Sadrnabavi A - Search Results

1

Ashrafzadeh F, Sadrnabavi A, Akhondian J, Beiraghi Toosi M, Mohammadi M, Hassanpour K. Ashrafzadeh F, et al. Among authors: sadrnabavi a. Iran J Child Neurol. 2016 Spring;10(2):86-9. Iran J Child Neurol. 2016. PMID: 27247589 Free PMC article.

2

Limb-girdle Muscular Dystrophy with New Mutation in Sarcoglycan Beta Gene: A Case Report.

Taghizadeh E, Abdolkarimi H, Boostani R, Sadrnabavi A. Taghizadeh E, et al. Among authors: sadrnabavi a. Iran J Public Health. 2018 Dec;47(12):1953-1957. Iran J Public Health. 2018. PMID: 30788312 Free PMC article.

3

Long-term exposure to electromagnetic radiation from mobile phones can cause considerable changes in the balance of Bax/Bcl2 mRNA expression in the hippocampus of mice.

Tohidi FZ, Sadr-Nabavi A, Haghir H, Fardid R, Rafatpanah H, Azimian H, Bahreyni-Toossi MH. Tohidi FZ, et al. Electromagn Biol Med. 2021 Jan 2;40(1):131-137. doi: 10.1080/15368378.2020.1830793. Epub 2020 Oct 20. Electromagn Biol Med. 2021. PMID: 33081559

4

Copy number analysis from whole-exome sequencing data revealed a novel homozygous deletion in PARK7 leads to severe early-onset Parkinson's disease.

Seyedtaghia MR, Soudyab M, Shariati M, Esfehani RJ, Vafadar S, Shalaei N, Nouri V, Zech M, Winkelmann J, Shoeibi A, Sadr-Nabavi A. Seyedtaghia MR, et al. Heliyon. 2023 Apr 8;9(4):e15393. doi: 10.1016/j.heliyon.2023.e15393. eCollection 2023 Apr. Heliyon. 2023. PMID: 37095917 Free PMC article.

5

Whole-Exome Sequencing Study of Consanguineous Parkinson's Disease Families and Related Phenotypes: Report of Twelve Novel Variants.

Soudyab M, Shariati M, Esfehani RJ, Shalaei N, Vafadar S, Nouri V, Zech M, Winkelmann J, Shoeibi A, Sadr-Nabavi A. Soudyab M, et al. J Mol Neurosci. 2022 Dec;72(12):2486-2496. doi: 10.1007/s12031-022-02085-9. Epub 2022 Dec 15. J Mol Neurosci. 2022. PMID: 36520381

6

AOPEP variants as a novel cause of recessive dystonia: Generalized dystonia and dystonia-parkinsonism.

Garavaglia B, Vallian S, Romito LM, Straccia G, Capecci M, Invernizzi F, Andrenelli E, Kazemi A, Boesch S, Kopajtich R, Olfati N, Shariati M, Shoeibi A, Sadr-Nabavi A, Prokisch H, Winkelmann J, Zech M. Garavaglia B, et al. Parkinsonism Relat Disord. 2022 Apr;97:52-56. doi: 10.1016/j.parkreldis.2022.03.007. Epub 2022 Mar 16. Parkinsonism Relat Disord. 2022. PMID: 35306330

7

Evaluation of COVID-19 Trend in Iran; Population Response to the Recent Pandemic Overtime.

Esfehani RJ, Shariati M, Sadr-Nabavi A, Bidkhori HR. Esfehani RJ, et al. Int J Prev Med. 2022 Jan 19;13:6. doi: 10.4103/ijpvm.IJPVM_367_20. eCollection 2022. Int J Prev Med. 2022. PMID: 35281986 Free PMC article.

8

Cardiac Tamponade: A Rare Manifestation of Familial Mediterranean Fever.

Malek A, Zeraati T, Sadr-Nabavi A, Vakili N, Abbaszadegan MR. Malek A, et al. Case Rep Rheumatol. 2022 Feb 7;2022:8334375. doi: 10.1155/2022/8334375. eCollection 2022. Case Rep Rheumatol. 2022. PMID: 35178266 Free PMC article.

9

PLA2G6 gene mutation and infantile neuroaxonal degeneration; report of three cases from Iran.

Jafarzadeh Esfehani R, Eslahi A, Beiraghi Toosi M, Sadr-Nabavi A, Kerachian MA, Asl Mohajeri MS, Farjami M, Alizade F, Mojarrad M. Jafarzadeh Esfehani R, et al. Iran J Basic Med Sci. 2021 Sep;24(9):1190-1195. doi: 10.22038/ijbms.2021.55082.12340. Iran J Basic Med Sci. 2021. PMID: 35083005 Free PMC article.

10

Exome sequencing identifies RASSF1 and KLK3 germline variants in an Iranian multiple-case breast cancer family.

Radmanesh H, Liu D, Geffers R, Shandiz FH, Sadr-Nabavi A, Hillemanns P, Park-Simon TW, Dörk T. Radmanesh H, et al. Eur J Med Genet. 2022 Mar;65(3):104425. doi: 10.1016/j.ejmg.2022.104425. Epub 2022 Jan 13. Eur J Med Genet. 2022. PMID: 35032689

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