For: | Chen SN, Wang YQ, Hao CL, Lu YH, Jiang WJ, Gao CY, Wu M. Multisystem smooth muscle dysfunction syndrome in a Chinese girl: A case report and review of the literature. World J Clin Cases 2019; 7(24): 4355-4365 [PMID: 31911919 DOI: 10.12998/wjcc.v7.i24.4355] |
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URL: | https://www.wjgnet.com/2307-8960/full/v7/i24/4355.htm |
Number | Citing Articles |
1 |
Xiaoyan Zhou, Yan Wang, Binbin Shao, Chen Wang, Ping Hu, Fengchang Qiao, Zhengfeng Xu. Molecular diagnostic in fetuses with isolated congenital anomalies of the kidney and urinary tract by whole‐exome sequencing. Journal of Clinical Laboratory Analysis 2020; 34(11) doi: 10.1002/jcla.23480
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2 |
Nicholas Houska, Michal Schafer, Kathryn C. Chatfield, Timothy J. Bernard, Richard J. Ing. Anesthetic Considerations for Children With Multisystem Smooth Muscle Dysfunction Syndrome and Review of the Literature. Journal of Cardiothoracic and Vascular Anesthesia 2022; 36(8): 3205 doi: 10.1053/j.jvca.2022.04.019
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3 |
Viviana Lupo, Maria Grazia Di Gregorio, Gerarda Mastrogiorgio, Monia Magliozzi, Maria Eleonora Scapillati, Vittorio Maglione, Ester Romanelli, Caterina Alegiani, Cristina Haass, Antonio Novelli. Neonatal diagnosis of ACTA2‐related disease: A case report and review of literature. American Journal of Medical Genetics Part A 2023; 191(4): 1111 doi: 10.1002/ajmg.a.63118
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4 |
Anthony Roylance, Stefan Spinty, Benedetta Pettorini. Communicating hydrocephalus and raised intracranial pressure in association with multi-systemic smooth muscle dysfunction syndrome (MSMDS). Child's Nervous System 2023; 39(3): 825 doi: 10.1007/s00381-022-05703-4
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5 |
Keita Kanamori, Yuri Sakaguchi, Kyoji Tsuda, Satoshi Ihara, Sahoko Miyama. Refractory cerebral infarction in a child with an ACTA2 mutation. Brain and Development 2021; 43(4): 585 doi: 10.1016/j.braindev.2020.12.001
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6 |
Rachel H. Ceron, Faviolla A. Báez-Cruz, Nicholas J. Palmer, Peter J. Carman, Malgorzata Boczkowska, Robert O. Heuckeroth, E. Michael Ostap, Roberto Dominguez. Molecular mechanisms linking missense ACTG2 mutations to visceral myopathy. Science Advances 2024; 10(22) doi: 10.1126/sciadv.adn6615
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7 |
Wen-Xian Yang, Hang-Hu Zhang, Jia-Ni Hu, Li Zhao, Yan-Yun Li, Xiao-Li Shao. <i>ACTA2</i> mutation is responsible for multisystemic smooth muscle dysfunction syndrome with seizures: A case report and review of literature. World Journal of Clinical Cases 2021; 9(29): 8789-8796 doi: 10.12998/wjcc.v9.i29.8789
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