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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: mohammadian s. Immunol Invest. 2022 Jan;51(1):170-181. doi: 10.1080/08820139.2020.1817068. Epub 2020 Sep 8. Immunol Invest. 2022. PMID: 32896191
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. Among authors: mohammadian s. 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.
The effect of recorded music on pain endurance (CRESCENDo) - A randomized controlled trial.
Billar R, Kappen P, Mohammadian S, van den Berg C, de Rijke Y, van den Akker E, van Rosmalen J, Schnater JM, Vincent A, Dirven C, Klimek M, Wijnen R, Jeekel J, Huygen F, Tiemensma J. Billar R, et al. Among authors: mohammadian s. Complement Ther Med. 2023 Oct;77:102969. doi: 10.1016/j.ctim.2023.102969. Epub 2023 Aug 12. Complement Ther Med. 2023. PMID: 37579996 Free article. Clinical Trial.
Parent's Satisfaction of Universal Newborn Hearing Screening Program in Iran.
Bayat A, Abdollahi FZ, Saki N, Khiavi FF, Mohammadian S, Bardsiri MM, Hoseinabadi R. Bayat A, et al. Among authors: mohammadian s. Indian J Otolaryngol Head Neck Surg. 2022 Aug;74(Suppl 1):517-522. doi: 10.1007/s12070-020-02355-1. Epub 2021 Jan 9. Indian J Otolaryngol Head Neck Surg. 2022. PMID: 36032845 Free PMC article.
43 results