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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2000 1
2002 3
2003 1
2004 1
2005 2
2006 1
2007 2
2009 1
2012 1
2013 3
2014 9
2015 12
2016 10
2017 7
2018 6
2019 6
2020 3
2021 5
2022 9
2023 6
2024 0

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76 results

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Page 1
Effects of Trehalose Administration in Patients with Mucopolysaccharidosis Type III.
Mobini M, Radbakhsh S, Kubaski F, Eshraghi P, Vakili S, Vakili R, Abbasifard M, Jamialahmadi T, Rajabi O, Emami SA, Tayarani-Najaran Z, Rizzo M, Eid AH, Banach M, Sahebkar A. Mobini M, et al. Among authors: vakili r. Curr Med Chem. 2023 Apr 6. doi: 10.2174/0929867330666230406102555. Online ahead of print. Curr Med Chem. 2023. PMID: 37038706
Acute Intermittent Porphyria: A Diagnostic Challenge.
Vakili R, Armanpoor P. Vakili R, et al. Iran J Pediatr. 2016 May 10;26(3):e5238. doi: 10.5812/ijp.5238. eCollection 2016 Jun. Iran J Pediatr. 2016. PMID: 27617074 Free PMC article. No abstract available.
Clinical Efficacy Evaluation of Sirolimus in Congenital Hyperinsulinism.
Hashemian S, Jafarzadeh Esfehani R, Karimdadi S, Vakili R, Zamanfar D, Sahebkar A. Hashemian S, et al. Among authors: vakili r. Int J Endocrinol. 2020 Jul 22;2020:7250406. doi: 10.1155/2020/7250406. eCollection 2020. Int J Endocrinol. 2020. PMID: 32774365 Free PMC article.
Atomistic simulations on the carbidisation processes in Pd nanoparticles.
Kordatos A, Mohammed K, Vakili R, Goguet A, Manyar H, Gibson E, Carravetta M, Wells P, Skylaris CK. Kordatos A, et al. Among authors: vakili r. RSC Adv. 2023 Feb 14;13(9):5619-5626. doi: 10.1039/d2ra07462a. eCollection 2023 Feb 14. RSC Adv. 2023. PMID: 36798744 Free PMC article.
Investigating Genetic Mutations in a Large Cohort of Iranian Patients with Congenital Hyperinsulinism.
Razzaghy-Azar M, Saeedi S, Dayani SB, Enayati S, Abbasi F, Hashemian S, Eshraghi P, Karimdadi S, Tajdini P, Vakili R, Amoli MM, Yaghootkar H. Razzaghy-Azar M, et al. Among authors: vakili r. J Clin Res Pediatr Endocrinol. 2022 Mar 3;14(1):87-95. doi: 10.4274/jcrpe.galenos.2021.2021.0071. Epub 2021 Dec 20. J Clin Res Pediatr Endocrinol. 2022. PMID: 34927408 Free PMC article.
Novel mutation in AIRE gene with autoimmune polyendocrine syndrome type 1.
Fardi Golyan F, Ghaemi N, Abbaszadegan MR, Dehghan Manshadi SH, Vakili R, Druley TE, Rahimi HR, Ghahraman M. Fardi Golyan F, et al. Among authors: vakili r. Immunobiology. 2019 Nov;224(6):728-733. doi: 10.1016/j.imbio.2019.09.004. Epub 2019 Sep 6. Immunobiology. 2019. PMID: 31526676
76 results