Filtros : "Albuquerque, Marco A. V." Limpar

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  • Source: Arquivos de Neuro-Psiquiatria. Unidade: FM

    Subjects: DISTROFIA MUSCULAR, MUTAÇÃO GENÉTICA, DOENÇAS MUSCULARES, ESTEROIDES

    Acesso à fonteAcesso à fonteDOIHow to cite
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    • ABNT

      ALBUQUERQUE, Marco A. V. et al. Clinical aspects of patients with sarcoglycanopathies under steroids therapy. Arquivos de Neuro-Psiquiatria, v. 72, n. 10, p. 768-772, 2014Tradução . . Disponível em: https://doi.org/10.1590/0004-282X20140126. Acesso em: 16 maio 2024.
    • APA

      Albuquerque, M. A. V., Abath-Neto, O., Maximino, J. R., Chadi, G., Zanoteli, E., & Reed, U. C. (2014). Clinical aspects of patients with sarcoglycanopathies under steroids therapy. Arquivos de Neuro-Psiquiatria, 72( 10), 768-772. doi:10.1590/0004-282X20140126
    • NLM

      Albuquerque MAV, Abath-Neto O, Maximino JR, Chadi G, Zanoteli E, Reed UC. Clinical aspects of patients with sarcoglycanopathies under steroids therapy [Internet]. Arquivos de Neuro-Psiquiatria. 2014 ; 72( 10): 768-772.[citado 2024 maio 16 ] Available from: https://doi.org/10.1590/0004-282X20140126
    • Vancouver

      Albuquerque MAV, Abath-Neto O, Maximino JR, Chadi G, Zanoteli E, Reed UC. Clinical aspects of patients with sarcoglycanopathies under steroids therapy [Internet]. Arquivos de Neuro-Psiquiatria. 2014 ; 72( 10): 768-772.[citado 2024 maio 16 ] Available from: https://doi.org/10.1590/0004-282X20140126
  • Source: Pediatric Neurology. Unidade: FM

    Subjects: DISTROFIA MUSCULAR, MUTAÇÃO GENÉTICA, MÚSCULO ESQUELÉTICO (ANORMALIDADES)

    Acesso à fonteDOIHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      ALBUQUERQUE, Marco A. V. et al. Phenotypic Intermediate Forms Overlapping to Emery-Dreifuss and Limb Girdle Muscular Dystrophies Caused by Lamin A/C Gene Mutations. Pediatric Neurology, v. 50, n. 5, p. e11-e12, 2014Tradução . . Disponível em: https://doi.org/10.1016/j.pediatrneurol.2014.01.036. Acesso em: 16 maio 2024.
    • APA

      Albuquerque, M. A. V., Pasqualin, L. M., Martins, C. A., Reed, U. C., & Zanoteli, E. (2014). Phenotypic Intermediate Forms Overlapping to Emery-Dreifuss and Limb Girdle Muscular Dystrophies Caused by Lamin A/C Gene Mutations. Pediatric Neurology, 50( 5), e11-e12. doi:10.1016/j.pediatrneurol.2014.01.036
    • NLM

      Albuquerque MAV, Pasqualin LM, Martins CA, Reed UC, Zanoteli E. Phenotypic Intermediate Forms Overlapping to Emery-Dreifuss and Limb Girdle Muscular Dystrophies Caused by Lamin A/C Gene Mutations [Internet]. Pediatric Neurology. 2014 ; 50( 5): e11-e12.[citado 2024 maio 16 ] Available from: https://doi.org/10.1016/j.pediatrneurol.2014.01.036
    • Vancouver

      Albuquerque MAV, Pasqualin LM, Martins CA, Reed UC, Zanoteli E. Phenotypic Intermediate Forms Overlapping to Emery-Dreifuss and Limb Girdle Muscular Dystrophies Caused by Lamin A/C Gene Mutations [Internet]. Pediatric Neurology. 2014 ; 50( 5): e11-e12.[citado 2024 maio 16 ] Available from: https://doi.org/10.1016/j.pediatrneurol.2014.01.036

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