Cardiomyopathy, an uncommon phenotype of congenital disorders of glycosylation: Recommendations for baseline screening and follow-up evaluation von Zemet, Roni, Hope, Kyle D., Edmondson, Andrew C., Shah, Rameen, Patino, Maria, Yesso, Abigail M., Berger, Justin H., Sarafoglou, Kyriakie, Larson, Austin, Lam, Christina, Morava, Eva, Scaglia, Fernando

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International Consensus on Differential Diagnosis and Management of Patients With Danon Disease von Hong, Kimberly N., Eshraghian, Emily A., Arad, Michael, Argirò, Alessia, Brambatti, Michela, Bui, Quan, Caspi, Oren, de Frutos, Fernando, Greenberg, Barry, Ho, Carolyn Y., Kaski, Juan Pablo, Olivotto, Iacopo, Taylor, Matthew R.G., Yesso, Abigail, Garcia-Pavia, Pablo, Adler, Eric D.

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International Consensus on Differential Diagnosis and Management of Patients With Danon Disease: JACC State-of-the-Art Review von Hong, Kimberly N, Eshraghian, Emily A, Arad, Michael, Argirò, Alessia, Brambatti, Michela, Bui, Quan, Caspi, Oren, de Frutos, Fernando, Greenberg, Barry, Ho, Carolyn Y, Kaski, Juan Pablo, Olivotto, Iacopo, Taylor, Matthew R G, Yesso, Abigail, Garcia-Pavia, Pablo, Adler, Eric D

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Arrhythmogenic cardiomyopathy is under‐recognized in end‐stage pediatric heart failure: A 36‐year single‐center experience von Tadros, Hanna J., Choudhry, Swati, Kearney, Debra L., Hope, Kyle, Yesso, Abigail, Miyake, Christina Y., Price, Jack, Spinner, Joseph, Tunuguntla, Hari, Puri, Kriti, Dreyer, William, Denfield, Susan W.

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