Tan D - Search Results

1

The serum IgG antibody level as a biomarker for clinical outcome in patients with cerebral sparganosis after treatment.

Xiang H, Wang J, Tan D, Xiong Y, Huang P, Shen Y, Xu Y, Gong Z, Hu F, Xu C, Wu J, Liu W, Liu J, Wan H, Hong D, Xie H. Xiang H, et al. Among authors: tan d. Front Immunol. 2023 Mar 27;14:1158635. doi: 10.3389/fimmu.2023.1158635. eCollection 2023. Front Immunol. 2023. PMID: 37051247 Free PMC article.

2

Variants in MME are associated with autosomal-recessive distal hereditary motor neuropathy.

Hong D, Fang P, Yao S, Chen J, Zhang X, Chen S, Zhang J, Tan D, Wang L, Han X, Xin L, Wang Y, Liu M, Cong L, Zhong S, Ouyang H, Gao X, Zhang J. Hong D, et al. Among authors: tan d. Ann Clin Transl Neurol. 2019 Sep;6(9):1728-1738. doi: 10.1002/acn3.50868. Epub 2019 Aug 20. Ann Clin Transl Neurol. 2019. PMID: 31429185 Free PMC article.

3

Skin biopsy and neuronal intranuclear inclusion disease.

Ren X, Tan D, Deng J, Wang Z, Hong D. Ren X, et al. Among authors: tan d. J Dermatol. 2023 Nov;50(11):1367-1372. doi: 10.1111/1346-8138.16966. Epub 2023 Sep 18. J Dermatol. 2023. PMID: 37718652 Review.

4

Homozygous variant in COQ7 causes autosomal recessive hereditary spastic paraplegia.

Qiu Y, Xiong Y, Wang L, Zhu M, Tan D, Hong D. Qiu Y, et al. Among authors: tan d. Ann Clin Transl Neurol. 2024 Apr;11(4):1067-1074. doi: 10.1002/acn3.52037. Epub 2024 Mar 4. Ann Clin Transl Neurol. 2024. PMID: 38439593 Free PMC article.

5

Encephalitis-like episodes with cortical edema and enhancement in patients with neuronal intranuclear inclusion disease.

Shen Y, Jiang K, Liang H, Xiong Y, Song Z, Wang B, Zhu M, Qiu Y, Tan D, Wu C, Deng J, Wang Z, Hong D. Shen Y, et al. Among authors: tan d. Neurol Sci. 2024 Mar 26. doi: 10.1007/s10072-024-07492-x. Online ahead of print. Neurol Sci. 2024. PMID: 38532189

6

CAG Repeat Expansion in THAP11 Is Associated with a Novel Spinocerebellar Ataxia.

Tan D, Wei C, Chen Z, Huang Y, Deng J, Li J, Liu Y, Bao X, Xu J, Hu Z, Wang S, Fan Y, Jiang Y, Wu Y, Wu Y, Wang S, Liu P, Zhang Y, Yang Z, Jiang Y, Zhang H, Hong D, Zhong N, Jiang H, Xiong H. Tan D, et al. Mov Disord. 2023 Jul;38(7):1282-1293. doi: 10.1002/mds.29412. Epub 2023 May 6. Mov Disord. 2023. PMID: 37148549

7

Phenotype and Genotype Study of Chinese POMT2-Related α-Dystroglycanopathy.

Chen XY, Song DY, Jiang L, Tan DD, Liu YD, Liu JY, Chang XZ, Xing GG, Toda T, Xiong H. Chen XY, et al. Front Genet. 2021 Aug 3;12:692479. doi: 10.3389/fgene.2021.692479. eCollection 2021. Front Genet. 2021. PMID: 34413876 Free PMC article.

8

Unique genotype-phenotype correlations within LAMA2-related limb girdle muscular dystrophy in Chinese patients.

Huang X, Tan D, Zhang Z, Ge L, Liu J, Ding J, Yang H, Wei C, Chang X, Yuan Y, Yan C, Xiong H. Huang X, et al. Among authors: tan d. Front Neurol. 2023 May 3;14:1158094. doi: 10.3389/fneur.2023.1158094. eCollection 2023. Front Neurol. 2023. PMID: 37206914 Free PMC article.

9

Genotype/phenotype analysis in Chinese laminin-α2 deficient congenital muscular dystrophy patients.

Xiong H, Tan D, Wang S, Song S, Yang H, Gao K, Liu A, Jiao H, Mao B, Ding J, Chang X, Wang J, Wu Y, Yuan Y, Jiang Y, Zhang F, Wu H, Wu X. Xiong H, et al. Among authors: tan d. Clin Genet. 2015 Mar;87(3):233-43. doi: 10.1111/cge.12366. Epub 2014 Mar 31. Clin Genet. 2015. PMID: 24611677

10

[Clinical and genetic characteristics of 9 rare cases with coexistence of dual genetic diagnoses].

Tan DD, Liu YD, Fan YB, Wei CJ, Song DY, Yang HP, Pan H, Cui WL, Mao SS, Xu XP, Yu XL, Cui B, Xiong H. Tan DD, et al. Zhonghua Er Ke Za Zhi. 2023 Apr 2;61(4):345-350. doi: 10.3760/cma.j.cn112140-20220922-00827. Zhonghua Er Ke Za Zhi. 2023. PMID: 37011981 Chinese.

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