Zhu W - Search Results

1

Clinical features and ETFDH mutation spectrum in a cohort of 90 Chinese patients with late-onset multiple acyl-CoA dehydrogenase deficiency.

Xi J, Wen B, Lin J, Zhu W, Luo S, Zhao C, Li D, Lin P, Lu J, Yan C. Xi J, et al. Among authors: zhu w. J Inherit Metab Dis. 2014 May;37(3):399-404. doi: 10.1007/s10545-013-9671-6. Epub 2013 Dec 20. J Inherit Metab Dis. 2014. PMID: 24357026

2

Clinical and pathological features in 15 Chinese patients with calpainopathy.

Luo SS, Xi JY, Lu JH, Zhao CB, Zhu WH, Lin J, Wang Y, Ren HM, Yin B, Andoni UJ. Luo SS, et al. Muscle Nerve. 2011 Mar;43(3):402-9. doi: 10.1002/mus.21908. Epub 2010 Dec 9. Muscle Nerve. 2011. PMID: 21321956

3

HLA-DQA1*03:02/DQB1*03:03:02 is strongly associated with susceptibility to childhood-onset ocular myasthenia gravis in Southern Han Chinese.

Zhu WH, Lu JH, Lin J, Xi JY, Lu J, Luo SS, Qiao K, Xiao BG, Lu CZ, Zhao CB. Zhu WH, et al. J Neuroimmunol. 2012 Jun 15;247(1-2):81-5. doi: 10.1016/j.jneuroim.2012.03.018. Epub 2012 Apr 13. J Neuroimmunol. 2012. PMID: 22503410

4

Genetic variability and clinical spectrum of Chinese patients with limb-girdle muscular dystrophy type 2A.

Luo SS, Xi JY, Zhu WH, Zhao CB, Lu JH, Lin J, Wang Y, Lu J, Qiao K. Luo SS, et al. Muscle Nerve. 2012 Nov;46(5):723-9. doi: 10.1002/mus.23381. Epub 2012 Aug 24. Muscle Nerve. 2012. PMID: 22926650

5

Novel mutations m.3959G>A and m.3995A>G in mitochondrial gene MT-ND1 associated with MELAS.

Lin J, Zhao CB, Lu JH, Wang HJ, Zhu WH, Xi JY, Lu J, Luo SS, Ma D, Wang Y, Xiao BG, Lu CZ. Lin J, et al. Mitochondrial DNA. 2014 Feb;25(1):56-62. doi: 10.3109/19401736.2013.779259. Epub 2013 Jul 8. Mitochondrial DNA. 2014. PMID: 23834081

6

Novel LAMP2 mutations in Chinese patients with Danon disease cause varying degrees of clinical severity.

Luo SS, Xi JY, Cai S, Zhao CB, Lu JH, Zhu WH, Lin J, Qiao K, Wang Y, Ye ZR. Luo SS, et al. Clin Neuropathol. 2014 Jul-Aug;33(4):284-91. doi: 10.5414/NP300668. Clin Neuropathol. 2014. PMID: 24691104

7

Giant cell polymyositis associated with myasthenia gravis and thymoma.

Lin J, Lu J, Zhao C, Qiao K, Zhu W, Yue D, Luo S, Wang Y, Fang W, Lu J. Lin J, et al. Among authors: zhu w. J Clin Neurosci. 2014 Dec;21(12):2252-4. doi: 10.1016/j.jocn.2014.04.027. Epub 2014 Aug 2. J Clin Neurosci. 2014. PMID: 25096712

8

New disease allele and de novo mutation indicate mutational vulnerability of titin exon 343 in hereditary myopathy with early respiratory failure.

Yue D, Gao M, Zhu W, Luo S, Xi J, Wang B, Li Y, Cai S, Li J, Wang Y, Lu J, Zhao C. Yue D, et al. Among authors: zhu w. Neuromuscul Disord. 2015 Feb;25(2):172-6. doi: 10.1016/j.nmd.2014.11.005. Epub 2014 Nov 18. Neuromuscul Disord. 2015. PMID: 25500009

9

Clinical heterogeneity and a high proportion of novel mutations in a Chinese cohort of patients with dysferlinopathy.

Xi J, Blandin G, Lu J, Luo S, Zhu W, Béroud C, Pécheux C, Labelle V, Lévy N, Urtizberea JA, Zhao C, Krahn M. Xi J, et al. Among authors: zhu w. Neurol India. 2014 Nov-Dec;62(6):635-9. doi: 10.4103/0028-3886.149386. Neurol India. 2014. PMID: 25591676 Free article.

10

Muscle pathology and whole-body MRI in a polyglucosan myopathy associated with a novel glycogenin-1 mutation.

Luo S, Zhu W, Yue D, Lin J, Wang Y, Zhu Z, Qiu W, Lu J, Hedberg-Oldfors C, Oldfors A, Zhao C. Luo S, et al. Among authors: zhu w, zhu z. Neuromuscul Disord. 2015 Oct;25(10):780-5. doi: 10.1016/j.nmd.2015.07.007. Epub 2015 Jul 15. Neuromuscul Disord. 2015. PMID: 26255073

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