Zhang H - Search Results

1

C9orf72 repeat expansions are not detected in Chinese patients with familial ALS.

Liu R, Tang L, Cai B, Liu X, Ye S, Ma Y, Zhang H, Fan D. Liu R, et al. Among authors: zhang h. Amyotroph Lateral Scler Frontotemporal Degener. 2013 Dec;14(7-8):630-1. doi: 10.3109/21678421.2013.817588. Epub 2013 Jul 22. Amyotroph Lateral Scler Frontotemporal Degener. 2013. PMID: 23869403 No abstract available.

2

ARHGEF28 gene exon 6/intron 6 junction mutations in Chinese amyotrophic lateral sclerosis cohort.

Ma Y, Tang L, Chen L, Zhang B, Deng P, Wang J, Yang Y, Liu R, Yang Y, Ye S, Liu X, Zhang H, Fan D. Ma Y, et al. Among authors: zhang b, zhang h. Amyotroph Lateral Scler Frontotemporal Degener. 2014 Jun;15(3-4):309-11. doi: 10.3109/21678421.2014.896926. Epub 2014 Apr 8. Amyotroph Lateral Scler Frontotemporal Degener. 2014. PMID: 24712971

3

[The association between angiogenin gene variations and familial amyotrophic lateral sclerosis in Chinese Han patients].

Zhang H, Zhang Y, Tang L, Zhang N, Fan D. Zhang H, et al. Among authors: zhang n, zhang y. Zhonghua Nei Ke Za Zhi. 2015 Feb;54(2):122-4. Zhonghua Nei Ke Za Zhi. 2015. PMID: 25907842 Chinese.

4

C9orf72 hexanucleotide repeat expansions in Chinese sporadic amyotrophic lateral sclerosis.

He J, Tang L, Benyamin B, Shah S, Hemani G, Liu R, Ye S, Liu X, Ma Y, Zhang H, Cremin K, Leo P, Wray NR, Visscher PM, Xu H, Brown MA, Bartlett PF, Mangelsdorf M, Fan D. He J, et al. Among authors: zhang h. Neurobiol Aging. 2015 Sep;36(9):2660.e1-8. doi: 10.1016/j.neurobiolaging.2015.06.002. Epub 2015 Jun 9. Neurobiol Aging. 2015. PMID: 26142124

5

[Association between VAPB mutations and familial amyotrophic lateral sclerosis in Chinese patients].

Zhang H, Tang L, Zhang N, Fan D. Zhang H, et al. Among authors: zhang n. Zhonghua Yi Xue Za Zhi. 2015 Jun 2;95(21):1667-70. Zhonghua Yi Xue Za Zhi. 2015. PMID: 26675796 Chinese.

6

Clinical Features of Isolated Bulbar Palsy of Amyotrophic Lateral Sclerosis in Chinese Population.

Zhang HG, Chen L, Tang L, Zhang N, Fan DS. Zhang HG, et al. Chin Med J (Engl). 2017 Aug 5;130(15):1768-1772. doi: 10.4103/0366-6999.211538. Chin Med J (Engl). 2017. PMID: 28748847 Free PMC article.

7

A rare Cu/Zn superoxide dismutase mutation causing familial amyotrophic lateral sclerosis with variable age of onset and incomplete penetrance in China.

Zhang H, Zhao H, Lu M, Zhang Y, Wang L, Zhang J, Ma D, Fan D. Zhang H, et al. Among authors: zhang j, zhang y. Amyotroph Lateral Scler Other Motor Neuron Disord. 2005 Dec;6(4):234-8. doi: 10.1080/14660820510044478. Amyotroph Lateral Scler Other Motor Neuron Disord. 2005. PMID: 16319027

8

VEGF C2578A polymorphism does not contribute to amyotrophic lateral sclerosis susceptibility in sporadic Chinese patients.

Zhang Y, Zhang H, Fu Y, Song H, Wang L, Zhang J, Fan D. Zhang Y, et al. Among authors: zhang j, zhang h. Amyotroph Lateral Scler. 2006 Jun;7(2):119-22. doi: 10.1080/14660820600600657. Amyotroph Lateral Scler. 2006. PMID: 16753977

9

[Ventilation function disorder of flail arm syndrome].

Zhang H, Tang L, Zhang N, Fan D. Zhang H, et al. Among authors: zhang n. Zhonghua Nei Ke Za Zhi. 2015 Sep;54(9):749-52. Zhonghua Nei Ke Za Zhi. 2015. PMID: 26674790 Chinese.

10

[Association between site of onset and ventilation dysfunction in patients with amyotrophic lateral sclerosis].

Zhang H, Tang L, Zhang N, Fan D. Zhang H, et al. Among authors: zhang n. Zhonghua Yi Xue Za Zhi. 2015 Nov 17;95(43):3496-500. Zhonghua Yi Xue Za Zhi. 2015. PMID: 26813271 Chinese.

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