Catalogo Articoli (Spogli Riviste)

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La ricerca find articoli where authors phrase all words 'NAOM I' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 13 riferimenti
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    1. Naom, I; D'Alessandro, M; Sewry, CA; Jardine, P; Ferlini, A; Moss, T; Dubowitz, J; Muntoni, F
      Mutations in the laminin alpha 2-chain gene in two children with early-onset muscular dystrophy

      BRAIN
    2. Brockington, M; Sewry, CA; Herrmann, R; Naom, I; Dearlove, A; Rhodes, M; Topaloglu, H; Dubowitz, V; Voit, T; Muntoni, F
      Assignment of a form of congenital muscular dystrophy with secondary merosin deficiency to chromosome 1q42

      AMERICAN JOURNAL OF HUMAN GENETICS
    3. D'Alessandro, M; Naom, I; Ferlini, A; Sewry, C; Dubowitz, V; Muntoni, F
      Is there selection in favour of heterozygotes in families with merosin-deficient congenital muscular dystrophy?

      HUMAN GENETICS
    4. NAOM I; DALESSANDRO M; SEWRY CA; PHILPOT J; MANZUR AY; DUBOWITZ V; MUNTONI F
      LAMININ ALPHA-2-CHAIN GENE-MUTATIONS IN 2 SIBLINGS PRESENTING WITH LIMB-GIRDLE MUSCULAR-DYSTROPHY

      Neuromuscular disorders
    5. BUSHBY K; ANDERSON LVB; POLLITT C; NAOM I; MUNTONI F; BINDOFF L
      ABNORMAL MEROSIN IN ADULTS - A NEW FORM OF LATE-ONSET MUSCULAR-DYSTROPHY NOT LINKED TO CHROMOSOME 6Q2

      Brain
    6. SEWRY CA; NAOM I; DALESSANDRO M; SOROKIN L; BRUNO S; WILSON LA; DUBOWITZ V; MUNTONI F
      VARIABLE CLINICAL PHENOTYPE IN MEROSIN-DEFICIENT CONGENITAL MUSCULAR-DYSTROPHY ASSOCIATED WITH DIFFERENTIAL IMMUNOLABELING OF 2 FRAGMENTS OF THE LAMININ ALPHA-2 CHAIN

      Neuromuscular disorders
    7. NAOM I; SEWRY C; DALESSANDRO M; TOPALOGLU H; FERLINI A; WILSON L; DUBOWITZ V; MUNTONI F
      PRENATAL-DIAGNOSIS IN MEROSIN-DEFICIENT CONGENITAL MUSCULAR-DYSTROPHY

      Neuromuscular disorders
    8. TAN E; TOPALOGLU H; SEWRY C; ZORLU Y; NAOM I; ERDEM S; DALESSANDRO M; MUNTONI F; DUBOWITZ V
      LATE-ONSET MUSCULAR-DYSTROPHY WITH CEREBRAL WHITE-MATTER CHANGES DUE TO PARTIAL MEROSIN DEFICIENCY

      Neuromuscular disorders
    9. NAOM I; DALESSANDRO M; SEWRY C; FERLINI A; TOPALOGLU H; HELBLINGLECLERC A; GUICHENEY P; SCHWARTZ K; AKCOREN Z; DUBOWITZ V; MUNTONI F
      THE ROLE OF IMMUNOCYTOCHEMISTRY AND LINKAGE ANALYSIS IN THE PRENATAL-DIAGNOSIS OF MEROSIN-DEFICIENT CONGENITAL MUSCULAR-DYSTROPHY

      Human genetics
    10. SEWRY CA; DALESSANDRO M; WILSON LA; SOROKIN LM; NAOM I; BRUNO S; FERLINI A; DUBOWITZ V; MUNTONI F
      EXPRESSION OF LAMININ CHAINS IN SKIN IN MEROSIN-DEFICIENT CONGENITAL MUSCULAR-DYSTROPHY

      Neuropediatrics
    11. SEWRY CA; PHILPOT J; SOROKIN LM; WILSON LA; NAOM I; GOODWIN F; DALESSANDRO M; DUBOWITZ V; MUNTONI F
      DIAGNOSIS OF MEROSIN (LAMININ-2) DEFICIENT CONGENITAL MUSCULAR-DYSTROPHY BY SKIN BIOPSY

      Lancet
    12. HUGOT JP; LAURENTPUIG P; GOWERROUSSEAU C; OLSON JM; LEE JC; BEAUGERIE L; NAOM I; DUPAS JL; VANGOSSUM A; ORHOLM M; BONAITIPELLIE C; WEISSENBACH J; MATHEW CG; LENNARDJONES JE; CORTOT A; COLOMBEL JF; THOMAS G
      MAPPING OF A SUSCEPTIBILITY LOCUS FOR CROHNS-DISEASE ON CHROMOSOME-16

      Nature
    13. NAOM I; LEE J; FORD D; BOWMAN SJ; LANCHBURY JS; HARIS I; HODGSON SV; EASTON D; LENNARDLONES J; MATHEW CG
      ANALYSIS OF THE CONTRIBUTION OF HLA GENES TO GENETIC PREDISPOSITION IN INFLAMMATORY BOWEL-DISEASE

      American journal of human genetics


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 04/08/20 alle ore 15:52:14