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Did you mean mohammad amin tabatabaeian (1 results)?
Monogenic etiologies of persistent human papillomavirus infections: A comprehensive systematic review.
Biglari S, Moghaddam AS, Tabatabaiefar MA, Sherkat R, Youssefian L, Saeidian AH, Vahidnezhad F, Tsoi LC, Gudjonsson JE, Hakonarson H, Casanova JL, Béziat V, Jouanguy E, Vahidnezhad H. Biglari S, et al. Among authors: tabatabaiefar ma. Genet Med. 2024 Feb;26(2):101028. doi: 10.1016/j.gim.2023.101028. Epub 2023 Nov 14. Genet Med. 2024. PMID: 37978863 Free PMC article.
Filaggrinopathies-FLG/FLG2: Diagnostic Complexities and Immunotherapy.
Nouri Z, Biglari S, Tabatabaiefar MA, Vahidnezhad F, Hozhabrpour A, March ME, Margolis DJ, Gudjonsson JE, Hakonarson H, Vahidnezhad H. Nouri Z, et al. Among authors: tabatabaiefar ma. J Invest Dermatol. 2025 Jul;145(7):1622-1632. doi: 10.1016/j.jid.2024.12.008. Epub 2025 Feb 7. J Invest Dermatol. 2025. PMID: 39927906 Free article. Review.
Epigenetics and Common Non Communicable Disease.
Tabatabaiefar MA, Sajjadi RS, Narrei S. Tabatabaiefar MA, et al. Adv Exp Med Biol. 2019;1121:7-20. doi: 10.1007/978-3-030-10616-4_2. Adv Exp Med Biol. 2019. PMID: 31392648
A novel TECTA mutation causes ARNSHL.
Asgharzade S, Tabatabaiefar MA, Modarressi MH, Ghahremani MH, Reiisi S, Tahmasebi P, Abdollahnejad F, Chaleshtori MH. Asgharzade S, et al. Among authors: tabatabaiefar ma. Int J Pediatr Otorhinolaryngol. 2017 Jan;92:88-93. doi: 10.1016/j.ijporl.2016.11.010. Epub 2016 Nov 15. Int J Pediatr Otorhinolaryngol. 2017. PMID: 28012541 Free article.
DOCK2 Deficiency and GATA2 Haploinsufficiency Can Underlie Critical Coronavirus Disease 2019 (COVID-19) Pneumonia.
Biglari S, Youssefian L, Tabatabaiefar MA, Saeidian AH, Abtahi-Naeini B, Khorram E, Sherkat R, Moghaddam AS, Mohaghegh F, Rahimi M, Rahimi H, Babaei S, Shahrooei M, Mozafari N, Zaresharifi S, Vahidnezhad F, Homayouni V, Tsoi LC, Gudjonsson JE, Hakonarson H, Casanova JL, Jouanguy E, Béziat V, Zhang Q, Cobat A, Vahidnezhad H. Biglari S, et al. Among authors: tabatabaiefar ma. J Clin Immunol. 2025 Mar 28;45(1):85. doi: 10.1007/s10875-025-01877-z. J Clin Immunol. 2025. PMID: 40153067 Free PMC article.
Bi-Allelic Variants in MICU1 Cause Myopathy With Extrapyramidal Signs: Case Series, Phenotypic Spectrum, and Genotype-Phenotype Correlations From 61 Patients.
Beheshti P, Akbarian F, Esmaeilzadeh E, Galehdari H, Khorrami M, Vallian S, Abdi A, Güngör Ö, Tuncel R, Aykut A, Ekmekci Ö, Akın H, Durmaz A, Moghaddam AS, Chamanrou N, Karimi F, Kazemi A, Habibi M, Tabatabaiefar MA, Khorshid HRK, Parvini F, Yiş U, Polat I, Youssefian L, Vahidnezhad H, Heidari M, Sarraf P, Karimiani EG, Maroofian R, Biglari S. Beheshti P, et al. Among authors: tabatabaiefar ma. Clin Genet. 2026 Mar;109(3):564-570. doi: 10.1111/cge.70062. Epub 2025 Sep 2. Clin Genet. 2026. PMID: 40898676
139 results