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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 1
2010 1
2011 1
2013 3
2014 2
2016 3
2017 4
2018 1
2020 3
2021 2
2022 5
2024 0

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22 results

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Page 1
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
Mutations in PPCS, Encoding Phosphopantothenoylcysteine Synthetase, Cause Autosomal-Recessive Dilated Cardiomyopathy.
Iuso A, Wiersma M, Schüller HJ, Pode-Shakked B, Marek-Yagel D, Grigat M, Schwarzmayr T, Berutti R, Alhaddad B, Kanon B, Grzeschik NA, Okun JG, Perles Z, Salem Y, Barel O, Vardi A, Rubinshtein M, Tirosh T, Dubnov-Raz G, Messias AC, Terrile C, Barshack I, Volkov A, Avivi C, Eyal E, Mastantuono E, Kumbar M, Abudi S, Braunisch M, Strom TM, Meitinger T, Hoffmann GF, Prokisch H, Haack TB, Brundel BJJM, Haas D, Sibon OCM, Anikster Y. Iuso A, et al. Among authors: salem y. Am J Hum Genet. 2018 Jun 7;102(6):1018-1030. doi: 10.1016/j.ajhg.2018.03.022. Epub 2018 May 10. Am J Hum Genet. 2018. PMID: 29754768 Free PMC article.
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.
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
Prenatal diagnosis of major aortopulmonary collateral arteries (MAPCA) in fetuses with pulmonary atresia with ventricular septal defect and agenesis of ductus arteriosus.
Gindes L, Salem Y, Gasnier R, Raucher A, Tamir A, Assa S, Weissman-Brenner A, Weisz B, Kasif E, Achiron R. Gindes L, et al. Among authors: salem y. J Matern Fetal Neonatal Med. 2022 Dec;35(25):5400-5408. doi: 10.1080/14767058.2021.1881475. Epub 2021 Feb 1. J Matern Fetal Neonatal Med. 2022. PMID: 33525939
Mutations in TMEM260 Cause a Pediatric Neurodevelopmental, Cardiac, and Renal Syndrome.
Ta-Shma A, Khan TN, Vivante A, Willer JR, Matak P, Jalas C, Pode-Shakked B, Salem Y, Anikster Y, Hildebrandt F, Katsanis N, Elpeleg O, Davis EE. Ta-Shma A, et al. Among authors: salem y. Am J Hum Genet. 2017 Apr 6;100(4):666-675. doi: 10.1016/j.ajhg.2017.02.007. Epub 2017 Mar 16. Am J Hum Genet. 2017. PMID: 28318500 Free PMC article.
22 results