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Year Number of Results
2009 2
2011 2
2012 4
2013 4
2014 2
2015 4
2016 4
2017 3
2018 5
2019 6
2020 7
2021 18
2022 15
2023 17
2024 5

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89 results

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Page 1
Genetic spectrum of renal disease for 1001 Chinese children based on a multicenter registration system.
Rao J, Liu X, Mao J, Tang X, Shen Q, Li G, Sun L, Bi Y, Wang X, Qian Y, Wu B, Wang H, Zhou W, Ma D, Zheng B, Shen Y, Chen Z, Luan J, Wang X, Wang M, Dang X, Wang Y, Wu Y, Hou L, Sun S, Li Q, Liu X, Bai H, Yang Y, Shao X, Li Y, Zheng S, Han M, Liu C, Cao G, Zhao L, Qiu S, Dong Y, Zhu Y, Wang F, Zhang D, Li Y, Zhao L, Yang C, Luo X, Chen L, Jiang X, Zhang A, Xu H; for “Internet Plus” Nephrology Alliance of National Center for Children's Care. Rao J, et al. Among authors: chen l. Clin Genet. 2019 Nov;96(5):402-410. doi: 10.1111/cge.13606. Epub 2019 Jul 25. Clin Genet. 2019. PMID: 31328266
Reply: UNC13B and focal epilepsy.
Qiao JD, Li X, Li J, Guo QH, Tang XQ, Chen LZ, Su T, Yi YH, Wang J, Liao WP. Qiao JD, et al. Brain. 2022 Apr 29;145(3):e13-e16. doi: 10.1093/brain/awab486. Brain. 2022. PMID: 35380625 No abstract available.
Heterozygous variants in USP25 cause genetic generalized epilepsy.
Fan CX, Liu XR, Mei DQ, Li BM, Li WB, Xie HC, Wang J, Shen NX, Ye ZL, You QL, Li LY, Qu XC, Chen LZ, Liang JJ, Zhang MR, He N, Li J, Gao JY, Deng WY, Liu WZ, Wang WT, Liao WP, Chen Q, Shi YW. Fan CX, et al. Brain. 2024 Jun 14:awae191. doi: 10.1093/brain/awae191. Online ahead of print. Brain. 2024. PMID: 38875478
Risk factors for renal outcomes in children with antineutrophil cytoplasmic antibody-associated vasculitis: a nationwide retrospective study in China.
Tan LW, Wan JL, Zhu CH, Xu H, Xia ZK, Chen LZ, Wu XC, Wang F, Liu XR, Zhao CG, Li XZ, Mao JH, Wang XW, Huang WY, Li YH, Zhang JJ, Feng SP, Yang J, Liu JJ, Gao CL, Rong LP, Shuai LJ, Xu K, Zhang HJ, Li Q, Zhang AH, Wang M. Tan LW, et al. World J Pediatr. 2024 May;20(5):506-516. doi: 10.1007/s12519-023-00753-3. Epub 2023 Oct 19. World J Pediatr. 2024. PMID: 37853276 Free PMC article.
89 results