BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

264 related articles for article (PubMed ID: 31268246)

  • 21. Next-generation sequencing (NGS) as a fast molecular diagnosis tool for left ventricular noncompaction in an infant with compound mutations in the MYBPC3 gene.
    Schaefer E; Helms P; Marcellin L; Desprez P; Billaud P; Chanavat V; Rousson R; Millat G
    Eur J Med Genet; 2014 Mar; 57(4):129-32. PubMed ID: 24602869
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Homozygous TNNI3 frameshift variant in a consanguineous family with lethal infantile dilated cardiomyopathy.
    Kraoua L; Louati A; Ahmed SB; Abida N; Khemiri M; Menif K; Mrad R; Zaffran S; Jaouadi H
    Mol Genet Genomic Med; 2024 Jun; 12(6):e2486. PubMed ID: 38924380
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [A case of dilated cardiomyopathy caused by FHL2 gene variant and a literature review].
    Yu C; Jia L; Hao C; Zuo B; Li W; Wang F; Guo J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Mar; 40(3):337-343. PubMed ID: 36854411
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Loss of Function Mutations in NNT Are Associated With Left Ventricular Noncompaction.
    Bainbridge MN; Davis EE; Choi WY; Dickson A; Martinez HR; Wang M; Dinh H; Muzny DM; Pignatelli R; Katsanis N; Boerwinkle E; Gibbs RA; Jefferies JL
    Circ Cardiovasc Genet; 2015 Aug; 8(4):544-52. PubMed ID: 26025024
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Left ventricular noncompaction: a cardiomyopathy often mistaken.
    Suvarna JC; Deshmukh CT; Hajela SA
    Indian J Med Sci; 2009 Jul; 63(7):303-7. PubMed ID: 19700911
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. Effects of cardiac resynchronization therapy on left ventricular remodeling and dyssynchrony in patients with left ventricular noncompaction and heart failure.
    Qiu Q; Chen YX; Mai JT; Yuan WL; Wei YL; Liu YM; Yang L; Wang JF
    Int J Cardiovasc Imaging; 2015 Feb; 31(2):329-37. PubMed ID: 25392055
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Whole-Exome Sequencing Reveals Novel Genetic Variation for Dilated Cardiomyopathy in Pediatric Chinese Patients.
    Dai G; Pu Z; Cheng X; Yin J; Chen J; Xu T; Zhang H; Li Z; Chen X; Chen J; Qin Y; Yang S
    Pediatr Cardiol; 2019 Jun; 40(5):950-957. PubMed ID: 30993396
    [TBL] [Abstract][Full Text] [Related]  

  • 29. VEZF1 loss-of-function mutation underlying familial dilated cardiomyopathy.
    Shi HY; Xie MS; Guo YH; Yang CX; Gu JN; Qiao Q; Di RM; Qiu XB; Xu YJ; Yang YQ
    Eur J Med Genet; 2023 Mar; 66(3):104705. PubMed ID: 36657711
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Cardiac Emerinopathy: A Nonsyndromic Nuclear Envelopathy With Increased Risk of Thromboembolic Stroke Due to Progressive Atrial Standstill and Left Ventricular Noncompaction.
    Ishikawa T; Mishima H; Barc J; Takahashi MP; Hirono K; Terada S; Kowase S; Sato T; Mukai Y; Yui Y; Ohkubo K; Kimoto H; Watanabe H; Hata Y; Aiba T; Ohno S; Chishaki A; Shimizu W; Horie M; Ichida F; Nogami A; Yoshiura KI; Schott JJ; Makita N
    Circ Arrhythm Electrophysiol; 2020 Oct; 13(10):e008712. PubMed ID: 32755394
    [TBL] [Abstract][Full Text] [Related]  

  • 31. The Desmin (
    Kulikova O; Brodehl A; Kiseleva A; Myasnikov R; Meshkov A; Stanasiuk C; Gärtner A; Divashuk M; Sotnikova E; Koretskiy S; Kharlap M; Kozlova V; Mershina E; Pilus P; Sinitsyn V; Milting H; Boytsov S; Drapkina O
    Genes (Basel); 2021 Jan; 12(1):. PubMed ID: 33478057
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Whole exome sequencing identified 1 base pair novel deletion in BCL2-associated athanogene 3 (BAG3) gene associated with severe dilated cardiomyopathy (DCM) requiring heart transplant in multiple family members.
    Rafiq MA; Chaudhry A; Care M; Spears DA; Morel CF; Hamilton RM
    Am J Med Genet A; 2017 Mar; 173(3):699-705. PubMed ID: 28211974
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Comparison of clinical and MRI features between dilated cardiomyopathy and left ventricular noncompaction].
    Yu JC; Zhao SH; Jiang SL; Wang LM; Wang ZF; Lu MJ; Ling J; Zhang Y; Yan CW; Liu Q; Cheng HB
    Zhonghua Xin Xue Guan Bing Za Zhi; 2010 May; 38(5):392-7. PubMed ID: 20654095
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 14-3-3ε gene variants in a Japanese patient with left ventricular noncompaction and hypoplasia of the corpus callosum.
    Chang B; Gorbea C; Lezin G; Li L; Shan L; Sakai N; Kogaki S; Otomo T; Okinaga T; Hamaoka A; Yu X; Hata Y; Nishida N; Yost HJ; Bowles NE; Brunelli L; Ichida F
    Gene; 2013 Feb; 515(1):173-80. PubMed ID: 23266643
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Value of Cardiac Magnetic Resonance Fractal Analysis Combined With Myocardial Strain in Discriminating Isolated Left Ventricular Noncompaction and Dilated Cardiomyopathy.
    Zheng T; Ma X; Li S; Ueda T; Wang Z; Lu A; Zhou W; Zou H; Zhao L; Gong L
    J Magn Reson Imaging; 2019 Jul; 50(1):153-163. PubMed ID: 30565346
    [TBL] [Abstract][Full Text] [Related]  

  • 36. MR -specific characteristics of left ventricular noncompaction and dilated cardiomyopathy.
    Gregor Z; Kiss AR; Grebur K; Szabó LE; Merkely B; Vágó H; Szűcs A
    Int J Cardiol; 2022 Jul; 359():69-75. PubMed ID: 35436556
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Clinical and mutational spectrum in a cohort of 105 unrelated patients with dilated cardiomyopathy.
    Millat G; Bouvagnet P; Chevalier P; Sebbag L; Dulac A; Dauphin C; Jouk PS; Delrue MA; Thambo JB; Le Metayer P; Seronde MF; Faivre L; Eicher JC; Rousson R
    Eur J Med Genet; 2011; 54(6):e570-5. PubMed ID: 21846512
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Novel compound heterozygous variants in EMC1: Overlapping phenotypes of left ventricular noncompaction and long QT syndrome warranting in-depth exploration.
    Dai X; Wang Y; Liu H; Chen J
    Prenat Diagn; 2024 Jun; 44(6-7):907-911. PubMed ID: 38161285
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Whole-exome sequencing identify a new mutation of MYH7 in a Chinese family with left ventricular noncompaction.
    Yang J; Zhu M; Wang Y; Hou X; Wu H; Wang D; Shen H; Hu Z; Zou J
    Gene; 2015 Mar; 558(1):138-42. PubMed ID: 25550050
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Genome-wide studies of copy number variation and exome sequencing identify rare variants in BAG3 as a cause of dilated cardiomyopathy.
    Norton N; Li D; Rieder MJ; Siegfried JD; Rampersaud E; Züchner S; Mangos S; Gonzalez-Quintana J; Wang L; McGee S; Reiser J; Martin E; Nickerson DA; Hershberger RE
    Am J Hum Genet; 2011 Mar; 88(3):273-82. PubMed ID: 21353195
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 14.