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ABNT
MORENO, Cristiane Araujo Martins et al. Congenital fiber type disproportion caused by TPM3 mutation: a report of two atypical cases. Neuromuscular disorders, v. 30, n. 1, p. 54-58, 2020Tradução . . Disponível em: https://observatorio.fm.usp.br/handle/OPI/35995. Acesso em: 01 jul. 2022.
APA
Moreno, C. A. M., Harms, M. B., Bonnemann, C., Zanoteli, E., Estephan, E. de P., Fappi, A., et al. (2020). Congenital fiber type disproportion caused by TPM3 mutation: a report of two atypical cases. Neuromuscular disorders, 30( 1), 54-58. doi:10.1016/j.nmd.2019.11.001
NLM
Moreno CAM, Harms MB, Bonnemann C, Zanoteli E, Estephan E de P, Fappi A, Monges S, Lubieniecki F, Abath Neto OL, Reed UC, Donkervoort S. Congenital fiber type disproportion caused by TPM3 mutation: a report of two atypical cases [Internet]. Neuromuscular disorders. 2020 ; 30( 1): 54-58.[citado 2022 jul. 01 ] Available from: https://observatorio.fm.usp.br/handle/OPI/35995
Vancouver
Moreno CAM, Harms MB, Bonnemann C, Zanoteli E, Estephan E de P, Fappi A, Monges S, Lubieniecki F, Abath Neto OL, Reed UC, Donkervoort S. Congenital fiber type disproportion caused by TPM3 mutation: a report of two atypical cases [Internet]. Neuromuscular disorders. 2020 ; 30( 1): 54-58.[citado 2022 jul. 01 ] Available from: https://observatorio.fm.usp.br/handle/OPI/35995
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ABNT
MIZIARA, Carmen Silvia Molleis Galego et al. Time Interval between First and Last Epileptic Seizures and Electroencephalogram Normalization in Benign Childhood Epilepsy with Centrotemporal Spikes: Influencing Factors. Journal of pediatric epilepsy, v. 9, n. 02, p. 31-35, 2020Tradução . . Disponível em: https://observatorio.fm.usp.br/handle/OPI/36911. Acesso em: 01 jul. 2022.
APA
Miziara, C. S. M. G., Micheletto, M. L. J., Serrano, V. A. G., Nakanishi, D. H., Serinolli, M. I., Manreza, M. L. G. de, & Reed, U. C. (2020). Time Interval between First and Last Epileptic Seizures and Electroencephalogram Normalization in Benign Childhood Epilepsy with Centrotemporal Spikes: Influencing Factors. Journal of pediatric epilepsy, 9( 02), 31-35. doi:10.1055/s-0040-1709187
NLM
Miziara CSMG, Micheletto MLJ, Serrano VAG, Nakanishi DH, Serinolli MI, Manreza MLG de, Reed UC. Time Interval between First and Last Epileptic Seizures and Electroencephalogram Normalization in Benign Childhood Epilepsy with Centrotemporal Spikes: Influencing Factors [Internet]. Journal of pediatric epilepsy. 2020 ; 9( 02): 31-35.[citado 2022 jul. 01 ] Available from: https://observatorio.fm.usp.br/handle/OPI/36911
Vancouver
Miziara CSMG, Micheletto MLJ, Serrano VAG, Nakanishi DH, Serinolli MI, Manreza MLG de, Reed UC. Time Interval between First and Last Epileptic Seizures and Electroencephalogram Normalization in Benign Childhood Epilepsy with Centrotemporal Spikes: Influencing Factors [Internet]. Journal of pediatric epilepsy. 2020 ; 9( 02): 31-35.[citado 2022 jul. 01 ] Available from: https://observatorio.fm.usp.br/handle/OPI/36911
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ABNT
MENDONCA, Rodrigo de Holanda et al. Intragenic variants in the SMN1 gene determine the clinical phenotype in 5q spinal muscular atrophy. Neurology-genetics, v. 6, n. 5, 2020Tradução . . Disponível em: https://observatorio.fm.usp.br/handle/OPI/38388. Acesso em: 01 jul. 2022.
APA
Mendonca, R. de H., Silva, A. M. S., Kulikowski, L., Dias, A. T., Zanardo, E. A., Kok, F., et al. (2020). Intragenic variants in the SMN1 gene determine the clinical phenotype in 5q spinal muscular atrophy. Neurology-genetics, 6( 5). doi:10.1212/NXG.0000000000000505
NLM
Mendonca R de H, Silva AMS, Kulikowski L, Dias AT, Zanardo EA, Kok F, Reed UC, Zanoteli E, Matsui Junior C, Polido GJ. Intragenic variants in the SMN1 gene determine the clinical phenotype in 5q spinal muscular atrophy [Internet]. Neurology-genetics. 2020 ; 6( 5):[citado 2022 jul. 01 ] Available from: https://observatorio.fm.usp.br/handle/OPI/38388
Vancouver
Mendonca R de H, Silva AMS, Kulikowski L, Dias AT, Zanardo EA, Kok F, Reed UC, Zanoteli E, Matsui Junior C, Polido GJ. Intragenic variants in the SMN1 gene determine the clinical phenotype in 5q spinal muscular atrophy [Internet]. Neurology-genetics. 2020 ; 6( 5):[citado 2022 jul. 01 ] Available from: https://observatorio.fm.usp.br/handle/OPI/38388
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ABNT
ZANOTELI, Edmar et al. Clinical features of collagen VI-related dystrophies: a large Brazilian cohort. Clinical neurology and neurosurgery, v. 192, 2020Tradução . . Disponível em: https://observatorio.fm.usp.br/handle/OPI/35998. Acesso em: 01 jul. 2022.
APA
Zanoteli, E., Soares, P. S., Silva, A. M. S. da, Camelo, C. G., Fonseca, A. T. Q. S. M., Albuquerque, M. A. V., et al. (2020). Clinical features of collagen VI-related dystrophies: a large Brazilian cohort. Clinical neurology and neurosurgery, 192. doi:10.1016/j.clineuro.2020.105734
NLM
Zanoteli E, Soares PS, Silva AMS da, Camelo CG, Fonseca ATQSM, Albuquerque MAV, Moreno CAM, Abath Neto OL, Novo Filho GM, Kulikowski LD, Reed UC. Clinical features of collagen VI-related dystrophies: a large Brazilian cohort [Internet]. Clinical neurology and neurosurgery. 2020 ; 192[citado 2022 jul. 01 ] Available from: https://observatorio.fm.usp.br/handle/OPI/35998
Vancouver
Zanoteli E, Soares PS, Silva AMS da, Camelo CG, Fonseca ATQSM, Albuquerque MAV, Moreno CAM, Abath Neto OL, Novo Filho GM, Kulikowski LD, Reed UC. Clinical features of collagen VI-related dystrophies: a large Brazilian cohort [Internet]. Clinical neurology and neurosurgery. 2020 ; 192[citado 2022 jul. 01 ] Available from: https://observatorio.fm.usp.br/handle/OPI/35998
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ABNT
REZENDE, Angelo R. T et al. Combining neuropsychological tests to improve the assessment of arithmetic difficulties in children with ADHD. Arquivos de Neuro-Psiquiatria, v. 78, n. 4, p. 193-198, 2020Tradução . . Disponível em: https://observatorio.fm.usp.br/handle/OPI/35915. Acesso em: 01 jul. 2022.
APA
Rezende, A. R. T., Pacheco, S. P., Branco, S. C. C., Fernandes, R. D. C., Boldrini, C. R., Doria Filho, U., et al. (2020). Combining neuropsychological tests to improve the assessment of arithmetic difficulties in children with ADHD. Arquivos de Neuro-Psiquiatria, 78( 4), 193-198. doi:10.1590/0004-282X20190178
NLM
Rezende ART, Pacheco SP, Branco SCC, Fernandes RDC, Boldrini CR, Doria Filho U, Bazan PR, Amaro Junior E, Reed UC, Casella EB. Combining neuropsychological tests to improve the assessment of arithmetic difficulties in children with ADHD [Internet]. Arquivos de Neuro-Psiquiatria. 2020 ; 78( 4): 193-198.[citado 2022 jul. 01 ] Available from: https://observatorio.fm.usp.br/handle/OPI/35915
Vancouver
Rezende ART, Pacheco SP, Branco SCC, Fernandes RDC, Boldrini CR, Doria Filho U, Bazan PR, Amaro Junior E, Reed UC, Casella EB. Combining neuropsychological tests to improve the assessment of arithmetic difficulties in children with ADHD [Internet]. Arquivos de Neuro-Psiquiatria. 2020 ; 78( 4): 193-198.[citado 2022 jul. 01 ] Available from: https://observatorio.fm.usp.br/handle/OPI/35915
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ABNT
MENDONCA, Rodrigo H et al. Global Central Nervous System Atrophy in Spinal Muscular Atrophy Type 0 [Carta]. Annals of neurology. Hoboken: Faculdade de Medicina, Universidade de São Paulo. Disponível em: http://observatorio.fm.usp.br/handle/OPI/34038. Acesso em: 01 jul. 2022. , 2019
APA
Mendonca, R. H., Rocha, A. J., Lozano-Arango, A., Diaz, A. B., Castiglioni, C., Silva, A. M. S., et al. (2019). Global Central Nervous System Atrophy in Spinal Muscular Atrophy Type 0 [Carta]. Annals of neurology. Hoboken: Faculdade de Medicina, Universidade de São Paulo. doi:10.1002/ana.25597
NLM
Mendonca RH, Rocha AJ, Lozano-Arango A, Diaz AB, Castiglioni C, Silva AMS, Reed UC, Kulikowski L, Paramonov I, Zanoteli E. Global Central Nervous System Atrophy in Spinal Muscular Atrophy Type 0 [Carta] [Internet]. Annals of neurology. 2019 ; 86( 5): 803-803.[citado 2022 jul. 01 ] Available from: http://observatorio.fm.usp.br/handle/OPI/34038
Vancouver
Mendonca RH, Rocha AJ, Lozano-Arango A, Diaz AB, Castiglioni C, Silva AMS, Reed UC, Kulikowski L, Paramonov I, Zanoteli E. Global Central Nervous System Atrophy in Spinal Muscular Atrophy Type 0 [Carta] [Internet]. Annals of neurology. 2019 ; 86( 5): 803-803.[citado 2022 jul. 01 ] Available from: http://observatorio.fm.usp.br/handle/OPI/34038
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ABNT
WINCKLER, Pablo B et al. Clinicogenetic lessons from 370 patients with autosomal recessive limb-girdle muscular dystrophy. Clinical genetics, v. 96, n. 4, p. 341-353, 2019Tradução . . Disponível em: http://observatorio.fm.usp.br/handle/OPI/34049. Acesso em: 01 jul. 2022.
APA
Winckler, P. B., Silva, A. M. S. da, Coimbra-Neto, A. R., Carvalho, E., Cavalcanti, E. B. U., Sobreira, C. F. R., et al. (2019). Clinicogenetic lessons from 370 patients with autosomal recessive limb-girdle muscular dystrophy. Clinical genetics, 96( 4), 341-353. doi:10.1111/cge.13597
NLM
Winckler PB, Silva AMS da, Coimbra-Neto AR, Carvalho E, Cavalcanti EBU, Sobreira CFR, Marrone CD, Machado-costa MC, Reed UC, Zanoteli E. Clinicogenetic lessons from 370 patients with autosomal recessive limb-girdle muscular dystrophy [Internet]. Clinical genetics. 2019 ; 96( 4): 341-353.[citado 2022 jul. 01 ] Available from: http://observatorio.fm.usp.br/handle/OPI/34049
Vancouver
Winckler PB, Silva AMS da, Coimbra-Neto AR, Carvalho E, Cavalcanti EBU, Sobreira CFR, Marrone CD, Machado-costa MC, Reed UC, Zanoteli E. Clinicogenetic lessons from 370 patients with autosomal recessive limb-girdle muscular dystrophy [Internet]. Clinical genetics. 2019 ; 96( 4): 341-353.[citado 2022 jul. 01 ] Available from: http://observatorio.fm.usp.br/handle/OPI/34049
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ABNT
MENDONCA, Rodrigo H et al. Severe brain involvement in 5q spinal muscular atrophy type 0. Annals of neurology, v. 86, n. 3, p. 458-462, 2019Tradução . . Disponível em: http://observatorio.fm.usp.br/handle/OPI/34443. Acesso em: 01 jul. 2022.
APA
Mendonca, R. H., Rocha, A. J., Lozano-arango, A., Diaz, A. B., Castiglioni, C., Silva, A. M. S., et al. (2019). Severe brain involvement in 5q spinal muscular atrophy type 0. Annals of neurology, 86( 3), 458-462. doi:10.1002/ana.25549
NLM
Mendonca RH, Rocha AJ, Lozano-arango A, Diaz AB, Castiglioni C, Silva AMS, Reed UC, Kulikowski L, Paramonov I, Zanoteli E. Severe brain involvement in 5q spinal muscular atrophy type 0 [Internet]. Annals of neurology. 2019 ; 86( 3): 458-462.[citado 2022 jul. 01 ] Available from: http://observatorio.fm.usp.br/handle/OPI/34443
Vancouver
Mendonca RH, Rocha AJ, Lozano-arango A, Diaz AB, Castiglioni C, Silva AMS, Reed UC, Kulikowski L, Paramonov I, Zanoteli E. Severe brain involvement in 5q spinal muscular atrophy type 0 [Internet]. Annals of neurology. 2019 ; 86( 3): 458-462.[citado 2022 jul. 01 ] Available from: http://observatorio.fm.usp.br/handle/OPI/34443
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POLIDO, Graziela Jorge et al. Cognitive performance of children with spinal muscular atrophy: a systematic review. Dementia & neuropsychologia, v. 13, n. 4, p. 436-443, 2019Tradução . . Disponível em: http://observatorio.fm.usp.br/handle/OPI/35304. Acesso em: 01 jul. 2022.
APA
Polido, G. J., Miranda, M. M. V. de, Carvas Junior, N., Mendonça, R. de H., Caromano, F. A., Reed, U. C., et al. (2019). Cognitive performance of children with spinal muscular atrophy: a systematic review. Dementia & neuropsychologia, 13( 4), 436-443. doi:10.1590/1980-57642018dn13-040011
NLM
Polido GJ, Miranda MMV de, Carvas Junior N, Mendonça R de H, Caromano FA, Reed UC, Zanoteli E, Voos MC. Cognitive performance of children with spinal muscular atrophy: a systematic review [Internet]. Dementia & neuropsychologia. 2019 ; 13( 4): 436-443.[citado 2022 jul. 01 ] Available from: http://observatorio.fm.usp.br/handle/OPI/35304
Vancouver
Polido GJ, Miranda MMV de, Carvas Junior N, Mendonça R de H, Caromano FA, Reed UC, Zanoteli E, Voos MC. Cognitive performance of children with spinal muscular atrophy: a systematic review [Internet]. Dementia & neuropsychologia. 2019 ; 13( 4): 436-443.[citado 2022 jul. 01 ] Available from: http://observatorio.fm.usp.br/handle/OPI/35304
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ABNT
SILVA, Andre M. S et al. Clinical and molecular findings in a cohort of ANO5-related myopathy. Annals of clinical and translational neurology, v. 6, n. 7, p. 1225-1238, 2019Tradução . . Disponível em: http://observatorio.fm.usp.br/handle/OPI/33500. Acesso em: 01 jul. 2022.
APA
Silva, A. M. S., Coimbra-neto, A. R., Souza, P. V. S., Winckler, P. B., Goncalves, M. V. M., Cavalcanti, E. B. U., et al. (2019). Clinical and molecular findings in a cohort of ANO5-related myopathy. Annals of clinical and translational neurology, 6( 7), 1225-1238. doi:10.1002/acn3.50801
NLM
Silva AMS, Coimbra-neto AR, Souza PVS, Winckler PB, Goncalves MVM, Cavalcanti EBU, Carvalho AADS, Sobreire CFDR, Reed UC, Zanoteli E. Clinical and molecular findings in a cohort of ANO5-related myopathy [Internet]. Annals of clinical and translational neurology. 2019 ; 6( 7): 1225-1238.[citado 2022 jul. 01 ] Available from: http://observatorio.fm.usp.br/handle/OPI/33500
Vancouver
Silva AMS, Coimbra-neto AR, Souza PVS, Winckler PB, Goncalves MVM, Cavalcanti EBU, Carvalho AADS, Sobreire CFDR, Reed UC, Zanoteli E. Clinical and molecular findings in a cohort of ANO5-related myopathy [Internet]. Annals of clinical and translational neurology. 2019 ; 6( 7): 1225-1238.[citado 2022 jul. 01 ] Available from: http://observatorio.fm.usp.br/handle/OPI/33500
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ABNT
CRUZ, Pedro M. Rodriguez et al. The clinical spectrum of the congenital myasthenic syndrome resulting from COL13A1 mutations. Brain, v. 142, p. 1547-1560, 2019Tradução . . Disponível em: http://observatorio.fm.usp.br/handle/OPI/33503. Acesso em: 01 jul. 2022.
APA
Cruz, P. M. R., Cossins, J., Estephan, E. de P., Munell, F., Selby, K., Hirano, M., et al. (2019). The clinical spectrum of the congenital myasthenic syndrome resulting from COL13A1 mutations. Brain, 142, 1547-1560. doi:10.1093/brain/awz107
NLM
Cruz PMR, Cossins J, Estephan E de P, Munell F, Selby K, Hirano M, Maroofin R, Mehrjardi MYV, Zanoteli E, Reed UC. The clinical spectrum of the congenital myasthenic syndrome resulting from COL13A1 mutations [Internet]. Brain. 2019 ; 142 1547-1560.[citado 2022 jul. 01 ] Available from: http://observatorio.fm.usp.br/handle/OPI/33503
Vancouver
Cruz PMR, Cossins J, Estephan E de P, Munell F, Selby K, Hirano M, Maroofin R, Mehrjardi MYV, Zanoteli E, Reed UC. The clinical spectrum of the congenital myasthenic syndrome resulting from COL13A1 mutations [Internet]. Brain. 2019 ; 142 1547-1560.[citado 2022 jul. 01 ] Available from: http://observatorio.fm.usp.br/handle/OPI/33503
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ABNT
DABAJ, Ivana e REED, Umbertina Conti e ZANOTELI, Edmar. Clinical and imaging hallmarks of the MYH7-related myopathy with severe axial involvement. Muscle & nerve, v. 58, n. 2, p. 224-234, 2018Tradução . . Disponível em: http://dx.doi.org/10.1002/mus.26137. Acesso em: 01 jul. 2022.
APA
Dabaj, I., Reed, U. C., & Zanoteli, E. (2018). Clinical and imaging hallmarks of the MYH7-related myopathy with severe axial involvement. Muscle & nerve, 58( 2), 224-234. doi:10.1002/mus.26137
NLM
Dabaj I, Reed UC, Zanoteli E. Clinical and imaging hallmarks of the MYH7-related myopathy with severe axial involvement [Internet]. Muscle & nerve. 2018 ; 58( 2): 224-234.[citado 2022 jul. 01 ] Available from: http://dx.doi.org/10.1002/mus.26137
Vancouver
Dabaj I, Reed UC, Zanoteli E. Clinical and imaging hallmarks of the MYH7-related myopathy with severe axial involvement [Internet]. Muscle & nerve. 2018 ; 58( 2): 224-234.[citado 2022 jul. 01 ] Available from: http://dx.doi.org/10.1002/mus.26137
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ABNT
CASTANEDA, Marisol Sampedro et al. A novel ATP1A2 mutation in a patient with hypokalaemic periodic paralysis and CNS symptoms. Brain, v. 141, p. 3308-3318, 2018Tradução . . Disponível em: http://observatorio.fm.usp.br/handle/OPI/30867. Acesso em: 01 jul. 2022.
APA
Castaneda, M. S., Zanoteli, E., Scalco, R. S., Scaramuzzi, V., Caldas, V. M., Reed, U. C., et al. (2018). A novel ATP1A2 mutation in a patient with hypokalaemic periodic paralysis and CNS symptoms. Brain, 141, 3308-3318. doi:10.1093/brain/awy283
NLM
Castaneda MS, Zanoteli E, Scalco RS, Scaramuzzi V, Caldas VM, Reed UC, Silva AMS da, O'callaghan B, Phadke R, Bugiardini E. A novel ATP1A2 mutation in a patient with hypokalaemic periodic paralysis and CNS symptoms [Internet]. Brain. 2018 ; 141 3308-3318.[citado 2022 jul. 01 ] Available from: http://observatorio.fm.usp.br/handle/OPI/30867
Vancouver
Castaneda MS, Zanoteli E, Scalco RS, Scaramuzzi V, Caldas VM, Reed UC, Silva AMS da, O'callaghan B, Phadke R, Bugiardini E. A novel ATP1A2 mutation in a patient with hypokalaemic periodic paralysis and CNS symptoms [Internet]. Brain. 2018 ; 141 3308-3318.[citado 2022 jul. 01 ] Available from: http://observatorio.fm.usp.br/handle/OPI/30867
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ESTEPHAN, Eduardo de Paula et al. Clinical variability of early-onset congenital myasthenic syndrome due to biallelic RAPSN mutations in Brazil. Neuromuscular disorders, v. 28, n. 11, p. 961-964, 2018Tradução . . Disponível em: http://observatorio.fm.usp.br/handle/OPI/29973. Acesso em: 01 jul. 2022.
APA
Estephan, E. de P., Zambon, A. A., Marchiori, P. E., Silva, A. M. S. da, Caldas, V. M., Moreno, C. A. M., et al. (2018). Clinical variability of early-onset congenital myasthenic syndrome due to biallelic RAPSN mutations in Brazil. Neuromuscular disorders, 28( 11), 961-964. doi:10.1016/j.nmd.2018.08.007
NLM
Estephan E de P, Zambon AA, Marchiori PE, Silva AMS da, Caldas VM, Moreno CAM, Reed UC, Horvath R, Topf A, Lochmueller H. Clinical variability of early-onset congenital myasthenic syndrome due to biallelic RAPSN mutations in Brazil [Internet]. Neuromuscular disorders. 2018 ; 28( 11): 961-964.[citado 2022 jul. 01 ] Available from: http://observatorio.fm.usp.br/handle/OPI/29973
Vancouver
Estephan E de P, Zambon AA, Marchiori PE, Silva AMS da, Caldas VM, Moreno CAM, Reed UC, Horvath R, Topf A, Lochmueller H. Clinical variability of early-onset congenital myasthenic syndrome due to biallelic RAPSN mutations in Brazil [Internet]. Neuromuscular disorders. 2018 ; 28( 11): 961-964.[citado 2022 jul. 01 ] Available from: http://observatorio.fm.usp.br/handle/OPI/29973
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ABNT
ESTEPHAN, Eduardo de Paula et al. A common CHRNE mutation in Brazilian patients with congenital myasthenic syndrome. Journal of neurology, v. 265, n. 3, p. 708-713, 2018Tradução . . Disponível em: http://dx.doi.org/10.1007/s00415-018-8736-8. Acesso em: 01 jul. 2022.
APA
Estephan, E. de P., Marchiori, P. E., Reed, U. C., & Zanoteli, E. (2018). A common CHRNE mutation in Brazilian patients with congenital myasthenic syndrome. Journal of neurology, 265( 3), 708-713. doi:10.1007/s00415-018-8736-8
NLM
Estephan E de P, Marchiori PE, Reed UC, Zanoteli E. A common CHRNE mutation in Brazilian patients with congenital myasthenic syndrome [Internet]. Journal of neurology. 2018 ; 265( 3): 708-713.[citado 2022 jul. 01 ] Available from: http://dx.doi.org/10.1007/s00415-018-8736-8
Vancouver
Estephan E de P, Marchiori PE, Reed UC, Zanoteli E. A common CHRNE mutation in Brazilian patients with congenital myasthenic syndrome [Internet]. Journal of neurology. 2018 ; 265( 3): 708-713.[citado 2022 jul. 01 ] Available from: http://dx.doi.org/10.1007/s00415-018-8736-8
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ESTEPHAN, Eduardo de Paula et al. Muscle biopsy with dystrophic pattern and rimmed vacuoles: GNE myopathy in a Brazilian patient. Arquivos de Neuro-Psiquiatria, v. 75, n. 1, p. 72-73, 2017Tradução . . Disponível em: http://www.scielo.br/pdf/anp/v75n1/0004-282X-anp-75-01-0072.pdf. Acesso em: 01 jul. 2022.
APA
Estephan, E. de P., Moreno, C. A. M., Silva, A. M. S. da, Mendonça, R. de H., Abath Neto, O., Nishimura, P. Y., et al. (2017). Muscle biopsy with dystrophic pattern and rimmed vacuoles: GNE myopathy in a Brazilian patient. Arquivos de Neuro-Psiquiatria, 75( 1), 72-73. doi:10.1590/0004-282X20160171
NLM
Estephan E de P, Moreno CAM, Silva AMS da, Mendonça R de H, Abath Neto O, Nishimura PY, Galindo LT, Zanoteli E, Reed UC. Muscle biopsy with dystrophic pattern and rimmed vacuoles: GNE myopathy in a Brazilian patient [Internet]. Arquivos de Neuro-Psiquiatria. 2017 ; 75( 1): 72-73.[citado 2022 jul. 01 ] Available from: http://www.scielo.br/pdf/anp/v75n1/0004-282X-anp-75-01-0072.pdf
Vancouver
Estephan E de P, Moreno CAM, Silva AMS da, Mendonça R de H, Abath Neto O, Nishimura PY, Galindo LT, Zanoteli E, Reed UC. Muscle biopsy with dystrophic pattern and rimmed vacuoles: GNE myopathy in a Brazilian patient [Internet]. Arquivos de Neuro-Psiquiatria. 2017 ; 75( 1): 72-73.[citado 2022 jul. 01 ] Available from: http://www.scielo.br/pdf/anp/v75n1/0004-282X-anp-75-01-0072.pdf
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SIMON, Valdecir Antonio et al. Translation and validation of the Life Satisfaction Index for Adolescents scale with neuromuscular disorders: LSI-A Brazil. Arquivos de Neuro-Psiquiatria, v. 75, n. 8, p. 553-562, 2017Tradução . . Disponível em: http://www.scielo.br/pdf/anp/v75n8/0004-282X-anp-75-08-0553.pdf. Acesso em: 01 jul. 2022.
APA
Simon, V. A., Zanoteli, E., Simon, M. A. V. P., Resende, M. B. D. de, & Reed, U. C. (2017). Translation and validation of the Life Satisfaction Index for Adolescents scale with neuromuscular disorders: LSI-A Brazil. Arquivos de Neuro-Psiquiatria, 75( 8), 553-562. doi:10.1590/0004-282X20170103 C
NLM
Simon VA, Zanoteli E, Simon MAVP, Resende MBD de, Reed UC. Translation and validation of the Life Satisfaction Index for Adolescents scale with neuromuscular disorders: LSI-A Brazil [Internet]. Arquivos de Neuro-Psiquiatria. 2017 ; 75( 8): 553-562.[citado 2022 jul. 01 ] Available from: http://www.scielo.br/pdf/anp/v75n8/0004-282X-anp-75-08-0553.pdf
Vancouver
Simon VA, Zanoteli E, Simon MAVP, Resende MBD de, Reed UC. Translation and validation of the Life Satisfaction Index for Adolescents scale with neuromuscular disorders: LSI-A Brazil [Internet]. Arquivos de Neuro-Psiquiatria. 2017 ; 75( 8): 553-562.[citado 2022 jul. 01 ] Available from: http://www.scielo.br/pdf/anp/v75n8/0004-282X-anp-75-08-0553.pdf
; Reed, Umbertina Conti 
