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Artigo de periodico
Primary Immunodeficiency Diseases in Different Age Groups: A Report on 1,008 Cases from a Single Brazilian Reference Center (2013)
Carneiro-Sampaio, Magda; Moraes-Vasconcelos, Dewton; Kokron, Cristina M.; Jacob, Cristina M. A.; Toledo-Barros, Myrthes; Dorna, Mayra B.; Watanabe, Letícia A.; Marinho, Ana Karolina B. B.; Castro, Ana Paula Moschione; Pastorino, Antonio C.; Silva, Clóvis Artur A.; Ferreira, Maurício D.; Rizzo, Luiz V.; Kalil, Jorge E.; Duarte, Alberto J. S.
Source: Journal of Clinical Immunology. Unidade: FM
Subjects: DOENÇAS IMUNOLÓGICAS (PREVALÊNCIA;EPIDEMIOLOGIA), ANTICORPOS (DEFICIÊNCIA)
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ABNT
CARNEIRO-SAMPAIO, Magda et al. Primary Immunodeficiency Diseases in Different Age Groups: A Report on 1,008 Cases from a Single Brazilian Reference Center. Journal of Clinical Immunology, v. 33, n. 4, p. 716-724, 2013Tradução . . Disponível em: http://link.springer.com/content/pdf/10.1007%2Fs10875-013-9865-6.pdf. Acesso em: 18 nov. 2024.
APA
Carneiro-Sampaio, M., Moraes-Vasconcelos, D., Kokron, C. M., Jacob, C. M. A., Toledo-Barros, M., Dorna, M. B., et al. (2013). Primary Immunodeficiency Diseases in Different Age Groups: A Report on 1,008 Cases from a Single Brazilian Reference Center. Journal of Clinical Immunology, 33( 4), 716-724. doi:10.1007%2Fs10875-013-9865-6
NLM
Carneiro-Sampaio M, Moraes-Vasconcelos D, Kokron CM, Jacob CMA, Toledo-Barros M, Dorna MB, Watanabe LA, Marinho AKBB, Castro APM, Pastorino AC, Silva CAA, Ferreira MD, Rizzo LV, Kalil JE, Duarte AJS. Primary Immunodeficiency Diseases in Different Age Groups: A Report on 1,008 Cases from a Single Brazilian Reference Center [Internet]. Journal of Clinical Immunology. 2013 ; 33( 4): 716-724.[citado 2024 nov. 18 ] Available from: http://link.springer.com/content/pdf/10.1007%2Fs10875-013-9865-6.pdf
Vancouver
Carneiro-Sampaio M, Moraes-Vasconcelos D, Kokron CM, Jacob CMA, Toledo-Barros M, Dorna MB, Watanabe LA, Marinho AKBB, Castro APM, Pastorino AC, Silva CAA, Ferreira MD, Rizzo LV, Kalil JE, Duarte AJS. Primary Immunodeficiency Diseases in Different Age Groups: A Report on 1,008 Cases from a Single Brazilian Reference Center [Internet]. Journal of Clinical Immunology. 2013 ; 33( 4): 716-724.[citado 2024 nov. 18 ] Available from: http://link.springer.com/content/pdf/10.1007%2Fs10875-013-9865-6.pdf
Artigo de periodico
Hereditary Autoinflammatory Syndromes: A Brazilian Multicenter Study (2012)
Jesus, Adriana A.; Fujihira, Erika; Watase, Mariana; Terreri, Maria T.; Hilario, Maria O.; Carneiro-Sampaio, Magda; Len, Claudio A.; Oliveira, Sheila K.; Rodrigues, Marta C.; Pereira, Rosa M.; Bica, Blanca; Silva, Nilzio A.; Cavalcanti, Andre; Marini, Roberto; Sztajnbok, Flavio; Quintero, Maria V.; Ferriani, Virginia P.; Moraes-Vasconcelos, Dewton; Silva, Clovis A.; Oliveira, Joao B.
Source: Journal of Clinical Immunology. Unidades: FM, FMRP
Subjects: DOENÇAS HEREDITÁRIAS (IMUNOLOGIA;EPIDEMIOLOGIA), FENÓTIPOS, INFLAMAÇÃO, DOENÇAS GENÉTICAS (IMUNOLOGIA;DIAGNÓSTICO;AVALIAÇÃO)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
JESUS, Adriana A. et al. Hereditary Autoinflammatory Syndromes: A Brazilian Multicenter Study. Journal of Clinical Immunology, v. 32, n. 5, p. 922-932, 2012Tradução . . Disponível em: https://doi.org/10.1007/s10875-012-9688-x. Acesso em: 18 nov. 2024.
APA
Jesus, A. A., Fujihira, E., Watase, M., Terreri, M. T., Hilario, M. O., Carneiro-Sampaio, M., et al. (2012). Hereditary Autoinflammatory Syndromes: A Brazilian Multicenter Study. Journal of Clinical Immunology, 32( 5), 922-932. doi:10.1007/s10875-012-9688-x
NLM
Jesus AA, Fujihira E, Watase M, Terreri MT, Hilario MO, Carneiro-Sampaio M, Len CA, Oliveira SK, Rodrigues MC, Pereira RM, Bica B, Silva NA, Cavalcanti A, Marini R, Sztajnbok F, Quintero MV, Ferriani VP, Moraes-Vasconcelos D, Silva CA, Oliveira JB. Hereditary Autoinflammatory Syndromes: A Brazilian Multicenter Study [Internet]. Journal of Clinical Immunology. 2012 ; 32( 5): 922-932.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1007/s10875-012-9688-x
Vancouver
Jesus AA, Fujihira E, Watase M, Terreri MT, Hilario MO, Carneiro-Sampaio M, Len CA, Oliveira SK, Rodrigues MC, Pereira RM, Bica B, Silva NA, Cavalcanti A, Marini R, Sztajnbok F, Quintero MV, Ferriani VP, Moraes-Vasconcelos D, Silva CA, Oliveira JB. Hereditary Autoinflammatory Syndromes: A Brazilian Multicenter Study [Internet]. Journal of Clinical Immunology. 2012 ; 32( 5): 922-932.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1007/s10875-012-9688-x
Artigo de periodico
Phenotype–Genotype Analysis of Cryopyrin-Associated Periodic Syndromes (CAPS): Description of a Rare Non-Exon 3 and a Novel CIAS1 Missense Mutation (2008)
Jesus, Adriana A.; Silva, Clovis A.; Segundo, Gesmar R.; Aksentijevich, Ivona; Fujihira, Erika; Watanabe, Mônica; Carneiro-Sampaio, Magda; Duarte, Alberto José da Silva; Oliveira, João B.
Source: Journal of Clinical Immunology. Unidade: FM
Subjects: FENÓTIPOS, DOENÇA CRÔNICA, MANIFESTAÇÕES CUTÂNEAS, FEBRE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
JESUS, Adriana A. et al. Phenotype–Genotype Analysis of Cryopyrin-Associated Periodic Syndromes (CAPS): Description of a Rare Non-Exon 3 and a Novel CIAS1 Missense Mutation. Journal of Clinical Immunology, v. 28, n. 2, p. 134-138, 2008Tradução . . Disponível em: https://doi.org/10.1007/s10875-007-9150-7. Acesso em: 18 nov. 2024.
APA
Jesus, A. A., Silva, C. A., Segundo, G. R., Aksentijevich, I., Fujihira, E., Watanabe, M., et al. (2008). Phenotype–Genotype Analysis of Cryopyrin-Associated Periodic Syndromes (CAPS): Description of a Rare Non-Exon 3 and a Novel CIAS1 Missense Mutation. Journal of Clinical Immunology, 28( 2), 134-138. doi:10.1007/s10875-007-9150-7
NLM
Jesus AA, Silva CA, Segundo GR, Aksentijevich I, Fujihira E, Watanabe M, Carneiro-Sampaio M, Duarte AJ da S, Oliveira JB. Phenotype–Genotype Analysis of Cryopyrin-Associated Periodic Syndromes (CAPS): Description of a Rare Non-Exon 3 and a Novel CIAS1 Missense Mutation [Internet]. Journal of Clinical Immunology. 2008 ; 28( 2): 134-138.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1007/s10875-007-9150-7
Vancouver
Jesus AA, Silva CA, Segundo GR, Aksentijevich I, Fujihira E, Watanabe M, Carneiro-Sampaio M, Duarte AJ da S, Oliveira JB. Phenotype–Genotype Analysis of Cryopyrin-Associated Periodic Syndromes (CAPS): Description of a Rare Non-Exon 3 and a Novel CIAS1 Missense Mutation [Internet]. Journal of Clinical Immunology. 2008 ; 28( 2): 134-138.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1007/s10875-007-9150-7
Trabalho de evento-resumo
Cryopyrin-associated periodic syndromes: Report of two brazilian cases, incluiding a rare non-exon 3 cias 1 mutation (2007)
Jesus, Adriana; Oliveira, J. B.; Silva, Clovis; Carneiro-Sampaio, Magda; Duarte, Alberto J.; Aksentijevich, I.
Source: Abstracts Book. Conference titles: Pediatric Rheumatology European Society Congress. Unidade: FM
Subjects: FEBRE (ETIOLOGIA), MUTAÇÃO GENÉTICA, IMAGEM POR RESSONÂNCIA MAGNÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
JESUS, Adriana et al. Cryopyrin-associated periodic syndromes: Report of two brazilian cases, incluiding a rare non-exon 3 cias 1 mutation. 2007, Anais.. Istanbul: Faculdade de Medicina, Universidade de São Paulo, 2007. . Acesso em: 18 nov. 2024.
APA
Jesus, A., Oliveira, J. B., Silva, C., Carneiro-Sampaio, M., Duarte, A. J., & Aksentijevich, I. (2007). Cryopyrin-associated periodic syndromes: Report of two brazilian cases, incluiding a rare non-exon 3 cias 1 mutation. In Abstracts Book. Istanbul: Faculdade de Medicina, Universidade de São Paulo.
NLM
Jesus A, Oliveira JB, Silva C, Carneiro-Sampaio M, Duarte AJ, Aksentijevich I. Cryopyrin-associated periodic syndromes: Report of two brazilian cases, incluiding a rare non-exon 3 cias 1 mutation. Abstracts Book. 2007 ;[citado 2024 nov. 18 ]
Vancouver
Jesus A, Oliveira JB, Silva C, Carneiro-Sampaio M, Duarte AJ, Aksentijevich I. Cryopyrin-associated periodic syndromes: Report of two brazilian cases, incluiding a rare non-exon 3 cias 1 mutation. Abstracts Book. 2007 ;[citado 2024 nov. 18 ]
Trabalho de evento-resumo
TNF receptor associated periodic fever syndrome (TRAPS) caused by a novel mutation (C30F) associated with a common (2007)
Oliveira, João B.; Jesus, Adriana A.; Silva, Clovis; Carneiro-Sampaio, Magda; Duarte, Alberto J.; Aksentijevich, I.
Source: Abstracts Book. Conference titles: Pediatric Rheumatology European Society Congress. Unidade: FM
Subjects: FEBRE (ETIOLOGIA), MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
OLIVEIRA, João B. et al. TNF receptor associated periodic fever syndrome (TRAPS) caused by a novel mutation (C30F) associated with a common. 2007, Anais.. Istanbul: Faculdade de Medicina, Universidade de São Paulo, 2007. . Acesso em: 18 nov. 2024.
APA
Oliveira, J. B., Jesus, A. A., Silva, C., Carneiro-Sampaio, M., Duarte, A. J., & Aksentijevich, I. (2007). TNF receptor associated periodic fever syndrome (TRAPS) caused by a novel mutation (C30F) associated with a common. In Abstracts Book. Istanbul: Faculdade de Medicina, Universidade de São Paulo.
NLM
Oliveira JB, Jesus AA, Silva C, Carneiro-Sampaio M, Duarte AJ, Aksentijevich I. TNF receptor associated periodic fever syndrome (TRAPS) caused by a novel mutation (C30F) associated with a common. Abstracts Book. 2007 ;[citado 2024 nov. 18 ]
Vancouver
Oliveira JB, Jesus AA, Silva C, Carneiro-Sampaio M, Duarte AJ, Aksentijevich I. TNF receptor associated periodic fever syndrome (TRAPS) caused by a novel mutation (C30F) associated with a common. Abstracts Book. 2007 ;[citado 2024 nov. 18 ]

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