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1.	Abed Abud, A., et al. (author) Searching for solar KDAR with DUNE 2021 In: Journal of Cosmology and Astroparticle Physics. - : IOP Publishing. - 1475-7516. ; 2021:10, s. 065-065 Journal article (peer-reviewed)
2.	Abolhassani, H, et al. (author) Clinical, immunologic, and genetic spectrum of 696 patients with combined immunodeficiency 2018 In: The Journal of allergy and clinical immunology. - : Elsevier BV. - 1097-6825 .- 0091-6749. ; 141:4, s. 1450-1458 Journal article (peer-reviewed)
3.	Abolhassani, H, et al. (author) Fourth Update on the Iranian National Registry of Primary Immunodeficiencies: Integration of Molecular Diagnosis 2018 In: Journal of clinical immunology. - : Springer Science and Business Media LLC. - 1573-2592 .- 0271-9142. ; 38:7, s. 816-832 Journal article (peer-reviewed)
4.	Aghamohammadi, A, et al. (author) Long-term evaluation of a historical cohort of Iranian common variable immunodeficiency patients 2014 In: Expert review of clinical immunology. - 1744-8409. ; 10:10, s. 1405-1417 Journal article (peer-reviewed)
5.	Alkhairy, OK, et al. (author) Spectrum of Phenotypes Associated with Mutations in LRBA 2016 In: Journal of clinical immunology. - : Springer Science and Business Media LLC. - 1573-2592 .- 0271-9142. ; 36:1, s. 33-45 Journal article (peer-reviewed)
6.	Mohammadinejad, P, et al. (author) Primary Antibody Deficiency in a Tertiary Referral Hospital: A 30-Year Experiment 2015 In: Journal of investigational allergology & clinical immunology. - 1018-9068. ; 25:6, s. 416-425 Journal article (peer-reviewed)
7.	Mohammadzadeh, I, et al. (author) A novel CD40 ligand mutation in a patient with pneumonia, neutropenia, and hyperimmunoglobulin M phenotype 2013 In: Journal of investigational allergology & clinical immunology. - 1018-9068. ; 23:1, s. 50-51 Journal article (peer-reviewed)
8.	Mohammadzadeh, I, et al. (author) IDENTIFICATION OF A NOVEL CD40 LIGAND MUTATION IN A PATIENT WITH HYPER IGM PHENOTYPE AND NEUTROPENIA 2012 In: JOURNAL OF CLINICAL IMMUNOLOGY. - 0271-9142. ; 32, s. 330-331 Conference paper (other academic/artistic)
9.	Nabilou, S, et al. (author) Genetic Study of Hereditary Angioedema Type I and Type II (First Report from Iranian Patients: Describing Three New Mutations) 2022 In: Immunological investigations. - : Informa UK Limited. - 1532-4311 .- 0882-0139. ; 51:1, s. 170-181 Journal article (peer-reviewed)
10.	Yazdani, R, et al. (author) Comparison of Common Monogenic Defects in a Large Predominantly Antibody Deficiency Cohort 2019 In: The journal of allergy and clinical immunology. In practice. - : Elsevier BV. - 2213-2201 .- 2213-2198. ; 7:3, s. 864- Journal article (peer-reviewed)

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Type of publication: journal article (9); conference paper (1)

Type of content: peer-reviewed (9); other academic/artistic (1)

Author/Editor: Mohammadzadeh, I (9); Rezaei, N (8); Aghamohammadi, A (8); Hammarstrom, L (7); Abolhassani, H (6); Parvaneh, N (5); show more...; Gharagozlou, M (5); Movahedi, M (5); Amin, R (5); Aleyasin, S (5); Faridhosseini, R (5); Jabbari-Azad, F (5); Nabavi, M (5); Bemanian, MH (5); Sherkat, R (5); Ghaffari, J (5); Shafiei, A (5); Cheraghi, T (4); Eslamian, MH (4); Chavoshzadeh, Z (4); Behniafard, N (4); Ahanchian, H (4); Khalili, A (4); Fayezi, A (4); Mohammadi, J (3); Tavassoli, M (3); Momen, T (3); Tavakol, M (3); Hamidieh, AA (3); Azizi, G (3); Yazdani, R (3); Mahdaviani, SA (3); Arshi, S (3); Molatefi, R (3); Mansouri, M (3); Mesdaghi, M (3); Babaie, D (3); Kalantari, N (3); Khoshkhui, M (3); Soheili, H (3); Dabbaghzadeh, A (3); Shirkani, A (3); Kalmarzi, RN (3); Mortazavi, SH (3); Tafaroji, J (3); Kashef, S (3); Zandieh, F (3); Sadeghi-Shabestari, ... (3); Zandkarimi, M (3); Moghtaderi, M (3); show less...

University: Karolinska Institutet (9); Royal Institute of Technology (1)

Language: English (10)

Research subject (UKÄ/SCB): Natural sciences (1)

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