Zhu M - Search Results

1

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: zhu m. 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.

2

A novel heterozygous deletion-insertion mutation in the desmin gene causes complete atrioventricular block and mild myopathy.

Cao L, Hong D, Zhu M, Li X, Wan H, Hong K. Cao L, et al. Among authors: zhu m. Clin Neuropathol. 2013 Jan-Feb;32(1):9-15. doi: 10.5414/NP300514. Clin Neuropathol. 2013. PMID: 23036309

3

Cerebral sparganosis in mainland Chinese patients.

Hong D, Xie H, Zhu M, Wan H, Xu R, Wu Y. Hong D, et al. Among authors: zhu m. J Clin Neurosci. 2013 Nov;20(11):1514-9. doi: 10.1016/j.jocn.2012.12.018. Epub 2013 Jul 30. J Clin Neurosci. 2013. PMID: 23911107

4

Sturge-Weber syndrome coexisting with episodes of rhabdomyolysis.

Zhu M, Li X, Zhou M, Wan H, Wu Y, Hong D. Zhu M, et al. BMC Neurol. 2013 Nov 11;13:169. doi: 10.1186/1471-2377-13-169. BMC Neurol. 2013. PMID: 24207015 Free PMC article.

5

Familial IBGC caused by SLC20A2 mutation presenting as paroxysmal kinesigenic dyskinesia.

Zhu M, Zhu X, Wan H, Hong D. Zhu M, et al. Among authors: zhu x. Parkinsonism Relat Disord. 2014 Mar;20(3):353-4. doi: 10.1016/j.parkreldis.2013.12.006. Epub 2013 Dec 28. Parkinsonism Relat Disord. 2014. PMID: 24411498 No abstract available.

6

Riboflavin-responsive multiple Acyl-CoA dehydrogenation deficiency in 13 cases, and a literature review in mainland Chinese patients.

Zhu M, Zhu X, Qi X, Weijiang D, Yu Y, Wan H, Hong D. Zhu M, et al. Among authors: zhu x. J Hum Genet. 2014 May;59(5):256-61. doi: 10.1038/jhg.2014.10. Epub 2014 Feb 13. J Hum Genet. 2014. PMID: 24522293 Review.

7

MAPT as a predisposing gene for sporadic amyotrophic lateral sclerosis in the Chinese Han population.

Fang P, Xu W, Wu C, Zhu M, Li X, Hong D. Fang P, et al. Among authors: zhu m. Neural Regen Res. 2013 Nov 25;8(33):3116-23. doi: 10.3969/j.issn.1673-5374.2013.33.005. Neural Regen Res. 2013. PMID: 25206632 Free PMC article.

8

[Clinical features of familial idiopathic basal ganglia calcification caused by a novel mutation in the SLC20A2 gene].

Zhu M, Fang C, Li X, Zhou M, Wan H, Hong D. Zhu M, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015 Feb;32(1):64-8. doi: 10.3760/cma.j.issn.1003-9406.2015.01.014. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015. PMID: 25636102 Chinese.

9

The clinical and genetic features in a cohort of mainland Chinese patients with thyrotoxic periodic paralysis.

Li X, Yao S, Xiang Y, Zhang X, Wu X, Luo L, Huang H, Zhu M, Wan H, Hong D. Li X, et al. Among authors: zhu m. BMC Neurol. 2015 Mar 21;15:38. doi: 10.1186/s12883-015-0290-8. BMC Neurol. 2015. PMID: 25885757 Free PMC article.

10

Diffuse leptomeningeal gliomatosis initially presenting with intraventricular hemorrhage: a case report and literature review.

Zhu M, Zheng J, Zhu Y, Wan H, Wu Y, Hong D. Zhu M, et al. Among authors: zhu y. BMC Neurol. 2015 May 10;15:77. doi: 10.1186/s12883-015-0341-1. BMC Neurol. 2015. PMID: 25957575 Free PMC article. Review.

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