PubMed for id: 4435

Year	Number of Results
1976	2
1979	1
1985	2
1991	1
1992	2
1994	2
1996	1
1998	1
1999	1
2002	1
2003	1
2005	2
2006	1
2007	1
2008	2
2010	2
2011	2
2013	5
2014	2
2015	5
2016	18
2017	70
2018	69
2019	68
2020	78
2021	73
2022	67
2023	75
2024	31

1

Heterozygous nonsense variants in laminin subunit 3α resulting in Ebstein's anomaly.

Zhou Z, Huang X, Tang X, Chen W, Chen Q, Zhang C, Li Y, Zhao D, Zheng Z, Hu S, Wang J, Kullo IJ, Ding K. Zhou Z, et al. HGG Adv. 2023 Jul 29;4(4):100227. doi: 10.1016/j.xhgg.2023.100227. eCollection 2023 Oct 12. HGG Adv. 2023. PMID: 37635785 Free PMC article.

2

Altered contractility, Ca²⁺ transients, and cell morphology seen in a patient-specific iPSC-CM model of Ebstein's anomaly with left ventricular noncompaction.

Thareja SK, Anfinson M, Cavanaugh M, Kim MS, Lamberton P, Radandt J, Brown R, Liang HL, Stamm K, Afzal MZ, Strande J, Frommelt MA, Lough JW, Fitts RH, Mitchell ME, Tomita-Mitchell A. Thareja SK, et al. Am J Physiol Heart Circ Physiol. 2023 Jul 1;325(1):H149-H162. doi: 10.1152/ajpheart.00658.2022. Epub 2023 May 19. Am J Physiol Heart Circ Physiol. 2023. PMID: 37204873

3

MYH7 variants cause complex congenital heart disease.

Ritter A, Leonard J, Gray C, Izumi K, Levinson K, Nair DR, O'Connor M, Rossano J, Shankar V, Chowns J, Marzolf A, Owens A, Ahrens-Nicklas RC. Ritter A, et al. Am J Med Genet A. 2022 Sep;188(9):2772-2776. doi: 10.1002/ajmg.a.62766. Epub 2022 May 2. Am J Med Genet A. 2022. PMID: 35491958

4

Ebstein Anomaly and Right Aortic Arch in Patient with Charge Syndrome.

Lubaua I, Teraudkalna M. Lubaua I, et al. Medicina (Kaunas). 2021 Nov 13;57(11):1239. doi: 10.3390/medicina57111239. Medicina (Kaunas). 2021. PMID: 34833458 Free PMC article.

5

Novel hemizygous loss-of-function variant in NONO identified in a South African boy.

Coetzer KC, Moosa S. Coetzer KC, et al. Am J Med Genet A. 2022 Jan;188(1):373-376. doi: 10.1002/ajmg.a.62509. Epub 2021 Sep 22. Am J Med Genet A. 2022. PMID: 34549882

6

Case Report of a 33-year-old with Ebstein malformation of tricuspid valve and hypertrophic cardiomyopathy.

Saedi S, Pashapour P, Houshmand G. Saedi S, et al. Cardiol Young. 2022 Apr;32(4):674-675. doi: 10.1017/S1047951121003644. Epub 2021 Sep 9. Cardiol Young. 2022. PMID: 34496998

7

A case of capillary malformation-arteriovenous malformation and Ebstein's anomaly in a child with EphB4 mutation.

Sherwani Y, Jenkins S, Adelanwa A, Burch DM, Chaudhuri NR, Zinn Z. Sherwani Y, et al. Pediatr Dermatol. 2021 Sep;38(5):1305-1307. doi: 10.1111/pde.14723. Epub 2021 Aug 2. Pediatr Dermatol. 2021. PMID: 34339071

8

Integrated microRNA and mRNA Expression Profiling Identifies Novel Targets and Networks Associated with Ebstein's Anomaly.

Abu-Halima M, Wagner V, Becker LS, Ayesh BM, Abd El-Rahman M, Fischer U, Meese E, Abdul-Khaliq H. Abu-Halima M, et al. Cells. 2021 Apr 30;10(5):1066. doi: 10.3390/cells10051066. Cells. 2021. PMID: 33946378 Free PMC article.

9

Differential diagnosis of arrhythmogenic cardiomyopathy: phenocopies versus disease variants.

Cipriani A, Perazzolo Marra M, Bariani R, Mattesi G, Vio R, Bettella N, DE Lazzari M, Motta R, Bauce B, Zorzi A, Corrado D. Cipriani A, et al. Minerva Med. 2021 Apr;112(2):269-280. doi: 10.23736/S0026-4806.20.06782-8. Epub 2020 Jul 22. Minerva Med. 2021. PMID: 32700864 Review.

10

Ebstein anomaly associated with cri du chat (cat's cry) syndrome and 20q duplication.

Olivella A, Manotas H, Payán-Gómez C, Piñeros JG. Olivella A, et al. BMJ Case Rep. 2020 Jun 1;13(6):e233766. doi: 10.1136/bcr-2019-233766. BMJ Case Rep. 2020. PMID: 32487530 Free PMC article.

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