Tan D - Search Results

1

Cortical venous thrombosis, multiple cortical infarctions, and vaginal bleeding in a Chinese family with hypofibrinogenemia caused by the FGG mutation c.1019C>T: a case report.

Nie H, Wu X, Bao B, Xia Z, Tan D. Nie H, et al. Among authors: tan d. Neurol Sci. 2020 Aug;41(8):2299-2301. doi: 10.1007/s10072-020-04346-0. Epub 2020 Mar 21. Neurol Sci. 2020. PMID: 32198656 No abstract available.

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

[Clinical and genetic study of a Chinese family affected with caveolinopathies].

Nie H, Wu X, Lyu J, Zhu J, Tan D. Nie H, et al. Among authors: tan d. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Oct 10;34(5):650-653. doi: 10.3760/cma.j.issn.1003-9406.2017.05.006. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 28981925 Chinese.

4

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.

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 Sep;45(9):4501-4511. doi: 10.1007/s10072-024-07492-x. Epub 2024 Mar 26. Neurol Sci. 2024. PMID: 38532189 Review.

6

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.

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

Clinical and genetic characteristics of myotonia congenita in Chinese population.

He Y, Qiu Y, Xiong Y, Shen Y, Jiang K, Yi H, Huang P, Zhu Y, Zhu M, Zhou M, Hong D, Tan D. He Y, et al. Among authors: tan d. Channels (Austin). 2024 Dec;18(1):2349823. doi: 10.1080/19336950.2024.2349823. Epub 2024 May 8. Channels (Austin). 2024. PMID: 38720415 Free PMC article.

9

A new phenotype of syndromic retinitis pigmentosa with myopathy is caused by mutations in retinol dehydrogenase 11.

Liu YD, Huang SS, Li M, Lek M, Song DY, Tan DD, Chen XY, Zhang H, Liu JY, Chang XZ, Xiong H. Liu YD, et al. Clin Genet. 2022 Apr;101(4):448-453. doi: 10.1111/cge.14108. Epub 2022 Jan 25. Clin Genet. 2022. PMID: 34988992

10

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.

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