Cited by

• Genetics and Clinical Features of Noncompaction Cardiomyopathy in the Fetal Population.

  Sun H, Hao X, Wang X, Zhou X, Zhang Y, Liu X, Han J, Gu X, Sun L, Zhao Y, Yi T, Zhang H, He Y. Sun H, et al. Front Cardiovasc Med. 2021 Jan 20;7:617561. doi: 10.3389/fcvm.2020.617561. eCollection 2020. Front Cardiovasc Med. 2021. PMID: 33553264 Free PMC article.
• Atypical form of left ventricular noncompaction resembling mass appearance in papillary muscles.

  Cagliyan CE, Akilli RE, Deniz A, Deveci OS, Demir S, Kanadasi M. Cagliyan CE, et al. Herz. 2015 Feb;40(1):76-8. doi: 10.1007/s00059-013-3903-2. Epub 2013 Aug 4. Herz. 2015. PMID: 23912970 No abstract available.
• Mutations in the NOTCH pathway regulator MIB1 cause left ventricular noncompaction cardiomyopathy.

  Luxán G, Casanova JC, Martínez-Poveda B, Prados B, D'Amato G, MacGrogan D, Gonzalez-Rajal A, Dobarro D, Torroja C, Martinez F, Izquierdo-García JL, Fernández-Friera L, Sabater-Molina M, Kong YY, Pizarro G, Ibañez B, Medrano C, García-Pavía P, Gimeno JR, Monserrat L, Jiménez-Borreguero LJ, de la Pompa JL. Luxán G, et al. Nat Med. 2013 Feb;19(2):193-201. doi: 10.1038/nm.3046. Epub 2013 Jan 13. Nat Med. 2013. PMID: 23314057
• Loss of Function Mutations in NNT Are Associated With Left Ventricular Noncompaction.

  Bainbridge MN, Davis EE, Choi WY, Dickson A, Martinez HR, Wang M, Dinh H, Muzny DM, Pignatelli R, Katsanis N, Boerwinkle E, Gibbs RA, Jefferies JL. Bainbridge MN, et al. Circ Cardiovasc Genet. 2015 Aug;8(4):544-52. doi: 10.1161/CIRCGENETICS.115.001026. Epub 2015 May 29. Circ Cardiovasc Genet. 2015. PMID: 26025024 Free PMC article.
• 16-kDa prolactin and bromocriptine in postpartum cardiomyopathy.

  Hilfiker-Kleiner D, Struman I, Hoch M, Podewski E, Sliwa K. Hilfiker-Kleiner D, et al. Curr Heart Fail Rep. 2012 Sep;9(3):174-82. doi: 10.1007/s11897-012-0095-7. Curr Heart Fail Rep. 2012. PMID: 22729360 Review.