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La ricerca find articoli where authors phrase all words ' Boespflug-Tanguy, O' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 7 riferimenti
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    1. Brenner, M; Johnson, AB; Boespflug-Tanguy, O; Rodriguez, D; Goldman, JE; Messing, A
      Mutations in GFAP, encoding glial fibrillary acidic protein, are associated with Alexander disease

      NATURE GENETICS
    2. Pingault, V; Bondurand, N; Le Caignec, C; Tardieu, S; Lemort, N; Dubourg, O; Le Guern, E; Goossens, M; Boespflug-Tanguy, O
      The SOX10 transcription factor: evaluation as a candidate gene for centraland peripheral hereditary myelin disorders

      JOURNAL OF NEUROLOGY
    3. Francalanci, P; Eymard-Pierre, E; Dionisi-Vici, C; Boldrini, R; Piemonte, F; Virgili, R; Fariello, G; Bosman, C; Santorelli, FM; Boespflug-Tanguy, O; Bertini, E
      Fatal infantile leukodystrophy - A severe variant of CACH/VWM syndrome, allelic to chromosome 3q27

      NEUROLOGY
    4. Bonavita, S; Schiffmann, R; Moore, DF; Frei, K; Choi, B; Patronas, N; Virta, A; Boespflug-Tanguy, O; Tedeschi, G
      Evidence for neuroaxonal injury in patients with proteolipid protein gene mutations

      NEUROLOGY
    5. Rodriguez, D; Gauthier, F; Bertini, E; Bugiani, M; Brenner, M; N'guyen, S; Goizet, C; Gelot, A; Surtees, R; Pedespan, JM; Hernandorena, X; Troncoso, M; Uziel, G; Messing, A; Ponsot, G; Pham-Dinh, D; Dautigny, A; Boespflug-Tanguy, O
      Infantile Alexander disease: Spectrum of GFAP mutations and genotype-phenotype correlation

      AMERICAN JOURNAL OF HUMAN GENETICS
    6. Cailloux, F; Gauthier-Barichard, F; Mimault, C; Isabelle, V; Courtois, V; Giraud, G; Dastugue, B; Boespflug-Tanguy, O
      Genotype-phenotype correlation in inherited brain myelination defects due to proteolipid protein gene mutations

      EUROPEAN JOURNAL OF HUMAN GENETICS
    7. Mimault, C; Giraud, G; Courtois, V; Cailloux, F; Boire, JY; Dastugue, B; Boespflug-Tanguy, O
      Proteolipoprotein gene analysis in 82 patients with sporadic Pelizaeus-Merzbacher disease: Duplications, the major cause of the disease, originate more frequently in male germ cells, but point mutations do not

      AMERICAN JOURNAL OF HUMAN GENETICS


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 10/08/20 alle ore 05:13:28