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Familial Occurrence of Isolated Late-onset Nasolacrimal Duct Obstruction in Two Unrelated Families.
Rambam Maimonides Med J. 2024 Jan 19;15(1):e0005. doi: 10.5041/RMMJ.10519.
Rambam Maimonides Med J. 2024.
PMID: 38261349
Free PMC article.
Partial penetrance and phenotypic variability of aplasia of lacrimal and salivary glands caused by a novel FGF10 donor splice-site mutation.
Freund O, Elsana B, Agam N, Jean MM, Safran A, Poleg T, Roguin N, Gradstein L, Tsumi E, Birk OS.
Freund O, et al. Among authors: elsana b.
Am J Med Genet A. 2023 Nov;191(11):2768-2774. doi: 10.1002/ajmg.a.63359. Epub 2023 Aug 24.
Am J Med Genet A. 2023.
PMID: 37615310
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Ocular manifestations among patients with congenital insensitivity to pain due to variants in PRDM12 and SCN9A genes.
Elsana B, Imtirat A, Yagev R, Gradstein L, Majdalani P, Iny O, Parvari R, Tsumi E.
Elsana B, et al.
Am J Med Genet A. 2022 Dec;188(12):3463-3468. doi: 10.1002/ajmg.a.62968. Epub 2022 Sep 16.
Am J Med Genet A. 2022.
PMID: 36111846
Free PMC article.
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Ocular manifestations of congenital insensitivity to pain: a long-term follow-up.
Elsana B, Gradstein L, Imtirat A, Yagev R, Barrett C, Ling G, Abu Tailakh M, Baidousi A, Tsumi E.
Elsana B, et al.
Br J Ophthalmol. 2022 Sep;106(9):1217-1221. doi: 10.1136/bjophthalmol-2020-317464. Epub 2021 Mar 22.
Br J Ophthalmol. 2022.
PMID: 33753408
Review.
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