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Artigo de periodico
The important role of hemispherotomy for rasmussen encephalitis: clinical and functional outcomes (2024)
Thome, Úrsula; Batista, Larissa A.; Rocha, Renata P.; Terra, Vera C.; Hamad, Ana Paula Andrade; Sakamoto, Américo Ceiki ; Santos, Antonio Carlos dos ; Santos, Marcelo Volpon ; Machado, Hélio Rubens
Fonte: Pediatric Neurology. Unidade: FMRP
Assuntos: ELETROENCEFALOGRAFIA, ENCEFALITE, DIAGNÓSTICO POR IMAGEM, QUALIDADE DE VIDA, CONVULSÕES, RESULTADO DE TRATAMENTO
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ABNT
THOME, Úrsula et al. The important role of hemispherotomy for rasmussen encephalitis: clinical and functional outcomes. Pediatric Neurology, v. 150, p. 82-90, 2024Tradução . . Disponível em: https://doi.org/10.1016/j.pediatrneurol.2023.10.016. Acesso em: 24 out. 2025.
APA
Thome, Ú., Batista, L. A., Rocha, R. P., Terra, V. C., Hamad, A. P. A., Sakamoto, A. C., et al. (2024). The important role of hemispherotomy for rasmussen encephalitis: clinical and functional outcomes. Pediatric Neurology, 150, 82-90. doi:10.1016/j.pediatrneurol.2023.10.016
NLM
Thome Ú, Batista LA, Rocha RP, Terra VC, Hamad APA, Sakamoto AC, Santos AC dos, Santos MV, Machado HR. The important role of hemispherotomy for rasmussen encephalitis: clinical and functional outcomes [Internet]. Pediatric Neurology. 2024 ; 150 82-90.[citado 2025 out. 24 ] Available from: https://doi.org/10.1016/j.pediatrneurol.2023.10.016
Vancouver
Thome Ú, Batista LA, Rocha RP, Terra VC, Hamad APA, Sakamoto AC, Santos AC dos, Santos MV, Machado HR. The important role of hemispherotomy for rasmussen encephalitis: clinical and functional outcomes [Internet]. Pediatric Neurology. 2024 ; 150 82-90.[citado 2025 out. 24 ] Available from: https://doi.org/10.1016/j.pediatrneurol.2023.10.016
Artigo de periodico
Babies with Pierre Robin sequence: neuropsychomotor development (2023)
Souza, Caroline Duchatsch Ribeiro de; Padovani, Leticia Faccim ; Ferreira-Donati, Grace Cristina ; Moraes, Márcia Cristina Almendros Fernandes ; Corrêa, Camila de Castro ; Maximino, Luciana Paula
Fonte: Pediatric Neurology. Unidades: FOB, HRAC
Assuntos: SÍNDROME DE PIERRE ROBIN, TERAPIA OCUPACIONAL, DESENVOLVIMENTO DA LINGUAGEM, DESENVOLVIMENTO INFANTIL
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ABNT
SOUZA, Caroline Duchatsch Ribeiro de et al. Babies with Pierre Robin sequence: neuropsychomotor development. Pediatric Neurology, v. 141, p. 72-76, 2023Tradução . . Disponível em: https://doi.org/10.1016/j.pediatrneurol.2023.01.010. Acesso em: 24 out. 2025.
APA
Souza, C. D. R. de, Padovani, L. F., Ferreira-Donati, G. C., Moraes, M. C. A. F., Corrêa, C. de C., & Maximino, L. P. (2023). Babies with Pierre Robin sequence: neuropsychomotor development. Pediatric Neurology, 141, 72-76. doi:10.1016/j.pediatrneurol.2023.01.010
NLM
Souza CDR de, Padovani LF, Ferreira-Donati GC, Moraes MCAF, Corrêa C de C, Maximino LP. Babies with Pierre Robin sequence: neuropsychomotor development [Internet]. Pediatric Neurology. 2023 ; 141 72-76.[citado 2025 out. 24 ] Available from: https://doi.org/10.1016/j.pediatrneurol.2023.01.010
Vancouver
Souza CDR de, Padovani LF, Ferreira-Donati GC, Moraes MCAF, Corrêa C de C, Maximino LP. Babies with Pierre Robin sequence: neuropsychomotor development [Internet]. Pediatric Neurology. 2023 ; 141 72-76.[citado 2025 out. 24 ] Available from: https://doi.org/10.1016/j.pediatrneurol.2023.01.010
Artigo de periodico
Clinical and Histologic Findings in ACTA1-Related Nemaline Myopathy: Case Series and Review of the Literature (2017)
Moreno, Cristiane de Araújo Martins; Abath Neto, Osório; Donkervoort, Sandra; Reed, Umbertina Conti; Oliveira, Acary Sousa Bulle; Bönnemann, Carsten; Zanoteli, Edmar
Fonte: Pediatric Neurology. Unidade: FM
Assuntos: DOENÇAS CONGÊNITAS, MUTAÇÃO GÊNICA, ESTUDOS DE COORTES, MIOPATIA, REVISÃO SISTEMÁTICA
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ABNT
MORENO, Cristiane de Araújo Martins et al. Clinical and Histologic Findings in ACTA1-Related Nemaline Myopathy: Case Series and Review of the Literature. Pediatric Neurology, v. 75, p. 11-16, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.pediatrneurol.2017.04.002. Acesso em: 24 out. 2025.
APA
Moreno, C. de A. M., Abath Neto, O., Donkervoort, S., Reed, U. C., Oliveira, A. S. B., Bönnemann, C., & Zanoteli, E. (2017). Clinical and Histologic Findings in ACTA1-Related Nemaline Myopathy: Case Series and Review of the Literature. Pediatric Neurology, 75, 11-16. doi:10.1016/j.pediatrneurol.2017.04.002
NLM
Moreno C de AM, Abath Neto O, Donkervoort S, Reed UC, Oliveira ASB, Bönnemann C, Zanoteli E. Clinical and Histologic Findings in ACTA1-Related Nemaline Myopathy: Case Series and Review of the Literature [Internet]. Pediatric Neurology. 2017 ; 75 11-16.[citado 2025 out. 24 ] Available from: https://doi.org/10.1016/j.pediatrneurol.2017.04.002
Vancouver
Moreno C de AM, Abath Neto O, Donkervoort S, Reed UC, Oliveira ASB, Bönnemann C, Zanoteli E. Clinical and Histologic Findings in ACTA1-Related Nemaline Myopathy: Case Series and Review of the Literature [Internet]. Pediatric Neurology. 2017 ; 75 11-16.[citado 2025 out. 24 ] Available from: https://doi.org/10.1016/j.pediatrneurol.2017.04.002
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
Fonte: Pediatric Neurology. Unidade: FM
Assuntos: DOENÇAS CONGÊNITAS, MUTAÇÃO GENÉTICA, MIOPIA, BRASILEIROS
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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: 24 out. 2025.
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 2025 out. 24 ] 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 2025 out. 24 ] Available from: https://doi.org/10.1016/j.pediatrneurol.2016.01.023
Artigo de periodico
Fingolimod prescribed for the treatment of multiple sclerosis in patients younger than age 18 years (2015)
Fragoso, Yara Dadalti; Alves-Leon, Soniza Vieira; Barreira, Amilton Antunes; Callegaro, Dagoberto; Ferreira, Maria Lucia Brito; Finkelsztejn, Alessandro; Gomes, Sidney; Gonçalves, Marcus Vinicius Magno; Machado, Maria Iris Moraes; Marques, Vanessa Daccach; Matta, Andre Palma Cunha; Papais-Alvarenga, Regina Maria; Pereira, Samira Luisa Apostolos; Tauil, Carlos Bernardo
Fonte: Pediatric Neurology. Unidade: FMRP
Assuntos: ESCLEROSE MÚLTIPLA, CRIANÇAS, ADOLESCENTES, FÁRMACOS IMUNOSSUPRESSORES
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ABNT
FRAGOSO, Yara Dadalti et al. Fingolimod prescribed for the treatment of multiple sclerosis in patients younger than age 18 years. Pediatric Neurology, v. 53, n. 2, p. 166-168, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.pediatrneurol.2015.03.024. Acesso em: 24 out. 2025.
APA
Fragoso, Y. D., Alves-Leon, S. V., Barreira, A. A., Callegaro, D., Ferreira, M. L. B., Finkelsztejn, A., et al. (2015). Fingolimod prescribed for the treatment of multiple sclerosis in patients younger than age 18 years. Pediatric Neurology, 53( 2), 166-168. doi:10.1016/j.pediatrneurol.2015.03.024
NLM
Fragoso YD, Alves-Leon SV, Barreira AA, Callegaro D, Ferreira MLB, Finkelsztejn A, Gomes S, Gonçalves MVM, Machado MIM, Marques VD, Matta APC, Papais-Alvarenga RM, Pereira SLA, Tauil CB. Fingolimod prescribed for the treatment of multiple sclerosis in patients younger than age 18 years [Internet]. Pediatric Neurology. 2015 ; 53( 2): 166-168.[citado 2025 out. 24 ] Available from: https://doi.org/10.1016/j.pediatrneurol.2015.03.024
Vancouver
Fragoso YD, Alves-Leon SV, Barreira AA, Callegaro D, Ferreira MLB, Finkelsztejn A, Gomes S, Gonçalves MVM, Machado MIM, Marques VD, Matta APC, Papais-Alvarenga RM, Pereira SLA, Tauil CB. Fingolimod prescribed for the treatment of multiple sclerosis in patients younger than age 18 years [Internet]. Pediatric Neurology. 2015 ; 53( 2): 166-168.[citado 2025 out. 24 ] Available from: https://doi.org/10.1016/j.pediatrneurol.2015.03.024
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
Fonte: Pediatric Neurology. Unidade: FM
Assuntos: PEDIATRIA, MUTAÇÃO GENÉTICA, DISTROFIA MUSCULAR, DOENÇAS CONGÊNITAS
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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: 24 out. 2025.
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 2025 out. 24 ] 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 2025 out. 24 ] 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
Fonte: Pediatric Neurology. Unidade: FM
Assuntos: DISTROFIA MUSCULAR, MUTAÇÃO GENÉTICA, MÚSCULO ESQUELÉTICO (ANORMALIDADES)
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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: 24 out. 2025.
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 2025 out. 24 ] 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 2025 out. 24 ] Available from: https://doi.org/10.1016/j.pediatrneurol.2014.01.036
Artigo de periodico
Outcomes of epileptic spasms in patients aged less than 3 years: single-center United States experience (2012)
Vendrame, Martina; Guilhoto, Laura Maria de Figueiredo Ferreira; Loddenkemper, T; Gregas, Matt; Bourgeois, Blaise F; Kothare, Sanjeev V
Fonte: Pediatric Neurology. Unidade: HU
Assuntos: EPILEPSIA, CRIANÇAS
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ABNT
VENDRAME, Martina et al. Outcomes of epileptic spasms in patients aged less than 3 years: single-center United States experience. Pediatric Neurology, v. 46, n. 5, p. 276-280, 2012Tradução . . Disponível em: https://doi.org/10.1016/j.pediatrneurol.2012.02.022. Acesso em: 24 out. 2025.
APA
Vendrame, M., Guilhoto, L. M. de F. F., Loddenkemper, T., Gregas, M., Bourgeois, B. F., & Kothare, S. V. (2012). Outcomes of epileptic spasms in patients aged less than 3 years: single-center United States experience. Pediatric Neurology, 46( 5), 276-280. doi:10.1016/j.pediatrneurol.2012.02.022
NLM
Vendrame M, Guilhoto LM de FF, Loddenkemper T, Gregas M, Bourgeois BF, Kothare SV. Outcomes of epileptic spasms in patients aged less than 3 years: single-center United States experience [Internet]. Pediatric Neurology. 2012 ; 46( 5): 276-280.[citado 2025 out. 24 ] Available from: https://doi.org/10.1016/j.pediatrneurol.2012.02.022
Vancouver
Vendrame M, Guilhoto LM de FF, Loddenkemper T, Gregas M, Bourgeois BF, Kothare SV. Outcomes of epileptic spasms in patients aged less than 3 years: single-center United States experience [Internet]. Pediatric Neurology. 2012 ; 46( 5): 276-280.[citado 2025 out. 24 ] Available from: https://doi.org/10.1016/j.pediatrneurol.2012.02.022
Artigo de periodico
Experience with lacosamide in a series of children with drug-resistant focal epilepsy (2011)
Guilhoto, Laura Maria de Figueiredo Ferreira; Loddenkemper, T; Gooty, V D; Rotenberg, A; Takeoka, M; Duffy, Frank H; Coulter, D; Urion, David; Bourgeois, Blaise F; Kothare, Sanjeev V
Fonte: Pediatric Neurology. Unidade: HU
Assuntos: EPILEPSIA, MEDICAMENTO
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ABNT
GUILHOTO, Laura Maria de Figueiredo Ferreira et al. Experience with lacosamide in a series of children with drug-resistant focal epilepsy. Pediatric Neurology, v. 44, n. 6, p. 414-419, 2011Tradução . . Disponível em: https://doi.org/10.1016/j.pediatrneurol.2010.12.003. Acesso em: 24 out. 2025.
APA
Guilhoto, L. M. de F. F., Loddenkemper, T., Gooty, V. D., Rotenberg, A., Takeoka, M., Duffy, F. H., et al. (2011). Experience with lacosamide in a series of children with drug-resistant focal epilepsy. Pediatric Neurology, 44( 6), 414-419. doi:10.1016/j.pediatrneurol.2010.12.003
NLM
Guilhoto LM de FF, Loddenkemper T, Gooty VD, Rotenberg A, Takeoka M, Duffy FH, Coulter D, Urion D, Bourgeois BF, Kothare SV. Experience with lacosamide in a series of children with drug-resistant focal epilepsy [Internet]. Pediatric Neurology. 2011 ; 44( 6): 414-419.[citado 2025 out. 24 ] Available from: https://doi.org/10.1016/j.pediatrneurol.2010.12.003
Vancouver
Guilhoto LM de FF, Loddenkemper T, Gooty VD, Rotenberg A, Takeoka M, Duffy FH, Coulter D, Urion D, Bourgeois BF, Kothare SV. Experience with lacosamide in a series of children with drug-resistant focal epilepsy [Internet]. Pediatric Neurology. 2011 ; 44( 6): 414-419.[citado 2025 out. 24 ] Available from: https://doi.org/10.1016/j.pediatrneurol.2010.12.003
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
Fonte: Pediatric Neurology. Unidade: FMRP
Assuntos: SISTEMA IMUNE, DOENÇAS, ASPERGILLUS, MUTAÇÃO GENÉTICA
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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: 24 out. 2025.
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 2025 out. 24 ]
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 2025 out. 24 ]
Artigo de periodico
Frontal Lobe Dysfunction in Children With Temporal Lobe Epilepsy (2007)
Rzezak, Patrícia; Fuentes, Daniel; Guimarães, Catarina A.; Thome-Souza, Sigride; Kuczynski, Evelyn; Li, Li M.; Franzon, Renata C.; Leite, Claudia C.; Guerreiro, Marilisa; Valente, Kette D.
Fonte: Pediatric Neurology. Unidade: FM
Assuntos: LOBO FRONTAL (FISIOPATOLOGIA), EPILEPSIA DO LOBO TEMPORAL (PATOLOGIA;DIAGNÓSTICO), COGNIÇÃO (TESTES), CRIANÇAS
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ABNT
RZEZAK, Patrícia et al. Frontal Lobe Dysfunction in Children With Temporal Lobe Epilepsy. Pediatric Neurology, v. 37, n. 3, p. 176-185, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.pediatrneurol.2007.05.009. Acesso em: 24 out. 2025.
APA
Rzezak, P., Fuentes, D., Guimarães, C. A., Thome-Souza, S., Kuczynski, E., Li, L. M., et al. (2007). Frontal Lobe Dysfunction in Children With Temporal Lobe Epilepsy. Pediatric Neurology, 37( 3), 176-185. doi:10.1016/j.pediatrneurol.2007.05.009
NLM
Rzezak P, Fuentes D, Guimarães CA, Thome-Souza S, Kuczynski E, Li LM, Franzon RC, Leite CC, Guerreiro M, Valente KD. Frontal Lobe Dysfunction in Children With Temporal Lobe Epilepsy [Internet]. Pediatric Neurology. 2007 ; 37( 3): 176-185.[citado 2025 out. 24 ] Available from: https://doi.org/10.1016/j.pediatrneurol.2007.05.009
Vancouver
Rzezak P, Fuentes D, Guimarães CA, Thome-Souza S, Kuczynski E, Li LM, Franzon RC, Leite CC, Guerreiro M, Valente KD. Frontal Lobe Dysfunction in Children With Temporal Lobe Epilepsy [Internet]. Pediatric Neurology. 2007 ; 37( 3): 176-185.[citado 2025 out. 24 ] Available from: https://doi.org/10.1016/j.pediatrneurol.2007.05.009
Artigo de periodico
Episodic somnolence in an infant with Riley-Day Syndrome (2005)
Casella, Erasmo B; Bousso, Albert; Corvello, Cassandra M; Fruchtengarten, Ligia V G; Diament, Aron J
Fonte: Pediatric Neurology. Unidade: HU
Assuntos: DOENÇAS DO SISTEMA NERVOSO PERIFÉRICO, CRIANÇAS
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ABNT
CASELLA, Erasmo B et al. Episodic somnolence in an infant with Riley-Day Syndrome. Pediatric Neurology, v. 32, n. 4, p. 273-274, 2005Tradução . . Disponível em: https://doi.org/10.1016/j.pediatrneurol.2004.09.010. Acesso em: 24 out. 2025.
APA
Casella, E. B., Bousso, A., Corvello, C. M., Fruchtengarten, L. V. G., & Diament, A. J. (2005). Episodic somnolence in an infant with Riley-Day Syndrome. Pediatric Neurology, 32( 4), 273-274. doi:10.1016/j.pediatrneurol.2004.09.010
NLM
Casella EB, Bousso A, Corvello CM, Fruchtengarten LVG, Diament AJ. Episodic somnolence in an infant with Riley-Day Syndrome [Internet]. Pediatric Neurology. 2005 ; 32( 4): 273-274.[citado 2025 out. 24 ] Available from: https://doi.org/10.1016/j.pediatrneurol.2004.09.010
Vancouver
Casella EB, Bousso A, Corvello CM, Fruchtengarten LVG, Diament AJ. Episodic somnolence in an infant with Riley-Day Syndrome [Internet]. Pediatric Neurology. 2005 ; 32( 4): 273-274.[citado 2025 out. 24 ] Available from: https://doi.org/10.1016/j.pediatrneurol.2004.09.010
Artigo de periodico
Language plasticity revealed by electroencephalogram mapping (2002)
Foz, Flávia B.; Lucchini Fábio L. P.; Palimieri, Samanta; Rocha, Armando F.; Rodella, Ednilson C.; Rondó, Andrea G.; Cardoso, Marly B.; Ramazzini, Patrícia B.; Leite, Claudia Costa
Fonte: Pediatric Neurology. Unidade: FM
Assuntos: ELETROENCEFALOGRAFIA, RADIOLOGIA
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ABNT
FOZ, Flávia B. et al. Language plasticity revealed by electroencephalogram mapping. Pediatric Neurology, v. 26, n. 2, p. 106-115, 2002Tradução . . Disponível em: https://doi.org/10.1016/s0887-8994(01)00368-x. Acesso em: 24 out. 2025.
APA
Foz, F. B., Lucchini Fábio L. P.,, Palimieri, S., Rocha, A. F., Rodella, E. C., Rondó, A. G., et al. (2002). Language plasticity revealed by electroencephalogram mapping. Pediatric Neurology, 26( 2), 106-115. doi:10.1016/s0887-8994(01)00368-x
NLM
Foz FB, Lucchini Fábio L. P., Palimieri S, Rocha AF, Rodella EC, Rondó AG, Cardoso MB, Ramazzini PB, Leite CC. Language plasticity revealed by electroencephalogram mapping [Internet]. Pediatric Neurology. 2002 ; 26( 2): 106-115.[citado 2025 out. 24 ] Available from: https://doi.org/10.1016/s0887-8994(01)00368-x
Vancouver
Foz FB, Lucchini Fábio L. P., Palimieri S, Rocha AF, Rodella EC, Rondó AG, Cardoso MB, Ramazzini PB, Leite CC. Language plasticity revealed by electroencephalogram mapping [Internet]. Pediatric Neurology. 2002 ; 26( 2): 106-115.[citado 2025 out. 24 ] Available from: https://doi.org/10.1016/s0887-8994(01)00368-x
Trabalho de evento-resumo periodico
Congenital structural myopathies: clinical and pathologic review of 13 patients (1994)
Reed, Umbertina Conti; Marie, Suely Kazue Nagahashi; Carvalho, M. S.; Delgado, M S; Diament, Aron Judka; Levy, J A
Fonte: Pediatric Neurology. Nome do evento: Congress of the International Child Neurology Association. Unidade: FM
Assunto: NEUROLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
REED, Umbertina Conti et al. Congenital structural myopathies: clinical and pathologic review of 13 patients. Pediatric Neurology. New York: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 24 out. 2025. , 1994
APA
Reed, U. C., Marie, S. K. N., Carvalho, M. S., Delgado, M. S., Diament, A. J., & Levy, J. A. (1994). Congenital structural myopathies: clinical and pathologic review of 13 patients. Pediatric Neurology. New York: Faculdade de Medicina, Universidade de São Paulo.
NLM
Reed UC, Marie SKN, Carvalho MS, Delgado MS, Diament AJ, Levy JA. Congenital structural myopathies: clinical and pathologic review of 13 patients. Pediatric Neurology. 1994 ;11( 2 ): 140-1.[citado 2025 out. 24 ]
Vancouver
Reed UC, Marie SKN, Carvalho MS, Delgado MS, Diament AJ, Levy JA. Congenital structural myopathies: clinical and pathologic review of 13 patients. Pediatric Neurology. 1994 ;11( 2 ): 140-1.[citado 2025 out. 24 ]
Trabalho de evento-resumo periodico
Limb defects with or without mobius sequence and misoprostol use in first trimester of pregnancy (1994)
Dias, M. J. M; Paz, J A; Gherpelli, J L D; Kim, C A; Leone, C R; Vargas, F R; Maldonado, M J; Ramos, G; Gonzalez, Claudette Hajaj
Fonte: Pediatric Neurology. Nome do evento: Congress of the International Child Neurology Association. Unidade: FM
Assunto: OBSTETRÍCIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
DIAS, M. J. M et al. Limb defects with or without mobius sequence and misoprostol use in first trimester of pregnancy. Pediatric Neurology. Chippewa Falls: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 24 out. 2025. , 1994
APA
Dias, M. J. M., Paz, J. A., Gherpelli, J. L. D., Kim, C. A., Leone, C. R., Vargas, F. R., et al. (1994). Limb defects with or without mobius sequence and misoprostol use in first trimester of pregnancy. Pediatric Neurology. Chippewa Falls: Faculdade de Medicina, Universidade de São Paulo.
NLM
Dias MJM, Paz JA, Gherpelli JLD, Kim CA, Leone CR, Vargas FR, Maldonado MJ, Ramos G, Gonzalez CH. Limb defects with or without mobius sequence and misoprostol use in first trimester of pregnancy. Pediatric Neurology. 1994 ;11( 2 ): 164.[citado 2025 out. 24 ]
Vancouver
Dias MJM, Paz JA, Gherpelli JLD, Kim CA, Leone CR, Vargas FR, Maldonado MJ, Ramos G, Gonzalez CH. Limb defects with or without mobius sequence and misoprostol use in first trimester of pregnancy. Pediatric Neurology. 1994 ;11( 2 ): 164.[citado 2025 out. 24 ]
Trabalho de evento-resumo periodico
Congenital muscular dystrophy: clinical and pathologic review of 24 patients (1994)
Reed, Umbertina Conti; Marie, Suely Kazue Nagahashi; Carvalho, A A S; Manreza, M L G; Salum, P N B; Diament, Aron Judka; Levy, J A
Fonte: Pediatric Neurology. Nome do evento: Congress of the International Child Neurology Association. Unidade: FM
Assunto: NEUROLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
REED, Umbertina Conti et al. Congenital muscular dystrophy: clinical and pathologic review of 24 patients. Pediatric Neurology. New York: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 24 out. 2025. , 1994
APA
Reed, U. C., Marie, S. K. N., Carvalho, A. A. S., Manreza, M. L. G., Salum, P. N. B., Diament, A. J., & Levy, J. A. (1994). Congenital muscular dystrophy: clinical and pathologic review of 24 patients. Pediatric Neurology. New York: Faculdade de Medicina, Universidade de São Paulo.
NLM
Reed UC, Marie SKN, Carvalho AAS, Manreza MLG, Salum PNB, Diament AJ, Levy JA. Congenital muscular dystrophy: clinical and pathologic review of 24 patients. Pediatric Neurology. 1994 ;11( 2 ): 141.[citado 2025 out. 24 ]
Vancouver
Reed UC, Marie SKN, Carvalho AAS, Manreza MLG, Salum PNB, Diament AJ, Levy JA. Congenital muscular dystrophy: clinical and pathologic review of 24 patients. Pediatric Neurology. 1994 ;11( 2 ): 141.[citado 2025 out. 24 ]
Trabalho de evento-resumo periodico
Congenital muscular dystrophy in two seblings with cataracts and slight cerebral involvement (1994)
Reed, Umbertina Conti; Marie, Suely Kazue Nagahashi; Tsanaclis, Ana Maria Crous; Carvalho, M. S.; Roinzenblat, J; Pedreira, C C; Diament, Aron Judka; Levy, J A
Fonte: Pediatric Neurology. Nome do evento: Congress of the International Child Neurology Association. Unidade: FM
Assunto: NEUROLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
REED, Umbertina Conti et al. Congenital muscular dystrophy in two seblings with cataracts and slight cerebral involvement. Pediatric Neurology. New York: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 24 out. 2025. , 1994
APA
Reed, U. C., Marie, S. K. N., Tsanaclis, A. M. C., Carvalho, M. S., Roinzenblat, J., Pedreira, C. C., et al. (1994). Congenital muscular dystrophy in two seblings with cataracts and slight cerebral involvement. Pediatric Neurology. New York: Faculdade de Medicina, Universidade de São Paulo.
NLM
Reed UC, Marie SKN, Tsanaclis AMC, Carvalho MS, Roinzenblat J, Pedreira CC, Diament AJ, Levy JA. Congenital muscular dystrophy in two seblings with cataracts and slight cerebral involvement. Pediatric Neurology. 1994 ;11( 2 ): 141.[citado 2025 out. 24 ]
Vancouver
Reed UC, Marie SKN, Tsanaclis AMC, Carvalho MS, Roinzenblat J, Pedreira CC, Diament AJ, Levy JA. Congenital muscular dystrophy in two seblings with cataracts and slight cerebral involvement. Pediatric Neurology. 1994 ;11( 2 ): 141.[citado 2025 out. 24 ]
Artigo de periodico
Congenital insensitivity to pain with anhidrosis (hereditary sensory and autonomic neuropathy type iv) (1994)
Rosemberg, Sérgio; Marie, Suely Kazue Nagahashi; Kliemann, S
Fonte: Pediatric Neurology. Unidade: FM
Assunto: NEUROLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ROSEMBERG, Sérgio e MARIE, Suely Kazue Nagahashi e KLIEMANN, S. Congenital insensitivity to pain with anhidrosis (hereditary sensory and autonomic neuropathy type iv). Pediatric Neurology, v. 11, n. 1 , p. 50-6, 1994Tradução . . Disponível em: https://doi.org/10.1016/0887-8994(94)90091-4. Acesso em: 24 out. 2025.
APA
Rosemberg, S., Marie, S. K. N., & Kliemann, S. (1994). Congenital insensitivity to pain with anhidrosis (hereditary sensory and autonomic neuropathy type iv). Pediatric Neurology, 11( 1 ), 50-6. doi:10.1016/0887-8994(94)90091-4
NLM
Rosemberg S, Marie SKN, Kliemann S. Congenital insensitivity to pain with anhidrosis (hereditary sensory and autonomic neuropathy type iv) [Internet]. Pediatric Neurology. 1994 ;11( 1 ): 50-6.[citado 2025 out. 24 ] Available from: https://doi.org/10.1016/0887-8994(94)90091-4
Vancouver
Rosemberg S, Marie SKN, Kliemann S. Congenital insensitivity to pain with anhidrosis (hereditary sensory and autonomic neuropathy type iv) [Internet]. Pediatric Neurology. 1994 ;11( 1 ): 50-6.[citado 2025 out. 24 ] Available from: https://doi.org/10.1016/0887-8994(94)90091-4

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