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Investigation of Chromosomal Abnormalities and Microdeletion/ Microduplication(s) in Fifty Iranian Patients with Multiple Congenital Anomalies.
Mohammadzadeh A, Akbaroghli S, Aghaei-Moghadam E, Mahdieh N, Badv RS, Jamali P, Kariminejad R, Chavoshzadeh Z, Ghasemi Firouzabadi S, Mansour Ghanaie R, Nozari A, Banihashemi S, Hadipour F, Hadipour Z, Kariminejad A, Najmabadi H, Shafeghati Y, Behjati F. Mohammadzadeh A, et al. Cell J. 2019 Oct;21(3):337-349. doi: 10.22074/cellj.2019.6053. Epub 2019 Jun 15. Cell J. 2019. PMID: 31210441 Free PMC article.
Little Hearts Are Affected by COVID19: Importance of the Myocardial Systolic Evaluation.
Mamishi S, Zeinaloo A, Haji Esmaeil Memar E, Khodabandeh M, Mirzaaghayan MR, Abdolsalehi MR, Eshaghi H, Gorji M, Ghamari A, Aghaei Moghadam E. Mamishi S, et al. Among authors: aghaei moghadam e. Front Pediatr. 2021 Sep 7;9:697213. doi: 10.3389/fped.2021.697213. eCollection 2021. Front Pediatr. 2021. PMID: 34557458 Free PMC article.
COVID-19: A New Horizon in Congenital Heart Diseases.
Aghaei Moghadam E, Mohammadzadeh S, Sattarzadeh Badkoubeh R, Ghamari A, Rabbani A, Mohebbi A, Zeinaloo A, Ashrafi M, Kamran N, Masoominasab P, Mahmoudi Z, Zamani Mehryan A, Mirzaaghayan MR. Aghaei Moghadam E, et al. Front Pediatr. 2021 Dec 8;9:582043. doi: 10.3389/fped.2021.582043. eCollection 2021. Front Pediatr. 2021. PMID: 34956968 Free PMC article.
A novel mutation in the ALS2 gene in an iranian kurdish family with juvenile amyotrophic lateral sclerosis.
Daneshmandpour Y, Bahmanpour Z, Kazeminasab S, Aghaei Moghadam E, Alehabib E, Chapi M, Tafakhori A, Aghaei N, Darvish H, Emamalizadeh B. Daneshmandpour Y, et al. Among authors: aghaei moghadam e. Amyotroph Lateral Scler Frontotemporal Degener. 2023 Feb;24(1-2):148-151. doi: 10.1080/21678421.2022.2100263. Epub 2022 Jul 19. Amyotroph Lateral Scler Frontotemporal Degener. 2023. PMID: 35852402
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