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Mitochondrial dysfunction in experimental Charcot-Marie-Tooth type 1A (CMT1A) neuropathy. 1-gen-2009 Nobbio, Lucilla; Fiorese, F.; Prada, V.; Ravera, Silvia; Nitti, Mariapaola; Schenone, Angelo
A morphological reappraisal of Tubifex blanchardi Vejdovský, 1891 (Clitellata: Tubificidae) 1-gen-2009 Marotta, Roberto; Angelica, Crottini; Prada, Valeria; Ferraguti, Marco
Immunohistochemical evidnce of HLA-G expression in extravillous trophoblast invading decidual tissues. 1-gen-2010 Prada, V.; Musizzano, Y.; Mora, M.; Puppo, Francesco; Fulcheri, Ezio
GAIN OR LOSS OF GLYCOSYLATION: THE SWEET SIDE OF MYELIN PROTEIN ZERO 1-gen-2011 Prada, V.; Passalacqua, Mario; Luzzi, Paola; Bono, M.; Bellone, Emilia; Mandich, Paola; Shy, M. E.; Schenone, Angelo; Grandis, Marina
Hyccin, the Molecule Mutated in the Leukodystrophy Hypomyelination and Congenital Cataract (HCC), Is a Neuronal Protein. 1-gen-2012 Gazzerro, E; Baldassari, Simona; Giacomini, C; Musante, V; Fruscione, Floriana; La Padula, V; Biancheri, R; Scarfi', Sonia; Prada, V; Sotgia, F; Duncan, Id; Zara, F; Werner, Hb; Lisanti, Mp; Nobbio, Lucilla; Corradi, ANNA MARGHERITA; Minetti, Carlo
Gain of glycosylation: a new pathomechanism of Myelin Protein Zero mutations 1-gen-2012 Prada, V1; Passalacqua, Mario; Bono, M; Luzzi, Paola; Scazzola, S; Nobbio, La; Capponi, Simona; Bellone, Emilia; Mandich, Paola; Mancardi, GIOVANNI LUIGI; Shy, M; Schenone, Angelo; Grandis, Marina
P2X7 TARGETING IMPROVES IN VITRO MYELINATION IN EXPERIMENTAL CHARCOT-MARIE-TOOTH TYPE 1A (CMT1A) 1-gen-2013 Nobbio, L; Visigalli, D; Mannino, E; Fiorese, F; Pareyson, D; Sereda, Mw; Prada, V; Mancardi, Gl; Zocchi, E; Bruzzone, S; Schenone, A
P2X7 RECEPTOR IMPLICATION IN CHARCOT-MARIE-TOOTH TYPE 1A (CMT1A) 1-gen-2013 Nobbio, L; Visigalli, D; Mannino, E; Pareyson, D; Sereda, Mw; Prada, V; Mancardi, G; Zocchi, E; Bruzzone, S; Schenone, A
The diadenosine homodinucleotide P18 improvesin vitromyelination in experimental Charcot-Marie-Tooth type 1A 1-gen-2014 Nobbio, Lucilla; Visigalli, Davide; Mannino, Elena; Fiorese, Fulvia; Matthias U., Kassack; Sturla, Laura; Prada, Valeria; Antonio De, Flora; Zocchi, Elena; Bruzzone, Santina; Schenone, Angelo
Innovative quantitative testing of hand function in Charcot-Marie-Tooth neuropathy 1-gen-2015 Alberti, M. A; Mori, Laura; Francini, Luca; Poggi, I; Monti Bragadin, M; Bellone, Emilia; Grandis, Marina; Maggi, G; Reni, L; Sormani, MARIA PIA; Tacchino, A; Padua, L; Prada, V; Bove, Marco; Schenone, Angelo
Sural nerve biopsy and functional studies support the pathogenic role of a novel MPZ mutation. 1-gen-2015 Prada, Valeria; Capponi, Simona; Ursino, Giulia; Alberti, A; Callegari, I; Passalacqua, Mario; Marotta, Riccardo; Mandich, Paola; Bellone, Emilia; Schenone, Angelo; Grandis, Marina
Sacral Nerve Stimulation for Fecal Incontinence in a Patient with Antiphospholipid Syndrome- Related Autonomic Neuropathy 1-gen-2016 Giorli, Elisa; Franciotta, Diego; Serventi, Alberto; Binda, Gian Andrea; Canepa, Giorgio; Siciliano, Gabriele; Giannini, Fabio; Prada, Valeria; Schenone, Angelo; Benedetti, Luana
Hand Rehabilitation Treatment for Charcot-Marie-Tooth Disease: An Open Label Pilot Study 1-gen-2018 Prada, Valeria; Schizzi, Sara; Poggi, Ilaria; Mori, Laura; Gemelli, Chiara; Hamedani, Mehrnaz; Accogli, Susanna; Maggi, Giovanni; Grandis, Marina; Mancardi, Giovanni; Schenone, Angelo
A novel prion protein gene-truncating mutation causing autonomic neuropathy and diarrhea 1-gen-2018 Bommarito, G.; Cellerino, M.; Prada, V.; Venturi, C.; Capellari, S.; Cortelli, P.; Mancardi, G. L.; Parchi, P.; Schenone, A.
Testing overwork weakness in Charcot-Marie-tooth disease: Is it true or false? 1-gen-2018 Prada, V; Mori, L; Accogli, S; Rivarola, M; Schizzi, S; Hamedani, M; Schenone, A.
OUTCOMES AFTER SINGLE-CYCLE RITUXIMAB MONOTHERAPY IN PATIENTS WITH ANTI-MAG ANTIBODY POLYNEUROPATHY: A 11 YEARS FOLLOW-UP ANALYSIS 1-gen-2019 Benedetti, L.; Franciotta, D.; Briani, C.; Demichelis, C.; Grandis, M.; Prada, V; Schenone, A.; Garnero, M.
Diagnostic Value of Sural Nerve Biopsy: Retrospective Analysis of Clinical Cases From 1981 to 2017 1-gen-2019 Prada, V.; Massucco, S.; Venturi, C.; Geroldi, A.; Bellone, E.; Mandich, P.; Minuto, M.; Varaldo, E.; Mancardi, G.; Grandis, M.; Schenone, A.
A novel mutation in the N-terminal acting-binding domain of Filamin C protein causing a distal myofibrillar myopathy 1-gen-2019 Gemelli, Chiara; Prada, Valeria; Fiorillo, Chiara; Fabbri, Sabrina; Maggi, Lorenzo; Geroldi, Alessandro; Gibertini, Sara; Mandich, Paola; Trevisan, Lucia; Fossa, Paola; Tagliafico, Alberto Stefano; Schenone, Angelo; Grandis, Marina.
Outcomes after single-cycle rituximab monotherapy in patients with anti-MAG polyneuropathy: A bi-center experience with an average follow-up of 11 years 1-gen-2019 Benedetti, L; Garnero, M; Demichelis, C; Grandis, M; Briani, C; Beltramini, S; Bellucci, M; Prada, V; Massa, F; Gastaldi, M; Schenone, A; Franciotta, D.
Mutation update for myelin protein zero-related neuropathies and the increasing role of variants causing a late-onset phenotype 1-gen-2019 Callegari, Ilaria; Gemelli, C; Geroldi, A; Veneri, F; Mandich, P; D'Antonio, M; Pareyson, D; Shy, M E; Schenone, A; Prada, V; Grandis, M
Mostrati risultati da 1 a 20 di 36
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