Filtros : "BRASILEIROS" "Dinamarca" Limpar

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  • Source: Clinical Genetics. Unidade: FM

    Subjects: DIABETES MELLITUS, BRASILEIROS, PREVALÊNCIA

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    • ABNT

      SANTANA, L. S. et al. Clinical application of ACMG-AMP guidelines in HNF1A and GCK variants in a cohort of MODY families. Clinical Genetics, v. 92, n. 4, p. 388-396, 2017Tradução . . Disponível em: https://doi.org/10.1111/cge.12897. Acesso em: 22 ago. 2024.
    • APA

      Santana, L. S., Caetano, L. A., Costa-Riquetto, A. D., Quedas, E. P. S., Nery, M., Collet-Solberg, P., et al. (2017). Clinical application of ACMG-AMP guidelines in HNF1A and GCK variants in a cohort of MODY families. Clinical Genetics, 92( 4), 388-396. doi:10.1111/cge.12897
    • NLM

      Santana LS, Caetano LA, Costa-Riquetto AD, Quedas EPS, Nery M, Collet-Solberg P, Boguszewski MCS, Vendramini VF, Crisostomo LG, Floh FO, Zarabia ZL, Kohara SK, Guastapaglia L, Passone CGB, Sewaybricker LE, Jorge AAL, Teles MG. Clinical application of ACMG-AMP guidelines in HNF1A and GCK variants in a cohort of MODY families [Internet]. Clinical Genetics. 2017 ; 92( 4): 388-396.[citado 2024 ago. 22 ] Available from: https://doi.org/10.1111/cge.12897
    • Vancouver

      Santana LS, Caetano LA, Costa-Riquetto AD, Quedas EPS, Nery M, Collet-Solberg P, Boguszewski MCS, Vendramini VF, Crisostomo LG, Floh FO, Zarabia ZL, Kohara SK, Guastapaglia L, Passone CGB, Sewaybricker LE, Jorge AAL, Teles MG. Clinical application of ACMG-AMP guidelines in HNF1A and GCK variants in a cohort of MODY families [Internet]. Clinical Genetics. 2017 ; 92( 4): 388-396.[citado 2024 ago. 22 ] Available from: https://doi.org/10.1111/cge.12897
  • Source: Bipolar Disorders. Conference titles: Annual Conference of the International Society for Bipolar Disorders. Unidade: FM

    Subjects: REDES DE INFORMAÇÃO, BRASILEIROS, TRANSTORNO BIPOLAR

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    • ABNT

      GOMES, F. et al. The Brazilian research network in bipolar disorder: main findings from the first 7 years of collaborative studies. Bipolar Disorders. Copenhagen: Faculdade de Medicina, Universidade de São Paulo. Disponível em: http://onlinelibrary.wiley.com/doi/10.1111/bdi.12480/epdf. Acesso em: 22 ago. 2024. , 2017
    • APA

      Gomes, F., Kapczinski, F., Miranda-Scippa, Â., Lafer, B., & Brietzke, E. (2017). The Brazilian research network in bipolar disorder: main findings from the first 7 years of collaborative studies. Bipolar Disorders. Copenhagen: Faculdade de Medicina, Universidade de São Paulo. doi:10.1111/bdi.12480
    • NLM

      Gomes F, Kapczinski F, Miranda-Scippa Â, Lafer B, Brietzke E. The Brazilian research network in bipolar disorder: main findings from the first 7 years of collaborative studies [Internet]. Bipolar Disorders. 2017 ; 19 139.[citado 2024 ago. 22 ] Available from: http://onlinelibrary.wiley.com/doi/10.1111/bdi.12480/epdf
    • Vancouver

      Gomes F, Kapczinski F, Miranda-Scippa Â, Lafer B, Brietzke E. The Brazilian research network in bipolar disorder: main findings from the first 7 years of collaborative studies [Internet]. Bipolar Disorders. 2017 ; 19 139.[citado 2024 ago. 22 ] Available from: http://onlinelibrary.wiley.com/doi/10.1111/bdi.12480/epdf
  • Source: Clinical Genetics. Unidade: FM

    Subjects: MUTAÇÃO GENÉTICA, ETNOBIOLOGIA, POPULAÇÃO, SÍNDROMES DE DEFICIÊNCIA IMUNOLÓGICA, BRASILEIROS

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    • ABNT

      SUZUKI, K. T. et al. New CBP mutations in Brazilian patients with Rubinstein–Taybi syndrome [Carta]. Clinical Genetics. Copenhagen: Faculdade de Medicina, Universidade de São Paulo. Disponível em: https://doi.org/10.1111/j.1399-0004.2012.01894.x. Acesso em: 22 ago. 2024. , 2013
    • APA

      Suzuki, K. T., Torres, L. C., Sugayama, S. M. M., Alves, B. da C. A., Moreira-Filho, C. A., & Carneiro-Sampaio, M. (2013). New CBP mutations in Brazilian patients with Rubinstein–Taybi syndrome [Carta]. Clinical Genetics. Copenhagen: Faculdade de Medicina, Universidade de São Paulo. doi:10.1111/j.1399-0004.2012.01894.x
    • NLM

      Suzuki KT, Torres LC, Sugayama SMM, Alves B da CA, Moreira-Filho CA, Carneiro-Sampaio M. New CBP mutations in Brazilian patients with Rubinstein–Taybi syndrome [Carta] [Internet]. Clinical Genetics. 2013 ; 83( 3): 291-292.[citado 2024 ago. 22 ] Available from: https://doi.org/10.1111/j.1399-0004.2012.01894.x
    • Vancouver

      Suzuki KT, Torres LC, Sugayama SMM, Alves B da CA, Moreira-Filho CA, Carneiro-Sampaio M. New CBP mutations in Brazilian patients with Rubinstein–Taybi syndrome [Carta] [Internet]. Clinical Genetics. 2013 ; 83( 3): 291-292.[citado 2024 ago. 22 ] Available from: https://doi.org/10.1111/j.1399-0004.2012.01894.x
  • Source: Journal of Oral Pathology and Medicine. Unidade: FO

    Subjects: BRASILEIROS, HIV, MANIFESTAÇÕES BUCAIS

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    • ABNT

      LÓPEZ ORTEGA, Karem e VALE, Daniela A. e MAGALHÃES, Marina Helena Cury Gallottini. Impact of PI and NNRTI HAART-based therapy on oral lesions of Brazilian HIV-infected patients. Journal of Oral Pathology and Medicine, v. 38, n. 6, p. 489-494, 2009Tradução . . Disponível em: https://doi.org/10.1111/j.1600-0714.2009.00783.x. Acesso em: 22 ago. 2024.
    • APA

      López Ortega, K., Vale, D. A., & Magalhães, M. H. C. G. (2009). Impact of PI and NNRTI HAART-based therapy on oral lesions of Brazilian HIV-infected patients. Journal of Oral Pathology and Medicine, 38( 6), 489-494. doi:10.1111/j.1600-0714.2009.00783.x
    • NLM

      López Ortega K, Vale DA, Magalhães MHCG. Impact of PI and NNRTI HAART-based therapy on oral lesions of Brazilian HIV-infected patients [Internet]. Journal of Oral Pathology and Medicine. 2009 ; 38( 6): 489-494.[citado 2024 ago. 22 ] Available from: https://doi.org/10.1111/j.1600-0714.2009.00783.x
    • Vancouver

      López Ortega K, Vale DA, Magalhães MHCG. Impact of PI and NNRTI HAART-based therapy on oral lesions of Brazilian HIV-infected patients [Internet]. Journal of Oral Pathology and Medicine. 2009 ; 38( 6): 489-494.[citado 2024 ago. 22 ] Available from: https://doi.org/10.1111/j.1600-0714.2009.00783.x
  • Source: Tissue Antigens. Unidade: FMRP

    Subjects: GENÉTICA DE POPULAÇÕES, BRASILEIROS

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    • ABNT

      COVAS, Dimas Tadeu et al. Variation in the Fc'gama'R3B gene among distinct Brazilian populations. Tissue Antigens, v. 65, p. 178-182, 2005Tradução . . Disponível em: https://doi.org/10.1111/j.1399-0039.2005.00352.x. Acesso em: 22 ago. 2024.
    • APA

      Covas, D. T., Kashima, S., Guerreiro, J. F., Santos, S. E. B. dos, & Zago, M. A. (2005). Variation in the Fc'gama'R3B gene among distinct Brazilian populations. Tissue Antigens, 65, 178-182. doi:10.1111/j.1399-0039.2005.00352.x
    • NLM

      Covas DT, Kashima S, Guerreiro JF, Santos SEB dos, Zago MA. Variation in the Fc'gama'R3B gene among distinct Brazilian populations [Internet]. Tissue Antigens. 2005 ; 65 178-182.[citado 2024 ago. 22 ] Available from: https://doi.org/10.1111/j.1399-0039.2005.00352.x
    • Vancouver

      Covas DT, Kashima S, Guerreiro JF, Santos SEB dos, Zago MA. Variation in the Fc'gama'R3B gene among distinct Brazilian populations [Internet]. Tissue Antigens. 2005 ; 65 178-182.[citado 2024 ago. 22 ] Available from: https://doi.org/10.1111/j.1399-0039.2005.00352.x

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