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Delayed diagnosis of hereditary angioedema with C1-inhibitor deficiency in iranian children and adolescents.
Ayazi M, Fazlollahi MR, Mohammadzadeh I, Fayezi A, Nabavi M, Mahdaviani SA, Movahedi M, Heidarzadeh M, Saghafi S, Shokouhi Shoormasti R, Mohammadian S, Farkas H, Pourpak Z. Ayazi M, et al. Pediatr Allergy Immunol. 2019 May;30(3):395-398. doi: 10.1111/pai.13028. Epub 2019 Mar 20. Pediatr Allergy Immunol. 2019. PMID: 30690789 No abstract available.
Genetic Study of Hereditary Angioedema Type I and Type II (First Report from Iranian Patients: Describing Three New Mutations).
Nabilou S, Pak F, Alizadeh Z, Fazlollahi MR, Houshmand M, Ayazi M, Mohammadzadeh I, Bemanian MH, Fayezi A, Nabavi M, Saghafi S, Mohammadian S, Kokhaei P, Moin M, Pourpak Z. Nabilou S, et al. Among authors: ayazi m. Immunol Invest. 2022 Jan;51(1):170-181. doi: 10.1080/08820139.2020.1817068. Epub 2020 Sep 8. Immunol Invest. 2022. PMID: 32896191
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