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La ricerca find articoli where authors phrase all words ' GIUNTI P' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 17 riferimenti
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    1. Gaspar, C; Lopes-Cendes, I; Hayes, S; Goto, J; Arvidsson, K; Dias, A; Silveira, I; Maciel, P; Coutinho, P; Lima, M; Zhou, YX; Soong, BW; Watanabe, M; Giunti, P; Stevanin, G; Riess, O; Sasaki, H; Hsieh, M; Nicholson, GA; Brunt, E; Higgins, JJ; Lauritzen, M; Tranebjaerg, L; Volpini, V; Wood, N; Ranum, L; Tsuji, S; Brice, A; Sequeiros, J; Rouleau, GA
      Ancestral origins of the Machado-Joseph disease mutation: A worldwide haplotype study

      AMERICAN JOURNAL OF HUMAN GENETICS
    2. Worth, PF; Houlden, H; Giunti, P; Davis, MB; Wood, NW
      Large, expanded repeats in SCA8 are not confined to patients with cerebellar ataxia

      NATURE GENETICS
    3. Stevanin, G; David, G; Durr, A; Giunti, P; Benomar, A; Abada-Bendib, M; Lee, MS; Agid, Y; Brice, A
      Multiple origins of the spinocerebellar ataxia 7 (SCA7) mutation revealed by linkage disequilibrium studies with closely flanking markers, including an intragenic polymorphism (G(3145)TG/A(3145)TG)

      EUROPEAN JOURNAL OF HUMAN GENETICS
    4. Worth, PF; Giunti, P; Gardner-Thorpe, C; Dixon, PH; Davis, MB; Wood, NW
      Autosomal dominant cerebellar ataxia type III: Linkage in a large British family to a 7.6-cM region on chromosome 15q14-21.3

      AMERICAN JOURNAL OF HUMAN GENETICS
    5. Giunti, P; Stevanin, G; Worth, PF; David, G; Brice, A; Wood, NW
      Molecular and clinical study of 18 families with ADCA type II: Evidence for genetic heterogeneity and De Novo mutation

      AMERICAN JOURNAL OF HUMAN GENETICS
    6. STEVANIN G; GIUNTI P; DAVID G; BELAL S; DURR A; RUBERG M; WOOD N; BRICE A
      DE-NOVO EXPANSION OF INTERMEDIATE ALLELES IN SPINOCEREBELLAR ATAXIA-7

      Human molecular genetics (Print)
    7. 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
    8. DAVID G; ABBAS N; STEVANIN G; DURR A; YVERT G; CANCEL G; WEBER C; IMBERT G; SAUDOU F; ANTONIOU E; DRABKIN H; GEMMILL R; GIUNTI P; BENOMAR A; WOOD N; RUBERG M; AGID Y; MANDEL JL; BRICE A
      CLONING OF THE SCA7 GENE REVEALS A HIGHLY UNSTABLE CAG REPEAT EXPANSION

      Nature genetics
    9. GIUNTI P; SWEENEY MG; DAVIS MB; WOOD NW
      CHARACTERIZATION OF THE SCA2 CAG REPEAT EXPANSION IN ADCA TYPE-I FAMILIES

      Journal of Medical Genetics
    10. SWEENEY M; GIUNTI P; WOOD NW; DAVIS MB
      GENETIC-ANALYSIS OF LATE-ONSET PURE CEREBELLAR-ATAXIA (SCA6)

      Journal of Medical Genetics
    11. 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
    12. GIUNTI P; SWEENEY MG; HARDING AE
      DETECTION OF THE MACHADO-JOSEPH DISEASE SPINOCEREBELLAR ATAXIA 3 TRINUCLEOTIDE REPEAT EXPANSION IN FAMILIES WITH AUTOSOMAL-DOMINANT MOTOR DISORDERS, INCLUDING THE DREW FAMILY OF WALWORTH

      Brain
    13. 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
    14. 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
    15. 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
    16. MALANDRINI A; VILLANOVA M; PIOMBONI P; COLLODEL G; SPADARO M; GIUNTI P; SALVADORI C; MOROCUTTI C; GUAZZI GC
      ULTRASTRUCTURAL SPERM ABNORMALITIES AND CEREBELLAR ATROPHY - DOES A CORRELATION EXIST - REPORT OF 2 CASES WITHOUT ENDOCRINE HYPOGONADISM

      Journal of submicroscopic cytology and pathology
    17. 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


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 21/10/20 alle ore 08:07:24