brindani; C., Lettieri; P., Bogani
A novel CX32 mutation with unusual phenotype 1-gen-2008 Mazzeo, Anna; Fabrizi, Gm; Taioli, F; Arena, G; Toscano, G; Vita, Giuseppe
A novel Cx32 mutation with unusual phenotype 1-gen-2008 Mazzeo, Anna; Fabrizi, G; Taioli, F; Arena, G; Toscano, A; Vita, Giuseppe
A novel CX32 mutation with unusual phenotype 1-gen-2008 Mazzeo, Anna; Fabrizi, Gm; Taioli, F; Arena, G; Toscano, G; Vita, Giuseppe
A novel Cx32 mutation with unusual phenotype. 1-gen-2008 Mazzeo, Anna; Fabrizi, G; Taioli, F; Arena, G; Toscano, Antonio; Vita, Giuseppe
A NOVEL MUTATION IN KIF5A GENE CAUSING HEREDITARY SPASTIC PARAPLEGIA WITH AXONAL NEUROPATHY; 1-gen-2009 Musumeci, Olimpia; Toscano, Antonio; Mazzeo, A.; Rossetto, Mg; Martinuzzi, A; Bassi, Mt
Acquired idiopathic generalized anhidrosis: a case report 1-gen-2006 Mazzeo, Anna; Nolano, M; DI LEO, R; Provitera, V; Santoro, L; Vita, Giuseppe
Acquired idiopathic generalized anhidrosis: a case report 1-gen-2006 DI LEO, R; Mazzeo, Anna; Nolano, M; Provitera, V; Santoro, L; Vita, Giuseppe
Acquired idiopathic generalized anhidrosis: a case report. 1-gen-2006 Mazzeo, Anna; Nolano, M; DI LEO, Rita; Provitera, V; Santoro, L; Vita, Giuseppe
Acquired idiopathic generalized anhidrosis: a case report. 1-gen-2006 DI LEO, Rita; Mazzeo, Anna; Nolano, M; Provitera, V; Santoro, L; Vita, Giuseppe
Activation and localization of transcription factor NF-KB in peripheral neuropathies of different origin. 1-gen-2002 Mazzeo, Anna; Aguennouz, M'Hammed; Vita, Giuseppe
Activation of nuclear factor-kappa B in inflammatory myopathies and Duchenne muscular dystrophy 1-gen-2003 Monici, Mc; Aguennouz, M'Hammed; Mazzeo, Anna; Messina, Corrado; Vita, Giuseppe
Activation of nuclear factor-κB in inflammatory myopathies and Duchenne muscular dystrophy 1-gen-2003 MONICI M., C; Mazzeo, A; Aguennouz, M'Hammed; AND VITA, G.
Adult polyglucosan body disease in a patient originally diagnosed with Fabry's disease. 1-gen-2014 Sagnelli, A; Savoiardo, M; Marchesi, C; Morandi, L; Mora, M; Morbin, M; Farina, L; Mazzeo, Anna; Toscano, Antonio; Pagliarani, S; Lucchiari, S; Comi, Gp; Salsano, E; Pareyson, D.
Advances in Treatment of ATTRv Amyloidosis: State of the Art and Future Prospects 1-gen-2020 Russo, Massimo; Gentile, Luca; Toscano, Antonio; Aguennouz, M'Hammed; Vita, Giuseppe; Mazzeo, Anna
Amyloid myopathy presenting with rhabdomyolisis: evidence of complement activation. 1-gen-2006 Rodolico, Carmelo; Musumeci, Olimpia; Toscano, Antonio; Mazzeo, Anna; Pastura, C; Maimone, D; Vita, Giuseppe
Amyloid myopathy presenting with rhabdomyolysis 1-gen-2005 Pastura, C; Rodolico, Carmelo; Toscano, A; Migliorato, A; Maimone, D; Mazzeo, Anna; Vita, Giuseppe