Bainter W - Search Results

1

Combined immunodeficiency due to a homozygous mutation in ORAI1 that deletes the C-terminus that interacts with STIM 1.

Badran YR, Massaad MJ, Bainter W, Cangemi B, Naseem SU, Javad H, Al-Tamemi S, Geha RS, Chou J. Badran YR, et al. Among authors: bainter w. Clin Immunol. 2016 May;166-167:100-2. doi: 10.1016/j.clim.2016.03.012. Epub 2016 Apr 6. Clin Immunol. 2016. PMID: 27063589

2

A novel mutation in FOXN1 resulting in SCID: a case report and literature review.

Chou J, Massaad MJ, Wakim RH, Bainter W, Dbaibo G, Geha RS. Chou J, et al. Among authors: bainter w. Clin Immunol. 2014 Nov;155(1):30-32. doi: 10.1016/j.clim.2014.08.005. Epub 2014 Aug 27. Clin Immunol. 2014. PMID: 25173801 Review. No abstract available.

3

A novel mutation in ORAI1 presenting with combined immunodeficiency and residual T-cell function.

Chou J, Badran YR, Yee CSK, Bainter W, Ohsumi TK, Al-Hammadi S, Pai SY, Feske S, Geha RS. Chou J, et al. Among authors: bainter w. J Allergy Clin Immunol. 2015 Aug;136(2):479-482.e1. doi: 10.1016/j.jaci.2015.03.050. Epub 2015 Jun 9. J Allergy Clin Immunol. 2015. PMID: 26070885 Free PMC article.

4

A novel mutation in NCF2 associated with autoimmune disease and a solitary late-onset infection.

Chou J, Hsu JT, Bainter W, Al-Attiyah R, Al-Herz W, Geha RS. Chou J, et al. Among authors: bainter w. Clin Immunol. 2015 Dec;161(2):128-30. doi: 10.1016/j.clim.2015.08.003. Epub 2015 Aug 10. Clin Immunol. 2015. PMID: 26272171

5

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. Among authors: bainter w. Clin Immunol. 2016 Oct;171:65-66. doi: 10.1016/j.clim.2016.08.016. Epub 2016 Aug 15. Clin Immunol. 2016. PMID: 27538774

6

A novel mutation in the JH4 domain of JAK3 causing severe combined immunodeficiency complicated by vertebral osteomyelitis.

Qamar F, Junejo S, Qureshi S, Seleman M, Bainter W, Massaad M, Chou J, Geha RS. Qamar F, et al. Among authors: bainter w. Clin Immunol. 2017 Oct;183:198-200. doi: 10.1016/j.clim.2017.09.007. Epub 2017 Sep 14. Clin Immunol. 2017. PMID: 28917720

7

Rethinking newborn screening for severe combined immunodeficiency: Lessons from an international partnership for patients with primary immunodeficiencies in Pakistan.

Wallace JG, Tipu HN, Stafstrom K, Alosaimi MF, Massaad MJ, Bainter W, Geha RS, Chou J. Wallace JG, et al. Among authors: bainter w. Clin Immunol. 2019 May;202:29-32. doi: 10.1016/j.clim.2019.03.004. Epub 2019 Mar 8. Clin Immunol. 2019. PMID: 30858051 No abstract available.

8

Combined immunodeficiency due to a mutation in the γ1 subunit of the coat protein I complex.

Bainter W, Platt CD, Park SY, Stafstrom K, Wallace JG, Peters ZT, Massaad MJ, Becuwe M, Salinas SA, Jones J, Beaussant-Cohen S, Jaber F, Yang JS, Walther TC, Orange JS, Rao C, Rakoff-Nahoum S, Tsokos M, Naseem SUR, Al-Tamemi S, Chou J, Hsu VW, Geha RS. Bainter W, et al. J Clin Invest. 2021 Feb 1;131(3):e140494. doi: 10.1172/JCI140494. J Clin Invest. 2021. PMID: 33529166 Free PMC article.

9

A novel mutation in ICOS presenting as hypogammaglobulinemia with susceptibility to opportunistic pathogens.

Chou J, Massaad MJ, Cangemi B, Bainter W, Platt C, Badran YR, Raphael BP, Kamin DS, Goldsmith JD, Pai SY, Al-Herz W, Geha RS. Chou J, et al. Among authors: bainter w. J Allergy Clin Immunol. 2015 Sep;136(3):794-797.e1. doi: 10.1016/j.jaci.2014.12.1940. Epub 2015 Feb 10. J Allergy Clin Immunol. 2015. PMID: 25678089 No abstract available.

10

Recurrent viral infections associated with a homozygous CORO1A mutation that disrupts oligomerization and cytoskeletal association.

Yee CS, Massaad MJ, Bainter W, Ohsumi TK, Föger N, Chan AC, Akarsu NA, Aytekin C, Ayvaz DÇ, Tezcan I, Sanal Ö, Geha RS, Chou J. Yee CS, et al. Among authors: bainter w. J Allergy Clin Immunol. 2016 Mar;137(3):879-88.e2. doi: 10.1016/j.jaci.2015.08.020. Epub 2015 Oct 21. J Allergy Clin Immunol. 2016. PMID: 26476480 Free PMC article.

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