Zhao DH - Search Results

1

[Clinical heterogeneity associated with mitochondrial DNA A8344G point mutation].

Zhao J, Zhao DH, Zhang W, Lü H, Yuan Y, Qi Y, Wang ZX. Zhao J, et al. Among authors: zhao dh. Zhonghua Yi Xue Za Zhi. 2012 Oct 30;92(40):2835-8. Zhonghua Yi Xue Za Zhi. 2012. PMID: 23290212 Chinese.

2

Mutations in mitochondrially encoded complex I enzyme as the second common cause in a cohort of Chinese patients with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes.

Zhao D, Hong D, Zhang W, Yao S, Qi X, Lv H, Zheng R, Feng L, Huang Y, Yuan Y, Wang Z. Zhao D, et al. J Hum Genet. 2011 Nov;56(11):759-64. doi: 10.1038/jhg.2011.96. Epub 2011 Aug 18. J Hum Genet. 2011. PMID: 21850008

3

MR evaluation of cerebral oxygen metabolism and blood flow in stroke-like episodes of MELAS.

Wang Z, Xiao J, Xie S, Zhao D, Liu X, Zhang J, Yuan Y, Huang Y. Wang Z, et al. J Neurol Sci. 2012 Dec 15;323(1-2):173-7. doi: 10.1016/j.jns.2012.09.011. Epub 2012 Oct 11. J Neurol Sci. 2012. PMID: 23062409

4

Chronic progressive external ophthalmoplegia coexistent with motor neuron disease in a patient with a novel large-scale mitochondrial DNA deletion.

Zhao D, Wang Z, Hong D, Zhang W, Yuan Y. Zhao D, et al. Clin Neurol Neurosurg. 2013 Aug;115(8):1490-2. doi: 10.1016/j.clineuro.2012.11.011. Epub 2012 Dec 23. Clin Neurol Neurosurg. 2013. PMID: 23266267 No abstract available.

5

[Audiologic features of mitochondrial DNA A3243G mutation and its correlation with mutation rate].

Xue JF, Chen L, Ma YN, Zhao DH, Duan JB, Wang ZX, Qi Y, Liu YH. Xue JF, et al. Among authors: zhao dh. Zhonghua Yi Xue Za Zhi. 2012 Oct 30;92(40):2830-4. Zhonghua Yi Xue Za Zhi. 2012. PMID: 23290211 Chinese.

6

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. Muscle Nerve. 2014 Aug;50(2):200-5. doi: 10.1002/mus.24130. Epub 2014 May 17. Muscle Nerve. 2014. PMID: 24273072

7

Novel collagen VI mutations identified in Chinese patients with Ullrich congenital muscular dystrophy.

Zhang YZ, Zhao DH, Yang HP, Liu AJ, Chang XZ, Hong DJ, Bonnemann C, Yuan Y, Wu XR, Xiong H. Zhang YZ, et al. Among authors: zhao dh. World J Pediatr. 2014 May;10(2):126-32. doi: 10.1007/s12519-014-0481-1. Epub 2014 May 7. World J Pediatr. 2014. PMID: 24801232

8

Audiological evaluation in Chinese patients with mitochondrial encephalomyopathies.

Liu Y, Xue J, Zhao D, Chen L, Yuan Y, Wang Z. Liu Y, et al. Chin Med J (Engl). 2014;127(12):2304-9. Chin Med J (Engl). 2014. PMID: 24931247

9

Severe sensory neuropathy in patients with adult-onset multiple acyl-CoA dehydrogenase deficiency.

Wang Z, Hong D, Zhang W, Li W, Shi X, Zhao D, Yang X, Lv H, Yuan Y. Wang Z, et al. Neuromuscul Disord. 2016 Feb;26(2):170-5. doi: 10.1016/j.nmd.2015.12.002. Epub 2015 Dec 18. Neuromuscul Disord. 2016. PMID: 26821934

10

Mitochondrial tRNA genes are hotspots for mutations in a cohort of patients with exercise intolerance and mitochondrial myopathy.

Lu Y, Zhao D, Yao S, Wu S, Hong D, Wang Q, Liu J, Smeitink JAM, Yuan Y, Wang Z. Lu Y, et al. J Neurol Sci. 2017 Aug 15;379:137-143. doi: 10.1016/j.jns.2017.05.056. Epub 2017 May 30. J Neurol Sci. 2017. PMID: 28716227

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