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

Year Number of Results
2005 1
2006 4
2007 4
2008 2
2010 3
2011 2
2012 2
2013 7
2014 6
2015 9
2016 11
2017 15
2018 17
2019 18
2020 16
2021 22
2022 18
2023 20
2024 28
2025 1

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185 results

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The following term was not found in PubMed: Momenjoo
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.
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 …
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.
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.
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 variants in SLC4A10 encoding a sodium-dependent bicarbonate transporter lead to a neurodevelopmental disorder.
Maroofian R, Zamani M, Kaiyrzhanov R, Liebmann L, Karimiani EG, Vona B, Huebner AK, Calame DG, Misra VK, Sadeghian S, Azizimalamiri R, Mohammadi MH, Zeighami J, Heydaran S, Toosi MB, Akhondian J, Babaei M, Hashemi N, Schnur RE, Suri M, Setzke J, Wagner M, Brunet T, Grochowski CM, Emrick L, Chung WK, Hellmich UA, Schmidts M, Lupski JR, Galehdari H, Severino M, Houlden H, Hübner CA. Maroofian R, et al. Genet Med. 2024 Mar;26(3):101034. doi: 10.1016/j.gim.2023.101034. Epub 2023 Dec 3. Genet Med. 2024. PMID: 38054405 Free PMC article.
185 results