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    1. Abbruzzese, G; Pigullo, S; Di Maria, E; Martinelli, P; Barone, P; Marchese, R; Scaglione, C; Assini, A; Lucetti, C; Berardelli, A; Calzetti, S; Bellone, E; Ajmar, F; Mandich, P
      Clinical and genetic study of essential tremor in the Italian population

      NEUROLOGICAL SCIENCES
    2. Musso, M; Balestra, P; Bellone, E; Cassandrini, D; Di Maria, E; Doria, LL; Grandis, M; Mancardi, G; Schenone, A; Levi, G; Ajmar, F; Mandich, P
      The D355V mutation decreases EGR2 binding to an element within the Cx32 promoter

      NEUROBIOLOGY OF DISEASE
    3. Pigullo, S; Di Maria, E; Marchese, R; Assini, A; Bellone, E; Scaglione, C; Vitale, C; Bonuccelli, U; Barone, P; Ajmar, F; Martinelli, P; Abbruzzese, G; Mandich, P
      No evidence of association between CAG expansions and essential tremor in a large cohort of Italian patients

      JOURNAL OF NEURAL TRANSMISSION
    4. Bellone, E; Hughes, JP; Guttorp, P
      A hidden Markov model for downscaling synoptic atmospheric patterns to precipitation amounts

      CLIMATE RESEARCH
    5. Battaglia, A; Ferraro, L; Lo Monaco, M; Palumbo, A; Mariani, M; Biadi, O; Boccalatte, A; Polimeno, S; De Rosa, V; Liguori, L; Cuomo, S; Boccanelli, A; Morosetti, P; D'Angelo, G; Bottiglieri, P; Brunelli, C; Spallarossa, P; Rolandi, A; Rossettini, PF; Campa, P; Barilla, F; De Biase, L; Biscosi, C; Zampino, D; Capponi, E; Buccolieri, M; Gattobigio, R; Capucci, A; Passerini, F; Piepoli, M; Castello, A; Chiariello, M; Betocchi, S; Ciampi, Q; Losi, M; Corsini, G; Melorio, S; Dalle Mule, J; Mazzella, M; Cristinziani, GR; Mario, L; De Luca, I; Fusco, F; Del Salvatore, B; Sorino, M; Delise, P; Mozzato, MG; Bilardo, G; Coro', L; Fantinel, M; Zasso, A; Fedele, F; Di Donato, D; Romano, S; De Pascale, F; Giasi, M; Ciarcia, L; Lizzardo, A; Mastursi, M; Giordano, A; Benigno, M; Zanelli, E; Campana, M; Giovannini, E; Lacche, A; Pulignano, G; Giuffrida, G; Montana, G; Licciardello, G; L'Abbate, A; Carpeggiani, C; Morales, A; Leghissa, R; Mandorla, S; Del Pinto, M; Borgioni, C; Mininni, N; Petrillo, ME; Moretti, G; Bonaglia, M; Zoni, A; Piscicelli, C; Orlandi, M; Panciroli, C; Oddone, A; Caizzi, V; Tartarini, G; Lattanzi, F; Reisenhofer, B; Pascotto, P; Zanocco, A; Dabizzi, RP; Bini, L; Mondanelli, D; Frascarelli, F; Pitscheider, W; Erlicher, A; Rauhe, W; Bonsante, E; Polimeni, M; Catananti, F; Guerrisi, G; Magnani, B; Rapezzi, C; Ferlito, M; Amati, S; Di Leo, L; Manzo, M; Baldi, C; De Cristofaro, M; Citro, R; Raviele, A; Turiano, G; Zuin, G; Rengo, F; Furgi, G; Papa, A; Rotiroti, D; Rosato, G; Siano, F; Pagliuca, MR; Rovelli, G; Heyman, J; Locati, I; Sanguinetti, M; Tomassini, F; Mantovani, R; Sanna, A; Marras, L; Crabu, E; Locci, G; Moio, N; Scilla, C; Tavazzi, L; Magrini, G; Bersano, C; Laudisa, ML; Trimarco, B; Argenziano, L; Silvestri, S; Valagussa, F; Ciro, E; Cantu, E; Trocino, G; Rossillo, A; Valagussa, L; Finocchi, G; Benvenuto, GM; Bonanno, C; Ometto, R; Risica, G; Gualandi, G; Facchin, L; Tenderini, P; Nicolosi, GL; Burelli, C; Macor, F; Bellone, E; Laiso, D; Carvalho, P; Peila, C; Fagiano, A; Gardiol, S; Ganci, B; Presutto, P; Fontanelli, A; Morgera, T; Scarpino, L; Barbuzzi, S; Capogrosso, V; Terrosu, PF; Contini, GM; Sabino, G; Pes, R; Uneddu, F; Mecca, D; De Tommaso, I; Rusconi, C; Brunazzi, MC; Codeluppi, P; Pasqualini, M; Gorni, R; Negrelli, M; Paparoni, S; Core, A; Pecce, P; Petrella, L; Zennaro, RG; Garuti, W; Alfano, G; Bacca, F; Petrucci, G; Paci, AM; Bigalli, G; Mangiameli, S; Gulizia, M; Cardillo, R; Ferrari, G; Tettamanti, F; Butti, E; Picchione, N; Sulla, A; Stroder, P; Perna, GP; Ricci, S; Generali, CA; Adornato, E; Ghisio, A; Tidu, M; Ferrari, R; Mele, D; Cicchitelli, G; Merli, E; Russa, O; Azcarate, JMA; Gonzales, PZ; Vilchez, F; Alonso, LFI; Montero, JMM; Zarzosa, CD; Martin, ES; de Ros, JO; Martinez, MH; Palau, VM; de Carranza, MST; Mayor, DJLB; Cocina, EG; Valderrama, JC; Jimenez, RP; Pardo, JAM; Cortada, JB; Lorente, LJ; Guerrero, JJG; Martinez, A; Coronado, JLB; Casado, RS; Cendon, AA; Cokkinos, D; Maounis, T; Karatasakis, G; Kremastinos, D; Iliodromitis, S; Karatzas, D; Georgiadis, M; Paraskevaidis, I; Toutouzas, P; Antoniadis, P; Angeli, C; Vadas, P; Kaleboubas, M; Stamatelopoulos, S; Nanas, I; Kanakakis, A; Dalianis, A; Zacharoulis, A; Fotiadis, I; Pyrgakis, V; Liata, O; Mazen, B; Kardaras, F; Kardara, D; Krokos, V; Sioras, H; Fousas, S; Stefanidis, A; Papadopoulos, G; Papadopoulos, C; Papagiannis, I; Karidas, I; Zobolos, S
      PREAMI: Perindopril and remodelling in elderly with acute myocardial infarction: Study rationale and design

      CARDIOVASCULAR DRUGS AND THERAPY
    6. Di Maria, E; Tabaton, M; Vigo, T; Abbruzzese, G; Bellone, E; Donati, C; Frasson, E; Marchese, R; Montagna, P; Munoz, DG; Pramstaller, PP; Zanusso, G; Ajmar, F; Mandich, P
      Corticobasal degeneration shares a common genetic background with progressive supranuclear palsy

      ANNALS OF NEUROLOGY
    7. Squitieri, F; Sabbadini, G; Mandich, P; Gellera, C; Di Maria, E; Bellone, E; Castellotti, B; Nargi, E; de Grazia, U; Frontali, M; Novelletto, A
      Family and molecular data for a fine analysis of age at onset in Huntington disease

      AMERICAN JOURNAL OF MEDICAL GENETICS
    8. Pizzuti, A; Novelli, G; Ratti, A; Amati, F; Bordoni, R; Mandich, P; Bellone, E; Conti, E; Bengala, M; Mari, A; Silani, V; Dallapiccola, B
      Isolation and characterization of a novel transcript embedded within HIRA,a gene deleted in DiGeorge syndrome

      MOLECULAR GENETICS AND METABOLISM
    9. Bellone, E
      Graduates from the Alps and Piedmont at the University of Pavia in the second half of the fifteenth century

      STUDI PIEMONTESI
    10. Mandich, P; Mancardi, GL; Varese, A; Soriani, S; Di Maria, E; Bellone, E; Bado, M; Gross, L; Windebank, AJ; Ajmar, F; Schenone, A
      Congenital hypomyelination due to myelin protein zero Q215X mutation

      ANNALS OF NEUROLOGY
    11. Mandich, P; Bellone, E; Di Maria, E; Pigullo, S; Pizzuti, A; Schenone, A; Soriani, S; Varese, A; Windebank, AJ; Ajmar, F
      Exclusion of the ninjurin gene as a candidate for hereditary sensory neuropathies type I and type II

      AMERICAN JOURNAL OF MEDICAL GENETICS
    12. MANDICH P; MONTERA M; BELLONE E; TROJANI A; DANIELE S; AJMAR F
      3 NOVEL MUTATIONS IN THE VON-HIPPEL-LINDAU TUMOR-SUPPRESSOR GENE IN ITALIAN PATIENTS

      Human mutation
    13. MANDICH P; JACOPINI G; DIMARIA E; SABBADINI G; ABBRUZZESE G; CHIMIRRI F; BELLONE E; NOVELLETTO A; AJMAR F; FRONTALI M
      PREDICTIVE TESTING FOR HUNTINGTONS-DISEASE - 10 YEARS EXPERIENCE IN 2ITALIAN CENTERS (VOL 19, PG 68, 1998)

      Italian journal of neurological sciences
    14. MANDICH P; JACOPINI G; DIMARIA E; SABBADINI G; CHIMIRRI F; BELLONE E; NOVELLETTO A; AJMAR F; FRONTALI M
      PREDICTIVE TESTING FOR HUNTINGTONS-DISEASE - 10 YEARS EXPERIENCE IN 2ITALIAN CENTERS

      Italian journal of neurological sciences
    15. BELLONE E
      DEGREES CONFERRED BY THE UNIVERSITA-DI-PAVIA DURING THE 2ND HALF OF THE QUATTROCENTO, VOL 1, (1450-1475) - ITALIAN - SOTTILI,A

      Studi piemontesi
    16. SCHENONE A; NOBBIO L; CAPONNETTO C; ABBRUZZESE M; MANDICH P; BELLONE E; AJMAR F; GHERARDI G; WINDEBANK AJ; MANCARDI G
      CORRELATION BETWEEN PMP-22 MESSENGER-RNA EXPRESSION AND PHENOTYPE IN HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES

      Annals of neurology
    17. MANDICH P; BELLONE E; MONTERA M; AJMAR F; SCHENONE A; NOBBIO L; MANCARDI G; PIZZUTI A; RATTI A; WINDEBANK AJ
      COMMENTS ON DAVAR ET-AL, PAIN, 67 (1996) 135-139

      Pain
    18. SCHITO AM; PIZZUTI A; DIMARIA E; SCHENONE A; RATTI A; DEFFERRARI R; BELLONE E; MANCARDI GL; AJMAR F; MANDICH P
      MESSENGER-RNA DISTRIBUTION IN ADULT HUMAN BRAIN OF GRIN2B, A N-METHYL-D-ASPARTATE (NMDA) RECEPTOR SUBUNIT

      Neuroscience letters
    19. SCHENONE A; NOBBIO L; MANDICH P; BELLONE E; ABBRUZZESE M; AYMAR F; MANCARDI GL; WINDEBANK AJ
      UNDEREXPRESSION OF MESSENGER-RNA FOR PERIPHERAL MYELIN PROTEIN-22 IN HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES

      Neurology
    20. NOVELLI G; PIZZUTI A; AMATI F; RATTI A; MARI A; FOGH I; CONTI E; BENGALA M; BORDONI R; BELLONE E; MANDICH P; COLOSIMO A; PANDOLFI F; DALLAPICCOLA B
      IDENTIFICATION OF A NOVEL NONCODING NUCLEAR-RNA FROM THE DIGEORGE-SYNDROME CRITICAL REGION AT 22Q11

      American journal of human genetics
    21. BELLONE E; MANDICH P; JAMES R; NELIS E; LAMBA LD; VANBROECKHOVEN C; AJMAR F
      IDENTIFICATION OF A 4 BP DELETION (1560DEL4) IN PO GENE IN A FAMILY WITH SEVERE CHARCOT-MARIE-TOOTH DISEASE

      Human mutation
    22. BELLONE E; SCHENONE A; MANCARDI G; NICHOLSON GA; ABBRUZZESE M; AJMAR F; MANDICH P
      USE OF COSH1 PROBE IN HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES - A RELIABLE GENETIC TEST FOR DEMONSTRATION OF IDENTICAL SIZE OF 17P11.2 DELETION IN UNRELATED PATIENTS

      Neuroscience letters
    23. SCHENONE AE; NOBBIO L; GROSS L; MANDICH P; BELLONE E; ABBRUZZESE M; MANCARDI GL; WINDEBANK AJ
      PERIPHERAL MYELIN PROTEIN-22 IS UNDEREXPRESSED IN PATIENTS WITH HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES

      Neurology
    24. MANDICH P; DIMARIA E; BELLONE E; AJMAR F; ABBRUZZESE G
      MOLECULAR ANALYSIS OF THE IT15 GENE IN PATIENTS WITH APPARENTLY SPORADIC HUNTINGTONS-DISEASE

      European neurology
    25. MANDICH P; BELLONE E; SCHENONE A; MANCARDI G; ABBRUZZESE M; AJMAR F
      DE-NOVO DUPLICATION IN CHARCOT-MARIE-TOOTH TYPE 1A

      American journal of human genetics
    26. MANDICH P; JAMES R; NASSANI S; DEFFERRARI R; BELLONE E; MANCARDI G; SCHENONE A; ABBRUZZESE M; ROCCHI M; AJMAR F; ARCHIDIACONO N
      MOLECULAR DIAGNOSIS OF HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES (HNPP) BY DETECTION OF 17P11.2 DELETION IN ITALIAN PATIENTS

      Journal of neurology
    27. JAMES R; BELLONE E; NELIS E; MANDICH P; SCHENONE A; MANCARDI G; VANBROECKHOVEN C; ABBRUZZESE M; AJMAR F
      MOLECULAR ANALYSIS OF 3 CASES WITH HEREDITARY MOTOR AND SENSORY NEUROPATHY WITH MYELIN OUTFOLDING

      Neuroscience letters
    28. MANCARDI GL; MANDICH P; NASSANI S; SCHENONE A; JAMES R; DEFFERRARI R; BELLONE E; GIUNCHEDI M; AJMAR F; ABBRUZZESE M
      PROGRESSIVE SENSORY-MOTOR POLYNEUROPATHY WITH TOMACULOUS CHANGES IS ASSOCIATED TO 17P11.2 DELETION

      Journal of the neurological sciences
    29. BELLONE E
      POPPER,KARL,RAIMUND

      Belfagor
    30. SCHENONE A; NOBBIO L; WINDEBANK AJ; MANDICH P; BELLONE E; ABBRUZZESE M; MANCARDI GL
      EXPRESSION OF PMP-22 IN SURAL NERVES OF PATIENTS WITH HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES (HNPP)

      American journal of human genetics
    31. NOVELLETTO A; PERSICHETTI F; SABBADINI G; MANDICH P; BELLONE E; AJMAR F; SQUITIERI F; CAMPANELLA G; BOZZA A; MACDONALD ME; GUSELLA JF; FRONTALI M
      POLYMORPHISM ANALYSIS OF THE HUNTINGTIN GENE IN ITALIAN FAMILIES AFFECTED WITH HUNTINGTON DISEASE

      Human molecular genetics
    32. NOVELLETTO A; PERSICHETTI F; SABBADINI G; MANDICH P; BELLONE E; AJMAR F; PERGOLA M; DELSENNO L; MACDONALD ME; GUSELLA JF; FRONTALI M
      ANALYSIS OF THE TRINUCLEOTIDE REPEAT EXPANSION IN ITALIAN FAMILIES AFFECTED WITH HUNTINGTON DISEASE

      Human molecular genetics
    33. MANDICH P; SCHITO AM; BELLONE E; ANTONACCI R; FINELLI P; ROCCHI M; AJMAR F
      MAPPING OF THE HUMAN NMDAR2B RECEPTOR SUBUNIT GENE (GRIN2B) TO CHROMOSOME 12P12

      Genomics
    34. SGHIRLANZONI A; PAREYSON D; MARAZZI R; CAVALETTI G; BELLONE E; MANDICH P; BALESTRINI MR; RIVA D
      HOMOZYGOUS HYPERTROPHIC HEREDITARY MOTOR AND SENSORY NEUROPATHIES

      Italian journal of neurological sciences
    35. SCHENONE A; ABBRUZZESE M; UCCELLI A; MANDICH P; JAMES R; BELLONE E; GIUNCHEDI M; ROLANDO S; CAPELLO E; MANCARDI GL
      HEREDITARY MOTOR AND SENSORY NEUROPATHY WITH MYELIN OUTFOLDING - CLINICAL, GENETIC AND NEUROPATHOLOGICAL STUDY OF 3 CASES (VOL 122, PG 20, 1994)

      Journal of the neurological sciences
    36. SCHENONE A; ABBRUZZESE M; UCCELLI A; MANDICH R; JAMES R; BELLONE E; GIUNCHEDI M; ROLANDO S; CAPELLO E; MANCARDI GL
      HEREDITARY MOTOR AND SENSORY NEUROPATHY WITH MYELIN OUTFOLDING - CLINICAL, GENETIC AND NEUROPATHOLOGICAL STUDY OF 3 CASES

      Journal of the neurological sciences
    37. MANCARDI GL; UCCELLI A; BELLONE E; SGHIRLANZONI A; MANDICH P; PAREYSON D; SCHENONE A; ABBRUZZESE M; AJMAR F
      17P11.2 DUPLICATION IS A COMMON FINDING IN SPORADIC CASES OF CHARCOT-MARIE-TOOTH TYPE-1

      European neurology
    38. BELLONE E
      ENGLISH GRADUATES OF THE UNIVERSITIES OF TURIN AND MONDOVI IN THE 16TH-CENTURY

      Studi piemontesi
    39. DALLAPICCOLA B; MANDICH P; BELLONE E; SELICORNI A; MOKIN V; AJMAR F; NOVELLI G
      PARENTAL ORIGIN OF CHROMOSOME-4P DELETION IN WOLF-HIRSCHHORN SYNDROME

      American journal of medical genetics
    40. SGHIRLANZONI A; PAREYSON D; BELLONE E; MARAZZI R; SCAIOLI V
      ABSENCE OF 17P11.2 DUPLICATION IN AUTOSOMAL RECESSIVE HYPERTROPHIC HMSN

      Neurology
    41. BELLONE E
      THE UNIVERSITY OF TURIN BETWEEN 1490 AND 1562

      Studi piemontesi


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 20/10/20 alle ore 09:10:21