For: | Yang WX, Zhang HH, Hu JN, Zhao L, Li YY, Shao XL. ACTA2 mutation is responsible for multisystemic smooth muscle dysfunction syndrome with seizures: A case report and review of literature. World J Clin Cases 2021; 9(29): 8789-8796 [PMID: 34734057 DOI: 10.12998/wjcc.v9.i29.8789] |
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URL: | https://www.wjgnet.com/2307-8960/full/v9/i29/8789.htm |
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1 |
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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2 |
Jessica Zucco, Federica Baldan, Lorenzo Allegri, Elisa Bregant, Nadia Passon, Alessandra Franzoni, Angela Valentina D’Elia, Flavio Faletra, Giuseppe Damante, Catia Mio. A bird’s eye view on the use of whole exome sequencing in rare congenital ophthalmic diseases. Journal of Human Genetics 2024; 69(6): 271 doi: 10.1038/s10038-024-01237-6
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3 |
David Andrew Prentice, Tejinder Singh, Paul Maria Parizel. Clinical and neuroimaging features of a familial pathogenic ACTA2 variant as a model of a vascular neurocristopathy. Neuroradiology 2022; 64(9): 1773 doi: 10.1007/s00234-022-02945-6
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4 |
Qianjia Wu, Yang Yang, Chongze Lin.
Exploration of Diagnostic Markers Associated with Inflammation in Chronic Kidney Disease Based on WGCNA and Machine Learning
. Critical Reviews in Immunology 2024; 44(5): 15 doi: 10.1615/CritRevImmunol.2024051277
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