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    1. Hoeltzenbein, M; Tome, FMS
      Oppenheim's myatonia congenita

      NEUROPEDIATRICS
    2. He, Y; Jones, KJ; Vignier, N; Morgan, G; Chevallay, M; Barois, A; Estournet-Mathiaud, B; Hori, H; Mizuta, T; Tome, FMS; North, KN; Guicheney, P
      Congenital muscular dystrophy with primary partial laminin alpha 2 chain deficiency: Molecular study

      NEUROLOGY
    3. Fayet, G; Rouche, A; Hogrel, JY; Tome, FMS; Fardeau, M
      Age-related morphological changes of the deltoid muscle from 50 to 79 years of age

      ACTA NEUROPATHOLOGICA
    4. 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
    5. Crosbie, RH; Lim, LE; Moore, SA; Hirano, M; Hays, AP; Maybaum, SW; Collin, H; Dovico, SA; Stolle, CA; Fardeau, M; Tome, FMS; Campbell, KP
      Molecular and genetic characterization of sarcospan: insights into sarcoglycan-sarcospan interactions

      HUMAN MOLECULAR GENETICS
    6. Fardeau, M; Vicart, P; Caron, A; Chateau, D; Chevallay, M; Collin, H; Chapon, F; Duboc, D; Eymard, B; Tome, FMS; Dupret, JM; Paulin, D; Guicheney, P
      Familial myopathy with desmin storage seen as a granulo-filamentar, electron-dense material with mutation of the alpha beta-cristallin gene

      REVUE NEUROLOGIQUE
    7. Eymard, B; Laforet, P; Tome, FMS; Collin, H; Leroy, JP; Hauw, JJ; Richard, I; Beckmann, J; Fardeau, M
      Miyoshi distal myopathy: specific signs and incidence.

      REVUE NEUROLOGIQUE
    8. 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
    9. Vilquin, JT; Guerette, B; Puymirat, J; Yaffe, D; Tome, FMS; Fardeau, M; Fiszman, M; Schwartz, K; Tremblay, JP
      Myoblast transplantations lead to the expression of the laminin alpha 2 chain in normal and dystrophic (dy/dy) mouse muscles

      GENE THERAPY
    10. 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
    11. Brais, B; Rouleau, GA; Bouchard, JP; Fardeau, M; Tome, FMS
      Oculopharyngeal muscular dystrophy

      SEMINARS IN NEUROLOGY
    12. Tome, FMS
      The saga of congenital muscular dystrophy

      NEUROPEDIATRICS
    13. TOME FMS; FARDEAU M
      HEREDITARY INCLUSION-BODY MYOPATHIES

      Current opinion in neurology
    14. 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
    15. MOGHADASZADEH B; DESGUERRE I; TOPALOGLU H; MUNTONI F; PAVEK S; MAYER M; SEWRY C; FARDEAU M; TOME FMS; GUICHENEY P
      IDENTIFICATION OF A NEW LOCUS FOR CONGENITAL MUSCULAR-DYSTROPHY WITH RIGID SPINE SYNDROME TO CHROMOSOME 1P35-36

      European journal of human genetics
    16. UYAMA E; UCHINO M; CHATEAU D; TOME FMS
      AUTOSOMAL RECESSIVE OCULOPHARYNGODISTAL MYOPATHY IN LIGHT OF DISTAL MYOPATHY WITH RIMMED VACUOLES AND OCULOPHARYNGEAL MUSCULAR-DYSTROPHY

      Neuromuscular disorders
    17. 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
    18. 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
    19. TOME FMS; HE Y; CHEVALLAY M; NICOLAS V; CRUAUD C; HORI H; MIZUTA T; ESTOURNET B; BAROIS A; FARDEAU M; GUICHENEY P
      CONGENITAL MUSCULAR-DYSTROPHY WITH PARTIAL LAMININ ALPHA-2 CHAIN (MEROSIN) DEFICIENCY - IMMUNOCYTOCHEMICAL AND MOLECULAR STUDIES

      Neurology
    20. GUICHENEY P; VIGNIER N; ZHANG X; HE Y; CRUAUD C; FREY V; HELBLINGLECLERC A; RICHARD P; ESTOURNET B; MERLINI L; TOPALOGLU H; MORA M; HARPEY JP; HAENGGELI CA; BAROIS A; HAINQUE B; SCHWARTZ K; TOME FMS; FARDEAU M; TRYGGVASON K
      PCR BASED MUTATION SCREENING OF THE LAMININ ALPHA-2 CHAIN GENE (LAMA2) - APPLICATION TO PRENATAL-DIAGNOSIS AND SEARCH FOR FOUNDER EFFECTS IN CONGENITAL MUSCULAR-DYSTROPHY

      Journal of Medical Genetics
    21. ANDERSON LVB; DAVISON K; MOSS JA; RICHARD I; FARDEAU M; TOME FMS; HUBNER C; LASA A; COLOMER J; BECKMANN JS
      CHARACTERIZATION OF MONOCLONAL-ANTIBODIES TO CALPAIN-3 AND PROTEIN EXPRESSION IN MUSCLE FROM PATIENTS WITH LIMB-GIRDLE MUSCULAR-DYSTROPHY TYPE 2A

      The American journal of pathology
    22. MOGHADASZADEH B; DESGUERRE I; TOPALOGLU H; MUNTONI FN; PAVEK S; SEWRY C; MAYER M; FARDEAU M; TOME FMS; GUICHENEY P
      IDENTIFICATION OF A NEW LOCUS FOR A PECULIAR FORM OF CONGENITAL MUSCULAR-DYSTROPHY WITH EARLY RIGIDITY OF THE SPINE, ON CHROMOSOME 1P35-36

      American journal of human genetics
    23. GUICHENEY P; VIGNIER N; HELBLINGLECLERC A; NISSINEN M; ZHANG X; CRUAUD C; LAMBERT JC; RICHELME C; TOPALOGLU H; MERLINI L; BAROIS A; SCHWARTZ K; TOME FMS; TRYGGVASON K; FARDEAU M
      GENETICS OF LAMININ ALPHA-2 CHAIN (OR MEROSIN) DEFICIENT CONGENITAL MUSCULAR-DYSTROPHY - FROM IDENTIFICATION OF MUTATIONS TO PRENATAL-DIAGNOSIS

      Neuromuscular disorders
    24. FARDEAU M; TOME FMS
      OCULOPHARYNGEAL MUSCULAR-DYSTROPHY IN FRANCE

      Neuromuscular disorders
    25. BRUNET G; TOME FMS; EYMARD B; ROBERT JM
      GENEALOGICAL STUDY OF OCULOPHARYNGEAL MUSCULAR-DYSTROPHY IN FRANCE

      Neuromuscular disorders
    26. UYAMA E; NOHIRA O; TOME FMS; CHATEAU D; TOKUNAGA M; ANDO M; MAKI M; OKABE T; UCHINO M
      OCULOPHARYNGEAL MUSCULAR-DYSTROPHY IN JAPAN

      Neuromuscular disorders
    27. MEOLA G; SANSONE V; ROTONDO G; TOME FMS; BOUCHARD JP
      OCULOPHARYNGEAL MUSCULAR-DYSTROPHY IN ITALY

      Neuromuscular disorders
    28. TOME FMS; CHATEAU D; HELBLINGLECLERC A; FARDEAU M
      MORPHOLOGICAL-CHANGES IN MUSCLE-FIBERS IN OCULOPHARYNGEAL MUSCULAR-DYSTROPHY

      Neuromuscular disorders
    29. 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
    30. 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
    31. FARDEAU M; EYMARD B; MIGNARD C; TOME FMS; RICHARD I; BECKMANN JS
      CHROMOSOME 15-LINKED LIMB-GIRDLE MUSCULAR-DYSTROPHY - COMPARISON OF THE CLINICAL PHENOTYPES IN REUNION ISLAND AND FRENCH METROPOLITAN COMMUNITIES

      Neurology
    32. 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
    33. KHURANA TS; SPECHT LA; BEGGS AH; TOME FMS; LETUREQ F; CHEVALLAY M; CHAFEY P; KUNKEL LM
      THE CONCOMITANT USE OF DYSTROPHIN AND UTROPHIN DYSTROPHIN RELATED PROTEIN ANTIBODIES TO REDUCE MISDIAGNOSIS OF DUCHENNE/BECKER-MUSCULAR-DYSTROPHY/

      Biochemical and biophysical research communications
    34. 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
    35. FARDEAU M; EYMARD B; MIGNARD C; TOME FMS; RICHARD I; BECKMANN JS
      CHROMOSOME 15-LINKED LIMB-GIRDLE MUSCULAR-DYSTROPHY - CLINICAL PHENOTYPES IN REUNION ISLAND AND FRENCH METROPOLITAN COMMUNITIES

      Neuromuscular disorders
    36. BECKMANN JS; RICHARD I; BROUX O; FOUGEROUSSE F; ALLAMAND V; CHIANNILKULCHAI N; LIM LE; DUCLOS F; BOURG N; BRENGUIER L; PASTURAUD P; QUETIER F; ROUDAUT C; SUNADA Y; MEYER J; DINCER P; LEFRANC G; MERLINI L; TOPALOGLU H; TOME FMS; COHEN D; JACKSON CE; CAMPBELL KP; FARDEAU M
      IDENTIFICATION OF MUSCLE-SPECIFIC CALPAIN AND BETA-SARCOGLYCAN GENES IN PROGRESSIVE AUTOSOMAL RECESSIVE MUSCULAR-DYSTROPHIES

      Neuromuscular disorders
    37. 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
    38. PINI A; MERLINI L; TOME FMS; CHEVALLAY M; GOBBI G
      MEROSIN-NEGATIVE CONGENITAL MUSCULAR-DYSTROPHY, OCCIPITAL EPILEPSY WITH PERIODIC SPASMS AND FOCAL CORTICAL DYSPLASIA - REPORT OF 3 ITALIAN CASES IN 2 FAMILIES

      Brain & development
    39. 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
    40. TREVISAN CP; MARTINELLO F; FERRUZZA E; FANIN M; CHEVALLAY M; TOME FMS
      BRAIN ALTERATIONS IN THE CLASSICAL FORM OF CONGENITAL MUSCULAR-DYSTROPHY - CLINICAL AND NEUROIMAGING FOLLOW-UP OF 12 CASES AND CORRELATION WITH THE EXPRESSION OF MEROSIN IN MUSCLE

      Child's nervous system
    41. FARDEAU M; TOME FMS; HELBLINGLECLERC A; EVANGELISTA T; OTTOLINI A; CHEVALLAY M; BAROIS A; ESTOURNET B; HARPEY JP; FAURE S; GUICHENEY P; HILLAIRE D
      CONGENITAL MUSCULAR-DYSTROPHY WITH MEROSI N DEFICIENCY - CLINICAL, HISTOPATHOLOGICAL, IMMUNOCYTOCHEMICAL AND GENETIC-STUDY

      Revue neurologique
    42. BLUMEN SC; SADEH M; KORCZYN AD; ROUCHE A; NISIPEANU P; ASHEROV A; TOME FMS
      INTRANUCLEAR INCLUSIONS IN OCULOPHARYNGEAL MUSCULAR-DYSTROPHY AMONG BUKHARA JEWS

      Neurology
    43. UYAMA E; NOHIRA O; CHATEAU D; TOKUNAGA M; UCHINO M; OKABE T; ANDO M; TOME FMS
      OCULOPHARYNGEAL MUSCULAR-DYSTROPHY 2 UNRELATED JAPANESE FAMILIES

      Neurology
    44. 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
    45. 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
    46. 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
    47. FARDEAU M; HILLAIRE D; MIGNARD C; FEINGOLD N; FEINGOLD J; MIGNARD D; DEUBEDA B; COLLIN H; TOME FMS; RICHARD I; BECKMANN J
      JUVENILE LIMB-GIRDLE MUSCULAR-DYSTROPHY CLINICAL, HISTOPATHOLOGICAL AND GENETIC DATA FROM A SMALL COMMUNITY LIVING IN THE REUNION-ISLAND

      Brain
    48. NISSINEN M; HELBLINGLECLERC A; ZHANG X; EVANGELISTA T; TOPALOGLU H; CRUAUD C; WEISSENBACH J; FARDEAU M; TOME FMS; SCHWARTZ K; TRYGGVASON K; GUICHENEY P
      SUBSTITUTION OF A CONSERVED CYSTEINE-996 IN A CYSTEINE-RICH MOTIF OF THE LAMININ ALPHA-2-CHAIN IN CONGENITAL MUSCULAR-DYSTROPHY WITH PARTIAL DEFICIENCY OF THE PROTEIN

      American journal of human genetics
    49. LIM LE; DUCLOS F; BROUX O; BOURG N; SUNADA Y; ALLAMAND V; MEYER J; RICHARD IZ; MOOMAW C; SLAUGHTER C; TOME FMS; FARDEAU M; JACKSON CE; BECKMANN JS; CAMPBELL KP
      BETA-SARCOGLYCAN - CHARACTERIZATION AND ROLE IN LIMB-GIRDLE MUSCULAR-DYSTROPHY LINKED TO 4Q12

      Nature genetics
    50. HELBLINGLECLERC A; ZHANG X; TOPALOGLU H; CRUAUD C; TESSON F; WEISSENBACH J; TOME FMS; SCHWARTZ K; FARDEAU M; TRYGGVASON K; GUICHENEY P
      MUTATIONS IN THE LAMININ ALPHA-2-CHAIN GENE (LAMA2) CAUSE MEROSIN-DEFICIENT CONGENITAL MUSCULAR-DYSTROPHY

      Nature genetics
    51. 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
    52. 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
    53. FARDEAU M; TOME FMS
      CONGENITAL MUSCULAR-DYSTROPHIES - A BREAKTHROUGH

      MS. Medecine sciences
    54. DUCLOS F; LIM LE; SUNADA Y; MEYER J; CAMPBELL KP; BROUX O; BOURG N; ALLAMAND V; RICHARD I; BECKMANN JS; MOOMAW C; SLAUGHTER C; TOME FMS; FARDEAU M; JACKSON CE
      BETA-SARCOGLYCAN - A PROTEIN OF THE DYSTR OPHIN-GLYCOPROTEINS COMPLEX, IS RESPONSIBLE FOR RECESSIVE LIMB-GIRDLE MUSCULAR-DYSTROPHY

      MS. Medecine sciences
    55. HELBLINGLECLERC A; TOPALOGLU H; TOME FMS; SEWRY C; GYAPAY G; NOAM I; MUNTONI F; DUBOWITZ V; BAROIS A; ESTOURNET B; URTIZBEREA JA; WEISSENBACH J; SCHWARTZ K; FARDEAU M; GUICHENEY P
      READJUSTING THE LOCALIZATION OF MEROSIN ( LAMININ ALPHA-2-CHAIN) DEFICIENT CONGENITAL MUSCULAR-DYSTROPHY LOCUS ON CHROMOSOME 6Q2

      Comptes rendus de l'Academie des sciences. Serie 3, Sciences de la vie
    56. VILLANOVA M; LOUBOUTIN JP; CHATEAU D; EYMARD B; SAGNIEZ M; TOME FMS; FARDEAU M
      X-LINKED VACUOLATED MYOPATHY - COMPLEMENT MEMBRANE ATTACK COMPLEX ON SURFACE-MEMBRANE OF INJURED MUSCLE-FIBERS

      Annals of neurology
    57. VANDENBERGH PYK; TOME FMS; FARDEAU M
      ETIOLOGY AND PATHOGENESIS OF THE MUSCULAR-DYSTROPHIES

      Acta neurologica belgica
    58. 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
    59. VILLANOVA M; LOUBOUTIN JP; SAGNIEZ M; CHATEAU D; EYMARD B; TOME FMS; FARDEAU M
      X-LINKED VACUOLATED MYOPATHY

      Neurology
    60. TOME FMS; LECLERC A; GUICHENEY P; CHEVALLAY M; HILLAIRE D; ESTOURNET B; BAROIS A; FARDEAU M
      MEROSIN-DEFICIENT CONGENITAL MUSCULAR-DYSTROPHIES

      Neurology
    61. 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
    62. KHURANA TS; PRENDERGAST RA; ALAMEDDINE HS; TOME FMS; FARDEAU M; ARAHATA K; SUGITA H; KUNKEL LM
      ABSENCE OF EXTRAOCULAR-MUSCLE PATHOLOGY IN DUCHENNES MUSCULAR-DYSTROPHY - ROLE FOR CALCIUM HOMEOSTASIS IN EXTRAOCULAR-MUSCLE SPARING

      The Journal of experimental medicine
    63. SEWRY CA; CHEVALLAY M; TOME FMS
      EXPRESSION OF LAMININ SUBUNITS IN HUMAN FETAL SKELETAL-MUSCLE

      Histochemical Journal
    64. JASMIN BJ; ALAMEDDINE H; LUNDE JA; STETZKOWSKIMARDEN F; COLLIN H; TINSLEY JM; DAVIES KE; TOME FMS; PARRY DJ; CARTAUD J
      EXPRESSION OF UTROPHIN AND ITS MESSENGER-RNA IN DENERVATED MDX MOUSE MUSCLE

      FEBS letters
    65. 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
    66. 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
    67. 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
    68. HILLAIRE D; LECLERC A; FAURE S; TOPALOGLU H; CHIANNILKULCHAI N; GUICHENEY P; GRINAS L; LEGOS P; PHILPOT J; EVANGELISTA T; ROUTON MC; MAYER M; PELLISSIER JF; ESTOURNET B; BAROIS A; HENTATI F; FEINGOLD N; BECKMANN JS; DUBOWITZ V; TOME FMS; FARDEAU M
      LOCALIZATION OF MEROSIN-NEGATIVE CONGENITAL MUSCULAR-DYSTROPHY TO CHROMOSOME 6Q2 BY HOMOZYGOSITY MAPPING

      Human molecular genetics
    69. TOME FMS; MATSUMURA K; CHEVALLAY M; CAMPBELL KP; FARDEAU M
      EXPRESSION OF DYSTROPHIN-ASSOCIATED GLYCOPROTEINS DURING HUMAN FETAL MUSCLE DEVELOPMENT - A PRELIMINARY IMMUNOCYTOCHEMICAL STUDY

      Neuromuscular disorders
    70. MATSUMURA K; TOME FMS; COLLIN H; LETURCQ F; JEANPIERRE M; KAPLAN JC; FARDEAU M; CAMPBELL KP
      EXPRESSION OF DYSTROPHIN-ASSOCIATED PROTEINS TN DYSTROPHIN-POSITIVE MUSCLE-FIBERS (REVERTANTS) IN DUCHENNE MUSCULAR-DYSTROPHY

      Neuromuscular disorders
    71. TOME FMS; EVANGELISTA T; LECLERC A; SUNADA Y; MANOLE E; ESTOURNET B; BAROIS A; CAMPBELL KP; FARDEAU M
      CONGENITAL MUSCULAR-DYSTROPHY WITH MEROSIN DEFICIENCY

      Comptes rendus de l'Academie des sciences. Serie 3, Sciences de la vie
    72. 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
    73. FARDEAU M; TOME FMS
      ULTRASTRUCTURE OF MUSCLE AND NEUROMUSCULAR-JUNCTION - AN HISTORICAL SURVEY OF THE EARLY FRENCH CONTRIBUTIONS

      Biology of the cell
    74. VOIT T; FARDEAU M; TOME FMS
      PRENATAL DETECTION OF MEROSIN EXPRESSION IN HUMAN PLACENTA

      Neuropediatrics
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ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 26/10/20 alle ore 08:48:56