Cardiomyopathy, Dilated

Displaying 1 - 8 of 8CSV
Wang, B. Z., Morsink, M. A. J., Kim, S. W., Luo, L. J., Zhang, X., Soni, R. K., Lock, R. I., Rao, J., Kim, Y., Zhang, A., Neyazi, M., Gorham, J. M., Kim, Y., Brown, K., DeLaughter, D. M., Zhang, Q., McDonough, B., Watkins, J. M., Cunningham, K. M., … Vunjak-Novakovic, G. (2025). Cardiac fibroblast BAG3 regulates TGFBR2 signaling and fibrosis in dilated cardiomyopathy. Journal of Clinical Investigation, 135(1). https://doi.org/10.1172/jci181630
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Kantor, P. F., Shi, L., Colan, S. D., Orav, E. J., Wilkinson, J. D., Hamza, T. H., Webber, S. A., Canter, C. E., Towbin, J. A., Everitt, M. D., Pahl, E., Ware, S. M., Rusconi, P. G., Lamour, J. M., Jefferies, J. L., Addonizio, L. J., & Lipshultz, S. E. (2024). Progressive Left Ventricular Remodeling for Predicting Mortality in Children With Dilated Cardiomyopathy: The Pediatric Cardiomyopathy Registry. Journal of the American Heart Association, 13(2). https://doi.org/10.1161/jaha.121.022557
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Souidi, M., Resta, J., Dridi, H., Sleiman, Y., Reiken, S., Formoso, K., Colombani, S., Amédro, P., Meyer, P., Charrabi, A., Vincenti, M., Liu, Y., Soni, R. K., Lezoualc’h, F., Stéphane Blot, D. V. M., Rivier, F., Cazorla, O., Parini, A., Marks, A. R., … Meli, A. C. (2024). Ryanodine receptor dysfunction causes senescence and fibrosis in Duchenne dilated cardiomyopathy. Journal of Cachexia, Sarcopenia and Muscle, 15(2), 536–551. Portico. https://doi.org/10.1002/jcsm.13411
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Kwiatkowski, D. M., Shezad, M., Barnes, A. P., Ploutz, M. S., Law, S. P., Zafar, F., Morales, D. L. S., & O’Connor, M. J. (2023). Impact of Weight on Ventricular Assist Device Outcomes in Dilated Cardiomyopathy Patients in Pediatric Centers: An ACTION Registry Study. ASAIO Journal, 69(5), 496–503. https://doi.org/10.1097/mat.0000000000001861
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Abrams, M., Magun, E., & DeFilippis, E. M. (2023). Considerations for specific cardiomyopathies during pregnancy. Current Opinion in Cardiology, 38(3), 233–240. https://doi.org/10.1097/hco.0000000000001033
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Xie, Z., Sun, C., Liu, C., Xie, Z., Wei, L., Yu, J., Ling, C., Guo, X., Liu, Y., Yu, M., Leng, Y., Meng, L., Sun, Y., Deng, J., Leal, S. M., Schrauwen, I., Wang, Z., & Yuan, Y. (2022). Clinical, muscle imaging, and genetic characteristics of dystrophinopathies with deep-intronic DMD variants. Journal of Neurology, 270(2), 925–937. https://doi.org/10.1007/s00415-022-11432-0
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Ware, S. M., Bhatnagar, S., Dexheimer, P. J., Wilkinson, J. D., Sridhar, A., Fan, X., Shen, Y., Tariq, M., Schubert, J. A., Colan, S. D., Shi, L., Canter, C. E., Hsu, D. T., Bansal, N., Webber, S. A., Everitt, M. D., Kantor, P. F., Rossano, J. W., Pahl, E., … Lipshultz, S. E. (2022). The genetic architecture of pediatric cardiomyopathy. The American Journal of Human Genetics, 109(2), 282–298. https://doi.org/10.1016/j.ajhg.2021.12.006
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