Found: 7
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Familial cardiomyopathy caused by a novel heterozygous mutation in the gene LMNA (c.1434dupG): a cardiac MRI-augmented segregation study.
- Published in:
- Acta Myologica, 2019, v. 38, n. 3, p. 159
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- Publication type:
- Article
Automated In-Line Artificial Intelligence Measured Global Longitudinal Shortening and Mitral Annular Plane Systolic Excursion: Reproducibility and Prognostic Significance.
- Published in:
- 2022
- By:
- Publication type:
- journal article
Myocardial Perfusion Defects in Hypertrophic Cardiomyopathy Mutation Carriers.
- Published in:
- 2021
- By:
- Publication type:
- journal article
Apical Hypertrophic Cardiomyopathy: The Variant Less Known.
- Published in:
- 2020
- By:
- Publication type:
- journal article
The myocardial phenotype of Fabry disease pre-hypertrophy and pre-detectable storage.
- Published in:
- European Heart Journal - Cardiovascular Imaging, 2021, v. 22, n. 7, p. 790, doi. 10.1093/ehjci/jeaa101
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- Publication type:
- Article
Dilated cardiomyopathy and arrhythmogenic left ventricular cardiomyopathy: a comprehensive genotype-imaging phenotype study.
- Published in:
- European Heart Journal - Cardiovascular Imaging, 2020, v. 21, n. 3, p. 326, doi. 10.1093/ehjci/jez188
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- Publication type:
- Article
Saturation-pulse prepared heart-rate independent inversion-recovery (SAPPHIRE) biventricular T1 mapping: inter-field strength, head-to-head comparison of diastolic, systolic and dark-blood measurements.
- Published in:
- BMC Medical Imaging, 2022, v. 22, n. 1, p. 1, doi. 10.1186/s12880-022-00843-0
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- Publication type:
- Article