Zhao Z - Search Results

1

Molecular landscape of DYSF mutations in dysferlinopathy: From a Chinese multicenter analysis to a worldwide perspective.

Zhong H, Yu M, Lin P, Zhao Z, Zheng X, Xi J, Zhu W, Zheng Y, Zhang W, Lv H, Yan C, Hu J, Wang Z, Lu J, Zhao C, Luo S, Yuan Y. Zhong H, et al. Among authors: zhao z, zhao c. Hum Mutat. 2021 Dec;42(12):1615-1623. doi: 10.1002/humu.24284. Epub 2021 Oct 11. Hum Mutat. 2021. PMID: 34559919

2

[A clinical and pathological analysis of inclusion body myositis].

Hu J, Li N, Yuan JH, Zhao Z, Shen HR, Mei L. Hu J, et al. Among authors: zhao z. Zhonghua Nei Ke Za Zhi. 2007 Aug;46(8):658-60. Zhonghua Nei Ke Za Zhi. 2007. PMID: 17967238 Chinese.

3

Genetically confirmed patients with merosin-deficient congenital muscular dystrophy in China.

Yuan J, Takashima H, Higuchi I, Arimura K, Li N, Zhao Z, Shen H, Hu J. Yuan J, et al. Among authors: zhao z. Neuropediatrics. 2008 Oct;39(5):264-7. doi: 10.1055/s-0029-1202288. Epub 2009 Mar 17. Neuropediatrics. 2008. PMID: 19294599

4

[Mutation analysis of a Chinese family with autosomal dominant Emery-Dreifuss muscular dystrophy].

Yuan JH, Hu J, Zhao Z, Shen HR, Li N, Bing Q. Yuan JH, et al. Among authors: zhao z. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2010 Apr;27(2):136-9. doi: 10.3760/cma.j.issn.1003-9406.2010.02.004. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2010. PMID: 20376791 Chinese.

5

Alanyl-tRNA synthetase mutation in a family with dominant distal hereditary motor neuropathy.

Zhao Z, Hashiguchi A, Hu J, Sakiyama Y, Okamoto Y, Tokunaga S, Zhu L, Shen H, Takashima H. Zhao Z, et al. Neurology. 2012 May 22;78(21):1644-9. doi: 10.1212/WNL.0b013e3182574f8f. Epub 2012 May 9. Neurology. 2012. PMID: 22573628 Free PMC article.

6

DYSF mutation analysis in a group of Chinese patients with dysferlinopathy.

Zhao Z, Hu J, Sakiyama Y, Okamoto Y, Higuchi I, Li N, Shen H, Takashima H. Zhao Z, et al. Clin Neurol Neurosurg. 2013 Aug;115(8):1234-7. doi: 10.1016/j.clineuro.2012.11.010. Epub 2012 Dec 14. Clin Neurol Neurosurg. 2013. PMID: 23254335

7

Clinical, pathological, and neuroimaging analyses of two cases of Leigh syndrome in a Chinese family.

Jin T, Shen H, Zhao Z, Hu J. Jin T, et al. Among authors: zhao z. J Child Neurol. 2014 Nov;29(11):NP143-8. doi: 10.1177/0883073813512524. Epub 2014 Jan 10. J Child Neurol. 2014. PMID: 24413359

8

Cardiac effects of the c.1583 C→G LMNA mutation in two families with Emery-Dreifuss muscular dystrophy.

Zhang L, Shen H, Zhao Z, Bing Q, Hu J. Zhang L, et al. Among authors: zhao z. Mol Med Rep. 2015 Oct;12(4):5065-71. doi: 10.3892/mmr.2015.4065. Epub 2015 Jul 8. Mol Med Rep. 2015. PMID: 26165385 Free PMC article.

9

Optimization PCR for Detection CTG/CCTG-Repeat Expansions in the Diagnosis of Myotonic Dystrophies.

Meng YX, Shen HR, Zhao Z, Bing Q, Li N, Hu J. Meng YX, et al. Among authors: zhao z. Ann Clin Lab Sci. 2015 Fall;45(5):502-7. Ann Clin Lab Sci. 2015. PMID: 26586700

10

Early myocardial damage assessment in dystrophinopathies using (99)Tc(m)-MIBI gated myocardial perfusion imaging.

Zhang L, Liu Z, Hu KY, Tian QB, Wei LG, Zhao Z, Shen HR, Hu J. Zhang L, et al. Among authors: zhao z. Ther Clin Risk Manag. 2015 Dec 10;11:1819-27. doi: 10.2147/TCRM.S89962. eCollection 2015. Ther Clin Risk Manag. 2015. PMID: 26677332 Free PMC article.

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