| For: | Xu HJ, Wen GD. Mixed porokeratosis with a novel mevalonate kinase gene mutation: A case report. World J Clin Cases 2022; 10(14): 4528-4534 [PMID: 35663074 DOI: 10.12998/wjcc.v10.i14.4528] |
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| URL: | https://www.wjgnet.com/2307-8960/full/v10/i14/4528.htm |
| Number | Citing Articles |
| 1 |
Qin Mei, Fengling Xing, Yue Yin, Chengda Yuan. Case Report: A Novel MVK Missense Mutation in the Sporadic Porokeratosis Ptychotropica in China. Clinical, Cosmetic and Investigational Dermatology 2023; doi: 10.2147/CCID.S408016
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| 2 |
Paweł Pietkiewicz, Katarzyna Korecka, Natalia Salwowska, Ihor Kohut, Adarsha Adhikari, Monika Bowszyc-Dmochowska, Anna Pogorzelska-Antkowiak, Cristian Navarrete-Dechent. Porokeratoses—A Comprehensive Review on the Genetics and Metabolomics, Imaging Methods and Management of Common Clinical Variants. Metabolites 2023; 13(12) doi: 10.3390/metabo13121176
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| 3 |
Yifan Yang, Jingwen Zhang, Shengru Zhou, Qicai Chen, Yihe Wang, Yuan Meng, Yuyang Gu, Zijing Ji, Xiaohui Zhang, Xuejun Zhang, Min Li. Germline and somatic second-hit changes in porokeratosis: comprehensive variant spectrum and genotype–phenotype correlation analysis. British Journal of Dermatology 2026; 194(3) doi: 10.1093/bjd/ljaf461
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| 4 |
Xiuping Wang, Xiaoliang Ouyang, Deng Zhang, Yunxia Zhu, Liang Wu, Zhen Xiao, Simin Yu, Wei Li, Chunming Li. Two Novel and Three Recurrent Mutations in the Mevalonate Pathway Genes in Chinese Patients with Porokeratosis. Clinical, Cosmetic and Investigational Dermatology 2024; doi: 10.2147/CCID.S444985
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| 5 |
Y. Jin, T. Wu, X. Xuan, J. Cao, S. Chen, C. Huang. Porokeratosis ptychotropica: Case reports and literature review. Annales de Dermatologie et de Vénéréologie 2025; 152(1) doi: 10.1016/j.annder.2024.103327
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| 6 |
Shuqin Lai, Wenjie Zhu, Chunli Lin, Zimeng Guo, Shiqi Chen, Lang Xie, Jie Liu, Zhaolin Zeng, Cong You, Longnian Li. Transcriptomic and proteomic analysis of MVK variant sites in two subtypes of porokeratosis. Journal of Applied Genetics 2026; doi: 10.1007/s13353-026-01076-5
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