Authors:
Del Bo, R
Torrente, Y
Corti, S
D'Angelo, MG
Comi, GP
Fagiolari, G
Salani, S
Cova, A
Pisati, F
Moggio, M
Ausenda, C
Scarlato, G
Bresolin, N
Citation: R. Del Bo et al., In vitro and in vivo tetracycline-controlled myogenic conversion of NIH-3T3 cells: Evidence of programmed cell death after muscle cell transplantation, CELL TRANSP, 10(2), 2001, pp. 209-221
Authors:
Cagliani, R
Comi, GP
Tancredi, L
Sironi, M
Fortunato, F
Giorda, R
Bardoni, A
Moggio, M
Prelle, A
Bresolin, N
Scarlato, G
Citation: R. Cagliani et al., Primary beta-sarcoglycanopathy manifesting as recurrent exercise-induced myoglobinuria, NEUROMUSC D, 11(4), 2001, pp. 389-394
Authors:
Savasta, S
Comi, GP
Perini, MP
Lupi, A
Strazzer, S
Rognoni, F
Rossoni, R
Citation: S. Savasta et al., Leigh disease: Clinical, neuroradiologic, and biochemical study of three new cases with cytochrome c oxidase deficiency, J CHILD NEU, 16(8), 2001, pp. 608-613
Authors:
Comi, GP
Fortunato, F
Lucchiari, S
Bordoni, A
Prelle, A
Jann, S
Keller, A
Ciscato, P
Galbiati, S
Chiveri, L
Torrente, Y
Scarlato, G
Bresolin, N
Citation: Gp. Comi et al., beta-enolase deficiency, a new metabolic myopathy of distal glycolysis, ANN NEUROL, 50(2), 2001, pp. 202-207
Authors:
Del Bo, R
Comi, GP
Perini, MP
Strazzer, S
Bresolin, N
Scarlato, G
Citation: R. Del Bo et al., Down's syndrome fibroblasts anticipate the accumulation of specific ageing-related mtDNA mutations, ANN NEUROL, 49(1), 2001, pp. 137-138
Authors:
Sironi, M
Pozzoli, U
Cagliani, R
Comi, GP
Bardoni, A
Bresolin, N
Citation: M. Sironi et al., Analysis of splicing parameters in the dystrophin gene: relevance for physiological and pathogenetic splicing mechanisms, HUM GENET, 109(1), 2001, pp. 73-84
Authors:
Sciacco, M
Prelle, A
Comi, GP
Napoli, L
Battistel, A
Bresolin, N
Tancredi, L
Lamperti, C
Bordoni, A
Fagiolari, G
Ciscato, P
Chiveri, L
Perini, MP
Fortunato, F
Adobbati, L
Messina, S
Toscano, A
Martinelli-Boneschi, F
Papadimitriou, A
Scarlato, G
Moggio, M
Citation: M. Sciacco et al., Retrospective study of patients affected of a large population with mitochondrial disorders: clinical, morphological and molecular genetic evaluation, J NEUROL, 248(9), 2001, pp. 778-788
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:
Torrente, Y
D'Angelo, MG
Li, Z
Del Bo, R
Corti, S
Mericskay, M
DeLiso, A
Fassati, A
Paulin, D
Comi, GP
Scarlato, G
Bresolin, N
Citation: Y. Torrente et al., Transplacental injection of somite-derived cells in mdx mouse embryos for the correction of dystrophin deficiency, HUM MOL GEN, 9(12), 2000, pp. 1843-1852
Authors:
Prelle, A
Sciacco, M
Comi, GP
Messina, S
Carpo, M
Ciscato, P
Orazio, EN
Fortunato, F
Mora, G
Bignotti, V
Fagiolari, G
Moggio, M
Scarlato, G
Citation: A. Prelle et al., A sporadic, atypical case of desminopathy: morphological and immunologicalcharacterization, CLIN NEUR, 19(4), 2000, pp. 208-212
Authors:
Musumeci, O
Andreu, AL
Shanske, S
Bresolin, N
Comi, GP
Rothstein, R
Schon, EA
DiMauro, S
Citation: O. Musumeci et al., Intragenic inversion of mtDNA: A new type of pathogenic mutation in a patient with mitochondrial myopathy, AM J HU GEN, 66(6), 2000, pp. 1900-1904
Authors:
Torrente, Y
D'Angelo, MG
Del Bo, R
DeLiso, A
Casati, R
Benti, R
Corti, S
Comi, GP
Gerundini, P
Anichini, A
Scarlato, G
Bresolin, N
Citation: Y. Torrente et al., Extracorporeal circulation as a new experimental pathway for myoblast implantation in mdx mice, CELL TRANSP, 8(3), 1999, pp. 247-258
Authors:
Tiranti, V
Jaksch, M
Hofmann, S
Galimberti, C
Hoertnagel, K
Lulli, L
Freisinger, P
Bindoff, L
Gerbitz, KD
Comi, GP
Uziel, G
Zeviani, M
Meitinger, T
Citation: V. Tiranti et al., Loss-of-function mutations of SURF-1 are specifically associated with Leigh syndrome with cytochrome c oxidase deficiency, ANN NEUROL, 46(2), 1999, pp. 161-166
Authors:
Hadjigeorgiou, GM
Comi, GP
Bordoni, A
Shen, J
Chen, YT
Salani, S
Toscano, A
Fortunato, F
Lucchiari, S
Bresolin, N
Rodolico, C
Piscaglia, MG
Franceschina, L
Papadimitriou, A
Scarlato, G
Citation: Gm. Hadjigeorgiou et al., Novel donor splice site mutations of AGL gene in glycogen storage disease type IIIa, J INH MET D, 22(6), 1999, pp. 762-763
Authors:
Kaukonen, J
Zeviani, M
Comi, GP
Piscaglia, MG
Peltonen, L
Suomalainen, A
Citation: J. Kaukonen et al., A third locus predisposing to multiple deletions of mtDNA in autosomal dominant progressive external ophthalmoplegia, AM J HU GEN, 65(1), 1999, pp. 256-261