Dilated Cardiomyopathy: Genetic Determinants and Mechanisms

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Leukocyte Nuclear Morphology Alterations in Dilated Cardiomyopathy Caused by a Lamin AC Truncating Mutation (LMNA/Ser431*) Are Modified by the Presence of a LAP2 Missense Polymorphism (TMPO/Arg690Cys)

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Are We Ready to Treat Dilated Cardiomyopathy Differently, Using LGE Guidance?

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Family Screening in DCM

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Novel Insights Into the Prevalence of TNNI3K -Mediated Dilated Cardiomyopathy and Putative Disease Mechanisms

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Integration of dilated cardiomyopathy genomics with transcriptomics from the human heart implicates regulatory molecular mechanismsPreprint

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Retinoid X receptor alpha is a spatiotemporally-specific therapeutic target for doxorubicin-induced cardiomyopathy in adult zebrafishPreprint

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Sudden Cardiac Death in Hereditary Dilated Cardiomyopathy

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Importance of Mitochondrial-Related Genes in Dilated Cardiomyopathy Based on Bioinformatics Analysis

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Differential Expression Profiles and Functional Analysis of Long Non-coding RNAs in Children With Dilated Cardiomyopathy

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The Role of Genetic Testing in the Evaluation of Dilated Cardiomyopathies

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IDIOPATINĖ DILATACINĖ KARDIOMIOPATIJA: KLINIKINIS ATVEJIS

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A Rare Case of Coexisting Mutation in Desmin and Thioredoxin Reductase 2 Genes Causing Dilated Cardiomyopathy

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CARDIOMIOPATIAS: CLASSIFICAÇÕES, DIAGNÓSTICOS E TRATAMENTOS

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CARDIOLOGIA EM FOCO: PREVENÇÃO, DIAGNÓSTICO E TRATAMENTOS ATUAIS

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Cardiomyopathy

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Diagnostics of combined hereditary cardiovascular pathology in a teenager

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24-year-old obese woman with dilated cardiomyopathy: a case report of obese cardiomyopathy

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Echocardiography to Assess Cardiac Structure and Function in Genetic Cardiomyopathies

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Recommendation: Precision therapy in dilated cardiomyopathy: Pipedream or paradigm shift? — R0/PR3

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Recommendation: Precision therapy in dilated cardiomyopathy: Pipedream or paradigm shift? — R2/PR9

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Recommendation: Precision therapy in dilated cardiomyopathy: Pipedream or paradigm shift? — R1/PR6

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Review: Precision therapy in dilated cardiomyopathy: Pipedream or paradigm shift? — R0/PR2

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Decision: Precision therapy in dilated cardiomyopathy: Pipedream or paradigm shift? — R1/PR7

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Author comment: Precision therapy in dilated cardiomyopathy: Pipedream or paradigm shift? — R1/PR5

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Decision: Precision therapy in dilated cardiomyopathy: Pipedream or paradigm shift? — R2/PR10

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Author comment: Precision therapy in dilated cardiomyopathy: Pipedream or paradigm shift? — R0/PR1

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Author comment: Precision therapy in dilated cardiomyopathy: Pipedream or paradigm shift? — R2/PR8

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Decision: Precision therapy in dilated cardiomyopathy: Pipedream or paradigm shift? — R0/PR4

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A silent interweaving: interatrial block and laminopathy

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Kardiomyopathien

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Recent Clinical Trials on Immunomodulatory Biomaterials Applications

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Real-World Genetic Characteristics of Candidates for Implantable Cardioverter-Defibrillators with Dilated CardiomyopathyPreprint

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Screening dilated cardiomyopathy core genes for pan-cancer analysis by machine learning

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Additional file 2 of Exploration of dilated cardiomyopathy for biomarkers and immune microenvironment: evidence from RNA-seq

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Additional file 3 of Genetic characterization of dilated cardiomyopathy patients undergoing heart transplantation in the Chinese population by whole-exome sequencing

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Additional file 3 of Identification and functional characterization of BICD2 as a candidate disease gene in an consanguineous family with dilated cardiomyopathy

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Additional file 4 of Identification and functional characterization of BICD2 as a candidate disease gene in an consanguineous family with dilated cardiomyopathy

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Additional file 2 of Identification and functional characterization of BICD2 as a candidate disease gene in an consanguineous family with dilated cardiomyopathy

Luo, K., Zheng, C., Luo, R., Cao, X., Sun, H., Ma, H., Huang, J., Yang, X., Wu, X., & Li, X. (2022) · Figshare · doi:10.6084/m9.figshare.21009584

Additional file 3 of Exploration of dilated cardiomyopathy for biomarkers and immune microenvironment: evidence from RNA-seq

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Additional file 5 of Identification and functional characterization of BICD2 as a candidate disease gene in an consanguineous family with dilated cardiomyopathy

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LMNA‐related muscular dystrophy presenting as an inflammatory myopathy

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