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Rare variant (p.Ser43Asn) of familial transthyretin amyloidosis associated with isolated cardiac phenotype: A case series with literature review.
Papathanasiou M, Carpinteiro A, Kersting D, Jakstaite AM, Hagenacker T, Schlosser TW, Rischpler C, Rassaf T, Luedike P. Papathanasiou M, et al. Among authors: jakstaite am. Mol Genet Genomic Med. 2021 Dec;9(12):e1581. doi: 10.1002/mgg3.1581. Epub 2020 Dec 20. Mol Genet Genomic Med. 2021. PMID: 33345470 Free PMC article. Review.
Clinical features and predictors of atrial fibrillation in patients with light-chain or transthyretin cardiac amyloidosis.
Papathanasiou M, Jakstaite AM, Oubari S, Siebermair J, Wakili R, Hoffmann J, Carpinteiro A, Hagenacker T, Thimm A, Rischpler C, Kessler L, Rassaf T, Luedike P. Papathanasiou M, et al. Among authors: jakstaite am. ESC Heart Fail. 2022 Jun;9(3):1740-1748. doi: 10.1002/ehf2.13851. Epub 2022 Feb 17. ESC Heart Fail. 2022. PMID: 35178887 Free PMC article.