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Journal Abstract Search

478 related items for PubMed ID: 23794396

  • 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. PubMed ID: 23794396
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  • 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. PubMed ID: 21127202
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  • 3. 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 03; 117(22):2893-901. PubMed ID: 18506004
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  • 6. 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 Dec 03; 228(4):301-4. PubMed ID: 23117287
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  • 7. 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 03; 148(5):e223-6. PubMed ID: 25444217
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  • 9. 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 03; 41(3):336-9. PubMed ID: 22859017
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  • 10. A rare case of Ebstein's anomaly with left ventricular noncompaction.
    Tourmousoglou C, Bogossian H, Ninios V, Ninios E.
    Asian Cardiovasc Thorac Ann; 2019 Mar 03; 27(3):208-209. PubMed ID: 30080103
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  • 14. Biallelic mutation in MYH7 and MYBPC3 leads to severe cardiomyopathy with left ventricular noncompaction phenotype.
    Kolokotronis K, Kühnisch J, Klopocki E, Dartsch J, Rost S, Huculak C, Mearini G, Störk S, Carrier L, Klaassen S, Gerull B.
    Hum Mutat; 2019 Aug 03; 40(8):1101-1114. PubMed ID: 30924982
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  • 15. A rare mutation in MYH7 gene occurs with overlapping phenotype.
    Ruggiero L, Fiorillo C, Gibertini S, De Stefano F, Manganelli F, Iodice R, Vitale F, Zanotti S, Galderisi M, Mora M, Santoro L.
    Biochem Biophys Res Commun; 2015 Feb 13; 457(3):262-6. PubMed ID: 25576864
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  • 16. 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. PubMed ID: 15982500
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