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Assessment of the CTNNA3 gene encoding human αT-catenin regarding its involvement in dilated cardiomyopathy.
- Published in:
- Human Genetics, 2003, v. 112, n. 3, p. 227, doi. 10.1007/s00439-002-0857-5
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- Publication type:
- Article
Outcomes of Congenital Heart Surgery Patients After Extracorporeal Life Support at Texas Children's Hospital.
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- Artificial Organs, 2004, v. 28, n. 10, p. 963, doi. 10.1111/j.1525-1594.2004.07378.x
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- Publication type:
- Article
Prevalence, predictors, and outcomes of cardiorenal syndrome in children with dilated cardiomyopathy: a report from the Pediatric Cardiomyopathy Registry.
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- Pediatric Nephrology, 2015, v. 30, n. 12, p. 2177, doi. 10.1007/s00467-015-3165-8
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- Publication type:
- Article
Incidence, Causes, and Outcomes of Dilated Cardiomyopathy in Children.
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- JAMA: Journal of the American Medical Association, 2006, v. 296, n. 15, p. 1867, doi. 10.1001/jama.296.15.1867
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- Publication type:
- Article
Risk of Aborted Cardiac Arrest or Sudden Cardiac Death During Adolescence in the Long-QT Syndrome.
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- JAMA: Journal of the American Medical Association, 2006, v. 296, n. 10, p. 1249, doi. 10.1001/jama.296.10.1249
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- Publication type:
- Article
Viral endomyocardial infection in the 1st year post transplant is associated with persistent inflammation in children who have undergone cardiac transplant.
- Published in:
- 2014
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- Publication type:
- Journal Article
Assessment and management of the failing heart in children.
- Published in:
- Cardiology in the Young, 2008, v. 18, n. S3, p. 63, doi. 10.1017/S1047951108003326
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- Publication type:
- Article
Concentrations of brain natriuretic peptide in the plasma predicts outcomes of treatment of children with decompensated heart failure admitted to the Intensive Care unit.
- Published in:
- Cardiology in the Young, 2007, v. 17, n. 4, p. 397, doi. 10.1017/S1047951107000601
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- Publication type:
- Article
Analysis of cardiac function and morphology in genetic reference population of BXD strains reveals associated eQTLs and candidate causal and modifier genes.
- Published in:
- FASEB Journal, 2022, v. 36, p. N.PAG, doi. 10.1096/fasebj.2022.36.S1.R3609
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- Publication type:
- Article
Corrigendum to: ‘HRS/EHRA Expert Consensus Statement on the State of Genetic Testing for the Channelopathies and Cardiomyopathies’ [Europace 2011;13:1077–109, doi: 10.1093/europace/eur245].
- Published in:
- EP: Europace, 2012, v. 14, n. 2, p. 277, doi. 10.1093/europace/eur413
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- Publication type:
- Article
HRS/EHRA Expert Consensus Statement on the State of Genetic Testing for the Channelopathies and Cardiomyopathies.
- Published in:
- EP: Europace, 2011, v. 13, n. 8, p. 1077, doi. 10.1093/europace/eur245
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- Publication type:
- Article
Tinman/Nkx2-5 acts via miR-1 and upstream of Cdc42 to regulate heart function across species.
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- Journal of Cell Biology, 2011, v. 193, n. 7, p. 1181, doi. 10.1083/jcb.201006114
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- Publication type:
- Article
Clinical approaches to tachyarrhythmias, volume 10: The brugada syndrome.
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- Clinical Cardiology, 2000, v. 23, n. 11, p. 873A, doi. 10.1002/clc.4960231122
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- Publication type:
- Article
Danon disease presenting with dilated cardiomyopathy and a complex phenotype.
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- Journal of Human Genetics, 2007, v. 52, n. 10, p. 830, doi. 10.1007/s10038-007-0184-8
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- Publication type:
- Article
Identification and functional characterization of NODAL rare variants in heterotaxy and isolated cardiovascular malformations.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 5, p. 861, doi. 10.1093/hmg/ddn411
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- Publication type:
- Article
NOTCH1 mutations in individuals with left ventricular outflow tract malformations reduce ligand-induced signaling.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 18, p. 2886, doi. 10.1093/hmg/ddn187
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- Publication type:
- Article
A cardiac myosin binding protein C mutation in the Maine Coon cat with familial hypertrophic cardiomyopathy.
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- Human Molecular Genetics, 2005, v. 14, n. 23, p. 3587, doi. 10.1093/hmg/ddi386
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- Publication type:
- Article
Expression Levels of the Tnni3k Gene in the Heart Are Highly Associated with Cardiac and Glucose Metabolism-Related Phenotypes and Functional Pathways.
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- International Journal of Molecular Sciences, 2023, v. 24, n. 16, p. 12759, doi. 10.3390/ijms241612759
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- Publication type:
- Article
Novel use of cangrelor in pediatrics: A pilot cohort study demonstrating use in ventricular assist devices.
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- Artificial Organs, 2021, v. 45, n. 1, p. 38, doi. 10.1111/aor.13782
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- Publication type:
- Article
Exploring the Regulation and Function of Rpl3l in the Development of Early-Onset Dilated Cardiomyopathy and Congestive Heart Failure Using Systems Genetics Approach.
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- Genes, 2024, v. 15, n. 1, p. 53, doi. 10.3390/genes15010053
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- Publication type:
- Article
Linkage analysis of left ventricular outflow tract malformations (aortic valve stenosis, coarctation of the aorta, and hypoplastic left heart syndrome).
- Published in:
- European Journal of Human Genetics, 2009, v. 17, n. 6, p. 811, doi. 10.1038/ejhg.2008.255
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- Publication type:
- Article
Arrhythmogenic right ventricular cardiomyopathy type 1 (ARVD1): confirmation of locus assignment and mutation screening of four candidate genes.
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- European Journal of Human Genetics, 2003, v. 11, n. 1, p. 69, doi. 10.1038/sj.ejhg.5200914
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- Publication type:
- Article
Neonatal presentation of ventricular tachycardia and a Reye-like syndrome episode associated with disturbed mitochondrial energy metabolism.
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- BMC Pediatrics, 2002, v. 2, p. 12, doi. 10.1186/1471-2431-2-12
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- Publication type:
- Article
Acquired and modifiable cardiovascular risk factors in patients treated for cancer.
- Published in:
- Journal of Thrombosis & Thrombolysis, 2021, v. 51, n. 4, p. 846, doi. 10.1007/s11239-020-02273-7
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- Publication type:
- Article
Concurrent Use of Calcium Chloride and Arginine Vasopressin Infusions in Pediatric Patients with Acute Cardiocirculatory Failure.
- Published in:
- Pediatric Cardiology, 2019, v. 40, n. 5, p. 1046, doi. 10.1007/s00246-019-02114-2
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- Publication type:
- Article
Strategies to Prevent Cast Formation in Patients with Plastic Bronchitis Undergoing Heart Transplantation.
- Published in:
- 2017
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- Publication type:
- Report
Utility of Echocardiography in the Assessment of Left Ventricular Diastolic Function and Restrictive Physiology in Children and Young Adults with Restrictive Cardiomyopathy: A Comparative Echocardiography-Catheterization Study.
- Published in:
- Pediatric Cardiology, 2017, v. 38, n. 2, p. 381, doi. 10.1007/s00246-016-1526-0
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- Publication type:
- Article
The Impact of Concomitant Left Ventricular Non-compaction with Congenital Heart Disease on Perioperative Outcomes.
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- Pediatric Cardiology, 2016, v. 37, n. 7, p. 1307, doi. 10.1007/s00246-016-1435-2
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- Publication type:
- Article
Fibrillin-1 Gene Mutations in Left Ventricular Non-compaction Cardiomyopathy.
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- Pediatric Cardiology, 2016, v. 37, n. 6, p. 1123, doi. 10.1007/s00246-016-1404-9
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- Publication type:
- Article
Medical Therapy Leads to Favorable Remodeling in Left Ventricular Non-compaction Cardiomyopathy: Dilated Phenotype.
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- Pediatric Cardiology, 2016, v. 37, n. 4, p. 674, doi. 10.1007/s00246-015-1330-2
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- Publication type:
- Article
Initial Observations of the Effects of Calcium Chloride Infusions in Pediatric Patients with Low Cardiac Output.
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- Pediatric Cardiology, 2016, v. 37, n. 3, p. 610, doi. 10.1007/s00246-015-1322-2
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- Publication type:
- Article
Parvovirus B19 Myocarditis Causes Significant Morbidity and Mortality in Children.
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- Pediatric Cardiology, 2013, v. 34, n. 2, p. 390, doi. 10.1007/s00246-012-0468-4
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- Publication type:
- Article
Left Ventricular Noncompaction Cardiomyopathy in Barth Syndrome: An Example of an Undulating Cardiac Phenotype Necessitating Mechanical Circulatory Support as a Bridge to Transplantation.
- Published in:
- 2012
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- Publication type:
- Report
PTPN11 Mutation Associated with Aortic Dilation and Hypertrophic Cardiomyopathy in a Pediatric Patient with Noonan Syndrome.
- Published in:
- Pediatric Cardiology, 2010, v. 31, n. 1, p. 114, doi. 10.1007/s00246-009-9537-8
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- Publication type:
- Article
The Efficacy of Mitral Valve Surgery in Children with Dilated Cardiomyopathy and Severe Mitral Regurgitation.
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- Pediatric Cardiology, 2008, v. 29, n. 1, p. 13, doi. 10.1007/s00246-007-9050-x
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- Publication type:
- Article
Detection of Viral Deoxyribonucleic Acid in Amniotic Fluid: Association with Fetal Malformation and Pregnancy Abnormalities.
- Published in:
- Fetal Diagnosis & Therapy, 2005, v. 20, n. 3, p. 203, doi. 10.1159/000083906
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- Publication type:
- Article
Dyslipidemia and cardiovascular disease among childhood cancer survivors: a St. Jude Lifetime Cohort report.
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- JNCI: Journal of the National Cancer Institute, 2024, v. 116, n. 3, p. 408, doi. 10.1093/jnci/djad222
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- Publication type:
- Article
Nesiritide Therapy in a Term Neonate with Renal Disease.
- Published in:
- Pharmacotherapy, 2006, v. 26, n. 2, p. 281, doi. 10.1592/phco.26.2.281
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- Publication type:
- Article
Administration of a Large Nesiritide Bolus Dose in a Pediatric Patient: Case Report and Review of Nesiritide Use in Pediatrics.
- Published in:
- Pharmacotherapy, 2006, v. 26, n. 2, p. 277, doi. 10.1592/phco.26.2.277
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- Publication type:
- Article
Intrauterine adenoviral infection associated with fetal non-immune hydrops.
- Published in:
- Prenatal Diagnosis, 1998, v. 18, n. 2, p. 182, doi. 10.1002/(SICI)1097-0223(199802)18:2<182::AID-PD225>3.0.CO;2-E
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- Publication type:
- Article
Myocardial deformation abnormalities in paediatric hypertrophic cardiomyopathy: are all aetiologies identical?
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- European Journal of Echocardiography, 2008, v. 9, n. 6, p. 784, doi. 10.1093/ejechocard/jen150
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- Publication type:
- Article
Genetic Modulation of Brugada Syndrome by a Common Polymorphism.
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- Journal of Cardiovascular Electrophysiology, 2009, v. 20, n. 10, p. 1137, doi. 10.1111/j.1540-8167.2009.01508.x
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- Publication type:
- Article
Mutations in Conserved Amino Acids in the KCNQ1 Channel and Risk of Cardiac Events in Type-1 Long-QT Syndrome.
- Published in:
- Journal of Cardiovascular Electrophysiology, 2009, v. 20, n. 8, p. 859, doi. 10.1111/j.1540-8167.2009.01455.x
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- Publication type:
- Article
A Common SCN5A Variant Alters the Responsiveness of Human Sodium Channels to Class I Antiarrhythmic Agents.
- Published in:
- Journal of Cardiovascular Electrophysiology, 2007, v. 18, n. 4, p. 434, doi. 10.1111/j.1540-8167.2007.00777.x
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- Publication type:
- Article
Clinical Course and Risk Stratification of Patients Affected with the Jervell and Lange-Nielsen Syndrome.
- Published in:
- Journal of Cardiovascular Electrophysiology, 2006, v. 17, n. 11, p. 1161, doi. 10.1111/j.1540-8167.2006.00587.x
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- Publication type:
- Article
Dilated Cardiomyopathy: A Tale of Cytoskeletal Proteins and Beyond.
- Published in:
- Journal of Cardiovascular Electrophysiology, 2006, v. 17, n. 8, p. 919, doi. 10.1111/j.1540-8167.2006.00530.x
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- Publication type:
- Article
Phenotypic Characterization of a Large European Family with Brugada Syndrome Displaying a Sudden Unexpected Death Syndrome Mutation in SCN5A: Female Predominance in the Signs and Symptoms of the Disease.
- Published in:
- Journal of Cardiovascular Electrophysiology, 2004, v. 15, n. 1, p. 64, doi. 10.1046/j.1540-8167.2004.03341.x
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- Publication type:
- Article
Location of Mutation in the KCNQ1 and Phenotypic Presentation of Long QT Syndrome.
- Published in:
- Journal of Cardiovascular Electrophysiology, 2003, v. 14, n. 11, p. 1149, doi. 10.1046/j.1540-8167.2003.03177.x
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- Publication type:
- Article
Ventricular Tachycardia or Conduction Disease: What is the Mechanism of Death Associated with SCN5A?
- Published in:
- Journal of Cardiovascular Electrophysiology, 2001, v. 12, n. 6, p. 637, doi. 10.1046/j.1540-8167.2001.00637.x
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- Publication type:
- Article
Cardiac Arrhythmias: The Genetic Connection.
- Published in:
- Journal of Cardiovascular Electrophysiology, 2000, v. 11, n. 5, p. 601, doi. 10.1111/j.1540-8167.2000.tb00016.x
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- Publication type:
- Article