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

Year Number of Results
1991 1
1997 1
2000 4
2002 2
2003 3
2004 1
2005 2
2006 8
2007 6
2008 4
2009 11
2010 12
2011 16
2012 12
2013 12
2014 17
2015 21
2016 18
2017 20
2018 20
2019 18
2020 11
2021 20
2022 17
2023 12
2024 9

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249 results

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Page 1
Nanovehicles for co-delivery of anticancer agents.
Zeinali M, Abbaspour-Ravasjani S, Ghorbani M, Babazadeh A, Soltanfam T, Santos AC, Hamishehkar H, Hamblin MR. Zeinali M, et al. Drug Discov Today. 2020 Aug;25(8):1416-1430. doi: 10.1016/j.drudis.2020.06.027. Epub 2020 Jul 2. Drug Discov Today. 2020. PMID: 32622880 Review.
Anxiety and depression among new cancer patients.
Safaie N, Zeinali H, Ghahramanfard F, Mirmohammadkhani M, Moonesan M. Safaie N, et al. J Family Med Prim Care. 2022 Aug;11(8):4146-4150. doi: 10.4103/jfmpc.jfmpc_1984_21. Epub 2022 Aug 30. J Family Med Prim Care. 2022. PMID: 36352942 Free PMC article. Review.
Frequency comparisons between the sub-groups were performed using the Chi-square test and, if necessary, Fisher's exact test. Moreover, the T-test or Mann-Whitney U test was used to compare numerical variables. ...
Frequency comparisons between the sub-groups were performed using the Chi-square test and, if necessary, Fisher's exact test. Moreover, the …
Molecular genetic study of Calpainopathy in Iran.
Mojbafan M, Khajeh A, Habibi H, Bagherian H, Zeinali S. Mojbafan M, et al. Gene. 2018 Nov 30;677:259-265. doi: 10.1016/j.gene.2018.07.067. Epub 2018 Jul 27. Gene. 2018. PMID: 30056071
In this study, mutations were found in 14 out of 16 families including 4 novel (c.1894A > T, c.567delG, c.2254-2256delAAC, and c.2373C > T) and 9 previously reported mutations consisting of 5 missense (c.2105C > T, c.2243G > A, c.1714C > T …
In this study, mutations were found in 14 out of 16 families including 4 novel (c.1894A > T, c.567delG, c.2254-2256delAAC, and c.2 …
Bi-allelic variants in OGDHL cause a neurodevelopmental spectrum disease featuring epilepsy, hearing loss, visual impairment, and ataxia.
Yap ZY, Efthymiou S, Seiffert S, Vargas Parra K, Lee S, Nasca A, Maroofian R, Schrauwen I, Pendziwiat M, Jung S, Bhoj E, Striano P, Mankad K, Vona B, Cuddapah S, Wagner A, Alvi JR, Davoudi-Dehaghani E, Fallah MS, Gannavarapu S, Lamperti C, Legati A, Murtaza BN, Nadeem MS, Rehman MU, Saeidi K, Salpietro V, von Spiczak S, Sandoval A, Zeinali S, Zeviani M, Reich A; SYNaPS Study Group; University of Washington Center for Mendelian Genomics; Jang C, Helbig I, Barakat TS, Ghezzi D, Leal SM, Weber Y, Houlden H, Yoon WH. Yap ZY, et al. Am J Hum Genet. 2021 Dec 2;108(12):2368-2384. doi: 10.1016/j.ajhg.2021.11.003. Epub 2021 Nov 19. Am J Hum Genet. 2021. PMID: 34800363 Free PMC article.
249 results