Management of cardiac involvement associated with neuromuscular diseases: a scientific statement from the American Heart Association

B Feingold, WT Mahle, S Auerbach, P Clemens… - Circulation, 2017 - Am Heart Assoc
For many neuromuscular diseases (NMDs), cardiac disease represents a major cause of
morbidity and mortality. The management of cardiac disease in NMDs is made challenging …

[HTML][HTML] Atenolol versus losartan in children and young adults with Marfan's syndrome

RV Lacro, HC Dietz, LA Sleeper… - … England Journal of …, 2014 - Mass Medical Soc
Background Aortic-root dissection is the leading cause of death in Marfan's syndrome.
Studies suggest that with regard to slowing aortic-root enlargement, losartan may be more …

Contemporary cardiac issues in Duchenne muscular dystrophy

EM McNally, JR Kaltman, DW Benson, CE Canter… - Circulation, 2015 - Am Heart Assoc
Muscular Dystrophy, convened a Working Group meeting on July 2014, in Bethesda, MD, to
explore clinical and research questions related to cardiac disease in patients with DMD. As …

Management of Kawasaki disease in adults

KJ Denby, DE Clark, LW Markham - Heart, 2017 - heart.bmj.com
Kawasaki disease is the most common childhood vasculitis in the USA and the most
common cause of acquired cardiac disease in children in developed countries. Since the …

Circumferential strain analysis identifies strata of cardiomyopathy in Duchenne muscular dystrophy: a cardiac magnetic resonance tagging study

KN Hor, J Wansapura, LW Markham, W Mazur… - Journal of the American …, 2009 - jacc.org
Objectives: This study sought to evaluate the natural history of occult cardiac dysfunction in
Duchenne muscular dystrophy (DMD). Background: Duchenne muscular dystrophy is …

Corticosteroid treatment retards development of ventricular dysfunction in Duchenne muscular dystrophy

LW Markham, K Kinnett, BL Wong, DW Benson… - Neuromuscular …, 2008 - Elsevier
Duchenne muscular dystrophy (DMD) is characterized by a predictable decline in cardiac
function with age that contributes to early death. Although corticosteroids are a clinically …

[HTML][HTML] Loss-of-function mutations in the X-linked biglycan gene cause a severe syndromic form of thoracic aortic aneurysms and dissections

JAN Meester, G Vandeweyer, I Pintelon… - Genetics in …, 2017 - nature.com
Purpose: Thoracic aortic aneurysm and dissection (TAAD) is typically inherited in an
autosomal dominant manner, but rare X-linked families have been described. So far, the …

[HTML][HTML] Increased myocardial native T1 and extracellular volume in patients with Duchenne muscular dystrophy

JH Soslow, SM Damon, K Crum, MA Lawson… - Journal of …, 2015 - Springer
Background Duchenne muscular dystrophy (DMD) cardiomyopathy is a progressive disease
for which there is no cure. Disease-specific therapies are needed that can be initiated before …

Current state of cardiac troponin testing in Duchenne muscular dystrophy cardiomyopathy: review and recommendations from the Parent Project Muscular Dystrophy …

CF Spurney, D Ascheim, L Charnas, L Cripe, K Hor… - Open …, 2021 - openheart.bmj.com
Cardiac disease is now the leading cause of death in Duchenne muscular dystrophy (DMD).
Clinical evaluations over time have demonstrated asymptomatic cardiac troponin elevations …

Correlation of heart rate and cardiac dysfunction in Duchenne muscular dystrophy

TO Thomas, TM Morgan, WB Burnette, LW Markham - Pediatric cardiology, 2012 - Springer
Sinus tachycardia is common in cases of Duchenne muscular dystrophy (DMD). The authors
hypothesized that an elevated heart rate would herald cardiomyopathy onset. A …