IRIS

BELLONE, EMILIA

BELLONE, EMILIA  

100009 - Dipartimento di Neuroscienze, Riabilitazione, Oftalmologia, Genetica e Scienze Materno-Infantili  

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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.
1993-2014: two decades of predictive testing for Huntington's disease at the Medical Genetics Unit of the University of Genoa. 1-gen-2017 Mandich, P; Lamp, M; Gotta, F; Gulli, R; Iacometti, A; Marchese, R; Bellone, E; Abbruzzese, G; Ferrandes, G
A CASE OF BIALLELIC SORD MUTATIONS ASSOCIATED WITH DISTAL WEAKNESS AND HISTOLOGICAL SIGNS OF MYOPATHY 1-gen-2023 Massucco, S; Fiorillo, C; Gemelli, C; Bellone, E; Patrone, S; Mandich, P; Scarsi, E; Faedo, E; Marinelli, L; Mongini, T; Traverso, M; Schenone, A; Grandis, M
A CMT2 family carrying the P7R mutation in the N- terminal region of the HSPB1 gene 1-gen-2017 Fortunato, Fernanda; Neri, Marcella; Geroldi, Alessandro; Bellone, Emilia; De Grandis, Domenico; Ferlini, Alessandra; Gualandi, Francesca
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, Emilia; Rodolico, C.; Toscano, A.; DI MARIA, Emilio; Cassandrini, D.; Pizzuti, A.; Pigullo, S.; Mazzeo, A.; Macaione, V.; Girlanda, P.; Vita, G.; Ajmar, Franco; Mandich, Paola
A misleading presentation of Mohr–Tranebjaerg syndrome: what is hidden behind an axonal neuropathy? 1-gen-2022 Geroldi, Alessandro; Trevisan, Lucia; Gaudio, Andrea; Gotta, Fabio; Patrone, Serena; Origone, Paola; Grandis, Marina; Gemelli, Chiara; Schenone, Angelo; Accogli, Andrea; Zara, Federico; Mandich, Paola; Bellone, Emilia
A novel autosomal dominant GDAP1 mutation in an Italian CMT2 family. 1-gen-2012 Manganelli, F; Pisciotta, C; Nolano, M; Capponi, Simona; Geroldi, Alessandro; Topa, A; Bellone, Emilia; Suls, A; Mandich, Paola; Santoro, L.
A novel de novo variant in POLR3B gene associated with a primary axonal involvement of the largest nerve fibers 1-gen-2023 Geroldi, A.; Tozza, S.; Fiorillo, C.; Nolano, M.; Fossa, P.; Vitale, F.; Domi, R.; Gaudio, A.; Mammi, A.; Patrone, S.; Barbera, A. L.; Origone, P.; Ponti, C.; Sanguineri, F.; Zara, F.; Cataldi, M.; Salpietro, V.; Venturi, C. B.; Massucco, S.; Schenone, A.; Manganelli, F.; Mandich, P.; Bellone, E.; Gotta, F.
A novel LITAF/SIMPLE mutation within a family with a demyelinating form of Charcot-Marie-Tooth disease. 1-gen-2014 Ciotti, P; Luigetti, M; Geroldi, Alessandro; Capponi, Simona; Pezzini, I; Gulli, R; Pazzaglia, C; Padua, L; Massa, R; Mandich, Paola; Bellone, Emilia
A novel mutation (D305V) in the early growth response 2 gene is associated with severe Charcot-Marie-Tooth type 1 disease. 1-gen-1999 Bellone, Emilia; DI MARIA, Emilio; Soriani, S; Varese, A; Doria, Ll; Ajmar, Franco; Mandich, Paola
A novel mutation of GDAP1 associated with Charcot-Marie-Tooth disease in three Italian families: evidence for a founder effect 1-gen-2004 DI MARIA, Emilio; Gulli, R.; Balestra, P.; Cassandrini, D.; Pigullo, S.; DORIA LAMBA, L.; Bado, M.; Schenone, Angelo; Ajmar, Franco; Mandich, Paola; Bellone, Emilia
A novel mutation of myelin protein zero associated with an axonal form of Charcot-Marie-Tooth disease 1-gen-2004 Santoro, L.; Manganelli, F.; DI MARIA, Emilio; Bordo, D.; Cassandrini, D.; Ajmar, Franco; Mandich, Paola; Bellone, Emilia
A novel mutation of Twinkle in Perrault syndrome: A not rare diagnosis? 1-gen-2020 Gotta, F; Lamp, M; Geroldi, A; Trevisan, L; Origone, P; Fugazza, G; Fabbri, S; Nesti, C; Rubegni, A; Morani, F; Santorelli, Fm; Bellone, E; Mandich, P.
A putative regulatory subunit (NR3A) of the NMDA receptor complex as candidate gene for susceptibility to schizophrenia: a case-control study 1-gen-2007 Gulli, R; Masnata, B; Bonvicini, C; Tura, Gb; Manglaviti, L; Vaggi, M; Mollica, M; Bellone, Emilia; Mandich, Paola; Gennarelli, M; DI MARIA, Emilio
Adult polycystic kidney disease: prenatal diagnosis with DNA polymorphic markers. 1-gen-1991 Bellone, Emilia; Mandich, Paola; P., Costa; L., Dalerba; Ajmar, Franco
Alternative Splicing in the Human PMP22 Gene: Implications in CMT1A Neuropathy 1-gen-2015 Visigalli, Davide; Castagnola, Patrizio; Capodivento, Giovanna; Geroldi, Alessandro; Bellone, Emilia; Mancardi, Gianluigi; Pareyson, Davide; Schenone, Angelo; Nobbio, Lucilla
An abnormal mRNA produced by a novel PMP22 splice site mutation associated with HNPP 1-gen-2006 Bellone, Emilia; Balestra, P; Ribizzi, G; Schenone, Angelo; Zocchi, G; DI MARIA, Emilio; Ajmar, Franco; Mandich, Paola
Analysis of the trinucleotide repeat expansion in Italian families affected with Huntington disease 1-gen-1994 Novelletto, A.; Persichetti, F.; Sabbadini, G.; Mandich, Paola; Bellone, Emilia; Ajmar, Franco; Pergola, M.; DEL SENNO, L.; MAC DONALD, M.; Gusella, J.; Frontali, M.
Autosomal dominant polycystic kidney disease: a linkage evaluation of heterogeneity in Italy. Italian Collaborative Group on Polycystic Kidney Disease. 1-gen-1990 Mandich, Paola; G., Restagno; G., Novelli; Bellone, Emilia; L., Potenza; O., Varetto; B., Dallapiccola; A., Carbonara; Ajmar, Franco
Autosomal-dominant transthyretin (TTR)-related amyloidosis is not a frequent CMT2 neuropathy "in disguise" 1-gen-2018 Grandis, M; Geroldi, A; Gulli, R; Manganelli, F; Gotta, F; Lamp, M; Origone, P; Trevisan, L; Gemelli, C; Fabbri, S; Schenone, A; Tozza, S; Santoro, L; Bellone, E; Mandich, P.