Guo J - Search Results

1

Batoclimab vs Placebo for Generalized Myasthenia Gravis: A Randomized Clinical Trial.

Yan C, Yue Y, Guan Y, Bu B, Ke Q, Duan R, Deng H, Xue Q, Jiang H, Xiao F, Yang H, Chang T, Zou Z, Li H, Tan S, Xiao H, Zhou H, Zhang H, Meng Q, Li W, Li W, Guo J, Zhang Y, Li Z, Tu J, Shi J, Li W, Lee M, Chen Y, Tao X, Zhao S, Li P, Zhao C; Batoclimab Study Team. Yan C, et al. Among authors: guo j. JAMA Neurol. 2024 Mar 4;81(4):336-45. doi: 10.1001/jamaneurol.2024.0044. Online ahead of print. JAMA Neurol. 2024. PMID: 38436998

2

Overlap of periodic paralysis and paramyotonia congenita caused by SCN4A gene mutations two family reports and literature review.

Huang S, Zhang W, Chang X, Guo J. Huang S, et al. Among authors: guo j. Channels (Austin). 2019 Dec;13(1):110-119. doi: 10.1080/19336950.2019.1600967. Channels (Austin). 2019. PMID: 30931713 Free PMC article. Review.

3

A childhood-onset nemaline myopathy caused by novel heterozygote variants in the nebulin gene with literature review.

Wen Q, Chang X, Guo J. Wen Q, et al. Among authors: guo j. Acta Neurol Belg. 2020 Dec;120(6):1351-1360. doi: 10.1007/s13760-019-01230-3. Epub 2019 Nov 6. Acta Neurol Belg. 2020. PMID: 31696431 Review.

4

The relationship between cognitive impairment and homocysteine in a B12 and folate deficient population in China: A cross-sectional study.

Meng H, Li Y, Zhang W, Zhao Y, Niu X, Guo J. Meng H, et al. Among authors: guo j. Medicine (Baltimore). 2019 Nov;98(47):e17970. doi: 10.1097/MD.0000000000017970. Medicine (Baltimore). 2019. PMID: 31764802 Free PMC article.

5

A meta-analysis and systematic review of Leigh syndrome: clinical manifestations, respiratory chain enzyme complex deficiency, and gene mutations.

Chang X, Wu Y, Zhou J, Meng H, Zhang W, Guo J. Chang X, et al. Among authors: guo j. Medicine (Baltimore). 2020 Jan;99(5):e18634. doi: 10.1097/MD.0000000000018634. Medicine (Baltimore). 2020. PMID: 32000367 Free PMC article.

6

Late-onset multiple acyl-CoA dehydrogenase deficiency with cardiac syncope: A case report.

Pan XQ, Chang XL, Zhang W, Meng HX, Zhang J, Shi JY, Guo JH. Pan XQ, et al. Among authors: guo jh. World J Clin Cases. 2020 Mar 6;8(5):995-1001. doi: 10.12998/wjcc.v8.i5.995. World J Clin Cases. 2020. PMID: 32190638 Free PMC article.

7

Whole-exome sequencing identifies a heterozygous mutation in SLC12A6 associated with hereditary sensory and motor neuropathy.

Shi J, Zhao F, Pang X, Huang S, Wang J, Chang X, Zhang J, Liu Y, Guo J, Zhang W. Shi J, et al. Among authors: guo j. Neuromuscul Disord. 2021 Feb;31(2):149-157. doi: 10.1016/j.nmd.2020.11.002. Epub 2020 Nov 18. Neuromuscul Disord. 2021. PMID: 33323309

8

A novel Q93H missense mutation in DCTN1 caused distal hereditary motor neuropathy type 7B and Perry syndrome from a Chinese family.

Zhang J, Wang H, Liu W, Wang J, Zhang J, Chang X, Huang S, Pang X, Guo J, Wang Q, Zhang W. Zhang J, et al. Among authors: guo j. Neurol Sci. 2021 Sep;42(9):3695-3705. doi: 10.1007/s10072-020-04962-w. Epub 2021 Jan 14. Neurol Sci. 2021. PMID: 33443672

9

Fasciculation score: a sensitive biomarker in amyotrophic lateral sclerosis.

Ma J, Wen Q, Pang X, Huang S, Zhang J, Wang J, Chang X, Guo J, Zhang W. Ma J, et al. Among authors: guo j. Neurol Sci. 2021 Nov;42(11):4657-4666. doi: 10.1007/s10072-021-05166-6. Epub 2021 Mar 11. Neurol Sci. 2021. PMID: 33704599

10

Pain in acute motor axonal neuropathy.

Zhao F, Wang J, Zhang J, Pang X, Huang S, Chang X, Guo J, Zhang W. Zhao F, et al. Among authors: guo j. Muscle Nerve. 2021 Dec;64(6):739-743. doi: 10.1002/mus.27414. Epub 2021 Sep 24. Muscle Nerve. 2021. PMID: 34506042

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