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ABNT
ARROJO, Maria Luiza et al. Tight junction gene expression in salivary gland tumors. Pathology, Research and Practice, 2022Tradução . . Disponível em: https://doi.org/10.1016/j.prp.2022.154113. Acesso em: 09 out. 2024.
APA
Arrojo, M. L., Oliveira, K. K., Bettim, B. B., Kowalski, L. P., Carraro, D. M., Meira, I. T. J. e, et al. (2022). Tight junction gene expression in salivary gland tumors. Pathology, Research and Practice. doi:10.1016/j.prp.2022.154113
NLM
Arrojo ML, Oliveira KK, Bettim BB, Kowalski LP, Carraro DM, Meira ITJ e, Torrezan GT, Lourenço SV, Camillo CMC. Tight junction gene expression in salivary gland tumors [Internet]. Pathology, Research and Practice. 2022 ;[citado 2024 out. 09 ] Available from: https://doi.org/10.1016/j.prp.2022.154113
Vancouver
Arrojo ML, Oliveira KK, Bettim BB, Kowalski LP, Carraro DM, Meira ITJ e, Torrezan GT, Lourenço SV, Camillo CMC. Tight junction gene expression in salivary gland tumors [Internet]. Pathology, Research and Practice. 2022 ;[citado 2024 out. 09 ] Available from: https://doi.org/10.1016/j.prp.2022.154113
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
UGOLINI-LOPES, Michelle Remiao et al. Enhanced type I interferon gene signature in primary antiphospholipid syndrome: association with earlier disease onset and preeclampsia. Autoimmunity reviews, v. 18, n. 4, p. 393-398, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.autrev.2018.11.004. Acesso em: 09 out. 2024.
APA
Ugolini-lopes, M. R., Torrezan, G. T., Gandara, A. P. R., Olivieri, E. H. R., Nascimento, I. S., Okazaki, E., et al. (2019). Enhanced type I interferon gene signature in primary antiphospholipid syndrome: association with earlier disease onset and preeclampsia. Autoimmunity reviews, 18( 4), 393-398. doi:10.1016/j.autrev.2018.11.004
NLM
Ugolini-lopes MR, Torrezan GT, Gandara APR, Olivieri EHR, Nascimento IS, Okazaki E, Bonfá ESD de O, Carraro DM, Andrade DCO de. Enhanced type I interferon gene signature in primary antiphospholipid syndrome: association with earlier disease onset and preeclampsia [Internet]. Autoimmunity reviews. 2019 ; 18( 4): 393-398.[citado 2024 out. 09 ] Available from: https://doi.org/10.1016/j.autrev.2018.11.004
Vancouver
Ugolini-lopes MR, Torrezan GT, Gandara APR, Olivieri EHR, Nascimento IS, Okazaki E, Bonfá ESD de O, Carraro DM, Andrade DCO de. Enhanced type I interferon gene signature in primary antiphospholipid syndrome: association with earlier disease onset and preeclampsia [Internet]. Autoimmunity reviews. 2019 ; 18( 4): 393-398.[citado 2024 out. 09 ] Available from: https://doi.org/10.1016/j.autrev.2018.11.004
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CUNHA, Isabela Werneck da et al. Expanding morphological and clinical aspects of hereditary leiomyomatosis and renal cell carcinoma (HLRCC): a case report in a patient with unusual morphology and clinical presentation. Virchows Archiv: the european journal of pathology, 2018Tradução . . Disponível em: https://doi.org/10.1007/s00428-018-2420-3. Acesso em: 09 out. 2024.
APA
Cunha, I. W. da, Costa, W. H. da, Morini, M. A., Bezerra, S. M., Carraro, D. M., Torrezan, G. T., et al. (2018). Expanding morphological and clinical aspects of hereditary leiomyomatosis and renal cell carcinoma (HLRCC): a case report in a patient with unusual morphology and clinical presentation. Virchows Archiv: the european journal of pathology. doi:10.1007/s00428-018-2420-3
NLM
Cunha IW da, Costa WH da, Morini MA, Bezerra SM, Carraro DM, Torrezan GT, Formiga MN da C, Guimarães GC, Zequi S de C, Soares FA. Expanding morphological and clinical aspects of hereditary leiomyomatosis and renal cell carcinoma (HLRCC): a case report in a patient with unusual morphology and clinical presentation [Internet]. Virchows Archiv: the european journal of pathology. 2018 ;[citado 2024 out. 09 ] Available from: https://doi.org/10.1007/s00428-018-2420-3
Vancouver
Cunha IW da, Costa WH da, Morini MA, Bezerra SM, Carraro DM, Torrezan GT, Formiga MN da C, Guimarães GC, Zequi S de C, Soares FA. Expanding morphological and clinical aspects of hereditary leiomyomatosis and renal cell carcinoma (HLRCC): a case report in a patient with unusual morphology and clinical presentation [Internet]. Virchows Archiv: the european journal of pathology. 2018 ;[citado 2024 out. 09 ] Available from: https://doi.org/10.1007/s00428-018-2420-3
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FERREIRA, Elisa Napolitano et al. A genomic case study of desmoplastic small round cell tumor: comprehensive analysis reveals insights into potential therapeutic targets and development of a monitoring tool for a rare and aggressive disease. Human Genomics, v. No 2016, p. 1-13, 2016Tradução . . Disponível em: https://doi.org/10.1186/s40246-016-0092-0. Acesso em: 09 out. 2024.
APA
Ferreira, E. N., Barros, B. D. F., Souza, J. E. de, Almeida, R. V., Torrezan, G. T., Garcia, S., et al. (2016). A genomic case study of desmoplastic small round cell tumor: comprehensive analysis reveals insights into potential therapeutic targets and development of a monitoring tool for a rare and aggressive disease. Human Genomics, No 2016, 1-13. doi:10.1186/s40246-016-0092-0
NLM
Ferreira EN, Barros BDF, Souza JE de, Almeida RV, Torrezan GT, Garcia S, Krepischi ACV, Mello CAL de, Cunha IW da, Pinto CAL, Soares FA, Dias Neto E, Lopes A, Souza SJ de, Carraro DM. A genomic case study of desmoplastic small round cell tumor: comprehensive analysis reveals insights into potential therapeutic targets and development of a monitoring tool for a rare and aggressive disease [Internet]. Human Genomics. 2016 ; No 2016 1-13.[citado 2024 out. 09 ] Available from: https://doi.org/10.1186/s40246-016-0092-0
Vancouver
Ferreira EN, Barros BDF, Souza JE de, Almeida RV, Torrezan GT, Garcia S, Krepischi ACV, Mello CAL de, Cunha IW da, Pinto CAL, Soares FA, Dias Neto E, Lopes A, Souza SJ de, Carraro DM. A genomic case study of desmoplastic small round cell tumor: comprehensive analysis reveals insights into potential therapeutic targets and development of a monitoring tool for a rare and aggressive disease [Internet]. Human Genomics. 2016 ; No 2016 1-13.[citado 2024 out. 09 ] Available from: https://doi.org/10.1186/s40246-016-0092-0