156 related articles for article (PubMed ID: 37280362)
1. The next step toward personalized recommendations for genetic cardiomyopathies.
Stroeks SLVM; Verdonschot JAJ
Eur J Hum Genet; 2023 Nov; 31(11):1201-1203. PubMed ID: 37280362
[No Abstract] [Full Text] [Related]
2. FLNC pathogenic variants in patients with cardiomyopathies: Prevalence and genotype-phenotype correlations.
Ader F; De Groote P; Réant P; Rooryck-Thambo C; Dupin-Deguine D; Rambaud C; Khraiche D; Perret C; Pruny JF; Mathieu-Dramard M; Gérard M; Troadec Y; Gouya L; Jeunemaitre X; Van Maldergem L; Hagège A; Villard E; Charron P; Richard P
Clin Genet; 2019 Oct; 96(4):317-329. PubMed ID: 31245841
[TBL] [Abstract][Full Text] [Related]
3. Short read (next-generation) sequencing: a tutorial with cardiomyopathy diagnostics as an exemplar.
Punetha J; Hoffman EP
Circ Cardiovasc Genet; 2013 Aug; 6(4):427-34. PubMed ID: 23852418
[No Abstract] [Full Text] [Related]
4. Cardiomyopathies: Genetic overlap between peripartum and dilated cardiomyopathies.
Lim GB
Nat Rev Cardiol; 2016 Mar; 13(3):121. PubMed ID: 26794013
[No Abstract] [Full Text] [Related]
5. Shared Genetic Predisposition in Peripartum and Dilated Cardiomyopathies.
Stergiopoulos K; Lima FV; Yang J
N Engl J Med; 2016 Jun; 374(26):2601. PubMed ID: 27355548
[No Abstract] [Full Text] [Related]
6. Shared Genetic Predisposition in Peripartum and Dilated Cardiomyopathies.
Biteker M
N Engl J Med; 2016 Jun; 374(26):2601. PubMed ID: 27355547
[No Abstract] [Full Text] [Related]
7. Shared Genetic Predisposition in Peripartum and Dilated Cardiomyopathies.
Ware JS; Seidman JG; Arany Z
N Engl J Med; 2016 Jun; 374(26):2601-2. PubMed ID: 27355546
[No Abstract] [Full Text] [Related]
8. Truncating mutations on myofibrillar myopathies causing genes as prevalent molecular explanations on patients with dilated cardiomyopathy.
Janin A; N'Guyen K; Habib G; Dauphin C; Chanavat V; Bouvagnet P; Eschalier R; Streichenberger N; Chevalier P; Millat G
Clin Genet; 2017 Dec; 92(6):616-623. PubMed ID: 28436997
[TBL] [Abstract][Full Text] [Related]
9. Value of cardiac magnetic resonance imaging in the setting of familiar cardiomyopathy: A step toward pre-clinical diagnosis.
Muser D; Puppato M; Proclemer A; Nucifora G
Int J Cardiol; 2016 Jan; 203():43-5. PubMed ID: 26492308
[No Abstract] [Full Text] [Related]
10. [Genotype-phenotype correlations of pathogenic variants in the FLNC gene].
Ader F; Villard E; Ledeuil C; Charron P; Richard P
Med Sci (Paris); 2018 Nov; 34 Hors série n°2():39-41. PubMed ID: 30418145
[No Abstract] [Full Text] [Related]
11. Filamin C Cardiomyopathy Variants Cause Protein and Lysosome Accumulation.
Agarwal R; Paulo JA; Toepfer CN; Ewoldt JK; Sundaram S; Chopra A; Zhang Q; Gorham J; DePalma SR; Chen CS; Gygi SP; Seidman CE; Seidman JG
Circ Res; 2021 Sep; 129(7):751-766. PubMed ID: 34405687
[TBL] [Abstract][Full Text] [Related]
12. Lymphocytic Myocarditis: A Genetically Predisposed Disease?
Artico J; Merlo M; Delcaro G; Cannatà A; Gentile P; De Angelis G; Paldino A; Bussani R; Ferro MD; Sinagra G
J Am Coll Cardiol; 2020 Jun; 75(24):3098-3100. PubMed ID: 32553263
[No Abstract] [Full Text] [Related]
13. Personalized medicine: genetic diagnosis for inherited cardiomyopathies/channelopathies.
Ackerman MJ; Marcou CA; Tester DJ
Rev Esp Cardiol (Engl Ed); 2013 Apr; 66(4):298-307. PubMed ID: 24775620
[TBL] [Abstract][Full Text] [Related]
14. Identification of a Novel Titin Variant Underlying Myocardial Involvement in Neurofibromatosis Type 1.
Kizawa M; Nakagama Y; Shindo T; Ogawa S; Inuzuka R
Can J Cardiol; 2018 Oct; 34(10):1369.e5-1369.e7. PubMed ID: 30269836
[TBL] [Abstract][Full Text] [Related]
15. Centronuclear myopathy with cardiomyopathy due to recessive titinopathy.
Martinez-Thompson JM; Winder TL; Liewluck T
Muscle Nerve; 2019 Apr; 59(4):E26-E27. PubMed ID: 30681174
[No Abstract] [Full Text] [Related]
16. Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic Cardiomyopathies.
Ortiz-Genga MF; Cuenca S; Dal Ferro M; Zorio E; Salgado-Aranda R; Climent V; Padrón-Barthe L; Duro-Aguado I; Jiménez-Jáimez J; Hidalgo-Olivares VM; García-Campo E; Lanzillo C; Suárez-Mier MP; Yonath H; Marcos-Alonso S; Ochoa JP; Santomé JL; García-Giustiniani D; Rodríguez-Garrido JL; Domínguez F; Merlo M; Palomino J; Peña ML; Trujillo JP; Martín-Vila A; Stolfo D; Molina P; Lara-Pezzi E; Calvo-Iglesias FE; Nof E; Calò L; Barriales-Villa R; Gimeno-Blanes JR; Arad M; García-Pavía P; Monserrat L
J Am Coll Cardiol; 2016 Dec; 68(22):2440-2451. PubMed ID: 27908349
[TBL] [Abstract][Full Text] [Related]
17. Inherited cardiomyopathies: molecular genetics and clinical genetic testing in the postgenomic era.
Teekakirikul P; Kelly MA; Rehm HL; Lakdawala NK; Funke BH
J Mol Diagn; 2013 Mar; 15(2):158-70. PubMed ID: 23274168
[TBL] [Abstract][Full Text] [Related]
18. Titin in muscular dystrophy and cardiomyopathy: Urinary titin as a novel marker.
Misaka T; Yoshihisa A; Takeishi Y
Clin Chim Acta; 2019 Aug; 495():123-128. PubMed ID: 30959043
[TBL] [Abstract][Full Text] [Related]
19. Filamin-C variant-associated cardiomyopathy: A pooled analysis of individual patient data to evaluate the clinical profile and risk of sudden cardiac death.
Celeghin R; Cipriani A; Bariani R; Bueno Marinas M; Cason M; Bevilacqua M; De Gaspari M; Rizzo S; Rigato I; Da Pozzo S; Zorzi A; Perazzolo Marra M; Thiene G; Iliceto S; Basso C; Corrado D; Pilichou K; Bauce B
Heart Rhythm; 2022 Feb; 19(2):235-243. PubMed ID: 34601126
[TBL] [Abstract][Full Text] [Related]
20. [Genetic diagnostics for cardiomyopathies].
Czepluch F; Wollnik B; Hasenfuß G
Dtsch Med Wochenschr; 2017 May; 142(9):657-664. PubMed ID: 28454199
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
