Catalogo Articoli (Spogli Riviste)

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La ricerca find articoli where authors phrase all words ' FELISARI G' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 16 riferimenti
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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
    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
    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
    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
    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
    6. Bardoni, A; Sironi, M; Felisari, G; Comi, GP; Bresolin, N
      Absence of brain Dp140 isoform and cognitive impairment in Becker musculardystrophy

      LANCET
    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
    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
    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
    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
    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
    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
    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
    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
    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
    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


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 20/01/21 alle ore 20:19:48