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Fetal liver T2* values: defining a standardized scale.
Goitein O, Eshet Y, Hoffmann C, Raviv-Zilka L, Salem Y, Hamdan A, Goitein D, Kushnir T, Eshed I, Di-Segni E, Konen E. Goitein O, et al. Among authors: salem y. J Magn Reson Imaging. 2013 Dec;38(6):1342-5. doi: 10.1002/jmri.24132. Epub 2013 Apr 10. J Magn Reson Imaging. 2013. PMID: 23576455
Primary Fetal Lung Hypoplasia (PFLH): Imaging and Clinical Characteristics.
Achiron R, Gilboa Y, Salem Y, Jacobson Y, Raviv-Zilka L, Cioca A, Kidron D, Kivilevitch Z. Achiron R, et al. Among authors: salem y. Ultraschall Med. 2017 Jun;38(3):301-309. doi: 10.1055/s-0042-124361. Epub 2017 Jun 14. Ultraschall Med. 2017. PMID: 28614860 English.
Whole-exome sequencing reveals a monogenic cause in 56% of individuals with laterality disorders and associated congenital heart defects.
Bolkier Y, Barel O, Marek-Yagel D, Atias-Varon D, Kagan M, Vardi A, Mishali D, Katz U, Salem Y, Tirosh-Wagner T, Jacobson JM, Raas-Rothschild A, Chorin O, Eliyahu A, Sarouf Y, Shlomovitz O, Veber A, Shalva N, Javasky E, Ben Moshe Y, Staretz-Chacham O, Rechavi G, Mane S, Anikster Y, Vivante A, Pode-Shakked B. Bolkier Y, et al. Among authors: salem y. J Med Genet. 2022 Jul;59(7):691-696. doi: 10.1136/jmedgenet-2021-107775. Epub 2021 Jul 2. J Med Genet. 2022. PMID: 34215651
A founder truncating variant in GDF1 causes autosomal-recessive right isomerism and associated congenital heart defects in multiplex Arab kindreds.
Marek-Yagel D, Bolkier Y, Barel O, Vardi A, Mishali D, Katz U, Salem Y, Abudi S, Nayshool O, Kol N, Raas-Rothschild A, Rechavi G, Anikster Y, Pode-Shakked B. Marek-Yagel D, et al. Among authors: salem y. Am J Med Genet A. 2020 May;182(5):987-993. doi: 10.1002/ajmg.a.61509. Epub 2020 Mar 7. Am J Med Genet A. 2020. PMID: 32144877
136 results