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Artigo de periodico
A Study of a Cohort of X-Linked Myotubular Myopathy at the Clinical, Histologic, and Genetic Levels (2016)
Abath Neto, Osorio; Silva, Marina Rodrigues e; Martins, Cristiane de Araújo; Oliveira, Acary de Souza Bulle; Reed, Umbertina Conti; Biancalana, Valérie; Pesquero, João Bosco; Laporte, Jocelyn; Zanoteli, Edmar
Source: Pediatric Neurology. Unidade: FM
Subjects: DOENÇAS CONGÊNITAS, MUTAÇÃO GENÉTICA, MIOPIA, BRASILEIROS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ABATH NETO, Osorio et al. A Study of a Cohort of X-Linked Myotubular Myopathy at the Clinical, Histologic, and Genetic Levels. Pediatric Neurology, v. 58, p. 107-112, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.pediatrneurol.2016.01.023. Acesso em: 02 nov. 2024.
APA
Abath Neto, O., Silva, M. R. e, Martins, C. de A., Oliveira, A. de S. B., Reed, U. C., Biancalana, V., et al. (2016). A Study of a Cohort of X-Linked Myotubular Myopathy at the Clinical, Histologic, and Genetic Levels. Pediatric Neurology, 58, 107-112. doi:10.1016/j.pediatrneurol.2016.01.023
NLM
Abath Neto O, Silva MR e, Martins C de A, Oliveira A de SB, Reed UC, Biancalana V, Pesquero JB, Laporte J, Zanoteli E. A Study of a Cohort of X-Linked Myotubular Myopathy at the Clinical, Histologic, and Genetic Levels [Internet]. Pediatric Neurology. 2016 ; 58 107-112.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1016/j.pediatrneurol.2016.01.023
Vancouver
Abath Neto O, Silva MR e, Martins C de A, Oliveira A de SB, Reed UC, Biancalana V, Pesquero JB, Laporte J, Zanoteli E. A Study of a Cohort of X-Linked Myotubular Myopathy at the Clinical, Histologic, and Genetic Levels [Internet]. Pediatric Neurology. 2016 ; 58 107-112.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1016/j.pediatrneurol.2016.01.023
Artigo de periodico
Congenital Muscular Dystrophy With Dropped Head Linked to the LMNA Gene in a Brazilian Cohort (2014)
Pasqualin, Lívia M. A.; Reed, Umbertina C.; Costa, Thais V. M. M.; Quedas, Elisângela; Albuquerque, Marco A .V.; Resende, Maria B. D.; Franzon, Renata C.; Rutkowski, Anne; Chadi, Gerson; Zanoteli, Edmar
Source: Pediatric Neurology. Unidade: FM
Subjects: PEDIATRIA, MUTAÇÃO GENÉTICA, DISTROFIA MUSCULAR, DOENÇAS CONGÊNITAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PASQUALIN, Lívia M. A. et al. Congenital Muscular Dystrophy With Dropped Head Linked to the LMNA Gene in a Brazilian Cohort. Pediatric Neurology, v. 50, n. 4, p. 400-406, 2014Tradução . . Disponível em: https://doi.org/10.1016/j.pediatrneurol.2013.11.010. Acesso em: 02 nov. 2024.
APA
Pasqualin, L. M. A., Reed, U. C., Costa, T. V. M. M., Quedas, E., Albuquerque, M. A. .V., Resende, M. B. D., et al. (2014). Congenital Muscular Dystrophy With Dropped Head Linked to the LMNA Gene in a Brazilian Cohort. Pediatric Neurology, 50( 4), 400-406. doi:10.1016/j.pediatrneurol.2013.11.010
NLM
Pasqualin LMA, Reed UC, Costa TVMM, Quedas E, Albuquerque MA .V, Resende MBD, Franzon RC, Rutkowski A, Chadi G, Zanoteli E. Congenital Muscular Dystrophy With Dropped Head Linked to the LMNA Gene in a Brazilian Cohort [Internet]. Pediatric Neurology. 2014 ; 50( 4): 400-406.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1016/j.pediatrneurol.2013.11.010
Vancouver
Pasqualin LMA, Reed UC, Costa TVMM, Quedas E, Albuquerque MA .V, Resende MBD, Franzon RC, Rutkowski A, Chadi G, Zanoteli E. Congenital Muscular Dystrophy With Dropped Head Linked to the LMNA Gene in a Brazilian Cohort [Internet]. Pediatric Neurology. 2014 ; 50( 4): 400-406.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1016/j.pediatrneurol.2013.11.010
Artigo de periodico
Phenotypic Intermediate Forms Overlapping to Emery-Dreifuss and Limb Girdle Muscular Dystrophies Caused by Lamin A/C Gene Mutations (2014)
Albuquerque, Marco A. V.; Pasqualin, Lívia M.; Martins, Cristiane A.; Reed, Umbertina C.; Zanoteli, Edmar
Source: Pediatric Neurology. Unidade: FM
Subjects: DISTROFIA MUSCULAR, MUTAÇÃO GENÉTICA, MÚSCULO ESQUELÉTICO (ANORMALIDADES)
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: 02 nov. 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 nov. 02 ] 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 nov. 02 ] Available from: https://doi.org/10.1016/j.pediatrneurol.2014.01.036
Artigo de periodico
Unusual presentation of brain aspergillosis in chronic granulomatous disease (2010)
Roxo Júnior, Pérsio; Menezes, Ulissis Pádua de; Condino-Neto, Antônio; Ferriani, Virgínia Paes Leme; Takayanagui, Osvaldo Massaiti
Source: Pediatric Neurology. Unidade: FMRP
Subjects: SISTEMA IMUNE, DOENÇAS, ASPERGILLUS, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ROXO JÚNIOR, Pérsio et al. Unusual presentation of brain aspergillosis in chronic granulomatous disease. Pediatric Neurology, v. 43, n. 6, p. 442-444, 2010Tradução . . Acesso em: 02 nov. 2024.
APA
Roxo Júnior, P., Menezes, U. P. de, Condino-Neto, A., Ferriani, V. P. L., & Takayanagui, O. M. (2010). Unusual presentation of brain aspergillosis in chronic granulomatous disease. Pediatric Neurology, 43( 6), 442-444.
NLM
Roxo Júnior P, Menezes UP de, Condino-Neto A, Ferriani VPL, Takayanagui OM. Unusual presentation of brain aspergillosis in chronic granulomatous disease. Pediatric Neurology. 2010 ; 43( 6): 442-444.[citado 2024 nov. 02 ]
Vancouver
Roxo Júnior P, Menezes UP de, Condino-Neto A, Ferriani VPL, Takayanagui OM. Unusual presentation of brain aspergillosis in chronic granulomatous disease. Pediatric Neurology. 2010 ; 43( 6): 442-444.[citado 2024 nov. 02 ]

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