These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

185 related articles for article (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
    [No Abstract]   [Full Text] [Related]  

  • 2. 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. PubMed ID: 23956225
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Ebstein's anomaly.
    Dima-Cozma C; Cojocaru DC; Chiriac S; Negru R; Mitu F
    Rev Med Chir Soc Med Nat Iasi; 2013; 117(3):674-9. PubMed ID: 24502034
    [TBL] [Abstract][Full Text] [Related]  

  • 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
    [TBL] [Abstract][Full Text] [Related]  

  • 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
    [No Abstract]   [Full Text] [Related]  

  • 7. 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; 228(4):301-4. PubMed ID: 23117287
    [TBL] [Abstract][Full Text] [Related]  

  • 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
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Partial atrioventricular septal defect associated with right atrioventricular valve Ebstein's disease].
    Romero-Rivera I; Andrade JL; Silva CC; Andrade JC; Carvalho AC
    Arq Bras Cardiol; 1997 May; 68(5):367-71. PubMed ID: 9497527
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Association Between Mutations in the NKX2.5 Homeobox, Atrial Septal Defects, Ventricular Noncompaction and Sudden Cardiac Death.
    Palomino Doza J; Salguero-Bodes R; de la Parte M; Arribas-Ynsaurriaga F
    Rev Esp Cardiol (Engl Ed); 2018 Jan; 71(1):53-55. PubMed ID: 28330612
    [No Abstract]   [Full Text] [Related]  

  • 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; 79(1):41-5. PubMed ID: 19545073
    [TBL] [Abstract][Full Text] [Related]  

  • 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
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Sarcomere mutations in cardiogenesis and ventricular noncompaction.
    McNally E; Dellefave L
    Trends Cardiovasc Med; 2009 Jan; 19(1):17-21. PubMed ID: 19467449
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Familial biventricular myocardial noncompaction associated with Ebstein's malformation.
    Sinkovec M; Kozelj M; Podnar T
    Int J Cardiol; 2005 Jul; 102(2):297-302. PubMed ID: 15982500
    [TBL] [Abstract][Full Text] [Related]  

  • 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
    [TBL] [Abstract][Full Text] [Related]  

  • 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
    [No Abstract]   [Full Text] [Related]  

  • 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; 117(22):2893-901. PubMed ID: 18506004
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 4(4):450-2. PubMed ID: 24327647
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 173(3):532-5. PubMed ID: 24726209
    [No Abstract]   [Full Text] [Related]  

  • 20. New skeletal myopathy and cardiomyopathy associated with a missense mutation in MYH7.
    Darin N; Tajsharghi H; Ostman-Smith I; Gilljam T; Oldfors A
    Neurology; 2007 Jun; 68(23):2041-2. PubMed ID: 17548557
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 10.