124 related articles for article (PubMed ID: 38423942)
1. 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]
2.
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]
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. 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]
5. 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]
6. Clinical Utility of a Phenotype-Enhanced
Mattivi CL; Bos JM; Bagnall RD; Nowak N; Giudicessi JR; Ommen SR; Semsarian C; Ackerman MJ
Circ Genom Precis Med; 2020 Oct; 13(5):453-459. PubMed ID: 32894683
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Determining pathogenicity of genetic variants in hypertrophic cardiomyopathy: importance of periodic reassessment.
Das K J; Ingles J; Bagnall RD; Semsarian C
Genet Med; 2014 Apr; 16(4):286-93. PubMed ID: 24113344
[TBL] [Abstract][Full Text] [Related]
9. 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]
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. 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]
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. 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]
14. 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]
15. 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]
16. Presence of Hypertrophic Cardiomyopathy Related Gene Mutations and Clinical Manifestations in Vietnamese Patients With Hypertrophic Cardiomyopathy.
Tran Vu MT; Nguyen TV; Huynh NV; Nguyen Thai HT; Pham Nguyen V; Ho Huynh TD
Circ J; 2019 Aug; 83(9):1908-1916. PubMed ID: 31308319
[TBL] [Abstract][Full Text] [Related]
17. [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]
18. [Hypertrophic cardiomyopathy: infrequent mutation of the cardiac beta-myosin heavy-chain gene].
Mora R; Merino JL; Peinado R; Olias F; García-Guereta L; del Cerro MJ; Tarín MN; Molano J
Rev Esp Cardiol; 2006 Aug; 59(8):846-9. PubMed ID: 16938236
[TBL] [Abstract][Full Text] [Related]
19. Lack of Phenotypic Differences by Cardiovascular Magnetic Resonance Imaging in MYH7 (β-Myosin Heavy Chain)- Versus MYBPC3 (Myosin-Binding Protein C)-Related Hypertrophic Cardiomyopathy.
Weissler-Snir A; Hindieh W; Gruner C; Fourey D; Appelbaum E; Rowin E; Care M; Lesser JR; Haas TS; Udelson JE; Manning WJ; Olivotto I; Tomberli B; Maron BJ; Maron MS; Crean AM; Rakowski H; Chan RH
Circ Cardiovasc Imaging; 2017 Feb; 10(2):. PubMed ID: 28193612
[TBL] [Abstract][Full Text] [Related]
20. Ultrasound and genetic detection of fetal hypertrophic cardiomyopathy in second trimester of pregnancy.
Soares C; Lourenço C; Nogueira RN; Carrico A
BMJ Case Rep; 2021 Jan; 14(1):. PubMed ID: 33408112
[No Abstract] [Full Text] [Related]
[Next] [New Search]
