| For: | Kobayashi S, Utsumi K, Tateno M, Iwamoto T, Murayama T, Sohma H, Ukai W, Hashimoto E, Kawanishi C. Longitudinal observation of ten family members with idiopathic basal ganglia calcification: A case report. World J Clin Cases 2019; 7(12): 1483-1491 [PMID: 31363477 DOI: 10.12998/wjcc.v7.i12.1483] |
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| URL: | https://www.wjgnet.com/2307-8960/full/v7/i12/1483.htm |
| Number | Citing Articles |
| 1 |
Moftah Alhagamhmad Sufrani. First case of Fahr’s disease with homozygous mutations of SLC20A2, among the Libyan children. BMC Pediatrics 2026; doi: 10.1186/s12887-026-06524-z
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| 2 |
Dehao Yang, Honghao Huang, Tian Zeng, Lebo Wang, Chenxin Ying, Xinhui Chen, Xinbo Zhou, Fangyue Sun, Yilin Chen, Shengqi Li, Bo Wang, Sheng Wu, Fei Xie, Zhidong Cen, Wei Luo. Unveiling distinct clinical manifestations of primary familial brain calcifications in Asian and European patients: A study based on 10-year individual-level data. Parkinsonism & Related Disorders 2025; 132: 107290 doi: 10.1016/j.parkreldis.2025.107290
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