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

Year Number of Results
1997 1
2002 1
2003 6
2004 11
2005 6
2006 11
2007 8
2008 11
2009 10
2010 4
2011 11
2012 12
2013 12
2014 12
2015 17
2016 17
2017 22
2018 19
2019 29
2020 23
2021 20
2022 28
2023 36
2024 20

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315 results

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Page 1
Photoredox-catalysed hydroaminoalkylation of on-DNA N-arylamines.
Mahdavi-Amiri Y, Hu MSJ, Frias N, Movahedi M, Csakai A, Marcaurelle LA, Hili R. Mahdavi-Amiri Y, et al. Among authors: movahedi m. Org Biomol Chem. 2023 Feb 15;21(7):1463-1467. doi: 10.1039/d2ob01956f. Org Biomol Chem. 2023. PMID: 36655521
Clinical and immunological characteristics of 69 leukocyte adhesion deficiency-I patients.
Fazlollahi MR, Hamidieh AA, Moradi L, Shokouhi Shoormati R, Sabetkish N, Esmaeili B, Badalzadeh M, Alizadeh Z, Shamlou S, Movahedi M, Mahloujirad M, Razaghian A, Arshi S, Gharagozlou M, Kalantari A, Bemanian MH, Safari M, Heidarzadeh Arani M, Nabavi M, Parvaneh N, Sadeghi-Shabestari M, Behfar M, Behniafard N, Sherkat R, Ahmadian Heris J, Shariat M, Radmehr R, Houshmand M, Kazemnejad A, Molitor A, Carapito R, Bahram S, Pourpak Z, Moin M. Fazlollahi MR, et al. Among authors: movahedi m. Pediatr Allergy Immunol. 2023 Jul;34(7):e13990. doi: 10.1111/pai.13990. Pediatr Allergy Immunol. 2023. PMID: 37492921
Wolff-Parkinson-White Syndrome and Peripartum Cardiomyopathy.
Ghaderian M, Movahedi M, Sabri MR, Dehghan B, Ahmadi A, Mahdavi C, Nejad DR, Esnaashari A. Ghaderian M, et al. Among authors: movahedi m. Heart Views. 2022 Jul-Sep;23(3):173-176. doi: 10.4103/heartviews.heartviews_13_22. Epub 2022 Oct 22. Heart Views. 2022. PMID: 36479164 Free PMC article.
Hypertrophic lichen planus on lip mimicking SCC.
Mozafari N, Bidari-Zerehpoosh F, Movahedi M, Dadkhahfar S. Mozafari N, et al. Among authors: movahedi m. Clin Case Rep. 2022 Aug 8;10(8):e6191. doi: 10.1002/ccr3.6191. eCollection 2022 Aug. Clin Case Rep. 2022. PMID: 35957792 Free PMC article.
Clinical, Immunological, and Genetic Findings in Iranian Patients with MHC-II Deficiency: Confirmation of c.162delG RFXANK Founder Mutation in the Iranian Population.
Mousavi Khorshidi MS, Seeleuthner Y, Chavoshzadeh Z, Behfar M, Hamidieh AA, Alimadadi H, Sherkat R, Momen T, Behniafard N, Eskandarzadeh S, Mansouri M, Behnam M, Mahdavi M, Heydarazad Zadeh M, Shokri M, Alizadeh F, Movahedi M, Momenilandi M, Keramatipour M, Casanova JL, Cobat A, Abel L, Shahrooei M, Parvaneh N. Mousavi Khorshidi MS, et al. Among authors: movahedi m. J Clin Immunol. 2023 Nov;43(8):1941-1952. doi: 10.1007/s10875-023-01562-z. Epub 2023 Aug 16. J Clin Immunol. 2023. PMID: 37584719
315 results