ReP USP - Resultado da busca

Filtros : "Moggio, Maurizio" Limpar

Filtros

Collaboration
Normalized affiliation
- university of massachusetts (umass) (~1)
Non normalized affiliation
- center for neuromuscular disease, university “g. d'annunzio,” chieti 66013, italy (1)
- department of biomedical sciences, university of modena and reggio emilia, modena 41125, italy (1)
- department of cell biology, university of texas southwestern medical center, dallas, tx 75390, usa (1)
- department of neurological sciences and vision, university of verona, verona 37134, italy (1)
- department of neurological sciences, university “federico ii,” naples 80131, italy (1)

Artigo de periodico
The effects of an intronic polymorphism in TOMM40 and APOE genotypes in sporadic inclusion body myositis (2015)
Gang, Qiang; Bettencourt, Conceicao; Machado, Pedro M.; Fox, Zoe; Brady, Stefen; Healy, Estelle; Parton, Matt; Holton, Janice L.; Hilton-Jones, David; Shieh, Perry B.; Zanoteli, Edmar; De Paepe, Boel; De Bleecker, Jan; Shaibani, Aziz; Ripolone, Michela; Violano, Raffaella; Moggio, Maurizio; Barohn, Richard J.; Dimachkie, Mazen M.; Mora, Marina; Mantegazza, Renato; Zanotti, Simona; Hanna, Michael G.; Houlden, Henry
Source: Neurobiology of aging. Unidade: FM
Subjects: DOENÇAS MUSCULARES, POLIMORFISMO, INTRONS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GANG, Qiang et al. The effects of an intronic polymorphism in TOMM40 and APOE genotypes in sporadic inclusion body myositis. Neurobiology of aging, v. 36, n. 4, p. 1766.e1–1766.e3, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.neurobiolaging.2013.09.029. Acesso em: 09 nov. 2024.
APA
Gang, Q., Bettencourt, C., Machado, P. M., Fox, Z., Brady, S., Healy, E., et al. (2015). The effects of an intronic polymorphism in TOMM40 and APOE genotypes in sporadic inclusion body myositis. Neurobiology of aging, 36( 4), 1766.e1–1766.e3. doi:10.1016/j.neurobiolaging.2013.09.029
NLM
Gang Q, Bettencourt C, Machado PM, Fox Z, Brady S, Healy E, Parton M, Holton JL, Hilton-Jones D, Shieh PB, Zanoteli E, De Paepe B, De Bleecker J, Shaibani A, Ripolone M, Violano R, Moggio M, Barohn RJ, Dimachkie MM, Mora M, Mantegazza R, Zanotti S, Hanna MG, Houlden H. The effects of an intronic polymorphism in TOMM40 and APOE genotypes in sporadic inclusion body myositis [Internet]. Neurobiology of aging. 2015 ; 36( 4): 1766.e1–1766.e3.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1016/j.neurobiolaging.2013.09.029
Vancouver
Gang Q, Bettencourt C, Machado PM, Fox Z, Brady S, Healy E, Parton M, Holton JL, Hilton-Jones D, Shieh PB, Zanoteli E, De Paepe B, De Bleecker J, Shaibani A, Ripolone M, Violano R, Moggio M, Barohn RJ, Dimachkie MM, Mora M, Mantegazza R, Zanotti S, Hanna MG, Houlden H. The effects of an intronic polymorphism in TOMM40 and APOE genotypes in sporadic inclusion body myositis [Internet]. Neurobiology of aging. 2015 ; 36( 4): 1766.e1–1766.e3.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1016/j.neurobiolaging.2013.09.029
Artigo de periodico
Large-scale population analysis challenges the current criteria for the molecular diagnosis of fascioscapulohumeral Muscular Dystrophy (2012)
Scionti, Isabella; Greco, Francesca; Ricci, Giulia; Govi, Monica; Arashiro, Patrícia; Vercelli, Liliana; Berardinelli, Angela; Angelini, Corrado; Antonini, Giovanni; Cao, Michelangelo; Muzio, Antonio Di; Moggio, Maurizio; Morandi, Lucia; Ricci, Enzo; Rodolico, Carmelo; Ruggiero, Lucia; Santoro, Lucio; Siciliano, Gabriele; Tomelleri, Giuliano; Trevisan, Carlo Pietro; Galluzzi, Giuliana; Wright, Woodring; Zatz, Mayana ; Tupler, Rosella
Source: American Journal of Human Genetics. Unidade: IB
Subjects: DISTROFIA MUSCULAR, DOENÇAS GENÉTICAS, GENÉTICA MOLECULAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SCIONTI, Isabella et al. Large-scale population analysis challenges the current criteria for the molecular diagnosis of fascioscapulohumeral Muscular Dystrophy. American Journal of Human Genetics, v. 90, n. 4, p. 628-635, 2012Tradução . . Disponível em: https://doi.org/10.1016/j.ajhg.2012.02.019. Acesso em: 09 nov. 2024.
APA
Scionti, I., Greco, F., Ricci, G., Govi, M., Arashiro, P., Vercelli, L., et al. (2012). Large-scale population analysis challenges the current criteria for the molecular diagnosis of fascioscapulohumeral Muscular Dystrophy. American Journal of Human Genetics, 90( 4), 628-635. doi:10.1016/j.ajhg.2012.02.019
NLM
Scionti I, Greco F, Ricci G, Govi M, Arashiro P, Vercelli L, Berardinelli A, Angelini C, Antonini G, Cao M, Muzio AD, Moggio M, Morandi L, Ricci E, Rodolico C, Ruggiero L, Santoro L, Siciliano G, Tomelleri G, Trevisan CP, Galluzzi G, Wright W, Zatz M, Tupler R. Large-scale population analysis challenges the current criteria for the molecular diagnosis of fascioscapulohumeral Muscular Dystrophy [Internet]. American Journal of Human Genetics. 2012 ; 90( 4): 628-635.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1016/j.ajhg.2012.02.019
Vancouver
Scionti I, Greco F, Ricci G, Govi M, Arashiro P, Vercelli L, Berardinelli A, Angelini C, Antonini G, Cao M, Muzio AD, Moggio M, Morandi L, Ricci E, Rodolico C, Ruggiero L, Santoro L, Siciliano G, Tomelleri G, Trevisan CP, Galluzzi G, Wright W, Zatz M, Tupler R. Large-scale population analysis challenges the current criteria for the molecular diagnosis of fascioscapulohumeral Muscular Dystrophy [Internet]. American Journal of Human Genetics. 2012 ; 90( 4): 628-635.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1016/j.ajhg.2012.02.019

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