Catalogo Articoli (Spogli Riviste)

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La ricerca find articoli where soggetti phrase all words 'SARCOGLYCANOPATHY' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 13 riferimenti
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    1. Dos Santos, MR; Vieira, EM; Lima, MR
      Molecular diagnosis and counseling in a family presenting compound heterozygosity for autosomal recessive limb-girdle muscular dystrophy

      GENETIC COUNSELING
    2. Cagliani, R; Comi, GP; Tancredi, L; Sironi, M; Fortunato, F; Giorda, R; Bardoni, A; Moggio, M; Prelle, A; Bresolin, N; Scarlato, G
      Primary beta-sarcoglycanopathy manifesting as recurrent exercise-induced myoglobinuria

      NEUROMUSCULAR DISORDERS
    3. Politano, L; Nigro, V; Passamano, L; Petretta, V; Comi, LI; Papparella, S; Nigro, G; Rambaldi, PF; Raia, P; Pini, A; Mora, M; Giugliano, MAM; Esposito, MG; Nigro, G
      Evaluation of cardiac and respiratory involvement in sarcoglycanopathies

      NEUROMUSCULAR DISORDERS
    4. Calvo, F; Teijeira, S; Fernandez, JM; Teijeiro, A; Fernandez-Hojas, R; Fernandez-Lopez, XA; Martin, E; Navarro, C
      Evaluation of heart involvement in gamma-sarcoglycanopathy (LGMD2C). A study of ten patients

      NEUROMUSCULAR DISORDERS
    5. Dincer, P; Bonnemann, CG; Aker, OE; Akcoren, Z; Nigro, V; Kunkel, LM; Topaloglu, H
      A homozygous nonsense mutation in delta-sarcoglycan exon 3 in a case of LGMD2F

      NEUROMUSCULAR DISORDERS
    6. Ginjaar, HB; van der Kooi, AJ; Ceelie, H; Kneppers, ALJ; van Meegen, M; Barth, PG; Busch, HFM; Wokke, JHJ; Anderson, LVB; Bonnemann, CG; Jeanpierre, M; Bolhuis, PA; Moorman, AFM; de Visser, M; Bakker, E; Von Ommen, GJB
      Sarcoglycanopathies in Dutch patients with autosomal recessive limb girdlemuscular dystrophy

      JOURNAL OF NEUROLOGY
    7. Merlini, L; Kaplan, JC; Navarro, C; Barois, A; Bonneau, D; Brasa, J; Echenne, B; Gallano, P; Jarre, L; Jeanpierre, M; Kalaydjieva, L; Leturcq, F; Levi-Gomes, A; Toutain, A; Tournev, I; Urtizberea, A; Vallat, JM; Voit, T; Warter, JM
      Homogeneous phenotype of the gypsy limb-girdle MD with the gamma-sarcoglycan C283Y mutation

      NEUROLOGY
    8. Noguchi, S; Wakabayashi, E; Imamura, M; Yoshida, M; Ozawa, E
      Formation of sarcoglycan complex with differentiation in cultured myocytes

      EUROPEAN JOURNAL OF BIOCHEMISTRY
    9. Matsumura, K; Saito, F; Yamada, H; Hase, A; Sunada, Y; Shimizu, T
      Sarcoglycan complex: A muscular supporter of dystroglycan-dystrophin interplay?

      CELLULAR AND MOLECULAR BIOLOGY
    10. BONNEMANN CG; WONG J; BENHAMIDA C; BENHAMIDA M; HENTATI F; KUNKEL LM
      LGMD 2E IN TUNISIA IS CAUSED BY A HOMOZYGOUS MISSENSE MUTATION IN BETA-SARCOGLYCAN EXON-3

      Neuromuscular disorders
    11. OZAWA E; NOGUCHI S; MIZUNO Y; HAGIWARA Y; YOSHIDA M
      INVITED REVIEW - FROM DYSTROPHINOPATHY TO SARCOGLYCANOPATHY - EVOLUTION OF A CONCEPT OF MUSCULAR-DYSTROPHY

      Muscle & nerve
    12. PRELLE A; COMI GP; TANCREDI L; RIGOLETTO C; CISCATO P; FORTUNATO F; NESTI S; SCIACCO M; ROBOTTI M; BAZZI P; FELISARI G; MOGGIO M; SCARLATO G
      SARCOGLYCAN DEFICIENCY IN A LARGE ITALIAN POPULATION OF MYOPATHIC PATIENTS

      Acta Neuropathologica
    13. HIGUCHI I; KAWAI H; UMAKI Y; KAWAJIRI M; ADACHI K; FUKUNAGA H; NAKAGAWA M; ARIMURA K; OSAME M
      DIFFERENT MANNERS OF SARCOGLYCAN EXPRESSION IN GENETICALLY PROVEN ALPHA-SARCOGLYCAN DEFICIENCY AND GAMMA-SARCOGLYCAN DEFICIENCY

      Acta Neuropathologica


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 20/01/21 alle ore 20:33:37