Evaluating Variation in the Cardiac Management of Children with Hereditary Thoracic Aortic Disease in the United States
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cardiology and Cardiovascular Medicine,Pediatrics, Perinatology and Child Health
Link
https://link.springer.com/content/pdf/10.1007/s00246-023-03305-8.pdf
Reference22 articles.
1. Isselbacher EM, Preventza O, HamiltonBlack J III et al (2022) 2022 ACC/AHA Guideline for the Diagnosis and Management of Aortic Disease: a report of the American Heart Association/American College of Cardiology Joint Committee on Clinical Practice Guidelines. J Am Coll Cardiol 80(24):e223–e393. https://doi.org/10.1016/j.jacc.2022.08.004
2. Shores J, Berger KR, Murphy EA, Pyeritz RE (1994) Progression of aortic dilatation and the benefit of long-term beta-adrenergic blockade in Marfan’s syndrome. N Engl J Med 330(19):1335–1341. https://doi.org/10.1056/NEJM199405123301902
3. Loeys BL, Schwarze U, Holm T et al (2006) Aneurysm syndromes caused by mutations in the TGF-beta receptor. N Engl J Med 355(8):788–798
4. Bergqvist D, Björck M, Wanhainen A (2013) Treatment of vascular Ehlers–Danlos syndrome: a systematic review. Ann Surg 258(2):257–261. https://doi.org/10.1097/SLA.0b013e31829c7a59
5. Tinkle BT, Saal HM (2013) Health supervision for children with Marfan syndrome. Pediatrics 132(4):e1059–e1072. https://doi.org/10.1542/peds.2013-2063
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