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Prediction of Parkinson's disease pathogenic variants using hybrid Machine learning systems and radiomic features.
Phys Med. 2023 Sep;113:102647. doi: 10.1016/j.ejmp.2023.102647. Epub 2023 Aug 12.
Phys Med. 2023.
PMID: 37579523
A Novel ARMC5 Germline Variant in Primary Macronodular Adrenal Hyperplasia Using Whole-Exome Sequencing.
Eghbali M, Cheraghi S, Samanian S, Rad I, Meghdadi J, Akbari H, Honardoost M.
Eghbali M, et al. Among authors: samanian s.
Diagnostics (Basel). 2022 Dec 2;12(12):3028. doi: 10.3390/diagnostics12123028.
Diagnostics (Basel). 2022.
PMID: 36553033
Free PMC article.
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Hyperphosphatemic familial tumoral calcinosis caused by a novel variant in the GALNT3 gene.
Mahjoubi F, Ghadir M, Samanian S, Heydari I, Honardoost M.
Mahjoubi F, et al. Among authors: samanian s.
J Endocrinol Invest. 2020 Aug;43(8):1125-1130. doi: 10.1007/s40618-020-01203-x. Epub 2020 Mar 3.
J Endocrinol Invest. 2020.
PMID: 32125652
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Extracellular matrix protein 1 gene (ECM1) mutations in nine Iranian families with lipoid proteinosis.
Izadi F, Mahjoubi F, Farhadi M, Kalayinia S, Bidmeshkipour A, Tavakoli MM, Samanian S.
Izadi F, et al. Among authors: samanian s.
Indian J Med Res. 2016 Mar;143(3):303-7. doi: 10.4103/0971-5916.182620.
Indian J Med Res. 2016.
PMID: 27241643
Free PMC article.
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A novel missense mutation in exon 7 of the ECM1 gene in an Iranian lipoid proteinosis patient.
Izadi F, Mahjoubi F, Farhadi M, Tavakoli MM, Samanian S.
Izadi F, et al. Among authors: samanian s.
Genet Mol Res. 2012 Nov 14;11(4):3955-60. doi: 10.4238/2012.November.14.2.
Genet Mol Res. 2012.
PMID: 23212332
Free article.
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MDR1 gene polymorphisms: possible association with its expression and clinicopathology characteristics in colorectal cancer patients.
Samanian S, Mahjoubi F, Mahjoubi B, Mirzaee R, Azizi R.
Samanian S, et al.
Asian Pac J Cancer Prev. 2011;12(11):3141-5.
Asian Pac J Cancer Prev. 2011.
PMID: 22394004
Free article.
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