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Parte de monografia/livro
Departamento de Neuropsiquiatria e Psicologia Médica: 1982 - 1992 (2022)
Marques Júnior, Wilson
Source: Faculdade de Medicina de Ribeirão Preto USP: quarta década. Unidade: FMRP
Subjects: UNIVERSIDADE PÚBLICA, ENSINO SUPERIOR, MEDICINA, ESTRUTURA ORGANIZACIONAL, NEUROPSIQUIATRIA, PSICOLOGIA MÉDICA
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MARQUES JÚNIOR, Wilson. Departamento de Neuropsiquiatria e Psicologia Médica: 1982 - 1992. Faculdade de Medicina de Ribeirão Preto USP: quarta década. Tradução . Ribeirão Preto: FUNPEC Editora, 2022. . Disponível em: https://www.fmrp.usp.br/wp-content/uploads/sites/356/2022/10/USP_Quarta_Decada.pdf. Acesso em: 08 jun. 2024.
APA
Marques Júnior, W. (2022). Departamento de Neuropsiquiatria e Psicologia Médica: 1982 - 1992. In Faculdade de Medicina de Ribeirão Preto USP: quarta década. Ribeirão Preto: FUNPEC Editora. Recuperado de https://www.fmrp.usp.br/wp-content/uploads/sites/356/2022/10/USP_Quarta_Decada.pdf
NLM
Marques Júnior W. Departamento de Neuropsiquiatria e Psicologia Médica: 1982 - 1992 [Internet]. In: Faculdade de Medicina de Ribeirão Preto USP: quarta década. Ribeirão Preto: FUNPEC Editora; 2022. [citado 2024 jun. 08 ] Available from: https://www.fmrp.usp.br/wp-content/uploads/sites/356/2022/10/USP_Quarta_Decada.pdf
Vancouver
Marques Júnior W. Departamento de Neuropsiquiatria e Psicologia Médica: 1982 - 1992 [Internet]. In: Faculdade de Medicina de Ribeirão Preto USP: quarta década. Ribeirão Preto: FUNPEC Editora; 2022. [citado 2024 jun. 08 ] Available from: https://www.fmrp.usp.br/wp-content/uploads/sites/356/2022/10/USP_Quarta_Decada.pdf
Artigo de periodico
Which factors in spinocerebellar ataxia type 3 patients are associated with restless legs syndrome/Willis-Ekbom disease? (2021)
Gitaí, Lívia Leite Góes; Eckeli, Alan Luiz ; Sobreira-Neto, Manoel Alves; Diniz, Paula Rejane Beserra; Santos, Antonio Carlos dos ; Marques Júnior, Wilson ; Fernandes, Regina Maria França
Source: The Cerebellum. Unidade: FMRP
Subjects: SÍNDROME DAS PERNAS INQUIETAS, DEGENERAÇÕES ESPINOCEREBELARES, RESSONÂNCIA MAGNÉTICA
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GITAÍ, Lívia Leite Góes et al. Which factors in spinocerebellar ataxia type 3 patients are associated with restless legs syndrome/Willis-Ekbom disease?. The Cerebellum, v. 20, n. 1, p. 21-30, 2021Tradução . . Disponível em: https://doi.org/10.1007/s12311-020-01170-2. Acesso em: 08 jun. 2024.
APA
Gitaí, L. L. G., Eckeli, A. L., Sobreira-Neto, M. A., Diniz, P. R. B., Santos, A. C. dos, Marques Júnior, W., & Fernandes, R. M. F. (2021). Which factors in spinocerebellar ataxia type 3 patients are associated with restless legs syndrome/Willis-Ekbom disease? The Cerebellum, 20( 1), 21-30. doi:10.1007/s12311-020-01170-2
NLM
Gitaí LLG, Eckeli AL, Sobreira-Neto MA, Diniz PRB, Santos AC dos, Marques Júnior W, Fernandes RMF. Which factors in spinocerebellar ataxia type 3 patients are associated with restless legs syndrome/Willis-Ekbom disease? [Internet]. The Cerebellum. 2021 ; 20( 1): 21-30.[citado 2024 jun. 08 ] Available from: https://doi.org/10.1007/s12311-020-01170-2
Vancouver
Gitaí LLG, Eckeli AL, Sobreira-Neto MA, Diniz PRB, Santos AC dos, Marques Júnior W, Fernandes RMF. Which factors in spinocerebellar ataxia type 3 patients are associated with restless legs syndrome/Willis-Ekbom disease? [Internet]. The Cerebellum. 2021 ; 20( 1): 21-30.[citado 2024 jun. 08 ] Available from: https://doi.org/10.1007/s12311-020-01170-2
Artigo de periodico
Acute inflammatory painful polyradiculoneuritis: an uncommon presentation related to COVID-19 (2021)
Dias, Francisco Antunes; Cunha, Ana Luiza Nunes; Pantoja, Patrícia Maria Pedrosa; Moreira, Carolina Lavigne; Tomaselli, Pedro José; Zotin, Maria Clara Zanon; Colleto, Francisco Antonio; Fábio, Soraia Ramos Cabette; Pontes Neto, Octávio Marques; Marques Júnior, Wilson
Source: Neurology: Clinical Practice. Unidade: FMRP
Subjects: COVID-19, INFECÇÕES POR CORONAVIRUS, NERVOS ESPINHAIS, DOENÇAS
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DIAS, Francisco Antunes et al. Acute inflammatory painful polyradiculoneuritis: an uncommon presentation related to COVID-19. Neurology: Clinical Practice, v. 11, n. 2, p. e205-e207, 2021Tradução . . Disponível em: https://doi.org/10.1212/CPJ.0000000000000910. Acesso em: 08 jun. 2024.
APA
Dias, F. A., Cunha, A. L. N., Pantoja, P. M. P., Moreira, C. L., Tomaselli, P. J., Zotin, M. C. Z., et al. (2021). Acute inflammatory painful polyradiculoneuritis: an uncommon presentation related to COVID-19. Neurology: Clinical Practice, 11( 2), e205-e207. doi:10.1212/CPJ.0000000000000910
NLM
Dias FA, Cunha ALN, Pantoja PMP, Moreira CL, Tomaselli PJ, Zotin MCZ, Colleto FA, Fábio SRC, Pontes Neto OM, Marques Júnior W. Acute inflammatory painful polyradiculoneuritis: an uncommon presentation related to COVID-19 [Internet]. Neurology: Clinical Practice. 2021 ; 11( 2): e205-e207.[citado 2024 jun. 08 ] Available from: https://doi.org/10.1212/CPJ.0000000000000910
Vancouver
Dias FA, Cunha ALN, Pantoja PMP, Moreira CL, Tomaselli PJ, Zotin MCZ, Colleto FA, Fábio SRC, Pontes Neto OM, Marques Júnior W. Acute inflammatory painful polyradiculoneuritis: an uncommon presentation related to COVID-19 [Internet]. Neurology: Clinical Practice. 2021 ; 11( 2): e205-e207.[citado 2024 jun. 08 ] Available from: https://doi.org/10.1212/CPJ.0000000000000910
Artigo de periodico
Dynamic plantar pressure patterns in children and adolescents with Charcot-Marie-Tooth disease (2021)
Cardoso, Juliana; Baptista, Cynthia Rogean de Jesus Alves de; Sartor, Cristina Dallemole; Elias, Adriana Helena do Nascimento; Marques Júnior, Wilson ; Martinez, Edson Zangiacomi ; Sacco, Isabel de Camargo Neves ; Mattiello-Sverzut, Ana Claudia
Source: Gait & Posture. Unidades: FM, FMRP
Subjects: DOENÇAS DEGENERATIVAS, PÉ, DEFORMIDADES DO PÉ, ESTUDOS TRANSVERSAIS, ADOLESCENTES
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CARDOSO, Juliana et al. Dynamic plantar pressure patterns in children and adolescents with Charcot-Marie-Tooth disease. Gait & Posture, v. 86, p. 112-119, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.gaitpost.2021.03.009. Acesso em: 08 jun. 2024.
APA
Cardoso, J., Baptista, C. R. de J. A. de, Sartor, C. D., Elias, A. H. do N., Marques Júnior, W., Martinez, E. Z., et al. (2021). Dynamic plantar pressure patterns in children and adolescents with Charcot-Marie-Tooth disease. Gait & Posture, 86, 112-119. doi:10.1016/j.gaitpost.2021.03.009
NLM
Cardoso J, Baptista CR de JA de, Sartor CD, Elias AH do N, Marques Júnior W, Martinez EZ, Sacco I de CN, Mattiello-Sverzut AC. Dynamic plantar pressure patterns in children and adolescents with Charcot-Marie-Tooth disease [Internet]. Gait & Posture. 2021 ; 86 112-119.[citado 2024 jun. 08 ] Available from: https://doi.org/10.1016/j.gaitpost.2021.03.009
Vancouver
Cardoso J, Baptista CR de JA de, Sartor CD, Elias AH do N, Marques Júnior W, Martinez EZ, Sacco I de CN, Mattiello-Sverzut AC. Dynamic plantar pressure patterns in children and adolescents with Charcot-Marie-Tooth disease [Internet]. Gait & Posture. 2021 ; 86 112-119.[citado 2024 jun. 08 ] Available from: https://doi.org/10.1016/j.gaitpost.2021.03.009
Artigo de periodico
GDAP1 mutations are frequent among Brazilian patients with autosomal recessive axonal Charcot-Marie-Tooth disease (2021)
Figueiredo, Fernanda Barbosa ; Silva Junior, Wilson Araújo da ; Giuliatti, Silvana ; Tomaselli, Pedro José; Lourenço, Charles Marques; Gouvêa, Silmara Paula; Covaleski, Anna Paula Paranhos Miranda; Hallak, Jaime Eduardo Cecilio ; Marques Júnior, Wilson
Source: Neuromuscular Disorders. Unidade: FMRP
Subjects: DOENÇAS DO SISTEMA NERVOSO, DOENÇAS DEGENERATIVAS, MUTAÇÃO GENÉTICA
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FIGUEIREDO, Fernanda Barbosa et al. GDAP1 mutations are frequent among Brazilian patients with autosomal recessive axonal Charcot-Marie-Tooth disease. Neuromuscular Disorders, v. 31, n. 6, p. 505-511, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.nmd.2021.03.005. Acesso em: 08 jun. 2024.
APA
Figueiredo, F. B., Silva Junior, W. A. da, Giuliatti, S., Tomaselli, P. J., Lourenço, C. M., Gouvêa, S. P., et al. (2021). GDAP1 mutations are frequent among Brazilian patients with autosomal recessive axonal Charcot-Marie-Tooth disease. Neuromuscular Disorders, 31( 6), 505-511. doi:10.1016/j.nmd.2021.03.005
NLM
Figueiredo FB, Silva Junior WA da, Giuliatti S, Tomaselli PJ, Lourenço CM, Gouvêa SP, Covaleski APPM, Hallak JEC, Marques Júnior W. GDAP1 mutations are frequent among Brazilian patients with autosomal recessive axonal Charcot-Marie-Tooth disease [Internet]. Neuromuscular Disorders. 2021 ; 31( 6): 505-511.[citado 2024 jun. 08 ] Available from: https://doi.org/10.1016/j.nmd.2021.03.005
Vancouver
Figueiredo FB, Silva Junior WA da, Giuliatti S, Tomaselli PJ, Lourenço CM, Gouvêa SP, Covaleski APPM, Hallak JEC, Marques Júnior W. GDAP1 mutations are frequent among Brazilian patients with autosomal recessive axonal Charcot-Marie-Tooth disease [Internet]. Neuromuscular Disorders. 2021 ; 31( 6): 505-511.[citado 2024 jun. 08 ] Available from: https://doi.org/10.1016/j.nmd.2021.03.005
Artigo de periodico
Presence of val30Met and val122ile mutations in a patient with hereditary amyloidosis (2020)
Silva-Batista, Jemima A. da; Marques Júnior, Wilson ; Oliveira, Mayala Thayrine de J. S.; Lins, Lucas Vergne C.; Galvão, Adilson Junior P.; Miguel, Diego Santana Chaves G.; Machado-Costa, Marcela Câmara
Source: Journal of Human Genetics. Unidade: FMRP
Subjects: AMILOIDOSE, GENÉTICA, FISIOPATOLOGIA, CARDIOPATIAS, MUTAÇÃO, LINHAGEM CELULAR
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SILVA-BATISTA, Jemima A. da et al. Presence of val30Met and val122ile mutations in a patient with hereditary amyloidosis. Journal of Human Genetics, v. 65, n. 8, p. 711-713, 2020Tradução . . Disponível em: https://doi.org/10.1038/s10038-020-0749-3. Acesso em: 08 jun. 2024.
APA
Silva-Batista, J. A. da, Marques Júnior, W., Oliveira, M. T. de J. S., Lins, L. V. C., Galvão, A. J. P., Miguel, D. S. C. G., & Machado-Costa, M. C. (2020). Presence of val30Met and val122ile mutations in a patient with hereditary amyloidosis. Journal of Human Genetics, 65( 8), 711-713. doi:10.1038/s10038-020-0749-3
NLM
Silva-Batista JA da, Marques Júnior W, Oliveira MT de JS, Lins LVC, Galvão AJP, Miguel DSCG, Machado-Costa MC. Presence of val30Met and val122ile mutations in a patient with hereditary amyloidosis [Internet]. Journal of Human Genetics. 2020 ; 65( 8): 711-713.[citado 2024 jun. 08 ] Available from: https://doi.org/10.1038/s10038-020-0749-3
Vancouver
Silva-Batista JA da, Marques Júnior W, Oliveira MT de JS, Lins LVC, Galvão AJP, Miguel DSCG, Machado-Costa MC. Presence of val30Met and val122ile mutations in a patient with hereditary amyloidosis [Internet]. Journal of Human Genetics. 2020 ; 65( 8): 711-713.[citado 2024 jun. 08 ] Available from: https://doi.org/10.1038/s10038-020-0749-3
Artigo de periodico
High glucose level as a modifier factor in CMT1A patients (2020)
Secchin, Juliana B.; Leal, Rita C. C.; Lourenço, Charles M.; Marques, Vanessa Daccach; Nogueira, Patricia T. L.; Santos, Andre C. J.; Tomaselli, Pedro J.; Marques Júnior, Wilson
Source: Journal of the Peripheral Nervous System. Unidade: FMRP
Subjects: GLICOSE, DIABETES MELLITUS, NEUROPATIAS DIABÉTICAS, DOENÇAS HEREDITÁRIAS, FENÓTIPOS, PRÁTICA CLÍNICA
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SECCHIN, Juliana B. et al. High glucose level as a modifier factor in CMT1A patients. Journal of the Peripheral Nervous System, v. 25, n. 2, p. 132-137, 2020Tradução . . Disponível em: https://doi.org/10.1111/jns.12379. Acesso em: 08 jun. 2024.
APA
Secchin, J. B., Leal, R. C. C., Lourenço, C. M., Marques, V. D., Nogueira, P. T. L., Santos, A. C. J., et al. (2020). High glucose level as a modifier factor in CMT1A patients. Journal of the Peripheral Nervous System, 25( 2), 132-137. doi:10.1111/jns.12379
NLM
Secchin JB, Leal RCC, Lourenço CM, Marques VD, Nogueira PTL, Santos ACJ, Tomaselli PJ, Marques Júnior W. High glucose level as a modifier factor in CMT1A patients [Internet]. Journal of the Peripheral Nervous System. 2020 ; 25( 2): 132-137.[citado 2024 jun. 08 ] Available from: https://doi.org/10.1111/jns.12379
Vancouver
Secchin JB, Leal RCC, Lourenço CM, Marques VD, Nogueira PTL, Santos ACJ, Tomaselli PJ, Marques Júnior W. High glucose level as a modifier factor in CMT1A patients [Internet]. Journal of the Peripheral Nervous System. 2020 ; 25( 2): 132-137.[citado 2024 jun. 08 ] Available from: https://doi.org/10.1111/jns.12379
Artigo de periodico
Leprosy in a prison population: A new active search strategy and a prospective clinical analysis (2020)
Bernardes Filho, Fred ; Santana, Jaci Maria; Almeida, Regina Coeli Palma; Voltan, Glauber; Paula, Natália Aparecida de; Leite, Marcel Nani ; Silva, Claudia Maria Lincoln; Tormena, Camila; Basoli, Lean; Menezes, Joelma; Silva, Moises Batista da; Spencer, John Stewart; Marques Júnior, Wilson ; Foss, Norma Tiraboschi ; Frade, Marco Andrey Cipriani
Source: PLOS Neglected Tropical Diseases. Unidades: FMRP, FM
Subjects: HANSENÍASE, PRISÕES, DOR, POPULAÇÃO CARCERÁRIA
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BERNARDES FILHO, Fred et al. Leprosy in a prison population: A new active search strategy and a prospective clinical analysis. PLOS Neglected Tropical Diseases, v. 14, n. 12, p. 1-17, 2020Tradução . . Disponível em: https://doi.org/10.1371/journal.pntd.0008917. Acesso em: 08 jun. 2024.
APA
Bernardes Filho, F., Santana, J. M., Almeida, R. C. P., Voltan, G., Paula, N. A. de, Leite, M. N., et al. (2020). Leprosy in a prison population: A new active search strategy and a prospective clinical analysis. PLOS Neglected Tropical Diseases, 14( 12), 1-17. doi:10.1371/journal.pntd.0008917
NLM
Bernardes Filho F, Santana JM, Almeida RCP, Voltan G, Paula NA de, Leite MN, Silva CML, Tormena C, Basoli L, Menezes J, Silva MB da, Spencer JS, Marques Júnior W, Foss NT, Frade MAC. Leprosy in a prison population: A new active search strategy and a prospective clinical analysis [Internet]. PLOS Neglected Tropical Diseases. 2020 ; 14( 12): 1-17.[citado 2024 jun. 08 ] Available from: https://doi.org/10.1371/journal.pntd.0008917
Vancouver
Bernardes Filho F, Santana JM, Almeida RCP, Voltan G, Paula NA de, Leite MN, Silva CML, Tormena C, Basoli L, Menezes J, Silva MB da, Spencer JS, Marques Júnior W, Foss NT, Frade MAC. Leprosy in a prison population: A new active search strategy and a prospective clinical analysis [Internet]. PLOS Neglected Tropical Diseases. 2020 ; 14( 12): 1-17.[citado 2024 jun. 08 ] Available from: https://doi.org/10.1371/journal.pntd.0008917
Artigo de periodico
Huntington’s disease-like 2: a phenocopy not to miss (2020)
Oliveira, Daniel Sabino de; Santos, Daniela Pereira; Araujo, Daniel Oliveira; Tomaselli, Pedro José; Marques Júnior, Wilson ; Vale, Thiago Cardoso
Source: Practical Neurology. Unidade: FMRP
Subjects: DOENÇAS CEREBRAIS, FENÓTIPOS, DOENÇA DE ALZHEIMER, DOENÇA DE PARKINSON, DOENÇAS DO SISTEMA NERVOSO PERIFÉRICO
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OLIVEIRA, Daniel Sabino de et al. Huntington’s disease-like 2: a phenocopy not to miss. Practical Neurology, v. 20, n. 6, p. 479-481, 2020Tradução . . Disponível em: https://doi.org/10.1136/practneurol-2020-002590. Acesso em: 08 jun. 2024.
APA
Oliveira, D. S. de, Santos, D. P., Araujo, D. O., Tomaselli, P. J., Marques Júnior, W., & Vale, T. C. (2020). Huntington’s disease-like 2: a phenocopy not to miss. Practical Neurology, 20( 6), 479-481. doi:10.1136/practneurol-2020-002590
NLM
Oliveira DS de, Santos DP, Araujo DO, Tomaselli PJ, Marques Júnior W, Vale TC. Huntington’s disease-like 2: a phenocopy not to miss [Internet]. Practical Neurology. 2020 ; 20( 6): 479-481.[citado 2024 jun. 08 ] Available from: https://doi.org/10.1136/practneurol-2020-002590
Vancouver
Oliveira DS de, Santos DP, Araujo DO, Tomaselli PJ, Marques Júnior W, Vale TC. Huntington’s disease-like 2: a phenocopy not to miss [Internet]. Practical Neurology. 2020 ; 20( 6): 479-481.[citado 2024 jun. 08 ] Available from: https://doi.org/10.1136/practneurol-2020-002590
Artigo de periodico
Intragenic variants in the SMN1 gene determine the clinical phenotype in 5q spinal muscular atrophy (2020)
Mendonca, Rodrigo de Holanda; Matsui Junior, Ciro; Polido, Graziela Jorge; Silva, Andre Macedo Serafim; Kulikowski, Leslie; Dias, Alexandre Torchio; Zanardo, Evelin Aline; Marques Júnior, Wilson ; Tomaselli, Pedro José; Kok, Fernando ; Reed, Umbertina Conti ; Zanoteli, Edmar
Source: Neurology-genetics. Unidades: FMRP, FM
Subjects: ATROFIA MUSCULAR, FENÓTIPOS, GENES
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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://doi.org/10.1212/NXG.0000000000000505. Acesso em: 08 jun. 2024.
APA
Mendonca, R. de H., Matsui Junior, C., Polido, G. J., Silva, A. M. S., Kulikowski, L., Dias, A. T., 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, Matsui Junior C, Polido GJ, Silva AMS, Kulikowski L, Dias AT, Zanardo EA, Marques Júnior W, Tomaselli PJ, Kok F, Reed UC, Zanoteli E. Intragenic variants in the SMN1 gene determine the clinical phenotype in 5q spinal muscular atrophy [Internet]. Neurology-genetics. 2020 ; 6( 5):[citado 2024 jun. 08 ] Available from: https://doi.org/10.1212/NXG.0000000000000505
Vancouver
Mendonca R de H, Matsui Junior C, Polido GJ, Silva AMS, Kulikowski L, Dias AT, Zanardo EA, Marques Júnior W, Tomaselli PJ, Kok F, Reed UC, Zanoteli E. Intragenic variants in the SMN1 gene determine the clinical phenotype in 5q spinal muscular atrophy [Internet]. Neurology-genetics. 2020 ; 6( 5):[citado 2024 jun. 08 ] Available from: https://doi.org/10.1212/NXG.0000000000000505
Artigo de periodico
Cerebellar ataxia, neuropathy, vestibular areflexia syndrome due to RFC1 repeat expansion (2020)
Cortese, Andrea; Tozza, Stefano; Yau, Wai Yan; Rossi, Salvatore; Beecroft, Sarah J; Jaunmuktane, Zane; Dyer, Zoe; Ravenscroft, Gianina; Lamont, Phillipa J; Mossman, Stuart; Chancellor, Andrew; Marques Júnior, Wilson
Source: Brain. Unidade: FMRP
Subjects: IDOSOS, ATAXIA, FISIOPATOLOGIA, SISTEMA NERVOSO PERIFÉRICO
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ABNT
CORTESE, Andrea et al. Cerebellar ataxia, neuropathy, vestibular areflexia syndrome due to RFC1 repeat expansion. Brain, v. 143, n. 2, p. 480-490, 2020Tradução . . Disponível em: https://doi.org/10.1093/brain/awz418. Acesso em: 08 jun. 2024.
APA
Cortese, A., Tozza, S., Yau, W. Y., Rossi, S., Beecroft, S. J., Jaunmuktane, Z., et al. (2020). Cerebellar ataxia, neuropathy, vestibular areflexia syndrome due to RFC1 repeat expansion. Brain, 143( 2), 480-490. doi:10.1093/brain/awz418
NLM
Cortese A, Tozza S, Yau WY, Rossi S, Beecroft SJ, Jaunmuktane Z, Dyer Z, Ravenscroft G, Lamont PJ, Mossman S, Chancellor A, Marques Júnior W. Cerebellar ataxia, neuropathy, vestibular areflexia syndrome due to RFC1 repeat expansion [Internet]. Brain. 2020 ; 143( 2): 480-490.[citado 2024 jun. 08 ] Available from: https://doi.org/10.1093/brain/awz418
Vancouver
Cortese A, Tozza S, Yau WY, Rossi S, Beecroft SJ, Jaunmuktane Z, Dyer Z, Ravenscroft G, Lamont PJ, Mossman S, Chancellor A, Marques Júnior W. Cerebellar ataxia, neuropathy, vestibular areflexia syndrome due to RFC1 repeat expansion [Internet]. Brain. 2020 ; 143( 2): 480-490.[citado 2024 jun. 08 ] Available from: https://doi.org/10.1093/brain/awz418
Artigo de periodico
CAG repeats ≥ 34 in Ataxin-1 gene are associated with amyotrophic lateral sclerosis in a Brazilian cohort (2020)
Gonçalves, João Pedro Nunes; Andrade, Helen Maia Tavares de; Cintra, Vívian Pedigone; Bonadia, Luciana Cardoso; Leoni, Tauana Bernardes; Albuquerque, Milena de; Martins, Melina Pazian; Borba, Fabrício Castro de; Couteiro, Rafael Esteves Duarte; Oliveira, Daniel Sabino de; Claudino, Rinaldo; Gonçalves, Marcos Vinicius Magno; Dourado, Mario Emilio; Souza, Leonardo Cruz de; Teixeira, Antônio Lúcio; Godoy Rousseff Prado, Laura de; Tumas, Vitor ; Oliveira, Acary Souza Bulle; Nucci, Anamarli; Lopes-Cendes, Iscia; Marques Júnior, Wilson ; França, Marcondes C.
Source: Journal of the Neurological Sciences. Unidade: FMRP
Subjects: ESCLEROSE AMIOTRÓFICA LATERAL, GENÉTICA DE POPULAÇÕES, DEMÊNCIA
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ABNT
GONÇALVES, João Pedro Nunes et al. CAG repeats ≥ 34 in Ataxin-1 gene are associated with amyotrophic lateral sclerosis in a Brazilian cohort. Journal of the Neurological Sciences, v. 414, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.jns.2020.116842. Acesso em: 08 jun. 2024.
APA
Gonçalves, J. P. N., Andrade, H. M. T. de, Cintra, V. P., Bonadia, L. C., Leoni, T. B., Albuquerque, M. de, et al. (2020). CAG repeats ≥ 34 in Ataxin-1 gene are associated with amyotrophic lateral sclerosis in a Brazilian cohort. Journal of the Neurological Sciences, 414. doi:10.1016/j.jns.2020.116842
NLM
Gonçalves JPN, Andrade HMT de, Cintra VP, Bonadia LC, Leoni TB, Albuquerque M de, Martins MP, Borba FC de, Couteiro RED, Oliveira DS de, Claudino R, Gonçalves MVM, Dourado ME, Souza LC de, Teixeira AL, Godoy Rousseff Prado L de, Tumas V, Oliveira ASB, Nucci A, Lopes-Cendes I, Marques Júnior W, França MC. CAG repeats ≥ 34 in Ataxin-1 gene are associated with amyotrophic lateral sclerosis in a Brazilian cohort [Internet]. Journal of the Neurological Sciences. 2020 ; 414[citado 2024 jun. 08 ] Available from: https://doi.org/10.1016/j.jns.2020.116842
Vancouver
Gonçalves JPN, Andrade HMT de, Cintra VP, Bonadia LC, Leoni TB, Albuquerque M de, Martins MP, Borba FC de, Couteiro RED, Oliveira DS de, Claudino R, Gonçalves MVM, Dourado ME, Souza LC de, Teixeira AL, Godoy Rousseff Prado L de, Tumas V, Oliveira ASB, Nucci A, Lopes-Cendes I, Marques Júnior W, França MC. CAG repeats ≥ 34 in Ataxin-1 gene are associated with amyotrophic lateral sclerosis in a Brazilian cohort [Internet]. Journal of the Neurological Sciences. 2020 ; 414[citado 2024 jun. 08 ] Available from: https://doi.org/10.1016/j.jns.2020.116842
Artigo de periodico
SPG15: a rare correlation with atypical juvenile parkinsonism responsive to levodopa (2020)
Araujo, Filipe Miranda Milagres; Marques Júnior, Wilson ; Tomaselli, Pedro José; Pimentel, Ângela V.; Brito, Manuelina C. Macruz; Tumas, Vitor
Source: Movement Disorders Clinical Practice. Unidade: FMRP
Subjects: DOENÇA DE PARKINSON, JOVENS, GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ARAUJO, Filipe Miranda Milagres et al. SPG15: a rare correlation with atypical juvenile parkinsonism responsive to levodopa. Movement Disorders Clinical Practice, v. 7, n. 7, p. 842-844, 2020Tradução . . Disponível em: https://doi.org/10.1002/mdc3.13027. Acesso em: 08 jun. 2024.
APA
Araujo, F. M. M., Marques Júnior, W., Tomaselli, P. J., Pimentel, Â. V., Brito, M. C. M., & Tumas, V. (2020). SPG15: a rare correlation with atypical juvenile parkinsonism responsive to levodopa. Movement Disorders Clinical Practice, 7( 7), 842-844. doi:10.1002/mdc3.13027
NLM
Araujo FMM, Marques Júnior W, Tomaselli PJ, Pimentel ÂV, Brito MCM, Tumas V. SPG15: a rare correlation with atypical juvenile parkinsonism responsive to levodopa [Internet]. Movement Disorders Clinical Practice. 2020 ; 7( 7): 842-844.[citado 2024 jun. 08 ] Available from: https://doi.org/10.1002/mdc3.13027
Vancouver
Araujo FMM, Marques Júnior W, Tomaselli PJ, Pimentel ÂV, Brito MCM, Tumas V. SPG15: a rare correlation with atypical juvenile parkinsonism responsive to levodopa [Internet]. Movement Disorders Clinical Practice. 2020 ; 7( 7): 842-844.[citado 2024 jun. 08 ] Available from: https://doi.org/10.1002/mdc3.13027
Artigo de periodico
The genetic landscape of axonal neuropathies in the middle-aged and elderly (2020)
Senderek, Jan; Lassuthova, Petra; Kabzińska, Dagmara; Abreu, Lisa; Baets, Jonathan; Beetz, Christian; Braathen, Geir J.; Brenner, David; Marques Júnior, Wilson
Source: Neurology. Unidade: FMRP
Subjects: IDOSOS, ENVELHECIMENTO, GENÉTICA, SEQUENCIAMENTO GENÉTICO, SANGUE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SENDEREK, Jan et al. The genetic landscape of axonal neuropathies in the middle-aged and elderly. Neurology, v. 95, n. 24, p. e3163-e3179, 2020Tradução . . Disponível em: https://doi.org/10.1212/WNL.0000000000011132. Acesso em: 08 jun. 2024.
APA
Senderek, J., Lassuthova, P., Kabzińska, D., Abreu, L., Baets, J., Beetz, C., et al. (2020). The genetic landscape of axonal neuropathies in the middle-aged and elderly. Neurology, 95( 24), e3163-e3179. doi:10.1212/WNL.0000000000011132
NLM
Senderek J, Lassuthova P, Kabzińska D, Abreu L, Baets J, Beetz C, Braathen GJ, Brenner D, Marques Júnior W. The genetic landscape of axonal neuropathies in the middle-aged and elderly [Internet]. Neurology. 2020 ; 95( 24): e3163-e3179.[citado 2024 jun. 08 ] Available from: https://doi.org/10.1212/WNL.0000000000011132
Vancouver
Senderek J, Lassuthova P, Kabzińska D, Abreu L, Baets J, Beetz C, Braathen GJ, Brenner D, Marques Júnior W. The genetic landscape of axonal neuropathies in the middle-aged and elderly [Internet]. Neurology. 2020 ; 95( 24): e3163-e3179.[citado 2024 jun. 08 ] Available from: https://doi.org/10.1212/WNL.0000000000011132
Artigo de periodico
Physical function and performance measures of children and adolescents with Charcot-Marie-Tooth disease (2019)
Baptista, Cyntia Rogean de Jesus Alves de ; Nascimento-Elias, Adriana Helena do ; Garcia, Beatriz; Testa, Amanda; Domingues, Paula Calori; Martinez, Edson Zangiacomi ; Marques Júnior, Wilson ; Mattiello-Sverzut, Ana Claudia
Source: Physiotherapy Theory and Practice. Unidade: FMRP
Subjects: DOENÇAS DO SISTEMA NERVOSO, FORÇA MUSCULAR, REABILITAÇÃO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BAPTISTA, Cyntia Rogean de Jesus Alves de et al. Physical function and performance measures of children and adolescents with Charcot-Marie-Tooth disease. Physiotherapy Theory and Practice, 2019Tradução . . Disponível em: https://doi.org/10.1080/09593985.2019.1603257. Acesso em: 08 jun. 2024.
APA
Baptista, C. R. de J. A. de, Nascimento-Elias, A. H. do, Garcia, B., Testa, A., Domingues, P. C., Martinez, E. Z., et al. (2019). Physical function and performance measures of children and adolescents with Charcot-Marie-Tooth disease. Physiotherapy Theory and Practice. doi:10.1080/09593985.2019.1603257
NLM
Baptista CR de JA de, Nascimento-Elias AH do, Garcia B, Testa A, Domingues PC, Martinez EZ, Marques Júnior W, Mattiello-Sverzut AC. Physical function and performance measures of children and adolescents with Charcot-Marie-Tooth disease [Internet]. Physiotherapy Theory and Practice. 2019 ;[citado 2024 jun. 08 ] Available from: https://doi.org/10.1080/09593985.2019.1603257
Vancouver
Baptista CR de JA de, Nascimento-Elias AH do, Garcia B, Testa A, Domingues PC, Martinez EZ, Marques Júnior W, Mattiello-Sverzut AC. Physical function and performance measures of children and adolescents with Charcot-Marie-Tooth disease [Internet]. Physiotherapy Theory and Practice. 2019 ;[citado 2024 jun. 08 ] Available from: https://doi.org/10.1080/09593985.2019.1603257
Artigo de periodico
Spinocerebellar ataxia: functional analysis of the stomatognathic system (2019)
Ferreira, Bruno; Palinkas, Marcelo ; Gonçalves, Lígia Maria Napolitano ; Silva, Gabriel Pádua da ; Arnoni, Veridiana Wanshi; Regalo, Isabela Hallak ; Vasconcelos, Paulo Batista de ; Marques Júnior, Wilson ; Hallak, Jaime Eduardo Cecilio ; Regalo, Simone Cecilio Hallak ; Siéssere, Selma
Source: Medicina Oral Patología Oral y Cirugia Bucal. Unidades: FORP, FMRP
Subjects: ATAXIA, ELETROMIOGRAFIA, FORÇA MUSCULAR, DOENÇAS DEGENERATIVAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FERREIRA, Bruno et al. Spinocerebellar ataxia: functional analysis of the stomatognathic system. Medicina Oral Patología Oral y Cirugia Bucal, v. 24, n. 2, p. e165-e171, 2019Tradução . . Disponível em: https://doi.org/10.4317/medoral.22839. Acesso em: 08 jun. 2024.
APA
Ferreira, B., Palinkas, M., Gonçalves, L. M. N., Silva, G. P. da, Arnoni, V. W., Regalo, I. H., et al. (2019). Spinocerebellar ataxia: functional analysis of the stomatognathic system. Medicina Oral Patología Oral y Cirugia Bucal, 24( 2), e165-e171. doi:10.4317/medoral.22839
NLM
Ferreira B, Palinkas M, Gonçalves LMN, Silva GP da, Arnoni VW, Regalo IH, Vasconcelos PB de, Marques Júnior W, Hallak JEC, Regalo SCH, Siéssere S. Spinocerebellar ataxia: functional analysis of the stomatognathic system [Internet]. Medicina Oral Patología Oral y Cirugia Bucal. 2019 ; 24( 2): e165-e171.[citado 2024 jun. 08 ] Available from: https://doi.org/10.4317/medoral.22839
Vancouver
Ferreira B, Palinkas M, Gonçalves LMN, Silva GP da, Arnoni VW, Regalo IH, Vasconcelos PB de, Marques Júnior W, Hallak JEC, Regalo SCH, Siéssere S. Spinocerebellar ataxia: functional analysis of the stomatognathic system [Internet]. Medicina Oral Patología Oral y Cirugia Bucal. 2019 ; 24( 2): e165-e171.[citado 2024 jun. 08 ] Available from: https://doi.org/10.4317/medoral.22839
Artigo de periodico
Sensory and motor conduction velocity in spontaneously hypertensive rats: sex and aging investigation (2019)
Fontanesi, Lucas Baptista; Fazan, Frederico Sassoli ; Dias, Fernando Jose ; Schiavoni, Maria Cristina Lopes; Marques Júnior, Wilson ; Fazan, Valéria Paula Sassoli
Source: Frontiers in Systems Neuroscience. Unidade: FMRP
Subjects: ENVELHECIMENTO, ELETROFISIOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FONTANESI, Lucas Baptista et al. Sensory and motor conduction velocity in spontaneously hypertensive rats: sex and aging investigation. Frontiers in Systems Neuroscience, v. 13, p. [10] , 2019Tradução . . Disponível em: https://doi.org/10.3389/fnsys.2019.00062. Acesso em: 08 jun. 2024.
APA
Fontanesi, L. B., Fazan, F. S., Dias, F. J., Schiavoni, M. C. L., Marques Júnior, W., & Fazan, V. P. S. (2019). Sensory and motor conduction velocity in spontaneously hypertensive rats: sex and aging investigation. Frontiers in Systems Neuroscience, 13, [10] . doi:10.3389/fnsys.2019.00062
NLM
Fontanesi LB, Fazan FS, Dias FJ, Schiavoni MCL, Marques Júnior W, Fazan VPS. Sensory and motor conduction velocity in spontaneously hypertensive rats: sex and aging investigation [Internet]. Frontiers in Systems Neuroscience. 2019 ; 13 [10] .[citado 2024 jun. 08 ] Available from: https://doi.org/10.3389/fnsys.2019.00062
Vancouver
Fontanesi LB, Fazan FS, Dias FJ, Schiavoni MCL, Marques Júnior W, Fazan VPS. Sensory and motor conduction velocity in spontaneously hypertensive rats: sex and aging investigation [Internet]. Frontiers in Systems Neuroscience. 2019 ; 13 [10] .[citado 2024 jun. 08 ] Available from: https://doi.org/10.3389/fnsys.2019.00062
Artigo de periodico
Alterations in the stomatognathic system due to amyotrophic lateral sclerosis (2018)
Gonçalves, Lígia Maria Napolitano ; Palinkas, Marcelo ; Hallak, Jaime Eduardo Cecilio ; Marques Júnior, Wilson ; Vasconcelos, Paulo Batista de ; Frota, Nicolly Parente Ribeiro ; Regalo, Isabela Hallak ; Siéssere, Selma ; Regalo, Simone Cecilio Hallak
Source: Journal of Applied Oral Science. Unidades: FMRP, FORP
Subjects: ESCLEROSE AMIOTRÓFICA LATERAL, MÚSCULOS MASTIGATÓRIOS, ELETROMIOGRAFIA, ULTRASSOM
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GONÇALVES, Lígia Maria Napolitano et al. Alterations in the stomatognathic system due to amyotrophic lateral sclerosis. Journal of Applied Oral Science, v. 26, p. [11 ], 2018Tradução . . Disponível em: https://doi.org/10.1590/1678-7757-2017-0408. Acesso em: 08 jun. 2024.
APA
Gonçalves, L. M. N., Palinkas, M., Hallak, J. E. C., Marques Júnior, W., Vasconcelos, P. B. de, Frota, N. P. R., et al. (2018). Alterations in the stomatognathic system due to amyotrophic lateral sclerosis. Journal of Applied Oral Science, 26, [11 ]. doi:10.1590/1678-7757-2017-0408
NLM
Gonçalves LMN, Palinkas M, Hallak JEC, Marques Júnior W, Vasconcelos PB de, Frota NPR, Regalo IH, Siéssere S, Regalo SCH. Alterations in the stomatognathic system due to amyotrophic lateral sclerosis [Internet]. Journal of Applied Oral Science. 2018 ; 26 [11 ].[citado 2024 jun. 08 ] Available from: https://doi.org/10.1590/1678-7757-2017-0408
Vancouver
Gonçalves LMN, Palinkas M, Hallak JEC, Marques Júnior W, Vasconcelos PB de, Frota NPR, Regalo IH, Siéssere S, Regalo SCH. Alterations in the stomatognathic system due to amyotrophic lateral sclerosis [Internet]. Journal of Applied Oral Science. 2018 ; 26 [11 ].[citado 2024 jun. 08 ] Available from: https://doi.org/10.1590/1678-7757-2017-0408
Artigo de periodico
Intermediate-length CAG repeat in ATXN2 is associated with increased risk for amyotrophic lateral sclerosis in Brazilian patients (2018)
Andrade, Helen Maia Tavares de; Cintra, Vívian Pedigone; Albuquerque, Milena de; Piccinin, Camila Callegari; Bonadia, Luciana Cardoso; Couteiro, Rafael Esteves Duarte; Oliveira, Daniel Sabino de; Claudino, Rinaldo; Gonçalves, Marcos Vinicius Magno; Dourado, Mario Emilio Teixeira; Souza, Leonardo Cruz de; Teixeira, Antônio Lúcio; Prado, Laura de Godoy Rousseff; Tumas, Vitor; Oliveira, Acary Souza Bulle; Nucci, Anamarli; Lopes-Cendes, Iscia; Marques Júnior, Wilson; França Júnior, Marcondes C.
Source: Neurobiology of Aging. Unidade: FMRP
Subjects: ESCLEROSE AMIOTRÓFICA LATERAL, GENES, NUCLEOTÍDEOS, POPULAÇÃO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ANDRADE, Helen Maia Tavares de et al. Intermediate-length CAG repeat in ATXN2 is associated with increased risk for amyotrophic lateral sclerosis in Brazilian patients. Neurobiology of Aging, v. 69, p. 292.e15-292.e18, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.neurobiolaging.2018.04.020. Acesso em: 08 jun. 2024.
APA
Andrade, H. M. T. de, Cintra, V. P., Albuquerque, M. de, Piccinin, C. C., Bonadia, L. C., Couteiro, R. E. D., et al. (2018). Intermediate-length CAG repeat in ATXN2 is associated with increased risk for amyotrophic lateral sclerosis in Brazilian patients. Neurobiology of Aging, 69, 292.e15-292.e18. doi:10.1016/j.neurobiolaging.2018.04.020
NLM
Andrade HMT de, Cintra VP, Albuquerque M de, Piccinin CC, Bonadia LC, Couteiro RED, Oliveira DS de, Claudino R, Gonçalves MVM, Dourado MET, Souza LC de, Teixeira AL, Prado L de GR, Tumas V, Oliveira ASB, Nucci A, Lopes-Cendes I, Marques Júnior W, França Júnior MC. Intermediate-length CAG repeat in ATXN2 is associated with increased risk for amyotrophic lateral sclerosis in Brazilian patients [Internet]. Neurobiology of Aging. 2018 ; 69 292.e15-292.e18.[citado 2024 jun. 08 ] Available from: https://doi.org/10.1016/j.neurobiolaging.2018.04.020
Vancouver
Andrade HMT de, Cintra VP, Albuquerque M de, Piccinin CC, Bonadia LC, Couteiro RED, Oliveira DS de, Claudino R, Gonçalves MVM, Dourado MET, Souza LC de, Teixeira AL, Prado L de GR, Tumas V, Oliveira ASB, Nucci A, Lopes-Cendes I, Marques Júnior W, França Júnior MC. Intermediate-length CAG repeat in ATXN2 is associated with increased risk for amyotrophic lateral sclerosis in Brazilian patients [Internet]. Neurobiology of Aging. 2018 ; 69 292.e15-292.e18.[citado 2024 jun. 08 ] Available from: https://doi.org/10.1016/j.neurobiolaging.2018.04.020
Artigo de periodico
Electromyographic characterisation of abdominal wall trigger points developed after caesarean section and response to local anaesthesia: an observational study (2018)
Poli Neto, Omero Benedicto; Chamochumbi, Carla Campos Martins; Toscano, Patrícia; Julio, Mônica Pitanguy; Marques Júnior, Wilson; Rosa e Silva, Júlio César; Reis, Francisco José Cândido dos; Nogueira, Antonio Alberto
Source: BJOG: An International Journal of Obstetrics & Gynaecology. Unidade: FMRP
Subjects: ABDOME, CESÁREA, PELVE, ANESTESIA LOCAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
POLI NETO, Omero Benedicto et al. Electromyographic characterisation of abdominal wall trigger points developed after caesarean section and response to local anaesthesia: an observational study. BJOG: An International Journal of Obstetrics & Gynaecology, v. 125, n. 10, p. 1313-1318, 2018Tradução . . Disponível em: https://doi.org/10.1111/1471-0528.15204. Acesso em: 08 jun. 2024.
APA
Poli Neto, O. B., Chamochumbi, C. C. M., Toscano, P., Julio, M. P., Marques Júnior, W., Rosa e Silva, J. C., et al. (2018). Electromyographic characterisation of abdominal wall trigger points developed after caesarean section and response to local anaesthesia: an observational study. BJOG: An International Journal of Obstetrics & Gynaecology, 125( 10), 1313-1318. doi:10.1111/1471-0528.15204
NLM
Poli Neto OB, Chamochumbi CCM, Toscano P, Julio MP, Marques Júnior W, Rosa e Silva JC, Reis FJC dos, Nogueira AA. Electromyographic characterisation of abdominal wall trigger points developed after caesarean section and response to local anaesthesia: an observational study [Internet]. BJOG: An International Journal of Obstetrics & Gynaecology. 2018 ; 125( 10): 1313-1318.[citado 2024 jun. 08 ] Available from: https://doi.org/10.1111/1471-0528.15204
Vancouver
Poli Neto OB, Chamochumbi CCM, Toscano P, Julio MP, Marques Júnior W, Rosa e Silva JC, Reis FJC dos, Nogueira AA. Electromyographic characterisation of abdominal wall trigger points developed after caesarean section and response to local anaesthesia: an observational study [Internet]. BJOG: An International Journal of Obstetrics & Gynaecology. 2018 ; 125( 10): 1313-1318.[citado 2024 jun. 08 ] Available from: https://doi.org/10.1111/1471-0528.15204

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