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Artigo de periodico-carta/editorial
Primary immunodeficiencies: a decade of progress and a promising future (2021)
Meyts, Isabelle ; Bousfiha, Aziz; Duff, Carla ; Singh, Surjit; Lau, Yu Lung ; Condino Neto, Antonio ; Bezrodnik, Liliana ; Ali, Adli ; Adeli, Mehdi ; Drabwell, José
Source: Frontiers in Immunology. Unidade: ICB
Subjects: IMUNOLOGIA, IMUNODEFICIÊNCIA DE VARIÁVEL COMUM, COVID-19, IMUNOGENÉTICA, INFECÇÕES POR CORONAVIRUS, SISTEMA IMUNE
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ABNT
MEYTS, Isabelle et al. Primary immunodeficiencies: a decade of progress and a promising future. Frontiers in Immunology. Lausanne: Instituto de Ciências Biomédicas, Universidade de São Paulo. Disponível em: https://doi.org/10.3389/fimmu.2020.625753. Acesso em: 02 nov. 2024. , 2021
APA
Meyts, I., Bousfiha, A., Duff, C., Singh, S., Lau, Y. L., Condino Neto, A., et al. (2021). Primary immunodeficiencies: a decade of progress and a promising future. Frontiers in Immunology. Lausanne: Instituto de Ciências Biomédicas, Universidade de São Paulo. doi:10.3389/fimmu.2020.625753
NLM
Meyts I, Bousfiha A, Duff C, Singh S, Lau YL, Condino Neto A, Bezrodnik L, Ali A, Adeli M, Drabwell J. Primary immunodeficiencies: a decade of progress and a promising future [Internet]. Frontiers in Immunology. 2021 ; 11 5 .[citado 2024 nov. 02 ] Available from: https://doi.org/10.3389/fimmu.2020.625753
Vancouver
Meyts I, Bousfiha A, Duff C, Singh S, Lau YL, Condino Neto A, Bezrodnik L, Ali A, Adeli M, Drabwell J. Primary immunodeficiencies: a decade of progress and a promising future [Internet]. Frontiers in Immunology. 2021 ; 11 5 .[citado 2024 nov. 02 ] Available from: https://doi.org/10.3389/fimmu.2020.625753
Artigo de periodico
Inherited GATA2 deficiency is dominant by haploinsufficiency and displays incomplete clinical penetrance (2021)
Quintas, Carmen Oleaga ; Oliveira Júnior, Edgar Borges de; Rosain, Jérémie ; Rapaport, Franck ; Deswarte, Caroline ; Guérin, Antoine; Sajjath, Sairaj Munavar ; Zhou, Yu Jerry ; Marot, Stéphane; Lozano, Claire ; Branco, Lidia ; Hidalgo, Nuria Fernández ; Lew, Dukhee Betty ; Brunel, Anne Sophiehttps ; Thomas, Caroline; Launay, Elise ; Arias, Andrés Augusto ; Cuffel, Alexis; Monjo, Vanesa Cunill ; Neehus, Anna-Lena ; Marques, Laura; Roynard, Manon; Vélez, Marcela Moncada ; Gerçeker, Bengü; Colobran, Roger ; Vigué, Marie-Gabrielle; Herrera, Gabriela Lopez ; Ruiz, Laura Berron ; Méndez, Nora Hilda Segura ; Romanillos, Patricia O’Farrill ; Voyer, Tom Le; Puel, Anne ; Chantelot, Christine Bellanné ; Ramirez, Kacy A.; Diaz, Lazaro Lorenzo ; Alejo, Noé Ramirez ; Diego, Rebeca Pérez de ; Condino Neto, Antonio ; Mellouli, Fethi ; Gallego, Carlos Rodriguez; Witte, Torsten ; Restrepo, José Franco; Jobim, Mariana ; Dupuis, Stéphanie Boisson ; Jeziorski, Eric ; Fieschi, Claire ; Vogt, Guillaume ; Donadieu, Jean ; Pasquet, Marlène ; Vasconcelos, Julia; Ardeniz, Fatma Omur; Gallo, Mónica Martínez ; Campos, Regis A.; Jobim, Luiz Fernando; Barricarte, Rubén Martínez ; Liu, Kang; Cobat, Aurélie; Abel, Laurent ; Casanova, Jean-Laurent ; Bustamante, Jacinta
Source: Journal of Clinical Immunology. Unidade: ICB
Subjects: IMUNOLOGIA, IMUNODEFICIÊNCIA DE VARIÁVEL COMUM, TUBERCULOSE, INTERLEUCINA 8, POLIMORFISMO, ALELOS, IMUNOGENÉTICA, MUTAÇÃO GENÉTICA, FENÓTIPOS
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QUINTAS, Carmen Oleaga et al. Inherited GATA2 deficiency is dominant by haploinsufficiency and displays incomplete clinical penetrance. Journal of Clinical Immunology, p. 19 , 2021Tradução . . Disponível em: https://doi.org/10.1007/s10875-020-00930-3. Acesso em: 02 nov. 2024.
APA
Quintas, C. O., Oliveira Júnior, E. B. de, Rosain, J., Rapaport, F., Deswarte, C., Guérin, A., et al. (2021). Inherited GATA2 deficiency is dominant by haploinsufficiency and displays incomplete clinical penetrance. Journal of Clinical Immunology, 19 . doi:10.1007/s10875-020-00930-3
NLM
Quintas CO, Oliveira Júnior EB de, Rosain J, Rapaport F, Deswarte C, Guérin A, Sajjath SM, Zhou YJ, Marot S, Lozano C, Branco L, Hidalgo NF, Lew DB, Brunel AS, Thomas C, Launay E, Arias AA, Cuffel A, Monjo VC, Neehus A-L, Marques L, Roynard M, Vélez MM, Gerçeker B, Colobran R, Vigué M-G, Herrera GL, Ruiz LB, Méndez NHS, Romanillos PO’F, Voyer TL, Puel A, Chantelot CB, Ramirez KA, Diaz LL, Alejo NR, Diego RP de, Condino Neto A, Mellouli F, Gallego CR, Witte T, Restrepo JF, Jobim M, Dupuis SB, Jeziorski E, Fieschi C, Vogt G, Donadieu J, Pasquet M, Vasconcelos J, Ardeniz FO, Gallo MM, Campos RA, Jobim LF, Barricarte RM, Liu K, Cobat A, Abel L, Casanova J-L, Bustamante J. Inherited GATA2 deficiency is dominant by haploinsufficiency and displays incomplete clinical penetrance [Internet]. Journal of Clinical Immunology. 2021 ;19 .[citado 2024 nov. 02 ] Available from: https://doi.org/10.1007/s10875-020-00930-3
Vancouver
Quintas CO, Oliveira Júnior EB de, Rosain J, Rapaport F, Deswarte C, Guérin A, Sajjath SM, Zhou YJ, Marot S, Lozano C, Branco L, Hidalgo NF, Lew DB, Brunel AS, Thomas C, Launay E, Arias AA, Cuffel A, Monjo VC, Neehus A-L, Marques L, Roynard M, Vélez MM, Gerçeker B, Colobran R, Vigué M-G, Herrera GL, Ruiz LB, Méndez NHS, Romanillos PO’F, Voyer TL, Puel A, Chantelot CB, Ramirez KA, Diaz LL, Alejo NR, Diego RP de, Condino Neto A, Mellouli F, Gallego CR, Witte T, Restrepo JF, Jobim M, Dupuis SB, Jeziorski E, Fieschi C, Vogt G, Donadieu J, Pasquet M, Vasconcelos J, Ardeniz FO, Gallo MM, Campos RA, Jobim LF, Barricarte RM, Liu K, Cobat A, Abel L, Casanova J-L, Bustamante J. Inherited GATA2 deficiency is dominant by haploinsufficiency and displays incomplete clinical penetrance [Internet]. Journal of Clinical Immunology. 2021 ;19 .[citado 2024 nov. 02 ] Available from: https://doi.org/10.1007/s10875-020-00930-3
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: 02 nov. 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 nov. 02 ] 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 nov. 02 ] Available from: https://doi.org/10.1016/j.jaci.2019.08.002
Artigo de periodico
X-linked agammaglobulinemia (XLA): phenotype, diagnosis, and therapeutic challenges around the world (2019)
El-Sayed, Zeinab A. ; Abramova, Irina ; Aldave, Juan Carlos ; Al-Herz, Waleed ; Bezrodnik, Liliana ; Boukari, Rachida ; Bousfilha, Ahmed Aziz; Cancrini, Caterina ; Dbaibo, Ghassan ; Derfalvi, Beata; Dogu, Figen ; Edgar, J. Davi M.; Eley, Brian ; El-Owaidy, Rasha Hasan ; Espinosa-Padilla, Sara Elva; Galal, Nermeen ; Haerynck, Filomeen ; Hanna-Wakim, Rima ; Hossny, Elham ; Ikinciogullari, Aydan ; Kamal, Ebtihal; Kanegane, Hirokaku ; Kechout, Nadia ; Lau, Yu Lung ; Morio, Tomohiro; Moschese, Viviana ; Neves, João Farela ; Quederni, Monia; Paganelli, Roberto ; Paris, Kenneth ; Pignata, Claudia; Plebani, Alessandro ; Qamar, Farah Naz; Qureshi, Sonia ; Radhakrishnan, Nita ; Rezaei, Nima; Rosario, Nelson ; Routes, John ; Sanchez, Berta; Sediva, Anna ; Seppanen, Mikko Risto Juhana ; Serrano, Edith Gonzalez ; Shcherbina, Anna ; Singh, Surjit ; Siniah, Sangeetha; Spadaro, Guiseppe; Tang, Mimi ; Vinet, Ana Maria; Volokha, Alla ; Sullivan, Kathleen E. ; Condino Neto, Antonio
Source: World Allergy Organization Journal. Unidade: ICB
Subjects: FENÓTIPOS, AGAMAGLOBULINEMIA, IMUNODEFICIÊNCIA DE VARIÁVEL COMUM, IMUNOGLOBULINAS, GENÉTICA APLICADA, ALERGIA E IMUNOLOGIA, VACINAS, LINFÓCITOS
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ABNT
EL-SAYED, Zeinab A. et al. X-linked agammaglobulinemia (XLA): phenotype, diagnosis, and therapeutic challenges around the world. World Allergy Organization Journal, v. 12, p. 9 , 2019Tradução . . Disponível em: https://doi.org/10.1016/j.waojou.2019.100018. Acesso em: 02 nov. 2024.
APA
El-Sayed, Z. A., Abramova, I., Aldave, J. C., Al-Herz, W., Bezrodnik, L., Boukari, R., et al. (2019). X-linked agammaglobulinemia (XLA): phenotype, diagnosis, and therapeutic challenges around the world. World Allergy Organization Journal, 12, 9 . doi:10.1016/j.waojou.2019.100018
NLM
El-Sayed ZA, Abramova I, Aldave JC, Al-Herz W, Bezrodnik L, Boukari R, Bousfilha AA, Cancrini C, Dbaibo G, Derfalvi B, Dogu F, Edgar JDM, Eley B, El-Owaidy RH, Espinosa-Padilla SE, Galal N, Haerynck F, Hanna-Wakim R, Hossny E, Ikinciogullari A, Kamal E, Kanegane H, Kechout N, Lau YL, Morio T, Moschese V, Neves JF, Quederni M, Paganelli R, Paris K, Pignata C, Plebani A, Qamar FN, Qureshi S, Radhakrishnan N, Rezaei N, Rosario N, Routes J, Sanchez B, Sediva A, Seppanen MRJ, Serrano EG, Shcherbina A, Singh S, Siniah S, Spadaro G, Tang M, Vinet AM, Volokha A, Sullivan KE, Condino Neto A. X-linked agammaglobulinemia (XLA): phenotype, diagnosis, and therapeutic challenges around the world [Internet]. World Allergy Organization Journal. 2019 ; 12 9 .[citado 2024 nov. 02 ] Available from: https://doi.org/10.1016/j.waojou.2019.100018
Vancouver
El-Sayed ZA, Abramova I, Aldave JC, Al-Herz W, Bezrodnik L, Boukari R, Bousfilha AA, Cancrini C, Dbaibo G, Derfalvi B, Dogu F, Edgar JDM, Eley B, El-Owaidy RH, Espinosa-Padilla SE, Galal N, Haerynck F, Hanna-Wakim R, Hossny E, Ikinciogullari A, Kamal E, Kanegane H, Kechout N, Lau YL, Morio T, Moschese V, Neves JF, Quederni M, Paganelli R, Paris K, Pignata C, Plebani A, Qamar FN, Qureshi S, Radhakrishnan N, Rezaei N, Rosario N, Routes J, Sanchez B, Sediva A, Seppanen MRJ, Serrano EG, Shcherbina A, Singh S, Siniah S, Spadaro G, Tang M, Vinet AM, Volokha A, Sullivan KE, Condino Neto A. X-linked agammaglobulinemia (XLA): phenotype, diagnosis, and therapeutic challenges around the world [Internet]. World Allergy Organization Journal. 2019 ; 12 9 .[citado 2024 nov. 02 ] Available from: https://doi.org/10.1016/j.waojou.2019.100018
Artigo de periodico
Culture-attenuated pathogenic Leptospira lose the ability to survive to complement-mediated-killing due to lower expression of factor H binding proteins (2019)
Torres, Azaf Moreno ; Jiménez, Irving R. Malvido; Moctezuma, Alejandro de la Peña ; Sánchez, Luz O. Castillo ; Fraga, Tatiana Rodrigues ; Barbosa, Angela Silva ; Isaac, Lourdes ; Ruiz, Alfredo Sahagún
Source: Microbes and Infection. Unidade: ICB
Subjects: IMUNOLOGIA, LEPTOSPIROSE, BACTÉRIAS GRAM-NEGATIVAS, PROTEÍNAS
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ABNT
TORRES, Azaf Moreno et al. Culture-attenuated pathogenic Leptospira lose the ability to survive to complement-mediated-killing due to lower expression of factor H binding proteins. Microbes and Infection, v. 21, n. 8–9, p. 377-385, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.micinf.2019.03.001. Acesso em: 02 nov. 2024.
APA
Torres, A. M., Jiménez, I. R. M., Moctezuma, A. de la P., Sánchez, L. O. C., Fraga, T. R., Barbosa, A. S., et al. (2019). Culture-attenuated pathogenic Leptospira lose the ability to survive to complement-mediated-killing due to lower expression of factor H binding proteins. Microbes and Infection, 21( 8–9), 377-385. doi:10.1016/j.micinf.2019.03.001
NLM
Torres AM, Jiménez IRM, Moctezuma A de la P, Sánchez LOC, Fraga TR, Barbosa AS, Isaac L, Ruiz AS. Culture-attenuated pathogenic Leptospira lose the ability to survive to complement-mediated-killing due to lower expression of factor H binding proteins [Internet]. Microbes and Infection. 2019 ; 21( 8–9): 377-385.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1016/j.micinf.2019.03.001
Vancouver
Torres AM, Jiménez IRM, Moctezuma A de la P, Sánchez LOC, Fraga TR, Barbosa AS, Isaac L, Ruiz AS. Culture-attenuated pathogenic Leptospira lose the ability to survive to complement-mediated-killing due to lower expression of factor H binding proteins [Internet]. Microbes and Infection. 2019 ; 21( 8–9): 377-385.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1016/j.micinf.2019.03.001
Artigo de periodico
Changing the lives of people with primary immunodeficiencies (PI) with early testing and diagnosis (2018)
Condino-Neto, Antonio; Espinosa-Rosales, Francisco Javier
Source: Frontiers in Immunology. Unidade: ICB
Subjects: IMUNODEFICIÊNCIA DE VARIÁVEL COMUM, MORBIDADE, MORTALIDADE
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CONDINO-NETO, Antonio e ESPINOSA-ROSALES, Francisco Javier. Changing the lives of people with primary immunodeficiencies (PI) with early testing and diagnosis. Frontiers in Immunology, v. 9, p. 4 , 2018Tradução . . Disponível em: https://doi.org/10.3389/fimmu.2018.01439. Acesso em: 02 nov. 2024.
APA
Condino-Neto, A., & Espinosa-Rosales, F. J. (2018). Changing the lives of people with primary immunodeficiencies (PI) with early testing and diagnosis. Frontiers in Immunology, 9, 4 . doi:10.3389/fimmu.2018.01439
NLM
Condino-Neto A, Espinosa-Rosales FJ. Changing the lives of people with primary immunodeficiencies (PI) with early testing and diagnosis [Internet]. Frontiers in Immunology. 2018 ; 9 4 .[citado 2024 nov. 02 ] Available from: https://doi.org/10.3389/fimmu.2018.01439
Vancouver
Condino-Neto A, Espinosa-Rosales FJ. Changing the lives of people with primary immunodeficiencies (PI) with early testing and diagnosis [Internet]. Frontiers in Immunology. 2018 ; 9 4 .[citado 2024 nov. 02 ] Available from: https://doi.org/10.3389/fimmu.2018.01439
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: 02 nov. 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 nov. 02 ] 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 nov. 02 ] Available from: https://doi.org/10.1126/sciimmunol.aau8714
Artigo de periodico
Hematopoietic stem cell transplantation in 29 patientshemizygous for hypomorphic IKBKG/NEMO mutations (2017)
Miot, Charline; Imai, Kohsuke; Imai, Chihaya; Mancini, Anthony J.; Kucuk, Zeynep Yesim; Kawai, Tokomki; Nishikomori, Ryuta; Ito, Etsuro; Pellier, Isabelle; Girod, Sophie Dupuis; Rosain, Jeremie; Sasaki, Shinya; Chandrakasan, Shanmuganathan; Schmid, Jana Pachlopnik; Okano, Tsubasa; Colin, Estelle; Olaya-Vargas, Alberto; Yamazaki-Nakashimada, Marco; Qasim, Waseem; Padilla, Sara Espinosa; Jones, Andrea; Krol, Alfons; Cole, Nyree; Jolles, Stephen; Bleesing, Jack; Vraetz, Thomas; Gennery, Andrew R.; Abinun, Mario; Güngör, Tayfun; Costa-Carvalho, Beatriz; Condino-Neto, Antonio; Veys, Paul; Holland, Steven M.; Uzel, Gulbu; Moshous, Despina; Neven, Benedicte; Blanche, Stéphane; Ehl, Stephan; Döffinger, Rainer; Patel, Smita Y.; Puel, Anne; Bustamante, Jacinta; Gelfand, Erwin W.; Casanova, Jean-Laurent; Orange, Jordan S.; Picard, Capucine
Source: Blood. Unidade: ICB
Assunto: IMUNOLOGIA
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ABNT
MIOT, Charline et al. Hematopoietic stem cell transplantation in 29 patientshemizygous for hypomorphic IKBKG/NEMO mutations. Blood, v. 130, n. 12, p. 1456-1467, 2017Tradução . . Disponível em: https://doi.org/10.1182/blood-2017-03-771600. Acesso em: 02 nov. 2024.
APA
Miot, C., Imai, K., Imai, C., Mancini, A. J., Kucuk, Z. Y., Kawai, T., et al. (2017). Hematopoietic stem cell transplantation in 29 patientshemizygous for hypomorphic IKBKG/NEMO mutations. Blood, 130( 12), 1456-1467. doi:10.1182/blood-2017-03-771600
NLM
Miot C, Imai K, Imai C, Mancini AJ, Kucuk ZY, Kawai T, Nishikomori R, Ito E, Pellier I, Girod SD, Rosain J, Sasaki S, Chandrakasan S, Schmid JP, Okano T, Colin E, Olaya-Vargas A, Yamazaki-Nakashimada M, Qasim W, Padilla SE, Jones A, Krol A, Cole N, Jolles S, Bleesing J, Vraetz T, Gennery AR, Abinun M, Güngör T, Costa-Carvalho B, Condino-Neto A, Veys P, Holland SM, Uzel G, Moshous D, Neven B, Blanche S, Ehl S, Döffinger R, Patel SY, Puel A, Bustamante J, Gelfand EW, Casanova J-L, Orange JS, Picard C. Hematopoietic stem cell transplantation in 29 patientshemizygous for hypomorphic IKBKG/NEMO mutations [Internet]. Blood. 2017 ; 130( 12): 1456-1467.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1182/blood-2017-03-771600
Vancouver
Miot C, Imai K, Imai C, Mancini AJ, Kucuk ZY, Kawai T, Nishikomori R, Ito E, Pellier I, Girod SD, Rosain J, Sasaki S, Chandrakasan S, Schmid JP, Okano T, Colin E, Olaya-Vargas A, Yamazaki-Nakashimada M, Qasim W, Padilla SE, Jones A, Krol A, Cole N, Jolles S, Bleesing J, Vraetz T, Gennery AR, Abinun M, Güngör T, Costa-Carvalho B, Condino-Neto A, Veys P, Holland SM, Uzel G, Moshous D, Neven B, Blanche S, Ehl S, Döffinger R, Patel SY, Puel A, Bustamante J, Gelfand EW, Casanova J-L, Orange JS, Picard C. Hematopoietic stem cell transplantation in 29 patientshemizygous for hypomorphic IKBKG/NEMO mutations [Internet]. Blood. 2017 ; 130( 12): 1456-1467.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1182/blood-2017-03-771600
Artigo de periodico
Mycobacterial disease in patients with chronic granulomatous disease: A retrospective analysis of 71 cases (2016)
Conti, Francesca; Reyes, Saul Oswaldo Lugo; Galicia, Lizbeth Blancas; He, Jianxin; Aksu, Güzide; Oliveira Junior, Edgar Borges de; Deswarte, Caroline; Hubeau, Marjorie; Karaca, Neslihan; Suremain, Maylis de; Guérin, Antoine; Baba, Laia Ait; Prando, Carolina; Guerrero, Gloria G; Emiroglu, Melike; Öz, Fatma Nur; Nakashimada, Marco Antonio Yamazaki; Serrano, Edith Gonzalez; Espinosa, Sara; Barlan, Isil; Pérez, Nestor; Regairaz, Lorena; Morales, Héctor Eduardo Guido; Bezrondnik, Liliana; Giovanni, Daniela Di; Dbaibo, Ghassan; Ailal, Fatima; Galicchio, Miguel; Oleastro, Matias; Chemli, Jalel; Danielian, Silvia; Perez, Laura; Ortega, Maria Claudia; Lavin, Susana Soto; Hertecant, Joseph; Anal, Ozden; Kechout, Nadia; Al-Idrissi, Eman; ElGhazali, Gehad; Bondareko, Anastasia; Chernyshova, Liudmyla; Ciznar, Peter; Herbigneaux, Rose-Marie; Diabate, Aminata; Ndaga, Stéphanie; Konte, Barik; Czarna, Ambre; Migaud, Mélanie; Sánchez, Sigifredo Pedraza; Zaidi, Mussaret Bano; Vogt, Guillaume; Blanche, Stéphane; Benmustapha, Imen; Mansouri, Davood; Abel, Laurent; Dupuis, Stéphanie Boisson; Mahlaoui, Nizar; Bousfiha, Ahmed Aziz; Picard, Capucine; Barbouche, Ridha; Al-Muhsen, Saleh; Rosales, Francisco J. Espinosa; Kütükçüler, Necil; Condino Neto, Antonio; Casanova, Jean-Laurent; Bustamante, Jacinta
Source: Journal of Allergy and Clinical Immunology. Unidade: ICB
Subjects: MYCOBACTERIUM, TUBERCULOSE, INFECÇÕES BACTERIANAS E MICOSES, GRANULOMA, IMUNOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CONTI, Francesca et al. Mycobacterial disease in patients with chronic granulomatous disease: A retrospective analysis of 71 cases. Journal of Allergy and Clinical Immunology, v. 138, n. 1, p. 214-248, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.jaci.2015.11.041. Acesso em: 02 nov. 2024.
APA
Conti, F., Reyes, S. O. L., Galicia, L. B., He, J., Aksu, G., Oliveira Junior, E. B. de, et al. (2016). Mycobacterial disease in patients with chronic granulomatous disease: A retrospective analysis of 71 cases. Journal of Allergy and Clinical Immunology, 138( 1), 214-248. doi:10.1016/j.jaci.2015.11.041
NLM
Conti F, Reyes SOL, Galicia LB, He J, Aksu G, Oliveira Junior EB de, Deswarte C, Hubeau M, Karaca N, Suremain M de, Guérin A, Baba LA, Prando C, Guerrero GG, Emiroglu M, Öz FN, Nakashimada MAY, Serrano EG, Espinosa S, Barlan I, Pérez N, Regairaz L, Morales HEG, Bezrondnik L, Giovanni DD, Dbaibo G, Ailal F, Galicchio M, Oleastro M, Chemli J, Danielian S, Perez L, Ortega MC, Lavin SS, Hertecant J, Anal O, Kechout N, Al-Idrissi E, ElGhazali G, Bondareko A, Chernyshova L, Ciznar P, Herbigneaux R-M, Diabate A, Ndaga S, Konte B, Czarna A, Migaud M, Sánchez SP, Zaidi MB, Vogt G, Blanche S, Benmustapha I, Mansouri D, Abel L, Dupuis SB, Mahlaoui N, Bousfiha AA, Picard C, Barbouche R, Al-Muhsen S, Rosales FJE, Kütükçüler N, Condino Neto A, Casanova J-L, Bustamante J. Mycobacterial disease in patients with chronic granulomatous disease: A retrospective analysis of 71 cases [Internet]. Journal of Allergy and Clinical Immunology. 2016 ;138( 1): 214-248.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1016/j.jaci.2015.11.041
Vancouver
Conti F, Reyes SOL, Galicia LB, He J, Aksu G, Oliveira Junior EB de, Deswarte C, Hubeau M, Karaca N, Suremain M de, Guérin A, Baba LA, Prando C, Guerrero GG, Emiroglu M, Öz FN, Nakashimada MAY, Serrano EG, Espinosa S, Barlan I, Pérez N, Regairaz L, Morales HEG, Bezrondnik L, Giovanni DD, Dbaibo G, Ailal F, Galicchio M, Oleastro M, Chemli J, Danielian S, Perez L, Ortega MC, Lavin SS, Hertecant J, Anal O, Kechout N, Al-Idrissi E, ElGhazali G, Bondareko A, Chernyshova L, Ciznar P, Herbigneaux R-M, Diabate A, Ndaga S, Konte B, Czarna A, Migaud M, Sánchez SP, Zaidi MB, Vogt G, Blanche S, Benmustapha I, Mansouri D, Abel L, Dupuis SB, Mahlaoui N, Bousfiha AA, Picard C, Barbouche R, Al-Muhsen S, Rosales FJE, Kütükçüler N, Condino Neto A, Casanova J-L, Bustamante J. Mycobacterial disease in patients with chronic granulomatous disease: A retrospective analysis of 71 cases [Internet]. Journal of Allergy and Clinical Immunology. 2016 ;138( 1): 214-248.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1016/j.jaci.2015.11.041
Artigo de periodico-carta/editorial
Into action: improving access to optimum care for all primary immunodeficiency patients (2016)
Espinosa-Rosales, Francisco J. ; Condino Neto, Antonio ; Franco, José L.; Sorensen, Ricardo U.
Source: Journal of Clinical Immunology. Unidade: ICB
Subjects: IMUNOLOGIA, IMUNODEFICIÊNCIA DE VARIÁVEL COMUM, INFLAMAÇÃO, DOENÇAS AUTOIMUNES, AUTOIMUNIDADE, IMUNOGENÉTICA, IMUNOGLOBULINAS, LINFÓCITOS T
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ESPINOSA-ROSALES, Francisco J. et al. Into action: improving access to optimum care for all primary immunodeficiency patients. Journal of Clinical Immunology. New York: Instituto de Ciências Biomédicas, Universidade de São Paulo. Disponível em: https://doi.org/10.1007/s10875-016-0277-2. Acesso em: 02 nov. 2024. , 2016
APA
Espinosa-Rosales, F. J., Condino Neto, A., Franco, J. L., & Sorensen, R. U. (2016). Into action: improving access to optimum care for all primary immunodeficiency patients. Journal of Clinical Immunology. New York: Instituto de Ciências Biomédicas, Universidade de São Paulo. doi:10.1007/s10875-016-0277-2
NLM
Espinosa-Rosales FJ, Condino Neto A, Franco JL, Sorensen RU. Into action: improving access to optimum care for all primary immunodeficiency patients [Internet]. Journal of Clinical Immunology. 2016 ; 36( 5): 415-417.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1007/s10875-016-0277-2
Vancouver
Espinosa-Rosales FJ, Condino Neto A, Franco JL, Sorensen RU. Into action: improving access to optimum care for all primary immunodeficiency patients [Internet]. Journal of Clinical Immunology. 2016 ; 36( 5): 415-417.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1007/s10875-016-0277-2
Artigo de periodico
Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery (2016)
Scott, Eric M.; Halees, A.; Itan, Y.; Spencer, E. G.; He,Y.; Azab, M. A.; Gabriel, S. B.; Belkadi, A.; Boisson, B.; Abel, L.; Clark, A. G.; Consortium, Greater Middle East Variome; Alkuraya, F. S.; Casanova, J. L.; Gleeson, J. G.; Rahim, S. A.; Abdel-Hadi, S.; Abdel-Salam, G.; Abdel-Salam, E.; Abdou, M.; Abhytankar, A.; Adimi, P.; Ahmad, J.; Akcakus, M.; Aksu, G.; Hajjar, S. A.; Juamaah, S. A.; Muhsen, S. A.; Sannaa, N. A.; Tameni, S. A.; Al-Aama, J.; Al-Allawi, N.; Al-Baradie, R.; Al-Gazali, L.; Al-Hashem, A.; Al-Herz, W.; Al-Jeaid, D.; Al-Tawari, A.; Alangari, A.; Alcais, A.; AlFawaz, T.; Alsum, Z.; Ammar-Khodja, A.; Amouian, S.; Ammar-Khodja, A.; Arikan, C.; Aryani, O.; Aslanger, A.; Aydogmus, C.; Aytekin, C.; Azam, M.; Bansagi, B.; Barbouche, M. R.; Bastaki, L.; Ben-Omran, T.; Bindu, P. S.; Blancas, L.; Boisson-Dupuis, S.; Bonnet, D.; Stambouli, O. B.; Bousfiha, A.; Boussafara, L.; Boutros, J.; Bustamante, J.; Caksen, H.; Camcioglu, Y.; Catherinot, E.; Celik, F. C.; Ciancanelli, M.; Cipe, F. E.; Clark, G.; Cobat, A.; Comu, S.; Condie, A.; Condino-Neto, A.; Desai, M.; Dobyns, W.; Dogu, F.; Domaia, M.; Egritas, O.; Azbaoui, S. E.; Baghdadi, J. E.; Ruby, M. E.; El-Harouni, A.; Elfeky,R. A.; Elghazali, G.; Faqeih, E.; Fenerci, E.; Fieschi, C.; Funda, C.; Gamal, I.; Gelik, U.; Genel, F.; Gezdirici, A.; Girisha, K. M.; Goldstein, A.; Grattan-Smith, P.; Gupta, N.; Hahn, J.; Hatipoglu, N.; Hennekam, R.; Houshmand, M.; Ichai, P.; Ikinciogullari, A.; Ismail, S.; Jalas, C.; Jouanguy, E.; Kabra, M.; Kalkan, G.; Kara, M.; Karaca, N.; Karaer, K.; Kariminejad, A.; Kayserili, H.; Keser-Emiroglu, M.; Kilic, S. S.; Kissani, N.; Kokron, C.; Koul, R.; Kutukculer, N.; Lanternier, F.; Mahdaviani, A.; Mahlaoui, N.; Mansour, L.; Mansouri, D.; Margari, L.; Valente, E. M.; Marzouki, N.; Masri, A.; Megahed, A.; Megahed, H.; Mekki, N.; Mesdaghi, M.; Mikati, M.; Mojahedi, F.; Mulley, J.; Nampoothiri, S.; Navarrete, C.; Omar, T.; Oraby, A.; Pandaluz, A.; Parvaneh, N.; Patiroglu, T.; Koc, Z. P.; Pellier, I.; Picard, C.; Puel, A.; Raas-Rothschild, A.; Rajab, A.; Raoult, D.; Reisli, I.; Rezaei, N.; Sabri, A.; Sahin, Y.; Saleem, L.; Salem, F.; AlSediq, N. S.; Sanal, O.; Sanger, T.; Shakankiry, H.; Shang, L.; Shehata, N.; Shembesh, N.; Shkalim, V.; Softah, A.; Sogaty, S.; Soliman, N.; Sonmez Aunaci, F.; Sztriha, L.; Taibi-Berrah, L.; Temtamy, S.; Tonekaboni, H.; Trauner, D.; Tuysuz, B.; Varan, A.; Vogt, G.; Walsh, C.; Woods, G.; Yesil, G.; Yildiran, A.; Yildiz, B.; Yuksel, A.; Zaki, M.; Zhang, S. Y.
Source: Nature Genetics. Unidade: ICB
Subjects: VARIAÇÃO GENÉTICA, GENÉTICA, GENÉTICA DE POPULAÇÕES, IMUNOLOGIA, ALELOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SCOTT, Eric M. et al. Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery. Nature Genetics, v. 48, n. 9, p. 1071-1076, 2016Tradução . . Disponível em: https://doi.org/10.1038/ng.3592. Acesso em: 02 nov. 2024.
APA
Scott, E. M., Halees, A., Itan, Y., Spencer, E. G., He, Y., Azab, M. A., et al. (2016). Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery. Nature Genetics, 48( 9), 1071-1076. doi:10.1038/ng.3592
NLM
Scott EM, Halees A, Itan Y, Spencer EG, He Y, Azab MA, Gabriel SB, Belkadi A, Boisson B, Abel L, Clark AG, Consortium GMEV, Alkuraya FS, Casanova JL, Gleeson JG, Rahim SA, Abdel-Hadi S, Abdel-Salam G, Abdel-Salam E, Abdou M, Abhytankar A, Adimi P, Ahmad J, Akcakus M, Aksu G, Hajjar SA, Juamaah SA, Muhsen SA, Sannaa NA, Tameni SA, Al-Aama J, Al-Allawi N, Al-Baradie R, Al-Gazali L, Al-Hashem A, Al-Herz W, Al-Jeaid D, Al-Tawari A, Alangari A, Alcais A, AlFawaz T, Alsum Z, Ammar-Khodja A, Amouian S, Ammar-Khodja A, Arikan C, Aryani O, Aslanger A, Aydogmus C, Aytekin C, Azam M, Bansagi B, Barbouche MR, Bastaki L, Ben-Omran T, Bindu PS, Blancas L, Boisson-Dupuis S, Bonnet D, Stambouli OB, Bousfiha A, Boussafara L, Boutros J, Bustamante J, Caksen H, Camcioglu Y, Catherinot E, Celik FC, Ciancanelli M, Cipe FE, Clark G, Cobat A, Comu S, Condie A, Condino-Neto A, Desai M, Dobyns W, Dogu F, Domaia M, Egritas O, Azbaoui SE, Baghdadi JE, Ruby ME, El-Harouni A, Elfeky RA, Elghazali G, Faqeih E, Fenerci E, Fieschi C, Funda C, Gamal I, Gelik U, Genel F, Gezdirici A, Girisha KM, Goldstein A, Grattan-Smith P, Gupta N, Hahn J, Hatipoglu N, Hennekam R, Houshmand M, Ichai P, Ikinciogullari A, Ismail S, Jalas C, Jouanguy E, Kabra M, Kalkan G, Kara M, Karaca N, Karaer K, Kariminejad A, Kayserili H, Keser-Emiroglu M, Kilic SS, Kissani N, Kokron C, Koul R, Kutukculer N, Lanternier F, Mahdaviani A, Mahlaoui N, Mansour L, Mansouri D, Margari L, Valente EM, Marzouki N, Masri A, Megahed A, Megahed H, Mekki N, Mesdaghi M, Mikati M, Mojahedi F, Mulley J, Nampoothiri S, Navarrete C, Omar T, Oraby A, Pandaluz A, Parvaneh N, Patiroglu T, Koc ZP, Pellier I, Picard C, Puel A, Raas-Rothschild A, Rajab A, Raoult D, Reisli I, Rezaei N, Sabri A, Sahin Y, Saleem L, Salem F, AlSediq NS, Sanal O, Sanger T, Shakankiry H, Shang L, Shehata N, Shembesh N, Shkalim V, Softah A, Sogaty S, Soliman N, Sonmez Aunaci F, Sztriha L, Taibi-Berrah L, Temtamy S, Tonekaboni H, Trauner D, Tuysuz B, Varan A, Vogt G, Walsh C, Woods G, Yesil G, Yildiran A, Yildiz B, Yuksel A, Zaki M, Zhang SY. Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery [Internet]. Nature Genetics. 2016 ; 48( 9): 1071-1076.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1038/ng.3592
Vancouver
Scott EM, Halees A, Itan Y, Spencer EG, He Y, Azab MA, Gabriel SB, Belkadi A, Boisson B, Abel L, Clark AG, Consortium GMEV, Alkuraya FS, Casanova JL, Gleeson JG, Rahim SA, Abdel-Hadi S, Abdel-Salam G, Abdel-Salam E, Abdou M, Abhytankar A, Adimi P, Ahmad J, Akcakus M, Aksu G, Hajjar SA, Juamaah SA, Muhsen SA, Sannaa NA, Tameni SA, Al-Aama J, Al-Allawi N, Al-Baradie R, Al-Gazali L, Al-Hashem A, Al-Herz W, Al-Jeaid D, Al-Tawari A, Alangari A, Alcais A, AlFawaz T, Alsum Z, Ammar-Khodja A, Amouian S, Ammar-Khodja A, Arikan C, Aryani O, Aslanger A, Aydogmus C, Aytekin C, Azam M, Bansagi B, Barbouche MR, Bastaki L, Ben-Omran T, Bindu PS, Blancas L, Boisson-Dupuis S, Bonnet D, Stambouli OB, Bousfiha A, Boussafara L, Boutros J, Bustamante J, Caksen H, Camcioglu Y, Catherinot E, Celik FC, Ciancanelli M, Cipe FE, Clark G, Cobat A, Comu S, Condie A, Condino-Neto A, Desai M, Dobyns W, Dogu F, Domaia M, Egritas O, Azbaoui SE, Baghdadi JE, Ruby ME, El-Harouni A, Elfeky RA, Elghazali G, Faqeih E, Fenerci E, Fieschi C, Funda C, Gamal I, Gelik U, Genel F, Gezdirici A, Girisha KM, Goldstein A, Grattan-Smith P, Gupta N, Hahn J, Hatipoglu N, Hennekam R, Houshmand M, Ichai P, Ikinciogullari A, Ismail S, Jalas C, Jouanguy E, Kabra M, Kalkan G, Kara M, Karaca N, Karaer K, Kariminejad A, Kayserili H, Keser-Emiroglu M, Kilic SS, Kissani N, Kokron C, Koul R, Kutukculer N, Lanternier F, Mahdaviani A, Mahlaoui N, Mansour L, Mansouri D, Margari L, Valente EM, Marzouki N, Masri A, Megahed A, Megahed H, Mekki N, Mesdaghi M, Mikati M, Mojahedi F, Mulley J, Nampoothiri S, Navarrete C, Omar T, Oraby A, Pandaluz A, Parvaneh N, Patiroglu T, Koc ZP, Pellier I, Picard C, Puel A, Raas-Rothschild A, Rajab A, Raoult D, Reisli I, Rezaei N, Sabri A, Sahin Y, Saleem L, Salem F, AlSediq NS, Sanal O, Sanger T, Shakankiry H, Shang L, Shehata N, Shembesh N, Shkalim V, Softah A, Sogaty S, Soliman N, Sonmez Aunaci F, Sztriha L, Taibi-Berrah L, Temtamy S, Tonekaboni H, Trauner D, Tuysuz B, Varan A, Vogt G, Walsh C, Woods G, Yesil G, Yildiran A, Yildiz B, Yuksel A, Zaki M, Zhang SY. Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery [Internet]. Nature Genetics. 2016 ; 48( 9): 1071-1076.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1038/ng.3592
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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 02 nov. 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 nov. 02 ] 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 nov. 02 ] Available from: https://doi.org/10.1002/pbc.25674

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