Tan D - Search Results

1

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.

2

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

3

Phenotype-Genotype Analysis of Chinese Patients with Early-Onset LMNA-Related Muscular Dystrophy.

Tan D, Yang H, Yuan Y, Bonnemann C, Chang X, Wang S, Wu Y, Wu X, Xiong H. Tan D, et al. PLoS One. 2015 Jun 22;10(6):e0129699. doi: 10.1371/journal.pone.0129699. eCollection 2015. PLoS One. 2015. PMID: 26098624 Free PMC article.

4

[Correlation between thigh muscle magnetic resonance imaging findings and clinical features of congenital muscular dystrophies: a preliminary study].

Wang LL, Du J, Fu XN, Fan YB, Wei CJ, Ding J, Tan DD, Xiao JX, Xiong H. Wang LL, et al. Among authors: tan dd. Zhonghua Er Ke Za Zhi. 2016 Oct 2;54(10):756-760. doi: 10.3760/cma.j.issn.0578-1310.2016.10.009. Zhonghua Er Ke Za Zhi. 2016. PMID: 27784478 Chinese.

5

Deletion of exon 4 in LAMA2 is the most frequent mutation in Chinese patients with laminin α2-related muscular dystrophy.

Ge L, Liu A, Gao K, Du R, Ding J, Mao B, Hua Y, Zhang X, Tan D, Yang H, Fu X, Fan Y, Zhang L, Song S, Wu J, Zhang F, Jiang Y, Wu X, Xiong H. Ge L, et al. Among authors: tan d. Sci Rep. 2018 Oct 9;8(1):14989. doi: 10.1038/s41598-018-33098-3. Sci Rep. 2018. PMID: 30301903 Free PMC article.

6

Clinical spectrum and genetic variations of LMNA-related muscular dystrophies in a large cohort of Chinese patients.

Fan Y, Tan D, Song D, Zhang X, Chang X, Wang Z, Zhang C, Chan SH, Wu Q, Wu L, Wang S, Yan H, Ge L, Yang H, Mao B, Bönnemann C, Liu J, Wang S, Yuan Y, Wu X, Zhang H, Xiong H. Fan Y, et al. Among authors: tan d. J Med Genet. 2021 May;58(5):326-333. doi: 10.1136/jmedgenet-2019-106671. Epub 2020 Jun 22. J Med Genet. 2021. PMID: 32571898 Free PMC article.

7

Nuclear Factor-κB Pathway Mediates the Molecular Pathogenesis of LMNA-Related Muscular Dystrophies.

Fan Y, Tan D, Zhang X, Song D, Chang X, Wang S, Yan H, Ge L, Yang H, Bönnemann C, Liu J, Wang S, Wu X, Zhang H, Xiong H. Fan Y, et al. Among authors: tan d. Biochem Genet. 2020 Dec;58(6):966-980. doi: 10.1007/s10528-020-09989-4. Epub 2020 Jul 23. Biochem Genet. 2020. PMID: 32705401

8

Novel mutations in B3GALNT2 gene causing α-dystroglycanopathy in Chinese patients.

Chen XY, Song DY, Fan YB, Tan DD, Chang XZ, Xiao JX, Toda T, Xiong H. Chen XY, et al. Chin Med J (Engl). 2020 Dec 7;134(12):1483-1485. doi: 10.1097/CM9.0000000000001283. Chin Med J (Engl). 2020. PMID: 33290285 Free PMC article. No abstract available.

9

Natural history and genetic study of LAMA2-related muscular dystrophy in a large Chinese cohort.

Tan D, Ge L, Fan Y, Chang X, Wang S, Wei C, Ding J, Liu A, Wang S, Li X, Gao K, Yang H, Que C, Huang Z, Li C, Zhu Y, Mao B, Jin B, Hua Y, Zhang X, Zhang B, Zhu W, Zhang C, Wang Y, Yuan Y, Jiang Y, Rutkowski A, Bönnemann CG, Wu X, Xiong H. Tan D, et al. Orphanet J Rare Dis. 2021 Jul 19;16(1):319. doi: 10.1186/s13023-021-01950-x. Orphanet J Rare Dis. 2021. PMID: 34281576 Free PMC article.

10

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.

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