Zheng Y - Search Results

1

Juvenile-onset PSAT1-related neuropathy: A milder phenotype of serine deficiency disorder.

Shen Y, Peng Y, Huang P, Zheng Y, Li S, Jiang K, Zhou M, Deng J, Zhu M, Hong D. Shen Y, et al. Among authors: zheng y. Front Genet. 2022 Aug 16;13:949038. doi: 10.3389/fgene.2022.949038. eCollection 2022. Front Genet. 2022. PMID: 36061210 Free PMC article.

2

[The value of muscle biopsy in rhabdomyolysis].

Zhao YW, Wang DQ, Deng JW, Yu M, Zheng YM, Leng YL, Zhang W, Wang ZX, Yuan Y. Zhao YW, et al. Among authors: zheng ym. Zhonghua Nei Ke Za Zhi. 2019 Dec 1;58(12):899-904. doi: 10.3760/cma.j.issn.0578-1426.2019.12.006. Zhonghua Nei Ke Za Zhi. 2019. PMID: 31775453 Chinese.

3

Benign monomelic amyotrophy of lower limb in a cohort of chinese patients.

Wang L, Wen H, Chen S, Wang H, Zheng Y, Chen R, Li J, Jiang K, Xiang H, Zhu M, Zhou M, Yao S, Hong D. Wang L, et al. Among authors: zheng y. Brain Behav. 2021 Apr;11(4):e02073. doi: 10.1002/brb3.2073. Epub 2021 Mar 2. Brain Behav. 2021. PMID: 33650811 Free PMC article.

4

Genetic origin of sporadic cases and RNA toxicity in neuronal intranuclear inclusion disease.

Deng J, Zhou B, Yu J, Han X, Fu J, Li X, Xie X, Zhu M, Zheng Y, Guo X, Li P, Wang Q, Liu J, Zhang W, Yuan Y, Yao S, Wang Z, Hong D. Deng J, et al. Among authors: zheng y. J Med Genet. 2022 May;59(5):462-469. doi: 10.1136/jmedgenet-2020-107649. Epub 2021 Mar 25. J Med Genet. 2022. PMID: 33766934

5

Diverse myopathological features in the congenital myasthenia syndrome with GFPT1 mutation.

Jiang K, Zheng Y, Lin J, Wu X, Yu Y, Zhu M, Fang X, Zhou M, Li X, Hong D. Jiang K, et al. Among authors: zheng y. Brain Behav. 2022 Feb;12(2):e2469. doi: 10.1002/brb3.2469. Epub 2022 Jan 3. Brain Behav. 2022. PMID: 34978387 Free PMC article.

6

Genetic spectrum in a cohort of patients with distal hereditary motor neuropathy.

Wu C, Xiang H, Chen R, Zheng Y, Zhu M, Chen S, Yu Y, Peng Y, Yu Y, Deng J, Zhou M, Hong D. Wu C, et al. Among authors: zheng y. Ann Clin Transl Neurol. 2022 May;9(5):633-643. doi: 10.1002/acn3.51543. Epub 2022 Mar 17. Ann Clin Transl Neurol. 2022. PMID: 35297556 Free PMC article.

7

Pathological changes of the sural nerve in patients with familial episodic pain syndrome.

Zheng Y, Huang P, Li S, Jiang K, Zhou B, Fang X, Zhou M, Hong D, Zhu M. Zheng Y, et al. Neurol Sci. 2022 Sep;43(9):5605-5614. doi: 10.1007/s10072-022-06107-7. Epub 2022 May 7. Neurol Sci. 2022. PMID: 35524925

8

The polyG diseases: a new disease entity.

Liufu T, Zheng Y, Yu J, Yuan Y, Wang Z, Deng J, Hong D. Liufu T, et al. Among authors: zheng y. Acta Neuropathol Commun. 2022 May 31;10(1):79. doi: 10.1186/s40478-022-01383-y. Acta Neuropathol Commun. 2022. PMID: 35642014 Free PMC article. Review.

9

Familial Episodic Pain Syndromes.

Shen Y, Zheng Y, Hong D. Shen Y, et al. Among authors: zheng y. J Pain Res. 2022 Aug 26;15:2505-2515. doi: 10.2147/JPR.S375299. eCollection 2022. J Pain Res. 2022. PMID: 36051609 Free PMC article. Review.

10

FUS Mutation Causes Disordered Lipid Metabolism in Skeletal Muscle Associated with ALS.

Zhou B, Zheng Y, Li X, Dong H, Yu J, Zou Y, Zhu M, Yu Y, Fang X, Zhou M, Zhang W, Yuan Y, Wang Z, Deng J, Hong D. Zhou B, et al. Among authors: zheng y. Mol Neurobiol. 2022 Dec;59(12):7265-7277. doi: 10.1007/s12035-022-03048-2. Epub 2022 Sep 28. Mol Neurobiol. 2022. PMID: 36169888

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