| For: | Wang Q, Hu F. Nemaline myopathy with dilated cardiomyopathy and severe heart failure: A case report. World J Clin Cases 2021; 9(11): 2569-2575 [PMID: 33889622 DOI: 10.12998/wjcc.v9.i11.2569] |
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| URL: | https://www.wjgnet.com/2307-8960/full/v9/i11/2569.htm |
| Number | Citing Articles |
| 1 |
Jucier Gonçalves Júnior, Samuel Katsuyuki Shinjo. Rituximab as a treatment for human immunodeficiency virus-associated nemaline myopathy: What does the literature have to tell us?. World Journal of Clinical Cases 2022; 10(4): 1454-1456 doi: 10.12998/wjcc.v10.i4.1454
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| 2 |
Guangyu Wang, Guiguan Yang, Yaru Wang, Chuanzhu Yan, Pengfei Lin. Activation of cryptic donor splice site due to an exonic MYPN variant in congenital myopathy. Journal of Human Genetics 2026; doi: 10.1038/s10038-026-01488-5
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| 3 |
E. S. Vasichkina, T. L. Vershinina, A. A. Morozov, P. A. Fedotov, T. S. Kovalchuk, D. Yu. Alekseeva, E. V. Grekhov, T. M. Pervunina. A clinical case of a combination of Ebstein’s anomaly and genetically determined cardiomyopathy in a child who required a heart transplantation in childhood. Russian Journal for Personalized Medicine 2023; 3(2) doi: 10.18705/2782-3806-2023-3-2139-147
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| 4 |
Lixin Chen, Jianbin Li, Mintai Gao, Danjun Zhu, Ruiyu Li, Ganghua Yang. Transesophageal echocardiography-guided anesthetic management of a patient with dilated cardiomyopathy, severe heart failure, and septic shock: a case report. Frontiers in Medicine 2026; 13 doi: 10.3389/fmed.2026.1853263
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| 5 |
Marion Onnée, Edoardo Malfatti. The widening genetic and myopathologic spectrum of congenital myopathies (CMYOs): a narrative review. Neuromuscular Disorders 2025; 49 doi: 10.1016/j.nmd.2025.105338
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