ReP USP - Resultado da busca

Artigo de periodico
1H NMR metabolomics and lipidomics to monitor positive responses in children with autism spectrum disorder following a guided parental Intervention: a pilot study (2023)
Correia, Banny Silva Barbosa; Pontes, Joao Guilherme de Moraes; Nani, Joao Victor Silva; Villalta, Fabian; Mor, Natalia Cristina; Bordini, Daniela; Brunoni, Decio; Brentani, Helena Paula ; Mari, Jair Jesus; Hayashi, Mirian A. F; Tasic, Ljubica
Source: Acs chemical neuroscience. Unidade: FM
Subjects: METABOLÔMICA, TRANSTORNO AUTÍSTICO, CRIANÇAS, TERAPIA CENTRADA NO CLIENTE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CORREIA, Banny Silva Barbosa et al. 1H NMR metabolomics and lipidomics to monitor positive responses in children with autism spectrum disorder following a guided parental Intervention: a pilot study. Acs chemical neuroscience, v. 14, n. 6, p. 1137-1145, 2023Tradução . . Disponível em: https://observatorio.fm.usp.br/handle/OPI/53072. Acesso em: 31 jul. 2024.
APA
Correia, B. S. B., Pontes, J. G. de M., Nani, J. V. S., Villalta, F., Mor, N. C., Bordini, D., et al. (2023). 1H NMR metabolomics and lipidomics to monitor positive responses in children with autism spectrum disorder following a guided parental Intervention: a pilot study. Acs chemical neuroscience, 14( 6), 1137-1145. doi:10.1021/acschemneuro.2c00735
NLM
Correia BSB, Pontes JG de M, Nani JVS, Villalta F, Mor NC, Bordini D, Brunoni D, Brentani HP, Mari JJ, Hayashi MAF, Tasic L. 1H NMR metabolomics and lipidomics to monitor positive responses in children with autism spectrum disorder following a guided parental Intervention: a pilot study [Internet]. Acs chemical neuroscience. 2023 ; 14( 6): 1137-1145.[citado 2024 jul. 31 ] Available from: https://observatorio.fm.usp.br/handle/OPI/53072
Vancouver
Correia BSB, Pontes JG de M, Nani JVS, Villalta F, Mor NC, Bordini D, Brunoni D, Brentani HP, Mari JJ, Hayashi MAF, Tasic L. 1H NMR metabolomics and lipidomics to monitor positive responses in children with autism spectrum disorder following a guided parental Intervention: a pilot study [Internet]. Acs chemical neuroscience. 2023 ; 14( 6): 1137-1145.[citado 2024 jul. 31 ] Available from: https://observatorio.fm.usp.br/handle/OPI/53072
Artigo de periodico
Procedures and compliance of a video modeling applied behavior analysis intervention for Brazilian parents of children with autism spectrum disorders (2017)
Bagaiolo, Leila F.; Mari, Jair de J.; Bordini, Daniela; Ribeiro, Tatiane C.; Martone, Maria Carolina C; Caetano, Sheila C.; Brunoni, Decio; Brentani, Helena; Paula, Cristiane S.
Source: Austim. Unidade: FM
Subjects: CRIANÇAS, AUTISMO, RELAÇÕES FAMILIARES, TÉCNICAS AUDIOVISUAIS DE EDUCAÇÃO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BAGAIOLO, Leila F. et al. Procedures and compliance of a video modeling applied behavior analysis intervention for Brazilian parents of children with autism spectrum disorders. Austim, v. 21, n. 5, p. 603-610, 2017Tradução . . Disponível em: http://journals.sagepub.com/doi/pdf/10.1177/1362361316677718. Acesso em: 31 jul. 2024.
APA
Bagaiolo, L. F., Mari, J. de J., Bordini, D., Ribeiro, T. C., Martone, M. C. C., Caetano, S. C., et al. (2017). Procedures and compliance of a video modeling applied behavior analysis intervention for Brazilian parents of children with autism spectrum disorders. Austim, 21( 5), 603-610. doi:10.1177/1362361316677718
NLM
Bagaiolo LF, Mari J de J, Bordini D, Ribeiro TC, Martone MCC, Caetano SC, Brunoni D, Brentani H, Paula CS. Procedures and compliance of a video modeling applied behavior analysis intervention for Brazilian parents of children with autism spectrum disorders [Internet]. Austim. 2017 ; 21( 5): 603-610.[citado 2024 jul. 31 ] Available from: http://journals.sagepub.com/doi/pdf/10.1177/1362361316677718
Vancouver
Bagaiolo LF, Mari J de J, Bordini D, Ribeiro TC, Martone MCC, Caetano SC, Brunoni D, Brentani H, Paula CS. Procedures and compliance of a video modeling applied behavior analysis intervention for Brazilian parents of children with autism spectrum disorders [Internet]. Austim. 2017 ; 21( 5): 603-610.[citado 2024 jul. 31 ] Available from: http://journals.sagepub.com/doi/pdf/10.1177/1362361316677718
Artigo de periodico
Clinical characterization of autosomal dominant and recessive variants of Robinow syndrome (2007)
Mazzeu, Juliana Forte; Pardono, Eliete; Vianna-Morgante, Angela M ; Richieri-Costa, Antonio; Kim, Chong Ae; Brunoni, Decio; Martelli, Lucia; Andrade, Carlos Eugenio F. de; Colin, Guilherme; Otto, Paulo A
Source: American Journal of Medical Genetics. Part A. Unidades: IB, HRAC, FM
Subjects: GENÉTICA, DIAGNÓSTICO DIFERENCIAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MAZZEU, Juliana Forte et al. Clinical characterization of autosomal dominant and recessive variants of Robinow syndrome. American Journal of Medical Genetics. Part A, v. 143 A, n. 4, p. 320-325, 2007Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.31592. Acesso em: 31 jul. 2024.
APA
Mazzeu, J. F., Pardono, E., Vianna-Morgante, A. M., Richieri-Costa, A., Kim, C. A., Brunoni, D., et al. (2007). Clinical characterization of autosomal dominant and recessive variants of Robinow syndrome. American Journal of Medical Genetics. Part A, 143 A( 4), 320-325. doi:10.1002/ajmg.a.31592
NLM
Mazzeu JF, Pardono E, Vianna-Morgante AM, Richieri-Costa A, Kim CA, Brunoni D, Martelli L, Andrade CEF de, Colin G, Otto PA. Clinical characterization of autosomal dominant and recessive variants of Robinow syndrome [Internet]. American Journal of Medical Genetics. Part A. 2007 ; 143 A( 4): 320-325.[citado 2024 jul. 31 ] Available from: https://doi.org/10.1002/ajmg.a.31592
Vancouver
Mazzeu JF, Pardono E, Vianna-Morgante AM, Richieri-Costa A, Kim CA, Brunoni D, Martelli L, Andrade CEF de, Colin G, Otto PA. Clinical characterization of autosomal dominant and recessive variants of Robinow syndrome [Internet]. American Journal of Medical Genetics. Part A. 2007 ; 143 A( 4): 320-325.[citado 2024 jul. 31 ] Available from: https://doi.org/10.1002/ajmg.a.31592
Artigo de periodico
Description of a new mutation and caracterization of FGFR1, FGFR2, and FGFR3 mutations among Brazilian patients with syndromic craniosynostoses (1998)
Passos-Bueno, Maria Rita ; Sertié, Andréa L; Richieri-Costa, Antonio; Alonso, Luís G; Zatz, Mayana ; Alonso, Nivaldo; Brunoni, Decio; Ribeiro, Sandra F M
Source: American Journal of Medical Genetics. Unidades: IB, HRAC
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PASSOS-BUENO, Maria Rita et al. Description of a new mutation and caracterization of FGFR1, FGFR2, and FGFR3 mutations among Brazilian patients with syndromic craniosynostoses. American Journal of Medical Genetics, v. 78, p. 237-241, 1998Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19980707)78:3%3C237::aid-ajmg5%3E3.0.co;2-m. Acesso em: 31 jul. 2024.
APA
Passos-Bueno, M. R., Sertié, A. L., Richieri-Costa, A., Alonso, L. G., Zatz, M., Alonso, N., et al. (1998). Description of a new mutation and caracterization of FGFR1, FGFR2, and FGFR3 mutations among Brazilian patients with syndromic craniosynostoses. American Journal of Medical Genetics, 78, 237-241. doi:10.1002/(sici)1096-8628(19980707)78:3%3C237::aid-ajmg5%3E3.0.co;2-m
NLM
Passos-Bueno MR, Sertié AL, Richieri-Costa A, Alonso LG, Zatz M, Alonso N, Brunoni D, Ribeiro SFM. Description of a new mutation and caracterization of FGFR1, FGFR2, and FGFR3 mutations among Brazilian patients with syndromic craniosynostoses [Internet]. American Journal of Medical Genetics. 1998 ; 78 237-241.[citado 2024 jul. 31 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19980707)78:3%3C237::aid-ajmg5%3E3.0.co;2-m
Vancouver
Passos-Bueno MR, Sertié AL, Richieri-Costa A, Alonso LG, Zatz M, Alonso N, Brunoni D, Ribeiro SFM. Description of a new mutation and caracterization of FGFR1, FGFR2, and FGFR3 mutations among Brazilian patients with syndromic craniosynostoses [Internet]. American Journal of Medical Genetics. 1998 ; 78 237-241.[citado 2024 jul. 31 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19980707)78:3%3C237::aid-ajmg5%3E3.0.co;2-m
Artigo de periodico
Deletion 9p and duplication 17p due to a translocation t(9;17)(p23;p13)pat (1996)
Melaragno, Maria Isabel; Gonzalez, Claudette Hajaj; Brunoni, Decio; Kim, Chong Ae
Source: Brazilian Journal of Genetics. Unidade: FM
Assunto: ORTOPEDIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MELARAGNO, Maria Isabel et al. Deletion 9p and duplication 17p due to a translocation t(9;17)(p23;p13)pat. Brazilian Journal of Genetics, v. 19, n. 3, p. 493-496, 1996Tradução . . Acesso em: 31 jul. 2024.
APA
Melaragno, M. I., Gonzalez, C. H., Brunoni, D., & Kim, C. A. (1996). Deletion 9p and duplication 17p due to a translocation t(9;17)(p23;p13)pat. Brazilian Journal of Genetics, 19( 3), 493-496.
NLM
Melaragno MI, Gonzalez CH, Brunoni D, Kim CA. Deletion 9p and duplication 17p due to a translocation t(9;17)(p23;p13)pat. Brazilian Journal of Genetics. 1996 ; 19( 3): 493-496.[citado 2024 jul. 31 ]
Vancouver
Melaragno MI, Gonzalez CH, Brunoni D, Kim CA. Deletion 9p and duplication 17p due to a translocation t(9;17)(p23;p13)pat. Brazilian Journal of Genetics. 1996 ; 19( 3): 493-496.[citado 2024 jul. 31 ]

USP Schools

ReP

Filtros

Authors

USP affiliated authors

Subjects