| scholarly article | Q13442814 |
| P2093 | author name string | Lizhang Chen | |
| Peng Huang | |||
| Tingting Wang | |||
| Lijuan Zhao | |||
| Tubao Yang | |||
| Jiabi Qin | |||
| Letao Chen | |||
| Lesan Wang | |||
| Senmao Zhang | |||
| Zan Zheng | |||
| Ziwei Ye | |||
| P2860 | cites work | The significance of ventriculo-coronary arterial connections in the setting of pulmonary atresia with an intact ventricular septum | Q36258138 |
| Ischemic Stroke in Children and Young Adults With Congenital Heart Disease | Q36713973 | ||
| Fkbp1a controls ventricular myocardium trabeculation and compaction by regulating endocardial Notch1 activity. | Q36783111 | ||
| Molecular mechanism of ventricular trabeculation/compaction and the pathogenesis of the left ventricular noncompaction cardiomyopathy (LVNC) | Q37051387 | ||
| Genetics of heart failure in congenital heart disease | Q38109319 | ||
| Factors associated with coronary artery disease and stroke in adults with congenital heart disease | Q38605191 | ||
| Chronic Heart Failure in Congenital Heart Disease: A Scientific Statement From the American Heart Association. | Q38703617 | ||
| Risk factors for excess mortality in adults with congenital heart diseases. | Q39026257 | ||
| 20-year survival of children born with congenital anomalies: a population-based study | Q39907766 | ||
| Post-Operative Outcomes in Children With and Without Congenital Heart Disease Undergoing Noncardiac Surgery | Q39985958 | ||
| Comorbidity, healthcare utilisation and process of care measures in patients with congenital heart disease in the UK: cross-sectional, population-based study with case-control analysis | Q40190821 | ||
| Long-Term Nationwide Follow-Up Study of Simple Congenital Heart Disease Diagnosed in Otherwise Healthy Children | Q40195093 | ||
| High mortality and morbidity among adults with congenital heart disease and type 2 diabetes | Q40509149 | ||
| Preferred reporting items for systematic reviews and meta-analyses: the PRISMA Statement | Q42035537 | ||
| Mutations in the NOTCH pathway regulator MIB1 cause left ventricular noncompaction cardiomyopathy | Q43487742 | ||
| Prevalence, timing of diagnosis and mortality of newborns with congenital heart defects: a population-based study | Q45234013 | ||
| Perioperative outcomes of major noncardiac surgery in adults with congenital heart disease. | Q46001711 | ||
| Prevalence of congenital heart disease | Q46130466 | ||
| A growing problem: maternal death and peripartum complications are higher in women with grown-up congenital heart disease | Q46326402 | ||
| Myocardial Infarction in Adults With Congenital Heart Disease | Q47624514 | ||
| Congenital heart disease in the general population: changing prevalence and age distribution | Q50182262 | ||
| Turner's syndrome and coronary artery disease. | Q51765413 | ||
| Incidence and Mortality of Adults With Pulmonary Hypertension and Congenital Heart Disease. | Q52588166 | ||
| Coronary events after arterial switch operation for transposition of the great arteries. | Q53918061 | ||
| Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene | Q55671357 | ||
| Pulse oximetry with clinical assessment to screen for congenital heart disease in neonates in China: a prospective study | Q56431330 | ||
| Coarctation of the Aorta and Coronary Artery Disease | Q58665719 | ||
| Mutations in the Sarcomere Gene MYH7 in Ebstein Anomaly | Q61650582 | ||
| Delivery of care for adult patients with congenital heart disease in Europe: results from the Euro Heart Survey. | Q64886282 | ||
| Anatomic variability in coronary arterial distribution with regard to the arterial switch procedure | Q78346369 | ||
| Prevalence of cardiovascular risk factors in adults with congenital heart disease | Q80013819 | ||
| Intracoronary ultrasound assessment late after the arterial switch operation for transposition of the great arteries | Q81864473 | ||
| Cardiac outcomes in young adult survivors of the arterial switch operation for transposition of the great arteries | Q84556891 | ||
| Risk of thromboembolic complications in adult congenital heart disease: A literature review | Q88958842 | ||
| Marfan's syndrome: natural history and long-term follow-up of cardiovascular involvement | Q93515227 | ||
| Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome | Q24291893 | ||
| Mutation in myosin heavy chain 6 causes atrial septal defect | Q24296801 | ||
| α-cardiac actin mutations produce atrial septal defects | Q24298075 | ||
| Mutation in the alpha-cardiac actin gene associated with apical hypertrophic cardiomyopathy, left ventricular non-compaction, and septal defects | Q24316985 | ||
| Meta-analysis of Observational Studies in Epidemiology: A Proposal for Reporting | Q27861077 | ||
| Transvenous pacing leads and systemic thromboemboli in patients with intracardiac shunts: a multicenter study | Q28218015 | ||
| Guidelines for the Management of Spontaneous Intracerebral Hemorrhage: A Guideline for Healthcare Professionals From the American Heart Association/American Stroke Association | Q28262545 | ||
| Mutations in sarcomeric protein genes not only lead to cardiomyopathy but also to congenital cardiovascular malformations | Q33327414 | ||
| Congenital heart disease: the original heart failure syndrome | Q35114340 | ||
| Major adverse cardiovascular events in adult congenital heart disease: a population-based follow-up study from Taiwan | Q35127429 | ||
| Medical and Obstetric Outcomes Among Pregnant Women With Congenital Heart Disease | Q36161526 | ||
| P433 | issue | 10 | |
| P921 | main subject | cardiovascular disease | Q389735 |
| congenital heart disease | Q939364 | ||
| P304 | page(s) | e012030 | |
| P577 | publication date | 2019-05-01 | |
| P1433 | published in | Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease | Q19880670 |
| P1476 | title | Congenital Heart Disease and Risk of Cardiovascular Disease: A Meta-Analysis of Cohort Studies. | |
| P478 | volume | 8 |
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