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Year Number of Results
2005 1
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2007 4
2008 2
2010 3
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2012 2
2013 7
2014 6
2015 9
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2017 15
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2020 16
2021 22
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The following term was not found in PubMed: Vahidniya
Page 1
Artificial Intelligence Explained for Nonexperts.
Razavian N, Knoll F, Geras KJ. Razavian N, et al. Semin Musculoskelet Radiol. 2020 Feb;24(1):3-11. doi: 10.1055/s-0039-3401041. Epub 2020 Jan 28. Semin Musculoskelet Radiol. 2020. PMID: 31991447 Free PMC article. Review.
Radioimmunotherapy (RIT) in Brain Tumors.
Gholamrezanezhad A, Shooli H, Jokar N, Nemati R, Assadi M. Gholamrezanezhad A, et al. Nucl Med Mol Imaging. 2019 Dec;53(6):374-381. doi: 10.1007/s13139-019-00618-6. Epub 2019 Nov 12. Nucl Med Mol Imaging. 2019. PMID: 31867072 Free PMC article. Review.
Phenotypic continuum of NFU1-related disorders.
Kaiyrzhanov R, Zaki MS, Lau T, Sen S, Azizimalamiri R, Zamani M, Sayin GY, Hilander T, Efthymiou S, Chelban V, Brown R, Thompson K, Scarano MI, Ganesh J, Koneev K, Gülaçar IM, Person R, Sadykova D, Maidyrov Y, Seifi T, Zadagali A, Bernard G, Allis K, Elloumi HZ, Lindy A, Taghiabadi E, Verma S, Logan R, Kirmse B, Bai R, Khalaf SM, Abdel-Hamid MS, Sedaghat A, Shariati G, Issa M, Zeighami J, Elbendary HM, Brown G, Taylor RW, Galehdari H, Gleeson JJ, Carroll CJ, Cowan JA, Moreno-De-Luca A, Houlden H, Maroofian R. Kaiyrzhanov R, et al. Ann Clin Transl Neurol. 2022 Dec;9(12):2025-2035. doi: 10.1002/acn3.51679. Epub 2022 Oct 18. Ann Clin Transl Neurol. 2022. PMID: 36256512 Free PMC article.
Biallelic MED27 variants lead to variable ponto-cerebello-lental degeneration with movement disorders.
Maroofian R, Kaiyrzhanov R, Cali E, Zamani M, Zaki MS, Ferla M, Tortora D, Sadeghian S, Saadi SM, Abdullah U, Karimiani EG, Efthymiou S, Yeşil G, Alavi S, Al Shamsi AM, Tajsharghi H, Abdel-Hamid MS, Saadi NW, Al Mutairi F, Alabdi L, Beetz C, Ali Z, Toosi MB, Rudnik-Schöneborn S, Babaei M, Isohanni P, Muhammad J, Khan S, Al Shalan M, Hickey SE, Marom D, Elhanan E, Kurian MA, Marafi D, Saberi A, Hamid M, Spaull R, Meng L, Lalani S, Maqbool S, Rahman F, Seeger J, Palculict TB, Lau T, Murphy D, Mencacci NE, Steindl K, Begemann A, Rauch A, Akbas S, Aslanger AD, Salpietro V, Yousaf H, Ben-Shachar S, Ejeskär K, Al Aqeel AI, High FA, Armstrong-Javors AE, Zahraei SM, Seifi T, Zeighami J, Shariati G, Sedaghat A, Asl SN, Shahrooei M, Zifarelli G, Burglen L, Ravelli C, Zschocke J, Schatz UA, Ghavideldarestani M, Kamel WA, Van Esch H, Hackenberg A, Taylor JC, Al-Gazali L, Bauer P, Gleeson JJ, Alkuraya FS, Lupski JR, Galehdari H, Azizimalamiri R, Chung WK, Baig SM, Houlden H, Severino M. Maroofian R, et al. Brain. 2023 Dec 1;146(12):5031-5043. doi: 10.1093/brain/awad257. Brain. 2023. PMID: 37517035 Free PMC article.
Multiple Sclerosis: Immunopathology and Treatment Update.
Dargahi N, Katsara M, Tselios T, Androutsou ME, de Courten M, Matsoukas J, Apostolopoulos V. Dargahi N, et al. Brain Sci. 2017 Jul 7;7(7):78. doi: 10.3390/brainsci7070078. Brain Sci. 2017. PMID: 28686222 Free PMC article. Review.
Peripheral Nervous System Manifestations Associated with COVID-19.
Andalib S, Biller J, Di Napoli M, Moghimi N, McCullough LD, Rubinos CA, O'Hana Nobleza C, Azarpazhooh MR, Catanese L, Elicer I, Jafari M, Liberati F, Camejo C, Torbey M, Divani AA. Andalib S, et al. Curr Neurol Neurosci Rep. 2021 Feb 14;21(3):9. doi: 10.1007/s11910-021-01102-5. Curr Neurol Neurosci Rep. 2021. PMID: 33586020 Free PMC article. Review.
Biallelic BORCS8 variants cause an infantile-onset neurodegenerative disorder with altered lysosome dynamics.
De Pace R, Maroofian R, Paimboeuf A, Zamani M, Zaki MS, Sadeghian S, Azizimalamiri R, Galehdari H, Zeighami J, Williamson CD, Fleming E, Zhou D, Gannon JL, Thiffault I, Roze E, Suri M, Zifarelli G, Bauer P, Houlden H, Severino M, Patten SA, Farrow E, Bonifacino JS. De Pace R, et al. Brain. 2023 Dec 21:awad427. doi: 10.1093/brain/awad427. Online ahead of print. Brain. 2023. PMID: 38128568
Hb Narges Lab, a Novel Hemoglobin Variant of the beta-Globin Gene.
Hamid M, Shahbazi Z, Keikhaei B, Galehdari H, Saberi A, Sedaghat A, Shariati G, Mohammadi-Anaei M. Hamid M, et al. Arch Iran Med. 2022 May 1;25(5):339-342. doi: 10.34172/aim.2022.55. Arch Iran Med. 2022. PMID: 35943011 Free article.
We report a novel mutation on the beta-globin gene (HBB), c.134 C>T; p.S44F variant, in the heterozygote state which was detected in a female of Persian ethnic origin in the Khuzestan province, southern Iran, that we named Hb Narges Lab (HbNL) variant. This mutation was …
We report a novel mutation on the beta-globin gene (HBB), c.134 C>T; p.S44F variant, in the heterozygote state which was detected in a fe …
168 results