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Trabalho de evento-resumo periodico
Deep learning classification of neuro-oncology medical documents (2019)
Wells, Michael; Sabedot, Thais; Malta, Tathiane Maistro; Snyder, James; Poisson, Laila; Noushmehr, Houtan
Source: Cancer Research. Conference titles: Annual Meeting American Association for Cancer Research - AACR. Unidade: FMRP
Subjects: NEUROLOGIA, ONCOLOGIA, REDES NEURAIS
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ABNT
WELLS, Michael et al. Deep learning classification of neuro-oncology medical documents. Cancer Research. Baltimore: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. Disponível em: https://doi.org/10.1158/1538-7445.AM2019-1640. Acesso em: 16 ago. 2024. , 2019
APA
Wells, M., Sabedot, T., Malta, T. M., Snyder, J., Poisson, L., & Noushmehr, H. (2019). Deep learning classification of neuro-oncology medical documents. Cancer Research. Baltimore: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. doi:10.1158/1538-7445.AM2019-1640
NLM
Wells M, Sabedot T, Malta TM, Snyder J, Poisson L, Noushmehr H. Deep learning classification of neuro-oncology medical documents [Internet]. Cancer Research. 2019 ; 79( 13):[citado 2024 ago. 16 ] Available from: https://doi.org/10.1158/1538-7445.AM2019-1640
Vancouver
Wells M, Sabedot T, Malta TM, Snyder J, Poisson L, Noushmehr H. Deep learning classification of neuro-oncology medical documents [Internet]. Cancer Research. 2019 ; 79( 13):[citado 2024 ago. 16 ] Available from: https://doi.org/10.1158/1538-7445.AM2019-1640
Artigo de periodico
Oncogenic signaling pathways in the cancer genome atlas (2018)
Sanchez-Vega, Francisco; Noushmehr, Houtan; Carlotti Júnior, Carlos Gilberto; Santos, José Sebastião dos; Kemp, Rafael; Sankarankutty, Ajith Kumar; Tirapelli, Daniela Pretti da Cunha
Source: Cell. Unidade: FMRP
Subjects: GENÔMICA, NEOPLASIAS, ONCOLOGIA, TERAPÊUTICA, CICLO CELULAR
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ABNT
SANCHEZ-VEGA, Francisco et al. Oncogenic signaling pathways in the cancer genome atlas. Cell, v. 173, n. 2, p. 321-337.e1-e4, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.cell.2018.03.035. Acesso em: 16 ago. 2024.
APA
Sanchez-Vega, F., Noushmehr, H., Carlotti Júnior, C. G., Santos, J. S. dos, Kemp, R., Sankarankutty, A. K., & Tirapelli, D. P. da C. (2018). Oncogenic signaling pathways in the cancer genome atlas. Cell, 173( 2), 321-337.e1-e4. doi:10.1016/j.cell.2018.03.035
NLM
Sanchez-Vega F, Noushmehr H, Carlotti Júnior CG, Santos JS dos, Kemp R, Sankarankutty AK, Tirapelli DP da C. Oncogenic signaling pathways in the cancer genome atlas [Internet]. Cell. 2018 ; 173( 2): 321-337.e1-e4.[citado 2024 ago. 16 ] Available from: https://doi.org/10.1016/j.cell.2018.03.035
Vancouver
Sanchez-Vega F, Noushmehr H, Carlotti Júnior CG, Santos JS dos, Kemp R, Sankarankutty AK, Tirapelli DP da C. Oncogenic signaling pathways in the cancer genome atlas [Internet]. Cell. 2018 ; 173( 2): 321-337.e1-e4.[citado 2024 ago. 16 ] Available from: https://doi.org/10.1016/j.cell.2018.03.035
Artigo de periodico
How much do smoking and alcohol consumption explain socioeconomic inequalities in head and neck cancer risk? (2011)
Boing, Antonio Fernando; Antunes, J. L. Ferreira; Carvalho, M. Brasilino de; Góis Filho, J. Francisco de; Kowalski, L. P; Michaluart Junior, Pedro; Eluf Neto, José; Boffeta, P; Wünsch Filho, Victor; Okamoto, Oswaldo Keith
Source: Journal of Epidemiology & Community Health. Unidades: IB, FM, FSP, FMRP
Subjects: NEOPLASIAS, ONCOLOGIA, FUMO
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ABNT
BOING, Antonio Fernando et al. How much do smoking and alcohol consumption explain socioeconomic inequalities in head and neck cancer risk?. Journal of Epidemiology & Community Health, v. 65, p. 709-714, 2011Tradução . . Disponível em: https://doi.org/10.1136/jech.2009.097691. Acesso em: 16 ago. 2024.
APA
Boing, A. F., Antunes, J. L. F., Carvalho, M. B. de, Góis Filho, J. F. de, Kowalski, L. P., Michaluart Junior, P., et al. (2011). How much do smoking and alcohol consumption explain socioeconomic inequalities in head and neck cancer risk? Journal of Epidemiology & Community Health, 65, 709-714. doi:10.1136/jech.2009.097691
NLM
Boing AF, Antunes JLF, Carvalho MB de, Góis Filho JF de, Kowalski LP, Michaluart Junior P, Eluf Neto J, Boffeta P, Wünsch Filho V, Okamoto OK. How much do smoking and alcohol consumption explain socioeconomic inequalities in head and neck cancer risk? [Internet]. Journal of Epidemiology & Community Health. 2011 ; 65 709-714.[citado 2024 ago. 16 ] Available from: https://doi.org/10.1136/jech.2009.097691
Vancouver
Boing AF, Antunes JLF, Carvalho MB de, Góis Filho JF de, Kowalski LP, Michaluart Junior P, Eluf Neto J, Boffeta P, Wünsch Filho V, Okamoto OK. How much do smoking and alcohol consumption explain socioeconomic inequalities in head and neck cancer risk? [Internet]. Journal of Epidemiology & Community Health. 2011 ; 65 709-714.[citado 2024 ago. 16 ] Available from: https://doi.org/10.1136/jech.2009.097691
Artigo de periodico
Lack of evidence for mutations or deletions in the CDKN2A/p16 and CDKN2B/p15 genes of Brazilian neuroblastoma patients (2004)
Bassi, C. L.; Martelli, Lúcia Regina; Cipolotti, R.; Scrideli, C. A.; Defavery, R.; Tone, Luiz Gonzaga
Source: Brazilian Journal of Medical and Biological Research. Unidade: FMRP
Subjects: ONCOLOGIA, PEDIATRIA, GENÉTICA
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ABNT
BASSI, C. L. et al. Lack of evidence for mutations or deletions in the CDKN2A/p16 and CDKN2B/p15 genes of Brazilian neuroblastoma patients. Brazilian Journal of Medical and Biological Research, v. 37, n. 11, p. 1683-1687, 2004Tradução . . Disponível em: https://doi.org/10.1590/s0100-879x2004001100014. Acesso em: 16 ago. 2024.
APA
Bassi, C. L., Martelli, L. R., Cipolotti, R., Scrideli, C. A., Defavery, R., & Tone, L. G. (2004). Lack of evidence for mutations or deletions in the CDKN2A/p16 and CDKN2B/p15 genes of Brazilian neuroblastoma patients. Brazilian Journal of Medical and Biological Research, 37( 11), 1683-1687. doi:10.1590/s0100-879x2004001100014
NLM
Bassi CL, Martelli LR, Cipolotti R, Scrideli CA, Defavery R, Tone LG. Lack of evidence for mutations or deletions in the CDKN2A/p16 and CDKN2B/p15 genes of Brazilian neuroblastoma patients [Internet]. Brazilian Journal of Medical and Biological Research. 2004 ; 37( 11): 1683-1687.[citado 2024 ago. 16 ] Available from: https://doi.org/10.1590/s0100-879x2004001100014
Vancouver
Bassi CL, Martelli LR, Cipolotti R, Scrideli CA, Defavery R, Tone LG. Lack of evidence for mutations or deletions in the CDKN2A/p16 and CDKN2B/p15 genes of Brazilian neuroblastoma patients [Internet]. Brazilian Journal of Medical and Biological Research. 2004 ; 37( 11): 1683-1687.[citado 2024 ago. 16 ] Available from: https://doi.org/10.1590/s0100-879x2004001100014
Trabalho de evento-resumo periodico
Acute monocytic leukemia and multiple abnormalities in a child with duplication of 1q detected by GTG-banding and SKY (2002)
Baruffi, Marcelo Razera; Scrideli, Carlos Alberto; Squire, J. A.; Karaskowa, J.; Ramos, Ester Silveira; Heck, B.; Tone, Luiz Gonzaga
Source: European Journal of Human Genetics. Conference titles: European Human Genetics Conference 2002. Unidade: FMRP
Subjects: ONCOLOGIA, PEDIATRIA, GENÉTICA MÉDICA
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ABNT
BARUFFI, Marcelo Razera et al. Acute monocytic leukemia and multiple abnormalities in a child with duplication of 1q detected by GTG-banding and SKY. European Journal of Human Genetics. New York: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 16 ago. 2024. , 2002
APA
Baruffi, M. R., Scrideli, C. A., Squire, J. A., Karaskowa, J., Ramos, E. S., Heck, B., & Tone, L. G. (2002). Acute monocytic leukemia and multiple abnormalities in a child with duplication of 1q detected by GTG-banding and SKY. European Journal of Human Genetics. New York: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Baruffi MR, Scrideli CA, Squire JA, Karaskowa J, Ramos ES, Heck B, Tone LG. Acute monocytic leukemia and multiple abnormalities in a child with duplication of 1q detected by GTG-banding and SKY. European Journal of Human Genetics. 2002 ; 10 91 res. P0082.[citado 2024 ago. 16 ]
Vancouver
Baruffi MR, Scrideli CA, Squire JA, Karaskowa J, Ramos ES, Heck B, Tone LG. Acute monocytic leukemia and multiple abnormalities in a child with duplication of 1q detected by GTG-banding and SKY. European Journal of Human Genetics. 2002 ; 10 91 res. P0082.[citado 2024 ago. 16 ]
Artigo de periodico
Osteoid osteomas with chromosome alterations involving 22q (2001)
Baruffi, Marcelo Razera; Volpon, José Batista; Barbieri Neto, José; Casartelli, Cacilda
Source: Cancer Genetics and Cytogenetics. Unidade: FMRP
Subjects: ONCOLOGIA, OSSO E OSSOS (CIRURGIA), CITOGENÉTICA
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ABNT
BARUFFI, Marcelo Razera et al. Osteoid osteomas with chromosome alterations involving 22q. Cancer Genetics and Cytogenetics, v. 124, p. 127-131, 2001Tradução . . Disponível em: https://doi.org/10.1016/s0165-4608(00)00327-7. Acesso em: 16 ago. 2024.
APA
Baruffi, M. R., Volpon, J. B., Barbieri Neto, J., & Casartelli, C. (2001). Osteoid osteomas with chromosome alterations involving 22q. Cancer Genetics and Cytogenetics, 124, 127-131. doi:10.1016/s0165-4608(00)00327-7
NLM
Baruffi MR, Volpon JB, Barbieri Neto J, Casartelli C. Osteoid osteomas with chromosome alterations involving 22q [Internet]. Cancer Genetics and Cytogenetics. 2001 ; 124 127-131.[citado 2024 ago. 16 ] Available from: https://doi.org/10.1016/s0165-4608(00)00327-7
Vancouver
Baruffi MR, Volpon JB, Barbieri Neto J, Casartelli C. Osteoid osteomas with chromosome alterations involving 22q [Internet]. Cancer Genetics and Cytogenetics. 2001 ; 124 127-131.[citado 2024 ago. 16 ] Available from: https://doi.org/10.1016/s0165-4608(00)00327-7
Artigo de periodico
Trisomy 4 in a case of gynecomastia (2000)
Burbano, Rommel Rodríguez; Barbieri Neto, José; Philbert, Paulo Meyer de Paula; Lemos, José Alexandre; Bahia, Marcelo; Casartelli, Cacilda
Source: Cancer Genetics Cytogenetics. Unidade: FMRP
Subjects: GENÉTICA MÉDICA, ONCOLOGIA, NEOPLASIAS, MAMA, DOENÇAS DOS GENITAIS FEMININOS
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ABNT
BURBANO, Rommel Rodríguez et al. Trisomy 4 in a case of gynecomastia. Cancer Genetics Cytogenetics, v. 117, p. 143-145, 2000Tradução . . Disponível em: http://probe.usp.br/cgi-bin/sciserv.pl?collection=journals&journal=01654608&issue=v117i0002&article=143_t4iacog&form=pdf&file=file.pdf. Acesso em: 16 ago. 2024.
APA
Burbano, R. R., Barbieri Neto, J., Philbert, P. M. de P., Lemos, J. A., Bahia, M., & Casartelli, C. (2000). Trisomy 4 in a case of gynecomastia. Cancer Genetics Cytogenetics, 117, 143-145. Recuperado de http://probe.usp.br/cgi-bin/sciserv.pl?collection=journals&journal=01654608&issue=v117i0002&article=143_t4iacog&form=pdf&file=file.pdf
NLM
Burbano RR, Barbieri Neto J, Philbert PM de P, Lemos JA, Bahia M, Casartelli C. Trisomy 4 in a case of gynecomastia [Internet]. Cancer Genetics Cytogenetics. 2000 ; 117 143-145.[citado 2024 ago. 16 ] Available from: http://probe.usp.br/cgi-bin/sciserv.pl?collection=journals&journal=01654608&issue=v117i0002&article=143_t4iacog&form=pdf&file=file.pdf
Vancouver
Burbano RR, Barbieri Neto J, Philbert PM de P, Lemos JA, Bahia M, Casartelli C. Trisomy 4 in a case of gynecomastia [Internet]. Cancer Genetics Cytogenetics. 2000 ; 117 143-145.[citado 2024 ago. 16 ] Available from: http://probe.usp.br/cgi-bin/sciserv.pl?collection=journals&journal=01654608&issue=v117i0002&article=143_t4iacog&form=pdf&file=file.pdf
Artigo de periodico
Cytogenetics of epithelial hyperplasias of the human breast (2000)
Burbano, Rommel Rodríguez; Medeiros, Arnaldo; Amorim, Marucia Irena Medeiros de; Lima, Eleonidas Moura; Mello, Adriano; Barbieri Neto, José; Casartelli, Cacilda
Source: Cancer Genetics Cytogenetics. Unidade: FMRP
Subjects: GENÉTICA MÉDICA, ONCOLOGIA, MAMA
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ABNT
BURBANO, Rommel Rodríguez et al. Cytogenetics of epithelial hyperplasias of the human breast. Cancer Genetics Cytogenetics, v. 119, p. 62-66, 2000Tradução . . Disponível em: http://probe.usp.br/cgi-bin/sciserv.pl?collection=journals&journal=01654608&issue=v119i0001&article=62_coehothb&form=pdf&file=file.pdf. Acesso em: 16 ago. 2024.
APA
Burbano, R. R., Medeiros, A., Amorim, M. I. M. de, Lima, E. M., Mello, A., Barbieri Neto, J., & Casartelli, C. (2000). Cytogenetics of epithelial hyperplasias of the human breast. Cancer Genetics Cytogenetics, 119, 62-66. Recuperado de http://probe.usp.br/cgi-bin/sciserv.pl?collection=journals&journal=01654608&issue=v119i0001&article=62_coehothb&form=pdf&file=file.pdf
NLM
Burbano RR, Medeiros A, Amorim MIM de, Lima EM, Mello A, Barbieri Neto J, Casartelli C. Cytogenetics of epithelial hyperplasias of the human breast [Internet]. Cancer Genetics Cytogenetics. 2000 ; 119 62-66.[citado 2024 ago. 16 ] Available from: http://probe.usp.br/cgi-bin/sciserv.pl?collection=journals&journal=01654608&issue=v119i0001&article=62_coehothb&form=pdf&file=file.pdf
Vancouver
Burbano RR, Medeiros A, Amorim MIM de, Lima EM, Mello A, Barbieri Neto J, Casartelli C. Cytogenetics of epithelial hyperplasias of the human breast [Internet]. Cancer Genetics Cytogenetics. 2000 ; 119 62-66.[citado 2024 ago. 16 ] Available from: http://probe.usp.br/cgi-bin/sciserv.pl?collection=journals&journal=01654608&issue=v119i0001&article=62_coehothb&form=pdf&file=file.pdf
Artigo de periodico
Investigation of single-strand conformational polymorphism of the TP53 gene in women with a family history of breast cancer (2000)
Burbano, R. R.; Medeiros, A. C.; Mello, A. A.; Lemos, José Alexandre; Bahia, Marcelo de Oliveira; Casartelli, Cacilda
Source: Brazilian Journal of Medical and Biological Research. Unidade: FMRP
Subjects: GENÉTICA MÉDICA, ONCOLOGIA, MAMA
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ABNT
BURBANO, R. R. et al. Investigation of single-strand conformational polymorphism of the TP53 gene in women with a family history of breast cancer. Brazilian Journal of Medical and Biological Research, v. 33, n. 11, p. 1325-1328, 2000Tradução . . Disponível em: https://doi.org/10.1590/s0100-879x2000001100010. Acesso em: 16 ago. 2024.
APA
Burbano, R. R., Medeiros, A. C., Mello, A. A., Lemos, J. A., Bahia, M. de O., & Casartelli, C. (2000). Investigation of single-strand conformational polymorphism of the TP53 gene in women with a family history of breast cancer. Brazilian Journal of Medical and Biological Research, 33( 11), 1325-1328. doi:10.1590/s0100-879x2000001100010
NLM
Burbano RR, Medeiros AC, Mello AA, Lemos JA, Bahia M de O, Casartelli C. Investigation of single-strand conformational polymorphism of the TP53 gene in women with a family history of breast cancer [Internet]. Brazilian Journal of Medical and Biological Research. 2000 ; 33( 11): 1325-1328.[citado 2024 ago. 16 ] Available from: https://doi.org/10.1590/s0100-879x2000001100010
Vancouver
Burbano RR, Medeiros AC, Mello AA, Lemos JA, Bahia M de O, Casartelli C. Investigation of single-strand conformational polymorphism of the TP53 gene in women with a family history of breast cancer [Internet]. Brazilian Journal of Medical and Biological Research. 2000 ; 33( 11): 1325-1328.[citado 2024 ago. 16 ] Available from: https://doi.org/10.1590/s0100-879x2000001100010

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