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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
   
   D. Choury et al., "Nucleotide sequence of the bla(RTG-2) (CARB-5) gene and phylogeny of a newgroup of carbenicillinases", ANTIM AG CH, 44(4), 2000, pp. 1070-1074
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
   
   D. Choury et al., "Characterization and nucleotide sequence of CARB-6, a new carbenicillin-hydrolyzing beta-lactamase from Vibrio cholerae", ANTIM AG CH, 43(2), 1999, pp. 297-301
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
   
   B. Eymard et al., "PRIMARY ADHALINOPATHY (ALPHA-SARCOGLYCANOPATHY) - CLINICAL, PATHOLOGICAL, AND GENETIC CORRELATION IN 20 PATIENTS WITH AUTOSOMAL RECESSIVE MUSCULAR-DYSTROPHY", Neurology, 48(5), 1997, pp. 1227-1234
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
   
   A. Carrie et al., "MUTATIONAL DIVERSITY AND HOT-SPOTS IN THE ALPHA-SARCOGLYCAN GENE IN AUTOSOMAL RECESSIVE MUSCULAR-DYSTROPHY (LGMD2D)", Journal of Medical Genetics, 34(6), 1997, pp. 470-475
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
   
   F. Piccolo et al., "A FOUNDER MUTATION IN THE GAMMA-SARCOGLYCAN GENE OF GYPSIES POSSIBLY PREDATING THEIR MIGRATION OUT OF INDIA", Human molecular genetics, 5(12), 1996, pp. 2019-2022
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
   
   M. Jeanpierre et al., "FROM ADHALINOPATHIES TO ALPHA-SARCOGLYCANOPATHIES - AN OVERVIEW", Neuromuscular disorders, 6(6), 1996, pp. 463-465
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
   
   B. Eymard et al., "ADHALIN-DEFICIENT MUSCULAR-DYSTROPHIES - CLINICAL, PATHOLOGICAL, AND GENETIC CORRELATIONS", Neurology, 46(2), 1996, pp. 68006-68006
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
   
   D. Jung et al., "ABSENCE OF GAMMA-SARCOGLYCAN (35-DAG) IN AUTOSOMAL RECESSIVE MUSCULAR-DYSTROPHY LINKED TO CHROMOSOME 13Q12", FEBS letters, 381(1-2), 1996, pp. 15-20
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
   
   F. Piccolo et al., "PRIMARY ADHALINOPATHY - A COMMON-CAUSE OF AUTOSOMAL RECESSIVE MUSCULAR-DYSTROPHY OF VARIABLE SEVERITY", Nature genetics, 10(2), 1995, pp. 243-245
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
    
    H. Yamada et al., "LAMININ ABNORMALITY IN SEVERE CHILDHOOD AUTOSOMAL RECESSIVE MUSCULAR-DYSTROPHY", Laboratory investigation, 72(6), 1995, pp. 715-722
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
    
    J.C. Kaplan et al., "ALLELIC AND PHENOTYPIC HETEROGENEITY OF PRIMARY ADHALINOPATHIES", American journal of human genetics, 57(4), 1995, pp. 103-103
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
    
    M. Jeanpierre et al., "REFINED MAPPING OF THE LGMD2C LOCUS TO A 1-CENTIMORGAN INTERVAL", American journal of human genetics, 57(4), 1995, pp. 1114-1114
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
    
    V. Allamand et al., "ADHALIN GENE POLYMORPHISM", Human molecular genetics, 3(12), 1994, pp. 2269-2269
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
    
    N.B. Romero et al., "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, 317(1), 1994, pp. 70-76
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
    
    F. Elkerch et al., "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, 31(4), 1994, pp. 342-343
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
    
    K. Azibi et al., "SEVERE CHILDHOOD AUTOSOMAL RECESSIVE MUSCULAR-DYSTROPHY WITH THE DEFICIENCY OF THE 50 KDA DYSTROPHIN-ASSOCIATED GLYCOPROTEIN MAPS TO CHROMOSOME-13Q12", Human molecular genetics, 2(9), 1993, pp. 1423-1428