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Targeted next-generation sequencing provides novel clues for associated epilepsy and cardiac conduction disorder/SUDEP.
- Published in:
- PLoS ONE, 2017, v. 12, n. 12, p. 1, doi. 10.1371/journal.pone.0189618
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- Publication type:
- Article
High-quality RNA improves sensitivity of SARS-CoV-2 detection by colorimetric RT-LAMP.
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- Experimental Biology & Medicine, 2022, v. 247, n. 4, p. 276, doi. 10.1177/15353702211054768
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- Publication type:
- Article
High-quality RNA improves sensitivity of SARS-CoV-2 detection by colorimetric RT-LAMP.
- Published in:
- Experimental Biology & Medicine, 2022, v. 247, n. 3, p. 276, doi. 10.1177/15353702211054768
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- Publication type:
- Article
Genetic analysis, in silico prediction, and family segregation in long QT syndrome.
- Published in:
- European Journal of Human Genetics, 2015, v. 23, n. 1, p. 79, doi. 10.1038/ejhg.2014.54
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- Publication type:
- Article
Implementing a New Algorithm for Reinterpretation of Ambiguous Variants in Genetic Dilated Cardiomyopathy.
- Published in:
- International Journal of Molecular Sciences, 2024, v. 25, n. 7, p. 3807, doi. 10.3390/ijms25073807
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- Article
A microRNA Signature for the Diagnosis of Statins Intolerance.
- Published in:
- International Journal of Molecular Sciences, 2022, v. 23, n. 15, p. 8146, doi. 10.3390/ijms23158146
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- Publication type:
- Article
miR-16-5p Suppression Protects Human Cardiomyocytes against Endoplasmic Reticulum and Oxidative Stress-Induced Injury.
- Published in:
- International Journal of Molecular Sciences, 2022, v. 23, n. 3, p. 1036, doi. 10.3390/ijms23031036
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- Publication type:
- Article
Rare Titin (TTN) Variants in Diseases Associated with Sudden Cardiac Death.
- Published in:
- International Journal of Molecular Sciences, 2015, v. 16, n. 10, p. 25773, doi. 10.3390/ijms161025773
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- Publication type:
- Article
A Novel Missense Mutation, I890T, in the Pore Region of Cardiac Sodium Channel Causes Brugada Syndrome.
- Published in:
- PLoS ONE, 2013, v. 8, n. 1, p. 1, doi. 10.1371/journal.pone.0053220
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- Publication type:
- Article
A sex determination protocol for the Iberian desman ( Galemys pyrenaicus) based on a three primer amplification of DBX and DBY fragments with non-invasive samples.
- Published in:
- 2010
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- Publication type:
- Report
Incomplete Penetrance and Variable Expressivity: Hallmarks in Channelopathies Associated with Sudden Cardiac Death.
- Published in:
- Biology (2079-7737), 2018, v. 7, n. 1, p. 3, doi. 10.3390/biology7010003
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- Publication type:
- Article
Additional value of screening for minor genes and copy number variants in hypertrophic cardiomyopathy.
- Published in:
- PLoS ONE, 2017, v. 12, n. 8, p. 1, doi. 10.1371/journal.pone.0181465
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- Publication type:
- Article
Correction: Natural and Undetermined Sudden Death: Value of Post-Mortem Genetic Investigation.
- Published in:
- 2017
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- Publication type:
- Correction Notice
Natural and Undetermined Sudden Death: Value of Post-Mortem Genetic Investigation.
- Published in:
- PLoS ONE, 2016, v. 11, n. 12, p. 1, doi. 10.1371/journal.pone.0167358
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- Publication type:
- Article
Large Genomic Imbalances in Brugada Syndrome.
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- PLoS ONE, 2016, v. 11, n. 9, p. 1, doi. 10.1371/journal.pone.0163514
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- Publication type:
- Article
Genetic differentiation between eastern and western Mediterranean swordfish revealed by phylogeographic analysis of the mitochondrial DNA control region.
- Published in:
- ICES Journal of Marine Science / Journal du Conseil, 2010, v. 67, n. 6, p. 1222, doi. 10.1093/icesjms/fsq031
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- Publication type:
- Article
Plasma microRNAs as biomarkers for Lamin A/C-related dilated cardiomyopathy.
- Published in:
- Journal of Molecular Medicine, 2018, v. 96, n. 8, p. 845, doi. 10.1007/s00109-018-1666-1
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- Publication type:
- Article
Genetic Variants as Sudden-Death Risk Markers in Inherited Arrhythmogenic Syndromes: Personalized Genetic Interpretation.
- Published in:
- Journal of Clinical Medicine, 2020, v. 9, n. 6, p. 1866, doi. 10.3390/jcm9061866
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- Publication type:
- Article
Discerning the Ambiguous Role of Missense TTN Variants in Inherited Arrhythmogenic Syndromes.
- Published in:
- Journal of Personalized Medicine, 2022, v. 12, n. 2, p. N.PAG, doi. 10.3390/jpm12020241
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- Publication type:
- Article
Rare Variants Associated with Arrhythmogenic Cardiomyopathy: Reclassification Five Years Later.
- Published in:
- Journal of Personalized Medicine, 2021, v. 11, n. 3, p. 162, doi. 10.3390/jpm11030162
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- Publication type:
- Article
Wolff-Parkinson-White Syndrome with Ventricular Hypertrophy in a Brazilian Family.
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- American Journal of Case Reports, 2017, v. 18, p. 766, doi. 10.12659/AJCR.904613
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- Publication type:
- Article
Familial Dilated Cardiomyopathy Caused by a Novel Frameshift in the BAG3 Gene.
- Published in:
- PLoS ONE, 2016, v. 11, n. 7, p. 1, doi. 10.1371/journal.pone.0158730
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- Publication type:
- Article
Comprehensive Genetic Characterization of a Spanish Brugada Syndrome Cohort.
- Published in:
- PLoS ONE, 2015, v. 10, n. 7, p. 1, doi. 10.1371/journal.pone.0132888
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- Publication type:
- Article