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La ricerca find articoli where authors phrase all words ' AZIBI K' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 16 riferimenti
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    1. Choury, D; Szajnert, MF; Joly-Guillou, ML; Azibi, K; Delpech, M; Paul, G
      Nucleotide sequence of the bla(RTG-2) (CARB-5) gene and phylogeny of a newgroup of carbenicillinases

      ANTIMICROBIAL AGENTS AND CHEMOTHERAPY
    2. Choury, D; Aubert, G; Szajnert, MF; Azibi, K; Delpech, M; Paul, G
      Characterization and nucleotide sequence of CARB-6, a new carbenicillin-hydrolyzing beta-lactamase from Vibrio cholerae

      ANTIMICROBIAL AGENTS AND CHEMOTHERAPY
    3. EYMARD B; ROMERO NB; LETURCQ F; PICCOLO F; CARRIE A; JEANPIERRE M; COLLIN H; DEBURGRAVE N; AZIBI K; CHAOUCH M; MERLINI L; THEMARNOEL C; PENISSON I; MAYER M; TANGUY O; CAMPBELL KP; KAPLAN JC; TOME FMS; FARDEAU M
      PRIMARY ADHALINOPATHY (ALPHA-SARCOGLYCANOPATHY) - CLINICAL, PATHOLOGICAL, AND GENETIC CORRELATION IN 20 PATIENTS WITH AUTOSOMAL RECESSIVE MUSCULAR-DYSTROPHY

      Neurology
    4. CARRIE A; PICCOLO F; LETURCQ F; DETOMA C; AZIBI K; BELDJORD C; VALLAT JM; MERLINI L; VOIT T; SEWRY C; URTIZBEREA JA; ROMERO N; TOME FMS; FARDEAU M; SUNADA Y; CAMPBELL KP; KAPLAN JC; JEANPIERRE M
      MUTATIONAL DIVERSITY AND HOT-SPOTS IN THE ALPHA-SARCOGLYCAN GENE IN AUTOSOMAL RECESSIVE MUSCULAR-DYSTROPHY (LGMD2D)

      Journal of Medical Genetics
    5. PICCOLO F; JEANPIERRE M; LETURCQ F; DODE C; AZIBI K; TOUTAIN A; MERLINI L; JARRE L; NAVARRO C; KRISHNAMOORTHY R; TOME FMS; URTIZBEREA JA; BECKMANN JS; CAMPBELL KP; KAPLAN JC
      A FOUNDER MUTATION IN THE GAMMA-SARCOGLYCAN GENE OF GYPSIES POSSIBLY PREDATING THEIR MIGRATION OUT OF INDIA

      Human molecular genetics
    6. JEANPIERRE M; CARRIE A; PICCOLO F; LETURCQ F; AZIBI K; DETOMA C; BELDJORD C; MERLINI L; VOIT T; ROMERO N; SUNADA Y; TOME FMS; FARDEAU M; CAMPBELL KP; KAPLAN JC
      FROM ADHALINOPATHIES TO ALPHA-SARCOGLYCANOPATHIES - AN OVERVIEW

      Neuromuscular disorders
    7. EYMARD B; ROMERO NB; LETURCQ F; CARRIE A; PICCOLO F; COLLIN H; KAPLAN JC; TOME FMS; FARDEAU M; AZIBI K; CHAOUCH M; MERLINI L; PENISSON I; SEFIANI A; CAMPBELL KP
      ADHALIN-DEFICIENT MUSCULAR-DYSTROPHIES - CLINICAL, PATHOLOGICAL, AND GENETIC CORRELATIONS

      Neurology
    8. JUNG D; LETURCQ F; SUNADA Y; DUCLOS F; TOME FMS; MOOMAW C; MERLINI L; AZIBI K; CHAOUCH M; SLAUGHTER C; FARDEAU M; KAPLAN JC; CAMPBELL KP
      ABSENCE OF GAMMA-SARCOGLYCAN (35-DAG) IN AUTOSOMAL RECESSIVE MUSCULAR-DYSTROPHY LINKED TO CHROMOSOME 13Q12

      FEBS letters
    9. PICCOLO F; ROBERDS SL; JEANPIERRE M; LETURCQ F; AZIBI K; BELDJORD C; CARRIE A; RECAN D; CHAOUCH M; REGHIS A; ELKERCH F; SEFIANI A; VOIT T; MERLINI L; COLLIN H; EYMARD B; BECKMANN JS; ROMERO NB; TOME FMS; FARDEAU M; CAMPBELL KP; KAPLAN JC
      PRIMARY ADHALINOPATHY - A COMMON-CAUSE OF AUTOSOMAL RECESSIVE MUSCULAR-DYSTROPHY OF VARIABLE SEVERITY

      Nature genetics
    10. YAMADA H; TOME FMS; HIGUCHI I; KAWAI H; AZIBI K; CHAOUCH M; ROBERDS SL; TANAKA T; FUJITA S; MITSUI T; FUKUNAGA H; MIYOSHI K; OSAME M; FARDEAU M; KAPLAN JC; SHIMIZU T; CAMPBELL KP; MATSUMURA K
      LAMININ ABNORMALITY IN SEVERE CHILDHOOD AUTOSOMAL RECESSIVE MUSCULAR-DYSTROPHY

      Laboratory investigation
    11. KAPLAN JC; CARRIE A; PICCOLO F; SUNADA Y; LETURCQ F; AZIBI K; ELKERCH F; BELDJORD C; MERLINI L; VOIT T; ROMERO N; TOME FMS; FARDEAU M; CAMPBELL KP; JEANPIERRE M
      ALLELIC AND PHENOTYPIC HETEROGENEITY OF PRIMARY ADHALINOPATHIES

      American journal of human genetics
    12. JEANPIERRE M; BECKMANN JS; AZIBI K; ELKERCH F; LETURCQ F; RECAN D; MERLINI L; TOUTAIN A; BONNEAU D; TOME FMS; FARDEAU M; KAPLAN JC; DODE C
      REFINED MAPPING OF THE LGMD2C LOCUS TO A 1-CENTIMORGAN INTERVAL

      American journal of human genetics
    13. ALLAMAND V; LETURCQ F; PICCOLO F; JEANPIERRE M; AZIBI K; ROBERDS SL; LIM LE; CAMPBELL KP; BECKMANN JS; KAPLAN JC
      ADHALIN GENE POLYMORPHISM

      Human molecular genetics
    14. ROMERO NB; TOME FMS; LETURCQ F; ELKERCH F; AZIBI K; BACHNER L; ANDERSON RD; ROBERDS SL; CAMPBELL KP; FARDEAU M; KAPLAN JC
      GENETIC-HETEROGENEITY OF SEVERE CHILDHOOD AUTOSOMAL RECESSIVE MUSCULAR-DYSTROPHY WITH ADHALIN (50 KDA DYSTROPHY-ASSOCIATED GLYCOPROTEIN) DEFICIENCY

      Comptes rendus de l'Academie des sciences. Serie 3, Sciences de la vie
    15. ELKERCH F; SEFIANI A; AZIBI K; BOUTALEB N; YAHYAOUI M; BENTAHILA A; VINET MC; LETURCQ F; BACHNER L; BECKMANN J; CAMPBELL KP; TOME FMS; FARDEAU M; KAPLAN JC
      LINKAGE ANALYSIS OF FAMILIES WITH SEVERE CHILDHOOD AUTOSOMAL RECESSIVE MUSCULAR-DYSTROPHY IN MOROCCO INDICATES GENETIC HOMOGENEITY OF THE DISEASE IN NORTH-AFRICA

      Journal of Medical Genetics
    16. AZIBI K; BACHNER L; BECKMANN JS; MATSUMURA K; HAMOUDA E; CHAOUCH M; CHAOUCH A; AITOUARAB R; VIGNAL A; WEISSENBACH J; VINET MC; LETURCQ F; COLLIN H; TOME FMS; REGHIS A; FARDEAU M; CAMPBELL KP; KAPLAN JC
      SEVERE CHILDHOOD AUTOSOMAL RECESSIVE MUSCULAR-DYSTROPHY WITH THE DEFICIENCY OF THE 50 KDA DYSTROPHIN-ASSOCIATED GLYCOPROTEIN MAPS TO CHROMOSOME-13Q12

      Human molecular genetics


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 18/01/21 alle ore 18:09:38