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Cardiology in the Young is a peer-reviewed journal published by Cambridge University Press, covering Congenital Heart Disease Studies, Coronary Artery Anomalies, Cardiac Structural Anomalies and Repair.
| Publisher | Cambridge University Press |
|---|---|
| Reference style | Numbered Numbered — [1], [2] in the text [1] A. Smith, B. Jones, and C. Lee, A representative article title, Cardiology in the Young 12 (2023) 45–58.
Formats any DOI in the closest standard style — Cardiology in the Young has no published style definition, so this is an approximation. No sign-up. |
| Publishes research in | Congenital Heart Disease Studies Coronary Artery Anomalies Cardiac Structural Anomalies and Repair Cardiac Arrhythmias and Treatments Cardiac Valve Diseases and Treatments |
| ISSN | 1047-9511 |
| Citation impact (2-yr) | 0.73 |
| h-index | 80 |
| i10-index | 2,127 |
| Total citations | 72,706 |
| Top institutions publishing here | Children's Hospital of Philadelphia |
| Journal website | journals.cambridge.org |
| You get | A submission-ready PDF and the editable LaTeX source — ready to submit. |
Citations each year’s papers have accumulated so far — the most recent years are still building up.
In 2000, The International Nomenclature Committee for Pediatric and Congenital Heart Disease was established. This committee eventually evolved into the International Society for Nomenclature of Paediatric and Congenital Heart Disease. The working component of this international nomenclature society has been The International Working Group for Mapping and Coding of Nomenclatures for Paediatric and Congenital Heart…
Over a decade ago, I co-authored a review in Cardiology in the Young regarding neurological outcomes following surgery for congenital cardiac disease. 1 In that review, I placed much emphasis on the conduct of cardiopulmonary bypass, and its role in neurodevelopmental disabilities. Much has been learned in the intervening years regarding the multifactorial causes of…
BACKGROUND: Women with Turner's syndrome have an increased risk of congenital cardiac malformations, ischaemic heart disease, hypertension and stroke. Aortic dissection seems to occur with increased frequency. AIM: To describe in more detail aortic dissection as encountered in Turner's syndrome, giving attention to clinical, histological and epidemiological aspects. MATERIALS AND METHODS: Based on a retrospective…
Normalization of the dimensions of cardiac structures to the size of the body, using so-called Z scores, is becoming increasingly common in the management of infants and children with congenital heart disease. Current published nomograms for the ascertainment of Z scores for cardiac structures in childhood are based largely on normal data obtained in formalin-fixed…
To judge whether an Amplatzer Septal Occluder can be used as standard therapy instead of surgery for closure of atrial septal defects we report our experiences in 200 patients. Of these patients, 127 had an atrial septal defect with haemodynamically significant left-to-right shunt, 68 patients a persistent oval foramen after presumed paradoxical embolism, and 5…
