Catalogo Articoli (Spogli Riviste)

HELP
ATTENZIONE: attualmente gli articoli Current Contents (fonte ISI) a partire dall'anno 2002 sono consultabili sulla Risorsa On-Line

Le informazioni sugli articoli di fonte ISI sono coperte da copyright

La ricerca find articoli where authors phrase all words ' FRONTALI M' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 40 riferimenti
Selezionare un intervallo

Per ulteriori informazioni selezionare i riferimenti di interesse.

    1. Valente, EM; Bentivoglio, AR; Cassetta, E; Dixon, PH; Davis, MB; Ferraris, A; Ialongo, T; Frontali, M; Wood, NW; Albanese, A
      Identification of a novel primary torsion dystonia loons (DYT13) on chromosome 1p36 in an Italian family with cranial-cervical or upper limb onset

      NEUROLOGICAL SCIENCES
    2. Valente, EM; Bentivoglio, AR; Cassetta, E; Dixon, PH; Davis, MB; Ferraris, A; Ialongo, T; Frontali, M; Wood, NW; Albanese, A
      DYT13, a novel primary torsion dystonia locus, maps to chromosome 1p36.13-36.32 in an Italian family with cranial cervical or upper limb onset

      ANNALS OF NEUROLOGY
    3. Frontali, M
      Spinocerebellar ataxia type 6: Channelopathy or glutamine repeat disorder?

      BRAIN RESEARCH BULLETIN
    4. Valente, EM; Bentivoglio, AR; Dixon, PH; Ferraris, A; Ialongo, T; Frontali, M; Albanese, A; Wood, NW
      Localization of a novel locus for autosomal recessive early-onset parkinsonism, PARK6, on human chromosome 1p35-p36

      AMERICAN JOURNAL OF HUMAN GENETICS
    5. Guida, S; Trettel, F; Pagnutti, S; Mantuano, E; Tottene, A; Veneziano, L; Fellin, T; Spadaro, M; Stauderman, KA; Williams, ME; Volsen, S; Ophoff, RA; Frants, RR; Jodice, C; Frontali, M; Pietrobon, D
      Complete loss of P/Q calcium channel activity caused by a CACNA1A missensemutation carried by patients with episodic ataxia type 2

      AMERICAN JOURNAL OF HUMAN GENETICS
    6. Stevanin, G; Herman, A; Durr, A; Jodice, C; Frontali, M; Agid, Y; Brice, A
      Are (CTG)(n) expansions at the SCA8 locus rare polymorphisms?

      NATURE GENETICS
    7. Trettel, F; Mantuano, E; Calabresi, V; Veneziano, L; Olsen, AS; Georgescu, A; Gordon, L; Sabbadini, G; Frontali, M; Jodice, C
      A fine physical map of the CACNA1A gene region on 19p13.1-p13.2 chromosome

      GENE
    8. Albanese, A; Bentivoglio, AR; Del Grosso, N; Cassetta, E; Frontali, M; Valente, EM; Tonali, P
      Phenotype variability of dystonia in monozygotic twins

      JOURNAL OF NEUROLOGY
    9. 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
    10. Frontali, M; Novelletto, A; Annesi, G; Jodice, C
      CAG repeat instability, cryptic sequence variation and pathogeneticity: evidence from different loci

      PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY OF LONDON SERIES B-BIOLOGICAL SCIENCES
    11. Cassetta, E; Del Grosso, N; Bentivoglio, AR; Valente, EM; Frontali, M; Albanese, A
      Italian family with cranial cervical dystonia: Clinical and genetic study

      MOVEMENT DISORDERS
    12. Jarman, PR; del Grosso, N; Valente, EM; Leube, B; Cassetta, E; Bentivoglio, AR; Waddy, HM; Uitti, RJ; Maraganore, DM; Albanese, A; Frontali, M; Auburger, G; Bressman, SB; Wood, NW; Nygaard, TG
      Primary torsion dystonia: the search for genes is not over

      JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
    13. TRETTEL F; MANTUANO E; VENEZIANO L; SABBADINI G; OLSEN A; OPHOFF RA; FRANTS RR; JODICE C; FRONTALI M
      MOLECULAR ANALYSIS OF THE GENE CACNA1A - REFINED MAPPING OF THE CONTAINING REGION AND SCREENING FOR MUTATIONS IN EA2

      European journal of human genetics
    14. Trowsdale, J; Beck, S; Boyle, JM; Campbell, D; Cann, HM; Edwards, Y; Frontali, M; Galibert, F; Le Gall, JY; Nizetic, D; Pontarotti; Ragoussis, J; Terrenato, L; Ziegler, A
      Physical Mapping of human chromosome 6

      HUMAN GENOME ANALYSIS
    15. 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
    16. 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
    17. MANTUANO E; TRETTEL F; OLSEN AS; LENNON G; FRONTALI M; JODICE C
      LOCALIZATION AND GENOMIC STRUCTURE OF HUMAN DEOXYHYPUSINE SYNTHASE GENE ON CHROMOSOME 19P13.2 DISTAL 19P13.1

      Gene
    18. SQUITIERI F; GELLERA C; RUGGIERI S; CASTELLOTTI B; FRONTALI M; MANDICH P; NACMIAS B; DELSENNO L; RAGONA G; DIDONATO P; AJMAR F; FRATI L; NOVELLETTO A
      A MODEL TO PREDICT THE ONSET AGE IN UNAFFECTED HUNTINGTONS-DISEASE MUTATION CARRIERS

      Annals of neurology
    19. MASCALCHI M; TOSETTI M; PLASMATI R; BIANCHI MC; TESSA C; SALVI F; FRONTALI M; VALZANIA F; BARTOLOZZI C; TASSINARI CA
      PROTON MAGNETIC-RESONANCE SPECTROSCOPY IN AN ITALIAN FAMILY WITH SPINOCEREBELLAR ATAXIA TYPE-1

      Annals of neurology
    20. GIUNTI P; SABBADINI G; SWEENEY MG; DAVIS MB; VENEZIANO L; MANTUANO E; FEDERICO A; PLASMATI R; FRONTALI M; WOOD NW
      THE ROLE OF THE SCA2 TRINUCLEOTIDE REPEAT EXPANSION IN 89 AUTOSOMAL-DOMINANT CEREBELLAR-ATAXIA FAMILIES - FREQUENCY, CLINICAL AND GENETIC CORRELATES

      Brain
    21. GIOVANNONE B; SABBADINI G; DIMAIO L; CALABRESE O; CASTALDO I; FRONTALI M; NOVELLETTO A; SQUITIERI F
      ANALYSIS OF (CAG)N SIZE HETEROGENEITY IN SOMATIC AND SPERM CELL-DNA FROM INTERMEDIATE AND EXPANDED HUNTINGTON-DISEASE GENE CARRIERS

      Human mutation
    22. JODICE C; MANTUANO E; VENEZIANO L; TRETTEL F; SABBADINI G; CALANDRIELLO L; FRANCIA A; SPADARO M; PIERELLI F; SALVI F; OPHOFF RA; FRANTS RR; FRONTALI M
      EPISODIC ATAXIA TYPE-2 (EA2) AND SPINOCEREBELLAR ATAXIA TYPE-6 (SCA6)DUE TO CAG REPEAT EXPANSION IN THE CACNA1A GENE ON CHROMOSOME 19P

      Human molecular genetics
    23. SQUITIERI F; GIOVANNONE B; SABBADINI G; FRONTALI M; NOVELLETTO A; DIMAIO L; CALABRESE O; CASTALDO I; CAMPANELLA G
      ANALYSIS OF (CAG)N SIZE HETEROGENEITY IN DNA FROM SOMATIC AND GERM-CELLS OF NORMAL, INTERMEDIATE AND EXPANDED HUNTINGTON DISEASE GENE CARRIERS

      Neurology
    24. BENTIVOGLIO AR; DELGROSSO N; ALBANESE A; CASSETTA E; TONALI P; FRONTALI M
      NON-DYT1 DYSTONIA IN A LARGE ITALIAN FAMILY

      Journal of Neurology, Neurosurgery and Psychiatry
    25. CALANDRIELLO L; VENEZIANO L; FRANCIA A; SABBADINI G; COLONNESE C; MANTUANO E; JODICE C; TRETTEL F; VIVIANI P; MANFREDI M; FRONTALI M
      ACETAZOLAMIDE-RESPONSIVE EPISODIC ATAXIA IN AN ITALIAN FAMILY REFINESGENE-MAPPING ON CHROMOSOME 19P13

      Brain
    26. TRETTEL F; MALASPINA P; BLASI P; JODICE C; NOVELLETTO A; SABBADINI G; VENEZIANO L; FRONTALI M; TERRENATO L
      ORDERING OF 44 GENETIC-MARKERS IN THE 6P22 CYTOGENETIC BAND

      DNA sequence
    27. MALASPINA P; ROETTO A; TRETTEL F; JODICE C; BLASI P; FRONTALI M; CARELLA M; FRANCO B; CAMASCHELLA C; NOVELLETO A
      CONSTRUCTION OF A YAC CONTIG COVERING HUMAN-CHROMOSOME 6P22

      Genomics
    28. BENTIVOGLIO AR; ALBANESE A; DELGROSSO N; CASSETTA E; ROMIGI A; FRONTALI M; TONALI P
      A LARGE ITALIAN FAMILY AFFECTED BY IDIOPATHIC TORSION DYSTONIA WITH COMPLETE PENETRANCE, NOT LINKED TO DYT1

      Neurology
    29. FRONTALI M; SABBADINI G; NOVELLETTO A; JODICE C; NASO F; SPADARO M; GIUNTI P; JACOPINI AG; VENEZIANO L; MANTUANO E; MALASPINA P; ULIZZI L; BRICE A; DURR A; TERRENATO L
      GENETIC FITNESS IN HUNTINGTONS-DISEASE AND SPINOCEREBELLAR ATAXIA-1 -A POPULATION-GENETICS MODEL FOR CAG REPEAT EXPANSIONS

      Annals of Human Genetics
    30. RUBINSZTEIN DC; LEGGO J; COLES R; ALMQVIST E; BIANCALANA V; CASSIMAN JJ; CHOTAI K; CONNARTY M; CRAUFURD D; CURTIS A; CURTIS D; DAVIDSON MJ; DIFFER AM; DODE C; DODGE A; FRONTALI M; RANEN NG; STINE OC; SHERR M; ABBOTT MH; FRANZ ML; GRAHAM CA; HARPER PS; HEDREEN JC; JACKSON A; KAPLAN JC; LOSEKOOT M; MACMILLAN JC; MORRISON P; TROTTIER Y; NOVELLETTO A; SIMPSON SA; THEILMANN J; WHITTAKER JL; FOLSTEIN SE; ROSS CA; HAYDEN MR
      PHENOTYPIC CHARACTERIZATION OF INDIVIDUALS WITH 30-40 CAG REPEATS IN THE HUNTINGTON DISEASE (HD) GENE REVEALS HD CASES WITH 36 REPEATS AND APPARENTLY NORMAL ELDERLY INDIVIDUALS WITH 36-39 REPEATS

      American journal of human genetics
    31. SABBADINI G; FRANCIA A; CALANDRIELLO L; DIBIASI C; TRASIMENI G; GUALDI GF; PALLADINI G; MANFREDI M; FRONTALI M
      CEREBRAL AUTOSOMAL-DOMINANT ARTERIOPATHY WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY (CADASIL) - CLINICAL, NEUROIMAGING, PATHOLOGICALAND GENETIC-STUDY OF A LARGE ITALIAN FAMILY

      Brain
    32. 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
    33. 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
    34. HARDING AE; GIUNTI P; SWEENEY MG; SPADARO M; JODICE C; NOVELLETTO A; MALASPINA P; FRONTALI M
      TRINUCLEOTIDE REPEAT EXPANSION ON CHROMOSOME 6P (SCA1) IN AUTOSOMAL-DOMINANT CEREBELLAR ATAXIAS

      Annals of neurology
    35. GIUNTI P; SWEENEY MG; SPADARO M; JODICE C; NOVELLETTO A; MALASPINA P; FRONTALI M; HARDING AE
      THE TRINUCLEOTIDE REPEAT EXPANSION ON CHROMOSOME 6P (SCA1) IN AUTOSOMAL-DOMINANT CEREBELLAR ATAXIAS

      Brain
    36. JODICE C; MALASPINA P; PERSICHETTI F; NOVELLETTO A; SPADARO M; GIUNTI P; MOROCUTTI C; TERRENATO L; HARDING AE; FRONTALI M
      EFFECT OF TRINUCLEOTIDE REPEAT LENGTH AND PARENTAL SEX ON PHENOTYPIC VARIATION IN SPINOCEREBELLAR ATAXIA-I

      American journal of human genetics
    37. DUYAO M; AMBROSE C; MYERS R; NOVELLETTO A; PERSICHETTI F; FRONTALI M; FOLSTEIN S; ROSS C; FRANZ M; ABBOTT M; GRAY J; CONNEALLY P; YOUNG A; PENNEY J; HOLLINGSWORTH Z; SHOULSON I; LAZZARINI A; FALEK A; KOROSHETZ W; SAX D; BIRD E; VONSATTEL J; BONILLA E; ALVIR J; CONDE JB; CHA JH; DURE L; GOMEZ F; RAMOS M; SANCHEZRAMOS J; SNODGRASS S; DEYOUNG M; WEXLER N; MOSCOWITZ C; PENCHASZADEH G; MACFARLANE H; ANDERSON M; JENKINS B; SRINIDHI J; BARNES G; GUSELLA J; MACDONALD M
      TRINUCLEOTIDE REPEAT LENGTH INSTABILITY AND AGE-OF-ONSET IN HUNTINGTONS-DISEASE

      Nature genetics
    38. JODICE C; FRONTALI M; PERSICHETTI F; NOVELLETTO A; PANDOLFO M; SPADARO M; GIUNTI P; SCHINAIA G; LULLI P; MALASPINA P; PLASMATI R; TOLA R; ANTONELLI A; DIDONATO S; MOROCUTTI C; WEISSENBACH J; CANN HM; TERRENATO L
      THE GENE FOR SPINAL CEREBELLAR ATAXIA-1 (SCA1) IS FLANKED BY 2 CLOSELY LINKED HIGHLY POLYMORPHIC MICROSATELLITE LOCI

      Human molecular genetics
    39. BALL D; HARPER PS; TYLER A; TIBBEN A; VEGTERVANDERVLIS M; CASSIMAN JJ; EVERSKIEBOOMS G; FRONTALI M; JACOPINI AG
      ETHICAL AND SOCIAL-ISSUES IN PRESYMPTOMATIC TESTING FOR HUNTINGTONS-DISEASE - A EUROPEAN-COMMUNITY COLLABORATIVE STUDY

      Journal of Medical Genetics
    40. KWIATKOWSKI TJ; ORR HT; BANFI S; MCCALL AE; JODICE C; PERSICHETTI F; NOVELLETTO A; LEBORGNEDEMARQUOY F; DUVICK LA; FRONTALI M; SUBRAMONY SH; BEAUDET AL; TERRENATO L; ZOGHBI HY; RANUM LPW
      THE GENE FOR AUTOSOMAL-DOMINANT SPINOCEREBELLAR ATAXIA (SCA1) MAPS CENTROMERIC TO D6S89 AND SHOWS NO RECOMBINATION, IN 9 LARGE KINDREDS, WITH A DINUCLEOTIDE REPEAT AT THE AM10 LOCUS

      American journal of human genetics


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 29/10/20 alle ore 19:31:41