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1. Sironi, M; Bardoni, A; Felisari, G; Cagliani, R; Robotti, M; Comi, GP; Moggio, M; Bresolin, N
   Transcriptional activation of the non-muscle, full-length dystrophin isoforms in Duchenne muscular dystrophy skeletal muscle
   JOURNAL OF THE NEUROLOGICAL SCIENCES
   
   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
2. Bonglia, MC; Giorda, R; Borgatti, R; Felisari, G; Gagliardi, C; Selicorni, A; Zuffardi, O
   Disruption of the ProSAP2 gene in a t(12;22)(q24.1;q13.3) is associated with the 22q13.3 deletion syndrome
   AMERICAN JOURNAL OF HUMAN GENETICS
   
   M.C. 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
3. Bardoni, A; Felisari, G; Sironi, M; Comi, G; Lai, M; Robotti, M; Bresolin, N
   Loss of Dp140 regulatory sequences is associated with cognitive impairmentin dystrophinopathies
   NEUROMUSCULAR DISORDERS
   
   A. Bardoni et al., "Loss of Dp140 regulatory sequences is associated with cognitive impairmentin dystrophinopathies", NEUROMUSC D, 10(3), 2000, pp. 194-199
4. Felisari, G; Boneschi, FM; Bardoni, A; Sironi, M; Comi, GP; Robotti, M; Turconi, AC; Lai, M; Corrao, G; Bresolin, N
   Loss of Dp140 dystrophin isoform and intellectual impairment in Duchenne dystrophy
   NEUROLOGY
   
   G. Felisari et al., "Loss of Dp140 dystrophin isoform and intellectual impairment in Duchenne dystrophy", NEUROLOGY, 55(4), 2000, pp. 559-564
5. Barresi, R; Di Blasi, C; Negri, T; Brugnoni, R; Vitali, A; Felisari, G; Salandi, A; Daniel, S; Cornelio, F; Morandi, L; Mora, M
   Disruption of heart sarcoglycan complex and severe cardiomyopathy caused by beta sarcoglycan mutations
   JOURNAL OF MEDICAL GENETICS
   
   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
6. Bardoni, A; Sironi, M; Felisari, G; Comi, GP; Bresolin, N
   Absence of brain Dp140 isoform and cognitive impairment in Becker musculardystrophy
   LANCET
   
   A. Bardoni et al., "Absence of brain Dp140 isoform and cognitive impairment in Becker musculardystrophy", LANCET, 353(9156), 1999, pp. 897-898
7. Turconi, AC; Benti, R; Castelli, E; Pochintesta, S; Felisari, G; Comi, G; Gagliardi, C; Del Piccolo, L; Bresolin, N
   Focal cognitive impairment in mitochondrial encephalomyopathies: a neuropsychological and neuroimaging study
   JOURNAL OF THE NEUROLOGICAL SCIENCES
   
   A.C. Turconi et al., "Focal cognitive impairment in mitochondrial encephalomyopathies: a neuropsychological and neuroimaging study", J NEUR SCI, 170(1), 1999, pp. 57-63
8. PICCININI L; FELISARI G; BRAMBILLA D; TURCONI AC; GAVIOLI C; BORGHI A; PARINI B; BRESOLIN N
   PATTERNS OF HEARING-LOSS AND AUDITORY PATHWAYS DYSFUNCTION IN ADULT MITOCHONDRIAL ENCEPHALOMYOPATHIES
   Neurology
   
   L. Piccinini et al., "PATTERNS OF HEARING-LOSS AND AUDITORY PATHWAYS DYSFUNCTION IN ADULT MITOCHONDRIAL ENCEPHALOMYOPATHIES", Neurology, 50(4), 1998, pp. 1011-1011
9. PRELLE A; COMI GP; TANCREDI L; RIGOLETTO C; CISCATO P; FORTUNATO F; NESTI S; SCIACCO M; ROBOTTI M; BAZZI P; FELISARI G; MOGGIO M; SCARLATO G
   SARCOGLYCAN DEFICIENCY IN A LARGE ITALIAN POPULATION OF MYOPATHIC PATIENTS
   Acta Neuropathologica
   
   A. Prelle et al., "SARCOGLYCAN DEFICIENCY IN A LARGE ITALIAN POPULATION OF MYOPATHIC PATIENTS", Acta Neuropathologica, 96(5), 1998, pp. 509-514
10. PRELLE A; COMI GP; RIGOLETTO C; TURCONI A; FELISARI G; CISCATO P; FORTUNATO F; MESSINA S; BRESOLIN N; MORA M; MOGGIO M; SCARLATO G
    AN ATYPICAL CASE OF PARTIAL MEROSIN DEFICIENCY CONGENITAL MUSCULAR-DYSTROPHY
    Journal of neurology
    
    A. Prelle et al., "AN ATYPICAL CASE OF PARTIAL MEROSIN DEFICIENCY CONGENITAL MUSCULAR-DYSTROPHY", Journal of neurology, 244(6), 1997, pp. 391-395
11. BENTI R; TURCONI AC; FELISARI G; MAROTTA G; CANZI C; BRUNO A; CASATI R; GASPARINI M; CASTELLANI M; RESCHINI E; LONGARI V; DIMAIO D; BRESOLIN N; GERUNDINI P
    TC-99M ECD SPECT PATTERN AND NEUROPSYCHOLOGICAL PROFILE IN MITOCHONDRIAL ENCEPHALOMYOPATHIES WITHOUT COGNITIVE IMPAIRMENT
    The Journal of nuclear medicine
    
    R. Benti et al., "TC-99M ECD SPECT PATTERN AND NEUROPSYCHOLOGICAL PROFILE IN MITOCHONDRIAL ENCEPHALOMYOPATHIES WITHOUT COGNITIVE IMPAIRMENT", The Journal of nuclear medicine, 38(5), 1997, pp. 1193-1193
12. PRELLE A; TANCREDI L; COMI GP; RIGOLETTO C; CISCATO P; FORTUNATO F; FELISARI G; MOGGIO M; SCARLATO G
    FREQUENCY OF ALPHA-SARCOGLYCAN AND GAMMA-SARCOGLYCAN DEFICIENCY IN A LARGE POPULATION OF MYOPATHIC PATIENTS
    Neurology
    
    A. Prelle et al., "FREQUENCY OF ALPHA-SARCOGLYCAN AND GAMMA-SARCOGLYCAN DEFICIENCY IN A LARGE POPULATION OF MYOPATHIC PATIENTS", Neurology, 48(3), 1997, pp. 3131-3131
13. MARTINELLI F; FELISARI G; TURCONI A; COMI GP; ROBOTTI M; AUSENDA CD; SCARLATO G; BRESOLIN N
    EPIDEMIOLOGIC EVALUATION OF CLINICAL HISTORY IN DUCHENNE MUSCULAR-DYSTROPHY
    Neurology
    
    F. Martinelli et al., "EPIDEMIOLOGIC EVALUATION OF CLINICAL HISTORY IN DUCHENNE MUSCULAR-DYSTROPHY", Neurology, 48(3), 1997, pp. 5040-5040
14. BRESOLIN N; CASTELLI E; COMI GP; FELISARI G; BARDONI A; PERANI D; GRASSI F; TURCONI A; MAZZUCCHELLI F; GALLOTTI D; MOGGIO M; PRELLE A; AUSENDA C; FAZIO G; SCARLATO G
    COGNITIVE IMPAIRMENT IN DUCHENNE MUSCULAR-DYSTROPHY
    Neuromuscular disorders
    
    N. Bresolin et al., "COGNITIVE IMPAIRMENT IN DUCHENNE MUSCULAR-DYSTROPHY", Neuromuscular disorders, 4(4), 1994, pp. 359-369
15. CIAFALONI E; COMI GP; BRESOLIN N; BARDONI A; DESILVA R; GARGHENTINO R; FELISARI G; ROBOTTI M; PRELLE A; ROSES A; SCARLATO G
    ABERRANT TRANSCRIPTS IN THE TERMINAL REGION OF DYSTROPHIN GENE IN A CONGENITAL MYOPATHY PATIENT
    Neurology
    
    E. Ciafaloni et al., "ABERRANT TRANSCRIPTS IN THE TERMINAL REGION OF DYSTROPHIN GENE IN A CONGENITAL MYOPATHY PATIENT", Neurology, 44(4), 1994, pp. 10000230-10000230
16. COMI GP; PRELLE A; BRESOLIN N; MOGGIO M; BARDONI A; GALLANTI A; VITA G; TOSCANO A; FERRO MT; BORDONI A; FORTUNATO F; CISCATO P; FELISARI G; TEDESCHI S; CASTELLI E; GARGHENTINO R; TURCONI A; FRASCHINI P; MARCHI E; NEGRETTO GG; ADOBBATI L; MEOLA G; TONIN P; PAPADIMITRIOU A; SCARLATO G
    CLINICAL VARIABILITY IN BECKER MUSCULAR-DYSTROPHY - GENETIC, BIOCHEMICAL AND IMMUNOHISTOCHEMICAL CORRELATES
    Brain
    
    G.P. Comi et al., "CLINICAL VARIABILITY IN BECKER MUSCULAR-DYSTROPHY - GENETIC, BIOCHEMICAL AND IMMUNOHISTOCHEMICAL CORRELATES", Brain, 117, 1994, pp. 1-14