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Results: 1 to 20 of 108

1.

Ebstein anomaly associated with left ventricular noncompaction: an autosomal dominant condition that can be caused by mutations in MYH7.

Vermeer AM, van Engelen K, Postma AV, Baars MJ, Christiaans I, De Haij S, Klaassen S, Mulder BJ, Keavney B.

Am J Med Genet C Semin Med Genet. 2013 Aug;163C(3):178-84. doi: 10.1002/ajmg.c.31365. Epub 2013 Jun 21. Review.

PMID:
23794396
[PubMed - indexed for MEDLINE]
2.

Mutations in the sarcomere gene MYH7 in Ebstein anomaly.

Postma AV, van Engelen K, van de Meerakker J, Rahman T, Probst S, Baars MJ, Bauer U, Pickardt T, Sperling SR, Berger F, Moorman AF, Mulder BJ, Thierfelder L, Keavney B, Goodship J, Klaassen S.

Circ Cardiovasc Genet. 2011 Feb;4(1):43-50. doi: 10.1161/CIRCGENETICS.110.957985. Epub 2010 Dec 2.

PMID:
21127202
[PubMed - indexed for MEDLINE]
Free Article
3.

Familial ebstein anomaly, left ventricular hypertrabeculation, and ventricular septal defect associated with a MYH7 mutation.

Bettinelli AL, Mulder TJ, Funke BH, Lafferty KA, Longo SA, Niyazov DM.

Am J Med Genet A. 2013 Dec;161A(12):3187-90. doi: 10.1002/ajmg.a.36182. Epub 2013 Aug 16.

PMID:
23956225
[PubMed - indexed for MEDLINE]
4.

Mutations in sarcomere protein genes in left ventricular noncompaction.

Klaassen S, Probst S, Oechslin E, Gerull B, Krings G, Schuler P, Greutmann M, Hürlimann D, Yegitbasi M, Pons L, Gramlich M, Drenckhahn JD, Heuser A, Berger F, Jenni R, Thierfelder L.

Circulation. 2008 Jun 3;117(22):2893-901. doi: 10.1161/CIRCULATIONAHA.107.746164. Epub 2008 May 27.

PMID:
18506004
[PubMed - indexed for MEDLINE]
Free Article
5.

Surgical repair of left ventricular noncompaction in a patient with a novel mutation of the myosin heavy chain 7 gene.

Uchiyama T, Yoshimura K, Kaneko K, Nemoto S, Ichida F, Hata Y, Nishida N.

Tohoku J Exp Med. 2012;228(4):301-4.

PMID:
23117287
[PubMed - indexed for MEDLINE]
Free Article
6.

Familial Ebstein's anomaly, left ventricular noncompaction, and ventricular septal defect associated with an MYH7 mutation.

Hirono K, Hata Y, Ibuki K, Yoshimura N.

J Thorac Cardiovasc Surg. 2014 Nov;148(5):e223-6. doi: 10.1016/j.jtcvs.2014.08.049. Epub 2014 Sep 6. No abstract available.

PMID:
25444217
[PubMed - indexed for MEDLINE]
7.

Prenatal ultrasound diagnosis of MYH7 non-compaction cardiomyopathy.

Hoedemaekers YM, Cohen-Overbeek TE, Frohn-Mulder IM, Dooijes D, Majoor-Krakauer DF.

Ultrasound Obstet Gynecol. 2013 Mar;41(3):336-9. doi: 10.1002/uog.12279.

PMID:
22859017
[PubMed - indexed for MEDLINE]
Free Article
8.

Ebstein's anomaly may be caused by mutations in the sarcomere protein gene MYH7.

van Engelen K, Postma AV, van de Meerakker JB, Roos-Hesselink JW, Helderman-van den Enden AT, Vliegen HW, Rahman T, Baars MJ, Sels JW, Bauer U, Pickardt T, Sperling SR, Moorman AF, Keavney B, Goodship J, Klaassen S, Mulder BJ.

Neth Heart J. 2013 Mar;21(3):113-7. doi: 10.1007/s12471-011-0141-1.

PMID:
21604106
[PubMed]
Free PMC Article
9.

Sarcomere mutations in cardiogenesis and ventricular noncompaction.

McNally E, Dellefave L.

Trends Cardiovasc Med. 2009 Jan;19(1):17-21. doi: 10.1016/j.tcm.2009.03.003. Review.

PMID:
19467449
[PubMed - indexed for MEDLINE]
10.

Noncompaction of the left ventricular myocardium in a boy with a novel chromosome 8p23.1 deletion.

Blinder JJ, Martinez HR, Craigen WJ, Belmont J, Pignatelli RH, Jefferies JL.

Am J Med Genet A. 2011 Sep;155A(9):2215-20. doi: 10.1002/ajmg.a.34129. Epub 2011 Aug 10.

PMID:
21834050
[PubMed - indexed for MEDLINE]
11.

Ebstein's anomaly.

Dima-Cozma C, Cojocaru DC, Chiriac S, Negru R, Mitu F.

Rev Med Chir Soc Med Nat Iasi. 2013 Jul-Sep;117(3):674-9.

PMID:
24502034
[PubMed - indexed for MEDLINE]
12.

Identification of a novel TPM1 mutation in a family with left ventricular noncompaction and sudden death.

Chang B, Nishizawa T, Furutani M, Fujiki A, Tani M, Kawaguchi M, Ibuki K, Hirono K, Taneichi H, Uese K, Onuma Y, Bowles NE, Ichida F, Inoue H, Matsuoka R, Miyawaki T; Noncompaction study collaborators.

Mol Genet Metab. 2011 Feb;102(2):200-6. doi: 10.1016/j.ymgme.2010.09.009. Epub 2010 Sep 29.

PMID:
20965760
[PubMed - indexed for MEDLINE]
13.

Familial biventricular myocardial noncompaction associated with Ebstein's malformation.

Sinkovec M, Kozelj M, Podnar T.

Int J Cardiol. 2005 Jul 10;102(2):297-302.

PMID:
15982500
[PubMed - indexed for MEDLINE]
14.

Left ventricular noncompaction associated with Ebstein's anomaly.

Saltik L, Eroğlu E, Bayrak F, Değertekin M.

Turk Kardiyol Dern Ars. 2009 Jun;37(4):269-72.

PMID:
19717963
[PubMed - indexed for MEDLINE]
15.

Digenic mutational inheritance of the integrin alpha 7 and the myosin heavy chain 7B genes causes congenital myopathy with left ventricular non-compact cardiomyopathy.

Esposito T, Sampaolo S, Limongelli G, Varone A, Formicola D, Diodato D, Farina O, Napolitano F, Pacileo G, Gianfrancesco F, Di Iorio G.

Orphanet J Rare Dis. 2013 Jun 21;8:91. doi: 10.1186/1750-1172-8-91.

PMID:
23800289
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

Sarcomere gene mutations in isolated left ventricular noncompaction cardiomyopathy do not predict clinical phenotype.

Probst S, Oechslin E, Schuler P, Greutmann M, Boyé P, Knirsch W, Berger F, Thierfelder L, Jenni R, Klaassen S.

Circ Cardiovasc Genet. 2011 Aug 1;4(4):367-74. doi: 10.1161/CIRCGENETICS.110.959270. Epub 2011 May 6.

PMID:
21551322
[PubMed - indexed for MEDLINE]
Free Article
17.

[Familial occurrence of Ebstein anomaly].

Margalit-Stashefski R, Lorber A, Margalit E.

Harefuah. 1998 May 15;134(10):762-4, 832. Hebrew.

PMID:
10909632
[PubMed - indexed for MEDLINE]
18.

The importance of genetic counseling, DNA diagnostics, and cardiologic family screening in left ventricular noncompaction cardiomyopathy.

Hoedemaekers YM, Caliskan K, Michels M, Frohn-Mulder I, van der Smagt JJ, Phefferkorn JE, Wessels MW, ten Cate FJ, Sijbrands EJ, Dooijes D, Majoor-Krakauer DF.

Circ Cardiovasc Genet. 2010 Jun;3(3):232-9. doi: 10.1161/CIRCGENETICS.109.903898. Epub 2010 Jun 8.

PMID:
20530761
[PubMed - indexed for MEDLINE]
Free Article
19.

Left ventricular non-compaction revisited: a distinct phenotype with genetic heterogeneity?

Oechslin E, Jenni R.

Eur Heart J. 2011 Jun;32(12):1446-56. doi: 10.1093/eurheartj/ehq508. Epub 2011 Jan 31. Review.

PMID:
21285074
[PubMed - indexed for MEDLINE]
Free Article
20.

Isolated left ventricular noncompaction in a newborn with Pierre-Robin sequence.

Aypar E, Sert A, Gokmen Z, Aslan E, Odabas D.

Pediatr Cardiol. 2013 Feb;34(2):452-4. doi: 10.1007/s00246-012-0294-8. Epub 2012 Mar 25.

PMID:
22447382
[PubMed - indexed for MEDLINE]
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