Meng L - Search Results

1

Vagus nerve ultrasound in transthyretin familial amyloid polyneuropathy: A pilot study.

Du K, Xu K, Chu X, Tang Y, Lv H, Zhang W, Wang Z, Yuan Y, Meng L. Du K, et al. Among authors: meng l. J Neuroimaging. 2022 Mar;32(2):285-291. doi: 10.1111/jon.12956. Epub 2021 Dec 29. J Neuroimaging. 2022. PMID: 34964197 Free PMC article.

2

Heterogeneity of axonal pathology in Chinese patients with giant axonal neuropathy.

Wang L, Zhao D, Wang Z, Zhang W, Lv H, Liu X, Meng L, Yuan Y. Wang L, et al. Among authors: meng l. Muscle Nerve. 2014 Aug;50(2):200-5. doi: 10.1002/mus.24130. Epub 2014 May 17. Muscle Nerve. 2014. PMID: 24273072

3

The C-1021T polymorphism of dopamine β-hydroxylase is not associated with orthostatic hypotension in a Chinese population.

Lu N, Chen J, Yuan Y, Cong X, Yang Y, Meng L, Sun K, Hui R, Zheng Y. Lu N, et al. Among authors: meng l. J Hum Hypertens. 2015 Mar;29(3):173-8. doi: 10.1038/jhh.2014.54. Epub 2014 Jul 3. J Hum Hypertens. 2015. PMID: 24990418

4

Hereditary Transthyretin Amyloidosis in Eight Chinese Families.

Meng LC, Lyu H, Zhang W, Liu J, Wang ZX, Yuan Y. Meng LC, et al. Chin Med J (Engl). 2015 Nov 5;128(21):2902-5. doi: 10.4103/0366-6999.168048. Chin Med J (Engl). 2015. PMID: 26521788 Free PMC article.

5

[The clinical and muscular pathological features of statin-induced myopathy].

Meng L, Lu Y, Zhang W, Wang Z, Lyu H, Yuan Y. Meng L, et al. Zhonghua Nei Ke Za Zhi. 2015 Aug;54(8):716-20. Zhonghua Nei Ke Za Zhi. 2015. PMID: 26674629 Chinese.

6

[Pathological features of muscles and peripheral nerves of Kennedy's disease: a report of 12 cases].

Meng L, Liu J, Liu X, Wang Z, Yuan Y, Zhang W. Meng L, et al. Zhonghua Yi Xue Za Zhi. 2015 Jun 2;95(21):1681-5. Zhonghua Yi Xue Za Zhi. 2015. PMID: 26675799 Chinese.

7

Heterogeneous characteristics of MRI changes of thigh muscles in patients with dysferlinopathy.

Jin S, Du J, Wang Z, Zhang W, Lv H, Meng L, Xiao J, Yuan Y. Jin S, et al. Among authors: meng l. Muscle Nerve. 2016 Dec;54(6):1072-1079. doi: 10.1002/mus.25207. Epub 2016 Oct 11. Muscle Nerve. 2016. PMID: 27251469

8

[Clinical and myopathological features of Jo-1 syndrome].

Meng LC, Li Y, Zhang W, Hao HJ, Gao F, Yuan Y. Meng LC, et al. Zhonghua Yi Xue Za Zhi. 2016 Aug 2;96(29):2352-5. doi: 10.3760/cma.j.issn.0376-2491.2016.29.014. Zhonghua Yi Xue Za Zhi. 2016. PMID: 27524195 Chinese.

9

HADHB mutations cause infantile-onset axonal Charcot-Marie-Tooth disease: A report of two cases.

Lu Y, Wu R, Meng L, Lv H, Liu J, Zuo Y, Zhang W, Yuan Y, Wang Z. Lu Y, et al. Among authors: meng l. Clin Neuropathol. 2018 Sep/Oct;37(5):232-238. doi: 10.5414/NP301097. Clin Neuropathol. 2018. PMID: 29956646

10

Novel mutations in HINT1 gene cause autosomal recessive axonal neuropathy with neuromyotonia in two cases of sensorimotor neuropathy and one case of motor neuropathy.

Meng L, Fu J, Lv H, Zhang W, Wang Z, Yuan Y. Meng L, et al. Neuromuscul Disord. 2018 Aug;28(8):646-651. doi: 10.1016/j.nmd.2018.05.003. Epub 2018 May 15. Neuromuscul Disord. 2018. PMID: 30001929

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