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  • Source: Autopsy and Case Reports. Unidade: HU

    Subjects: IMUNOGLOBULINAS, LINFONODOS

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      OLMOS, Rodrigo Diaz et al. IgG4-related disease: a diagnostic challenge. Autopsy and Case Reports, v. 11, p. e2021312, 2021Tradução . . Disponível em: https://doi.org/10.4322/acr.2021.312. Acesso em: 10 out. 2024.
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      Olmos, R. D., Rodrigues, M. A. V., Ferreira, C. R., Etrusco, R. de C. F., & Romagnolli, C. (2021). IgG4-related disease: a diagnostic challenge. Autopsy and Case Reports, 11, e2021312. doi:10.4322/acr.2021.312
    • NLM

      Olmos RD, Rodrigues MAV, Ferreira CR, Etrusco R de CF, Romagnolli C. IgG4-related disease: a diagnostic challenge [Internet]. Autopsy and Case Reports. 2021 ; 11 e2021312.[citado 2024 out. 10 ] Available from: https://doi.org/10.4322/acr.2021.312
    • Vancouver

      Olmos RD, Rodrigues MAV, Ferreira CR, Etrusco R de CF, Romagnolli C. IgG4-related disease: a diagnostic challenge [Internet]. Autopsy and Case Reports. 2021 ; 11 e2021312.[citado 2024 out. 10 ] Available from: https://doi.org/10.4322/acr.2021.312
  • Source: Autopsy and Case Reports. Unidades: HU, FO

    Subjects: PATOLOGIA BUCAL, ARTICULAÇÃO TEMPOROMANDIBULAR

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      BARRETTO, Matheus Dantas de Araújo et al. Surgical treatment of a rare bilateral synovial chondromatosis. Autopsy and Case Reports, v. 10, n. 4, p. Se 2020, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.pdpdt.2020.101651. Acesso em: 10 out. 2024.
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      Barretto, M. D. de A., Kaba, S. C. P., Elias, F. M., & Deboni, M. C. Z. (2020). Surgical treatment of a rare bilateral synovial chondromatosis. Autopsy and Case Reports, 10( 4), Se 2020. doi:10.1016/j.pdpdt.2020.101651
    • NLM

      Barretto MD de A, Kaba SCP, Elias FM, Deboni MCZ. Surgical treatment of a rare bilateral synovial chondromatosis [Internet]. Autopsy and Case Reports. 2020 ; 10( 4): Se 2020.[citado 2024 out. 10 ] Available from: https://doi.org/10.1016/j.pdpdt.2020.101651
    • Vancouver

      Barretto MD de A, Kaba SCP, Elias FM, Deboni MCZ. Surgical treatment of a rare bilateral synovial chondromatosis [Internet]. Autopsy and Case Reports. 2020 ; 10( 4): Se 2020.[citado 2024 out. 10 ] Available from: https://doi.org/10.1016/j.pdpdt.2020.101651
  • Source: Autopsy and Case Reports. Unidades: HU, ICB

    Subjects: DOENÇAS CEREBRAIS, INFECÇÕES POR VÍRUS DE DNA, ENCEFALITE, SÍNDROME DE IMUNODEFICIÊNCIA ADQUIRIDA, AUTÓPSIA

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      LOPES, Cesar Castello Branco et al. Progressive multifocal leukoencephalopathy: a challenging diagnosis established at autopsy. Autopsy and Case Reports, v. 9, n. ja/mar. 2019, p. e2018063, 2019Tradução . . Disponível em: https://doi.org/10.4322/acr.2018.063. Acesso em: 10 out. 2024.
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      Lopes, C. C. B., Crivillari, M., Prado, J. C. M., Ferreira, C. R., Santos Neto, P. J. dos, Takayasu, V., & Laborda, L. S. (2019). Progressive multifocal leukoencephalopathy: a challenging diagnosis established at autopsy. Autopsy and Case Reports, 9( ja/mar. 2019), e2018063. doi:10.4322/acr.2018.063
    • NLM

      Lopes CCB, Crivillari M, Prado JCM, Ferreira CR, Santos Neto PJ dos, Takayasu V, Laborda LS. Progressive multifocal leukoencephalopathy: a challenging diagnosis established at autopsy [Internet]. Autopsy and Case Reports. 2019 ; 9( ja/mar. 2019): e2018063.[citado 2024 out. 10 ] Available from: https://doi.org/10.4322/acr.2018.063
    • Vancouver

      Lopes CCB, Crivillari M, Prado JCM, Ferreira CR, Santos Neto PJ dos, Takayasu V, Laborda LS. Progressive multifocal leukoencephalopathy: a challenging diagnosis established at autopsy [Internet]. Autopsy and Case Reports. 2019 ; 9( ja/mar. 2019): e2018063.[citado 2024 out. 10 ] Available from: https://doi.org/10.4322/acr.2018.063
  • Source: Autopsy and Case Reports. Unidades: FM, HU

    Subjects: LÚPUS ERITEMATOSO SISTÊMICO, VESÍCULA BILIAR, FARMÁCIA

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      PADRÃO, Eduardo Messias Hirano et al. Bullous systemic lupus erythematosus: a case report. Autopsy and Case Reports, v. 9, n. ja/mar. 2019, p. e2018069, 2019Tradução . . Disponível em: https://doi.org/10.4322/acr.2018.069. Acesso em: 10 out. 2024.
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      Padrão, E. M. H., Teixeira, L. F., Maruta, C. W., Aoki, V., Felipe-Silva, A., Kim, E. I. M., & Smeili, L. A. A. (2019). Bullous systemic lupus erythematosus: a case report. Autopsy and Case Reports, 9( ja/mar. 2019), e2018069. doi:10.4322/acr.2018.069
    • NLM

      Padrão EMH, Teixeira LF, Maruta CW, Aoki V, Felipe-Silva A, Kim EIM, Smeili LAA. Bullous systemic lupus erythematosus: a case report [Internet]. Autopsy and Case Reports. 2019 ; 9( ja/mar. 2019): e2018069.[citado 2024 out. 10 ] Available from: https://doi.org/10.4322/acr.2018.069
    • Vancouver

      Padrão EMH, Teixeira LF, Maruta CW, Aoki V, Felipe-Silva A, Kim EIM, Smeili LAA. Bullous systemic lupus erythematosus: a case report [Internet]. Autopsy and Case Reports. 2019 ; 9( ja/mar. 2019): e2018069.[citado 2024 out. 10 ] Available from: https://doi.org/10.4322/acr.2018.069
  • Source: Autopsy and Case Reports. Unidade: HU

    Subjects: BAÇO, DOENÇAS SANGUÍNEAS E LINFÁTICAS, NEOPLASIAS, HEMANGIOMA

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      FIORENTINO, Matheus Dalben et al. Primary splenic angiosarcoma: a rare entity often associated with rupture and hemoperitoneum. Autopsy and Case Reports, v. 9, n. 3, p. jul./se 2019, 2019Tradução . . Disponível em: https://doi.org/10.4322/acr.2019.100. Acesso em: 10 out. 2024.
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      Fiorentino, M. D., Monteiro, J. M. C., Siqueira, R. E. B. de, Kim, E. I. M., Curi, A. P., Ferreira, C. R., et al. (2019). Primary splenic angiosarcoma: a rare entity often associated with rupture and hemoperitoneum. Autopsy and Case Reports, 9( 3), jul./se 2019. doi:10.4322/acr.2019.100
    • NLM

      Fiorentino MD, Monteiro JMC, Siqueira REB de, Kim EIM, Curi AP, Ferreira CR, Nardo M, Campos FPF de. Primary splenic angiosarcoma: a rare entity often associated with rupture and hemoperitoneum [Internet]. Autopsy and Case Reports. 2019 ; 9( 3): jul./se 2019.[citado 2024 out. 10 ] Available from: https://doi.org/10.4322/acr.2019.100
    • Vancouver

      Fiorentino MD, Monteiro JMC, Siqueira REB de, Kim EIM, Curi AP, Ferreira CR, Nardo M, Campos FPF de. Primary splenic angiosarcoma: a rare entity often associated with rupture and hemoperitoneum [Internet]. Autopsy and Case Reports. 2019 ; 9( 3): jul./se 2019.[citado 2024 out. 10 ] Available from: https://doi.org/10.4322/acr.2019.100
  • Source: Autopsy and Case Reports. Unidade: HU

    Subjects: ESTENOSE TRAQUEAL, INTUBAÇÃO INTRATRAQUEAL, PRÓTESE

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      GASPAR, Márcio Teodoro da Costa et al. Tracheal stenosis due to endotracheal tube cuff hyperinflation: a preventable complication. Autopsy and Case Reports, v. 9, n. ja/mar. 2019, p. e2018072, 2019Tradução . . Disponível em: https://doi.org/10.4322/acr.2018.072. Acesso em: 10 out. 2024.
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      Gaspar, M. T. da C., Maximiano, L. F., Minamoto, H., & Otoch, J. P. (2019). Tracheal stenosis due to endotracheal tube cuff hyperinflation: a preventable complication. Autopsy and Case Reports, 9( ja/mar. 2019), e2018072. doi:10.4322/acr.2018.072
    • NLM

      Gaspar MT da C, Maximiano LF, Minamoto H, Otoch JP. Tracheal stenosis due to endotracheal tube cuff hyperinflation: a preventable complication [Internet]. Autopsy and Case Reports. 2019 ; 9( ja/mar. 2019): e2018072.[citado 2024 out. 10 ] Available from: https://doi.org/10.4322/acr.2018.072
    • Vancouver

      Gaspar MT da C, Maximiano LF, Minamoto H, Otoch JP. Tracheal stenosis due to endotracheal tube cuff hyperinflation: a preventable complication [Internet]. Autopsy and Case Reports. 2019 ; 9( ja/mar. 2019): e2018072.[citado 2024 out. 10 ] Available from: https://doi.org/10.4322/acr.2018.072
  • Source: Autopsy and Case Reports. Unidade: HU

    Subjects: ESOFAGOPATIAS, DIABETES MELLITUS, SEPSE, AUTÓPSIA

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      MONTEIRO, Jean Michell Correia et al. Black esophagus. Autopsy and Case Reports, v. 9, n. ja/mar. 2019, p. e20180077, 2019Tradução . . Disponível em: https://doi.org/10.4322/acr.2018.077. Acesso em: 10 out. 2024.
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      Monteiro, J. M. C., Castelo, L. F., Fischer, W. G. G., & Felipe-Silva, A. (2019). Black esophagus. Autopsy and Case Reports, 9( ja/mar. 2019), e20180077. doi:10.4322/acr.2018.077
    • NLM

      Monteiro JMC, Castelo LF, Fischer WGG, Felipe-Silva A. Black esophagus [Internet]. Autopsy and Case Reports. 2019 ; 9( ja/mar. 2019): e20180077.[citado 2024 out. 10 ] Available from: https://doi.org/10.4322/acr.2018.077
    • Vancouver

      Monteiro JMC, Castelo LF, Fischer WGG, Felipe-Silva A. Black esophagus [Internet]. Autopsy and Case Reports. 2019 ; 9( ja/mar. 2019): e20180077.[citado 2024 out. 10 ] Available from: https://doi.org/10.4322/acr.2018.077
  • Source: Autopsy and Case Reports. Unidade: HU

    Subjects: NECROSE, ESOFAGITE, CANDIDÍASE, MICOSES

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      PIUBELLI, Mario Luiz Marques et al. Fatal necrotizing Candida esophagitis in a patient with leukocytoclastic cutaneous vasculitis and ankylosing spondylitis. Autopsy and Case Reports, v. 9, n. apr./ju 2019, p. e2018070, 2019Tradução . . Disponível em: https://doi.org/10.4322/acr.2018.070. Acesso em: 10 out. 2024.
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      Piubelli, M. L. M., Felipe-Silva, A., Kanegae, M. Y., & Campos, F. P. F. de. (2019). Fatal necrotizing Candida esophagitis in a patient with leukocytoclastic cutaneous vasculitis and ankylosing spondylitis. Autopsy and Case Reports, 9( apr./ju 2019), e2018070. doi:10.4322/acr.2018.070
    • NLM

      Piubelli MLM, Felipe-Silva A, Kanegae MY, Campos FPF de. Fatal necrotizing Candida esophagitis in a patient with leukocytoclastic cutaneous vasculitis and ankylosing spondylitis [Internet]. Autopsy and Case Reports. 2019 ; 9( apr./ju 2019): e2018070.[citado 2024 out. 10 ] Available from: https://doi.org/10.4322/acr.2018.070
    • Vancouver

      Piubelli MLM, Felipe-Silva A, Kanegae MY, Campos FPF de. Fatal necrotizing Candida esophagitis in a patient with leukocytoclastic cutaneous vasculitis and ankylosing spondylitis [Internet]. Autopsy and Case Reports. 2019 ; 9( apr./ju 2019): e2018070.[citado 2024 out. 10 ] Available from: https://doi.org/10.4322/acr.2018.070
  • Source: Autopsy and Case Reports. Unidade: HU

    Subjects: CITOGENÉTICA, LEUCEMIA MIELOIDE AGUDA, POLIMORFISMO, ANÁLISE SEQUENCIAL, DNA

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      NORONHA, Thiago Rodrigo de e MITNE-NETO, Miguel e CHAUFFAILLE, Maria de Lourdes. JAK2-mutated acute myeloid leukemia: comparison of next-generation sequencing (NGS) and single nucleotide polymorphism array (SNPa) findings between two cases. Autopsy and Case Reports, v. 9, n. apr./ju 2019, p. e2018084, 2019Tradução . . Disponível em: https://doi.org/10.4322/acr.2018.084. Acesso em: 10 out. 2024.
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      Noronha, T. R. de, Mitne-Neto, M., & Chauffaille, M. de L. (2019). JAK2-mutated acute myeloid leukemia: comparison of next-generation sequencing (NGS) and single nucleotide polymorphism array (SNPa) findings between two cases. Autopsy and Case Reports, 9( apr./ju 2019), e2018084. doi:10.4322/acr.2018.084
    • NLM

      Noronha TR de, Mitne-Neto M, Chauffaille M de L. JAK2-mutated acute myeloid leukemia: comparison of next-generation sequencing (NGS) and single nucleotide polymorphism array (SNPa) findings between two cases [Internet]. Autopsy and Case Reports. 2019 ; 9( apr./ju 2019): e2018084.[citado 2024 out. 10 ] Available from: https://doi.org/10.4322/acr.2018.084
    • Vancouver

      Noronha TR de, Mitne-Neto M, Chauffaille M de L. JAK2-mutated acute myeloid leukemia: comparison of next-generation sequencing (NGS) and single nucleotide polymorphism array (SNPa) findings between two cases [Internet]. Autopsy and Case Reports. 2019 ; 9( apr./ju 2019): e2018084.[citado 2024 out. 10 ] Available from: https://doi.org/10.4322/acr.2018.084
  • Source: Autopsy and Case Reports. Unidade: HU

    Subjects: COMUNICAÇÃO CIENTÍFICA, EDITORAÇÃO, DOCUMENTOS ELETRÔNICOS

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      CAMPOS, Fernando Peixoto Ferraz de. Continuous publication: changing the publishing model [Editorial]. Autopsy and Case Reports. São Paulo: Hospital Universitário, Universidade de São Paulo. Disponível em: https://doi.org/10.4322/acr.2018.017. Acesso em: 10 out. 2024. , 2018
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      Campos, F. P. F. de. (2018). Continuous publication: changing the publishing model [Editorial]. Autopsy and Case Reports. São Paulo: Hospital Universitário, Universidade de São Paulo. doi:10.4322/acr.2018.017
    • NLM

      Campos FPF de. Continuous publication: changing the publishing model [Editorial] [Internet]. Autopsy and Case Reports. 2018 ; 8( ja/mar. 2018): e2018017.[citado 2024 out. 10 ] Available from: https://doi.org/10.4322/acr.2018.017
    • Vancouver

      Campos FPF de. Continuous publication: changing the publishing model [Editorial] [Internet]. Autopsy and Case Reports. 2018 ; 8( ja/mar. 2018): e2018017.[citado 2024 out. 10 ] Available from: https://doi.org/10.4322/acr.2018.017
  • Source: Autopsy and Case Reports. Unidade: HU

    Subjects: DOENÇA CELÍACA, SÍNDROME DE MALABSORÇÃO, DIARREIA

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      VALE, Rômulo Ribeiro do et al. Celiac Crisis: an unusual presentation of gluten-sensitive enteropathy. Autopsy and Case Reports, v. 8, n. 3, p. jul./se 2018, 2018Tradução . . Disponível em: https://doi.org/10.4322/acr.2018.027. Acesso em: 10 out. 2024.
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      Vale, R. R. do, Conci, N. da S., Santana, A. P., Pereira, M. B., Menezes, N. Y. H., Takayasu, V., et al. (2018). Celiac Crisis: an unusual presentation of gluten-sensitive enteropathy. Autopsy and Case Reports, 8( 3), jul./se 2018. doi:10.4322/acr.2018.027
    • NLM

      Vale RR do, Conci N da S, Santana AP, Pereira MB, Menezes NYH, Takayasu V, Laborda LS, Felipe-Silva A. Celiac Crisis: an unusual presentation of gluten-sensitive enteropathy [Internet]. Autopsy and Case Reports. 2018 ; 8( 3): jul./se 2018.[citado 2024 out. 10 ] Available from: https://doi.org/10.4322/acr.2018.027
    • Vancouver

      Vale RR do, Conci N da S, Santana AP, Pereira MB, Menezes NYH, Takayasu V, Laborda LS, Felipe-Silva A. Celiac Crisis: an unusual presentation of gluten-sensitive enteropathy [Internet]. Autopsy and Case Reports. 2018 ; 8( 3): jul./se 2018.[citado 2024 out. 10 ] Available from: https://doi.org/10.4322/acr.2018.027
  • Source: Autopsy and Case Reports. Unidade: HU

    Subjects: PROLIFERAÇÃO CELULAR, DERMATOPATIAS, DOENÇAS RARAS

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      MAXIMIANO, Linda Ferreira e GASPAR, Márcio Teodoro e NAKAHIRA, Evelyn Sue. Madelung disease (multiple symmetric lipomatosis). Autopsy and Case Reports, v. 8, n. 3, p. jul./se 2018, 2018Tradução . . Disponível em: https://doi.org/10.4322/acr.2018.030. Acesso em: 10 out. 2024.
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      Maximiano, L. F., Gaspar, M. T., & Nakahira, E. S. (2018). Madelung disease (multiple symmetric lipomatosis). Autopsy and Case Reports, 8( 3), jul./se 2018. doi:10.4322/acr.2018.030
    • NLM

      Maximiano LF, Gaspar MT, Nakahira ES. Madelung disease (multiple symmetric lipomatosis) [Internet]. Autopsy and Case Reports. 2018 ; 8( 3): jul./se 2018.[citado 2024 out. 10 ] Available from: https://doi.org/10.4322/acr.2018.030
    • Vancouver

      Maximiano LF, Gaspar MT, Nakahira ES. Madelung disease (multiple symmetric lipomatosis) [Internet]. Autopsy and Case Reports. 2018 ; 8( 3): jul./se 2018.[citado 2024 out. 10 ] Available from: https://doi.org/10.4322/acr.2018.030
  • Source: Autopsy and Case Reports. Unidade: HU

    Subjects: HISTOPLASMA, PNEUMOPATIAS, GRANULOMA

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      MATOS, Paulo Marcelo Pontes Gomes de e FELIPE-SILVA, Aloisio e OTOCH, José Pinhata. Pulmonary histoplasmoma: a disguised malady. Autopsy and Case Reports, v. 8, n. 4, p. e2018065, 2018Tradução . . Disponível em: https://doi.org/10.4322/acr.2018.065. Acesso em: 10 out. 2024.
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      Matos, P. M. P. G. de, Felipe-Silva, A., & Otoch, J. P. (2018). Pulmonary histoplasmoma: a disguised malady. Autopsy and Case Reports, 8( 4), e2018065. doi:10.4322/acr.2018.065
    • NLM

      Matos PMPG de, Felipe-Silva A, Otoch JP. Pulmonary histoplasmoma: a disguised malady [Internet]. Autopsy and Case Reports. 2018 ; 8( 4): e2018065.[citado 2024 out. 10 ] Available from: https://doi.org/10.4322/acr.2018.065
    • Vancouver

      Matos PMPG de, Felipe-Silva A, Otoch JP. Pulmonary histoplasmoma: a disguised malady [Internet]. Autopsy and Case Reports. 2018 ; 8( 4): e2018065.[citado 2024 out. 10 ] Available from: https://doi.org/10.4322/acr.2018.065
  • Source: Autopsy and Case Reports. Unidade: HU

    Subjects: ENDOCARDITE, EMBOLIA PULMONAR, ESTENOSE DA VALVA AÓRTICA, INSUFICIÊNCIA CARDÍACA

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      CAMPOS, Fernando Peixoto Ferraz de et al. Non-infectious thrombotic endocarditis. Autopsy and Case Reports, v. 8, n. abr./ju 2018, p. e2018020, 2018Tradução . . Disponível em: https://doi.org/10.4322/acr.2018.020. Acesso em: 10 out. 2024.
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      Campos, F. P. F. de, Takayasu, V., Kim, E. I. M., & Benvenuti, L. A. (2018). Non-infectious thrombotic endocarditis. Autopsy and Case Reports, 8( abr./ju 2018), e2018020. doi:10.4322/acr.2018.020
    • NLM

      Campos FPF de, Takayasu V, Kim EIM, Benvenuti LA. Non-infectious thrombotic endocarditis [Internet]. Autopsy and Case Reports. 2018 ; 8( abr./ju 2018): e2018020.[citado 2024 out. 10 ] Available from: https://doi.org/10.4322/acr.2018.020
    • Vancouver

      Campos FPF de, Takayasu V, Kim EIM, Benvenuti LA. Non-infectious thrombotic endocarditis [Internet]. Autopsy and Case Reports. 2018 ; 8( abr./ju 2018): e2018020.[citado 2024 out. 10 ] Available from: https://doi.org/10.4322/acr.2018.020
  • Source: Autopsy and Case Reports. Unidades: HU, FM

    Subjects: ACIDENTE VASCULAR CEREBRAL, ISQUEMIA CEREBRAL, PROCEDIMENTOS CIRÚRGICOS OPERATÓRIOS

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      CAMPOS, Fernando Peixoto Ferraz de et al. Traumatic injury to the internal carotid artery by the hyoid bone: a rare cause of ischemic stroke. Autopsy and Case Reports, v. 8, n. ja/mar. 2018, p. e2018010, 2018Tradução . . Disponível em: https://doi.org/10.4322/acr.2018.010. Acesso em: 10 out. 2024.
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      Campos, F. P. F. de, Kanegae, M. Y., Aiello, V. D., Santos Neto, P. J. dos, Gratão, T. C., & Silva, E. S. da. (2018). Traumatic injury to the internal carotid artery by the hyoid bone: a rare cause of ischemic stroke. Autopsy and Case Reports, 8( ja/mar. 2018), e2018010. doi:10.4322/acr.2018.010
    • NLM

      Campos FPF de, Kanegae MY, Aiello VD, Santos Neto PJ dos, Gratão TC, Silva ES da. Traumatic injury to the internal carotid artery by the hyoid bone: a rare cause of ischemic stroke [Internet]. Autopsy and Case Reports. 2018 ; 8( ja/mar. 2018): e2018010.[citado 2024 out. 10 ] Available from: https://doi.org/10.4322/acr.2018.010
    • Vancouver

      Campos FPF de, Kanegae MY, Aiello VD, Santos Neto PJ dos, Gratão TC, Silva ES da. Traumatic injury to the internal carotid artery by the hyoid bone: a rare cause of ischemic stroke [Internet]. Autopsy and Case Reports. 2018 ; 8( ja/mar. 2018): e2018010.[citado 2024 out. 10 ] Available from: https://doi.org/10.4322/acr.2018.010
  • Source: Autopsy and Case Reports. Unidade: HU

    Subjects: NEOPLASIAS ABDOMINAIS, CARCINOMA, MEDULA ÓSSEA, METÁSTASE NEOPLÁSICA

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      TAKAYASU, Vilma et al. Bicytopenia and leukoerythroblastosis: a rare initial presentation of signet ring cell gastric adenocarcinoma. Autopsy and Case Reports, v. 7, n. abr./ju 2017, p. 55-60, 2017Tradução . . Disponível em: https://doi.org/10.4322/acr.2017.014. Acesso em: 10 out. 2024.
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      Takayasu, V., Goto, E. H., Casagrande, M. Z., Miranda, P. G. de A., Diniz, G. B. de F., Monteiro, M. F., & Felipe-Silva, A. (2017). Bicytopenia and leukoerythroblastosis: a rare initial presentation of signet ring cell gastric adenocarcinoma. Autopsy and Case Reports, 7( abr./ju 2017), 55-60. doi:10.4322/acr.2017.014
    • NLM

      Takayasu V, Goto EH, Casagrande MZ, Miranda PG de A, Diniz GB de F, Monteiro MF, Felipe-Silva A. Bicytopenia and leukoerythroblastosis: a rare initial presentation of signet ring cell gastric adenocarcinoma [Internet]. Autopsy and Case Reports. 2017 ; 7( abr./ju 2017): 55-60.[citado 2024 out. 10 ] Available from: https://doi.org/10.4322/acr.2017.014
    • Vancouver

      Takayasu V, Goto EH, Casagrande MZ, Miranda PG de A, Diniz GB de F, Monteiro MF, Felipe-Silva A. Bicytopenia and leukoerythroblastosis: a rare initial presentation of signet ring cell gastric adenocarcinoma [Internet]. Autopsy and Case Reports. 2017 ; 7( abr./ju 2017): 55-60.[citado 2024 out. 10 ] Available from: https://doi.org/10.4322/acr.2017.014
  • Source: Autopsy and Case Reports. Unidade: HU

    Subjects: ACTINOMICOSE, ABSCESSO, FÍSTULA

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    • ABNT

      NAKAHIRA, Evelyn Sue et al. Abdominal and pelvic actinomycosis due to longstanding intrauterine device: a slow and devastating infection. Autopsy and Case Reports, v. 7, n. ja/mar. 2017, p. 43-47, 2017Tradução . . Disponível em: https://doi.org/10.4322/acr.2017.001. Acesso em: 10 out. 2024.
    • APA

      Nakahira, E. S., Maximiano, L. F., Lima, F. R., & Ussami, E. Y. (2017). Abdominal and pelvic actinomycosis due to longstanding intrauterine device: a slow and devastating infection. Autopsy and Case Reports, 7( ja/mar. 2017), 43-47. doi:10.4322/acr.2017.001
    • NLM

      Nakahira ES, Maximiano LF, Lima FR, Ussami EY. Abdominal and pelvic actinomycosis due to longstanding intrauterine device: a slow and devastating infection [Internet]. Autopsy and Case Reports. 2017 ; 7( ja/mar. 2017): 43-47.[citado 2024 out. 10 ] Available from: https://doi.org/10.4322/acr.2017.001
    • Vancouver

      Nakahira ES, Maximiano LF, Lima FR, Ussami EY. Abdominal and pelvic actinomycosis due to longstanding intrauterine device: a slow and devastating infection [Internet]. Autopsy and Case Reports. 2017 ; 7( ja/mar. 2017): 43-47.[citado 2024 out. 10 ] Available from: https://doi.org/10.4322/acr.2017.001
  • Source: Autopsy and Case Reports. Unidade: HU

    Subjects: HEMOGLOBINAS, MEDULA ÓSSEA, NECROSE, EMBOLIA

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    • ABNT

      TARGUETA, Eduardo Pelegrineti et al. Bone marrow necrosis and fat embolism syndrome: a dreadful complication of hemoglobin sickle cell disease. Autopsy and Case Reports, v. 7, n. 4, p. 42-50, 2017Tradução . . Disponível em: https://doi.org/10.4322/acr.2017.043. Acesso em: 10 out. 2024.
    • APA

      Targueta, E. P., Hirano, A. C. de G., Campos, F. P. F. de, Martines, J. A. dos S., Lovisolo, S. M., & Felipe-Silva, A. (2017). Bone marrow necrosis and fat embolism syndrome: a dreadful complication of hemoglobin sickle cell disease. Autopsy and Case Reports, 7( 4), 42-50. doi:10.4322/acr.2017.043
    • NLM

      Targueta EP, Hirano AC de G, Campos FPF de, Martines JA dos S, Lovisolo SM, Felipe-Silva A. Bone marrow necrosis and fat embolism syndrome: a dreadful complication of hemoglobin sickle cell disease [Internet]. Autopsy and Case Reports. 2017 ; 7( 4): 42-50.[citado 2024 out. 10 ] Available from: https://doi.org/10.4322/acr.2017.043
    • Vancouver

      Targueta EP, Hirano AC de G, Campos FPF de, Martines JA dos S, Lovisolo SM, Felipe-Silva A. Bone marrow necrosis and fat embolism syndrome: a dreadful complication of hemoglobin sickle cell disease [Internet]. Autopsy and Case Reports. 2017 ; 7( 4): 42-50.[citado 2024 out. 10 ] Available from: https://doi.org/10.4322/acr.2017.043
  • Source: Autopsy and Case Reports. Unidade: HU

    Subjects: ACIDENTE VASCULAR CEREBRAL, ENXAQUECA

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    • ABNT

      KRELING, Gabriel Afonso Dutra e ALMEIDA NETO, Neuro Rodrigues e SANTOS NETO, Pedro José dos. Migrainous infarction: a rare and often overlooked diagnosis. Autopsy and Case Reports, v. 7, n. abr./ju 2017, p. 61-68, 2017Tradução . . Disponível em: https://doi.org/10.4322/acr.2017.018. Acesso em: 10 out. 2024.
    • APA

      Kreling, G. A. D., Almeida Neto, N. R., & Santos Neto, P. J. dos. (2017). Migrainous infarction: a rare and often overlooked diagnosis. Autopsy and Case Reports, 7( abr./ju 2017), 61-68. doi:10.4322/acr.2017.018
    • NLM

      Kreling GAD, Almeida Neto NR, Santos Neto PJ dos. Migrainous infarction: a rare and often overlooked diagnosis [Internet]. Autopsy and Case Reports. 2017 ; 7( abr./ju 2017): 61-68.[citado 2024 out. 10 ] Available from: https://doi.org/10.4322/acr.2017.018
    • Vancouver

      Kreling GAD, Almeida Neto NR, Santos Neto PJ dos. Migrainous infarction: a rare and often overlooked diagnosis [Internet]. Autopsy and Case Reports. 2017 ; 7( abr./ju 2017): 61-68.[citado 2024 out. 10 ] Available from: https://doi.org/10.4322/acr.2017.018
  • Source: Autopsy and Case Reports. Unidade: HU

    Subjects: ENFISEMA PULMONAR, FIBROSE PULMONAR, HIPERTENSÃO PULMONAR, DOENÇA CARDIOPULMONAR, AUTÓPSIA

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      HIRANO, André Carramenha de Góes et al. Severe pulmonary hypertension due to combined pulmonary fibrosis and emphysema: another cause of death among smokers. Autopsy and Case Reports, v. 7, n. abr./ju 2017, p. 15-26, 2017Tradução . . Disponível em: https://doi.org/10.4322/acr.2017.022. Acesso em: 10 out. 2024.
    • APA

      Hirano, A. C. de G., Targueta, E. P., Campos, F. P. F. de, Martines, J. A. dos S., Andrade, D., Lovisolo, S. M., & Felipe-Silva, A. (2017). Severe pulmonary hypertension due to combined pulmonary fibrosis and emphysema: another cause of death among smokers. Autopsy and Case Reports, 7( abr./ju 2017), 15-26. doi:10.4322/acr.2017.022
    • NLM

      Hirano AC de G, Targueta EP, Campos FPF de, Martines JA dos S, Andrade D, Lovisolo SM, Felipe-Silva A. Severe pulmonary hypertension due to combined pulmonary fibrosis and emphysema: another cause of death among smokers [Internet]. Autopsy and Case Reports. 2017 ; 7( abr./ju 2017): 15-26.[citado 2024 out. 10 ] Available from: https://doi.org/10.4322/acr.2017.022
    • Vancouver

      Hirano AC de G, Targueta EP, Campos FPF de, Martines JA dos S, Andrade D, Lovisolo SM, Felipe-Silva A. Severe pulmonary hypertension due to combined pulmonary fibrosis and emphysema: another cause of death among smokers [Internet]. Autopsy and Case Reports. 2017 ; 7( abr./ju 2017): 15-26.[citado 2024 out. 10 ] Available from: https://doi.org/10.4322/acr.2017.022

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