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Page 1
Inherited IFNAR1 Deficiency in a Child with Both Critical COVID-19 Pneumonia and Multisystem Inflammatory Syndrome.
Abolhassani H, Landegren N, Bastard P, Materna M, Modaresi M, Du L, Aranda-Guillén M, Sardh F, Zuo F, Zhang P, Marcotte H, Marr N, Khan T, Ata M, Al-Ali F, Pescarmona R, Belot A, Béziat V, Zhang Q, Casanova JL, Kämpe O, Zhang SY, Hammarström L, Pan-Hammarström Q. Abolhassani H, et al. J Clin Immunol. 2022 Apr;42(3):471-483. doi: 10.1007/s10875-022-01215-7. Epub 2022 Jan 28. J Clin Immunol. 2022. PMID: 35091979 Free PMC article.
Autosomal recessive agammaglobulinemia: a novel non-sense mutation in CD79a.
Khalili A, Plebani A, Vitali M, Abolhassani H, Lougaris V, Mirminachi B, Rezaei N, Aghamohammadi A. Khalili A, et al. Among authors: abolhassani h. J Clin Immunol. 2014 Feb;34(2):138-41. doi: 10.1007/s10875-014-9989-3. Epub 2014 Feb 1. J Clin Immunol. 2014. PMID: 24481606
Long-term evaluation of a historical cohort of Iranian common variable immunodeficiency patients.
Aghamohammadi A, Abolhassani H, Latif A, Tabassomi F, Shokuhfar T, Torabi Sagvand B, Shahinpour S, Mirminachi B, Parvaneh N, Movahedi M, Gharagozlou M, Sherkat R, Amin R, Aleyasin S, Faridhosseini R, Jabbari-Azad F, Cheraghi T, Eslamian MH, Khalili A, Kalantari N, Shafiei A, Dabbaghzade A, Khayatzadeh A, Ebrahimi M, Razavinejad D, Bazregari S, Ebrahimi M, Ghaffari J, Bemanian MH, Behniafard N, Kashef S, Mohammadzadeh I, Hammarström L, Rezaei N. Aghamohammadi A, et al. Among authors: abolhassani h. Expert Rev Clin Immunol. 2014 Oct;10(10):1405-17. doi: 10.1586/1744666X.2014.958469. Expert Rev Clin Immunol. 2014. PMID: 25225775
RAC2 loss-of-function mutation in 2 siblings with characteristics of common variable immunodeficiency.
Alkhairy OK, Rezaei N, Graham RR, Abolhassani H, Borte S, Hultenby K, Wu C, Aghamohammadi A, Williams DA, Behrens TW, Hammarström L, Pan-Hammarström Q. Alkhairy OK, et al. Among authors: abolhassani h. J Allergy Clin Immunol. 2015 May;135(5):1380-4.e1-5. doi: 10.1016/j.jaci.2014.10.039. Epub 2014 Dec 12. J Allergy Clin Immunol. 2015. PMID: 25512081 Free PMC article.
Novel mutations in TNFRSF7/CD27: Clinical, immunologic, and genetic characterization of human CD27 deficiency.
Alkhairy OK, Perez-Becker R, Driessen GJ, Abolhassani H, van Montfrans J, Borte S, Choo S, Wang N, Tesselaar K, Fang M, Bienemann K, Boztug K, Daneva A, Mechinaud F, Wiesel T, Becker C, Dückers G, Siepermann K, van Zelm MC, Rezaei N, van der Burg M, Aghamohammadi A, Seidel MG, Niehues T, Hammarström L. Alkhairy OK, et al. Among authors: abolhassani h. J Allergy Clin Immunol. 2015 Sep;136(3):703-712.e10. doi: 10.1016/j.jaci.2015.02.022. Epub 2015 Apr 3. J Allergy Clin Immunol. 2015. PMID: 25843314
379 results