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SERAPHIM, Carlos Eduardo. Investigação dos aspectos metabólicos da puberdade precoce central. 2024. Tese (Doutorado) – Universidade de São Paulo, São Paulo, 2024. Disponível em: https://www.teses.usp.br/teses/disponiveis/5/5135/tde-19062024-165829/. Acesso em: 19 out. 2024.
APA
Seraphim, C. E. (2024). Investigação dos aspectos metabólicos da puberdade precoce central (Tese (Doutorado). Universidade de São Paulo, São Paulo. Recuperado de https://www.teses.usp.br/teses/disponiveis/5/5135/tde-19062024-165829/
NLM
Seraphim CE. Investigação dos aspectos metabólicos da puberdade precoce central [Internet]. 2024 ;[citado 2024 out. 19 ] Available from: https://www.teses.usp.br/teses/disponiveis/5/5135/tde-19062024-165829/
Vancouver
Seraphim CE. Investigação dos aspectos metabólicos da puberdade precoce central [Internet]. 2024 ;[citado 2024 out. 19 ] Available from: https://www.teses.usp.br/teses/disponiveis/5/5135/tde-19062024-165829/
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MACHADO, Rafael Rahal Guaragna et al. Immune evasion of SARS-CoV-2 omicron subvariants XBB.1.5, XBB.1.16 and EG.5.1 in a cohort of older adults after ChAdOx1-S vaccination and BA.4/5 bivalent Booster. Vaccines, v. 12, n. 2, 2024Tradução . . Disponível em: https://doi.org/10.3390/vaccines12020144. Acesso em: 19 out. 2024.
APA
Machado, R. R. G., Candido, E. D. de O., Aguiar, A. S., Chalup, V. N., Sanches, P. R., Dorlass, E. G., et al. (2024). Immune evasion of SARS-CoV-2 omicron subvariants XBB.1.5, XBB.1.16 and EG.5.1 in a cohort of older adults after ChAdOx1-S vaccination and BA.4/5 bivalent Booster. Vaccines, 12( 2). doi:10.3390/vaccines12020144
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Machado RRG, Candido ED de O, Aguiar AS, Chalup VN, Sanches PR, Dorlass EG, Amgarten DE, Pinho JRR, Oliveira DBL de. Immune evasion of SARS-CoV-2 omicron subvariants XBB.1.5, XBB.1.16 and EG.5.1 in a cohort of older adults after ChAdOx1-S vaccination and BA.4/5 bivalent Booster [Internet]. Vaccines. 2024 ; 12( 2):[citado 2024 out. 19 ] Available from: https://doi.org/10.3390/vaccines12020144
Vancouver
Machado RRG, Candido ED de O, Aguiar AS, Chalup VN, Sanches PR, Dorlass EG, Amgarten DE, Pinho JRR, Oliveira DBL de. Immune evasion of SARS-CoV-2 omicron subvariants XBB.1.5, XBB.1.16 and EG.5.1 in a cohort of older adults after ChAdOx1-S vaccination and BA.4/5 bivalent Booster [Internet]. Vaccines. 2024 ; 12( 2):[citado 2024 out. 19 ] Available from: https://doi.org/10.3390/vaccines12020144
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MENDONÇA, Leonardo et al. What is needed to diagnose an autoinflammatory disease? From clinical manifestations to genomic sequencing: the Brazilian experience. Clinical Immunology, v. 262, p. 51-52, 2024Tradução . . Disponível em: https://doi.org/10.1016/j.clim.2024.110132. Acesso em: 19 out. 2024.
APA
Mendonça, L., Pontillo, A., Freschi-Barros, S., Melato, A., Cunha, A. L., Ianhez, M., et al. (2024). What is needed to diagnose an autoinflammatory disease? From clinical manifestations to genomic sequencing: the Brazilian experience. Clinical Immunology, 262, 51-52. doi:https://doi.org/10.1016/j.clim.2024.110132
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Mendonça L, Pontillo A, Freschi-Barros S, Melato A, Cunha AL, Ianhez M, Osaku F, Carvalho LM de, Didier F, Cavalcanti A, Carlos LR, Takano O, Robazzi T, Alcantara C, Francescantonio I, Frèmond M-L, Kalil Filho JE. What is needed to diagnose an autoinflammatory disease? From clinical manifestations to genomic sequencing: the Brazilian experience [Internet]. Clinical Immunology. 2024 ; 262 51-52.[citado 2024 out. 19 ] Available from: https://doi.org/10.1016/j.clim.2024.110132
Vancouver
Mendonça L, Pontillo A, Freschi-Barros S, Melato A, Cunha AL, Ianhez M, Osaku F, Carvalho LM de, Didier F, Cavalcanti A, Carlos LR, Takano O, Robazzi T, Alcantara C, Francescantonio I, Frèmond M-L, Kalil Filho JE. What is needed to diagnose an autoinflammatory disease? From clinical manifestations to genomic sequencing: the Brazilian experience [Internet]. Clinical Immunology. 2024 ; 262 51-52.[citado 2024 out. 19 ] Available from: https://doi.org/10.1016/j.clim.2024.110132
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PARDUCCI, Natalia Sudan et al. Antineoplastic effects of pharmacological inhibitors of aurora kinases in CSF3RT618I-driven cells. BLOOD CELLS MOLECULES AND DISEASES, v. 104, 2024Tradução . . Disponível em: https://observatorio.fm.usp.br/handle/OPI/58756. Acesso em: 19 out. 2024.
APA
Parducci, N. S., Garnique, A. D. M. B., Lima, K. C. de, Carlos, J. A. E. G., Fonseca, N. P., Miranda, L. B. L. D., et al. (2024). Antineoplastic effects of pharmacological inhibitors of aurora kinases in CSF3RT618I-driven cells. BLOOD CELLS MOLECULES AND DISEASES, 104. doi:10.1016/j.bcmd.2023.102799
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Parducci NS, Garnique ADMB, Lima KC de, Carlos JAEG, Fonseca NP, Miranda LBLD, Almeida BO de, Rego EM, Traina F, Machado Neto JA. Antineoplastic effects of pharmacological inhibitors of aurora kinases in CSF3RT618I-driven cells [Internet]. BLOOD CELLS MOLECULES AND DISEASES. 2024 ; 104[citado 2024 out. 19 ] Available from: https://observatorio.fm.usp.br/handle/OPI/58756
Vancouver
Parducci NS, Garnique ADMB, Lima KC de, Carlos JAEG, Fonseca NP, Miranda LBLD, Almeida BO de, Rego EM, Traina F, Machado Neto JA. Antineoplastic effects of pharmacological inhibitors of aurora kinases in CSF3RT618I-driven cells [Internet]. BLOOD CELLS MOLECULES AND DISEASES. 2024 ; 104[citado 2024 out. 19 ] Available from: https://observatorio.fm.usp.br/handle/OPI/58756
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PINTO, Emilia M et al. Multiple TP53 p.R337H haplotypes and implications for tumor susceptibility. Human genetics and genomics advances, v. 5, n. 1, 2024Tradução . . Disponível em: https://observatorio.fm.usp.br/handle/OPI/57446. Acesso em: 19 out. 2024.
APA
Pinto, E. M., Rave, C. F., Figueiredo, B. C., Salvador, H., Teixeira, M. R., Pinto, C., et al. (2024). Multiple TP53 p.R337H haplotypes and implications for tumor susceptibility. Human genetics and genomics advances, 5( 1). doi:10.1016/j.xhgg.2023.100244
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Pinto EM, Rave CF, Figueiredo BC, Salvador H, Teixeira MR, Pinto C, Pinheiro M, Kratz CP, Lavarino C, Legal EAMF. Multiple TP53 p.R337H haplotypes and implications for tumor susceptibility [Internet]. Human genetics and genomics advances. 2024 ; 5( 1):[citado 2024 out. 19 ] Available from: https://observatorio.fm.usp.br/handle/OPI/57446
Vancouver
Pinto EM, Rave CF, Figueiredo BC, Salvador H, Teixeira MR, Pinto C, Pinheiro M, Kratz CP, Lavarino C, Legal EAMF. Multiple TP53 p.R337H haplotypes and implications for tumor susceptibility [Internet]. Human genetics and genomics advances. 2024 ; 5( 1):[citado 2024 out. 19 ] Available from: https://observatorio.fm.usp.br/handle/OPI/57446
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MENDONÇA, Leonardo Oliveira et al. Unexplained fever with consumptive syndrome in the elderly: two cases of VEXAS syndrome with inflammasome dysregulation. Clinical and Experimental Immunology, p. 21 , 2024Tradução . . Disponível em: https://doi.org/10.1093/cei/uxae069. Acesso em: 19 out. 2024.
APA
Mendonça, L. O., Leal, V. N. C., Roa, M. E. G. V., Barros, S. F. de, Kalil Filho, J. E., & Pontillo, A. (2024). Unexplained fever with consumptive syndrome in the elderly: two cases of VEXAS syndrome with inflammasome dysregulation. Clinical and Experimental Immunology, 21 . doi:10.1093/cei/uxae069
NLM
Mendonça LO, Leal VNC, Roa MEGV, Barros SF de, Kalil Filho JE, Pontillo A. Unexplained fever with consumptive syndrome in the elderly: two cases of VEXAS syndrome with inflammasome dysregulation [Internet]. Clinical and Experimental Immunology. 2024 ;21 .[citado 2024 out. 19 ] Available from: https://doi.org/10.1093/cei/uxae069
Vancouver
Mendonça LO, Leal VNC, Roa MEGV, Barros SF de, Kalil Filho JE, Pontillo A. Unexplained fever with consumptive syndrome in the elderly: two cases of VEXAS syndrome with inflammasome dysregulation [Internet]. Clinical and Experimental Immunology. 2024 ;21 .[citado 2024 out. 19 ] Available from: https://doi.org/10.1093/cei/uxae069
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HOSOMI, Silverio Shindi e SALLES, Igor Caitano e BACHEGA, Tania Aparecida Sartori Sanchez. Mutation distributions among patients with congenital adrenal hyperplasia from five regions of Brazil: a systematic review. Archives of endocrinology metabolism, v. 67, n. 3, p. 427-441, 2023Tradução . . Disponível em: https://observatorio.fm.usp.br/handle/OPI/53798. Acesso em: 19 out. 2024.
APA
Hosomi, S. S., Salles, I. C., & Bachega, T. A. S. S. (2023). Mutation distributions among patients with congenital adrenal hyperplasia from five regions of Brazil: a systematic review. Archives of endocrinology metabolism, 67( 3), 427-441. doi:10.20945/2359-3997000000593
NLM
Hosomi SS, Salles IC, Bachega TASS. Mutation distributions among patients with congenital adrenal hyperplasia from five regions of Brazil: a systematic review [Internet]. Archives of endocrinology metabolism. 2023 ; 67( 3): 427-441.[citado 2024 out. 19 ] Available from: https://observatorio.fm.usp.br/handle/OPI/53798
Vancouver
Hosomi SS, Salles IC, Bachega TASS. Mutation distributions among patients with congenital adrenal hyperplasia from five regions of Brazil: a systematic review [Internet]. Archives of endocrinology metabolism. 2023 ; 67( 3): 427-441.[citado 2024 out. 19 ] Available from: https://observatorio.fm.usp.br/handle/OPI/53798
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MAGNOTTO, John C et al. Novel MKRN3 missense mutations associated with central precocious puberty reveal distinct effects on ubiquitination. Journal of clinical endocrinology & metabolism, v. 108, n. 7, p. 1646-1656, 2023Tradução . . Disponível em: https://observatorio.fm.usp.br/handle/OPI/54585. Acesso em: 19 out. 2024.
APA
Magnotto, J. C., Mancini, A., Bird, K., Montenegro, L., Tutunculer, F., Pereira, S. A., et al. (2023). Novel MKRN3 missense mutations associated with central precocious puberty reveal distinct effects on ubiquitination. Journal of clinical endocrinology & metabolism, 108( 7), 1646-1656. doi:10.1210/clinem/dgad151
NLM
Magnotto JC, Mancini A, Bird K, Montenegro L, Tutunculer F, Pereira SA, Simas V, Garcia L, Roberts SA, Xavier ACL. Novel MKRN3 missense mutations associated with central precocious puberty reveal distinct effects on ubiquitination [Internet]. Journal of clinical endocrinology & metabolism. 2023 ; 108( 7): 1646-1656.[citado 2024 out. 19 ] Available from: https://observatorio.fm.usp.br/handle/OPI/54585
Vancouver
Magnotto JC, Mancini A, Bird K, Montenegro L, Tutunculer F, Pereira SA, Simas V, Garcia L, Roberts SA, Xavier ACL. Novel MKRN3 missense mutations associated with central precocious puberty reveal distinct effects on ubiquitination [Internet]. Journal of clinical endocrinology & metabolism. 2023 ; 108( 7): 1646-1656.[citado 2024 out. 19 ] Available from: https://observatorio.fm.usp.br/handle/OPI/54585
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FAGUNDES, Gustavo F. C et al. Evidence for a Founder Effect of SDHB Exon 1 Deletion in Brazilian Patients With Paraganglioma. Journal of clinical endocrinology & metabolism, v. 108, n. 8, p. 2105-2114, 2023Tradução . . Disponível em: https://observatorio.fm.usp.br/handle/OPI/54605. Acesso em: 19 out. 2024.
APA
Fagundes, G. F. C., Freitas-Castro, F., Santana, L. S., Afonso, A. C. F., Petenuci, J., Funari, M. F. A., et al. (2023). Evidence for a Founder Effect of SDHB Exon 1 Deletion in Brazilian Patients With Paraganglioma. Journal of clinical endocrinology & metabolism, 108( 8), 2105-2114. doi:10.1210/clinem/dgad028
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Fagundes GFC, Freitas-Castro F, Santana LS, Afonso ACF, Petenuci J, Funari MFA, Guimaraes AG, Ledesma FL, Xavier ACL, Mendonca BB de. Evidence for a Founder Effect of SDHB Exon 1 Deletion in Brazilian Patients With Paraganglioma [Internet]. Journal of clinical endocrinology & metabolism. 2023 ; 108( 8): 2105-2114.[citado 2024 out. 19 ] Available from: https://observatorio.fm.usp.br/handle/OPI/54605
Vancouver
Fagundes GFC, Freitas-Castro F, Santana LS, Afonso ACF, Petenuci J, Funari MFA, Guimaraes AG, Ledesma FL, Xavier ACL, Mendonca BB de. Evidence for a Founder Effect of SDHB Exon 1 Deletion in Brazilian Patients With Paraganglioma [Internet]. Journal of clinical endocrinology & metabolism. 2023 ; 108( 8): 2105-2114.[citado 2024 out. 19 ] Available from: https://observatorio.fm.usp.br/handle/OPI/54605
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CASTRO, Mateus Vidigal de et al. Corrigendum: follow-up of young adult monozygotic twins after simultaneous critical coronavirus disease 2019: a case report. Frontiers in Medicine, v. 10, 2023Tradução . . Disponível em: https://doi.org/10.3389/fmed.2023.1185833. Acesso em: 19 out. 2024.
APA
Castro, M. V. de, Silva, M. V. R., Soares, F. B., Coria, V. R., Naslavsky, M., Scliar, M. O., et al. (2023). Corrigendum: follow-up of young adult monozygotic twins after simultaneous critical coronavirus disease 2019: a case report. Frontiers in Medicine, 10. doi:10.3389/fmed.2023.1185833
NLM
Castro MV de, Silva MVR, Soares FB, Coria VR, Naslavsky M, Scliar MO, Castelli EC, Oliveira JR de, Medeiros GX de, Sasahara GL, Santos KS, Cunha Neto E, Kalil J, Zatz M. Corrigendum: follow-up of young adult monozygotic twins after simultaneous critical coronavirus disease 2019: a case report [Internet]. Frontiers in Medicine. 2023 ; 10[citado 2024 out. 19 ] Available from: https://doi.org/10.3389/fmed.2023.1185833
Vancouver
Castro MV de, Silva MVR, Soares FB, Coria VR, Naslavsky M, Scliar MO, Castelli EC, Oliveira JR de, Medeiros GX de, Sasahara GL, Santos KS, Cunha Neto E, Kalil J, Zatz M. Corrigendum: follow-up of young adult monozygotic twins after simultaneous critical coronavirus disease 2019: a case report [Internet]. Frontiers in Medicine. 2023 ; 10[citado 2024 out. 19 ] Available from: https://doi.org/10.3389/fmed.2023.1185833
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TINANO, Flavia Rezende et al. Clinical and Genetic Characterization of Familial Central Precocious Puberty. Journal of clinical endocrinology & metabolism, v. 108, n. 7, p. 1758-1767, 2023Tradução . . Disponível em: https://observatorio.fm.usp.br/handle/OPI/54565. Acesso em: 19 out. 2024.
APA
Tinano, F. R., Canton, A. P. M., Montenegro, L. R., Leal, A. de C., Faria, A. G., Seraphim, C. E., et al. (2023). Clinical and Genetic Characterization of Familial Central Precocious Puberty. Journal of clinical endocrinology & metabolism, 108( 7), 1758-1767. doi:10.1210/clinem/dgac763
NLM
Tinano FR, Canton APM, Montenegro LR, Leal A de C, Faria AG, Seraphim CE, Brauner R, Jorge AA de L, Mendonca BB de, Xavier ACL. Clinical and Genetic Characterization of Familial Central Precocious Puberty [Internet]. Journal of clinical endocrinology & metabolism. 2023 ; 108( 7): 1758-1767.[citado 2024 out. 19 ] Available from: https://observatorio.fm.usp.br/handle/OPI/54565
Vancouver
Tinano FR, Canton APM, Montenegro LR, Leal A de C, Faria AG, Seraphim CE, Brauner R, Jorge AA de L, Mendonca BB de, Xavier ACL. Clinical and Genetic Characterization of Familial Central Precocious Puberty [Internet]. Journal of clinical endocrinology & metabolism. 2023 ; 108( 7): 1758-1767.[citado 2024 out. 19 ] Available from: https://observatorio.fm.usp.br/handle/OPI/54565
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HOMAN, Claire C et al. Somatic mutational landscape of hereditary hematopoietic malignancies caused by germline variants in RUNX1, GATA2, and DDX41. Blood advances, v. 7, n. 20, p. 6092-6107, 2023Tradução . . Disponível em: https://observatorio.fm.usp.br/handle/OPI/57340. Acesso em: 19 out. 2024.
APA
Homan, C. C., Drazer, M. W., Yu, K., Lawrence, D. M., Feng, J., Arriola-Martinez, L., et al. (2023). Somatic mutational landscape of hereditary hematopoietic malignancies caused by germline variants in RUNX1, GATA2, and DDX41. Blood advances, 7( 20), 6092-6107. doi:10.1182/bloodadvances.2023010045
NLM
Homan CC, Drazer MW, Yu K, Lawrence DM, Feng J, Arriola-Martinez L, Pozsgai MJ, Mcneely KE, Ha T, Velloso EDRP. Somatic mutational landscape of hereditary hematopoietic malignancies caused by germline variants in RUNX1, GATA2, and DDX41 [Internet]. Blood advances. 2023 ; 7( 20): 6092-6107.[citado 2024 out. 19 ] Available from: https://observatorio.fm.usp.br/handle/OPI/57340
Vancouver
Homan CC, Drazer MW, Yu K, Lawrence DM, Feng J, Arriola-Martinez L, Pozsgai MJ, Mcneely KE, Ha T, Velloso EDRP. Somatic mutational landscape of hereditary hematopoietic malignancies caused by germline variants in RUNX1, GATA2, and DDX41 [Internet]. Blood advances. 2023 ; 7( 20): 6092-6107.[citado 2024 out. 19 ] Available from: https://observatorio.fm.usp.br/handle/OPI/57340
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BRITO, Vinicius N et al. The congenital and acquired mechanisms implicated in the etiology of central precocious puberty. Endocrine reviews, v. 44, n. 2, p. 193-221, 2023Tradução . . Disponível em: https://observatorio.fm.usp.br/handle/OPI/52867. Acesso em: 19 out. 2024.
APA
Brito, V. N., Canton, A. P. M., Seraphim, C. E., Abreu, A. P., Macedo, D. B., Mendonca, B. B. de, et al. (2023). The congenital and acquired mechanisms implicated in the etiology of central precocious puberty. Endocrine reviews, 44( 2), 193-221. doi:10.1210/endrev/bnac020
NLM
Brito VN, Canton APM, Seraphim CE, Abreu AP, Macedo DB, Mendonca BB de, Kaiser UB, Argente J, Xavier ACL. The congenital and acquired mechanisms implicated in the etiology of central precocious puberty [Internet]. Endocrine reviews. 2023 ; 44( 2): 193-221.[citado 2024 out. 19 ] Available from: https://observatorio.fm.usp.br/handle/OPI/52867
Vancouver
Brito VN, Canton APM, Seraphim CE, Abreu AP, Macedo DB, Mendonca BB de, Kaiser UB, Argente J, Xavier ACL. The congenital and acquired mechanisms implicated in the etiology of central precocious puberty [Internet]. Endocrine reviews. 2023 ; 44( 2): 193-221.[citado 2024 out. 19 ] Available from: https://observatorio.fm.usp.br/handle/OPI/52867
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SOUZA, Rodrigo Barbosa de et al. Extracellular matrix and vascular dynamics in the kidney of a murine model for Marfan syndrome. PLoS ONE, v. 18, n. 5, 2023Tradução . . Disponível em: https://doi.org/10.1371/journal.pone.0285418. Acesso em: 19 out. 2024.
APA
Souza, R. B. de, Lemes, R. B., Foresto Neto, O., Cassiano, L. L., Reinhardt, D. P., Meek, K. M., et al. (2023). Extracellular matrix and vascular dynamics in the kidney of a murine model for Marfan syndrome. PLoS ONE, 18( 5). doi:10.1371/journal.pone.0285418
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Souza RB de, Lemes RB, Foresto Neto O, Cassiano LL, Reinhardt DP, Meek KM, Koh IHJ, Lewis PN, Pereira L da V. Extracellular matrix and vascular dynamics in the kidney of a murine model for Marfan syndrome [Internet]. PLoS ONE. 2023 ; 18( 5):[citado 2024 out. 19 ] Available from: https://doi.org/10.1371/journal.pone.0285418
Vancouver
Souza RB de, Lemes RB, Foresto Neto O, Cassiano LL, Reinhardt DP, Meek KM, Koh IHJ, Lewis PN, Pereira L da V. Extracellular matrix and vascular dynamics in the kidney of a murine model for Marfan syndrome [Internet]. PLoS ONE. 2023 ; 18( 5):[citado 2024 out. 19 ] Available from: https://doi.org/10.1371/journal.pone.0285418
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SONNE, Alexander et al. Abnormal myosin post-translational modifications and ATP turnover time associated with human congenital myopathy-related RYR1 mutations. Acta physiologica, v. 239, n. 2, 2023Tradução . . Disponível em: https://observatorio.fm.usp.br/handle/OPI/57449. Acesso em: 19 out. 2024.
APA
Sonne, A., Antonovic, A. K., Melhedegaard, E., Akter, F., Andersen, J. L., Jungbluth, H., et al. (2023). Abnormal myosin post-translational modifications and ATP turnover time associated with human congenital myopathy-related RYR1 mutations. Acta physiologica, 239( 2). doi:10.1111/apha.14035
NLM
Sonne A, Antonovic AK, Melhedegaard E, Akter F, Andersen JL, Jungbluth H, Witting N, Vissing J, Zanoteli E, Fornili A, Ochala J. Abnormal myosin post-translational modifications and ATP turnover time associated with human congenital myopathy-related RYR1 mutations [Internet]. Acta physiologica. 2023 ; 239( 2):[citado 2024 out. 19 ] Available from: https://observatorio.fm.usp.br/handle/OPI/57449
Vancouver
Sonne A, Antonovic AK, Melhedegaard E, Akter F, Andersen JL, Jungbluth H, Witting N, Vissing J, Zanoteli E, Fornili A, Ochala J. Abnormal myosin post-translational modifications and ATP turnover time associated with human congenital myopathy-related RYR1 mutations [Internet]. Acta physiologica. 2023 ; 239( 2):[citado 2024 out. 19 ] Available from: https://observatorio.fm.usp.br/handle/OPI/57449
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LEITE, Ana Kober Nogueira et al. Profile of MicroRNAs associated with death due to disease progression in metastatic papillary Thyroid Carcinoma patients. Cancers, v. 15, n. 3, p. 1-12, 2023Tradução . . Disponível em: https://doi.org/10.3390/cancers15030869. Acesso em: 19 out. 2024.
APA
Leite, A. K. N., Saito, K. C., Theodoro, T. R., Pasini, F. S., Camilo, L. P., Rossetti, C. A., et al. (2023). Profile of MicroRNAs associated with death due to disease progression in metastatic papillary Thyroid Carcinoma patients. Cancers, 15( 3), 1-12. doi:10.3390/cancers15030869
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Leite AKN, Saito KC, Theodoro TR, Pasini FS, Camilo LP, Rossetti CA, Cavalheiro BG, Alves VAF, Kowalski LP, Kimura ET, Matos LL. Profile of MicroRNAs associated with death due to disease progression in metastatic papillary Thyroid Carcinoma patients [Internet]. Cancers. 2023 ; 15( 3): 1-12.[citado 2024 out. 19 ] Available from: https://doi.org/10.3390/cancers15030869
Vancouver
Leite AKN, Saito KC, Theodoro TR, Pasini FS, Camilo LP, Rossetti CA, Cavalheiro BG, Alves VAF, Kowalski LP, Kimura ET, Matos LL. Profile of MicroRNAs associated with death due to disease progression in metastatic papillary Thyroid Carcinoma patients [Internet]. Cancers. 2023 ; 15( 3): 1-12.[citado 2024 out. 19 ] Available from: https://doi.org/10.3390/cancers15030869
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SILVA, Fernanda Jardim da et al. Salivary glands adenoid cystic carcinoma: a molecular profile update and potential implications. Frontiers in Oncology, v. 13, p. 1-14, 2023Tradução . . Disponível em: https://doi.org/10.3389/fonc.2023.1191218. Acesso em: 19 out. 2024.
APA
Silva, F. J. da, Azevedo Junior, J. C. de, Ralph, A. C. L., Pinheiro, J. de J. V., Calcagno, D. Q., & Freitas, V. M. (2023). Salivary glands adenoid cystic carcinoma: a molecular profile update and potential implications. Frontiers in Oncology, 13, 1-14. doi:10.3389/fonc.2023.1191218
NLM
Silva FJ da, Azevedo Junior JC de, Ralph ACL, Pinheiro J de JV, Calcagno DQ, Freitas VM. Salivary glands adenoid cystic carcinoma: a molecular profile update and potential implications [Internet]. Frontiers in Oncology. 2023 ; 13 1-14.[citado 2024 out. 19 ] Available from: https://doi.org/10.3389/fonc.2023.1191218
Vancouver
Silva FJ da, Azevedo Junior JC de, Ralph ACL, Pinheiro J de JV, Calcagno DQ, Freitas VM. Salivary glands adenoid cystic carcinoma: a molecular profile update and potential implications [Internet]. Frontiers in Oncology. 2023 ; 13 1-14.[citado 2024 out. 19 ] Available from: https://doi.org/10.3389/fonc.2023.1191218
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ABNT
CHAGAS, Pablo Ferreira das et al. Identification of ITPR1 as a Hub Gene of Group 3 Medulloblastoma and Coregulated Genes with Potential Prognostic Values. Journal of molecular neuroscience, v. 72, n. 3, p. 633-641, 2022Tradução . . Disponível em: https://doi.org/10.1007/s12031-021-01942-3. Acesso em: 19 out. 2024.
APA
Chagas, P. F. das, Sousa, G. R. de, Veronez, L. C., Martins-da-Silva, A., Correa, C. A. P., Cruzeiro, G. A. V., et al. (2022). Identification of ITPR1 as a Hub Gene of Group 3 Medulloblastoma and Coregulated Genes with Potential Prognostic Values. Journal of molecular neuroscience, 72( 3), 633-641. doi:10.1007/s12031-021-01942-3
NLM
Chagas PF das, Sousa GR de, Veronez LC, Martins-da-Silva A, Correa CAP, Cruzeiro GAV, Nagano LFP, Queiroz RG de P, Marie SKN, Brandalise SR. Identification of ITPR1 as a Hub Gene of Group 3 Medulloblastoma and Coregulated Genes with Potential Prognostic Values [Internet]. Journal of molecular neuroscience. 2022 ; 72( 3): 633-641.[citado 2024 out. 19 ] Available from: https://doi.org/10.1007/s12031-021-01942-3
Vancouver
Chagas PF das, Sousa GR de, Veronez LC, Martins-da-Silva A, Correa CAP, Cruzeiro GAV, Nagano LFP, Queiroz RG de P, Marie SKN, Brandalise SR. Identification of ITPR1 as a Hub Gene of Group 3 Medulloblastoma and Coregulated Genes with Potential Prognostic Values [Internet]. Journal of molecular neuroscience. 2022 ; 72( 3): 633-641.[citado 2024 out. 19 ] Available from: https://doi.org/10.1007/s12031-021-01942-3
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SILVA, Andre Macedo Serafim et al. The location of disease-causing DES variants determines the severity of phenotype and the morphology of sarcoplasmic aggregates. Journal of neuropathology and experimental neurology, v. 81, n. 9, p. 746-757, 2022Tradução . . Disponível em: https://doi.org/10.1093/jnen/nlac063. Acesso em: 19 out. 2024.
APA
Silva, A. M. S., Rodrigo, P., Moreno, C. A. M., Mendonca, R. de H., Estephan, E. de P., Camelo, C. G., et al. (2022). The location of disease-causing DES variants determines the severity of phenotype and the morphology of sarcoplasmic aggregates. Journal of neuropathology and experimental neurology, 81( 9), 746-757. doi:10.1093/jnen/nlac063
NLM
Silva AMS, Rodrigo P, Moreno CAM, Mendonca R de H, Estephan E de P, Camelo CG, Campos ED, Dias AT, Reed UC, Zanoteli E. The location of disease-causing DES variants determines the severity of phenotype and the morphology of sarcoplasmic aggregates [Internet]. Journal of neuropathology and experimental neurology. 2022 ; 81( 9): 746-757.[citado 2024 out. 19 ] Available from: https://doi.org/10.1093/jnen/nlac063
Vancouver
Silva AMS, Rodrigo P, Moreno CAM, Mendonca R de H, Estephan E de P, Camelo CG, Campos ED, Dias AT, Reed UC, Zanoteli E. The location of disease-causing DES variants determines the severity of phenotype and the morphology of sarcoplasmic aggregates [Internet]. Journal of neuropathology and experimental neurology. 2022 ; 81( 9): 746-757.[citado 2024 out. 19 ] Available from: https://doi.org/10.1093/jnen/nlac063
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CASTRO, Mateus Vidigal de et al. Follow-up of young adult monozygotic twins after simultaneous critical coronavirus disease 2019: a case report. Frontiers in Medicine, v. 9, 2022Tradução . . Disponível em: https://doi.org/10.3389/fmed.2022.1008585. Acesso em: 19 out. 2024.
APA
Castro, M. V. de, Silva, M. V. R., Soares, F. B., Coria, V. R., Naslavsky, M., Scliar, M. O., et al. (2022). Follow-up of young adult monozygotic twins after simultaneous critical coronavirus disease 2019: a case report. Frontiers in Medicine, 9. doi:10.3389/fmed.2022.1008585
NLM
Castro MV de, Silva MVR, Soares FB, Coria VR, Naslavsky M, Scliar MO, Castelli EC, Oliveira JR de, Medeiros GX de, Sasahara GL, Santos KS, Cunha Neto E, Kalil J, Zatz M. Follow-up of young adult monozygotic twins after simultaneous critical coronavirus disease 2019: a case report [Internet]. Frontiers in Medicine. 2022 ; 9[citado 2024 out. 19 ] Available from: https://doi.org/10.3389/fmed.2022.1008585
Vancouver
Castro MV de, Silva MVR, Soares FB, Coria VR, Naslavsky M, Scliar MO, Castelli EC, Oliveira JR de, Medeiros GX de, Sasahara GL, Santos KS, Cunha Neto E, Kalil J, Zatz M. Follow-up of young adult monozygotic twins after simultaneous critical coronavirus disease 2019: a case report [Internet]. Frontiers in Medicine. 2022 ; 9[citado 2024 out. 19 ] Available from: https://doi.org/10.3389/fmed.2022.1008585