BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

131 related articles for article (PubMed ID: 35862010)

  • 1. Early Childhood-Onset Hypertrophic Cardiomyopathy in a Family With an In-Frame
    Field E; Lopes LR; Dady K; Kaski JP
    Circ Genom Precis Med; 2022 Aug; 15(4):e003667. PubMed ID: 35862010
    [No Abstract]   [Full Text] [Related]  

  • 2. A novel mutation of the MYH7 gene in a patient with hypertrophic cardiomyopathy.
    Goel N; Huddleston CB; Fiore AC
    Turk J Pediatr; 2018; 60(3):315-318. PubMed ID: 30511546
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Symptomatic distal myopathy with cardiomyopathy due to a MYH7 mutation.
    Overeem S; Schelhaas HJ; Blijham PJ; Grootscholten MI; ter Laak HJ; Timmermans J; van den Wijngaard A; Zwarts MJ
    Neuromuscul Disord; 2007 Jun; 17(6):490-3. PubMed ID: 17383184
    [TBL] [Abstract][Full Text] [Related]  

  • 4.
    Dias GM; Lamounier Júnior A; Seifert M; Barájas-Martinez H; Barr D; Sternick EB; Medina-Acosta E; Campos de Carvalho AC; Cruz Filho FES
    Circ Genom Precis Med; 2021 Oct; 14(5):e003476. PubMed ID: 34555931
    [No Abstract]   [Full Text] [Related]  

  • 5. Genes frequently associated with sudden death in primary hypertrophic cardiomyopathy.
    Herrera-Rodríguez DL; Totomoch-Serra A; Rosas-Madrigal S; Luna-Limón C; Marroquín-Ramírez D; Carnevale A; Rosendo-Gutiérrez R; Villarreal-Molina MT; Márquez-Murillo MF
    Arch Cardiol Mex; 2020; 90(1):58-68. PubMed ID: 31996869
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Hypertrophic cardiomyopathy: New pathogenic variant in MYH7.
    Vargas-Ursúa F; Melendo-Viu M; Íñiguez-Romo A
    Med Clin (Barc); 2024 Jun; 162(11):563-564. PubMed ID: 38423942
    [No Abstract]   [Full Text] [Related]  

  • 7. Cranial, axial and proximal myopathy and hypertrophic cardiomyopathy caused by a mutation in the globular head region of the MYH7 gene.
    Díaz-Manera J; Alejaldre A; Llauger J; Mirabet S; Rojas-García R; Ramos-Fransi A; Gallardo E; Illa I
    Eur J Neurol; 2014 Jun; 21(6):e51-2. PubMed ID: 24805292
    [No Abstract]   [Full Text] [Related]  

  • 8. A novel de novo mutation of β-cardiac myosin heavy chain gene found in a twelve-year-old boy with hypertrophic cardiomyopathy.
    Okada S; Suzuki Y; Arimura T; Kimura A; Narumi H; Hasegawa S
    J Genet; 2014 Aug; 93(2):557-60. PubMed ID: 25189259
    [No Abstract]   [Full Text] [Related]  

  • 9. Ventricular fibrillation in MYH7-related hypertrophic cardiomyopathy before onset of ventricular hypertrophy.
    Christiaans I; Lekanne dit Deprez RH; van Langen IM; Wilde AA
    Heart Rhythm; 2009 Sep; 6(9):1366-9. PubMed ID: 19539541
    [No Abstract]   [Full Text] [Related]  

  • 10. Genotype-phenotype correlation of R870H mutation in hypertrophic cardiomyopathy.
    Tanjore RR; Sikindlapuram AD; Calambur N; Thakkar B; Kerkar PG; Nallari P
    Clin Genet; 2006 May; 69(5):434-6. PubMed ID: 16650083
    [No Abstract]   [Full Text] [Related]  

  • 11. Utility of genetics for risk stratification in pediatric hypertrophic cardiomyopathy.
    Mathew J; Zahavich L; Lafreniere-Roula M; Wilson J; George K; Benson L; Bowdin S; Mital S
    Clin Genet; 2018 Feb; 93(2):310-319. PubMed ID: 29053178
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Myocardial Deformation Analysis in
    Höller V; Seebacher H; Zach D; Schwegel N; Ablasser K; Kolesnik E; Gollmer J; Waltl G; Rainer PP; Verheyen S; Zirlik A; Verheyen N
    Genes (Basel); 2021 Sep; 12(10):. PubMed ID: 34680864
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Generation of a hiPSC line ZZUNEUi007-A from a patient with hypertrophic cardiomyopathy caused by mutation in MYH7.
    Li X; Liu Y; Liu F; Wang X; Liu M; Du W; Zhao J; Wang M; Hu L; Wang C; Fu W; Dong J; Zhao X
    Stem Cell Res; 2020 Mar; 43():101699. PubMed ID: 31931472
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Clinical phenotypic characteristics in patients carrying MYH7-R143Q mutation with hypertrophic cardiomyopathy.
    Zhang L; Zhang Y; Wang J; Ta S; Zhao J; Yao L; Han C; Liu J; Zhao X; Yuan J; Li R; Shan B; Wang Y; Qin Y; Wang B; Liu L
    Curr Probl Cardiol; 2024 Jan; 49(1 Pt C):102164. PubMed ID: 37907184
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Shedding Light on the Darkness of MYH7 Cardiomyopathies.
    Kantor PF
    JACC Heart Fail; 2024 Jan; 12(1):148-149. PubMed ID: 37804309
    [No Abstract]   [Full Text] [Related]  

  • 16. Screening of MYH7, MYBPC3, and TNNT2 genes in Brazilian patients with hypertrophic cardiomyopathy.
    Marsiglia JD; Credidio FL; de Oliveira TG; Reis RF; Antunes Mde O; de Araujo AQ; Pedrosa RP; Barbosa-Ferreira JM; Mady C; Krieger JE; Arteaga-Fernandez E; Pereira Ada C
    Am Heart J; 2013 Oct; 166(4):775-82. PubMed ID: 24093860
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Coexistence of Digenic Mutations in Both Thin (TPM1) and Thick (MYH7) Filaments of Sarcomeric Genes Leads to Severe Hypertrophic Cardiomyopathy in a South Indian FHCM.
    Selvi Rani D; Nallari P; Dhandapany PS; Rani J; Meraj K; Ganesan M; Narasimhan C; Thangaraj K
    DNA Cell Biol; 2015 May; 34(5):350-9. PubMed ID: 25607779
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Troponin T and beta-myosin mutations have distinct cardiac functional effects in hypertrophic cardiomyopathy patients without hypertrophy.
    Revera M; van der Merwe L; Heradien M; Goosen A; Corfield VA; Brink PA; Moolman-Smook JC
    Cardiovasc Res; 2008 Mar; 77(4):687-94. PubMed ID: 18029407
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Association of variants in MYH7, MYBPC3 and TNNT2 with sudden cardiac death-related risk factors in Brazilian patients with hypertrophic cardiomyopathy.
    Mori AA; Castro LR; Bortolin RH; Bastos GM; Oliveira VF; Ferreira GM; Hirata TDC; Fajardo CM; Sampaio MF; Moreira DAR; Pachón-Mateos JC; Correia EB; Sousa AGMR; Brión M; Carracedo A; Hirata RDC; Hirata MH
    Forensic Sci Int Genet; 2021 May; 52():102478. PubMed ID: 33588347
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Hypertrophic cardiomyopathy: never-ending complexity].
    Navarro-López F
    Rev Esp Cardiol; 2006 Oct; 59(10):994-6. PubMed ID: 17125707
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.