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Artigo de periodico
CLOCK Polymorphisms in attention-deficit/hyperactivity disorder (ADHD): further evidence linking sleep and circadian disturbances and ADHD (2019)
Carpena, Marina Xavier; Hutz, Mara H; Salatino-Oliveira, Angelica; Polanczyk, Guilherme V; Zeni, Cristian; Schmitz, Marcelo; Chazan, Rodrigo; Genro, Julia P; Rohde, Luis Augusto; Tovo-Rodrigues, Luciana
Source: Genes. Unidade: FM
Subjects: POLIMORFISMO, TRANSTORNO DO DEFICIT DE ATENÇÃO COM HIPERATIVIDADE, TRANSTORNOS DO SONO, RITMO CIRCADIANO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CARPENA, Marina Xavier et al. CLOCK Polymorphisms in attention-deficit/hyperactivity disorder (ADHD): further evidence linking sleep and circadian disturbances and ADHD. Genes, v. 10, n. 2, 2019Tradução . . Disponível em: https://doi.org/10.3390/genes10020088. Acesso em: 01 nov. 2024.
APA
Carpena, M. X., Hutz, M. H., Salatino-Oliveira, A., Polanczyk, G. V., Zeni, C., Schmitz, M., et al. (2019). CLOCK Polymorphisms in attention-deficit/hyperactivity disorder (ADHD): further evidence linking sleep and circadian disturbances and ADHD. Genes, 10( 2). doi:10.3390/genes10020088
NLM
Carpena MX, Hutz MH, Salatino-Oliveira A, Polanczyk GV, Zeni C, Schmitz M, Chazan R, Genro JP, Rohde LA, Tovo-Rodrigues L. CLOCK Polymorphisms in attention-deficit/hyperactivity disorder (ADHD): further evidence linking sleep and circadian disturbances and ADHD [Internet]. Genes. 2019 ; 10( 2):[citado 2024 nov. 01 ] Available from: https://doi.org/10.3390/genes10020088
Vancouver
Carpena MX, Hutz MH, Salatino-Oliveira A, Polanczyk GV, Zeni C, Schmitz M, Chazan R, Genro JP, Rohde LA, Tovo-Rodrigues L. CLOCK Polymorphisms in attention-deficit/hyperactivity disorder (ADHD): further evidence linking sleep and circadian disturbances and ADHD [Internet]. Genes. 2019 ; 10( 2):[citado 2024 nov. 01 ] Available from: https://doi.org/10.3390/genes10020088
Artigo de periodico
NOS1 and SNAP25 polymorphisms are associated with Attention-Deficit/Hyperactivity Disorder symptoms in adults but not in children (2016)
Salatino-Oliveira, Angélica; Akutagava-Martins, Glaucia C.; Bruxel, Estela M.; Genro, Julia P.; Polanczyk, Guilherme V.; Zeni, Cristian; Kieling, Christian; Karam, Rafael G.; Rovaris, Diego Luiz ; Contini, Verônica; Cupertino, Renata B.; Mota, Nina R.; Grevet, Eugenio H.; Bau, Claiton H.; Rohde, Luis A.; Hutz, Mara H.
Source: Journal of Psychiatric Research. Unidade: FM
Subjects: SINAIS E SINTOMAS, POLIMORFISMO, CRIANÇAS, HIPERATIVIDADE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SALATINO-OLIVEIRA, Angélica et al. NOS1 and SNAP25 polymorphisms are associated with Attention-Deficit/Hyperactivity Disorder symptoms in adults but not in children. Journal of Psychiatric Research, v. 75, p. 75-81, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.jpsychires.2015.01.018. Acesso em: 01 nov. 2024.
APA
Salatino-Oliveira, A., Akutagava-Martins, G. C., Bruxel, E. M., Genro, J. P., Polanczyk, G. V., Zeni, C., et al. (2016). NOS1 and SNAP25 polymorphisms are associated with Attention-Deficit/Hyperactivity Disorder symptoms in adults but not in children. Journal of Psychiatric Research, 75, 75-81. doi:10.1016/j.jpsychires.2015.01.018
NLM
Salatino-Oliveira A, Akutagava-Martins GC, Bruxel EM, Genro JP, Polanczyk GV, Zeni C, Kieling C, Karam RG, Rovaris DL, Contini V, Cupertino RB, Mota NR, Grevet EH, Bau CH, Rohde LA, Hutz MH. NOS1 and SNAP25 polymorphisms are associated with Attention-Deficit/Hyperactivity Disorder symptoms in adults but not in children [Internet]. Journal of Psychiatric Research. 2016 ; 75 75-81.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.jpsychires.2015.01.018
Vancouver
Salatino-Oliveira A, Akutagava-Martins GC, Bruxel EM, Genro JP, Polanczyk GV, Zeni C, Kieling C, Karam RG, Rovaris DL, Contini V, Cupertino RB, Mota NR, Grevet EH, Bau CH, Rohde LA, Hutz MH. NOS1 and SNAP25 polymorphisms are associated with Attention-Deficit/Hyperactivity Disorder symptoms in adults but not in children [Internet]. Journal of Psychiatric Research. 2016 ; 75 75-81.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.jpsychires.2015.01.018
Parte de monografia/livro
Transtorno de déficit de atenção/hiperoatividade (2014)
Polanczyk, Guilherme Vanoni; Rohde, Luis Augusto
Source: Clínica psiquiátrica de bolso. Unidade: FM
Subjects: SINAIS E SINTOMAS, POLIMORFISMO, PREVALÊNCIA, HIPERATIVIDADE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
POLANCZYK, Guilherme Vanoni e ROHDE, Luis Augusto. Transtorno de déficit de atenção/hiperoatividade. Clínica psiquiátrica de bolso. Tradução . Barueri, S P: Manole, 2014. . . Acesso em: 01 nov. 2024.
APA
Polanczyk, G. V., & Rohde, L. A. (2014). Transtorno de déficit de atenção/hiperoatividade. In Clínica psiquiátrica de bolso. Barueri, S P: Manole.
NLM
Polanczyk GV, Rohde LA. Transtorno de déficit de atenção/hiperoatividade. In: Clínica psiquiátrica de bolso. Barueri, S P: Manole; 2014. [citado 2024 nov. 01 ]
Vancouver
Polanczyk GV, Rohde LA. Transtorno de déficit de atenção/hiperoatividade. In: Clínica psiquiátrica de bolso. Barueri, S P: Manole; 2014. [citado 2024 nov. 01 ]
Artigo de periodico
Gene–environment interaction in externalizing problems among adolescents: evidence from the Pelotas 1993 Birth Cohort Study (2013)
Kieling, Christian; Hutz, Mara H.; Genro, Júlia P.; Polanczyk, Guilherme V.; Anselmi, Luciana; Camey, Suzi; Hallal, Pedro C.; Barros, Fernando C.; Victora, Cesar G.; Menezes, Ana M. B.; Rohde, Luis Augusto
Source: Journal of Child Psychology and Psychiatry. Unidade: FM
Subjects: GENES, ADOLESCENTES, POLIMORFISMO, FATORES DE RISCO, TRANSTORNOS MENTAIS, MAUS-TRATOS INFANTIS, ESTUDOS PROSPECTIVOS, MEIO AMBIENTE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
KIELING, Christian et al. Gene–environment interaction in externalizing problems among adolescents: evidence from the Pelotas 1993 Birth Cohort Study. Journal of Child Psychology and Psychiatry, v. 54, n. 3, p. 298-304, 2013Tradução . . Disponível em: http://onlinelibrary.wiley.com/doi/10.1111/jcpp.12022/pdf. Acesso em: 01 nov. 2024.
APA
Kieling, C., Hutz, M. H., Genro, J. P., Polanczyk, G. V., Anselmi, L., Camey, S., et al. (2013). Gene–environment interaction in externalizing problems among adolescents: evidence from the Pelotas 1993 Birth Cohort Study. Journal of Child Psychology and Psychiatry, 54( 3), 298-304. doi:10.1111/jcpp.12022
NLM
Kieling C, Hutz MH, Genro JP, Polanczyk GV, Anselmi L, Camey S, Hallal PC, Barros FC, Victora CG, Menezes AMB, Rohde LA. Gene–environment interaction in externalizing problems among adolescents: evidence from the Pelotas 1993 Birth Cohort Study [Internet]. Journal of Child Psychology and Psychiatry. 2013 ; 54( 3): 298-304.[citado 2024 nov. 01 ] Available from: http://onlinelibrary.wiley.com/doi/10.1111/jcpp.12022/pdf
Vancouver
Kieling C, Hutz MH, Genro JP, Polanczyk GV, Anselmi L, Camey S, Hallal PC, Barros FC, Victora CG, Menezes AMB, Rohde LA. Gene–environment interaction in externalizing problems among adolescents: evidence from the Pelotas 1993 Birth Cohort Study [Internet]. Journal of Child Psychology and Psychiatry. 2013 ; 54( 3): 298-304.[citado 2024 nov. 01 ] Available from: http://onlinelibrary.wiley.com/doi/10.1111/jcpp.12022/pdf
Artigo de periodico
Association of a carboxylesterase 1 polymorphism with appetite reduction in children and adolescents with attention-deficit/hyperactivity disorder treated with methylphenidate (2013)
Bruxel, E. M.; Salatino-Oliveira, A.; Genro, J. P.; Zeni, C. P.; Polanczyk, G. V.; Chazan, R.; Rohde, L. A.; Hutz, M. H.
Source: The Pharmacogenomics Journal. Unidade: FM
Subjects: POLIMORFISMO, CRIANÇAS, ADOLESCENTES, FARMACOGENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BRUXEL, E. M. et al. Association of a carboxylesterase 1 polymorphism with appetite reduction in children and adolescents with attention-deficit/hyperactivity disorder treated with methylphenidate. The Pharmacogenomics Journal, v. 13, n. 5, p. 476-480, 2013Tradução . . Disponível em: https://doi.org/10.1038/tpj.2012.25. Acesso em: 01 nov. 2024.
APA
Bruxel, E. M., Salatino-Oliveira, A., Genro, J. P., Zeni, C. P., Polanczyk, G. V., Chazan, R., et al. (2013). Association of a carboxylesterase 1 polymorphism with appetite reduction in children and adolescents with attention-deficit/hyperactivity disorder treated with methylphenidate. The Pharmacogenomics Journal, 13( 5), 476-480. doi:10.1038/tpj.2012.25
NLM
Bruxel EM, Salatino-Oliveira A, Genro JP, Zeni CP, Polanczyk GV, Chazan R, Rohde LA, Hutz MH. Association of a carboxylesterase 1 polymorphism with appetite reduction in children and adolescents with attention-deficit/hyperactivity disorder treated with methylphenidate [Internet]. The Pharmacogenomics Journal. 2013 ; 13( 5): 476-480.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1038/tpj.2012.25
Vancouver
Bruxel EM, Salatino-Oliveira A, Genro JP, Zeni CP, Polanczyk GV, Chazan R, Rohde LA, Hutz MH. Association of a carboxylesterase 1 polymorphism with appetite reduction in children and adolescents with attention-deficit/hyperactivity disorder treated with methylphenidate [Internet]. The Pharmacogenomics Journal. 2013 ; 13( 5): 476-480.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1038/tpj.2012.25
Artigo de periodico
Cathechol-O-methyltransferase Val158Met polymorphism is associated with disruptive behavior disorders among children and adolescents with ADHD (2012)
Salatino-Oliveira, Angélica; Genro, Julia P.; Guimarães, Ana P.; Chazan, Rodrigo; Zeni, Cristian; Schmitz, Marcelo; Polanczyk, Guilherme; Roman, Tatiana; Rohde, Luis A.; Hutz, Mara H.
Source: Journal of Neural Transmission. Unidade: FM
Subjects: SINAIS E SINTOMAS, CRIANÇAS, ADOLESCENTES, HIPERATIVIDADE, POLIMORFISMO, CÉREBRO (QUÍMICA), DISTÚRBIOS DO COMPORTAMENTO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SALATINO-OLIVEIRA, Angélica et al. Cathechol-O-methyltransferase Val158Met polymorphism is associated with disruptive behavior disorders among children and adolescents with ADHD. Journal of Neural Transmission, v. 119, n. 6, p. 729-733, 2012Tradução . . Disponível em: https://doi.org/10.1007/s00702-012-0766-2. Acesso em: 01 nov. 2024.
APA
Salatino-Oliveira, A., Genro, J. P., Guimarães, A. P., Chazan, R., Zeni, C., Schmitz, M., et al. (2012). Cathechol-O-methyltransferase Val158Met polymorphism is associated with disruptive behavior disorders among children and adolescents with ADHD. Journal of Neural Transmission, 119( 6), 729-733. doi:10.1007/s00702-012-0766-2
NLM
Salatino-Oliveira A, Genro JP, Guimarães AP, Chazan R, Zeni C, Schmitz M, Polanczyk G, Roman T, Rohde LA, Hutz MH. Cathechol-O-methyltransferase Val158Met polymorphism is associated with disruptive behavior disorders among children and adolescents with ADHD [Internet]. Journal of Neural Transmission. 2012 ; 119( 6): 729-733.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1007/s00702-012-0766-2
Vancouver
Salatino-Oliveira A, Genro JP, Guimarães AP, Chazan R, Zeni C, Schmitz M, Polanczyk G, Roman T, Rohde LA, Hutz MH. Cathechol-O-methyltransferase Val158Met polymorphism is associated with disruptive behavior disorders among children and adolescents with ADHD [Internet]. Journal of Neural Transmission. 2012 ; 119( 6): 729-733.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1007/s00702-012-0766-2
Artigo de periodico
Catechol-O-Methyltransferase Valine158Methionine Polymorphism Moderates Methylphenidate Effects on Oppositional Symptoms in Boys with Attention-Deficit/Hyperactivity Disorder (2011)
Salatino-Oliveira, Angélica; Genro, Julia P.; Zeni, Cristian; Polanczyk, Guilherme V.; Chazan, Rodrigo; Guimarães, Ana P.; Callegari-Jacques, Sidia M.; Rohde, Luis A.; Hutz, Mara H.
Source: Biological Psychiatry. Unidade: FM
Subjects: CRIANÇAS, HIPERATIVIDADE, RECEPTORES DE DOPAMINA, POLIMORFISMO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SALATINO-OLIVEIRA, Angélica et al. Catechol-O-Methyltransferase Valine158Methionine Polymorphism Moderates Methylphenidate Effects on Oppositional Symptoms in Boys with Attention-Deficit/Hyperactivity Disorder. Biological Psychiatry, v. 70, n. 3, p. 216-221, 2011Tradução . . Disponível em: https://doi.org/10.1016/j.biopsych.2011.03.025. Acesso em: 01 nov. 2024.
APA
Salatino-Oliveira, A., Genro, J. P., Zeni, C., Polanczyk, G. V., Chazan, R., Guimarães, A. P., et al. (2011). Catechol-O-Methyltransferase Valine158Methionine Polymorphism Moderates Methylphenidate Effects on Oppositional Symptoms in Boys with Attention-Deficit/Hyperactivity Disorder. Biological Psychiatry, 70( 3), 216-221. doi:10.1016/j.biopsych.2011.03.025
NLM
Salatino-Oliveira A, Genro JP, Zeni C, Polanczyk GV, Chazan R, Guimarães AP, Callegari-Jacques SM, Rohde LA, Hutz MH. Catechol-O-Methyltransferase Valine158Methionine Polymorphism Moderates Methylphenidate Effects on Oppositional Symptoms in Boys with Attention-Deficit/Hyperactivity Disorder [Internet]. Biological Psychiatry. 2011 ; 70( 3): 216-221.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.biopsych.2011.03.025
Vancouver
Salatino-Oliveira A, Genro JP, Zeni C, Polanczyk GV, Chazan R, Guimarães AP, Callegari-Jacques SM, Rohde LA, Hutz MH. Catechol-O-Methyltransferase Valine158Methionine Polymorphism Moderates Methylphenidate Effects on Oppositional Symptoms in Boys with Attention-Deficit/Hyperactivity Disorder [Internet]. Biological Psychiatry. 2011 ; 70( 3): 216-221.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.biopsych.2011.03.025

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