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Journal Abstract Search

186 related items for PubMed ID: 25444217

  • 1. 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. PubMed ID: 25444217
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  • 4. Ebstein's anomaly.
    Dima-Cozma C, Cojocaru DC, Chiriac S, Negru R, Mitu F.
    Rev Med Chir Soc Med Nat Iasi; 2013 Nov; 117(3):674-9. PubMed ID: 24502034
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  • 5. 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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  • 6. Novel mutation in exon 14 of the sarcomere gene MYH7 in familial left ventricular noncompaction with bicuspid aortic valve.
    Basu R, Hazra S, Shanks M, Paterson DI, Oudit GY.
    Circ Heart Fail; 2014 Nov; 7(6):1059-62. PubMed ID: 25415959
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  • 8. Ebstein's anomaly. Genetic study of 26 families.
    Emanuel R, O'Brien K, Ng R.
    Br Heart J; 1976 Jan; 38(1):5-7. PubMed ID: 943167
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  • 11. [Ebstein's anomaly and interventricular communication, a rare association].
    PatiñoBahena E, Yabur Espitia M, Muñoz Castellanos L, Calderón Colmenero J, Buendía Hernández A.
    Arch Cardiol Mex; 2009 Jan; 79(1):41-5. PubMed ID: 19545073
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  • 12. 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.
    Am J Med Genet A; 2022 Sep; 188(9):2772-2776. PubMed ID: 35491958
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  • 15. Novel KLHL26 variant associated with a familial case of Ebstein's anomaly and left ventricular noncompaction.
    Samudrala SSK, North LM, Stamm KD, Earing MG, Frommelt MA, Willes R, Tripathi S, Dsouza NR, Zimmermann MT, Mahnke DK, Liang HL, Lund M, Lin CW, Geddes GC, Mitchell ME, Tomita-Mitchell A.
    Mol Genet Genomic Med; 2020 Apr; 8(4):e1152. PubMed ID: 31985165
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  • 16. The presence of multiple variants affects the clinical phenotype and prognosis in left ventricular noncompaction after surgery.
    Hirono K, Sakai T, Hata Y, Nishida N.
    J Thorac Cardiovasc Surg; 2018 Mar; 155(3):e101-e109. PubMed ID: 29203216
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  • 17. 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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  • 18. Secondary repair of Ebstein's anomaly with atrioventricular septal defect using the cone technique.
    Kumar G, Panda BR, Gooi A, Alphonso N, Karl TR.
    World J Pediatr Congenit Heart Surg; 2013 Oct 03; 4(4):450-2. PubMed ID: 24327647
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  • 19. Novel MYH7 mutation associated with mild myopathy but life-threatening ventricular arrhythmias and noncompaction.
    Finsterer J, Stöllberger C, Brandau O, Laccone F, Bichler K, Laing NG.
    Int J Cardiol; 2014 May 15; 173(3):532-5. PubMed ID: 24726209
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