Larry Wayne Markham

26-A-16543-ACC RIGHT VENTRICULAR MEASURES OF ALL-CAUSE MORTALITY IN DUCHENNE MUSCULAR DYSTROPHY

Jasmine Ragoowansi, Mei HU, Meng Xu, James Slaughter et autres

26-A-9100-ACC DETECTION OF NOVEL PROTEIN BIOMARKERS IN DUCHENNE MUSCULAR DYSTROPHY CARDIOMYOPATHY

Greigory Dimailig, Mark M. Naguib, Bryan Burnette, Jaclyn G. Tamaroff et autres

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26-CCC-17044-ACC FONTAN FAILURE WITH NORMAL HEMODYNAMICS: TAKING THE ROAD LESS TRAVELED

Kyle Saysana, Christopher Baron, Thomas P. Doyle, Michael G. Earing et autres

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Empagliflozin preserves cardiac function and modulates metabolism in a mouse model of Duchenne muscular dystrophy

B. Zeidler, Connor R Thomas, John P Salvas, Areli Jannes S. Javier et autres

Abstract Duchenne muscular dystrophy (DMD) is a fatal genetic disorder characterized by skeletal muscle degeneration and cardiomyopathy without a cure. This study examined the therapeutic potential of the sodium-glucose cotransporter 2 (SGLT2) inhibitor empagliflozin (EMPA) on cardiac function in the dystrophin-deficient mdx …

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Variant burden and severity of cardiomyopathy in patients with DMD-related Duchenne muscular dystrophy

Gabrielle C. Geddes, Stephanie M. Ware, Tae-Hwi Linus Schwantes-An, Marco A. Abreu et autres

BACKGROUND: This study was designed to identify genes for further study as modifiers of the severity of cardiomyopathy in DMD-related Duchenne Muscular Dystrophy (DMD). METHODS: We evaluated genome sequencing results in a well-phenotyped DMD cohort with severe cardiomyopathy against those with less …

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Novel 4D Strain Associates with Mortality in Duchenne Muscular Dystrophy Cardiomyopathy

Kristen George‐Durrett, Jonathan H. Soslow, Marco Aurélio Prado, Conner C. Earl et autres

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Net4DMD: A Deep Learning Framework for 4D CMR Left Ventricle Strain Analysis in Duchenne Muscular Dystrophy

Marco Aurélio Prado, Conner C. Earl, Madison Sullivan, Guang Lin et autres

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Heart Transplantation and Ventricular Assist Device in Duchenne Muscular Dystrophy: A New Era

David N. Rosenthal, A. Amodeo, Russell J. Butterfield, Ryan J. Butts et autres

Duchenne muscular dystrophy (DMD) is an X-linked genetic neuromuscular disorder that is caused by a mutation in the dystrophin gene. The disease is characterized by progressive weakness of skeletal muscle, resulting in loss of ambulation and eventually respiratory insufficiency. Cardiac muscle is …

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Six-Minute Activity-95th Centile, a Novel Wearable-Derived Clinical Outcome Assessment for Duchenne Muscular Dystrophy

Nicholas Joy, Jonathan H. Soslow, William Bryan Burnette, Andrew Liu et autres

The six-minute walk test and quantitative muscle testing are commonly used skeletal muscle assessments in Duchenne muscular dystrophy; however, they present challenges in non-ambulatory patients. Our objective was to evaluate whether six-minute activity- 95 th centile, a novel accelerometry metric capturing a …

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Abstract 4366789: Natural History Nomograms of Duchenne Cardiomyopathy by Cardiac Magnetic Resonance Imaging

Jordan Noble, Larry Wayne Markham, Carol A. Wittlieb‐Weber, Jennifer S.Y. Li et autres

Introduction: Duchenne Muscular Dystrophy (DMD), an X-linked disorder resulting in skeletal and cardiac myopathy, typically leads to death from 20-40 years of age. Cardiac magnetic resonance (CMR) imaging is the gold standard for assessment of cardiac progression. However, it can be difficult …

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Prevalence and Predictors of Neurocognitive Dysfunction in Adults With Congenital Heart Disease

Scott B. Cohen, Michelle Z. Gurvitz, Kristin M. Burns, Olivia A. Wheaton et autres

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Switch to Success: Heart Transplant After the Mustard Operation

Michael J. Wilde, Syed Talal Hussain, Robert K. Darragh, Larry Wayne Markham et autres

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