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Cardiac fibrosis in mice with hypertrophic cardiomyopathy is mediated by non-myocyte proliferation and requires Tgf-β.
- Published in:
- 2010
- By:
- Publication type:
- journal article
Calsequestrin 2 (CASQ2) mutations increase expression of calreticulin and ryanodine receptors, causing catecholaminergic polymorphic ventricular tachycardia.
- Published in:
- Journal of Clinical Investigation, 2007, v. 117, n. 7, p. 1814, doi. 10.1172/JCI31080
- By:
- Publication type:
- Article
Calsequestrin 2 (CASQ2) mutations increase expression of calreticulin and ryanodine receptors, causing catecholaminergic polymorphic ventricular tachycardia.
- Published in:
- Journal of Clinical Investigation, 2007, v. 117, p. 1814, doi. 10.1172/JCI31080
- By:
- Publication type:
- Article
Reclassification of genetic variants in children with long QT syndrome.
- Published in:
- Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 9, p. 1, doi. 10.1002/mgg3.1300
- By:
- Publication type:
- Article
Genetic and phenotypic spectrum in the NONO‐associated syndromic disorder.
- Published in:
- American Journal of Medical Genetics. Part A, 2023, v. 191, n. 2, p. 469, doi. 10.1002/ajmg.a.63044
- By:
- Publication type:
- Article
Epicardioid single-cell genomics uncovers principles of human epicardium biology in heart development and disease.
- Published in:
- Nature Biotechnology, 2023, v. 41, n. 12, p. 1787, doi. 10.1038/s41587-023-01718-7
- By:
- Publication type:
- Article
Differentiating primary sarcomeric hypertrophic cardiomyopathy from Noonan syndrome: can the electrocardiogram be of use?
- Published in:
- Cardiology in the Young, 2024, v. 34, n. 3, p. 597, doi. 10.1017/S1047951123003177
- By:
- Publication type:
- Article
Low-molecular-weight heparin administered by subcutaneous catheter is a safe and effective anti-coagulation regimen in selected inpatient infants and children with complex congenital heart disease.
- Published in:
- Cardiology in the Young, 2021, v. 31, n. 9, p. 1439, doi. 10.1017/S1047951121000317
- By:
- Publication type:
- Article
Cytoplasmic CUG RNA Foci Are Insufficient to Elicit Key DM1 Features.
- Published in:
- PLoS ONE, 2008, v. 3, n. 12, p. 1, doi. 10.1371/journal.pone.0003968
- By:
- Publication type:
- Article
Neointimal hyperplasia in systemic-to-pulmonary shunts of children with complex cyanotic congenital heart disease.
- Published in:
- European Journal of Cardio-Thoracic Surgery, 2022, v. 62, n. 6, p. 1, doi. 10.1093/ejcts/ezac431
- By:
- Publication type:
- Article
No increased extracellular volume fraction or conduction time after childhood septal myectomy.
- Published in:
- European Journal of Cardio-Thoracic Surgery, 2020, v. 57, n. 5, p. 958, doi. 10.1093/ejcts/ezz356
- By:
- Publication type:
- Article
Clinical long-term outcome of septal myectomy for obstructive hypertrophic cardiomyopathy in infants.
- Published in:
- European Journal of Cardio-Thoracic Surgery, 2018, v. 53, n. 3, p. 538, doi. 10.1093/ejcts/ezx369
- By:
- Publication type:
- Article
Fetal Bradycardia Caused by Monogenic Disorders—A Review of the Literature.
- Published in:
- Journal of Clinical Medicine, 2022, v. 11, n. 23, p. 6880, doi. 10.3390/jcm11236880
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- Publication type:
- Article
Compound Mutation in Cardiac Sarcomere Proteins Is Associated with Increased Risk for Major Arrhythmic Events in Pediatric Onset Hypertrophic Cardiomyopathy.
- Published in:
- Journal of Clinical Medicine, 2021, v. 10, n. 22, p. 5256, doi. 10.3390/jcm10225256
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- Publication type:
- Article
Response to the editor:.
- Published in:
- Journal of Cardiovascular Electrophysiology, 2006, v. 17, n. 9, p. E6, doi. 10.1111/j.1540-8167.2006.00564.x
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- Publication type:
- Article
Inherited Conduction System Abnormalities—One Group of Diseases, Many Genes.
- Published in:
- Journal of Cardiovascular Electrophysiology, 2006, v. 17, n. 4, p. 446, doi. 10.1111/j.1540-8167.2006.00427.x
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- Publication type:
- Article
A SCALY RASH.
- Published in:
- Contemporary Pediatrics, 2007, v. 24, n. 10, p. 56
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- Publication type:
- Article
EGFR and MMP-9 are associated with neointimal hyperplasia in systemic-to-pulmonary shunts in children with complex cyanotic heart disease.
- Published in:
- Mammalian Genome, 2023, v. 34, n. 2, p. 285, doi. 10.1007/s00335-023-09982-3
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- Publication type:
- Article
Peak Oxygen Uptake on Cardiopulmonary Exercise Test Is a Predictor for Severe Arrhythmic Events during Three-Year Follow-Up in Patients with Complex Congenital Heart Disease.
- Published in:
- Journal of Cardiovascular Development & Disease (JCDD), 2022, v. 9, n. 7, p. 215, doi. 10.3390/jcdd9070215
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- Publication type:
- Article
Bioactive adrenomedullin (bio-ADM) is associated with endothelial dysfunction in infants and children with complex congenital heart disease undergoing open-heart surgery on cardiopulmonary bypass.
- Published in:
- Clinical Chemistry & Laboratory Medicine, 2024, v. 62, n. 3, p. 551, doi. 10.1515/cclm-2023-0511
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- Publication type:
- Article