BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

226 related articles for article (PubMed ID: 28855170)

  • 21. Phenotype/Genotype Relationship in Left Ventricular Noncompaction: Ion Channel Gene Mutations Are Associated With Preserved Left Ventricular Systolic Function and Biventricular Noncompaction: Phenotype/Genotype of Noncompaction.
    Cambon-Viala M; Gerard H; Nguyen K; Richard P; Ader F; Pruny JF; Donal E; Eicher JC; Huttin O; Selton-Suty C; Raud-Raynier P; Jondeau G; Mansencal N; Sawka C; Casalta AC; Michel N; Donghi V; Martel H; Faivre L; Charron P; Habib G
    J Card Fail; 2021 Jun; 27(6):677-681. PubMed ID: 34088380
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. A Splice Variant of the
    Myasnikov RP; Kulikova OV; Meshkov AN; Bukaeva AA; Kiseleva AV; Ershova AI; Petukhova AV; Divashuk MG; Zotova ED; Sotnikova EA; Abisheva AA; Muraveva AV; Koretskiy SN; Popov SV; Utkina MV; Snigir EA; Mitrofanov SI; Konureeva KD; Mershina EA; Sinitsyn VE; Yudin SM; Drapkina OM
    Genes (Basel); 2022 Sep; 13(10):. PubMed ID: 36292635
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Genotype-Positive Status Is Associated With Poor Prognoses in Patients With Left Ventricular Noncompaction Cardiomyopathy.
    Li S; Zhang C; Liu N; Bai H; Hou C; Wang J; Song L; Pu J
    J Am Heart Assoc; 2018 Oct; 7(20):e009910. PubMed ID: 30371277
    [TBL] [Abstract][Full Text] [Related]  

  • 25. A novel de novo CASZ1 heterozygous frameshift variant causes dilated cardiomyopathy and left ventricular noncompaction cardiomyopathy.
    Guo J; Li Z; Hao C; Guo R; Hu X; Qian S; Zeng J; Gao H; Li W
    Mol Genet Genomic Med; 2019 Aug; 7(8):e828. PubMed ID: 31268246
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Whole exome sequencing identifies novel candidate mutations in a Chinese family with left ventricular noncompaction.
    Zhou Y; Qian Z; Yang J; Zhu M; Hou X; Wang Y; Wu H; Zou J
    Mol Med Rep; 2018 May; 17(5):7325-7330. PubMed ID: 29568952
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. 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]  

  • 29. Clinical implications of sarcomere and nonsarcomere gene variants in patients with left ventricular noncompaction cardiomyopathy.
    Li S; Zhang C; Liu N; Bai H; Hou C; Pu J
    Mol Genet Genomic Med; 2019 Sep; 7(9):e874. PubMed ID: 31397097
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Identification of a novel TPM1 mutation in a family with left ventricular noncompaction and sudden death.
    Chang B; Nishizawa T; Furutani M; Fujiki A; Tani M; Kawaguchi M; Ibuki K; Hirono K; Taneichi H; Uese K; Onuma Y; Bowles NE; Ichida F; Inoue H; Matsuoka R; Miyawaki T;
    Mol Genet Metab; 2011 Feb; 102(2):200-6. PubMed ID: 20965760
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Left ventricular noncompaction associated with a pathogenic mutation in the MYH7 gene: Known mutation, different phenotype.
    Oliveira M; Azevedo O; Faria B; von Hafe P; Dias G; Faria R; Sanfins V; Lourenço M; Miltenberger-Miltenyi G; Lourenço A
    Rev Port Cardiol; 2022 Mar; 41(3):253-259. PubMed ID: 36062655
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. Left ventricular noncompaction in a family with lamin A/C gene mutation.
    Parent JJ; Towbin JA; Jefferies JL
    Tex Heart Inst J; 2015 Feb; 42(1):73-6. PubMed ID: 25873806
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Role of
    Amor-Salamanca A; Santana Rodríguez A; Rasoul H; Rodríguez-Palomares JF; Moldovan O; Hey TM; Delgado MG; Cuenca DL; de Castro Campos D; Basurte-Elorz MT; Macías-Ruiz R; Fuentes Cañamero ME; Galvin J; Bilbao Quesada R; de la Higuera Romero L; Trujillo-Quintero JP; García-Cruz LM; Cárdenas-Reyes I; Jiménez-Jáimez J; García-Hernández S; Valverde-Gómez M; Gómez-Díaz I; Limeres Freire J; García-Pinilla JM; Gimeno-Blanes JR; Savattis K; García-Pavía P; Ochoa JP
    Circ Genom Precis Med; 2024 Apr; 17(2):e004404. PubMed ID: 38353104
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Left Ventricular Noncompaction and Congenital Heart Disease Increases the Risk of Congestive Heart Failure.
    Hirono K; Hata Y; Miyao N; Okabe M; Takarada S; Nakaoka H; Ibuki K; Ozawa S; Yoshimura N; Nishida N; Ichida F; Lvnc Study Collaborators
    J Clin Med; 2020 Mar; 9(3):. PubMed ID: 32183154
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Targeted panel sequencing in adult patients with left ventricular non-compaction reveals a large genetic heterogeneity.
    Richard P; Ader F; Roux M; Donal E; Eicher JC; Aoutil N; Huttin O; Selton-Suty C; Coisne D; Jondeau G; Damy T; Mansencal N; Casalta AC; Michel N; Haentjens J; Faivre L; Lavoute C; Nguyen K; Tregouët DA; Habib G; Charron P
    Clin Genet; 2019 Mar; 95(3):356-367. PubMed ID: 30471092
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Prevalence and Prognostic Significance of Left Ventricular Noncompaction in Patients Referred for Cardiac Magnetic Resonance Imaging.
    Ivanov A; Dabiesingh DS; Bhumireddy GP; Mohamed A; Asfour A; Briggs WM; Ho J; Khan SA; Grossman A; Klem I; Sacchi TJ; Heitner JF
    Circ Cardiovasc Imaging; 2017 Sep; 10(9):. PubMed ID: 28899950
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Genetic Basis of Left Ventricular Noncompaction.
    Rojanasopondist P; Nesheiwat L; Piombo S; Porter GA; Ren M; Phoon CKL
    Circ Genom Precis Med; 2022 Jun; 15(3):e003517. PubMed ID: 35549379
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Novel α-Actin Gene Mutation p.(Ala21Val) Causing Familial Hypertrophic Cardiomyopathy, Myocardial Noncompaction, and Transmural Crypts. Clinical-Pathologic Correlation.
    Frustaci A; De Luca A; Guida V; Biagini T; Mazza T; Gaudio C; Letizia C; Russo MA; Galea N; Chimenti C
    J Am Heart Assoc; 2018 Feb; 7(4):. PubMed ID: 29440008
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 12.