AAAAAA

   
Results: 1-6 |
Results: 6

Authors: Gellera, C Castellotti, B Riggio, MC Silani, V Morandi, L Testa, D Casali, C Taroni, F Di Donato, S Zeviani, M Mariotti, C
Citation: C. Gellera et al., Superoxide dismutase gene mutations in Italian patients with familial and sporadic amyotrophic lateral sclerosis: identification of three novel missense mutations, NEUROMUSC D, 11(4), 2001, pp. 404-410

Authors: Sander, T Schulz, H Saar, K Gennaro, E Riggio, MC Bianchi, A Zara, F Luna, D Bulteau, C Kaminska, A Ville, D Cieuta, C Picard, F Prud'homme, JF Bate, L Sundquist, A Gardiner, RM Janssen, GAMAJ de Haan, GJ Kasteleijn-Nolst-Trenite, DGA Bader, A Lindhout, D Riess, O Wienker, TF Janz, D Reis, A
Citation: T. Sander et al., Genome search for susceptibility loci of common idiopathic generalised epilepsies, HUM MOL GEN, 9(10), 2000, pp. 1465-1472

Authors: Filla, A Mariotti, C Caruso, G Coppola, G Cocozza, S Castaldo, I Calabrese, O Salvatore, E De Michele, G Riggio, MC Pareyson, D Gellera, C Di Donato, S
Citation: A. Filla et al., Relative frequencies of CAG expansions in spinocerebellar ataxia and dentatorubropallidoluysian atrophy in 116 Italian families, EUR NEUROL, 44(1), 2000, pp. 31-36

Authors: Pareyson, D Gellera, C Castellotti, B Antonelli, A Riggio, MC Mazzucchelli, F Girotti, F Pietrini, V Mariotti, C Di Donato, S
Citation: D. Pareyson et al., Clinical and molecular studies of 73 Italian families with autosomal dominant cerebellar ataxia type I: SCA1 and SCA2 are the most common genotypes, J NEUROL, 246(5), 1999, pp. 389-393

Authors: Gennaro, E Malacarne, M Carbone, I Riggio, MC Bianchi, A Bonanni, P Boniver, C Dalla Bernardina, B De Marco, P Giordano, L Guerrini, R Santorum, E Sebastianelli, R Vecchi, M Veggiotti, P Vigevano, F Bricarelli, FD Zara, F
Citation: E. Gennaro et al., No evidence of a major locus for benign familial infantile convulsions on chromosome 19q12-q13.1, EPILEPSIA, 40(12), 1999, pp. 1799-1803

Authors: Pietrini, V Godani, M Calzetti, S Negrotti, A Castellotti, B Riggio, MC Toffoli, C
Citation: V. Pietrini et al., Clinical and genetic study of a family with spinocerebellar ataxia type 1 (SCA1) and beta-thalassemia, ITAL J NEUR, 19(6), 1998, pp. 345-350
Risultati: 1-6 |