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La ricerca find articoli where authors phrase all words ' CISCATO P' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 15 riferimenti
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    1. 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
      beta-enolase deficiency, a new metabolic myopathy of distal glycolysis

      ANNALS OF NEUROLOGY
    2. 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
      Retrospective study of patients affected of a large population with mitochondrial disorders: clinical, morphological and molecular genetic evaluation

      JOURNAL OF NEUROLOGY
    3. 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
      A sporadic, atypical case of desminopathy: morphological and immunologicalcharacterization

      CLINICAL NEUROPATHOLOGY
    4. Tredici, G; Buccellato, FR; Braga, M; Cavaletti, G; Ciscato, P; Moggio, A; Scalabrino, G
      Polyneuropathy due to cobalamin deficiency in the rat (vol 156, pg 18, 1998)

      JOURNAL OF THE NEUROLOGICAL SCIENCES
    5. TREDICI G; BUCCELLATO FR; BRAGA M; CAVALETTI G; CISCATO P; MOGGIO A; SCALABRINO G
      POLYNEUROPATHY DUE TO COBALAMIN DEFICIENCY IN THE RAT

      Journal of the neurological sciences
    6. 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
    7. 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
    8. 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
    9. COMI GP; CIAFALONI E; DESILVA HAR; PRELLE A; BARDONI A; RIGOLETTO C; ROBOTTI M; BRESOLIN N; MOGGIO M; FORTUNATO F; CISCATO P; TURCONI A; ROSES AD; SCARLATO G
      A G(-]A TRANSVERSION AT THE 5'-SPLICE-SITE OF INTRON-69 OF THE DYSTROPHIN GENE CAUSING THE ABSENCE OF PERIPHERAL-NERVE DP116 AND SEVERE CLINICAL INVOLVEMENT IN A DMD PATIENT (VOL 4, PG 2171, 1995)(1))

      Human molecular genetics
    10. PRELLE A; RIGOLETTO C; MOGGIO M; SCIACCO M; COMI GP; CISCATO P; FAGIOLARI G; RAPUZZI S; BIGNOTTI V; SCARLATO G
      ASYMPTOMATIC FAMILIAL HYPERCKEMIA ASSOCIATED WITH DESMIN ACCUMULATIONIN SKELETAL-MUSCLE

      Journal of the neurological sciences
    11. COMI GP; CIAFALONI E; DESILVA HAR; PRELLE A; BARDONI A; RIGOLETTO C; ROBOTTI M; BRESOLIN N; MOGGIO M; FORTUNATO F; CISCATO P; TURCONI A; ROSE AD; SCARLATO G
      A G(-]A TRANSVERSION AT THE 5'-SPLICE-SITE OF INTRON-69 OF THE DYSTROPHIN GENE CAUSING THE ABSENCE OF PERIPHERAL-NERVE DP116 AND SEVERE CLINICAL INVOLVEMENT IN A DMD PATIENT(1))

      Human molecular genetics
    12. RIGOLETTO C; PRELLE A; CISCATO P; MOGGIO M; COMI G; FORTUNATO F; SCARLATO G
      UTROPHIN EXPRESSION DURING HUMAN FETAL DEVELOPMENT

      International journal of developmental neuroscience
    13. RAPUZZI S; PRELLE A; MOGGIO M; RIGOLETTO C; CISCATO P; COMI G; FRANCESCA F; SCARLATO G
      HIGH SERUM CREATINE-KINASE LEVELS ASSOCIATED WITH CYLINDRICAL SPIRALSAT MUSCLE BIOPSY

      Acta Neuropathologica
    14. MOGGIO M; PRELLE A; FAGIOLARI G; CHECCARELLI N; SCIACCO M; CISCATO P; SCARLATO G
      ANIONIC PHOSPHOLIPIDS CALCIUM-BINDING SITES IN DUCHENNE AND MURINE X-LINKED MUSCULAR-DYSTROPHY

      Muscle & nerve
    15. 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 20:04:59