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Results:
1-9
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Results: 9
Authors:
Feriotto, G
Ferlini, A
Ravani, A
Calzolari, E
Mischiati, C
Bianchi, N
Gambari, R
Citation: G. Feriotto et al., Biosensor technology for real-time detection of the cystic fibrosis W1282Xmutation in CFTR, HUM MUTAT, 18(1), 2001, pp. 70-81
Authors:
Bastianutto, C
Bestard, JA
Lahnakoski, K
Broere, D
De Visser, M
Zaccolo, M
Pozzan, T
Ferlini, A
Muntoni, F
Patarnello, T
Citation: C. Bastianutto et al., Dystrophin muscle enhancer 1 is implicated in the activation of non-muscleisoforms in the skeletal muscle of patients with X-linked dilated cardiomyopathy, HUM MOL GEN, 10(23), 2001, pp. 2627-2635
Authors:
Vacca, M
Filippini, F
Budillon, A
Rossi, V
Mercadante, G
Manzati, E
Gualandi, F
Bigoni, S
Trabanelli, C
Pini, G
Calzolari, E
Ferlini, A
Meloni, I
Hayek, G
Zappella, M
Renieri, A
D'Urso, M
D'Esposito, M
MacDonald, F
Kerr, A
Dhanjal, S
Hulten, M
Citation: M. Vacca et al., Mutation analysis of the MECP2 gene in British and Italian Rett syndrome females, J MOL MED-J, 78(11), 2001, pp. 648
Authors:
Ferlini, A
Obici, L
Manzati, E
Biadi, O
Tarantino, E
Conigli, P
Merlini, G
D'Alessandro, M
Mazzaferro, V
Tassinari, CA
Salvi, F
Citation: A. Ferlini et al., Mutation and transcription analysis of transthyretin gene in Italian families with hereditary amyloidosis: a putative novel 'hot spot' in codon 47, CLIN GENET, 57(4), 2000, pp. 284-290
Authors:
Naom, I
D'Alessandro, M
Sewry, CA
Jardine, P
Ferlini, A
Moss, T
Dubowitz, J
Muntoni, F
Citation: I. Naom et al., Mutations in the laminin alpha 2-chain gene in two children with early-onset muscular dystrophy, BRAIN, 123, 2000, pp. 31-41
Authors:
Torelli, S
Ferlini, A
Obici, L
Sewry, C
Muntoni, F
Citation: S. Torelli et al., Expression, regulation and localisation of dystrophin isoforms in human foetal skeletal and cardiac muscle, NEUROMUSC D, 9(8), 1999, pp. 541-551
Authors:
Ferlini, A
Sewry, C
Melis, MA
Mateddu, A
Muntoni, F
Citation: A. Ferlini et al., X-linked dilated cardiomyopathy and the dystrophin gene, NEUROMUSC D, 9(5), 1999, pp. 339-346
Authors:
D'Alessandro, M
Naom, I
Ferlini, A
Sewry, C
Dubowitz, V
Muntoni, F
Citation: M. D'Alessandro et al., Is there selection in favour of heterozygotes in families with merosin-deficient congenital muscular dystrophy?, HUM GENET, 105(4), 1999, pp. 308-313
Authors:
Mascalchi, M
Salvi, FP
Pirini, MG
D'Errico, A
Ferlini, A
Lolli, F
Plasmati, R
Tessa, C
Villari, N
Tassinari, CA
Citation: M. Mascalchi et al., Transthyretin amyloidosis and superficial siderosis of the CNS, NEUROLOGY, 53(7), 1999, pp. 1498-1503
Risultati:
1-9
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