IRIS

MAZZEO, Anna

MAZZEO, Anna  

Dipartimento di Medicina Clinica e Sperimentale  

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"Dropped- head" syndrome due to isolated myositis of neck extensor muscles: MRI findings 1-gen-2006 Gaeta, Michele; Mazziotti, Silvio; Toscano, Antonio; Rodolico, Carmelo; Mazzeo, Anna; Blandino, Alfredo
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 15-year consolidated overview of data in over 6000 patients from the Transthyretin Amyloidosis Outcomes Survey (THAOS) 1-gen-2023 Gentile, Luca; Coelho, Teresa; Dispenzieri, Angela; Conceição, Isabel; Waddington-Cruz, Márcia; Kristen, Arnt; Wixner, Jonas; Diemberger, Igor; Gonzalez-Moreno, Juan; Cariou, Eve; Maurer, Mathew S; Planté-Bordeneuve, Violaine; Garcia-Pavia, Pablo; Tournev, Ivailo; Gonzalez-Costello, Jose; Duarte, Alejandra Gonzalez; Grogan, Martha; Mazzeo, Anna; Chapman, Doug; Gupta, Pritam; Glass, Oliver; Amass, Leslie
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 family with autosomal dominant mutilating neuropathy not linked to either Charcot-Marie-Tooth disease type 2B (CMT2B) or hereditary sensory neuropathy type I (HSN I) loci 1-gen-2002 Bellone, E.; Rodolico, Carmelo; Toscano, Antonio; DI MARIA, E.; Cassandrini, D.; Pizzuti, A.; Pigullo, S.; Mazzeo, Anna; Macaione, Vincenzo; Girlanda, Paolo; Vita, Giuseppe; Ajmar, F.; Mandich, P.
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 multicentric study of the disease risks and first manifestations in Hereditary transthyretin amyloidosis (ATTRv): insights for an earlier diagnosis 1-gen-2023 Planté-Bordeneuve, Violaine; Gorram, Farida; Olsson, Malin; Anan, Intissar; Mazzeo, Anna; Gentile, Luca; Cisneros-Barroso, Eugenia; Gonzalez-Moreno, Juan; Losada, Ines; Waddington-Cruz, Marcia; Pinto, Luiz Felipe; Parman, Yeşim; Fanen, Pascale; Alarcon, Flora; Nuel, Gregory
A nationwide retrospective analysis on the effect of immune therapies in patients with chronic inflammatory demyelinating polyradiculoneuropathy 1-gen-2010 Cocito, D; Paolasso, I.; Antonini, G.; Benedetti, L.; Briani, C.; Comi, C.; Fazio, R.; Jann, S.; Matà, S.; Mazzeo, Anna; Sabatelli, M.; Nobile Orazio, E.
A nationwide retrospective analysis on the effect of immune therapies in patients with chronic inflammatory demyelinating polyradiculoneuropathy 1-gen-2010 Cocito, D; Paolasso, I; Antonini, G; Benedetti, L; Briani, C; Comi, C; Fazio, R; Jann, S; Matà, S; Mazzeo, Anna; Sabatelli, M; Nobile Orazio, E; Italian Network for CIDP, Register
A Nouvel serum MicroRNA signature to screen ATTR 1-gen-2017 Aguennouz, M; Mazzeo, A; Gentile, L; Stancanelli, C; Russo, M; Polito, F; Ragusa, M; DI GIORGIO, Rosa Maria; Vita, G
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-2011 Musumeci, Olimpia; Bassi, M. T.; Mazzeo, Anna; Grandis, M.; Crimella, C.; Martinuzzi, A.; Toscano, Antonio
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
A NOVEL SERUM MICRORNA SIGNATURE TO SCREEN TRANSTHYRETIN-RELATED FAMILIAL AMYLOID POLYNEUROPATHY 1-gen-2017 Aguennouz, M; Mazzeo, A; Gentile, L; Stancanelli, C; Russo, M; Polito, F; Ragusa, M; DI GIORGIO, Rosa Maria; Vita, G
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