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Results:
1-7
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Results: 7
Authors:
Sironi, M
Bardoni, A
Felisari, G
Cagliani, R
Robotti, M
Comi, GP
Moggio, M
Bresolin, N
Citation: M. Sironi et al., Transcriptional activation of the non-muscle, full-length dystrophin isoforms in Duchenne muscular dystrophy skeletal muscle, J NEUR SCI, 186(1-2), 2001, pp. 51-57
Authors:
Bonglia, MC
Giorda, R
Borgatti, R
Felisari, G
Gagliardi, C
Selicorni, A
Zuffardi, O
Citation: Mc. Bonglia et al., Disruption of the ProSAP2 gene in a t(12;22)(q24.1;q13.3) is associated with the 22q13.3 deletion syndrome, AM J HU GEN, 69(2), 2001, pp. 261-268
Authors:
Bardoni, A
Felisari, G
Sironi, M
Comi, G
Lai, M
Robotti, M
Bresolin, N
Citation: A. Bardoni et al., Loss of Dp140 regulatory sequences is associated with cognitive impairmentin dystrophinopathies, NEUROMUSC D, 10(3), 2000, pp. 194-199
Authors:
Felisari, G
Boneschi, FM
Bardoni, A
Sironi, M
Comi, GP
Robotti, M
Turconi, AC
Lai, M
Corrao, G
Bresolin, N
Citation: G. Felisari et al., Loss of Dp140 dystrophin isoform and intellectual impairment in Duchenne dystrophy, NEUROLOGY, 55(4), 2000, pp. 559-564
Authors:
Barresi, R
Di Blasi, C
Negri, T
Brugnoni, R
Vitali, A
Felisari, G
Salandi, A
Daniel, S
Cornelio, F
Morandi, L
Mora, M
Citation: R. Barresi et al., Disruption of heart sarcoglycan complex and severe cardiomyopathy caused by beta sarcoglycan mutations, J MED GENET, 37(2), 2000, pp. 102-107
Authors:
Bardoni, A
Sironi, M
Felisari, G
Comi, GP
Bresolin, N
Citation: A. Bardoni et al., Absence of brain Dp140 isoform and cognitive impairment in Becker musculardystrophy, LANCET, 353(9156), 1999, pp. 897-898
Authors:
Turconi, AC
Benti, R
Castelli, E
Pochintesta, S
Felisari, G
Comi, G
Gagliardi, C
Del Piccolo, L
Bresolin, N
Citation: Ac. Turconi et al., Focal cognitive impairment in mitochondrial encephalomyopathies: a neuropsychological and neuroimaging study, J NEUR SCI, 170(1), 1999, pp. 57-63
Risultati:
1-7
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