Huang X - Search Results

1

Hereditary and idiopathic spastic paraparesis: preliminary findings of a single center experience.

Cui F, Sun L, Qiao J, Xiong J, Zhao Y, Li J, Li M, Chen S, Huang X. Cui F, et al. Among authors: huang x. Neurol Res. 2018 Dec;40(12):1088-1093. doi: 10.1080/01616412.2018.1522412. Neurol Res. 2018. PMID: 30352018

2

[Acute panautonomic neuropathy: a report of 4 cases].

Cui F, Huang XS, Zhou ZB. Cui F, et al. Nan Fang Yi Ke Da Xue Xue Bao. 2010 Apr;30(4):900-2. Nan Fang Yi Ke Da Xue Xue Bao. 2010. PMID: 20423877 Chinese.

3

Distal myopathy with rimmed vacuoles: clinical and muscle morphological characteristics and spectrum of GNE gene mutations in 53 Chinese patients.

Lu X, Pu C, Huang X, Liu J, Mao Y. Lu X, et al. Among authors: huang x. Neurol Res. 2011 Dec;33(10):1025-31. doi: 10.1179/1743132811Y.0000000070. Neurol Res. 2011. PMID: 22196754

4

[Electrophysiological features of patients with myotonic dystrophy type 1].

Li M, Wang ZJ, Cui F, Yang F, Chen ZH, Ling L, Huang XS. Li M, et al. Zhonghua Yi Xue Za Zhi. 2013 Jan 29;93(5):345-7. Zhonghua Yi Xue Za Zhi. 2013. PMID: 23660205 Chinese.

5

Coexistence of peripheral myelin protein 22 and dystrophin mutations in a chinese boy.

Wang Z, Cui F, Chen D, Pu C, Chen Z, Yang F, Wu H, Huang X. Wang Z, et al. Among authors: huang x. Muscle Nerve. 2013 Dec;48(6):979-83. doi: 10.1002/mus.23918. Epub 2013 Jun 26. Muscle Nerve. 2013. PMID: 23740413

6

New mutation in the SOD1 (copper/zinc superoxide dismutase-1) gene in a Chinese amyotrophic lateral sclerosis (ALS) patient.

Cui F, Cai W, Wang Z, Ren Y, Li M, Sun Z, Huang X. Cui F, et al. Among authors: huang x. Amyotroph Lateral Scler Frontotemporal Degener. 2013 Dec;14(7-8):635-7. doi: 10.3109/21678421.2013.817589. Epub 2013 Jul 29. Amyotroph Lateral Scler Frontotemporal Degener. 2013. PMID: 23889606

7

Exome sequencing identifies novel compound heterozygous mutations in SPG11 that cause autosomal recessive hereditary spastic paraplegia.

Zhao W, Zhu QY, Zhang JT, Liu H, Wang LJ, Chen ZQ, Guan LP, Huang XS, Yang L, Yu SY. Zhao W, et al. J Neurol Sci. 2013 Dec 15;335(1-2):112-7. doi: 10.1016/j.jns.2013.09.004. Epub 2013 Sep 10. J Neurol Sci. 2013. PMID: 24090761

8

Identification of a novel missense (C7W) mutation of SOD1 in a large familial amyotrophic lateral sclerosis pedigree.

Wang Z, Cai W, Cui F, Cai T, Chen Z, Mao F, Teng H, Chen L, Wang J, Sun Z, Huang X, Yu P. Wang Z, et al. Among authors: huang x. Neurobiol Aging. 2014 Mar;35(3):725.e11-5. doi: 10.1016/j.neurobiolaging.2013.08.024. Epub 2013 Oct 1. Neurobiol Aging. 2014. PMID: 24094577

9

Prolonged thiamphenicol treatment associated sensory axonal polyneuropathy.

Cui F, Rao Q, Zhang Y, Ren M, Yang Y, Chen Z, Huang X. Cui F, et al. Among authors: huang x. Neurol India. 2013 Nov-Dec;61(6):657-8. doi: 10.4103/0028-3886.125277. Neurol India. 2013. PMID: 24441338 Free article. No abstract available.

10

Investigation of molecular diagnosis in Chinese patients with myotonic dystrophy type 1.

Li M, Wang Z, Cui F, Yang F, Chen Z, Ling L, Pu C, Huang X. Li M, et al. Among authors: huang x. Chin Med J (Engl). 2014;127(6):1084-8. Chin Med J (Engl). 2014. PMID: 24622439

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