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Clinical and genetic screening in a large Iranian family with Marfan syndrome: A case study.
Health Sci Rep. 2023 Oct 23;6(10):e1647. doi: 10.1002/hsr2.1647. eCollection 2023 Oct.
Health Sci Rep. 2023.
PMID: 37877128
Free PMC article.
Clinical Manifestations Associated with the Domain-Containing Protein 2 Gene Mutation in an Iranian Family with Spastic Paraplegia 54.
Yari A, Etesam S, Zarifi S, Parvizpour S, Miri-Moghaddam E.
Yari A, et al. Among authors: etesam s.
Neurodegener Dis. 2022;22(3-4):139-150. doi: 10.1159/000530375. Epub 2023 Mar 28.
Neurodegener Dis. 2022.
PMID: 36977391
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The Barriers and Facilitators of Gastric Cancer Screening: a Systematic Review.
Hatamian S, Etesam S, Mazidimoradi A, Momenimovahed Z, Salehiniya H.
Hatamian S, et al. Among authors: etesam s.
J Gastrointest Cancer. 2021 Sep;52(3):839-845. doi: 10.1007/s12029-021-00652-8. Epub 2021 Jun 14.
J Gastrointest Cancer. 2021.
PMID: 34128198
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Identification and In Silico Characterization of a Novel Point Mutation within the Phosphatidylinositol Glycan Anchor Biosynthesis Class G Gene in an Iranian Family with Intellectual Disability.
Parsamanesh N, Safarpour H, Etesam S, Shadmehri AA, Miri-Moghaddam E.
Parsamanesh N, et al. Among authors: etesam s.
J Mol Neurosci. 2019 Dec;69(4):538-545. doi: 10.1007/s12031-019-01376-y. Epub 2019 Aug 14.
J Mol Neurosci. 2019.
PMID: 31414351
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