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Parte de monografia/livro
Innovation in services: the case of Fleury - a diagnostic medical center (2014)
Vasconcellos, Eduardo; Guedes, Liliana Vasconcellos ; Franco, Rendrik; Maeda, Patricia Yumi; Guedes, Luís F. A; Bruno, Marcos C.
Source: Managing consumer services : factory or theater?. Unidade: FEA
Subjects: INOVAÇÕES TECNOLÓGICAS, SERVIÇOS
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ABNT
VASCONCELLOS, Eduardo et al. Innovation in services: the case of Fleury - a diagnostic medical center. Managing consumer services : factory or theater? Tradução . Heidelberg: Springer, 2014. . . Acesso em: 01 nov. 2024.
APA
Vasconcellos, E., Guedes, L. V., Franco, R., Maeda, P. Y., Guedes, L. F. A., & Bruno, M. C. (2014). Innovation in services: the case of Fleury - a diagnostic medical center. In Managing consumer services : factory or theater?. Heidelberg: Springer.
NLM
Vasconcellos E, Guedes LV, Franco R, Maeda PY, Guedes LFA, Bruno MC. Innovation in services: the case of Fleury - a diagnostic medical center. In: Managing consumer services : factory or theater? Heidelberg: Springer; 2014. [citado 2024 nov. 01 ]
Vancouver
Vasconcellos E, Guedes LV, Franco R, Maeda PY, Guedes LFA, Bruno MC. Innovation in services: the case of Fleury - a diagnostic medical center. In: Managing consumer services : factory or theater? Heidelberg: Springer; 2014. [citado 2024 nov. 01 ]
Artigo de periodico
Hereditary hemochromatosis in a Brazilian university hospital in São Paulo State (1990-2000) (2005)
Martinelli, Ana Lourdes Candolo; Filho, Rui; Cruz, Samantha; Franco, Rendrik; Tavella, Marli; Secaf, Marie; Ramalho, Leandra Naíra Zambelli; Zucoloto, Sérgio; Rodrigues, Sandra; Zago, Marcos Antônio
Source: Genetics and Molecular Research. Unidade: FMRP
Subjects: HEMOCROMATOSE, DOENÇAS GENÉTICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MARTINELLI, Ana Lourdes Candolo et al. Hereditary hemochromatosis in a Brazilian university hospital in São Paulo State (1990-2000). Genetics and Molecular Research, v. 4, n. 1, p. 31-38, 2005Tradução . . Acesso em: 01 nov. 2024.
APA
Martinelli, A. L. C., Filho, R., Cruz, S., Franco, R., Tavella, M., Secaf, M., et al. (2005). Hereditary hemochromatosis in a Brazilian university hospital in São Paulo State (1990-2000). Genetics and Molecular Research, 4( 1), 31-38.
NLM
Martinelli ALC, Filho R, Cruz S, Franco R, Tavella M, Secaf M, Ramalho LNZ, Zucoloto S, Rodrigues S, Zago MA. Hereditary hemochromatosis in a Brazilian university hospital in São Paulo State (1990-2000). Genetics and Molecular Research. 2005 ; 4( 1): 31-38.[citado 2024 nov. 01 ]
Vancouver
Martinelli ALC, Filho R, Cruz S, Franco R, Tavella M, Secaf M, Ramalho LNZ, Zucoloto S, Rodrigues S, Zago MA. Hereditary hemochromatosis in a Brazilian university hospital in São Paulo State (1990-2000). Genetics and Molecular Research. 2005 ; 4( 1): 31-38.[citado 2024 nov. 01 ]
Artigo de periodico
Heterogeneous ethnic distribution of the factor V leiden mutation (1999)
Franco, Rendrik; Elion, Jacques; Santos, Sidney E. B.; Araújo, Amélia G.; Tavella, Marli Haydee; Zago, Marco Antônio
Source: Genetics and Molecular Biology. Unidade: FMRP
Assunto: GENÉTICA MÉDICA
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ABNT
FRANCO, Rendrik et al. Heterogeneous ethnic distribution of the factor V leiden mutation. Genetics and Molecular Biology, v. 22, n. 2, p. 143-145, 1999Tradução . . Disponível em: https://doi.org/10.1590/s1415-47571999000200001. Acesso em: 01 nov. 2024.
APA
Franco, R., Elion, J., Santos, S. E. B., Araújo, A. G., Tavella, M. H., & Zago, M. A. (1999). Heterogeneous ethnic distribution of the factor V leiden mutation. Genetics and Molecular Biology, 22( 2), 143-145. doi:10.1590/s1415-47571999000200001
NLM
Franco R, Elion J, Santos SEB, Araújo AG, Tavella MH, Zago MA. Heterogeneous ethnic distribution of the factor V leiden mutation [Internet]. Genetics and Molecular Biology. 1999 ; 22( 2): 143-145.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1590/s1415-47571999000200001
Vancouver
Franco R, Elion J, Santos SEB, Araújo AG, Tavella MH, Zago MA. Heterogeneous ethnic distribution of the factor V leiden mutation [Internet]. Genetics and Molecular Biology. 1999 ; 22( 2): 143-145.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1590/s1415-47571999000200001
Artigo de periodico
The frequency of 844ins68 mutation in the cystathionine 'beta'-synthase gene is not increased in patients with venous thrombosis (1998)
Franco, Rendrik; Maffei, Francisco; Lourenço, Dayse; Piccinato, Carlos Eli; Morelli, Vânia; Thomazini, Isolete; Zago, Marco Antonio
Source: Haematologica. Unidade: FMRP
Assunto: DOENÇAS VASCULARES (CIRURGIA)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FRANCO, Rendrik et al. The frequency of 844ins68 mutation in the cystathionine 'beta'-synthase gene is not increased in patients with venous thrombosis. Haematologica, v. 83, p. 1006-1008, 1998Tradução . . Acesso em: 01 nov. 2024.
APA
Franco, R., Maffei, F., Lourenço, D., Piccinato, C. E., Morelli, V., Thomazini, I., & Zago, M. A. (1998). The frequency of 844ins68 mutation in the cystathionine 'beta'-synthase gene is not increased in patients with venous thrombosis. Haematologica, 83, 1006-1008.
NLM
Franco R, Maffei F, Lourenço D, Piccinato CE, Morelli V, Thomazini I, Zago MA. The frequency of 844ins68 mutation in the cystathionine 'beta'-synthase gene is not increased in patients with venous thrombosis. Haematologica. 1998 ; 83 1006-1008.[citado 2024 nov. 01 ]
Vancouver
Franco R, Maffei F, Lourenço D, Piccinato CE, Morelli V, Thomazini I, Zago MA. The frequency of 844ins68 mutation in the cystathionine 'beta'-synthase gene is not increased in patients with venous thrombosis. Haematologica. 1998 ; 83 1006-1008.[citado 2024 nov. 01 ]

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