Clinical Exome Sequencing Revealed a De Novo FLNC Mutation in a Child with Restrictive Cardiomyopathy.
- Published in:
- Cardiogenetics, 2022, v. 12, n. 2, p. 206, doi. 10.3390/cardiogenetics12020019
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- Publication type:
- Article
Works matching IS 20358253 AND DT 2022 AND VI 12 AND IP 2
Results: 6
1
2
Genetic Screening of a Large Panel of Genes Associated with Cardiac Disease in a Spanish Heart Transplanted Cohort.
- Published in:
- Cardiogenetics, 2022, v. 12, n. 2, p. 198, doi. 10.3390/cardiogenetics12020018
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- Publication type:
- Article
3
Modified Body Mass Index as a Novel Nutritional and Prognostic Marker in Patients with Cardiac Amyloidosis.
- Published in:
- Cardiogenetics, 2022, v. 12, n. 2, p. 185, doi. 10.3390/cardiogenetics12020017
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- Publication type:
- Article
4
Left Ventricular Non-Compaction Spectrum in Adults and Children: From a Morphological Trait to a Structural Muscular Disease.
- Published in:
- Cardiogenetics, 2022, v. 12, n. 2, p. 170, doi. 10.3390/cardiogenetics12020016
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- Publication type:
- Article
5
Clinical Phenotypes of Cardiovascular and Heart Failure Diseases Can Be Reversed? The Holistic Principle of Systems Biology in Multifaceted Heart Diseases.
- Published in:
- Cardiogenetics, 2022, v. 12, n. 2, p. 142, doi. 10.3390/cardiogenetics12020015
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- Publication type:
- Article
6
Pancarditis as the Clinical Presentation of Eosinophilic Granulomatosis with Polyangiitis: A Multimodality Approach to Diagnosis.
- Published in:
- Cardiogenetics, 2022, v. 12, n. 2, p. 133, doi. 10.3390/cardiogenetics12020014
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- Publication type:
- Article