BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

193 related articles for article (PubMed ID: 26108892)

  • 1. Left Ventricular Non-compaction: Is It Genetic?
    Ting TW; Jamuar SS; Brett MS; Tan ES; Cham BW; Lim JY; Law HY; Tan EC; Choo JT; Lai AH
    Pediatr Cardiol; 2015 Dec; 36(8):1565-72. PubMed ID: 26108892
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Left-ventricular non-compaction (LVNC): a clinical feature more often observed in terminal deletion 1p36 than previously expected.
    Cremer K; Lüdecke HJ; Ruhr F; Wieczorek D
    Eur J Med Genet; 2008; 51(6):685-8. PubMed ID: 18721913
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A neonatal case of left ventricular noncompaction associated with trisomy 18.
    Beken S; Cevik A; Turan O; Hirfanoğlu IM; Unal S; Altuntaş N; Pektas A; Türkyilmaz C; Tunaoğlu S
    Genet Couns; 2011; 22(2):161-4. PubMed ID: 21848008
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Non-compaction cardiomyopathy: a genetically and clinically heterogeneous disorder.
    Rooms I; Dujardin K; De Sutter J
    Acta Cardiol; 2015 Dec; 70(6):625-31. PubMed ID: 26717209
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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. PubMed ID: 21834050
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Left ventricular non-compaction revisited: a distinct phenotype with genetic heterogeneity?
    Oechslin E; Jenni R
    Eur Heart J; 2011 Jun; 32(12):1446-56. PubMed ID: 21285074
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Defects in Trabecular Development Contribute to Left Ventricular Noncompaction.
    Choquet C; Kelly RG; Miquerol L
    Pediatr Cardiol; 2019 Oct; 40(7):1331-1338. PubMed ID: 31342111
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Left-ventricular non-compaction in a patient with monosomy 1p36.
    Thienpont B; Mertens L; Buyse G; Vermeesch JR; Devriendt K
    Eur J Med Genet; 2007; 50(3):233-6. PubMed ID: 17337261
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Left ventricular noncompaction cardiomyopathy: updated review.
    Udeoji DU; Philip KJ; Morrissey RP; Phan A; Schwarz ER
    Ther Adv Cardiovasc Dis; 2013 Oct; 7(5):260-73. PubMed ID: 24132556
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Do mitochondria contribute to left ventricular non-compaction cardiomyopathy? New findings from myocardium of patients with left ventricular non-compaction cardiomyopathy.
    Liu S; Bai Y; Huang J; Zhao H; Zhang X; Hu S; Wei Y
    Mol Genet Metab; 2013 May; 109(1):100-6. PubMed ID: 23465694
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Congenital left ventricular aneurysm coexisting with left ventricular non-compaction in a newborn.
    Ootani K; Shimada J; Kitagawa Y; Konno Y; Miura F; Takahashi T; Ito E; Ichinose K; Yonesaka S
    Pediatr Int; 2014 Oct; 56(5):e72-4. PubMed ID: 25336015
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Left ventricular noncompaction.
    Malla R; Sharma R; Rauniyar B; Kc MB; Maskey A; Joshi D; Hamal S
    JNMA J Nepal Med Assoc; 2009; 48(174):180-4. PubMed ID: 20387366
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Left ventricular non - compaction: contemporary view of genetic background, clinical course, diagnostic and treatment].
    Streltsova AA; Gudkova AY; Kostareva AA
    Ter Arkh; 2019 Dec; 91(12):90-97. PubMed ID: 32598595
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Left ventricular noncompaction cardiomyopathy: adult association with 1p36 deletion syndrome.
    Lee J; Rinehart S; Polsani V
    Methodist Debakey Cardiovasc J; 2014; 10(4):258-9. PubMed ID: 25624984
    [No Abstract]   [Full Text] [Related]  

  • 15. Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy.
    Arndt AK; Schafer S; Drenckhahn JD; Sabeh MK; Plovie ER; Caliebe A; Klopocki E; Musso G; Werdich AA; Kalwa H; Heinig M; Padera RF; Wassilew K; Bluhm J; Harnack C; Martitz J; Barton PJ; Greutmann M; Berger F; Hubner N; Siebert R; Kramer HH; Cook SA; MacRae CA; Klaassen S
    Am J Hum Genet; 2013 Jul; 93(1):67-77. PubMed ID: 23768516
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Molecular mechanism of ventricular trabeculation/compaction and the pathogenesis of the left ventricular noncompaction cardiomyopathy (LVNC).
    Zhang W; Chen H; Qu X; Chang CP; Shou W
    Am J Med Genet C Semin Med Genet; 2013 Aug; 163C(3):144-56. PubMed ID: 23843320
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Cutis laxa in a patient with 1p36 deletion syndrome.
    Zhang Z; Wang J; Li N; Yao R; Chen J
    J Dermatol; 2018 Jul; 45(7):871-873. PubMed ID: 29611295
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Supplementary Diagnostic Landmarks of Left Ventricular Non-Compaction on Magnetic Resonance Imaging.
    Boban M; Pesa V; Beck N; Manola S; Zulj M; Rotim A; Vcev A
    Yonsei Med J; 2018 Jan; 59(1):63-71. PubMed ID: 29214778
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Exon 3 deletion of RYR2 encoding cardiac ryanodine receptor is associated with left ventricular non-compaction.
    Ohno S; Omura M; Kawamura M; Kimura H; Itoh H; Makiyama T; Ushinohama H; Makita N; Horie M
    Europace; 2014 Nov; 16(11):1646-54. PubMed ID: 24394973
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 10.