IRIS

SIMONE, Isabella Laura

SIMONE, Isabella Laura  

DIPARTIMENTO DI SCIENZE MEDICHE DI BASE, NEUROSCIENZE ED ORGANI DI SENSO (attivo dal 06/09/2012 al 30/09/2022)  

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Risultati 1 - 20 di 226 (tempo di esecuzione: 0.028 secondi).
Titolo Data di pubblicazione Autore(i) File
. Amyotrophic lateral sclerosis: a new missense mutation in the SOD1 gene 1-gen-2013 Tortelli, R; Conforti, Fl; Cortese, R; D'Errico, E; Distaso, E; Mazzei, R; Ungaro, C; Magariello, A; Gambardella, A; Simone, Isabella Laura; Logroscino, Giancarlo
1H-MR Spectroscopy profiles in normal appearing white matter(NAWM) of clinically isolated sindromes suggestive of multiple sclerosis(CIS) 1-gen-2001 Simone, Isabella Laura; C., Tortorella; D., Carrara; D., Mezzapesa; Federico, Francesco; A., Bellacosa; A., Ceccarelli; P., Livrea
1H-MRSA comparison of normal appearing white matter in different clinical MS subgroups 1-gen-2001 Simone, Isabella Laura; D., Carrara; C., Tortorella; Federico, Francesco; A., Bellacosa; D., Mezzapesa; A., Ceccarelli; P., Livrea
99mTc-HM-PAO SPET and proton magnetic resonance spectroscopy in patients with ischaemic cerebral infarction 1-gen-1994 A., D'Addabbo; F., Federico; F., Lauriero; Rubini, Giuseppe; D., Rubini; C., Conte; V., Inchingolo; Simone, Isabella Laura
99Tcm-HMPAO SPET and 1H-MRS (Proton Magnetic Resonance Spectroscopy) in patients with ischaemic cerebral infarction 1-gen-1996 F., Lauriero; F., Federico; Rubini, Giuseppe; C., Conte; Simone, Isabella Laura; V., Inchingolo; A., D'Addabbo
A case of Landau-Kleffner syndrome secondary to inflammatory demyelinating disease 1-gen-1993 Perniola, T; Margari, Lucia; Buttiglione, M; Andreula, C; Simone, Isabella Laura; Santostasi, R.
A 71-nucleotide deletion in the periaxin gene in an Italian patient with late-onset slowly progressive demyelinating CMT 1-gen-2020 Citrigno, L; Zoccolella, S; Lastella, P; Simone, Il; Muglia, M
A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis. 1-gen-2014 Fogh, I; Ratti, A; Gellera, C; Lin, K; Tiloca, C; Moskvina, V; Corrado, L; Sorarù, G; Cereda, C; Corti, S; Gentilini, D; Calini, D; Castellotti, B; Mazzini, L; Querin, G; Gagliardi, S; Del Bo, R; Conforti, Fl; Siciliano, G; Inghilleri, M; Saccà, F; Bongioanni, P; Penco, S; Corbo, M; Sorbi, S; Filosto, M; Ferlini, A; Di Blasio, Am; Signorini, S; Shatunov, A; Jones, A; Shaw, Pj; Morrison, Ke; Farmer, Ae; Van Damme, P; Robberecht, W; Chiò, A; Traynor, Bj; Sendtner, M; Melki, J; Meininger, V; Hardiman, O; Andersen, Pm; Leigh, Np; Glass, Jd; Overste, D; Diekstra, Fp; Veldink, Jh; van Es, Ma; Shaw, Ce; Weale, Me; Lewis, Cm; Williams, J; Brown, Rh; Landers, Je; Ticozzi, N; Ceroni, M; Pegoraro, E; Comi, Gp; D'Alfonso, S; van den Berg, Lh; Taroni, F; Al Chalabi, A; Powell, J; Silani, V; Slagen, Consortium; Collaborators, ; ITALSGEN Consortium: Brescia Morra, V; Filla, A; Massimo, F; Marsili, A; Viviana, P; Puorro, G; La Bella, V; Logroscino, Giancarlo; Monsurrò, Mr; Quattrone, A; Simone, Isabella Laura; Ahmeti, Kb; Ajroud Driss, S; Armstrong, J; Birve, A; Blauw, Hm; Bruijn, L; Chen, W; Comeau, Mc; Cronin, S; Soraya, Ga; Grab, Jd; Groen, Ej; Haines, Jl; Heller, S; Huang, J; Hung, Wy; Jaworski, Jm; Khan, H; Langefeld, Cd; Marion, Mc; Mclaughlin, Rl; Miller, Jw; Mora, G; Pericak Vance, Ma; Rampersaud, E; Siddique, N; Siddique, T; Smith, Bn; Sufit, R; Topp, S; Vance, C; van Vught, P; Yang, Y; Zheng, J. G.
A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD 1-gen-2011 Renton, Ae; Majounie, E; Waite, A; Simón Sánchez, J; Rollinson, S; Gibbs, Jr; Schymick, Jc; Laaksovirta, H; van Swieten, Jc; Myllykangas, L; Kalimo, H; Paetau, A; Abramzon, Y; Remes, Am; Kaganovich, A; Scholz, Sw; Duckworth, J; Ding, J; Harmer, Dw; Hernandez, Dg; Johnson, Jo; Mok, K; Ryten, M; Trabzuni, D; Guerreiro, Rj; Orrell, Rw; Neal, J; Murray, A; Pearson, J; Jansen, Ie; Sondervan, D; Seelaar, H; Blake, D; Young, K; Halliwell, N; Callister, Jb; Toulson, G; Richardson, A; Gerhard, A; Snowden, J; Mann, D; Neary, D; Nalls, Ma; Peuralinna, T; Jansson, L; Isoviita, Vm; Kaivorinne, Al; Hölttä Vuori, M; Ikonen, E; Sulkava, R; Benatar, M; Wuu, J; Chiò, A; Restagno, G; Borghero, G; Sabatelli, M; The ITALSGEN, Consortium; Simone, Isabella Laura; Heckerman, D; Rogaeva, E; Zinman, L; Rothstein, Jd; Sendtner, M; Drepper, C; Eichler, Ee; Alkan, C; Abdullaev, Z; Pack, Sd; Dutra, A; Pak, E; Hardy, J; Singleton, A; Williams, Nm; Heutink, P; Pickering Brown, S; Morris, Hr; Tienari, Pj; Traynor, Bj
A novel Angiogenin gene mutation in a sporadic patient with amyotrophic lateral sclerosis from southern Italy 1-gen-2008 Conforti, Fl; Sprovieri, T; Mazzei, R; Ungaro, C; LA BELLA, V; Tessitore, A; Patitucci, A; Magariello, A; Gabriele, Al; Tedeschi, G; Simone, Isabella Laura; Majorana, G; Valentino, P; Condino, F; Bono, F; Monsurrò, Mr; Muglia, M; Quattrone, A.
A Novel CSF1R Mutation in a Patient with Clinical and Neuroradiological Features of Hereditary Diffuse Leukoencephalopathy with Axonal Spheroids 1-gen-2015 Di Donato, Ilaria; Stabile, Carmen; Bianchi, Silvia; Taglia, Ilaria; Mignarri, Andrea; Salvatore, Simona; Giorgio, Elisa; Brusco, Alfredo; Simone, Isabella Laura; Dotti, Maria Teresa; Federico, Antonio
A novel KIF5A mutation in an Italian family marked by spastic paraparesis and congenital deafness 1-gen-2014 Muglia, M; Citrigno, L.; D'Errico, Eustachio; Magariello, A.; Distaso, Eugenio; Gasparro, A. A.; Scarafino, Antonio; Patitucci, A.; Conforti, F. L.; Mazzei, Rosaria; Cortese, R.; Tortelli, Rosanna; Simone, Isabella Laura
A rare association between multiple sclerosis and Charcot-Marie-Tooth type 1B 1-gen-2016 Cortese, Rosa; Zoccolella, Stefano; Muglia, Maria; Patitucci, Alessandra; Scarafino, Antonio; Paolicelli, Damiano; Simone, Isabella Laura
Acute changes in blood-CSF barrier permselectivity to serum proteins after intrathecal methotrexate and CNS irradiation 1-gen-1985 Troiano, Maria; Simone, Isabella Laura; Zimatore, Gb; Logroscino, Giancarlo; Pisicchio, L; Lojacono, G; Colella, R; Ceci, A.; Livrea, Paolo
Adherence to riluzole in patients with amyotrophic lateral sclerosis: An observational study 1-gen-2018 Introna, Alessandro; D’Errico, Eustachio; Modugno, Boris; Scarafino, Antonio; Fraddosio, Angela; Distaso, Eugenio; Tempesta, Irene; Mastronardi, Antonella; Simone, Isabella Laura
Adult-onset Rasmussen's encephalitis: anatomical-electrographic-clinical features of 7 Italian cases 1-gen-2006 Villani, F; Pincherle, A; Antozzi, C; Chiapparini, L; Granata, T; Michelucci, R; Rubboli, G; Simone, Isabella Laura; Bellomo, R; Spreafico, R.
Age-related gadolinium-enhancement of MRI brain lesions in multiple sclerosis. 1-gen-2005 Tortorella, C; Bellacosa, A; Paolicelli, Damiano; Fuiani, A; Di Monte, E; Simone, Isabella Laura; Giaquinto, P; Livrea, Paolo; Troiano, Maria
ALS multidisciplinary clinic and survival. Results from a population-based study in Southern Italy 1-gen-2007 Zoccolella, S; Beghi, E; Palagano, G; Fraddosio, A; Guerra, V; Lepore, V; Simone, Isabella Laura; Lamberti, P; Serlenga, L; Logroscino, Giancarlo
Alzheimer disease: comparison of 99mTc-HMPAO SPET and 1H-MRS data 1-gen-1996 F., Lauriero; F., Federico; Rubini, Giuseppe; D., Rubini; V., Inchigolo; V., Lucivero; Simone, Isabella Laura; A., D'Addabbo
An exploration of anger phenomenology in multiple sclerosis 1-gen-2009 Nocentini, U; Tedeschi, G; Migliaccio, R; Dinacci, D; Lavorgna, L; Bonavita, S; Bresciamorra, V; Comanducci, G; Coniglio, G; Livrea, Paolo; Mannu, R; Orefice, G; Paciello, M; Patti, F; Quattrone, A; Salemi, G; Savettieri, G; Simone, Isabella Laura; Valentino, P; Zappia, M; Bonavita, V; Musicco, M; Caltagirone, C.