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