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Artigo de periodico-carta/editorial
Newborn screening for inborn errors of immunity in Brazil [Carta] (2025)
Aranda, Carolina Sanchez ; Pimentel, Mariana de Gouveia-Pereira ; Guimarães, Rafaela Rôla Leite; Fernandes, Juliana Folloni ; Rizzo, Maria Candida Faria Varanda ; Ishizuka, Edson Kiyotaka ; Oliveira Junior, Edgar Borges de ; Hadachi, Sonia Marchezi ; Hayashi, Giselle Yuri ; Andrade, Carlos Eugênio Fernandez de ; Mauro, Athenê Maria de Marco França ; Solé, Dirceu ; Condino Neto, Antonio
Fonte: Pediatric Allergy and Immunology. Unidade: ICB
Assuntos: IMUNOLOGIA, IMUNODEFICIÊNCIA DE VARIÁVEL COMUM, CRIANÇAS, TRIAGEM, IMUNIDADE, IMUNOFENOTIPAGEM
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ABNT
ARANDA, Carolina Sanchez et al. Newborn screening for inborn errors of immunity in Brazil [Carta]. Pediatric Allergy and Immunology. Chichester: Instituto de Ciências Biomédicas, Universidade de São Paulo. Disponível em: https://doi.org/10.1111/pai.70047. Acesso em: 14 out. 2025. , 2025
APA
Aranda, C. S., Pimentel, M. de G. -P., Guimarães, R. R. L., Fernandes, J. F., Rizzo, M. C. F. V., Ishizuka, E. K., et al. (2025). Newborn screening for inborn errors of immunity in Brazil [Carta]. Pediatric Allergy and Immunology. Chichester: Instituto de Ciências Biomédicas, Universidade de São Paulo. doi:10.1111/pai.70047
NLM
Aranda CS, Pimentel M de G-P, Guimarães RRL, Fernandes JF, Rizzo MCFV, Ishizuka EK, Oliveira Junior EB de, Hadachi SM, Hayashi GY, Andrade CEF de, Mauro AM de MF, Solé D, Condino Neto A. Newborn screening for inborn errors of immunity in Brazil [Carta] [Internet]. Pediatric Allergy and Immunology. 2025 ; 36( 2): 4 .[citado 2025 out. 14 ] Available from: https://doi.org/10.1111/pai.70047
Vancouver
Aranda CS, Pimentel M de G-P, Guimarães RRL, Fernandes JF, Rizzo MCFV, Ishizuka EK, Oliveira Junior EB de, Hadachi SM, Hayashi GY, Andrade CEF de, Mauro AM de MF, Solé D, Condino Neto A. Newborn screening for inborn errors of immunity in Brazil [Carta] [Internet]. Pediatric Allergy and Immunology. 2025 ; 36( 2): 4 .[citado 2025 out. 14 ] Available from: https://doi.org/10.1111/pai.70047
Artigo de periodico
Nutritional status and metabolic alterations in patients with ataxia-telangiectasia (2025)
Leon, Cristiano do Amaral de ; Amantea, Sérgio Luis ; Pereira, Renan Augusto ; Dantas, Ellen O.; Loekmanwidjaja, Jéssica; Costa-Carvalho, Beatriz T. ; Mazzucchelli, Juliana Themudo Lessa; Aranda, Carolina Sanchez ; Gonzalez-Serrano, Maria Edith ; Cordoba, Elizabeth Alejandra De La Cruz ; Bezrodnik, Liliana ; Moreira, Ileana ; Ferreira, Janáira Fernandes Severo ; Dantas, Vera Maria ; Sales, Valéria S. F.; Navarrete, Carmen Luz; Vilela, Maria Marluce dos Santos ; Motta, Isabella P.; Franco, Jose Luis; Orrengo-Arango, Julio Cesar ; Álvarez-Álvarez, Jesús Armando ; Riaño Cardozo, Lina Rocio; Orellana, Julio Cesar ; Kokron, Cristina Maria ; Barros, Myrthes Toledo ; Regairaz, Lorena ; Cabanillas, Diana ; Suarez, Carmen L. N.; Rosario Filho, Nelson Augusto ; Chong Neto, Herberto José ; Takano, Olga Akiko ; Nadaf, Maria Isabel S. Valdomir ; Moraes, Lillian S. L. ; Tavares, Fabíola Scancetti ; Rabelo, Flaviane; Escobar, Jessica Pino ; Calderon, Wilmer C.; Mendoza-Quispe, Daniel; Goudouris, Ekaterini Simões ; Patiño, Virginia ; Montenegro, Cecilia; Souza, Monica S.; Branco, Aniela B. Xexe Castelo ; Forte, Wilma Carvalho Neves ; Carvalho, Flavia Amendola Anisio de ; Segundo, Gesmar Rodrigues Silva ; Cheik, Marina F. A. ; Roxo Júnior, Pérsio ; Peres, Maryanna; Oliveira, Annie M.; Neto, Arnaldo C. P.; Ortega-López, Maria Claudia ; Lozano, Alejandro ; Lozano, Natalia Andrea ; Hernández-Nieto, Leticia ; Grumach, Anete Sevciovi ; Costa, Daniele C.; Antunes, Nelma Maria Neves ; Nudelman, Victor ; Pereira, Camila T. M.; Martinez, Maria D. M.; Quiroz, Francisco J. R.; Cardona, Aristóteles Álvarez ; Nuñez-Nuñez, Maria Enriqueta ; Rodriguez, Jairo A.; Cuellar, Célia M.; Vijoditz, Gustavo ; Bichuetti-Silva, Danielli Christinni ; Prando, Carolina Cardoso de Mello ; Condino Neto, Antonio
Fonte: Orphanet Journal of Rare Diseases. Unidades: FM, FMRP, ICB
Assuntos: IMUNOLOGIA, DOENÇAS GENÉTICAS, DOENÇAS HEREDITÁRIAS, DOENÇAS METABÓLICAS, REPARAÇÃO DE DNA, DESNUTRIÇÃO, VASOS SANGUÍNEOS, HEPATOPATIAS, COORDENAÇÃO MOTORA
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ABNT
LEON, Cristiano do Amaral de et al. Nutritional status and metabolic alterations in patients with ataxia-telangiectasia. Orphanet Journal of Rare Diseases, v. 20, n. 1, p. 9 , 2025Tradução . . Disponível em: https://doi.org/10.1186/s13023-025-03785-2. Acesso em: 14 out. 2025.
APA
Leon, C. do A. de, Amantea, S. L., Pereira, R. A., Dantas, E. O., Loekmanwidjaja, J., Costa-Carvalho, B. T., et al. (2025). Nutritional status and metabolic alterations in patients with ataxia-telangiectasia. Orphanet Journal of Rare Diseases, 20( 1), 9 . doi:10.1186/s13023-025-03785-2
NLM
Leon C do A de, Amantea SL, Pereira RA, Dantas EO, Loekmanwidjaja J, Costa-Carvalho BT, Mazzucchelli JTL, Aranda CS, Gonzalez-Serrano ME, Cordoba EADLC, Bezrodnik L, Moreira I, Ferreira JFS, Dantas VM, Sales VSF, Navarrete CL, Vilela MM dos S, Motta IP, Franco JL, Orrengo-Arango JC, Álvarez-Álvarez JA, Riaño Cardozo LR, Orellana JC, Kokron CM, Barros MT, Regairaz L, Cabanillas D, Suarez CLN, Rosario Filho NA, Chong Neto HJ, Takano OA, Nadaf MISV, Moraes LSL, Tavares FS, Rabelo F, Escobar JP, Calderon WC, Mendoza-Quispe D, Goudouris ES, Patiño V, Montenegro C, Souza MS, Branco ABXC, Forte WCN, Carvalho FAA de, Segundo GRS, Cheik MFA, Roxo Júnior P, Peres M, Oliveira AM, Neto ACP, Ortega-López MC, Lozano A, Lozano NA, Hernández-Nieto L, Grumach AS, Costa DC, Antunes NMN, Nudelman V, Pereira CTM, Martinez MDM, Quiroz FJR, Cardona AÁ, Nuñez-Nuñez ME, Rodriguez JA, Cuellar CM, Vijoditz G, Bichuetti-Silva DC, Prando CC de M, Condino Neto A. Nutritional status and metabolic alterations in patients with ataxia-telangiectasia [Internet]. Orphanet Journal of Rare Diseases. 2025 ; 20( 1): 9 .[citado 2025 out. 14 ] Available from: https://doi.org/10.1186/s13023-025-03785-2
Vancouver
Leon C do A de, Amantea SL, Pereira RA, Dantas EO, Loekmanwidjaja J, Costa-Carvalho BT, Mazzucchelli JTL, Aranda CS, Gonzalez-Serrano ME, Cordoba EADLC, Bezrodnik L, Moreira I, Ferreira JFS, Dantas VM, Sales VSF, Navarrete CL, Vilela MM dos S, Motta IP, Franco JL, Orrengo-Arango JC, Álvarez-Álvarez JA, Riaño Cardozo LR, Orellana JC, Kokron CM, Barros MT, Regairaz L, Cabanillas D, Suarez CLN, Rosario Filho NA, Chong Neto HJ, Takano OA, Nadaf MISV, Moraes LSL, Tavares FS, Rabelo F, Escobar JP, Calderon WC, Mendoza-Quispe D, Goudouris ES, Patiño V, Montenegro C, Souza MS, Branco ABXC, Forte WCN, Carvalho FAA de, Segundo GRS, Cheik MFA, Roxo Júnior P, Peres M, Oliveira AM, Neto ACP, Ortega-López MC, Lozano A, Lozano NA, Hernández-Nieto L, Grumach AS, Costa DC, Antunes NMN, Nudelman V, Pereira CTM, Martinez MDM, Quiroz FJR, Cardona AÁ, Nuñez-Nuñez ME, Rodriguez JA, Cuellar CM, Vijoditz G, Bichuetti-Silva DC, Prando CC de M, Condino Neto A. Nutritional status and metabolic alterations in patients with ataxia-telangiectasia [Internet]. Orphanet Journal of Rare Diseases. 2025 ; 20( 1): 9 .[citado 2025 out. 14 ] Available from: https://doi.org/10.1186/s13023-025-03785-2
Artigo de periodico-carta/editorial
Editorial: Community series in primary immunodeficiencies worldwide, volume II (2025)
Condino Neto, Antonio ; Korganow, Anne-Sophie; Kanegane, Hirokazu
Fonte: Frontiers in Immunology. Unidade: ICB
Assuntos: IMUNOLOGIA, IMUNODEFICIÊNCIA DE VARIÁVEL COMUM, DOENÇAS IMUNOLÓGICAS, SÍNDROMES DE DEFICIÊNCIA IMUNOLÓGICA, IMUNIDADE, TRIAGEM, RECÉM-NASCIDO, EPIDEMIOLOGIA
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ABNT
CONDINO NETO, Antonio e KORGANOW, Anne-Sophie e KANEGANE, Hirokazu. Editorial: Community series in primary immunodeficiencies worldwide, volume II. Frontiers in Immunology. Lausanne: Instituto de Ciências Biomédicas, Universidade de São Paulo. Disponível em: https://doi.org/10.3389/fimmu.2025.1564959. Acesso em: 14 out. 2025. , 2025
APA
Condino Neto, A., Korganow, A. -S., & Kanegane, H. (2025). Editorial: Community series in primary immunodeficiencies worldwide, volume II. Frontiers in Immunology. Lausanne: Instituto de Ciências Biomédicas, Universidade de São Paulo. doi:10.3389/fimmu.2025.1564959
NLM
Condino Neto A, Korganow A-S, Kanegane H. Editorial: Community series in primary immunodeficiencies worldwide, volume II [Internet]. Frontiers in Immunology. 2025 ; 16 3 .[citado 2025 out. 14 ] Available from: https://doi.org/10.3389/fimmu.2025.1564959
Vancouver
Condino Neto A, Korganow A-S, Kanegane H. Editorial: Community series in primary immunodeficiencies worldwide, volume II [Internet]. Frontiers in Immunology. 2025 ; 16 3 .[citado 2025 out. 14 ] Available from: https://doi.org/10.3389/fimmu.2025.1564959
Artigo de periodico
The Latin American Society for Immunodeficiencies Registry (2025)
Seminario, Gisela; Gonzalez-Serrano, Maria Edith ; Aranda, Carolina Sanchez ; Grumach, Anete Sevciovic ; Segundo, Gesmar Rodrigues Silva ; Regairaz, Lorena ; Cardona, Aristóteles Álvarez ; Becerra, Juan Carlos Aldave ; Poli, Cecilia; King, Alejandra ; Fernandes, Fatima Rodrigues ; Leiva, Lily; Franco, Jose Luis; Espinosa-Rosales, Francisco Javier ; Sorensen, Ricardo; Carvalho, Beatriz Tavares Costa ; Bezrodnik, Liliana ; Condino Neto, Antonio
Fonte: Journal of Clinical Immunology. Unidade: ICB
Assuntos: IMUNOLOGIA, IMUNODEFICIÊNCIA DE VARIÁVEL COMUM, HEMATOPOESE, ANTICORPOS, CÉLULAS-TRONCO
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ABNT
SEMINARIO, Gisela et al. The Latin American Society for Immunodeficiencies Registry. Journal of Clinical Immunology, v. 45, n. 1, p. 9 , 2025Tradução . . Disponível em: https://doi.org/10.1007/s10875-024-01822-6. Acesso em: 14 out. 2025.
APA
Seminario, G., Gonzalez-Serrano, M. E., Aranda, C. S., Grumach, A. S., Segundo, G. R. S., Regairaz, L., et al. (2025). The Latin American Society for Immunodeficiencies Registry. Journal of Clinical Immunology, 45( 1), 9 . doi:10.1007/s10875-024-01822-6
NLM
Seminario G, Gonzalez-Serrano ME, Aranda CS, Grumach AS, Segundo GRS, Regairaz L, Cardona AÁ, Becerra JCA, Poli C, King A, Fernandes FR, Leiva L, Franco JL, Espinosa-Rosales FJ, Sorensen R, Carvalho BTC, Bezrodnik L, Condino Neto A. The Latin American Society for Immunodeficiencies Registry [Internet]. Journal of Clinical Immunology. 2025 ; 45( 1): 9 .[citado 2025 out. 14 ] Available from: https://doi.org/10.1007/s10875-024-01822-6
Vancouver
Seminario G, Gonzalez-Serrano ME, Aranda CS, Grumach AS, Segundo GRS, Regairaz L, Cardona AÁ, Becerra JCA, Poli C, King A, Fernandes FR, Leiva L, Franco JL, Espinosa-Rosales FJ, Sorensen R, Carvalho BTC, Bezrodnik L, Condino Neto A. The Latin American Society for Immunodeficiencies Registry [Internet]. Journal of Clinical Immunology. 2025 ; 45( 1): 9 .[citado 2025 out. 14 ] Available from: https://doi.org/10.1007/s10875-024-01822-6
Artigo de periodico
First Brazilian case report of unrelated patients with identical ISG15 mutation (2025)
Napoleão, Sarah Maria da Silva ; Salgado, Ranieri Coelho ; Ferreira, Janáira Fernandes Severo ; Dorna, Mayra de Barros ; Moura, Thais Costa Lima de; França, Tábata Takahashi ; Barreiros, Lucila Akune ; Gomes, Lillian Nunes ; Gomes, Lillian Nunes ; Condino Neto, Antonio
Fonte: Journal of Clinical Immunology. Unidade: ICB
Assuntos: IMUNOLOGIA, MYCOBACTERIUM, INFECÇÕES BACTERIANAS GRAM-POSITIVAS, IMUNODEFICIÊNCIA DE VARIÁVEL COMUM, CITOCINAS, CRIANÇAS EM IDADE PRÉ-ESCOLAR, VARIAÇÃO GENÉTICA, MUTAÇÃO GENÉTICA, PREDISPOSIÇÃO GENÉTICA PARA DOENÇA
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NAPOLEÃO, Sarah Maria da Silva et al. First Brazilian case report of unrelated patients with identical ISG15 mutation. Journal of Clinical Immunology, v. 45, n. 21, p. 21 , 2025Tradução . . Disponível em: https://doi.org/10.1007/s10875-024-01811-9. Acesso em: 14 out. 2025.
APA
Napoleão, S. M. da S., Salgado, R. C., Ferreira, J. F. S., Dorna, M. de B., Moura, T. C. L. de, França, T. T., et al. (2025). First Brazilian case report of unrelated patients with identical ISG15 mutation. Journal of Clinical Immunology, 45( 21), 21 . doi:10.1007/s10875-024-01811-9
NLM
Napoleão SM da S, Salgado RC, Ferreira JFS, Dorna M de B, Moura TCL de, França TT, Barreiros LA, Gomes LN, Gomes LN, Condino Neto A. First Brazilian case report of unrelated patients with identical ISG15 mutation [Internet]. Journal of Clinical Immunology. 2025 ; 45( 21): 21 .[citado 2025 out. 14 ] Available from: https://doi.org/10.1007/s10875-024-01811-9
Vancouver
Napoleão SM da S, Salgado RC, Ferreira JFS, Dorna M de B, Moura TCL de, França TT, Barreiros LA, Gomes LN, Gomes LN, Condino Neto A. First Brazilian case report of unrelated patients with identical ISG15 mutation [Internet]. Journal of Clinical Immunology. 2025 ; 45( 21): 21 .[citado 2025 out. 14 ] Available from: https://doi.org/10.1007/s10875-024-01811-9
Artigo de periodico-carta/editorial
Duplication of exons 8–9 in NCF2 leading to incomplete clinical penetrance in Chronic Granulomatous Disease (2024)
Hernandez, Marco Antonio Venancio ; Flores, Carlos Sanchez ; Juárez, María Jiménez ; Galicia, Lizbeth Blancas ; Espinosa-Padilla, Sara ; Condino Neto, Antonio
Fonte: Journal of Clinical Immunology. Unidade: ICB
Assuntos: IMUNOLOGIA, DOENÇAS GENÉTICAS, MUTAÇÃO GENÉTICA, NEUTRÓFILOS, EXONS, OXIDAÇÃO
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ABNT
HERNANDEZ, Marco Antonio Venancio et al. Duplication of exons 8–9 in NCF2 leading to incomplete clinical penetrance in Chronic Granulomatous Disease. Journal of Clinical Immunology. New York: Springer New York LLC. Disponível em: https://doi.org/10.1007/s10875-023-01624-2. Acesso em: 14 out. 2025. , 2024
APA
Hernandez, M. A. V., Flores, C. S., Juárez, M. J., Galicia, L. B., Espinosa-Padilla, S., & Condino Neto, A. (2024). Duplication of exons 8–9 in NCF2 leading to incomplete clinical penetrance in Chronic Granulomatous Disease. Journal of Clinical Immunology. New York: Springer New York LLC. doi:10.1007/s10875-023-01624-2
NLM
Hernandez MAV, Flores CS, Juárez MJ, Galicia LB, Espinosa-Padilla S, Condino Neto A. Duplication of exons 8–9 in NCF2 leading to incomplete clinical penetrance in Chronic Granulomatous Disease [Internet]. Journal of Clinical Immunology. 2024 ; 44( 1): 4 .[citado 2025 out. 14 ] Available from: https://doi.org/10.1007/s10875-023-01624-2
Vancouver
Hernandez MAV, Flores CS, Juárez MJ, Galicia LB, Espinosa-Padilla S, Condino Neto A. Duplication of exons 8–9 in NCF2 leading to incomplete clinical penetrance in Chronic Granulomatous Disease [Internet]. Journal of Clinical Immunology. 2024 ; 44( 1): 4 .[citado 2025 out. 14 ] Available from: https://doi.org/10.1007/s10875-023-01624-2
Artigo de periodico
Newborn screening for inborn errors of immunity: the status worldwide (2024)
Chong Neto, Herberto José ; Radwan, Nesrine ; Condino Neto, Antonio ; Rosário Filho, Nelson Augusto ; Martell, José Antonio Ortega ; El-Sayed, Zeinab A.
Fonte: World Allergy Organization Journal. Unidade: ICB
Assuntos: IMUNOLOGIA, NEONATOLOGIA, IMUNIDADE MATERNO-ADQUIRIDA, IMUNOGLOBULINAS, IMUNODEFICIÊNCIA DE VARIÁVEL COMUM, IMUNOGENÉTICA, CÉLULAS-TRONCO, ESTUDOS DE COORTES
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ABNT
CHONG NETO, Herberto José et al. Newborn screening for inborn errors of immunity: the status worldwide. World Allergy Organization Journal, v. 17, n. 6, p. 12 , 2024Tradução . . Disponível em: https://doi.org/10.1016/j.waojou.2024.100920. Acesso em: 14 out. 2025.
APA
Chong Neto, H. J., Radwan, N., Condino Neto, A., Rosário Filho, N. A., Martell, J. A. O., & El-Sayed, Z. A. (2024). Newborn screening for inborn errors of immunity: the status worldwide. World Allergy Organization Journal, 17( 6), 12 . doi:10.1016/j.waojou.2024.100920
NLM
Chong Neto HJ, Radwan N, Condino Neto A, Rosário Filho NA, Martell JAO, El-Sayed ZA. Newborn screening for inborn errors of immunity: the status worldwide [Internet]. World Allergy Organization Journal. 2024 ; 17( 6): 12 .[citado 2025 out. 14 ] Available from: https://doi.org/10.1016/j.waojou.2024.100920
Vancouver
Chong Neto HJ, Radwan N, Condino Neto A, Rosário Filho NA, Martell JAO, El-Sayed ZA. Newborn screening for inborn errors of immunity: the status worldwide [Internet]. World Allergy Organization Journal. 2024 ; 17( 6): 12 .[citado 2025 out. 14 ] Available from: https://doi.org/10.1016/j.waojou.2024.100920
Artigo de periodico
Heterozygous BTNL8 variants in individuals with multisystem inflammatory syndrome in children (MIS-C) (2024)
Bellos, Evangelos ; Santillo, Dilys ; Vantourout, Pierre ; Jackson, Heather R. ; Duret, Amedine ; Hearn, Henry ; Seeleuthner, Yoann ; Talouarn, Estelle ; Hodeib, Stephanie ; Patel, Harsita ; Powell, Oliver ; Yeoh, Sophya ; Mustafa, Sobia ; Habgood-Coote, Dominic ; Nichols, Samuel ; Elorrieta, Leire Estramiana ; D’Souza, Giselle ; Wright, Victoria J. ; Estrada-Rivadeneyra, Diego ; Tremoulet, Adriana H. ; Dummer, Kirsten B. ; Netea, Stejara A. ; Lau, Yu Lung ; Núñez Cuadros, Esmeralda ; Toubiana, Julie ; Holanda-Peña, Marisol Holanda ; Rieux-Laucat, Frédéric ; Luyt, Charles-Edouard ; Haerynck, Filomeen ; Mège, Jean Louis ; Chakravorty, Samya ; Haddad, Elie ; Morin, Marie-Paule ; Akcan, Özge Metin ; Keles, Sevgi ; Emiroglu, Melike ; Alkan, Gulsum ; Öz, Sadiye Kübra Tüter ; Bozdemir, Sefika Elmas ; Morelle, Guillaume ; Volokha, Alla ; Kendir-Demirkol, Yasemin ; Sözeri, Betul ; Coskuner, Taner ; Yahsi, Aysun; Gülhan, Belgin ; Kanik-Yuksek, Saliha ; Bayhan, Gulsum Iclal ; Ozkaya-Parlakay, Aslinur ; Yesilbas, Osman ; Hatipoglu, Nevin ; Ozcelik, Tayfun ; Belot, Alexandre ; Chopin, Emilie ; Barlogis, Vincent ; Sevketoglu, Esra ; Menentoglu, Emim ; Aydin, Zeynep Gokce Gayretli ; Bloomfield, Markéta ; AlKhater, Suzan A. ; Cyrus, Cyril ; Stepanovskiy, Yuriy ; Bondarenko, Anastasiia ; Öz, Fatma Nur ; Polat, Meltem ; Fremuth, Jiří ; Lebl, Jan ; Geraldo, Amyrath ; Jouanguy, Emmanuelle ; Carter, Michael J. ; Wellman, Paul ; Peters, Mark ; Diego, Rebeca Pérez de ; Edwards, Lindsey Ann ; Chiu, Christopher ; Noursadeghi, Mahdad ; Bolze, Alexandre ; Shimizu, Chisato ; Kaforou, Myrsini ; Hamilton, Melissa Shea ; Herberg, Jethro A. ; Schmitt, Erica G. ; Rodriguez-Palmero, Agusti ; Pujol, Aurora ; Kim, Jihoon ; Cobat, Aurélie ; Abel, Laurent ; Zhang, Shen-Ying ; Casanova, Jean-Laurent ; Kuijpers, Taco W. ; Burns, Jane C. ; Levin, Michael ; Hayday, Adrian C. ; Sancho-Shimizu, Vanessa ; Condino Neto, Antonio
Fonte: The Journal of Experimental Medicine. Unidade: ICB
Assuntos: IMUNOLOGIA, VARIAÇÃO GENÉTICA, PREDISPOSIÇÃO GENÉTICA PARA DOENÇA, COVID-19, SEQUENCIAMENTO GENÉTICO, ALELOS, HOMEOSTASE, CÉLULAS EPITELIAIS, LINFÓCITOS T, ESTUDOS DE COORTES
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ABNT
BELLOS, Evangelos et al. Heterozygous BTNL8 variants in individuals with multisystem inflammatory syndrome in children (MIS-C). The Journal of Experimental Medicine, v. 221, n. 12, p. 31 , 2024Tradução . . Disponível em: https://doi.org/10.1084/jem.20240699. Acesso em: 14 out. 2025.
APA
Bellos, E., Santillo, D., Vantourout, P., Jackson, H. R., Duret, A., Hearn, H., et al. (2024). Heterozygous BTNL8 variants in individuals with multisystem inflammatory syndrome in children (MIS-C). The Journal of Experimental Medicine, 221( 12), 31 . doi:10.1084/jem.20240699
NLM
Bellos E, Santillo D, Vantourout P, Jackson HR, Duret A, Hearn H, Seeleuthner Y, Talouarn E, Hodeib S, Patel H, Powell O, Yeoh S, Mustafa S, Habgood-Coote D, Nichols S, Elorrieta LE, D’Souza G, Wright VJ, Estrada-Rivadeneyra D, Tremoulet AH, Dummer KB, Netea SA, Lau YL, Núñez Cuadros E, Toubiana J, Holanda-Peña MH, Rieux-Laucat F, Luyt C-E, Haerynck F, Mège JL, Chakravorty S, Haddad E, Morin M-P, Akcan ÖM, Keles S, Emiroglu M, Alkan G, Öz SKT, Bozdemir SE, Morelle G, Volokha A, Kendir-Demirkol Y, Sözeri B, Coskuner T, Yahsi A, Gülhan B, Kanik-Yuksek S, Bayhan GI, Ozkaya-Parlakay A, Yesilbas O, Hatipoglu N, Ozcelik T, Belot A, Chopin E, Barlogis V, Sevketoglu E, Menentoglu E, Aydin ZGG, Bloomfield M, AlKhater SA, Cyrus C, Stepanovskiy Y, Bondarenko A, Öz FN, Polat M, Fremuth J, Lebl J, Geraldo A, Jouanguy E, Carter MJ, Wellman P, Peters M, Diego RP de, Edwards LA, Chiu C, Noursadeghi M, Bolze A, Shimizu C, Kaforou M, Hamilton MS, Herberg JA, Schmitt EG, Rodriguez-Palmero A, Pujol A, Kim J, Cobat A, Abel L, Zhang S-Y, Casanova J-L, Kuijpers TW, Burns JC, Levin M, Hayday AC, Sancho-Shimizu V, Condino Neto A. Heterozygous BTNL8 variants in individuals with multisystem inflammatory syndrome in children (MIS-C) [Internet]. The Journal of Experimental Medicine. 2024 ; 221( 12): 31 .[citado 2025 out. 14 ] Available from: https://doi.org/10.1084/jem.20240699
Vancouver
Bellos E, Santillo D, Vantourout P, Jackson HR, Duret A, Hearn H, Seeleuthner Y, Talouarn E, Hodeib S, Patel H, Powell O, Yeoh S, Mustafa S, Habgood-Coote D, Nichols S, Elorrieta LE, D’Souza G, Wright VJ, Estrada-Rivadeneyra D, Tremoulet AH, Dummer KB, Netea SA, Lau YL, Núñez Cuadros E, Toubiana J, Holanda-Peña MH, Rieux-Laucat F, Luyt C-E, Haerynck F, Mège JL, Chakravorty S, Haddad E, Morin M-P, Akcan ÖM, Keles S, Emiroglu M, Alkan G, Öz SKT, Bozdemir SE, Morelle G, Volokha A, Kendir-Demirkol Y, Sözeri B, Coskuner T, Yahsi A, Gülhan B, Kanik-Yuksek S, Bayhan GI, Ozkaya-Parlakay A, Yesilbas O, Hatipoglu N, Ozcelik T, Belot A, Chopin E, Barlogis V, Sevketoglu E, Menentoglu E, Aydin ZGG, Bloomfield M, AlKhater SA, Cyrus C, Stepanovskiy Y, Bondarenko A, Öz FN, Polat M, Fremuth J, Lebl J, Geraldo A, Jouanguy E, Carter MJ, Wellman P, Peters M, Diego RP de, Edwards LA, Chiu C, Noursadeghi M, Bolze A, Shimizu C, Kaforou M, Hamilton MS, Herberg JA, Schmitt EG, Rodriguez-Palmero A, Pujol A, Kim J, Cobat A, Abel L, Zhang S-Y, Casanova J-L, Kuijpers TW, Burns JC, Levin M, Hayday AC, Sancho-Shimizu V, Condino Neto A. Heterozygous BTNL8 variants in individuals with multisystem inflammatory syndrome in children (MIS-C) [Internet]. The Journal of Experimental Medicine. 2024 ; 221( 12): 31 .[citado 2025 out. 14 ] Available from: https://doi.org/10.1084/jem.20240699
Artigo de periodico
Severe combined immunodeficiency diagnosis and genetic defects (2024)
Aranda, Carolina Sanchez ; Pereira, Mariana Pimentel Gouveia ; Silva, Celso Jose Mendanha da; Rizzo, Maria Candida Faria Varanda; Ishizuka, Edson Kiyotaka ; Oliveira, Edgar Borges de; Condino Neto, Antonio
Fonte: Immunological Reviews. Unidade: ICB
Assuntos: IMUNOLOGIA, IMUNODEFICIÊNCIA DE VARIÁVEL COMUM, HEMATOPOESE, AGAMAGLOBULINEMIA, LINFÓCITOS T, IMUNOGENÉTICA, CÉLULAS-TRONCO, CRIANÇAS, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ARANDA, Carolina Sanchez et al. Severe combined immunodeficiency diagnosis and genetic defects. Immunological Reviews, v. 322, n. 1, p. 138-147, 2024Tradução . . Disponível em: https://doi.org/10.1111/imr.13310. Acesso em: 14 out. 2025.
APA
Aranda, C. S., Pereira, M. P. G., Silva, C. J. M. da, Rizzo, M. C. F. V., Ishizuka, E. K., Oliveira, E. B. de, & Condino Neto, A. (2024). Severe combined immunodeficiency diagnosis and genetic defects. Immunological Reviews, 322( 1), 138-147. doi:10.1111/imr.13310
NLM
Aranda CS, Pereira MPG, Silva CJM da, Rizzo MCFV, Ishizuka EK, Oliveira EB de, Condino Neto A. Severe combined immunodeficiency diagnosis and genetic defects [Internet]. Immunological Reviews. 2024 ; 322( 1): 138-147.[citado 2025 out. 14 ] Available from: https://doi.org/10.1111/imr.13310
Vancouver
Aranda CS, Pereira MPG, Silva CJM da, Rizzo MCFV, Ishizuka EK, Oliveira EB de, Condino Neto A. Severe combined immunodeficiency diagnosis and genetic defects [Internet]. Immunological Reviews. 2024 ; 322( 1): 138-147.[citado 2025 out. 14 ] Available from: https://doi.org/10.1111/imr.13310
Artigo de periodico
Autosomal recessive IL-12p40 deficiency due to a mutation in the IL12B gene: report of a Brazilian patient with lymph node mycobacterial infection (2024)
Melo, Karina Mescouto de ; Tavares, Fabíola Scancetti ; Antunes, Thales Silva ; Segundo, Gesmar Rodrigues Silva ; Macedo, Antônio Carlos Tanajura de; Ferreira, Alexandre Paz; Valente, Cláudia França Cavalcante ; Condino Neto, Antonio
Fonte: Pediatric Allergy, Immunology, and Pulmonology. Unidade: ICB
Assuntos: IMUNOLOGIA, MYCOBACTERIUM, LINFONODOS, MUTAÇÃO GENÉTICA, INTERLEUCINAS, CITOCINAS, INTERFERONS, CRIANÇAS, IMUNODEFICIÊNCIA DE VARIÁVEL COMUM, INFECÇÕES BACTERIANAS GRAM-POSITIVAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MELO, Karina Mescouto de et al. Autosomal recessive IL-12p40 deficiency due to a mutation in the IL12B gene: report of a Brazilian patient with lymph node mycobacterial infection. Pediatric Allergy, Immunology, and Pulmonology, v. 37, n. 1, p. 33-36, 2024Tradução . . Disponível em: https://doi.org/10.1089/ped.2022.0206. Acesso em: 14 out. 2025.
APA
Melo, K. M. de, Tavares, F. S., Antunes, T. S., Segundo, G. R. S., Macedo, A. C. T. de, Ferreira, A. P., et al. (2024). Autosomal recessive IL-12p40 deficiency due to a mutation in the IL12B gene: report of a Brazilian patient with lymph node mycobacterial infection. Pediatric Allergy, Immunology, and Pulmonology, 37( 1), 33-36. doi:10.1089/ped.2022.0206
NLM
Melo KM de, Tavares FS, Antunes TS, Segundo GRS, Macedo ACT de, Ferreira AP, Valente CFC, Condino Neto A. Autosomal recessive IL-12p40 deficiency due to a mutation in the IL12B gene: report of a Brazilian patient with lymph node mycobacterial infection [Internet]. Pediatric Allergy, Immunology, and Pulmonology. 2024 ; 37( 1): 33-36.[citado 2025 out. 14 ] Available from: https://doi.org/10.1089/ped.2022.0206
Vancouver
Melo KM de, Tavares FS, Antunes TS, Segundo GRS, Macedo ACT de, Ferreira AP, Valente CFC, Condino Neto A. Autosomal recessive IL-12p40 deficiency due to a mutation in the IL12B gene: report of a Brazilian patient with lymph node mycobacterial infection [Internet]. Pediatric Allergy, Immunology, and Pulmonology. 2024 ; 37( 1): 33-36.[citado 2025 out. 14 ] Available from: https://doi.org/10.1089/ped.2022.0206
Artigo de periodico-carta/editorial
Human PLCG2 haploinsufficiency results in a novel NK cell immunodeficiency (2024)
Condino Neto, Antonio
Fonte: Journal of Allergy and Clinical Immunology. Unidade: ICB
Assuntos: IMUNOLOGIA, HAPLOTIPOS, IMUNODEFICIÊNCIA DE VARIÁVEL COMUM, IMUNIDADE, DOENÇAS CONGÊNITAS, HERPES SIMPLES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CONDINO NETO, Antonio. Human PLCG2 haploinsufficiency results in a novel NK cell immunodeficiency. Journal of Allergy and Clinical Immunology. Philadelphia, PA: Elsevier Inc. Disponível em: https://doi.org/10.1016/j.jaci.2023.12.005. Acesso em: 14 out. 2025. , 2024
APA
Condino Neto, A. (2024). Human PLCG2 haploinsufficiency results in a novel NK cell immunodeficiency. Journal of Allergy and Clinical Immunology. Philadelphia, PA: Elsevier Inc. doi:10.1016/j.jaci.2023.12.005
NLM
Condino Neto A. Human PLCG2 haploinsufficiency results in a novel NK cell immunodeficiency [Internet]. Journal of Allergy and Clinical Immunology. 2024 ; 153( 2): 1 .[citado 2025 out. 14 ] Available from: https://doi.org/10.1016/j.jaci.2023.12.005
Vancouver
Condino Neto A. Human PLCG2 haploinsufficiency results in a novel NK cell immunodeficiency [Internet]. Journal of Allergy and Clinical Immunology. 2024 ; 153( 2): 1 .[citado 2025 out. 14 ] Available from: https://doi.org/10.1016/j.jaci.2023.12.005
Artigo de periodico
Calculated globulin can be used as a screening test for antibody deficiency in children and adolescents (2024)
Piza, Cristina Frias Sartorelli de Toledo ; Aranda, Carolina Sanchez ; Sole, Dirceu ; Jolles, Stephen ; Condino Neto, Antonio
Fonte: Frontiers in Immunology. Unidade: ICB
Assuntos: IMUNOLOIGIA, IMUNOGLOBULINAS, GLOBULINAS, IMUNODEFICIÊNCIA DE VARIÁVEL COMUM, SÍNDROMES DE DEFICIÊNCIA IMUNOLÓGICA, PROTEÍNAS SANGUÍNEAS, ANTICORPOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PIZA, Cristina Frias Sartorelli de Toledo et al. Calculated globulin can be used as a screening test for antibody deficiency in children and adolescents. Frontiers in Immunology, v. 15, p. 6 , 2024Tradução . . Disponível em: https://doi.org/10.3389/fimmu.2024.1495564. Acesso em: 14 out. 2025.
APA
Piza, C. F. S. de T., Aranda, C. S., Sole, D., Jolles, S., & Condino Neto, A. (2024). Calculated globulin can be used as a screening test for antibody deficiency in children and adolescents. Frontiers in Immunology, 15, 6 . doi:10.3389/fimmu.2024.1495564
NLM
Piza CFS de T, Aranda CS, Sole D, Jolles S, Condino Neto A. Calculated globulin can be used as a screening test for antibody deficiency in children and adolescents [Internet]. Frontiers in Immunology. 2024 ; 15 6 .[citado 2025 out. 14 ] Available from: https://doi.org/10.3389/fimmu.2024.1495564
Vancouver
Piza CFS de T, Aranda CS, Sole D, Jolles S, Condino Neto A. Calculated globulin can be used as a screening test for antibody deficiency in children and adolescents [Internet]. Frontiers in Immunology. 2024 ; 15 6 .[citado 2025 out. 14 ] Available from: https://doi.org/10.3389/fimmu.2024.1495564
Artigo de periodico
Higher COVID-19 pneumonia risk associated with anti-IFN-α than with anti-IFN-ω auto-Abs in children (2024)
Bastard, Paul ; Adrian, Gervais ; Taniguchi, Maki ; Saare, Liisa ; Särekannu, Karita ; Voyer, Tom Le ; Philippot, Quentin ; Rosain, Jérémie ; Bizien, Lucy ; Asano, Takaki Asano ; Garcia-Prat, Marina ; Parra-Martínez, Alba ; Migaud, Mélanie ; Tsumura, Miyuki ; Conti, Francesca ; Belot, Alexandre ; Rivière, Jacques G. ; Morio, Tomohiro ; Tanaka, Junko ; Javouhey, Etienne ; Haerynck, Filomeen ; Duvlis, Sotirija ; Ozcelik, Tayfun ; Keles, Sevgi ; Redondo, Yacine Tandjaoui-Lambiotte ; Escoda, Simon ; Husain, Maya ; Pan-Hammarström, Qiang ; Hammarström, Lennart ; Ahlijah, Gloria ; Haidar, Anthony Abi ; Soudee, Camile ; Arsegue, Vincent; Abolhassani, Hassan ; Sahanic, Sabina ; Tancevsk, Ivan ; Nukui, Yoko ; Hayakawa, Seiichi ; Chrousos, George P. ; Michos, Athanasios ; Tatsi, Elizabeth-Barbara ; Filippatos, Filippos ; Seuma, Agusti Rodriguez-Palmero ; Garcia, Jésus Troya ; Tipu, Imran ; Meyts, Isabelle ; Roussel, Lucie ; Ostrowski, Sisse Rye ; Schidlowski, Laire ; Prando, Carolina ; Cheikh, Nathalie ; Bousfiha, Ahmed Aziz ; Bakkouri, Jalila El ; Peterson, Pärt ; Pujol, Aurora ; Lévy, Romain ; Quartier, Pierre ; Vinh, Donalod C. ; Boisson, Bertrand ; Béziat, Vivien ; Zhang, Shen-Ying ; Borghesi, Alessandro ; Pession, Andrea ; Andreakos, Evangelos ; Marr, Nico ; Mentis, Alexios-Fotios A. ; Mogensen, Trine Hyrup ; Rodríiguez-Gallego, Carlos ; Soler-Palacín, Pere ; Colobran, Roger ; Tillmann, Vallo ; Neven, Bénédicte ; Trouillet-Assant, Sophie ; Brodin, Peter ; Abel, Laurent ; Jouanguy, Emmanuelle ; Zhang, Qian ; Martinón-Torres, Federico ; Ellacuriaga, Antonio Sallas ; Gómez-Carballa, Alberto ; Gonzalez-Granado, Luis Ignacio ; Kisan, Kai ; Okada, Satoshi ; Puel, Anne ; Cobat, Aurélie ; Casanova, Jean-Laurent ; Condino Neto, Antonio
Fonte: The Journal of Experimental Medicine. Unidade: ICB
Assuntos: IMUNOLOGIA, AUTOANTICORPOS, COVID-19, PNEUMONIA, PNEUMOPATIAS, INTERFERON TIPO I, INTERFERONS, CRIANÇAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BASTARD, Paul et al. Higher COVID-19 pneumonia risk associated with anti-IFN-α than with anti-IFN-ω auto-Abs in children. The Journal of Experimental Medicine, v. 221, n. 2, p. 45 , 2024Tradução . . Disponível em: https://doi.org/10.1084/jem.20231353. Acesso em: 14 out. 2025.
APA
Bastard, P., Adrian, G., Taniguchi, M., Saare, L., Särekannu, K., Voyer, T. L., et al. (2024). Higher COVID-19 pneumonia risk associated with anti-IFN-α than with anti-IFN-ω auto-Abs in children. The Journal of Experimental Medicine, 221( 2), 45 . doi:10.1084/jem.20231353
NLM
Bastard P, Adrian G, Taniguchi M, Saare L, Särekannu K, Voyer TL, Philippot Q, Rosain J, Bizien L, Asano TA, Garcia-Prat M, Parra-Martínez A, Migaud M, Tsumura M, Conti F, Belot A, Rivière JG, Morio T, Tanaka J, Javouhey E, Haerynck F, Duvlis S, Ozcelik T, Keles S, Redondo YT-L, Escoda S, Husain M, Pan-Hammarström Q, Hammarström L, Ahlijah G, Haidar AA, Soudee C, Arsegue V, Abolhassani H, Sahanic S, Tancevsk I, Nukui Y, Hayakawa S, Chrousos GP, Michos A, Tatsi E-B, Filippatos F, Seuma AR-P, Garcia JT, Tipu I, Meyts I, Roussel L, Ostrowski SR, Schidlowski L, Prando C, Cheikh N, Bousfiha AA, Bakkouri JE, Peterson P, Pujol A, Lévy R, Quartier P, Vinh DC, Boisson B, Béziat V, Zhang S-Y, Borghesi A, Pession A, Andreakos E, Marr N, Mentis A-FA, Mogensen TH, Rodríiguez-Gallego C, Soler-Palacín P, Colobran R, Tillmann V, Neven B, Trouillet-Assant S, Brodin P, Abel L, Jouanguy E, Zhang Q, Martinón-Torres F, Ellacuriaga AS, Gómez-Carballa A, Gonzalez-Granado LI, Kisan K, Okada S, Puel A, Cobat A, Casanova J-L, Condino Neto A. Higher COVID-19 pneumonia risk associated with anti-IFN-α than with anti-IFN-ω auto-Abs in children [Internet]. The Journal of Experimental Medicine. 2024 ; 221( 2): 45 .[citado 2025 out. 14 ] Available from: https://doi.org/10.1084/jem.20231353
Vancouver
Bastard P, Adrian G, Taniguchi M, Saare L, Särekannu K, Voyer TL, Philippot Q, Rosain J, Bizien L, Asano TA, Garcia-Prat M, Parra-Martínez A, Migaud M, Tsumura M, Conti F, Belot A, Rivière JG, Morio T, Tanaka J, Javouhey E, Haerynck F, Duvlis S, Ozcelik T, Keles S, Redondo YT-L, Escoda S, Husain M, Pan-Hammarström Q, Hammarström L, Ahlijah G, Haidar AA, Soudee C, Arsegue V, Abolhassani H, Sahanic S, Tancevsk I, Nukui Y, Hayakawa S, Chrousos GP, Michos A, Tatsi E-B, Filippatos F, Seuma AR-P, Garcia JT, Tipu I, Meyts I, Roussel L, Ostrowski SR, Schidlowski L, Prando C, Cheikh N, Bousfiha AA, Bakkouri JE, Peterson P, Pujol A, Lévy R, Quartier P, Vinh DC, Boisson B, Béziat V, Zhang S-Y, Borghesi A, Pession A, Andreakos E, Marr N, Mentis A-FA, Mogensen TH, Rodríiguez-Gallego C, Soler-Palacín P, Colobran R, Tillmann V, Neven B, Trouillet-Assant S, Brodin P, Abel L, Jouanguy E, Zhang Q, Martinón-Torres F, Ellacuriaga AS, Gómez-Carballa A, Gonzalez-Granado LI, Kisan K, Okada S, Puel A, Cobat A, Casanova J-L, Condino Neto A. Higher COVID-19 pneumonia risk associated with anti-IFN-α than with anti-IFN-ω auto-Abs in children [Internet]. The Journal of Experimental Medicine. 2024 ; 221( 2): 45 .[citado 2025 out. 14 ] Available from: https://doi.org/10.1084/jem.20231353
Artigo de periodico
Newborn Screening (NBS) for Inborn Errors of Immunity (IEI) – first real-life experience of a reference center in Brazil (2024)
Lopes, Luisa; Silvestre, Katherine Costa; Gurgel, Luma; Trevisol, Leticia; Said, Larissa; Pimentel, Mariana; Aranda, Carolina; Sole, Dirceu ; Condino Neto, Antonio
Fonte: Journal of Allergy and Clinical Immunology ISSN:1097-6825. Nome do evento: Annual Meeting American Academy of Allergy Asthma & Immunology [AAAAI], 2024. Unidade: ICB
Assuntos: IMUNOLOGIA, IMUNIDADE, ANORMALIDADES CONGÊNITAS, ANORMALIDADES CROMOSSÔMICAS, NEONATOLOGIA, DOENÇAS IMUNOLÓGICAS, ESTUDOS RETROSPECTIVOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LOPES, Luisa et al. Newborn Screening (NBS) for Inborn Errors of Immunity (IEI) – first real-life experience of a reference center in Brazil. Journal of Allergy and Clinical Immunology ISSN:1097-6825, v. 153, n. supl. 2, p. AB143, 2024Tradução . . Disponível em: https://doi.org/10.1016/j.jaci.2023.11.472. Acesso em: 14 out. 2025.
APA
Lopes, L., Silvestre, K. C., Gurgel, L., Trevisol, L., Said, L., Pimentel, M., et al. (2024). Newborn Screening (NBS) for Inborn Errors of Immunity (IEI) – first real-life experience of a reference center in Brazil. Journal of Allergy and Clinical Immunology ISSN:1097-6825, 153( supl. 2), AB143. doi:10.1016/j.jaci.2023.11.472
NLM
Lopes L, Silvestre KC, Gurgel L, Trevisol L, Said L, Pimentel M, Aranda C, Sole D, Condino Neto A. Newborn Screening (NBS) for Inborn Errors of Immunity (IEI) – first real-life experience of a reference center in Brazil [Internet]. Journal of Allergy and Clinical Immunology ISSN:1097-6825. 2024 ; 153( supl. 2): AB143.[citado 2025 out. 14 ] Available from: https://doi.org/10.1016/j.jaci.2023.11.472
Vancouver
Lopes L, Silvestre KC, Gurgel L, Trevisol L, Said L, Pimentel M, Aranda C, Sole D, Condino Neto A. Newborn Screening (NBS) for Inborn Errors of Immunity (IEI) – first real-life experience of a reference center in Brazil [Internet]. Journal of Allergy and Clinical Immunology ISSN:1097-6825. 2024 ; 153( supl. 2): AB143.[citado 2025 out. 14 ] Available from: https://doi.org/10.1016/j.jaci.2023.11.472
Artigo de periodico
Correction: Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19 (2024)
Matuozzo, Daniela ; Talouarn, Estelle ; Marchal, Astrid; Manry, Jeremy; Seeleuthner, Yoann; Zhang, Yu; Bolze, Alexandre ; Chaldebas, Matthieu; Condino Neto, Antonio ; Zatz, Mayana
Fonte: Genome Medicine. Unidades: IB, ICB
Assuntos: IMUNOLOGIA, COVID-19
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MATUOZZO, Daniela et al. Correction: Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19. Genome Medicine, v. 16, 2024Tradução . . Disponível em: https://doi.org/10.1186/s13073-023-01278-0. Acesso em: 14 out. 2025.
APA
Matuozzo, D., Talouarn, E., Marchal, A., Manry, J., Seeleuthner, Y., Zhang, Y., et al. (2024). Correction: Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19. Genome Medicine, 16. Recuperado de https://doi.org/10.1186/s13073-023-01278-0
NLM
Matuozzo D, Talouarn E, Marchal A, Manry J, Seeleuthner Y, Zhang Y, Bolze A, Chaldebas M, Condino Neto A, Zatz M. Correction: Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19 [Internet]. Genome Medicine. 2024 ; 16[citado 2025 out. 14 ] Available from: https://doi.org/10.1186/s13073-023-01278-0
Vancouver
Matuozzo D, Talouarn E, Marchal A, Manry J, Seeleuthner Y, Zhang Y, Bolze A, Chaldebas M, Condino Neto A, Zatz M. Correction: Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19 [Internet]. Genome Medicine. 2024 ; 16[citado 2025 out. 14 ] Available from: https://doi.org/10.1186/s13073-023-01278-0
Artigo de periodico
Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19 (2023)
Matuozzo, Daniela ; Talouarn, Estelle ; Marchal, Astrid; Manry, Jeremy; Seeleuthner, Yoann; Zhang, Yu; Bolze, Alexandre ; Chaldebas, Matthieu; Condino Neto, Antonio ; Zatz, Mayana
Fonte: Genome Medicine. Unidades: IB, ICB
Assuntos: IMUNOLOGIA, COVID-19
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MATUOZZO, Daniela et al. Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19. Genome Medicine, v. 15, p. 1-25, 2023Tradução . . Disponível em: https://doi.org/10.1186/s13073-023-01173-8. Acesso em: 14 out. 2025.
APA
Matuozzo, D., Talouarn, E., Marchal, A., Manry, J., Seeleuthner, Y., Zhang, Y., et al. (2023). Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19. Genome Medicine, 15, 1-25. doi:10.1186/s13073-023-01173-8
NLM
Matuozzo D, Talouarn E, Marchal A, Manry J, Seeleuthner Y, Zhang Y, Bolze A, Chaldebas M, Condino Neto A, Zatz M. Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19 [Internet]. Genome Medicine. 2023 ; 15 1-25.[citado 2025 out. 14 ] Available from: https://doi.org/10.1186/s13073-023-01173-8
Vancouver
Matuozzo D, Talouarn E, Marchal A, Manry J, Seeleuthner Y, Zhang Y, Bolze A, Chaldebas M, Condino Neto A, Zatz M. Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19 [Internet]. Genome Medicine. 2023 ; 15 1-25.[citado 2025 out. 14 ] Available from: https://doi.org/10.1186/s13073-023-01173-8
Artigo de periodico
Allergy, asthma, and proteomics: opportunities with immediate impact (2023)
Cruz, Renata Harumi; Pontes, Leticia Gomes de ; Condino Neto, Antonio
Fonte: Allergol Immunopathol. Unidade: ICB
Assuntos: IMUNOLOGIA, ASMA, HIPERSENSIBILIDADE, INFLAMAÇÃO, PROTEÔMICA, ESPECTROMETRIA DE MASSAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CRUZ, Renata Harumi e PONTES, Leticia Gomes de e CONDINO NETO, Antonio. Allergy, asthma, and proteomics: opportunities with immediate impact. Allergol Immunopathol, v. 51, n. 1, p. 16–21, 2023Tradução . . Disponível em: https://doi.org/10.15586/aei.v51i1.567. Acesso em: 14 out. 2025.
APA
Cruz, R. H., Pontes, L. G. de, & Condino Neto, A. (2023). Allergy, asthma, and proteomics: opportunities with immediate impact. Allergol Immunopathol, 51( 1), 16–21. doi:10.15586/aei.v51i1.567
NLM
Cruz RH, Pontes LG de, Condino Neto A. Allergy, asthma, and proteomics: opportunities with immediate impact [Internet]. Allergol Immunopathol. 2023 ; 51( 1): 16–21.[citado 2025 out. 14 ] Available from: https://doi.org/10.15586/aei.v51i1.567
Vancouver
Cruz RH, Pontes LG de, Condino Neto A. Allergy, asthma, and proteomics: opportunities with immediate impact [Internet]. Allergol Immunopathol. 2023 ; 51( 1): 16–21.[citado 2025 out. 14 ] Available from: https://doi.org/10.15586/aei.v51i1.567
Artigo de periodico
A novel insight on SARS-CoV-2 S-derived fragments in the control of the host immunity (2023)
Bastos, Thais Sibioni Berti ; Paula, André Guilherme Portela de ; Luz, Rebeca Bosso dos Santos ; Garnique, Anali M. B. ; Belo, Marco A. A. ; Eto, Silas Fernandes ; Fernandes, Dayanne Carla ; Ferraris, Fausto Klabund ; Pontes, Leticia Gomes de ; França, Tábata Takahashi ; Ferraris, Fausto Klabund ; Pontes, Leticia Gomes de ; França, Tábata Takahashi ; Barcellos, Leonardo José Gil ; Veras, Flavio P. ; Bermejo, Pamela ; Guidelli, Giovanna ; Maneira, Carla ; Mello, Fellipe da Silveira Bezerra de ; Teixeira, Gleidson ; Pereira, Gonçalo Amarante Guimarães ; Fernandes, Bianca Helena Ventura ; Sanches, Paulo R. S. ; Braz, Helyson Lucas Bezerra ; Jorge, Roberta Jeane Bezerra ; Malafaia, Guilherme ; Cilli, Eduardo M. ; Olivier, Danilo da Silva ; Amaral, Marcos Serrou do ; Medeiros, Renata J. ; Carvalho, Luciani R. ; Charlie-Silva, Ives ; Galindo-Villegas, Jorge ; Braga, Tarcio Teodoro ; Condino Neto, Antonio ; Machado-Santelli, Glaucia Maria
Fonte: Scientifc Reports. Unidades: ICB, FM, FMRP
Assuntos: IMUNOLOGIA, BIOLOGIA CELULAR, COVID-19, TELEOSTEI, MODELOS ANIMAIS DE DOENÇAS, PROTEÍNAS RECOMBINANTES, MACRÓFAGOS, TOXICIDADE EM ANIMAL, ESTRESSE OXIDATIVO, MICROSCOPIA CONFOCAL, IMUNIDADE, NEUTRÓFILOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BASTOS, Thais Sibioni Berti et al. A novel insight on SARS-CoV-2 S-derived fragments in the control of the host immunity. Scientifc Reports, v. 13, p. 1-15, 2023Tradução . . Disponível em: https://doi.org/10.1038/s41598-023-29588-8. Acesso em: 14 out. 2025.
APA
Bastos, T. S. B., Paula, A. G. P. de, Luz, R. B. dos S., Garnique, A. M. B., Belo, M. A. A., Eto, S. F., et al. (2023). A novel insight on SARS-CoV-2 S-derived fragments in the control of the host immunity. Scientifc Reports, 13, 1-15. doi:10.1038/s41598-023-29588-8
NLM
Bastos TSB, Paula AGP de, Luz RB dos S, Garnique AMB, Belo MAA, Eto SF, Fernandes DC, Ferraris FK, Pontes LG de, França TT, Ferraris FK, Pontes LG de, França TT, Barcellos LJG, Veras FP, Bermejo P, Guidelli G, Maneira C, Mello F da SB de, Teixeira G, Pereira GAG, Fernandes BHV, Sanches PRS, Braz HLB, Jorge RJB, Malafaia G, Cilli EM, Olivier D da S, Amaral MS do, Medeiros RJ, Carvalho LR, Charlie-Silva I, Galindo-Villegas J, Braga TT, Condino Neto A, Machado-Santelli GM. A novel insight on SARS-CoV-2 S-derived fragments in the control of the host immunity [Internet]. Scientifc Reports. 2023 ; 13 1-15.[citado 2025 out. 14 ] Available from: https://doi.org/10.1038/s41598-023-29588-8
Vancouver
Bastos TSB, Paula AGP de, Luz RB dos S, Garnique AMB, Belo MAA, Eto SF, Fernandes DC, Ferraris FK, Pontes LG de, França TT, Ferraris FK, Pontes LG de, França TT, Barcellos LJG, Veras FP, Bermejo P, Guidelli G, Maneira C, Mello F da SB de, Teixeira G, Pereira GAG, Fernandes BHV, Sanches PRS, Braz HLB, Jorge RJB, Malafaia G, Cilli EM, Olivier D da S, Amaral MS do, Medeiros RJ, Carvalho LR, Charlie-Silva I, Galindo-Villegas J, Braga TT, Condino Neto A, Machado-Santelli GM. A novel insight on SARS-CoV-2 S-derived fragments in the control of the host immunity [Internet]. Scientifc Reports. 2023 ; 13 1-15.[citado 2025 out. 14 ] Available from: https://doi.org/10.1038/s41598-023-29588-8
Artigo de periodico
Correction to: Screening for antibody Deficiencies in adults by serum electrophoresis and calculated globulin (2023)
Piza, Cristina Frias Sartorelli de Toledo ; Aranda, Carolina Sanchez ; Sole, Dirceu ; Jolles, Stephen ; Condino Neto, Antonio
Fonte: Journal of Clinical Immunology. Unidade: ICB
Assuntos: IMUNOLOGIA, ANTICORPOS, ELETROFORESE, HEMOGLOBINAS, IMUNOGLOBULINAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PIZA, Cristina Frias Sartorelli de Toledo et al. Correction to: Screening for antibody Deficiencies in adults by serum electrophoresis and calculated globulin. Journal of Clinical Immunology, p. 1-8, 2023Tradução . . Disponível em: https://doi.org/10.1007/s10875-023-01536-1. Acesso em: 14 out. 2025.
APA
Piza, C. F. S. de T., Aranda, C. S., Sole, D., Jolles, S., & Condino Neto, A. (2023). Correction to: Screening for antibody Deficiencies in adults by serum electrophoresis and calculated globulin. Journal of Clinical Immunology, 1-8. doi:10.1007/s10875-023-01536-1
NLM
Piza CFS de T, Aranda CS, Sole D, Jolles S, Condino Neto A. Correction to: Screening for antibody Deficiencies in adults by serum electrophoresis and calculated globulin [Internet]. Journal of Clinical Immunology. 2023 ; 1-8.[citado 2025 out. 14 ] Available from: https://doi.org/10.1007/s10875-023-01536-1
Vancouver
Piza CFS de T, Aranda CS, Sole D, Jolles S, Condino Neto A. Correction to: Screening for antibody Deficiencies in adults by serum electrophoresis and calculated globulin [Internet]. Journal of Clinical Immunology. 2023 ; 1-8.[citado 2025 out. 14 ] Available from: https://doi.org/10.1007/s10875-023-01536-1
Artigo de periodico
Autoantibodies against type I IFNs in humans with alternative NF-κB pathway deficiency (2023)
Voyer, Tom Le ; Parent, Audrey V ; Liu, Xian ; Cederholm, Axel ; Condino Neto, Antonio ; Vidigal, Mateus; Zatz, Mayana
Fonte: Nature. Unidades: ICB, IB
Assuntos: AUTOANTICORPOS, IMUNOLOGIA, DOENÇAS AUTOIMUNES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VOYER, Tom Le et al. Autoantibodies against type I IFNs in humans with alternative NF-κB pathway deficiency. Nature, v. 623, p. 803–813, 2023Tradução . . Disponível em: https://doi-org.ez67.periodicos.capes.gov.br/10.1038/s41586-023-06717-x. Acesso em: 14 out. 2025.
APA
Voyer, T. L., Parent, A. V., Liu, X., Cederholm, A., Condino Neto, A., Vidigal, M., & Zatz, M. (2023). Autoantibodies against type I IFNs in humans with alternative NF-κB pathway deficiency. Nature, 623, 803–813. doi:10.1038/s41586-023-06717-x
NLM
Voyer TL, Parent AV, Liu X, Cederholm A, Condino Neto A, Vidigal M, Zatz M. Autoantibodies against type I IFNs in humans with alternative NF-κB pathway deficiency [Internet]. Nature. 2023 ; 623 803–813.[citado 2025 out. 14 ] Available from: https://doi-org.ez67.periodicos.capes.gov.br/10.1038/s41586-023-06717-x
Vancouver
Voyer TL, Parent AV, Liu X, Cederholm A, Condino Neto A, Vidigal M, Zatz M. Autoantibodies against type I IFNs in humans with alternative NF-κB pathway deficiency [Internet]. Nature. 2023 ; 623 803–813.[citado 2025 out. 14 ] Available from: https://doi-org.ez67.periodicos.capes.gov.br/10.1038/s41586-023-06717-x

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