ReP USP - Resultado da busca

Parte de monografia/livro
Pulmonary manifestations of defects in innate immunity (2019)
Roxo-Junior, Pérsio ; Mina, Isabela; Martins, Catherine Sonaly Ferreira
Source: Pulmonary manifestations of primary immunodeficiency diseases. Unidade: FMRP
Subjects: PNEUMOPATIAS, DOENÇAS IMUNOLÓGICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ROXO-JUNIOR, Pérsio e MINA, Isabela e MARTINS, Catherine Sonaly Ferreira. Pulmonary manifestations of defects in innate immunity. Pulmonary manifestations of primary immunodeficiency diseases. Tradução . Cham: Springer Nature, 2019. . Disponível em: https://doi.org/10.1007/978-3-030-00880-2. Acesso em: 23 maio 2024.
APA
Roxo-Junior, P., Mina, I., & Martins, C. S. F. (2019). Pulmonary manifestations of defects in innate immunity. In Pulmonary manifestations of primary immunodeficiency diseases. Cham: Springer Nature. doi:10.1007/978-3-030-00880-2
NLM
Roxo-Junior P, Mina I, Martins CSF. Pulmonary manifestations of defects in innate immunity [Internet]. In: Pulmonary manifestations of primary immunodeficiency diseases. Cham: Springer Nature; 2019. [citado 2024 maio 23 ] Available from: https://doi.org/10.1007/978-3-030-00880-2
Vancouver
Roxo-Junior P, Mina I, Martins CSF. Pulmonary manifestations of defects in innate immunity [Internet]. In: Pulmonary manifestations of primary immunodeficiency diseases. Cham: Springer Nature; 2019. [citado 2024 maio 23 ] Available from: https://doi.org/10.1007/978-3-030-00880-2
Artigo de periodico
Curcuma longa L. ameliorates asthma control in children and adolescents: arandomized, double-blind, controlled trial (2019)
Manarin, Gabriel; Anderson, Daniela; Silva, Jorgete Maria e; Coppede, Juliana da Silva; Roxo-Junior, Pérsio ; Pereira, Ana Maria Soares ; Carmona, Fabio
Source: Journal of Ethnopharmacology. Unidade: FMRP
Subjects: ASMA, PEDIATRIA, AÇAFRÃO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MANARIN, Gabriel et al. Curcuma longa L. ameliorates asthma control in children and adolescents: arandomized, double-blind, controlled trial. Journal of Ethnopharmacology, v. 238, p. art. 111882 [6] , 2019Tradução . . Disponível em: https://doi.org/10.1016/j.jep.2019.111882. Acesso em: 23 maio 2024.
APA
Manarin, G., Anderson, D., Silva, J. M. e, Coppede, J. da S., Roxo-Junior, P., Pereira, A. M. S., & Carmona, F. (2019). Curcuma longa L. ameliorates asthma control in children and adolescents: arandomized, double-blind, controlled trial. Journal of Ethnopharmacology, 238, art. 111882 [6] . doi:10.1016/j.jep.2019.111882
NLM
Manarin G, Anderson D, Silva JM e, Coppede J da S, Roxo-Junior P, Pereira AMS, Carmona F. Curcuma longa L. ameliorates asthma control in children and adolescents: arandomized, double-blind, controlled trial [Internet]. Journal of Ethnopharmacology. 2019 ; 238 art. 111882 [6] .[citado 2024 maio 23 ] Available from: https://doi.org/10.1016/j.jep.2019.111882
Vancouver
Manarin G, Anderson D, Silva JM e, Coppede J da S, Roxo-Junior P, Pereira AMS, Carmona F. Curcuma longa L. ameliorates asthma control in children and adolescents: arandomized, double-blind, controlled trial [Internet]. Journal of Ethnopharmacology. 2019 ; 238 art. 111882 [6] .[citado 2024 maio 23 ] Available from: https://doi.org/10.1016/j.jep.2019.111882
Artigo de periodico-carta/editorial
Genotype‐phenotype correlations in Brazilian patients with hereditary angioedema due to C1 inhibitor deficiency. [Carta] (2019)
Maia, Luana Sella Motta ; Moreno, Adriana Santos ; Ferriani, Mariana Paes Leme; Nunes, Fernanda Leonel; Ferraro, Maria Fernanda; Dias, Marina Mendonça; Roxo-Junior, Pérsio ; Dias, Fabrício Moura; Valle, Solange Oliveira Rodrigues; Levy, Soloni ; Alonso, Maria Luiza Oliva; França, Alfeu Tavares; Serpa, Faradiba Sarquis; Motta, Antônio Abílio; Maia, Felipe Gonçalves Motta ; Aragon, Davi Casale ; Sarti, Willy; Silva Junior, Wilson Araújo da ; Bork, Konrad ; Cichon, Sven; Arruda, Luisa Karla de Paula
Source: Allergy. Unidades: FMRP, FM, ICB
Subjects: BRADICININA, ANGIOEDEMA, DOENÇAS HEREDITÁRIAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MAIA, Luana Sella Motta et al. Genotype‐phenotype correlations in Brazilian patients with hereditary angioedema due to C1 inhibitor deficiency. [Carta]. Allergy. West Sussex: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. Disponível em: https://doi.org/10.1111/all.13699. Acesso em: 23 maio 2024. , 2019
APA
Maia, L. S. M., Moreno, A. S., Ferriani, M. P. L., Nunes, F. L., Ferraro, M. F., Dias, M. M., et al. (2019). Genotype‐phenotype correlations in Brazilian patients with hereditary angioedema due to C1 inhibitor deficiency. [Carta]. Allergy. West Sussex: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. doi:10.1111/all.13699
NLM
Maia LSM, Moreno AS, Ferriani MPL, Nunes FL, Ferraro MF, Dias MM, Roxo-Junior P, Dias FM, Valle SOR, Levy S , Alonso MLO, França AT, Serpa FS, Motta AA, Maia FGM, Aragon DC, Sarti W, Silva Junior WA da, Bork K , Cichon S, Arruda LK de P. Genotype‐phenotype correlations in Brazilian patients with hereditary angioedema due to C1 inhibitor deficiency. [Carta] [Internet]. Allergy. 2019 ; 74( 5): 1013-1016.[citado 2024 maio 23 ] Available from: https://doi.org/10.1111/all.13699
Vancouver
Maia LSM, Moreno AS, Ferriani MPL, Nunes FL, Ferraro MF, Dias MM, Roxo-Junior P, Dias FM, Valle SOR, Levy S , Alonso MLO, França AT, Serpa FS, Motta AA, Maia FGM, Aragon DC, Sarti W, Silva Junior WA da, Bork K , Cichon S, Arruda LK de P. Genotype‐phenotype correlations in Brazilian patients with hereditary angioedema due to C1 inhibitor deficiency. [Carta] [Internet]. Allergy. 2019 ; 74( 5): 1013-1016.[citado 2024 maio 23 ] Available from: https://doi.org/10.1111/all.13699
Artigo de periodico
A novel homozygous JAK3 mutation leading to T-B+NK– SCID in two brazilian patients (2018)
Barreiros, Lucila Akune ; Segundo, Gesmar R. S.; Grumach, Anete S.; Roxo-Junior, Pérsio ; Torgerson, Troy R.; Ochs, Hans D.; Condino Neto, Antonio
Source: Frontiers in Pediatrics. Unidades: FMRP, ICB
Subjects: TRIAGEM, NEONATOLOGIA, SEQUENCIAMENTO GENÉTICO, SISTEMA IMUNE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BARREIROS, Lucila Akune et al. A novel homozygous JAK3 mutation leading to T-B+NK– SCID in two brazilian patients. Frontiers in Pediatrics, v. 6, 2018Tradução . . Disponível em: https://doi.org/10.3389/fped.2018.00230. Acesso em: 23 maio 2024.
APA
Barreiros, L. A., Segundo, G. R. S., Grumach, A. S., Roxo-Junior, P., Torgerson, T. R., Ochs, H. D., & Condino Neto, A. (2018). A novel homozygous JAK3 mutation leading to T-B+NK– SCID in two brazilian patients. Frontiers in Pediatrics, 6. doi:10.3389/fped.2018.00230
NLM
Barreiros LA, Segundo GRS, Grumach AS, Roxo-Junior P, Torgerson TR, Ochs HD, Condino Neto A. A novel homozygous JAK3 mutation leading to T-B+NK– SCID in two brazilian patients [Internet]. Frontiers in Pediatrics. 2018 ; 6[citado 2024 maio 23 ] Available from: https://doi.org/10.3389/fped.2018.00230
Vancouver
Barreiros LA, Segundo GRS, Grumach AS, Roxo-Junior P, Torgerson TR, Ochs HD, Condino Neto A. A novel homozygous JAK3 mutation leading to T-B+NK– SCID in two brazilian patients [Internet]. Frontiers in Pediatrics. 2018 ; 6[citado 2024 maio 23 ] Available from: https://doi.org/10.3389/fped.2018.00230
Artigo de periodico
Phenotypic IgA deficit (SIgAD) or probably (PIgAD) and related diseases associations during 4 years of research in Latin-American kids (2018)
Fernández, Carmen; Roxo-Junior, Pérsio ; Marina, S. C.; Juan, C. A. B.; Felipe, M. B.; Deysi, L. A. F.; Lorena, B.
Source: Journal of Clinical Immunology and Research. Unidade: FMRP
Subjects: ALERGIA E IMUNOLOGIA, ASMA, LEITE, VITILIGO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FERNÁNDEZ, Carmen et al. Phenotypic IgA deficit (SIgAD) or probably (PIgAD) and related diseases associations during 4 years of research in Latin-American kids. Journal of Clinical Immunology and Research, v. 1, n. 1, p. [5 ], 2018Tradução . . Disponível em: https://www.scitechnol.com/peer-review/phenotypic-iga-deficit-sigad-or-probably-pigad-and-related-diseases-associations-during-4-years-of-research-in-latinamerican-kids-axjk.pdf. Acesso em: 23 maio 2024.
APA
Fernández, C., Roxo-Junior, P., Marina, S. C., Juan, C. A. B., Felipe, M. B., Deysi, L. A. F., & Lorena, B. (2018). Phenotypic IgA deficit (SIgAD) or probably (PIgAD) and related diseases associations during 4 years of research in Latin-American kids. Journal of Clinical Immunology and Research, 1( 1), [5 ]. Recuperado de https://www.scitechnol.com/peer-review/phenotypic-iga-deficit-sigad-or-probably-pigad-and-related-diseases-associations-during-4-years-of-research-in-latinamerican-kids-axjk.pdf
NLM
Fernández C, Roxo-Junior P, Marina SC, Juan CAB, Felipe MB, Deysi LAF, Lorena B. Phenotypic IgA deficit (SIgAD) or probably (PIgAD) and related diseases associations during 4 years of research in Latin-American kids [Internet]. Journal of Clinical Immunology and Research. 2018 ; 1( 1): [5 ].[citado 2024 maio 23 ] Available from: https://www.scitechnol.com/peer-review/phenotypic-iga-deficit-sigad-or-probably-pigad-and-related-diseases-associations-during-4-years-of-research-in-latinamerican-kids-axjk.pdf
Vancouver
Fernández C, Roxo-Junior P, Marina SC, Juan CAB, Felipe MB, Deysi LAF, Lorena B. Phenotypic IgA deficit (SIgAD) or probably (PIgAD) and related diseases associations during 4 years of research in Latin-American kids [Internet]. Journal of Clinical Immunology and Research. 2018 ; 1( 1): [5 ].[citado 2024 maio 23 ] Available from: https://www.scitechnol.com/peer-review/phenotypic-iga-deficit-sigad-or-probably-pigad-and-related-diseases-associations-during-4-years-of-research-in-latinamerican-kids-axjk.pdf

USP Schools

ReP

Filtros

Authors

USP affiliated authors

Subjects

Indexado em

Non normalized affiliation

Countries of institutions of collaboration