Left Atrial Phasic Function via Cardiac Magnetic Resonance Imaging in Patients with Duchenne Muscular Dystrophy
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/s00246-023-03327-2.pdf
Reference25 articles.
1. Muntoni F, Torelli S, Ferlini A (2003) Dystrophin and mutations: one gene, several proteins, multiple phenotypes. Lancet Neurol 2(12):731–740. https://doi.org/10.1016/s1474-4422(03)00585-4
2. Centers for Disease C, Prevention, (2009) Prevalence of Duchenne/Becker muscular dystrophy among males aged 5–24 years—four states, 2007. MMWR Morb Mortal Wkly Rep 58(40):1119–1122
3. Eagle M, Baudouin SV, Chandler C, Giddings DR, Bullock R, Bushby K (2002) Survival in Duchenne muscular dystrophy: improvements in life expectancy since 1967 and the impact of home nocturnal ventilation. Neuromuscul Disord 12(10):926–929. https://doi.org/10.1016/s0960-8966(02)00140-2
4. Connuck DM, Sleeper LA, Colan SD et al (2008) Characteristics and outcomes of cardiomyopathy in children with duchenne or becker muscular dystrophy: a comparative study from the pediatric cardiomyopathy registry. Am Heart J 155(6):998–1005. https://doi.org/10.1016/j.ahj.2008.01.018
5. Power A, Poonja S, Disler D et al (2017) Echocardiographic image quality deteriorates with age in children and young adults with duchenne muscular dystrophy. Front Cardiovasc Med 4:82. https://doi.org/10.3389/fcvm.2017.00082
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