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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
Fonte: Journal of Clinical Immunology. Unidade: ICB
Assuntos: IMUNOLOGIA, IMUNODEFICIÊNCIA DE VARIÁVEL COMUM, TUBERCULOSE, INTERLEUCINA 8, POLIMORFISMO, ALELOS, IMUNOGENÉTICA, MUTAÇÃO GENÉTICA, FENÓTIPOS
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ABNT
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: 11 maio 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 maio 11 ] 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 maio 11 ] Available from: https://doi.org/10.1007/s10875-020-00930-3
Artigo de periodico
Hematologically important mutations: X-linked chronic granulomatous disease (fourth update) (2021)
Roos, Dirk; Leeuwen, Karin van; Hsu, Amy P.; Priel, Debra Long ; Begtrup, Amber ; Brandon, Rhonda; Stasia, Marie José ; Bakri, Faris Ghalib ; Köker, Nezihe ; Köker, Mustafa Yavuz ; Madkaika, Manisha; Boer, Martin de ; Morato, Maria Bravo Garcia ; Shephard, Juan Luis Valdivieso; Roesler, Joachim ; Kanegane, Hirokazu ; Kawai, Toshinao ; Matteo, Gigliola Di ; Shahrooei, Mohammad ; Bustamante, Jacinta ; Rawat, Amit ; Vignesh, Pandiarajan ; Mortaz, Esmaeil ; Fayezi, Abbas; Cagdas, Deniz ; Tezcan, Ilhan ; Kitcharoensakkul, Maleewan ; Dinauer, Mary C. ; Meyts, Isabelle; Wolach, Baruch; Condino Neto, Antonio ; Zerbe, Christa S. ; Holland, Steven M.; Malech, Harry L. ; Gallin, John I.; Kuhns, Douglas B.
Fonte: Blood Cells, Molecules and Diseases. Unidade: ICB
Assuntos: IMUNOLOGIA, IMUNODEFICIÊNCIA DE VARIÁVEL COMUM, MUTAÇÃO GENÉTICA, DOENÇAS SANGUÍNEAS E LINFÁTICAS, SUPERÓXIDO DISMUTASE, ATIVAÇÃO ENZIMÁTICA, IMUNOGENÉTICA, ENZIMAS
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ROOS, Dirk et al. Hematologically important mutations: X-linked chronic granulomatous disease (fourth update). Blood Cells, Molecules and Diseases, v. 90, p. 1-36, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.bcmd.2021.102587. Acesso em: 11 maio 2024.
APA
Roos, D., Leeuwen, K. van, Hsu, A. P., Priel, D. L., Begtrup, A., Brandon, R., et al. (2021). Hematologically important mutations: X-linked chronic granulomatous disease (fourth update). Blood Cells, Molecules and Diseases, 90, 1-36. doi:10.1016/j.bcmd.2021.102587
NLM
Roos D, Leeuwen K van, Hsu AP, Priel DL, Begtrup A, Brandon R, Stasia MJ, Bakri FG, Köker N, Köker MY, Madkaika M, Boer M de, Morato MBG, Shephard JLV, Roesler J, Kanegane H, Kawai T, Matteo GD, Shahrooei M, Bustamante J, Rawat A, Vignesh P, Mortaz E, Fayezi A, Cagdas D, Tezcan I, Kitcharoensakkul M, Dinauer MC, Meyts I, Wolach B, Condino Neto A, Zerbe CS, Holland SM, Malech HL, Gallin JI, Kuhns DB. Hematologically important mutations: X-linked chronic granulomatous disease (fourth update) [Internet]. Blood Cells, Molecules and Diseases. 2021 ; 90 1-36.[citado 2024 maio 11 ] Available from: https://doi.org/10.1016/j.bcmd.2021.102587
Vancouver
Roos D, Leeuwen K van, Hsu AP, Priel DL, Begtrup A, Brandon R, Stasia MJ, Bakri FG, Köker N, Köker MY, Madkaika M, Boer M de, Morato MBG, Shephard JLV, Roesler J, Kanegane H, Kawai T, Matteo GD, Shahrooei M, Bustamante J, Rawat A, Vignesh P, Mortaz E, Fayezi A, Cagdas D, Tezcan I, Kitcharoensakkul M, Dinauer MC, Meyts I, Wolach B, Condino Neto A, Zerbe CS, Holland SM, Malech HL, Gallin JI, Kuhns DB. Hematologically important mutations: X-linked chronic granulomatous disease (fourth update) [Internet]. Blood Cells, Molecules and Diseases. 2021 ; 90 1-36.[citado 2024 maio 11 ] Available from: https://doi.org/10.1016/j.bcmd.2021.102587
Artigo de periodico
Hematologically important mutations: the autosomal forms of chronic granulomatous disease (third update) (2021)
Roos, Dirk ; Leeuwen, Karin van ; Hsu, Amy P. ; Priel, Debra Long ; Begtrup, Amber ; Brandon, Rhonda; Rawat, Amit ; Vignesh, Pandiarajan ; Madkaikar, Manesha ; Stasia, Marie José ; Bakri, Faris Ghalib ; Boer, Martin de ; Roesler, Joachim ; Köker, Nezihe ; Köker, Mustafa Yavuz ; Jakobsen, Marianne ; Bustamante, Jacinta ; Morato, Maria Bravo Garcia ; Condino Neto, Antonio
Fonte: Blood Cells, Molecules and Diseases. Unidade: ICB
Assuntos: IMUNOLOGIA, DOENÇAS GENÉTICAS, IMUNODEFICIÊNCIA DE VARIÁVEL COMUM, IMUNOGENÉTICA, MUTAÇÃO GENÉTICA, POLIMORFISMO, INIBIDORES DE ENZIMAS, PERÓXIDO DE HIDROGÊNIO, APOPTOSE, HERANÇA GENÉTICA
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ABNT
ROOS, Dirk et al. Hematologically important mutations: the autosomal forms of chronic granulomatous disease (third update). Blood Cells, Molecules and Diseases, v. 92, p. 1-16, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.bcmd.2021.102596. Acesso em: 11 maio 2024.
APA
Roos, D., Leeuwen, K. van, Hsu, A. P., Priel, D. L., Begtrup, A., Brandon, R., et al. (2021). Hematologically important mutations: the autosomal forms of chronic granulomatous disease (third update). Blood Cells, Molecules and Diseases, 92, 1-16. doi:10.1016/j.bcmd.2021.102596
NLM
Roos D, Leeuwen K van, Hsu AP, Priel DL, Begtrup A, Brandon R, Rawat A, Vignesh P, Madkaikar M, Stasia MJ, Bakri FG, Boer M de, Roesler J, Köker N, Köker MY, Jakobsen M, Bustamante J, Morato MBG, Condino Neto A. Hematologically important mutations: the autosomal forms of chronic granulomatous disease (third update) [Internet]. Blood Cells, Molecules and Diseases. 2021 ; 92 1-16.[citado 2024 maio 11 ] Available from: https://doi.org/10.1016/j.bcmd.2021.102596
Vancouver
Roos D, Leeuwen K van, Hsu AP, Priel DL, Begtrup A, Brandon R, Rawat A, Vignesh P, Madkaikar M, Stasia MJ, Bakri FG, Boer M de, Roesler J, Köker N, Köker MY, Jakobsen M, Bustamante J, Morato MBG, Condino Neto A. Hematologically important mutations: the autosomal forms of chronic granulomatous disease (third update) [Internet]. Blood Cells, Molecules and Diseases. 2021 ; 92 1-16.[citado 2024 maio 11 ] Available from: https://doi.org/10.1016/j.bcmd.2021.102596
Artigo de periodico
Sweet dreams: therapeutic insights, targeting imaging and physiologic evidence linking sleep, melatonin and diabetic nephropathy (2020)
Afsar, Baris; Afsar, Rengin Elsurer; Sag, Alan A. ; Kanbay, Asiye ; Korkmaz, Hakan ; Covic, Adrian ; Ortiz, Alberto; Kanbay, Mehmet ; Cipolla Neto, José
Fonte: Clinical Kidney Journal. Unidade: ICB
Assuntos: FISIOLOGIA, MELATONINA, DIABETES MELLITUS, NEFROPATIAS, ESTRESSE OXIDATIVO, INFLAMAÇÃO, RITMO CIRCADIANO, SONO, GLICOSE, COLESTEROL
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ABNT
AFSAR, Baris et al. Sweet dreams: therapeutic insights, targeting imaging and physiologic evidence linking sleep, melatonin and diabetic nephropathy. Clinical Kidney Journal, v. 13, n. 4, p. 522-530, 2020Tradução . . Disponível em: https://doi.org/10.1093/ckj/sfz198. Acesso em: 11 maio 2024.
APA
Afsar, B., Afsar, R. E., Sag, A. A., Kanbay, A., Korkmaz, H., Covic, A., et al. (2020). Sweet dreams: therapeutic insights, targeting imaging and physiologic evidence linking sleep, melatonin and diabetic nephropathy. Clinical Kidney Journal, 13( 4), 522-530. doi:10.1093/ckj/sfz198
NLM
Afsar B, Afsar RE, Sag AA, Kanbay A, Korkmaz H, Covic A, Ortiz A, Kanbay M, Cipolla Neto J. Sweet dreams: therapeutic insights, targeting imaging and physiologic evidence linking sleep, melatonin and diabetic nephropathy [Internet]. Clinical Kidney Journal. 2020 ; 13( 4): 522-530.[citado 2024 maio 11 ] Available from: https://doi.org/10.1093/ckj/sfz198
Vancouver
Afsar B, Afsar RE, Sag AA, Kanbay A, Korkmaz H, Covic A, Ortiz A, Kanbay M, Cipolla Neto J. Sweet dreams: therapeutic insights, targeting imaging and physiologic evidence linking sleep, melatonin and diabetic nephropathy [Internet]. Clinical Kidney Journal. 2020 ; 13( 4): 522-530.[citado 2024 maio 11 ] Available from: https://doi.org/10.1093/ckj/sfz198
Artigo de periodico-carta/editorial
U100: an innovative USERN platform for education and research without borders (2020)
Momtazmanesh, Sara ; Rahmani, Farzaneh ; Delavari, Farnaz; Vahedi, Zahra; Ebadirad, Saleheh; Fathi, Mahsa Keshavarz ; Moallemian, Marjan; Ashkevarian, Saboura; Kolahi, Mohammad Reza; Samimiat, Alireza ; Raei, Nahid ; Rouzrokh, Pouria ; Alesaeid, Samira; Jaberipour, Ali; Bakhshi, Sara; Zanjani, Sasan Paryad; Perc, Matjaz ; Uddin, Lucina Q. ; Allali, Abdelkader; Sullivan, Kathleen; Taher, Abbas; Baris, Safa ; Ozen, Ahmet; Aydiner, Elif Karakoc ; Aldave, Juan Carlo ; Latiff, Amir Hamzah Abdul ; Herz, Waleed Al ; Phantumvanit, Prathi ; Stashchak, Anzhel ; Kryvenko, Oleksandr; Stashchak, Mykola; Utomo, Didik ; Salunke, Deepak ; Kelishadi, Roya; Hedayati, Mojtaba; MirzaHossein, Shahrokh; Bondarenko, Anastasiia ; Goudouris, Ekaterini ; Condino Neto, Antonio ; Vieira, Duarte Nuno ; Ulrichs, Timo ; Pavalkis, Dainius; Rosivall, László ; Ochs, Hans ; Rezaei, Nima
Fonte: Acta Medica Iranica. Unidade: ICB
Assuntos: IMUNOLOGIA, EDUCAÇÃO MÉDICA, PESQUISA CIENTÍFICA, INFORMAÇÃO EM SAÚDE
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MOMTAZMANESH, Sara et al. U100: an innovative USERN platform for education and research without borders. Acta Medica Iranica. Tehran: Instituto de Ciências Biomédicas, Universidade de São Paulo. Disponível em: https://doi.org/10.18502/acta.v58i1.3698. Acesso em: 11 maio 2024. , 2020
APA
Momtazmanesh, S., Rahmani, F., Delavari, F., Vahedi, Z., Ebadirad, S., Fathi, M. K., et al. (2020). U100: an innovative USERN platform for education and research without borders. Acta Medica Iranica. Tehran: Instituto de Ciências Biomédicas, Universidade de São Paulo. doi:10.18502/acta.v58i1.3698
NLM
Momtazmanesh S, Rahmani F, Delavari F, Vahedi Z, Ebadirad S, Fathi MK, Moallemian M, Ashkevarian S, Kolahi MR, Samimiat A, Raei N, Rouzrokh P, Alesaeid S, Jaberipour A, Bakhshi S, Zanjani SP, Perc M, Uddin LQ, Allali A, Sullivan K, Taher A, Baris S, Ozen A, Aydiner EK, Aldave JC, Latiff AHA, Herz WA, Phantumvanit P, Stashchak A, Kryvenko O, Stashchak M, Utomo D, Salunke D, Kelishadi R, Hedayati M, MirzaHossein S, Bondarenko A, Goudouris E, Condino Neto A, Vieira DN, Ulrichs T, Pavalkis D, Rosivall L, Ochs H, Rezaei N. U100: an innovative USERN platform for education and research without borders [Internet]. Acta Medica Iranica. 2020 ; 58( 1): 1-3.[citado 2024 maio 11 ] Available from: https://doi.org/10.18502/acta.v58i1.3698
Vancouver
Momtazmanesh S, Rahmani F, Delavari F, Vahedi Z, Ebadirad S, Fathi MK, Moallemian M, Ashkevarian S, Kolahi MR, Samimiat A, Raei N, Rouzrokh P, Alesaeid S, Jaberipour A, Bakhshi S, Zanjani SP, Perc M, Uddin LQ, Allali A, Sullivan K, Taher A, Baris S, Ozen A, Aydiner EK, Aldave JC, Latiff AHA, Herz WA, Phantumvanit P, Stashchak A, Kryvenko O, Stashchak M, Utomo D, Salunke D, Kelishadi R, Hedayati M, MirzaHossein S, Bondarenko A, Goudouris E, Condino Neto A, Vieira DN, Ulrichs T, Pavalkis D, Rosivall L, Ochs H, Rezaei N. U100: an innovative USERN platform for education and research without borders [Internet]. Acta Medica Iranica. 2020 ; 58( 1): 1-3.[citado 2024 maio 11 ] Available from: https://doi.org/10.18502/acta.v58i1.3698
Artigo de periodico
All together to fight COVID-19 (2020)
Momtazmanesh, Sara ; Ochs, Hans D.; Uddin, Lucina Q. ; Perc, Matjaz ; Routes, John M. ; Vieira, Duarte Nuno ; Al-Herz, Waleed ; Baris, Safa ; Prando, Carolina ; Rosivall, Laszlo ; Latiff, Amir Hamzah Abdul ; Ulrichs, Timo ; Roudenok, Vasili; Becerra, Juan Carlos Aldave; Salunke, Deepak B. ; Goudouris, Ekaterini ; Condino Neto, Antonio ; Stashchak, Anzhela ; Kryvenko, Oleksandr; Stashchak, Mykola; Bondarenko, Anastasia; Rezaei, Nima
Fonte: American Journal of Tropical Medicine and Hygiene. Unidade: ICB
Assuntos: IMUNOLOGIA, INFECÇÕES RESPIRATÓRIAS, DOENÇAS RESPIRATÓRIAS, VÍRUS DE RNA
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ABNT
MOMTAZMANESH, Sara et al. All together to fight COVID-19. American Journal of Tropical Medicine and Hygiene, v. 102, n. 6, p. 1181 - 1183, 2020Tradução . . Disponível em: https://doi.org/10.4269/ajtmh.20-0281. Acesso em: 11 maio 2024.
APA
Momtazmanesh, S., Ochs, H. D., Uddin, L. Q., Perc, M., Routes, J. M., Vieira, D. N., et al. (2020). All together to fight COVID-19. American Journal of Tropical Medicine and Hygiene, 102( 6), 1181 - 1183. doi:10.4269/ajtmh.20-0281
NLM
Momtazmanesh S, Ochs HD, Uddin LQ, Perc M, Routes JM, Vieira DN, Al-Herz W, Baris S, Prando C, Rosivall L, Latiff AHA, Ulrichs T, Roudenok V, Becerra JCA, Salunke DB, Goudouris E, Condino Neto A, Stashchak A, Kryvenko O, Stashchak M, Bondarenko A, Rezaei N. All together to fight COVID-19 [Internet]. American Journal of Tropical Medicine and Hygiene. 2020 ; 102( 6): 1181 - 1183.[citado 2024 maio 11 ] Available from: https://doi.org/10.4269/ajtmh.20-0281
Vancouver
Momtazmanesh S, Ochs HD, Uddin LQ, Perc M, Routes JM, Vieira DN, Al-Herz W, Baris S, Prando C, Rosivall L, Latiff AHA, Ulrichs T, Roudenok V, Becerra JCA, Salunke DB, Goudouris E, Condino Neto A, Stashchak A, Kryvenko O, Stashchak M, Bondarenko A, Rezaei N. All together to fight COVID-19 [Internet]. American Journal of Tropical Medicine and Hygiene. 2020 ; 102( 6): 1181 - 1183.[citado 2024 maio 11 ] Available from: https://doi.org/10.4269/ajtmh.20-0281
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
Fonte: World Allergy Organization Journal. Unidade: ICB
Assuntos: 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: 11 maio 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 maio 11 ] 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 maio 11 ] Available from: https://doi.org/10.1016/j.waojou.2019.100018
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
Fonte: Science Immunology. Unidade: ICB
Assuntos: 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: 11 maio 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 maio 11 ] 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 maio 11 ] 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.
Fonte: Journal of Allergy and Clinical Immunology. Unidade: ICB
Assuntos: 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: 11 maio 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 maio 11 ] 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 maio 11 ] Available from: https://doi.org/10.1016/j.jaci.2016.07.039
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
Fonte: Journal of Allergy and Clinical Immunology. Unidade: ICB
Assuntos: 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: 11 maio 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 maio 11 ] 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 maio 11 ] Available from: https://doi.org/10.1016/j.jaci.2015.11.041
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.
Fonte: Nature Genetics. Unidade: ICB
Assuntos: 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: 11 maio 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 maio 11 ] 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 maio 11 ] Available from: https://doi.org/10.1038/ng.3592

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