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For: Song S, Shi A, Lian H, Hu S, Nie Y. Filamin C in cardiomyopathy: from physiological roles to DNA variants. Heart Fail Rev 2021. [PMID: 34535832 DOI: 10.1007/s10741-021-10172-z] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
Number Citing Articles
1 Ripoll-Vera T. Cardiac filaminopathies: lights and shadows in the phenotype associated with the FLNC gene. Rev Esp Cardiol (Engl Ed) 2022:S1885-5857(22)00326-7. [PMID: 36539187 DOI: 10.1016/j.rec.2022.12.005] [Reference Citation Analysis]
2 Ripoll-vera T. Filaminopatías cardiacas: luces y sombras en el fenotipo asociado con el gen FLNC. Revista Española de Cardiología 2022. [DOI: 10.1016/j.recesp.2022.09.018] [Reference Citation Analysis]
3 Baban A, Alesi V, Magliozzi M, Parlapiano G, Genovese S, Cicenia M, Loddo S, Lodato V, Di Chiara L, Fattori F, D'Amico A, Francalanci P, Amodeo A, Novelli A, Drago F. Cardiovascular Involvement in Pediatric FLNC Variants: A Case Series of Fourteen Patients. J Cardiovasc Dev Dis 2022;9:332. [PMID: 36286284 DOI: 10.3390/jcdd9100332] [Reference Citation Analysis]
4 Girolami F, Passantino S, Ballerini A, Gozzini A, Porcedda G, Olivotto I, Favilli S. Clinical Exome Sequencing Revealed a De Novo FLNC Mutation in a Child with Restrictive Cardiomyopathy. Cardiogenetics 2022;12:206-211. [DOI: 10.3390/cardiogenetics12020019] [Reference Citation Analysis]
5 van Wijk SW, Su W, Wijdeveld LFJM, Ramos KS, Brundel BJJM. Cytoskeletal Protein Variants Driving Atrial Fibrillation: Potential Mechanisms of Action. Cells 2022;11:416. [PMID: 35159226 DOI: 10.3390/cells11030416] [Reference Citation Analysis]
6 Castrichini M, Eldemire R, Groves DW, Taylor MR, Miyamoto S, Mestroni L. Clinical and genetic features of arrhythmogenic cardiomyopathy: diagnosis, management and the heart failure perspective. Prog Pediatr Cardiol 2021;63:101459. [PMID: 34970070 DOI: 10.1016/j.ppedcard.2021.101459] [Reference Citation Analysis]