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La ricerca find articoli where authors phrase all words ' Brais, B' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 27 riferimenti
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    1. Fan, XP; Dion, P; Laganiere, J; Brais, B; Rouleau, GA
      Oligomerization of polyalanine expanded PABPN1 facilitates nuclear proteinaggregation that is associated with cell death

      HUMAN MOLECULAR GENETICS
    2. Calado, A; Tome, FMS; Brais, B; Rouleau, G; Kuhn, U; Wahle, E; Carmo-Fonseca, M
      Nuclear inclusions in oculopharyngeal muscular dystrophy consist of poly(A) binding protein 2 aggregates which sequester poly(A) RNA

      HUMAN MOLECULAR GENETICS
    3. Gaspar, C; Jannatipour, M; Dion, P; Laganiere, J; Sequeiros, J; Brais, B; Rouleau, GA
      CAG tract of MJD-1 may be prone to frameshifts causing polyalanine accumulation

      HUMAN MOLECULAR GENETICS
    4. Shanmugam, V; Dion, P; Rochefort, D; Laganiere, J; Brais, B; Rouleau, GA
      PABP2 polyalanine tract expansion causes intranuclear inclusions in oculopharyngeal muscular dystrophy

      ANNALS OF NEUROLOGY
    5. Blumen, SC; Korczyn, AD; Lavoie, H; Medynski, S; Chapman, J; Asherov, A; Nisipeanu, P; Inzelberg, R; Carasso, RL; Bouchard, JP; Tome, FMS; Rouleau, GA; Brais, B
      Oculopharyngeal MD among Bukhara Jews is due to a founder (GCG)9 mutation in the PABP2 gene

      NEUROLOGY
    6. Blumen, SC; Brais, B; Korczyn, AD; Medinsky, S; Chapman, J; Asherov, A; Nisipeanu, P; Codere, F; Bouchard, JP; Fardeau, M; Tome, FMS; Rouleau, GA
      Homozygotes for oculopharyngeal muscular dystrophy have a severe form of the disease

      ANNALS OF NEUROLOGY
    7. Brais, B; Rouleau, GA; Bouchard, JP; Fardeau, M; Tome, FMS
      Oculopharyngeal muscular dystrophy

      SEMINARS IN NEUROLOGY
    8. Mezei, MM; Mankodi, A; Brais, B; Marineau, C; Thornton, CA; Rouleau, GA; Karpati, G
      Minimal expansion of the GCG repeat in the PABP2 gene does not predispose to sporadic inclusion body myositis

      NEUROLOGY
    9. BRAIS B
      SHORT GCG EXPANSIONS IN THE PABP2 GENE CAUSE OCULOPHARYNGEAL MUSCULAR-DYSTROPHY (VOL 18, PG 164, 1998)

      Nature genetics
    10. BRAIS B; BOUCHARD JP; XIE YG; ROCHEFORT DL; CHRETIEN N; TOME FMS; LAFRENIERE RG; ROMMENS JM; UYAMA E; NOHIRA O; BLUMEN S; KORCYN AD; HEUTINK P; MATHIEU J; DURANCEAU A; CODERE F; FARDEAU M; ROULEAU GA
      SHORT GCG EXPANSIONS IN THE PABP2 GENE CAUSE OCULOPHARYNGEAL MUSCULAR-DYSTROPHY

      Nature genetics
    11. XIE YG; ROCHEFORT D; BRAIS B; HOWARD H; HAN FY; GOU LP; MACIEL P; THE BT; LARSSON C; ROULEAU GA
      RESTRICTION MAP OF A YAC AND COSMID CONTIG ENCOMPASSING THE OCULOPHARYNGEAL MUSCULAR-DYSTROPHY CANDIDATE REGION ON CHROMOSOME 14Q11.2-Q13

      Genomics (San Diego, Calif.)
    12. BRAIS B; BOUCHARD JP; TOME FMS; FARDEAU M; CODERE F; DURANCEAU A; ROULEAU GA
      GENETIC-EVIDENCE FOR THE INVOLVEMENT OF OTHER GENES IN MODULATING THESEVERITY OF OCULOPHARYNGEAL MUSCULAR-DYSTROPHY

      Annals of neurology
    13. UYAMA E; BRAIS B; NOHIRA O; TOKUNAGA M; CHATEAU D; TOME FMS; ROULEAU GA; UCHINO M
      OCULOPHARYNGEAL MUSCULAR-DYSTROPHY - PHENOTYPE GENOTYPE DIFFERENCE IN2 UNRELATED JAPANESE FAMILIES/

      Annals of neurology
    14. FEIT H; SILBERGLEIT A; SCHNEIDER LB; GUTIERREZ JA; ROULEAU GA; BRAIS B; JACKSON CE
      AUTOSOMAL-DOMINANT DISTAL MYOPATHY WITH PHARYNGEAL AND VOCAL CORD WEAKNESS

      Neurology
    15. Feit, H; Silbergleit, A; Schneider, LB; Gutierrez, JA; Fitoussi, RP; Reyes, C; Rouleau, GA; Brais, B; Jackson, CE; Beckmann, JS; Seboun, E
      Vocal cord and pharyngeal weakness with autosomal dominant distal myopathy: Clinical description and gene localization to 5q31

      AMERICAN JOURNAL OF HUMAN GENETICS
    16. BOUCHARD JP; BRAIS B; BRUNET D; GOULD PV; ROULEAU GA
      RECENT STUDIES ON OCULOPHARYNGEAL MUSCULAR-DYSTROPHY IN QUEBEC

      Neuromuscular disorders
    17. BRAIS B; BOUCHARD JP; GOSSELIN F; XIE YG; FARDEAU M; TOME FMS; ROULEAU GA
      USING THE FULL POWER OF LINKAGE ANALYSIS IN 11 FRENCH-CANADIAN FAMILIES TO FINE MAP THE OCULOPHARYNGEAL MUSCULAR-DYSTROPHY GENE

      Neuromuscular disorders
    18. MATHIEU J; LAPOINTE G; BRASSARD A; TREMBLAY C; BRAIS B; ROULEAU GA; BOUCHARD JP
      A PILOT-STUDY ON UPPER ESOPHAGEAL SPHINCTER DILATATION FOR THE TREATMENT OF DYSPHAGIA IN PATIENTS WITH OCULOPHARYNGEAL MUSCULAR-DYSTROPHY

      Neuromuscular disorders
    19. NEETENS A; MARTIN JJ; BRAIS B; WEIN B; DREUW B; TIJSSEN CC; CEUTERICK C
      OCULOPHARYNGEAL MUSCULAR-DYSTROPHY (OPMD)

      Neuro-ophthalmology
    20. KIBAR Z; DERKALOUSTIAN VM; BRAIS B; HANI V; FRASER FC; ROULEAU GA
      THE GENE RESPONSIBLE FOR CLOUSTON HIDROTIC ECTODERMAL DYSPLASIA MAPS TO THE PERICENTROMERIC REGION OF CHROMOSOME 13Q

      Human molecular genetics
    21. UYAMA E; NOHIRA O; BRAIS B; TOME FMS; TOKUNAGA M; OKABE T; ROULEAU GA; CHATEAU D; UCHINO M
      OCULOPHARYNGEAL MUSCULAR-DYSTROPHY IN JAPANESE - CLINICOPATHOLOGICAL AND GENETIC-STUDIES

      Annals of neurology
    22. BRAIS B; TOME FMS; FARDEAU M; XIE YG; ROULEAU GA; BOUCHARD JP
      THE NATURAL-HISTORY OF OCULOPHARYNGEAL MUSCULAR-DYSTROPHY BASED ON THE STUDY OF A LARGE COHORT OF FRENCH-CANADIAN MUTATION CARRIERS

      Neurology
    23. BRAIS B; XIE YG; SANSON M; MORGAN K; WEISSENBACH J; KORCZYN AD; BLUMEN SC; FARDEAU M; TOME FMS; BOUCHARD JP; ROULEAU GA
      THE OCULOPHARYNGEAL MUSCULAR-DYSTROPHY LOCUS MAPS TO THE REGION OF THE CARDIAC ALPHA-MYOSIN AND BETA-MYOSIN HEAVY-CHAIN GENES ON CHROMOSOME14Q11.2-Q13

      Human molecular genetics
    24. BRAIS B; BOUCHARD JP; XIE YG; TOME FMS; FARDEAU M; ROULEAU GA
      A MORE SEVERE FORM OF OCULOPHARYNGEAL MUSCULAR-DYSTROPHY (OPMD) IS DOCUMENTED IN A GENETICALLY PROVEN HOMOZYGOUS PATIENT

      Neurology
    25. BRAIS B; MORGAN K; XIE Y; TOME FMS; FARDEAU M; BOUCHARD JP; ROULEAU GA
      STRONG LINKAGE DISEQUILIBRIUM SUGGEST ONE FOUNDER MUTATION IS RESPONSIBLE FOR ALL CASES OF OCULOPHARYNGEAL MUSCULAR-DYSTROPHY (OPMD) IN THEFRENCH-CANADIAN POPULATION

      American journal of human genetics
    26. BRAIS B
      CHARCOT,JEAN,MARTIN AND APHASIA - TREADING THE LINE BETWEEN EXPERIMENTAL PHYSIOLOGY AND PATHOLOGICAL ANATOMY

      Brain and language
    27. BRAIS B; ROULEAU GA; SANSON M; GOSSELIN F; BOUCHARD JP
      OCULOPHARYNGEAL MUSCULAR-DYSTROPHY REVISITED - DIAGNOSTIC-CRITERIA AND VARIABILITY IN PHENOTYPE

      Neurology


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 05/08/20 alle ore 10:22:27