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Artigo de periodico
The first Iranian cohort of pediatric patients with activated phosphoinositide 3-kinase-δ (PI3Kδ) syndrome (APDS) (2021)
Fekrvand, Saba ; Delavaria, Samaneh; Chavoshzadehbb, Zahra; Sherkat, Roya; Mahadavianian, Seyed Alireza; Shabestarie, Mahnaz Sadeghi; Azizif, Gholamreza; Arzanian, Mohammad Taghi; Shamsian, Bibi Shahin; Eskandarzadeh, Shabnam; Eslami, Narges ; Rae, William ; Mohammadik, Javad; Abolhassani, Hassan ; Yazdani, Reza ; Aghamohammadi, Asghar ; Condino Neto, Antonio
Source: Immunological Investigations. Unidade: ICB
Subjects: PROTEÍNAS QUINASES, IMUNODEFICIÊNCIA DE VARIÁVEL COMUM, ESTUDOS DE COORTES, INFECÇÕES RESPIRATÓRIAS, DOENÇAS RESPIRATÓRIAS, LINFOMA, MUTAÇÃO GENÉTICA, IMUNOGENÉTICA, GENÓTIPOS, FENÓTIPOS
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ABNT
FEKRVAND, Saba et al. The first Iranian cohort of pediatric patients with activated phosphoinositide 3-kinase-δ (PI3Kδ) syndrome (APDS). Immunological Investigations, p. 16 , 2021Tradução . . Disponível em: https://doi.org/10.1080/08820139.2020.1863982. Acesso em: 09 nov. 2024.
APA
Fekrvand, S., Delavaria, S., Chavoshzadehbb, Z., Sherkat, R., Mahadavianian, S. A., Shabestarie, M. S., et al. (2021). The first Iranian cohort of pediatric patients with activated phosphoinositide 3-kinase-δ (PI3Kδ) syndrome (APDS). Immunological Investigations, 16 . doi:10.1080/08820139.2020.1863982
NLM
Fekrvand S, Delavaria S, Chavoshzadehbb Z, Sherkat R, Mahadavianian SA, Shabestarie MS, Azizif G, Arzanian MT, Shamsian BS, Eskandarzadeh S, Eslami N, Rae W, Mohammadik J, Abolhassani H, Yazdani R, Aghamohammadi A, Condino Neto A. The first Iranian cohort of pediatric patients with activated phosphoinositide 3-kinase-δ (PI3Kδ) syndrome (APDS) [Internet]. Immunological Investigations. 2021 ;16 .[citado 2024 nov. 09 ] Available from: https://doi.org/10.1080/08820139.2020.1863982
Vancouver
Fekrvand S, Delavaria S, Chavoshzadehbb Z, Sherkat R, Mahadavianian SA, Shabestarie MS, Azizif G, Arzanian MT, Shamsian BS, Eskandarzadeh S, Eslami N, Rae W, Mohammadik J, Abolhassani H, Yazdani R, Aghamohammadi A, Condino Neto A. The first Iranian cohort of pediatric patients with activated phosphoinositide 3-kinase-δ (PI3Kδ) syndrome (APDS) [Internet]. Immunological Investigations. 2021 ;16 .[citado 2024 nov. 09 ] Available from: https://doi.org/10.1080/08820139.2020.1863982
Artigo de periodico
Global systematic review of primary immunodeficiency registries (2020)
Abolhassani, Hassan ; Azizi, Gholamreza ; Sharifi, Laleh ; Yazdani, Reza ; Mohsenzadegan, Monireh; Delavari, Samaneh ; Sohani, Mahsa ; Shirmast, Paniz ; Chavoshzadeh, Zahra ; Mahdavian, Seyed Alireza ; Kalantar, Arash; Tavako, Marzieh; Azad, Farahzad Jabbari ; Ahanchian, Hamid ; Momen, Tooba ; Sherkat, Roya; Shabestari, Mahnaz Sadeghi ; Aleyasin, Soheila; Esmaeilzadeh, Hossein ; Herz, Waleed Al ; Bousfiha, Ahmed Aziz ; Condino Neto, Antonio ; Seppänen, Mikko ; Sullivan, Kathleen E. ; Hammarström, Lennart ; Modell, Vicki; Modell, Fred; Quinn, Jessica ; Orange, Jordan S. ; Aghamohammadi, Asghar
Source: Expert Review of Clinical Immunology. Unidade: ICB
Subjects: IMUNOLOGIA, IMUNODEFICIÊNCIA DE VARIÁVEL COMUM, DOENÇAS IMUNOLÓGICAS, REVISÃO SISTEMÁTICA, DANO AO DNA, IMUNOGENÉTICA, IMUNOENSAIO
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ABNT
ABOLHASSANI, Hassan et al. Global systematic review of primary immunodeficiency registries. Expert Review of Clinical Immunology, v. 16, n. 7, p. 717-732, 2020Tradução . . Disponível em: https://doi.org/10.1080/1744666X.2020.1801422. Acesso em: 09 nov. 2024.
APA
Abolhassani, H., Azizi, G., Sharifi, L., Yazdani, R., Mohsenzadegan, M., Delavari, S., et al. (2020). Global systematic review of primary immunodeficiency registries. Expert Review of Clinical Immunology, 16( 7), 717-732. doi:10.1080/1744666X.2020.1801422
NLM
Abolhassani H, Azizi G, Sharifi L, Yazdani R, Mohsenzadegan M, Delavari S, Sohani M, Shirmast P, Chavoshzadeh Z, Mahdavian SA, Kalantar A, Tavako M, Azad FJ, Ahanchian H, Momen T, Sherkat R, Shabestari MS, Aleyasin S, Esmaeilzadeh H, Herz WA, Bousfiha AA, Condino Neto A, Seppänen M, Sullivan KE, Hammarström L, Modell V, Modell F, Quinn J, Orange JS, Aghamohammadi A. Global systematic review of primary immunodeficiency registries [Internet]. Expert Review of Clinical Immunology. 2020 ; 16( 7): 717-732.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1080/1744666X.2020.1801422
Vancouver
Abolhassani H, Azizi G, Sharifi L, Yazdani R, Mohsenzadegan M, Delavari S, Sohani M, Shirmast P, Chavoshzadeh Z, Mahdavian SA, Kalantar A, Tavako M, Azad FJ, Ahanchian H, Momen T, Sherkat R, Shabestari MS, Aleyasin S, Esmaeilzadeh H, Herz WA, Bousfiha AA, Condino Neto A, Seppänen M, Sullivan KE, Hammarström L, Modell V, Modell F, Quinn J, Orange JS, Aghamohammadi A. Global systematic review of primary immunodeficiency registries [Internet]. Expert Review of Clinical Immunology. 2020 ; 16( 7): 717-732.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1080/1744666X.2020.1801422
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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 09 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. 09 ] 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. 09 ] Available from: https://doi.org/10.1126/sciimmunol.aau8714
Artigo de periodico
Long-term outcomes of 176 patients with X-linked hyper-IgM syndrome treated with or without hematopoietic cell transplantation (2017)
Morena, Maria Teresa de la ; Leonard, David; Torgerson, Troy R.; Marques, Otavio Cabral; Slatter, Mary Anne; Aghamohammadi, Asghar ; Chandra, Sharat; Favela, Luis Murguia ; Bonilla, Francisco A. ; Kanariou, Maria; Damrongwatanasuk, Rongras; Kuo, Caroline Y.; Dvorak, Christopher C. ; Meyts, Isabelle; Chen, Karin ; Kobrynski, Lisa ; Kapoor, Neena; Richter, Darko ; DiGiovanni, Daniela; Dhalla, Fatima ; Farmaki, Evangelia ; Speckmann, Carsten ; Español, Teresa; Shcherbina, Anna YU ; Hanson, Imelda Celine Guerra; Litzman, Jiri ; Routes, John M. ; Wong, Melanie; Fuleihan, Ramsay ; Seneviratne, Suranjith L. ; Small, Trudy N.; Janda, Ales ; Bezrodnik, Liliana; Seger, Reinhard; Raccio, Andrea Gomez; Edgar, John David M. ; Chou, Janet ; Abbott, Jordan Keith ; Montfrans, Joris van ; Granado, Luis Ignacio González ; Bunin, Nancy; Kutukculer, Necil ; Gray, Paul ; Seminario, Gisela; Pasic, Srdjan ; Aquino, Victor; Wysocki, Christian ; Abolhassani, Hassan ; Dorsey, Morna ; Rundles, Charlotte Cunningham ; Knutsen, Alan Paul ; Sleasman, John William ; Carvalho, Beatriz Tavares Costa ; Condino-Neto, Antonio ; Grunebaum, Eyal ; Chapel, Helen ; Ochs, Hans Dieter; Filipovich, Alexandra Hult; Cowan, Mort; Gennery, Andrew ; Cant, Andrew James ; Notarangelo, Luigi D. ; Roifman, Chaim M.
Source: Journal of Allergy and Clinical Immunology. Unidade: ICB
Subjects: IMUNOLOGIA, CÉLULAS-TRONCO, IMUNODEFICIÊNCIA DE VARIÁVEL COMUM, HEMATOPOESE, CÉLULAS SANGUÍNEAS, IMUNOLOGIA CELULAR, DOENÇAS AUTOIMUNES, DOENÇAS IMUNOLÓGICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MORENA, Maria Teresa de la et al. Long-term outcomes of 176 patients with X-linked hyper-IgM syndrome treated with or without hematopoietic cell transplantation. Journal of Allergy and Clinical Immunology, v. 139, n. 4, p. 1282-1292, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.jaci.2016.07.039. Acesso em: 09 nov. 2024.
APA
Morena, M. T. de la, Leonard, D., Torgerson, T. R., Marques, O. C., Slatter, M. A., Aghamohammadi, A., et al. (2017). Long-term outcomes of 176 patients with X-linked hyper-IgM syndrome treated with or without hematopoietic cell transplantation. Journal of Allergy and Clinical Immunology, 139( 4), 1282-1292. doi:10.1016/j.jaci.2016.07.039
NLM
Morena MT de la, Leonard D, Torgerson TR, Marques OC, Slatter MA, Aghamohammadi A, Chandra S, Favela LM, Bonilla FA, Kanariou M, Damrongwatanasuk R, Kuo CY, Dvorak CC, Meyts I, Chen K, Kobrynski L, Kapoor N, Richter D, DiGiovanni D, Dhalla F, Farmaki E, Speckmann C, Español T, Shcherbina AYU, Hanson ICG, Litzman J, Routes JM, Wong M, Fuleihan R, Seneviratne SL, Small TN, Janda A, Bezrodnik L, Seger R, Raccio AG, Edgar JDM, Chou J, Abbott JK, Montfrans J van, Granado LIG, Bunin N, Kutukculer N, Gray P, Seminario G, Pasic S, Aquino V, Wysocki C, Abolhassani H, Dorsey M, Rundles CC, Knutsen AP, Sleasman JW, Carvalho BTC, Condino-Neto A, Grunebaum E, Chapel H, Ochs HD, Filipovich AH, Cowan M, Gennery A, Cant AJ, Notarangelo LD, Roifman CM. Long-term outcomes of 176 patients with X-linked hyper-IgM syndrome treated with or without hematopoietic cell transplantation [Internet]. Journal of Allergy and Clinical Immunology. 2017 ; 139( 4): 1282-1292.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1016/j.jaci.2016.07.039
Vancouver
Morena MT de la, Leonard D, Torgerson TR, Marques OC, Slatter MA, Aghamohammadi A, Chandra S, Favela LM, Bonilla FA, Kanariou M, Damrongwatanasuk R, Kuo CY, Dvorak CC, Meyts I, Chen K, Kobrynski L, Kapoor N, Richter D, DiGiovanni D, Dhalla F, Farmaki E, Speckmann C, Español T, Shcherbina AYU, Hanson ICG, Litzman J, Routes JM, Wong M, Fuleihan R, Seneviratne SL, Small TN, Janda A, Bezrodnik L, Seger R, Raccio AG, Edgar JDM, Chou J, Abbott JK, Montfrans J van, Granado LIG, Bunin N, Kutukculer N, Gray P, Seminario G, Pasic S, Aquino V, Wysocki C, Abolhassani H, Dorsey M, Rundles CC, Knutsen AP, Sleasman JW, Carvalho BTC, Condino-Neto A, Grunebaum E, Chapel H, Ochs HD, Filipovich AH, Cowan M, Gennery A, Cant AJ, Notarangelo LD, Roifman CM. Long-term outcomes of 176 patients with X-linked hyper-IgM syndrome treated with or without hematopoietic cell transplantation [Internet]. Journal of Allergy and Clinical Immunology. 2017 ; 139( 4): 1282-1292.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1016/j.jaci.2016.07.039

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