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Page 1
Epidermodysplasia verruciformis as a manifestation of ARTEMIS deficiency in a young adult.
Tahiat A, Badran YR, Chou J, Cangemi B, Lefranc G, Labgaa ZM, Oussalam S, Kaddouri-Slimani A, Belarbi A, Bendissari-Bouzid K, Gharnaout M, Geha RS, Djidjik R, Massaad MJ. Tahiat A, et al. Among authors: badran yr. J Allergy Clin Immunol. 2017 Jan;139(1):372-375.e4. doi: 10.1016/j.jaci.2016.07.024. Epub 2016 Aug 24. J Allergy Clin Immunol. 2017. PMID: 27568080 No abstract available.
Mutations in pyrin masquerading as a primary immunodeficiency.
Badran YR, Rajab M, Hanna-Wakim R, Bainter W, Cangemi B, Massaad MJ, Dbaibo G, Geha RS, Chou J. Badran YR, et al. Clin Immunol. 2016 Oct;171:65-66. doi: 10.1016/j.clim.2016.08.016. Epub 2016 Aug 15. Clin Immunol. 2016. PMID: 27538774
Advances in basic and clinical immunology in 2016.
Chinen J, Badran YR, Geha RS, Chou JS, Fried AJ. Chinen J, et al. Among authors: badran yr. J Allergy Clin Immunol. 2017 Oct;140(4):959-973. doi: 10.1016/j.jaci.2017.07.023. Epub 2017 Aug 19. J Allergy Clin Immunol. 2017. PMID: 28826774 Review.
Hypomorphic variants in AK2 reveal the contribution of mitochondrial function to B-cell activation.
Chou J, Alazami AM, Jaber F, Hoyos-Bachiloglu R, Jones J, Weeks S, Alosaimi MF, Bainter W, Cangemi B, Badran YR, Mohammed R, Alroqi F, Almutairi A, Al-Onazi N, AlAjaji S, Al-Saud B, Arnaout R, Elkins M, Devana S, Imperial J, Li B, Drexhage L, Abdel Rahman AM, Jacob M, Haddad H, Hanna-Wakim R, Dbaibo G, Massaad MJ, Dasouki M, Mikhael R, Baz Z, Geha RS, Al-Mousa H. Chou J, et al. Among authors: badran yr. J Allergy Clin Immunol. 2020 Jul;146(1):192-202. doi: 10.1016/j.jaci.2019.12.004. Epub 2019 Dec 17. J Allergy Clin Immunol. 2020. PMID: 31862378 Clinical Trial.
Leucine-rich repeat containing 8A (LRRC8A)-dependent volume-regulated anion channel activity is dispensable for T-cell development and function.
Platt CD, Chou J, Houlihan P, Badran YR, Kumar L, Bainter W, Poliani PL, Perez CJ, Dent SYR, Clapham DE, Benavides F, Geha RS. Platt CD, et al. Among authors: badran yr. J Allergy Clin Immunol. 2017 Dec;140(6):1651-1659.e1. doi: 10.1016/j.jaci.2016.12.974. Epub 2017 Feb 10. J Allergy Clin Immunol. 2017. PMID: 28192143 Free PMC article.
Combined immunodeficiency with autoimmunity caused by a homozygous missense mutation in inhibitor of nuclear factor 𝛋B kinase alpha (IKKα).
Bainter W, Lougaris V, Wallace JG, Badran Y, Hoyos-Bachiloglu R, Peters Z, Wilkie H, Das M, Janssen E, Beano A, Farhat KB, Kam C, Bercich L, Incardona P, Villanacci V, Bondioni MP, Meini A, Baronio M, Abarzua P, Parolini S, Tabellini G, Maio S, Schmidt B, Goldsmith JD, Murphy G, Hollander G, Plebani A, Chou J, Geha RS. Bainter W, et al. Sci Immunol. 2021 Sep 17;6(63):eabf6723. doi: 10.1126/sciimmunol.abf6723. Epub 2021 Sep 17. Sci Immunol. 2021. PMID: 34533979 Free PMC article.
21 results