Authors:
di Barletta, MR
Ricci, E
Galluzzi, G
Tonali, P
Mora, M
Morandi, L
Romorini, A
Voit, T
Orstavik, KH
Merlini, L
Trevisan, C
Biancalana, V
Housmanowa-Petrusewicz, I
Bione, S
Ricotti, R
Schwartz, K
Bonne, G
Toniolo, D
Citation: Mr. Di Barletta et al., Different mutations in the LMNA gene cause autosomal dominant and autosomal recessive Emery-Dreifuss muscular dystrophy, AM J HU GEN, 66(4), 2000, pp. 1407-1412
Authors:
Galluzzi, G
Deidda, G
Cacurri, S
Colantoni, L
Piazzo, N
Vigneti, E
Ricci, E
Servidei, S
Merico, B
Pachi, A
Brambati, B
Mangiola, F
Tonali, P
Felicetti, L
Citation: G. Galluzzi et al., Molecular analysis of 4q35 rearrangements in facioscapulohumeral muscular dystrophy (FSHD): application to family studies for a correct genetic advice and a reliable prenatal diagnosis of the disease, NEUROMUSC D, 9(3), 1999, pp. 190-198
Authors:
Ricci, E
Galluzzi, G
Deidda, G
Cacurri, S
Colantoni, L
Merico, B
Piazzo, N
Servidei, S
Vigneti, E
Pasceri, V
Silvestri, G
Mirabella, M
Mangiola, F
Tonali, P
Felicetti, L
Citation: E. Ricci et al., Progress in the molecular diagnosis of facioscapulohumeral muscular dystrophy and correlation between the number of KpnI repeats at the 4q35 locus and clinical phenotype, ANN NEUROL, 45(6), 1999, pp. 751-757
Authors:
Murillo, FM
Kobayashi, H
Pegoraro, E
Galluzzi, G
Creel, G
Mariani, C
Farina, E
Ricci, E
Alfonso, G
Pauli, RM
Hoffman, EP
Citation: Fm. Murillo et al., Genetic localization of a new locus for recessive familial spastic paraparesis to 15q13-15, NEUROLOGY, 53(1), 1999, pp. 50-56