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Results: 1-4 |
Results: 4

Authors: Bruno, C Bado, M Minetti, C Cordone, G DiMauro, S
Citation: C. Bruno et al., Novel mutation in the CPT II gene in a child with periodic febrile myalgiaand myoglobinuria, J CHILD NEU, 15(6), 2000, pp. 390-393

Authors: Carbone, I Bruno, C Sotgia, F Bado, M Broda, P Masetti, E Panella, A Zara, F Bricarelli, FD Cordone, G Lisanti, MP Minetti, C
Citation: I. Carbone et al., Mutation in the CAV3 gene causes partial caveolin-3 deficiency and hyperCKemia, NEUROLOGY, 54(6), 2000, pp. 1373-1376

Authors: Mandich, P Mancardi, GL Varese, A Soriani, S Di Maria, E Bellone, E Bado, M Gross, L Windebank, AJ Ajmar, F Schenone, A
Citation: P. Mandich et al., Congenital hypomyelination due to myelin protein zero Q215X mutation, ANN NEUROL, 45(5), 1999, pp. 676-678

Authors: Repetto, S Bado, M Broda, P Lucania, G Masetti, E Sotgia, F Carbone, I Pavan, A Bonilla, E Cordone, G Lisanti, MP Minetti, C
Citation: S. Repetto et al., Increased number of caveolae and caveolin-3 overexpression in Duchenne muscular dystrophy, BIOC BIOP R, 261(3), 1999, pp. 547-550
Risultati: 1-4 |