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Page 1
Angiotensin-Converting Enzyme Gene Polymorphism in Children with Idiopathic Nephrotic Syndrome, Effect on Biopsy Findings.
Monajemzadeh M, Hesami M, Shahsiah R, Vasei M, Hooshmand S, Tanzifi P, Hajizadeh N, Ataei N, Mehrkash M, Javadi Larijani F, Moghtaderi M, Bazargani B, Khorvash R, Soleimanifar N. Monajemzadeh M, et al. Among authors: khorvash r. Fetal Pediatr Pathol. 2017 Aug;36(4):265-275. doi: 10.1080/15513815.2017.1287229. Epub 2017 May 8. Fetal Pediatr Pathol. 2017. PMID: 28481137
Frequency of diencephalic syndrome in NMOSD.
Etemadifar M, Nouri H, Khorvash R, Salari M, Ghafari K, Aghababaee A. Etemadifar M, et al. Among authors: khorvash r. Acta Neurol Belg. 2022 Aug;122(4):961-967. doi: 10.1007/s13760-021-01792-1. Epub 2021 Sep 13. Acta Neurol Belg. 2022. PMID: 34515964
SARS-CoV-2 serology among people with multiple sclerosis on disease-modifying therapies after BBIBP-CorV (Sinopharm) inactivated virus vaccination: Same story, different vaccine.
Etemadifar M, Sedaghat N, Nouri H, Lotfi N, Chitsaz A, Khorvash R, Zolfaghari H, Ghasemi Movaghar A, Pourabbas M, Salari M. Etemadifar M, et al. Among authors: khorvash r. Mult Scler Relat Disord. 2022 Jan;57:103417. doi: 10.1016/j.msard.2021.103417. Epub 2021 Nov 22. Mult Scler Relat Disord. 2022. PMID: 34875487 Free PMC article.
Seizure incidence among neuromyelitis optica spectrum disorder patients.
Etemadifar M, Sabeti F, Khorvash R, Mirbagheri M, Nouri H, Salari M. Etemadifar M, et al. Among authors: khorvash r. Rev Neurol (Paris). 2021 Jun;177(6):655-659. doi: 10.1016/j.neurol.2020.08.011. Epub 2021 Jan 8. Rev Neurol (Paris). 2021. PMID: 33431266 Review.