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Artigo de periodico
Latin American consensus on the supportive management of patients with severe combined immunodeficiency (2019)
Ogando, Juan Carlos Bustamante ; Gaytán, Armando Partida ; Becerra, Juan Carlos Aldave ; Cardona, Aristóteles Álvarez ; Bezrodnik, Liliana ; Borzutzky, Arturo ; Galicia, Lizbeth Blancas ; Cabanillas, Diana; Ranero, Agustín de Colsa ; Padilla, Sara Espinosa; Fernandes, Juliana Folloni; Campos, Jorge Alberto Garcia; Tello, Héctor Gómez; Serrano, María Edith González ; Hernández, Alonso Gutiérrez; Bautista, Víctor Manuel Hernández; Escoto, Gabriele Ivankovich ; King, Alejandra; Mazzucchelli, Juliana Lessa; Guillén, Beatriz Adriana Llamas; Reyes, Saul Oswaldo Lugo ; Espinosa, Sarbelio Moreno ; Oleastro, Matías; Mendonza, Francisco Otero ; Harlowe, María Cecilia Poli ; Porras, Oscar; Uribe, Nideshda Ramirez; Regairaz, Lorean; Larrauri, Francisco Rivas ; Weber, Federico José Saracho ; Grumach, Anete S. ; Boone, Tamara Staines; Costa-Carvalho, Beatriz Tavares ; Nakashimada, Marco Antonio Yamazaki ; Rosales, Francisco Javier Espinosa ; Condino Neto, Antonio
Source: Journal of Allergy and Clinical Immunology: In Practice. Unidade: ICB
Subjects: IMUNODEFICIÊNCIA DE VARIÁVEL COMUM, SÍNDROME DE IMUNODEFICIÊNCIA ADQUIRIDA, CÉLULAS-TRONCO, IMUNOGENÉTICA, PACIENTES
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OGANDO, Juan Carlos Bustamante et al. Latin American consensus on the supportive management of patients with severe combined immunodeficiency. Journal of Allergy and Clinical Immunology: In Practice, v. 144, n. 4, p. 897-905, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.jaci.2019.08.002. Acesso em: 03 out. 2024.
APA
Ogando, J. C. B., Gaytán, A. P., Becerra, J. C. A., Cardona, A. Á., Bezrodnik, L., Borzutzky, A., et al. (2019). Latin American consensus on the supportive management of patients with severe combined immunodeficiency. Journal of Allergy and Clinical Immunology: In Practice, 144( 4), 897-905. doi:10.1016/j.jaci.2019.08.002
NLM
Ogando JCB, Gaytán AP, Becerra JCA, Cardona AÁ, Bezrodnik L, Borzutzky A, Galicia LB, Cabanillas D, Ranero A de C, Padilla SE, Fernandes JF, Campos JAG, Tello HG, Serrano MEG, Hernández AG, Bautista VMH, Escoto GI, King A, Mazzucchelli JL, Guillén BAL, Reyes SOL, Espinosa SM, Oleastro M, Mendonza FO, Harlowe MCP, Porras O, Uribe NR, Regairaz L, Larrauri FR, Weber FJS, Grumach AS, Boone TS, Costa-Carvalho BT, Nakashimada MAY, Rosales FJE, Condino Neto A. Latin American consensus on the supportive management of patients with severe combined immunodeficiency [Internet]. Journal of Allergy and Clinical Immunology: In Practice. 2019 ; 144( 4): 897-905.[citado 2024 out. 03 ] Available from: https://doi.org/10.1016/j.jaci.2019.08.002
Vancouver
Ogando JCB, Gaytán AP, Becerra JCA, Cardona AÁ, Bezrodnik L, Borzutzky A, Galicia LB, Cabanillas D, Ranero A de C, Padilla SE, Fernandes JF, Campos JAG, Tello HG, Serrano MEG, Hernández AG, Bautista VMH, Escoto GI, King A, Mazzucchelli JL, Guillén BAL, Reyes SOL, Espinosa SM, Oleastro M, Mendonza FO, Harlowe MCP, Porras O, Uribe NR, Regairaz L, Larrauri FR, Weber FJS, Grumach AS, Boone TS, Costa-Carvalho BT, Nakashimada MAY, Rosales FJE, Condino Neto A. Latin American consensus on the supportive management of patients with severe combined immunodeficiency [Internet]. Journal of Allergy and Clinical Immunology: In Practice. 2019 ; 144( 4): 897-905.[citado 2024 out. 03 ] Available from: https://doi.org/10.1016/j.jaci.2019.08.002
Artigo de periodico-carta/editorial
In Time: the value and global implications of newborn screening for severe combined immunodeficiency [Editorial] (2018)
Meehan, Cristina ; Bonfim, Carmem Maria Sales ; Dasso, Joseph F. ; Costa-Carvalho, Beatriz Tavares ; Walter, Jolan ; Condino Neto, Antonio
Source: Revista Paulista de Pediatria (Online). Unidade: ICB
Subjects: NEONATOLOGIA, IMUNODEFICIÊNCIA DE VARIÁVEL COMUM, INFECÇÕES BACTERIANAS, RECÉM-NASCIDO
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MEEHAN, Cristina et al. In Time: the value and global implications of newborn screening for severe combined immunodeficiency [Editorial]. Revista Paulista de Pediatria (Online). São Paulo: Instituto de Ciências Biomédicas, Universidade de São Paulo. Disponível em: https://doi.org/10.1590/1984-0462/;2018;36;4;00020. Acesso em: 03 out. 2024. , 2018
APA
Meehan, C., Bonfim, C. M. S., Dasso, J. F., Costa-Carvalho, B. T., Walter, J., & Condino Neto, A. (2018). In Time: the value and global implications of newborn screening for severe combined immunodeficiency [Editorial]. Revista Paulista de Pediatria (Online). São Paulo: Instituto de Ciências Biomédicas, Universidade de São Paulo. doi:10.1590/1984-0462/;2018;36;4;00020
NLM
Meehan C, Bonfim CMS, Dasso JF, Costa-Carvalho BT, Walter J, Condino Neto A. In Time: the value and global implications of newborn screening for severe combined immunodeficiency [Editorial] [Internet]. Revista Paulista de Pediatria (Online). 2018 ; 36( 4):´ 388-397.[citado 2024 out. 03 ] Available from: https://doi.org/10.1590/1984-0462/;2018;36;4;00020
Vancouver
Meehan C, Bonfim CMS, Dasso JF, Costa-Carvalho BT, Walter J, Condino Neto A. In Time: the value and global implications of newborn screening for severe combined immunodeficiency [Editorial] [Internet]. Revista Paulista de Pediatria (Online). 2018 ; 36( 4):´ 388-397.[citado 2024 out. 03 ] Available from: https://doi.org/10.1590/1984-0462/;2018;36;4;00020
Artigo de periodico
CD40 ligand deficiency causes functional defects of peripheral neutrophils that are improved by exogenous IFN-γ (2018)
Cabral-Marques Otavio; França, Tabata Takahashi; Al-Sbiei, Ashraf; Schimke, Lena Friederike; Khan, Taj Ali; Feriotti, Claudia; Costa, Tania Alves da; Reis Junior, Oswaldo; Weber, Cristina Worm; Ferreira, Janaira Fernandes; Tavares, Fabiola Scancetti; Valente, Claudia; Gesu, Regina Sumiko Watanabe Di; Iqbal, Asif; Riemekasten, Gabriela; Costa-Carvalho, Beatriz Tavares; Pereira, Paulo Vitor Soeiro; Fernandez-Cabezudo, Maria J.; Notarangelo, Luigi; Togerson, Troy R.; Al-Ramadi; Ochs, Hans D.; Calich, Vera Lucia Garcia; Condino-Neto, Antonio; Amarante-Mendes, João Gustavo Pessini ; Barbuto, José Alexandre Marzagão
Source: Journal of Allergy and Clinical Immunology. Unidades: ICB, IQ
Subjects: NEUTRÓFILOS, CÉLULAS SANGUÍNEAS, IMUNOGLOBULINAS, EXPRESSÃO GÊNICA, CAMUNDONGOS, CITOCINAS, PATOGENIA ANIMAL, PROLIFERAÇÃO CELULAR
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CABRAL-MARQUES OTAVIO, et al. CD40 ligand deficiency causes functional defects of peripheral neutrophils that are improved by exogenous IFN-γ. Journal of Allergy and Clinical Immunology, v. 142, n. 5, p. 1571-1588.e9, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.jaci.2018.02.026. Acesso em: 03 out. 2024.
APA
Cabral-Marques Otavio,, França, T. T., Al-Sbiei, A., Schimke, L. F., Khan, T. A., Feriotti, C., et al. (2018). CD40 ligand deficiency causes functional defects of peripheral neutrophils that are improved by exogenous IFN-γ. Journal of Allergy and Clinical Immunology, 142( 5), 1571-1588.e9. doi:10.1016/j.jaci.2018.02.026
NLM
Cabral-Marques Otavio, França TT, Al-Sbiei A, Schimke LF, Khan TA, Feriotti C, Costa TA da, Reis Junior O, Weber CW, Ferreira JF, Tavares FS, Valente C, Gesu RSWD, Iqbal A, Riemekasten G, Costa-Carvalho BT, Pereira PVS, Fernandez-Cabezudo MJ, Notarangelo L, Togerson TR, Al-Ramadi, Ochs HD, Calich VLG, Condino-Neto A, Amarante-Mendes JGP, Barbuto JAM. CD40 ligand deficiency causes functional defects of peripheral neutrophils that are improved by exogenous IFN-γ [Internet]. Journal of Allergy and Clinical Immunology. 2018 ; 142( 5): 1571-1588.e9.[citado 2024 out. 03 ] Available from: https://doi.org/10.1016/j.jaci.2018.02.026
Vancouver
Cabral-Marques Otavio, França TT, Al-Sbiei A, Schimke LF, Khan TA, Feriotti C, Costa TA da, Reis Junior O, Weber CW, Ferreira JF, Tavares FS, Valente C, Gesu RSWD, Iqbal A, Riemekasten G, Costa-Carvalho BT, Pereira PVS, Fernandez-Cabezudo MJ, Notarangelo L, Togerson TR, Al-Ramadi, Ochs HD, Calich VLG, Condino-Neto A, Amarante-Mendes JGP, Barbuto JAM. CD40 ligand deficiency causes functional defects of peripheral neutrophils that are improved by exogenous IFN-γ [Internet]. Journal of Allergy and Clinical Immunology. 2018 ; 142( 5): 1571-1588.e9.[citado 2024 out. 03 ] Available from: https://doi.org/10.1016/j.jaci.2018.02.026
Artigo de periodico
Tuberculosis and impaired IL-23–dependent IFN-γ immunity in humans homozygous for a common TYK2 missense variant (2018)
Boisson-Dupuis, Stéphanie; Ramires-Alejo, Noe; Li, Zhi; Patin, Etienne; Rao, Geetha; Kerner, Gaspard; Lim, Che Kang; Krementsov, Dimitry N.; Hernandez, Nicholas; Ma, Cidy S.; Zhang, Qian; Markle, Janet; Martinez-Barricarte, Ruben; Payne, Kathryn; Fisch, Robert; Deswarte, Caroline; Halpern, Joshua; Bouaziz, Matthieu; Mulwa, Jeanette; Sivanesan, Durga; Lazarov, Tomi; Naves, Rodrigo; Garcia, Patricia; Itan, Yuval; Boisson, Bertrand; Checci, Alix; Jabot-Hanin, Fabienne; Cobat, Aurélie; Guennoun, Andrea; Jackson, Carolyn C.; Pekcan, Sevai; Caliskaner, Zafer; Inostroza, Jaime; Costa-Carvalho, Beatriz Tavares; Albuquerque, José Antonio Tavares de; Gacia-Ortiz, Humberto; Orozco, Lorena; Ozcelik, Tayfun; Abid, Ahmed; Rhorfi, Ismail Abderahmani; Souhi, Hicham; Amrani, Hicham Naji; Zegmout, Adil; Geissmann, Frédéric; Michnick, Stephen W.; Muller-Fleckenstein, Ingrid; Fleckenstein, Bernhard; Puel, Anne; Ciancanelli, Michael J.; Marr, Nico; Abolhassani, Hassan; Balcells, Maria Elvira; Strickler, Alexis; Abarca, Katia; Teuscher, Cory; Ochs, Hans D.; Reisli, Ismail; Sayar, Esra H.; El-Baghdadi, Jamila; Bustamante, Jacinta; Hammarströn, Lennart; Tangye, Stuart G.; Pellegrini, Sandra; Quintana-Murci, Lluis; Abel, Laurent; Casanova, Jean-Laurent; Condino-Neto, Antonio
Source: Science Immunology. Unidade: ICB
Subjects: TUBERCULOSE, VARIAÇÃO GENÉTICA, IMUNIDADE, CITOCINAS, DIFERENCIAÇÃO CELULAR, ATIVAÇÃO ENZIMÁTICA, IMUNOGENÉTICA
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ABNT
BOISSON-DUPUIS, Stéphanie et al. Tuberculosis and impaired IL-23–dependent IFN-γ immunity in humans homozygous for a common TYK2 missense variant. Science Immunology, v. 3, 2018Tradução . . Disponível em: https://doi.org/10.1126/sciimmunol.aau8714. Acesso em: 03 out. 2024.
APA
Boisson-Dupuis, S., Ramires-Alejo, N., Li, Z., Patin, E., Rao, G., Kerner, G., et al. (2018). Tuberculosis and impaired IL-23–dependent IFN-γ immunity in humans homozygous for a common TYK2 missense variant. Science Immunology, 3. doi:10.1126/sciimmunol.aau8714
NLM
Boisson-Dupuis S, Ramires-Alejo N, Li Z, Patin E, Rao G, Kerner G, Lim CK, Krementsov DN, Hernandez N, Ma CS, Zhang Q, Markle J, Martinez-Barricarte R, Payne K, Fisch R, Deswarte C, Halpern J, Bouaziz M, Mulwa J, Sivanesan D, Lazarov T, Naves R, Garcia P, Itan Y, Boisson B, Checci A, Jabot-Hanin F, Cobat A, Guennoun A, Jackson CC, Pekcan S, Caliskaner Z, Inostroza J, Costa-Carvalho BT, Albuquerque JAT de, Gacia-Ortiz H, Orozco L, Ozcelik T, Abid A, Rhorfi IA, Souhi H, Amrani HN, Zegmout A, Geissmann F, Michnick SW, Muller-Fleckenstein I, Fleckenstein B, Puel A, Ciancanelli MJ, Marr N, Abolhassani H, Balcells ME, Strickler A, Abarca K, Teuscher C, Ochs HD, Reisli I, Sayar EH, El-Baghdadi J, Bustamante J, Hammarströn L, Tangye SG, Pellegrini S, Quintana-Murci L, Abel L, Casanova J-L, Condino-Neto A. Tuberculosis and impaired IL-23–dependent IFN-γ immunity in humans homozygous for a common TYK2 missense variant [Internet]. Science Immunology. 2018 ; 3[citado 2024 out. 03 ] Available from: https://doi.org/10.1126/sciimmunol.aau8714
Vancouver
Boisson-Dupuis S, Ramires-Alejo N, Li Z, Patin E, Rao G, Kerner G, Lim CK, Krementsov DN, Hernandez N, Ma CS, Zhang Q, Markle J, Martinez-Barricarte R, Payne K, Fisch R, Deswarte C, Halpern J, Bouaziz M, Mulwa J, Sivanesan D, Lazarov T, Naves R, Garcia P, Itan Y, Boisson B, Checci A, Jabot-Hanin F, Cobat A, Guennoun A, Jackson CC, Pekcan S, Caliskaner Z, Inostroza J, Costa-Carvalho BT, Albuquerque JAT de, Gacia-Ortiz H, Orozco L, Ozcelik T, Abid A, Rhorfi IA, Souhi H, Amrani HN, Zegmout A, Geissmann F, Michnick SW, Muller-Fleckenstein I, Fleckenstein B, Puel A, Ciancanelli MJ, Marr N, Abolhassani H, Balcells ME, Strickler A, Abarca K, Teuscher C, Ochs HD, Reisli I, Sayar EH, El-Baghdadi J, Bustamante J, Hammarströn L, Tangye SG, Pellegrini S, Quintana-Murci L, Abel L, Casanova J-L, Condino-Neto A. Tuberculosis and impaired IL-23–dependent IFN-γ immunity in humans homozygous for a common TYK2 missense variant [Internet]. Science Immunology. 2018 ; 3[citado 2024 out. 03 ] Available from: https://doi.org/10.1126/sciimmunol.aau8714
Artigo de periodico
Human CD40 ligand deficiency dysregulates the macrophage transcriptome causing functional defects that are improved by exogenous IFN-γ (2017)
Cabral-Marques, Otavio; Ramos, Rodrigo Nalio; Schimke, Lena Friederick; Khan, Taj Ali; Amaral, Eduardo Pinheiro; Bomfim, Caio César Barbosa; Reis Junior, Osvaldo; França, Tabata Takahashi; Kubo, Christina Arslanian; Lima, Joanna Darck Carola Correia; Weber, Cristina Worm; Ferreira, Janaíra Fernandes; Tavares, Fabiola Scancetti; Sun, Jing; Lima, Maria Regina D'Império ; Seelaender, Marília; Calich, Vera Lucia Garcia; Barbuto, José Alexandre Marzagão ; Costa-Carvalho, Beatriz Tavares; Riemekasten, Gabriela; Seminario, Gisela; Bezrodnik, Liliana; Notarangelo, Luigi; Torgerson, Troy R.; Ochs, Hans D.; Condino-Neto, Antonio
Source: Journal of Allergy and Clinical Immunology. Unidade: ICB
Subjects: HISTOLOGIA, IMUNOLOGIA, MACRÓFAGOS, ADJUVANTES IMUNOLÓGICOS, CITOCINAS
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ABNT
CABRAL-MARQUES, Otavio et al. Human CD40 ligand deficiency dysregulates the macrophage transcriptome causing functional defects that are improved by exogenous IFN-γ. Journal of Allergy and Clinical Immunology, v. 139, n. 3, p. 900-912, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.jaci.2016.07.018. Acesso em: 03 out. 2024.
APA
Cabral-Marques, O., Ramos, R. N., Schimke, L. F., Khan, T. A., Amaral, E. P., Bomfim, C. C. B., et al. (2017). Human CD40 ligand deficiency dysregulates the macrophage transcriptome causing functional defects that are improved by exogenous IFN-γ. Journal of Allergy and Clinical Immunology, 139( 3), 900-912. doi:10.1016/j.jaci.2016.07.018
NLM
Cabral-Marques O, Ramos RN, Schimke LF, Khan TA, Amaral EP, Bomfim CCB, Reis Junior O, França TT, Kubo CA, Lima JDCC, Weber CW, Ferreira JF, Tavares FS, Sun J, Lima MRD'I, Seelaender M, Calich VLG, Barbuto JAM, Costa-Carvalho BT, Riemekasten G, Seminario G, Bezrodnik L, Notarangelo L, Torgerson TR, Ochs HD, Condino-Neto A. Human CD40 ligand deficiency dysregulates the macrophage transcriptome causing functional defects that are improved by exogenous IFN-γ [Internet]. Journal of Allergy and Clinical Immunology. 2017 ; 139( 3): 900-912.[citado 2024 out. 03 ] Available from: https://doi.org/10.1016/j.jaci.2016.07.018
Vancouver
Cabral-Marques O, Ramos RN, Schimke LF, Khan TA, Amaral EP, Bomfim CCB, Reis Junior O, França TT, Kubo CA, Lima JDCC, Weber CW, Ferreira JF, Tavares FS, Sun J, Lima MRD'I, Seelaender M, Calich VLG, Barbuto JAM, Costa-Carvalho BT, Riemekasten G, Seminario G, Bezrodnik L, Notarangelo L, Torgerson TR, Ochs HD, Condino-Neto A. Human CD40 ligand deficiency dysregulates the macrophage transcriptome causing functional defects that are improved by exogenous IFN-γ [Internet]. Journal of Allergy and Clinical Immunology. 2017 ; 139( 3): 900-912.[citado 2024 out. 03 ] Available from: https://doi.org/10.1016/j.jaci.2016.07.018
Artigo de periodico
II Brazilian Consensus on the use of human immunoglobulin in patients with primary immunodeficiencies (2017)
Goudouris, Ekaterini Simões; Silva, Almerinda Maria do Rego; Ouricuri, Aluce Loureiro; Grumach, Anete Sevciovic; Condino-Neto, Antonio; Costa-Carvalho, Beatriz Tavares; Prando, Carolina Cardoso de Mello; Kokron, Cristina Maria; Vasconcelos, Dewton de Moraes; Tavares, Fabíola Scancetti; Segundo, Gesmar Rodrigues Silva; Barreto, Irma Cecília Douglas Paes; Dorna, Mayra de Barros; Barros, Myrthes Anna Maragna Toledo; Forte, Wilma Carvalho Neves
Source: Einstein. Unidade: ICB
Subjects: IMUNOLOGIA, IMUNIZAÇÃO PASSIVA, SISTEMA IMUNE, DOENÇAS IMUNOLÓGICAS, IMUNOGLOBULINAS INTRAVENOSAS, SÍNDROMES DE DEFICIÊNCIA IMUNOLÓGICA
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ABNT
GOUDOURIS, Ekaterini Simões et al. II Brazilian Consensus on the use of human immunoglobulin in patients with primary immunodeficiencies. Einstein, v. 15, n. 1, p. 1-16, 2017Tradução . . Disponível em: https://doi.org/10.1590/S1679-45082017AE3844. Acesso em: 03 out. 2024.
APA
Goudouris, E. S., Silva, A. M. do R., Ouricuri, A. L., Grumach, A. S., Condino-Neto, A., Costa-Carvalho, B. T., et al. (2017). II Brazilian Consensus on the use of human immunoglobulin in patients with primary immunodeficiencies. Einstein, 15( 1), 1-16. doi:10.1590/S1679-45082017AE3844
NLM
Goudouris ES, Silva AM do R, Ouricuri AL, Grumach AS, Condino-Neto A, Costa-Carvalho BT, Prando CC de M, Kokron CM, Vasconcelos D de M, Tavares FS, Segundo GRS, Barreto ICDP, Dorna M de B, Barros MAMT, Forte WCN. II Brazilian Consensus on the use of human immunoglobulin in patients with primary immunodeficiencies [Internet]. Einstein. 2017 ; 15( 1): 1-16.[citado 2024 out. 03 ] Available from: https://doi.org/10.1590/S1679-45082017AE3844
Vancouver
Goudouris ES, Silva AM do R, Ouricuri AL, Grumach AS, Condino-Neto A, Costa-Carvalho BT, Prando CC de M, Kokron CM, Vasconcelos D de M, Tavares FS, Segundo GRS, Barreto ICDP, Dorna M de B, Barros MAMT, Forte WCN. II Brazilian Consensus on the use of human immunoglobulin in patients with primary immunodeficiencies [Internet]. Einstein. 2017 ; 15( 1): 1-16.[citado 2024 out. 03 ] Available from: https://doi.org/10.1590/S1679-45082017AE3844
Artigo de periodico
Neonatal screening for severe combined immunodeficiency in Brazil (2016)
Kanegae, Marilia Pyles Patto; Barreiros, Lucila Akune; Mazzucchelli, Juliana Themudo Lessa; Hadachi, Sonia Marchezi; Guilhoto, Laura Maria de Figueiredo Ferreira; Acquesta, Ana Lúcia; Genov, Isabel Rugue; Holanda, Silvia Maia; Di Gesu, Regina Sumiko Watanabe; Goulart, Ana Lucia; Santos, Amélia Miyashiro Nunes dos; Bellesi, Newton; Costa-Carvalho, Beatriz Tavares; Condino Neto, Antonio
Source: Jornal de Pediatria. Unidades: HU, ICB
Subjects: DOENÇAS IMUNOLÓGICAS, LINFÓCITOS T, TESTES IMUNOLÓGICOS, RECÉM-NASCIDO, IMUNOLOGIA
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ABNT
KANEGAE, Marilia Pyles Patto et al. Neonatal screening for severe combined immunodeficiency in Brazil. Jornal de Pediatria, v. 92, n. 4, p. 374-380, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.ped.2015.10.006. Acesso em: 03 out. 2024.
APA
Kanegae, M. P. P., Barreiros, L. A., Mazzucchelli, J. T. L., Hadachi, S. M., Guilhoto, L. M. de F. F., Acquesta, A. L., et al. (2016). Neonatal screening for severe combined immunodeficiency in Brazil. Jornal de Pediatria, 92( 4), 374-380. doi:10.1016/j.ped.2015.10.006
NLM
Kanegae MPP, Barreiros LA, Mazzucchelli JTL, Hadachi SM, Guilhoto LM de FF, Acquesta AL, Genov IR, Holanda SM, Di Gesu RSW, Goulart AL, Santos AMN dos, Bellesi N, Costa-Carvalho BT, Condino Neto A. Neonatal screening for severe combined immunodeficiency in Brazil [Internet]. Jornal de Pediatria. 2016 ; 92( 4): 374-380.[citado 2024 out. 03 ] Available from: https://doi.org/10.1016/j.ped.2015.10.006
Vancouver
Kanegae MPP, Barreiros LA, Mazzucchelli JTL, Hadachi SM, Guilhoto LM de FF, Acquesta AL, Genov IR, Holanda SM, Di Gesu RSW, Goulart AL, Santos AMN dos, Bellesi N, Costa-Carvalho BT, Condino Neto A. Neonatal screening for severe combined immunodeficiency in Brazil [Internet]. Jornal de Pediatria. 2016 ; 92( 4): 374-380.[citado 2024 out. 03 ] Available from: https://doi.org/10.1016/j.ped.2015.10.006
Artigo de periodico
Neutrophil oxidative burst activates ATM to regulate cytokine production and apoptosis (2015)
Harbort, C. J.; Soeiro-Pereira, Paulo Vitor; Bernuth, Horst von; Kaindl, Angela M.; Costa-Carvalho, Beatriz Tavares; Condino-Neto, Antonio; Reichenbach, Janine; Roesler, Joachim; Zychlinsky, Arturo; Amulic, Borko
Source: Blood. Unidade: ICB
Subjects: IMUNOLOGIA, APOPTOSE, NEUTRÓFILOS, CITOCINAS
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ABNT
HARBORT, C. J. et al. Neutrophil oxidative burst activates ATM to regulate cytokine production and apoptosis. Blood, v. 126, n. 26, p. 2842-2851, 2015Tradução . . Disponível em: https://doi.org/10.1182/blood-2015-05-645424. Acesso em: 03 out. 2024.
APA
Harbort, C. J., Soeiro-Pereira, P. V., Bernuth, H. von, Kaindl, A. M., Costa-Carvalho, B. T., Condino-Neto, A., et al. (2015). Neutrophil oxidative burst activates ATM to regulate cytokine production and apoptosis. Blood, 126( 26), 2842-2851. doi:10.1182/blood-2015-05-645424
NLM
Harbort CJ, Soeiro-Pereira PV, Bernuth H von, Kaindl AM, Costa-Carvalho BT, Condino-Neto A, Reichenbach J, Roesler J, Zychlinsky A, Amulic B. Neutrophil oxidative burst activates ATM to regulate cytokine production and apoptosis [Internet]. Blood. 2015 ; 126( 26): 2842-2851.[citado 2024 out. 03 ] Available from: https://doi.org/10.1182/blood-2015-05-645424
Vancouver
Harbort CJ, Soeiro-Pereira PV, Bernuth H von, Kaindl AM, Costa-Carvalho BT, Condino-Neto A, Reichenbach J, Roesler J, Zychlinsky A, Amulic B. Neutrophil oxidative burst activates ATM to regulate cytokine production and apoptosis [Internet]. Blood. 2015 ; 126( 26): 2842-2851.[citado 2024 out. 03 ] Available from: https://doi.org/10.1182/blood-2015-05-645424
Artigo de periodico
Clinical and genotypic spectrum of chronic granulomatous disease in 71 Latin American patients: first report from the LASID registry (2015)
Oliveira-Junior, Edgar Borges de; Zurro, Nuria Bengala; Prando, Carolina; Cabral-Marques, Otavio; Pereira, Paulo Vitor Soeiro; Schimke, Lena-Friederick; Klaver, Stefanie; Buzolin, Marcia; Blancas-Galicia, Lizbeth; Santos-Argumedo, Leopoldo; Pietropaolo-Cienfuegos, Dino Roberto; Espinosa-Rosales, Francisco; King, Alejandra; Sorensen, Ricardo; Porras, Oscar; Roxo Junior, Persio; Forte, Wilma Carvalho Neves; Orellana, Julio Cesar; Lozano, Alejandro; Galicchio, Miguel; Regairaz, Lorena; Grumach, Anete Sevciovic; Costa-Carvalho, Beatriz Tavares; Bustamante, Jacinta; Bezrodnik, Liliana; Oleastro, Matias; Danielian, Silvia; Condino Neto, Antonio
Source: Pediatric Blood & Cancer. Unidades: FMRP, ICB
Subjects: GENÉTICA MÉDICA, MUTAÇÃO, INFECÇÕES BACTERIANAS
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ABNT
OLIVEIRA-JUNIOR, Edgar Borges de et al. Clinical and genotypic spectrum of chronic granulomatous disease in 71 Latin American patients: first report from the LASID registry. Pediatric Blood & Cancer, v. 62, n. 12, p. 2101-2107, 2015Tradução . . Disponível em: https://doi.org/10.1002/pbc.25674. Acesso em: 03 out. 2024.
APA
Oliveira-Junior, E. B. de, Zurro, N. B., Prando, C., Cabral-Marques, O., Pereira, P. V. S., Schimke, L. -F., et al. (2015). Clinical and genotypic spectrum of chronic granulomatous disease in 71 Latin American patients: first report from the LASID registry. Pediatric Blood & Cancer, 62( 12), 2101-2107. doi:10.1002/pbc.25674
NLM
Oliveira-Junior EB de, Zurro NB, Prando C, Cabral-Marques O, Pereira PVS, Schimke L-F, Klaver S, Buzolin M, Blancas-Galicia L, Santos-Argumedo L, Pietropaolo-Cienfuegos DR, Espinosa-Rosales F, King A, Sorensen R, Porras O, Roxo Junior P, Forte WCN, Orellana JC, Lozano A, Galicchio M, Regairaz L, Grumach AS, Costa-Carvalho BT, Bustamante J, Bezrodnik L, Oleastro M, Danielian S, Condino Neto A. Clinical and genotypic spectrum of chronic granulomatous disease in 71 Latin American patients: first report from the LASID registry [Internet]. Pediatric Blood & Cancer. 2015 ; 62( 12): 2101-2107.[citado 2024 out. 03 ] Available from: https://doi.org/10.1002/pbc.25674
Vancouver
Oliveira-Junior EB de, Zurro NB, Prando C, Cabral-Marques O, Pereira PVS, Schimke L-F, Klaver S, Buzolin M, Blancas-Galicia L, Santos-Argumedo L, Pietropaolo-Cienfuegos DR, Espinosa-Rosales F, King A, Sorensen R, Porras O, Roxo Junior P, Forte WCN, Orellana JC, Lozano A, Galicchio M, Regairaz L, Grumach AS, Costa-Carvalho BT, Bustamante J, Bezrodnik L, Oleastro M, Danielian S, Condino Neto A. Clinical and genotypic spectrum of chronic granulomatous disease in 71 Latin American patients: first report from the LASID registry [Internet]. Pediatric Blood & Cancer. 2015 ; 62( 12): 2101-2107.[citado 2024 out. 03 ] Available from: https://doi.org/10.1002/pbc.25674
Artigo de periodico
Attending to warning signs of primary immunodeficiency diseases across the range of clinical practice (2014)
Costa-Carvalho, Beatriz Tavares; Grumach, Anete Sevciovic; Franco, José Luis; Espinosa-Rosales, Francisco Javier; Leiva, Lily E.; King, Alejandra; Porras, Oscar; Bezrodnik, Liliana; Oleastro, Mathias; Sorensen, Ricardo U.; Condino-Neto, Antonio
Source: Journal of Clinical Immunology. Unidade: ICB
Assunto: IMUNOLOGIA
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ABNT
COSTA-CARVALHO, Beatriz Tavares et al. Attending to warning signs of primary immunodeficiency diseases across the range of clinical practice. Journal of Clinical Immunology, v. 34, n. 1, p. 10-22, 2014Tradução . . Disponível em: https://doi.org/10.1007/s10875-013-9954-6. Acesso em: 03 out. 2024.
APA
Costa-Carvalho, B. T., Grumach, A. S., Franco, J. L., Espinosa-Rosales, F. J., Leiva, L. E., King, A., et al. (2014). Attending to warning signs of primary immunodeficiency diseases across the range of clinical practice. Journal of Clinical Immunology, 34( 1), 10-22. doi:10.1007/s10875-013-9954-6
NLM
Costa-Carvalho BT, Grumach AS, Franco JL, Espinosa-Rosales FJ, Leiva LE, King A, Porras O, Bezrodnik L, Oleastro M, Sorensen RU, Condino-Neto A. Attending to warning signs of primary immunodeficiency diseases across the range of clinical practice [Internet]. Journal of Clinical Immunology. 2014 ; 34( 1): 10-22.[citado 2024 out. 03 ] Available from: https://doi.org/10.1007/s10875-013-9954-6
Vancouver
Costa-Carvalho BT, Grumach AS, Franco JL, Espinosa-Rosales FJ, Leiva LE, King A, Porras O, Bezrodnik L, Oleastro M, Sorensen RU, Condino-Neto A. Attending to warning signs of primary immunodeficiency diseases across the range of clinical practice [Internet]. Journal of Clinical Immunology. 2014 ; 34( 1): 10-22.[citado 2024 out. 03 ] Available from: https://doi.org/10.1007/s10875-013-9954-6
Artigo de periodico
High-performance liquid chromatography under partially denaturing conditions (dHPLC) is a fast and cost effective method for screening molecular defects: four novel mutations found in x-linked chronic granulomatous disease (2012)
Oliveira-Junior, Edgar Borges de; Prando, Carolina; López, Juan Alvaro; Arango, Julian Camilo; Buzolin, Marcia; Rehder, Jussara; Pedroza, Luis Alberto; Frazão, Josias Brito; Dantas, Vera Maria; Roxo Junior, Persio; Grumach, Anete Sevciovic; Costa-Carvalho, Beatriz Tavares; Bustamante, Jacinta; Condino-Neto, Antonio
Source: Scandinavian Journal of Immunology. Unidades: FMRP, ICB
Subjects: DOENÇAS GENÉTICAS, GRANULOMA, CROMATOGRAFIA LÍQUIDA, MUTAÇÃO GENÉTICA (ANÁLISE)
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ABNT
OLIVEIRA-JUNIOR, Edgar Borges de et al. High-performance liquid chromatography under partially denaturing conditions (dHPLC) is a fast and cost effective method for screening molecular defects: four novel mutations found in x-linked chronic granulomatous disease. Scandinavian Journal of Immunology, v. 76, n. 2, p. 158-166, 2012Tradução . . Disponível em: https://doi.org/10.1111/j.1365-3083.2012.02714.x. Acesso em: 03 out. 2024.
APA
Oliveira-Junior, E. B. de, Prando, C., López, J. A., Arango, J. C., Buzolin, M., Rehder, J., et al. (2012). High-performance liquid chromatography under partially denaturing conditions (dHPLC) is a fast and cost effective method for screening molecular defects: four novel mutations found in x-linked chronic granulomatous disease. Scandinavian Journal of Immunology, 76( 2), 158-166. doi:10.1111/j.1365-3083.2012.02714.x
NLM
Oliveira-Junior EB de, Prando C, López JA, Arango JC, Buzolin M, Rehder J, Pedroza LA, Frazão JB, Dantas VM, Roxo Junior P, Grumach AS, Costa-Carvalho BT, Bustamante J, Condino-Neto A. High-performance liquid chromatography under partially denaturing conditions (dHPLC) is a fast and cost effective method for screening molecular defects: four novel mutations found in x-linked chronic granulomatous disease [Internet]. Scandinavian Journal of Immunology. 2012 ; 76( 2): 158-166.[citado 2024 out. 03 ] Available from: https://doi.org/10.1111/j.1365-3083.2012.02714.x
Vancouver
Oliveira-Junior EB de, Prando C, López JA, Arango JC, Buzolin M, Rehder J, Pedroza LA, Frazão JB, Dantas VM, Roxo Junior P, Grumach AS, Costa-Carvalho BT, Bustamante J, Condino-Neto A. High-performance liquid chromatography under partially denaturing conditions (dHPLC) is a fast and cost effective method for screening molecular defects: four novel mutations found in x-linked chronic granulomatous disease [Internet]. Scandinavian Journal of Immunology. 2012 ; 76( 2): 158-166.[citado 2024 out. 03 ] Available from: https://doi.org/10.1111/j.1365-3083.2012.02714.x
Artigo de periodico
Allogeneic hematopoietic stem cell transplantation in children with primary immunodeficiencies: Hospital Israelita Albert Einstein experience (2011)
Fernandes, Juliana Folloni; Kerbauy, Fabio Rodrigues; Ribeiro, Andreza Alice Feitosa; Kutner, Jose Mauro; Camargo, Luis Fernando Aranha; Stape, Adalberto; Troster, Eduardo Juan; Zamperlini-Netto, Gabriele; Azambuja, Alessandra Milani Prandini de; Carvalho, Bruna; Dorna, Mayra de Barros; Vilela, Marluce dos Santos; Jacob, Cristina Miuki Abe; Costa-Carvalho, Beatriz Tavares; Cunha, Jose Marcos; Carneiro-Sampaio, Magda Maria; Hamerschlak, Nelson
Source: Einstein. Unidade: FM
Subjects: CELULAS-TRONCO (TRANSPLANTE), HEMATOPOESE, DOENÇAS IMUNOLÓGICAS (IMUNOLOGIA)
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ABNT
FERNANDES, Juliana Folloni et al. Allogeneic hematopoietic stem cell transplantation in children with primary immunodeficiencies: Hospital Israelita Albert Einstein experience. Einstein, v. 9, n. 2, p. 140-144, 2011Tradução . . Disponível em: https://doi.org/10.1590/s1679-45082011ao2007. Acesso em: 03 out. 2024.
APA
Fernandes, J. F., Kerbauy, F. R., Ribeiro, A. A. F., Kutner, J. M., Camargo, L. F. A., Stape, A., et al. (2011). Allogeneic hematopoietic stem cell transplantation in children with primary immunodeficiencies: Hospital Israelita Albert Einstein experience. Einstein, 9( 2), 140-144. doi:10.1590/s1679-45082011ao2007
NLM
Fernandes JF, Kerbauy FR, Ribeiro AAF, Kutner JM, Camargo LFA, Stape A, Troster EJ, Zamperlini-Netto G, Azambuja AMP de, Carvalho B, Dorna M de B, Vilela M dos S, Jacob CMA, Costa-Carvalho BT, Cunha JM, Carneiro-Sampaio MM, Hamerschlak N. Allogeneic hematopoietic stem cell transplantation in children with primary immunodeficiencies: Hospital Israelita Albert Einstein experience [Internet]. Einstein. 2011 ; 9( 2): 140-144.[citado 2024 out. 03 ] Available from: https://doi.org/10.1590/s1679-45082011ao2007
Vancouver
Fernandes JF, Kerbauy FR, Ribeiro AAF, Kutner JM, Camargo LFA, Stape A, Troster EJ, Zamperlini-Netto G, Azambuja AMP de, Carvalho B, Dorna M de B, Vilela M dos S, Jacob CMA, Costa-Carvalho BT, Cunha JM, Carneiro-Sampaio MM, Hamerschlak N. Allogeneic hematopoietic stem cell transplantation in children with primary immunodeficiencies: Hospital Israelita Albert Einstein experience [Internet]. Einstein. 2011 ; 9( 2): 140-144.[citado 2024 out. 03 ] Available from: https://doi.org/10.1590/s1679-45082011ao2007
Artigo de periodico
Imunodeficiências primárias na prática clínica do especialista em alergia e imunologia clínica do Brasil (2011)
Costa-Carvalho, Beatriz Tavares; Sano, Flávio; Rosario, Nelson A.; Condino-Neto, Antonio; Solé, Dirceu
Source: Revista Brasileira de Alergia e Imunopatologia. Unidade: ICB
Assunto: IMUNOLOGIA
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ABNT
COSTA-CARVALHO, Beatriz Tavares et al. Imunodeficiências primárias na prática clínica do especialista em alergia e imunologia clínica do Brasil. Revista Brasileira de Alergia e Imunopatologia, v. 34, p. 241-250, 2011Tradução . . Acesso em: 03 out. 2024.
APA
Costa-Carvalho, B. T., Sano, F., Rosario, N. A., Condino-Neto, A., & Solé, D. (2011). Imunodeficiências primárias na prática clínica do especialista em alergia e imunologia clínica do Brasil. Revista Brasileira de Alergia e Imunopatologia, 34, 241-250.
NLM
Costa-Carvalho BT, Sano F, Rosario NA, Condino-Neto A, Solé D. Imunodeficiências primárias na prática clínica do especialista em alergia e imunologia clínica do Brasil. Revista Brasileira de Alergia e Imunopatologia. 2011 ; 34 241-250.[citado 2024 out. 03 ]
Vancouver
Costa-Carvalho BT, Sano F, Rosario NA, Condino-Neto A, Solé D. Imunodeficiências primárias na prática clínica do especialista em alergia e imunologia clínica do Brasil. Revista Brasileira de Alergia e Imunopatologia. 2011 ; 34 241-250.[citado 2024 out. 03 ]
Artigo de periodico
Skipping of exon 30 in C5 gene results in complete human C5 deficiency and demonstrates the importance of C5d and CUB domains for stability (2009)
Aguilar-Ramirez, Priscilia; Reis, Edimara da Silva; Florido, Marlene P. C.; Barbosa, Angela Silva; Farah, Chuck Shaker ; Costa-Carvalho, Beatriz Tavares; Isaac, Lourdes
Source: Molecular Immunology. Unidades: IQ, ICB
Subjects: MENINGITE, IMUNOLOGIA
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ABNT
AGUILAR-RAMIREZ, Priscilia et al. Skipping of exon 30 in C5 gene results in complete human C5 deficiency and demonstrates the importance of C5d and CUB domains for stability. Molecular Immunology, v. 46, n. 10, p. 2116-2123, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.molimm.2008.10.035. Acesso em: 03 out. 2024.
APA
Aguilar-Ramirez, P., Reis, E. da S., Florido, M. P. C., Barbosa, A. S., Farah, C. S., Costa-Carvalho, B. T., & Isaac, L. (2009). Skipping of exon 30 in C5 gene results in complete human C5 deficiency and demonstrates the importance of C5d and CUB domains for stability. Molecular Immunology, 46( 10), 2116-2123. doi:10.1016/j.molimm.2008.10.035
NLM
Aguilar-Ramirez P, Reis E da S, Florido MPC, Barbosa AS, Farah CS, Costa-Carvalho BT, Isaac L. Skipping of exon 30 in C5 gene results in complete human C5 deficiency and demonstrates the importance of C5d and CUB domains for stability [Internet]. Molecular Immunology. 2009 ; 46( 10): 2116-2123.[citado 2024 out. 03 ] Available from: https://doi.org/10.1016/j.molimm.2008.10.035
Vancouver
Aguilar-Ramirez P, Reis E da S, Florido MPC, Barbosa AS, Farah CS, Costa-Carvalho BT, Isaac L. Skipping of exon 30 in C5 gene results in complete human C5 deficiency and demonstrates the importance of C5d and CUB domains for stability [Internet]. Molecular Immunology. 2009 ; 46( 10): 2116-2123.[citado 2024 out. 03 ] Available from: https://doi.org/10.1016/j.molimm.2008.10.035
Trabalho de evento-resumo
Essencial role of nuclear factor kappa B (NF-'kapa'B) on NCF1 and NCF2 gene expression in normal, anhidrotic ectodermal dysplasia with immunodeficiency (EDA-ID), and chronic granulomatous disease (CGD) leukocytes (2008)
Aragão-Filho, Walmir Cutrim; Moreira, Juliana; Oliveira-Júnior, Edgar Borges de; Frazão, Josias Brito; Pereira, Paulo Vítor Soeiro; Errante, Paolo Ruggero; Costa-Carvalho, Beatriz Tavares; Bustamante, Jacinta; Casanova, Jean-Laurent; Newburger, Peter E.; Condino Neto, Antonio
Source: Resumos. Conference titles: Congress of the Brazilian Society for Immunology - SBI. Unidade: ICB
Assunto: IMUNOLOGIA
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ABNT
ARAGÃO-FILHO, Walmir Cutrim et al. Essencial role of nuclear factor kappa B (NF-'kapa'B) on NCF1 and NCF2 gene expression in normal, anhidrotic ectodermal dysplasia with immunodeficiency (EDA-ID), and chronic granulomatous disease (CGD) leukocytes. 2008, Anais.. Ribeirão Preto: Instituto de Ciências Biomédicas, Universidade de São Paulo, 2008. . Acesso em: 03 out. 2024.
APA
Aragão-Filho, W. C., Moreira, J., Oliveira-Júnior, E. B. de, Frazão, J. B., Pereira, P. V. S., Errante, P. R., et al. (2008). Essencial role of nuclear factor kappa B (NF-'kapa'B) on NCF1 and NCF2 gene expression in normal, anhidrotic ectodermal dysplasia with immunodeficiency (EDA-ID), and chronic granulomatous disease (CGD) leukocytes. In Resumos. Ribeirão Preto: Instituto de Ciências Biomédicas, Universidade de São Paulo.
NLM
Aragão-Filho WC, Moreira J, Oliveira-Júnior EB de, Frazão JB, Pereira PVS, Errante PR, Costa-Carvalho BT, Bustamante J, Casanova J-L, Newburger PE, Condino Neto A. Essencial role of nuclear factor kappa B (NF-'kapa'B) on NCF1 and NCF2 gene expression in normal, anhidrotic ectodermal dysplasia with immunodeficiency (EDA-ID), and chronic granulomatous disease (CGD) leukocytes. Resumos. 2008 ;[citado 2024 out. 03 ]
Vancouver
Aragão-Filho WC, Moreira J, Oliveira-Júnior EB de, Frazão JB, Pereira PVS, Errante PR, Costa-Carvalho BT, Bustamante J, Casanova J-L, Newburger PE, Condino Neto A. Essencial role of nuclear factor kappa B (NF-'kapa'B) on NCF1 and NCF2 gene expression in normal, anhidrotic ectodermal dysplasia with immunodeficiency (EDA-ID), and chronic granulomatous disease (CGD) leukocytes. Resumos. 2008 ;[citado 2024 out. 03 ]
Artigo de periodico
Primary Immunodeficiency Diseases in Latin America: The Second Report of the LAGID1 Registry (2007)
Leiva, Lily E.; Zelasco, Marta; Oleastro, Matías; Carneiro-Sampaio, Magda; Condino-Neto, Antonio; Costa-Carvalho, Beatriz Tavares; Grumach, Anete Sevciovic; Quezada, Arnoldo; Patiño, Pablo; Franco, José Luiz; Porras, Oscar; Rodriguez, Francisco Javier; Espinosa-Rosales, Francisco Javier; Espinosa-Padilla, Sara Elva; Almillategui, Diva; Martinez, Celia; Tafur, Juan Rodriguez; Valentín, Marilyn; Benarroch, Lorena; Barroso, Rosy; Sorensen, Ricardo U.
Source: Journal of Clinical Immunology. Unidades: FM, ICB
Subjects: DOENÇAS IMUNOLÓGICAS (IMUNOLOGIA), AMÉRICA LATINA, DOENÇAS IMUNOLÓGICAS (EPIDEMIOLOGIA)
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ABNT
LEIVA, Lily E. et al. Primary Immunodeficiency Diseases in Latin America: The Second Report of the LAGID1 Registry. Journal of Clinical Immunology, v. 27, n. 1, p. 101-108, 2007Tradução . . Disponível em: https://doi.org/10.1007/s10875-006-9052-0. Acesso em: 03 out. 2024.
APA
Leiva, L. E., Zelasco, M., Oleastro, M., Carneiro-Sampaio, M., Condino-Neto, A., Costa-Carvalho, B. T., et al. (2007). Primary Immunodeficiency Diseases in Latin America: The Second Report of the LAGID1 Registry. Journal of Clinical Immunology, 27( 1), 101-108. doi:10.1007/s10875-006-9052-0
NLM
Leiva LE, Zelasco M, Oleastro M, Carneiro-Sampaio M, Condino-Neto A, Costa-Carvalho BT, Grumach AS, Quezada A, Patiño P, Franco JL, Porras O, Rodriguez FJ, Espinosa-Rosales FJ, Espinosa-Padilla SE, Almillategui D, Martinez C, Tafur JR, Valentín M, Benarroch L, Barroso R, Sorensen RU. Primary Immunodeficiency Diseases in Latin America: The Second Report of the LAGID1 Registry [Internet]. Journal of Clinical Immunology. 2007 ; 27( 1): 101-108.[citado 2024 out. 03 ] Available from: https://doi.org/10.1007/s10875-006-9052-0
Vancouver
Leiva LE, Zelasco M, Oleastro M, Carneiro-Sampaio M, Condino-Neto A, Costa-Carvalho BT, Grumach AS, Quezada A, Patiño P, Franco JL, Porras O, Rodriguez FJ, Espinosa-Rosales FJ, Espinosa-Padilla SE, Almillategui D, Martinez C, Tafur JR, Valentín M, Benarroch L, Barroso R, Sorensen RU. Primary Immunodeficiency Diseases in Latin America: The Second Report of the LAGID1 Registry [Internet]. Journal of Clinical Immunology. 2007 ; 27( 1): 101-108.[citado 2024 out. 03 ] Available from: https://doi.org/10.1007/s10875-006-9052-0
Artigo de periodico
Primary immunodeficiency diseases in Latin America: the second report of the lagid registry (2007)
Leiva, Lily E.; Zelazco, Marta; Oleastro, Matías; Carneiro-Sampaio, Magda Maria Sales; Condino-Neto, Antonio; Costa-Carvalho, Beatriz Tavares; Grumach, Anete Sevciovic; Quezada, Arnoldo; Patiño, Pablo; Franco, José Luis; Porras, Oscar; Rodríguez, Francisco Javier; Espinosa-Rosales, Francisco Javier; Espinosa-Padilla, Sara Elva; Almillategui, Diva; Martínez, Celia; Tafur, Juan Rodríguez; Valentín, Marilyn; Benarroch, Lorena; Barroso, Rosy; Sorensen, Ricardo U.
Source: Journal of Clinical Immunology. Unidades: ICB, FM
Assunto: IMUNOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LEIVA, Lily E. et al. Primary immunodeficiency diseases in Latin America: the second report of the lagid registry. Journal of Clinical Immunology, v. 27, n. 1, p. 101-108, 2007Tradução . . Acesso em: 03 out. 2024.
APA
Leiva, L. E., Zelazco, M., Oleastro, M., Carneiro-Sampaio, M. M. S., Condino-Neto, A., Costa-Carvalho, B. T., et al. (2007). Primary immunodeficiency diseases in Latin America: the second report of the lagid registry. Journal of Clinical Immunology, 27( 1), 101-108.
NLM
Leiva LE, Zelazco M, Oleastro M, Carneiro-Sampaio MMS, Condino-Neto A, Costa-Carvalho BT, Grumach AS, Quezada A, Patiño P, Franco JL, Porras O, Rodríguez FJ, Espinosa-Rosales FJ, Espinosa-Padilla SE, Almillategui D, Martínez C, Tafur JR, Valentín M, Benarroch L, Barroso R, Sorensen RU. Primary immunodeficiency diseases in Latin America: the second report of the lagid registry. Journal of Clinical Immunology. 2007 ; 27( 1): 101-108.[citado 2024 out. 03 ]
Vancouver
Leiva LE, Zelazco M, Oleastro M, Carneiro-Sampaio MMS, Condino-Neto A, Costa-Carvalho BT, Grumach AS, Quezada A, Patiño P, Franco JL, Porras O, Rodríguez FJ, Espinosa-Rosales FJ, Espinosa-Padilla SE, Almillategui D, Martínez C, Tafur JR, Valentín M, Benarroch L, Barroso R, Sorensen RU. Primary immunodeficiency diseases in Latin America: the second report of the lagid registry. Journal of Clinical Immunology. 2007 ; 27( 1): 101-108.[citado 2024 out. 03 ]
Trabalho de evento-resumo
Subpopulação de linfócitos T em vinte e dois pacientes com ataxia telengiectasia (AT) (2007)
Lawrence, Tatiana Cristina; Dantas, Ellen; Rullo, Vera; Almeida, Lisiane C.; Condino-Neto, antonio; Carneiro-Sampaio, Magda M. S.; Nudelman, Victor; Moraes-Pinto, Maria Isabel; Costa-Carvalho, Beatriz Tavares
Source: Resumos. Conference titles: Congresso Paulista de Pediatria. Unidade: FM
Subjects: ATAXIA, LINFÓCITOS T, FORMAÇÃO DE ANTICORPOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LAWRENCE, Tatiana Cristina et al. Subpopulação de linfócitos T em vinte e dois pacientes com ataxia telengiectasia (AT). 2007, Anais.. São Paulo: SPSP, 2007. . Acesso em: 03 out. 2024.
APA
Lawrence, T. C., Dantas, E., Rullo, V., Almeida, L. C., Condino-Neto, antonio, Carneiro-Sampaio, M. M. S., et al. (2007). Subpopulação de linfócitos T em vinte e dois pacientes com ataxia telengiectasia (AT). In Resumos. São Paulo: SPSP.
NLM
Lawrence TC, Dantas E, Rullo V, Almeida LC, Condino-Neto antonio, Carneiro-Sampaio MMS, Nudelman V, Moraes-Pinto MI, Costa-Carvalho BT. Subpopulação de linfócitos T em vinte e dois pacientes com ataxia telengiectasia (AT). Resumos. 2007 ;[citado 2024 out. 03 ]
Vancouver
Lawrence TC, Dantas E, Rullo V, Almeida LC, Condino-Neto antonio, Carneiro-Sampaio MMS, Nudelman V, Moraes-Pinto MI, Costa-Carvalho BT. Subpopulação de linfócitos T em vinte e dois pacientes com ataxia telengiectasia (AT). Resumos. 2007 ;[citado 2024 out. 03 ]
Artigo de periodico
Chronic granulomatous disease in latin american patients: clinical spectrum and molecular genetics (2006)
Agudo-Flórez, Piedad; Prando-Andrade, Carolina Cardoso; López, Juan Alvaro; Costa-Carvalho, Beatriz Tavares; Quezada, Arnoldo; Espinosa, Francisco Jose; Paiva, Maria Aparecida de Souza; Roxo, Persio; Grumach, Anete; Jacob, Cristina Abe; Carneiro-Sampaio, Magda Maria Salles; Newburger, Peter E.; Condino-Neto, Antonio
Source: Pediatric Blood & Cancer. Unidades: ICB, FM
Assunto: IMUNOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
AGUDO-FLÓREZ, Piedad et al. Chronic granulomatous disease in latin american patients: clinical spectrum and molecular genetics. Pediatric Blood & Cancer, v. 46, n. 2, p. 243-252, 2006Tradução . . Disponível em: https://doi.org/10.1002/pbc.20455. Acesso em: 03 out. 2024.
APA
Agudo-Flórez, P., Prando-Andrade, C. C., López, J. A., Costa-Carvalho, B. T., Quezada, A., Espinosa, F. J., et al. (2006). Chronic granulomatous disease in latin american patients: clinical spectrum and molecular genetics. Pediatric Blood & Cancer, 46( 2), 243-252. doi:10.1002/pbc.20455
NLM
Agudo-Flórez P, Prando-Andrade CC, López JA, Costa-Carvalho BT, Quezada A, Espinosa FJ, Paiva MA de S, Roxo P, Grumach A, Jacob CA, Carneiro-Sampaio MMS, Newburger PE, Condino-Neto A. Chronic granulomatous disease in latin american patients: clinical spectrum and molecular genetics [Internet]. Pediatric Blood & Cancer. 2006 ; 46( 2): 243-252.[citado 2024 out. 03 ] Available from: https://doi.org/10.1002/pbc.20455
Vancouver
Agudo-Flórez P, Prando-Andrade CC, López JA, Costa-Carvalho BT, Quezada A, Espinosa FJ, Paiva MA de S, Roxo P, Grumach A, Jacob CA, Carneiro-Sampaio MMS, Newburger PE, Condino-Neto A. Chronic granulomatous disease in latin american patients: clinical spectrum and molecular genetics [Internet]. Pediatric Blood & Cancer. 2006 ; 46( 2): 243-252.[citado 2024 out. 03 ] Available from: https://doi.org/10.1002/pbc.20455
Artigo de periodico
Hyperresponsiveness of neutrophils from gp 91(phox) deficient patients to lipopolysaccharide and serum amyloid A (2004)
Hatanaka, Elaine; Costa-Carvalho, Beatriz Tavares; Condino-Neto, Antonio; Campa, Ana
Source: Immunology Letters. Unidade: FCF
Subjects: NEUTRÓFILOS, INTERLEUCINA 8, MONÓCITOS, CITOCINAS
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ABNT
HATANAKA, Elaine et al. Hyperresponsiveness of neutrophils from gp 91(phox) deficient patients to lipopolysaccharide and serum amyloid A. Immunology Letters, v. 94, n. 1-2, p. 43-46, 2004Tradução . . Disponível em: https://doi.org/10.1016/j.imlet.2004.04.016. Acesso em: 03 out. 2024.
APA
Hatanaka, E., Costa-Carvalho, B. T., Condino-Neto, A., & Campa, A. (2004). Hyperresponsiveness of neutrophils from gp 91(phox) deficient patients to lipopolysaccharide and serum amyloid A. Immunology Letters, 94( 1-2), 43-46. doi:10.1016/j.imlet.2004.04.016
NLM
Hatanaka E, Costa-Carvalho BT, Condino-Neto A, Campa A. Hyperresponsiveness of neutrophils from gp 91(phox) deficient patients to lipopolysaccharide and serum amyloid A [Internet]. Immunology Letters. 2004 ; 94( 1-2): 43-46.[citado 2024 out. 03 ] Available from: https://doi.org/10.1016/j.imlet.2004.04.016
Vancouver
Hatanaka E, Costa-Carvalho BT, Condino-Neto A, Campa A. Hyperresponsiveness of neutrophils from gp 91(phox) deficient patients to lipopolysaccharide and serum amyloid A [Internet]. Immunology Letters. 2004 ; 94( 1-2): 43-46.[citado 2024 out. 03 ] Available from: https://doi.org/10.1016/j.imlet.2004.04.016

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