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Artigo de periodico
Affected female carriers of MTM1 mutations display a wide spectrum of clinical and pathological involvement: delineating diagnostic clues (2017)
Biancalana, Valérie; Zanoteli, Edmar
Source: Acta neuropathologica. Unidade: FM
Subjects: MIOPATIAS CONGÊNITAS ESTRUTURAIS, MUTAÇÃO GENÉTICA, DIAGNÓSTICO, DOENÇAS CONGÊNITAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BIANCALANA, Valérie e ZANOTELI, Edmar. Affected female carriers of MTM1 mutations display a wide spectrum of clinical and pathological involvement: delineating diagnostic clues. Acta neuropathologica, v. 134, p. 889-904, 2017Tradução . . Disponível em: https://doi.org/10.1007/s00401-017-1748-0. Acesso em: 04 nov. 2024.
APA
Biancalana, V., & Zanoteli, E. (2017). Affected female carriers of MTM1 mutations display a wide spectrum of clinical and pathological involvement: delineating diagnostic clues. Acta neuropathologica, 134, 889-904. doi:10.1007/s00401-017-1748-0
NLM
Biancalana V, Zanoteli E. Affected female carriers of MTM1 mutations display a wide spectrum of clinical and pathological involvement: delineating diagnostic clues [Internet]. Acta neuropathologica. 2017 ; 134 889-904.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1007/s00401-017-1748-0
Vancouver
Biancalana V, Zanoteli E. Affected female carriers of MTM1 mutations display a wide spectrum of clinical and pathological involvement: delineating diagnostic clues [Internet]. Acta neuropathologica. 2017 ; 134 889-904.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1007/s00401-017-1748-0
Artigo de periodico-carta/editorial
Nonlethal CHRNA1-Related Congenital Myasthenic Syndrome with a Homozygous Null Mutation [Carta] (2017)
Abath Neto, Osorio; Heise, Carlos Otto; Moreno, Cristiane de Araújo Martins; Estephan, Eduardo de Paula; Mesrob, Lilia; Lechner, Doris; Boland, Anne; Deleuze, Jean-François; Oliveira, Acary Souza Bulle; Reed, Umbertina Conti; Biancalana, Valérie; Laporte, Jocelyn; Zanoteli, Edmar
Source: Canadian journal of neurological sciences. Unidade: FM
Subjects: MUTAÇÃO GENÉTICA, MIASTENIA GRAVIS, DOENÇAS NEURODEGENERATIVAS, GENES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ABATH NETO, Osorio et al. Nonlethal CHRNA1-Related Congenital Myasthenic Syndrome with a Homozygous Null Mutation [Carta]. Canadian journal of neurological sciences. Winnipeg: Faculdade de Medicina, Universidade de São Paulo. Disponível em: https://doi.org/10.1017/cjn.2016.322. Acesso em: 04 nov. 2024. , 2017
APA
Abath Neto, O., Heise, C. O., Moreno, C. de A. M., Estephan, E. de P., Mesrob, L., Lechner, D., et al. (2017). Nonlethal CHRNA1-Related Congenital Myasthenic Syndrome with a Homozygous Null Mutation [Carta]. Canadian journal of neurological sciences. Winnipeg: Faculdade de Medicina, Universidade de São Paulo. doi:10.1017/cjn.2016.322
NLM
Abath Neto O, Heise CO, Moreno C de AM, Estephan E de P, Mesrob L, Lechner D, Boland A, Deleuze J-F, Oliveira ASB, Reed UC, Biancalana V, Laporte J, Zanoteli E. Nonlethal CHRNA1-Related Congenital Myasthenic Syndrome with a Homozygous Null Mutation [Carta] [Internet]. Canadian journal of neurological sciences. 2017 ; 44( 1): 125-127.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1017/cjn.2016.322
Vancouver
Abath Neto O, Heise CO, Moreno C de AM, Estephan E de P, Mesrob L, Lechner D, Boland A, Deleuze J-F, Oliveira ASB, Reed UC, Biancalana V, Laporte J, Zanoteli E. Nonlethal CHRNA1-Related Congenital Myasthenic Syndrome with a Homozygous Null Mutation [Carta] [Internet]. Canadian journal of neurological sciences. 2017 ; 44( 1): 125-127.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1017/cjn.2016.322
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: 04 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. 04 ] 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. 04 ] Available from: https://doi.org/10.1016/j.pediatrneurol.2016.01.023
Artigo de periodico
Integrative data mining highlights candidate genes for monogenic myopathies (2014)
Abath Neto, Osorio; Tassy, Olivier; Biancalana, Valérie; Zanoteli, Edmar; Pourquié, Olivier; Laporte, Jocelyn
Source: PLOS ONE. Unidade: FM
Subjects: DOENÇAS MUSCULARES, MINERAÇÃO DE DADOS, GENES, GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ABATH NETO, Osorio et al. Integrative data mining highlights candidate genes for monogenic myopathies. PLOS ONE, v. 9, n. 10, p. e110888, 2014Tradução . . Disponível em: https://doi.org/10.1371/journal.pone.0110888. Acesso em: 04 nov. 2024.
APA
Abath Neto, O., Tassy, O., Biancalana, V., Zanoteli, E., Pourquié, O., & Laporte, J. (2014). Integrative data mining highlights candidate genes for monogenic myopathies. PLOS ONE, 9( 10), e110888. doi:10.1371/journal.pone.0110888
NLM
Abath Neto O, Tassy O, Biancalana V, Zanoteli E, Pourquié O, Laporte J. Integrative data mining highlights candidate genes for monogenic myopathies [Internet]. PLOS ONE. 2014 ; 9( 10): e110888.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1371/journal.pone.0110888
Vancouver
Abath Neto O, Tassy O, Biancalana V, Zanoteli E, Pourquié O, Laporte J. Integrative data mining highlights candidate genes for monogenic myopathies [Internet]. PLOS ONE. 2014 ; 9( 10): e110888.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1371/journal.pone.0110888

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