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Rare single-nucleotide variants of MLH1 and MSH2 genes in patients with Lynch syndrome.
Mirabdolhosseini SM, Yaghoob Taleghani M, Rejali L, Sadeghi H, Fatemi N, Tavallaei M, Famil Meyari A, Saeidi N, Ketabi Moghadam P, Sadeghi A, Asadzadeh Aghdaei H, Zali MR, Nazemalhosseini Mojarad E. Mirabdolhosseini SM, et al. Among authors: tavallaei m. Cancer Rep (Hoboken). 2024 Jan;7(1):e1930. doi: 10.1002/cnr2.1930. Epub 2023 Nov 2. Cancer Rep (Hoboken). 2024. PMID: 37919876 Free PMC article.
A novel stop codon mutation in STK11 gene is associated with Peutz-Jeghers Syndrome and elevated cancer risk: a case study.
Khanabadi B, Najafgholizadeh Seyfi D, Rejali L, Taleghani MY, Tavallaei M, Shahrokh S, Daskar Abkenar E, Naderi Noukabadi F, Asadzadeh Aghdaei H, Nazemalhosseini Mojarad E. Khanabadi B, et al. Among authors: tavallaei m. Gastroenterol Hepatol Bed Bench. 2023;16(3):341-346. doi: 10.22037/ghfbb.v16i2.2751. Gastroenterol Hepatol Bed Bench. 2023. PMID: 37767326 Free PMC article.
The CathCam: A Novel Angioscopic Solution for Endovascular Interventions.
Tahmasebi M, Alawneh Y, Miller J, Sewani A, Kayssi A, Dueck A, Wright G, Gu X, Tavallaei MA. Tahmasebi M, et al. Among authors: tavallaei ma. Ann Biomed Eng. 2023 Dec;51(12):2812-2823. doi: 10.1007/s10439-023-03344-5. Epub 2023 Aug 10. Ann Biomed Eng. 2023. PMID: 37561231
Multiple sclerosis and ulcerative colitis: A systematic review and meta-analysis.
Nabizadeh F, Azizi A, Hejrati L, Mousavi M, Mehranzadeh A, Badihian S, Tavallaei MJ, Rahmanian V, Shateri Amiri B, Rafiei-Sefiddashti R, Hejrati A. Nabizadeh F, et al. Among authors: tavallaei mj. Mult Scler J Exp Transl Clin. 2023 Jul 19;9(3):20552173231186516. doi: 10.1177/20552173231186516. eCollection 2023 Jul-Sep. Mult Scler J Exp Transl Clin. 2023. PMID: 37483528 Free PMC article. Review.
67 results