Zhang L - Search Results

1

[Clinical and genetic analysis of a patient with Krabbe disease presented as peripheral neuropathy].

Wang W, Qin Y, Wang R, Zhang W, Zhang L, Cui L, Jin M, Jiao Y, Jiao J. Wang W, et al. Among authors: zhang l, zhang w. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Aug 10;36(8):821-825. doi: 10.3760/cma.j.issn.1003-9406.2019.08.017. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 31400137 Chinese.

2

Myotonic dystrophy type 1 associated with white matter hyperintense lesions: clinic, imaging, and genetic analysis.

Liu L, Liu HM, Liu ZJ, Zhang LW, Gu WH, Wang RB. Liu L, et al. Among authors: zhang lw. Chin Med J (Engl). 2015 May 20;128(10):1412-4. doi: 10.4103/0366-6999.156812. Chin Med J (Engl). 2015. PMID: 25963366 Free PMC article. No abstract available.

3

A case report of SPG11 mutations in a Chinese ARHSP-TCC family.

Zhang L, McFarland KN, Jiao J, Jiao Y. Zhang L, et al. BMC Neurol. 2016 Jun 3;16:87. doi: 10.1186/s12883-016-0604-5. BMC Neurol. 2016. PMID: 27256065 Free PMC article.

4

Etiological, clinical, and radiological features of longitudinally extensive myelopathy in Chinese patients.

Zhang W, Jiao Y, Cui L, Liu L, Zhang L, Jiao J. Zhang W, et al. Among authors: zhang l. J Clin Neurosci. 2016 Oct;32:61-6. doi: 10.1016/j.jocn.2015.12.048. Epub 2016 Aug 12. J Clin Neurosci. 2016. PMID: 27526974

5

Plasma Exchange for Neuromyelitis Optica Spectrum Disorders in Chinese Patients and Factors Predictive of Short-term Outcome.

Jiao Y, Cui L, Zhang W, Zhang Y, Wang W, Zhang L, Tang W, Jiao J. Jiao Y, et al. Among authors: zhang l, zhang w, zhang y. Clin Ther. 2018 Apr;40(4):603-612. doi: 10.1016/j.clinthera.2018.03.007. Epub 2018 Mar 30. Clin Ther. 2018. PMID: 29606515

6

[Analysis of fragile X mental retardation 1 gene premutation in multiple system atrophy patients].

Zhang LW, Gu WH, Wang GX, Chen YY, Hao Y, Zhang J, Wang K, Jin M. Zhang LW, et al. Zhonghua Yi Xue Za Zhi. 2013 Dec 17;93(47):3744-7. Zhonghua Yi Xue Za Zhi. 2013. PMID: 24548388 Chinese.

7

Clinical and genetic study of ataxia with vitamin E deficiency: A case report.

Zhang LW, Liu B, Peng DT. Zhang LW, et al. World J Clin Cases. 2022 Aug 16;10(23):8271-8276. doi: 10.12998/wjcc.v10.i23.8271. World J Clin Cases. 2022. PMID: 36159513 Free PMC article.

8

SPG7 and Impaired Emotional Communication.

Zhang L, McFarland KN, Subramony SH, Heilman KM, Ashizawa T. Zhang L, et al. Cerebellum. 2017 Apr;16(2):595-598. doi: 10.1007/s12311-016-0818-5. Cerebellum. 2017. PMID: 27557734 Free PMC article.

9

Primary coenzyme Q10 deficiency due to COQ8A gene mutations.

Zhang L, Ashizawa T, Peng D. Zhang L, et al. Mol Genet Genomic Med. 2020 Oct;8(10):e1420. doi: 10.1002/mgg3.1420. Epub 2020 Aug 2. Mol Genet Genomic Med. 2020. PMID: 32743982 Free PMC article.

10

Altered cerebral blood flow in patients with spinocerebellar degeneration.

Liu B, Yang A, Gao W, Chen Y, Wang Y, Liu X, Lv K, Zhang L, Ma G. Liu B, et al. Among authors: zhang l. Front Neurosci. 2022 Sep 13;16:977145. doi: 10.3389/fnins.2022.977145. eCollection 2022. Front Neurosci. 2022. PMID: 36177360 Free PMC article.

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