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Results: 1-13 |
Results: 13

Authors: Melacini, P Gambino, A Caforio, A Barchitta, A Valente, ML Angelini, A Fanin, M Thiene, G Angelini, C Casarotto, D Danieli, GA Dalla-Volta, S
Citation: P. Melacini et al., Heart transplantation in patients with inherited myopathies associated with end-stage cardiomyopathy: Molecular and biochemical defects on cardiac and skeletal muscle, TRANSPLAN P, 33(1-2), 2001, pp. 1596-1599

Authors: Fanin, M Pegoraro, E Matsuda-Asada, C Brown, RH Angelini, C
Citation: M. Fanin et al., Calpain-3 and dysferlin protein screening in patients with limb-girdle dystrophy and myopathy, NEUROLOGY, 56(5), 2001, pp. 660-665

Authors: Fanin, M Hoffman, EP Angelini, C Pegoraro, E
Citation: M. Fanin et al., Private beta- and gamma-sarcoglycan gene mutations: Evidence of a founder effect in northern Italy, HUM MUTAT, 16(1), 2000, pp. 13-17

Authors: Salviati, L Laverda, AM Zancan, L Fanin, M Angelini, C Meznaric-Petrusa, N
Citation: L. Salviati et al., Acute quadriplegic myopathy in a 17-month-old boy, J CHILD NEU, 15(1), 2000, pp. 63-66

Authors: Bonifati, DM Ori, C Rossi, CR Caira, S Fanin, M Angelini, C
Citation: Dm. Bonifati et al., Neuromuscular damage after hyperthermic isolated limb perfusion in patients with melanoma or sarcoma treated with chemotherapeutic agents, CANC CHEMOT, 46(6), 2000, pp. 517-522

Authors: Pegoraro, E Fanin, M Trevisan, CP Angelini, C Hoffman, EP
Citation: E. Pegoraro et al., A novel laminin alpha 2 isoform in severe laminin alpha 2 deficient congenital muscular dystrophy, NEUROLOGY, 55(8), 2000, pp. 1128-1134

Authors: Pegoraro, E Fanin, M Angelini, C Hoffman, EP
Citation: E. Pegoraro et al., Prenatal diagnosis in a family affected with beta-sarcoglycan muscular dystrophy, NEUROMUSC D, 9(5), 1999, pp. 323-325

Authors: Melacini, P Fanin, M Duggan, DJ Freda, MP Berardinelli, A Danieli, GA Barchitta, A Hoffman, EP Dalla Volta, S Angelini, C
Citation: P. Melacini et al., Heart involvement in muscular dystrophies due to sarcoglycan gene mutations, MUSCLE NERV, 22(4), 1999, pp. 473-479

Authors: Angelini, C Fanin, M Freda, MP Duggan, DJ Siciliano, G Hoffman, EP
Citation: C. Angelini et al., The clinical spectrum of sarcoglycanopathies, NEUROLOGY, 52(1), 1999, pp. 176-179

Authors: Fanin, M Angelini, C
Citation: M. Fanin et C. Angelini, Regeneration in sarcoglycanopathies: expression studies of sarcoglycans and other muscle proteins, J NEUR SCI, 165(2), 1999, pp. 170-177

Authors: Fanin, M Melacini, P Angelini, C Danieli, GA
Citation: M. Fanin et al., Could utrophin rescue the myocardium of patients with dystrophin gene mutations?, J MOL CEL C, 31(8), 1999, pp. 1501-1508

Authors: Martinuzzi, A Schievano, G Nascimbeni, A Fanin, M
Citation: A. Martinuzzi et al., McArdle's disease - The unsolved mystery of the reappearing enzyme, AM J PATH, 154(6), 1999, pp. 1893-1897

Authors: Melacini, P Fanin, M Angelini, A Pegoraro, E Livi, U Danieli, GA Hoffman, EP Thiene, G Dalla Volta, S Angelini, C
Citation: P. Melacini et al., Cardiac transplantation in a Duchenne muscular dystrophy carrier, NEUROMUSC D, 8(8), 1998, pp. 585-590
Risultati: 1-13 |