| For: | Cao LX, Liu Y, Song ZJ, Zhang BR, Long WY, Zhao GH. Compound heterozygous mutations in the neuraminidase 1 gene in type 1 sialidosis: A case report and review of literature. World J Clin Cases 2021; 9(3): 623-631 [PMID: 33553400 DOI: 10.12998/wjcc.v9.i3.623] |
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| URL: | https://www.wjgnet.com/2307-8960/full/v9/i3/623.htm |
| Number | Citing Articles |
| 1 |
Yuan Ding, Ming Cheng, Chunxiu Gong. Two cases of type I sialidosis and a literature review. Orphanet Journal of Rare Diseases 2024; 19(1) doi: 10.1186/s13023-024-03431-3
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| 2 |
Mei-Ling Peng, Siu-Fung Chau, Jia-Ying Chien, Peng-Yeong Woon, Yu-Chen Chen, Wai-Man Cheang, Hsien-Yang Tsai, Shun-Ping Huang. Genetic Insights and Clinical Implications of NEU1 Mutations in Sialidosis. Genes 2025; 16(2): 151 doi: 10.3390/genes16020151
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| 3 |
Janina Gburek‐Augustat, I‐Chun Lee, Marica Rubino, Vehap Topçu, Melissa Chavez‐Castillo, Shao Ching Tu, Marwan Shinawi, Isabel Alfradique‐Dunham, Manouela Valtcheva, Astrid Adarmes‐Gómez, Daniel Macias‐Garcia, Laura Laura Muñoz‐Delgado, Silvia Jesús, Pablo Mir, Andreas Merkenschlager, Antonietta Coppola. Sialidosis type I: How to alleviate disabling myoclonic seizures?—A multicenter analysis of eight cases and review of the literature. Epilepsia Open 2026; 11(2): 577 doi: 10.1002/epi4.70233
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| 4 |
Mustafa Kılıç, Suzan İcil, Abdullah Sezer, Öznur Kaya-Güneş, Selim S. Comoğlu. Sialidosis type 1 in a Turkish family: a case report and review of literatures. Journal of Pediatric Endocrinology and Metabolism 2025; 38(2): 176 doi: 10.1515/jpem-2024-0468
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