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For: Cade WT, Laforest R, Bohnert KL, Reeds DN, Bittel AJ, de Las Fuentes L, Bashir A, Woodard PK, Pacak CA, Byrne BJ, Gropler RJ, Peterson LR. Myocardial glucose and fatty acid metabolism is altered and associated with lower cardiac function in young adults with Barth syndrome. J Nucl Cardiol 2021;28:1649-59. [PMID: 31705425 DOI: 10.1007/s12350-019-01933-3] [Cited by in Crossref: 8] [Cited by in F6Publishing: 7] [Article Influence: 2.7] [Reference Citation Analysis]
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2 Kumar TR, Reusch JEB, Kohrt WM, Regensteiner JG. Sex Differences Across the Lifespan: A Focus on Cardiometabolism. J Womens Health (Larchmt) 2020;29:899-909. [PMID: 32423340 DOI: 10.1089/jwh.2020.8408] [Reference Citation Analysis]
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4 Greenwell AA, Gopal K, Altamimi TR, Saed CT, Wang F, Tabatabaei Dakhili SA, Ho KL, Zhang L, Eaton F, Kruger J, Al Batran R, Lopaschuk GD, Oudit GY, Ussher JR. Barth syndrome-related cardiomyopathy is associated with a reduction in myocardial glucose oxidation. Am J Physiol Heart Circ Physiol 2021;320:H2255-69. [PMID: 33929899 DOI: 10.1152/ajpheart.00873.2020] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
5 Greenwell AA, Gopal K, Ussher JR. Myocardial Energy Metabolism in Non-ischemic Cardiomyopathy. Front Physiol 2020;11:570421. [PMID: 33041869 DOI: 10.3389/fphys.2020.570421] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
6 Wasmus C, Dudek J. Metabolic Alterations Caused by Defective Cardiolipin Remodeling in Inherited Cardiomyopathies. Life (Basel) 2020;10:E277. [PMID: 33187128 DOI: 10.3390/life10110277] [Cited by in Crossref: 4] [Cited by in F6Publishing: 6] [Article Influence: 2.0] [Reference Citation Analysis]
7 Chatfield KC, Sparagna GC, Specht KS, Whitcomb LA, Omar AK, Miyamoto SD, Wolfe LM, Chicco AJ. Long-chain fatty acid oxidation and respiratory complex I deficiencies distinguish Barth Syndrome from idiopathic pediatric cardiomyopathy. J Inherit Metab Dis 2021. [PMID: 34821394 DOI: 10.1002/jimd.12459] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
8 Bohnert KL, Ditzenberger G, Bittel AJ, de Las Fuentes L, Corti M, Pacak CA, Taylor C, Byrne BJ, Reeds DN, Cade WT. Resistance exercise training with protein supplementation improves skeletal muscle strength and improves quality of life in late adolescents and young adults with Barth syndrome: A pilot study. JIMD Rep 2021;62:74-84. [PMID: 34765401 DOI: 10.1002/jmd2.12244] [Reference Citation Analysis]
9 Thompson R, Jefferies J, Wang S, Pu WT, Takemoto C, Hornby B, Heyman A, Chin MT, Vernon HJ. Current and future treatment approaches for Barth syndrome. J Inherit Metab Dis 2021. [PMID: 34713454 DOI: 10.1002/jimd.12453] [Reference Citation Analysis]
10 Mason C, Gimblet GR, Lapi SE, Lewis JS. Novel Tracers and Radionuclides in PET Imaging. Radiol Clin North Am 2021;59:887-918. [PMID: 34392925 DOI: 10.1016/j.rcl.2021.05.012] [Reference Citation Analysis]
11 Cade WT, Bohnert KL, Bittel AJ, Chacko SJ, Patterson BW, Pacak CA, Byrne BJ, Vernon HJ, Reeds DN. Arginine kinetics are altered in a pilot sample of adolescents and young adults with Barth syndrome. Mol Genet Metab Rep 2020;25:100675. [PMID: 33204638 DOI: 10.1016/j.ymgmr.2020.100675] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
12 Brunken RC. Mitochondrial dysfunction in heart failure. Lessons from a hereditary mitochondrial disease. J Nucl Cardiol 2021;28:1660-3. [PMID: 31845308 DOI: 10.1007/s12350-019-01980-w] [Reference Citation Analysis]