Liu Z - Search Results

1

The clinical and genetic characteristics in children with mitochondrial disease in China.

Fang F, Liu Z, Fang H, Wu J, Shen D, Sun S, Ding C, Han T, Wu Y, Lv J, Yang L, Li S, Lv J, Shen Y. Fang F, et al. Among authors: liu z. Sci China Life Sci. 2017 Jul;60(7):746-757. doi: 10.1007/s11427-017-9080-y. Epub 2017 Jun 16. Sci China Life Sci. 2017. PMID: 28639102

2

Liu Z, Fang F, Ding C, Wu H, Lyu J, Wu Y. Liu Z, et al. Zhonghua Er Ke Za Zhi. 2014 Nov;52(11):817-21. Zhonghua Er Ke Za Zhi. 2014. PMID: 25582465 Review. Chinese.

3

[Challenges and developments in diagnosis of mitochondrial diseases in children].

Fang F, Liu Z. Fang F, et al. Among authors: liu z. Zhonghua Er Ke Za Zhi. 2015 Oct;53(10):723-5. Zhonghua Er Ke Za Zhi. 2015. PMID: 26758104 Chinese. No abstract available.

4

[Diagnosis of mitochondrial disorders in children with next generation sequencing].

Liu Z, Fang F, Ding C, Zhang W, Li J, Yang X, Wang X, Wu Y, Wang H, Liu L, Han T, Wang X, Chen C, Lyu J, Wu H. Liu Z, et al. Among authors: liu l. Zhonghua Er Ke Za Zhi. 2015 Oct;53(10):747-53. Zhonghua Er Ke Za Zhi. 2015. PMID: 26758110 Chinese.

5

[Clinical and genetic characteristics of children with Leigh syndrome].

Fang F, Shen Y, Shen DM, Liu ZM, Ding CH, Zhang WC, Sun SZ, Lyu JL, Han TL, Wang XH, Zhang WH, Yang XY, Li JW, Wu HS. Fang F, et al. Among authors: liu zm. Zhonghua Er Ke Za Zhi. 2017 Mar 2;55(3):205-209. doi: 10.3760/cma.j.issn.0578-1310.2017.03.008. Zhonghua Er Ke Za Zhi. 2017. PMID: 28273704 Chinese.

6

Erratum to: The clinical and genetic characteristics in children with mitochondrial disease in China.

Fang F, Liu Z, Fang H, Wu J, Shen D, Sun S, Ding C, Han T, Wu Y, Lv J, Yang L, Li S, Lv J, Shen Y. Fang F, et al. Among authors: liu z. Sci China Life Sci. 2018 Dec;61(12):1606. doi: 10.1007/s11427-017-9130-4. Sci China Life Sci. 2018. PMID: 28730341

7

[Clinical and genetic characteristics of congenital myasthenia syndrome with episodic apnea caused by CHAT gene mutation: a report of 2 cases].

Liu ZM, Fang F, Ding CH, Zhang WH, Deng J, Chen CH, Wang X, Liu J, Li Z, Jia XL, Zeng JS, Qian SY. Liu ZM, et al. Among authors: liu j. Zhonghua Er Ke Za Zhi. 2018 Mar 2;56(3):216-220. doi: 10.3760/cma.j.issn.0578-1310.2018.03.012. Zhonghua Er Ke Za Zhi. 2018. PMID: 29518833 Chinese.

8

[Phenotype and genotype of twelve Chinese children with mitochondrial DNA depletion syndromes].

Dai LF, Fang F, Liu ZM, Shen DM, Ding CH, Li JW, Ren XT, Wu HS. Dai LF, et al. Among authors: liu zm. Zhonghua Er Ke Za Zhi. 2019 Mar 2;57(3):211-216. doi: 10.3760/cma.j.issn.0578-1310.2019.03.011. Zhonghua Er Ke Za Zhi. 2019. PMID: 30818899 Chinese.

9

Compound Heterozygous CHAT Gene Mutations of a Large Deletion and a Missense Variant in a Chinese Patient With Severe Congenital Myasthenic Syndrome With Episodic Apnea.

Liu Z, Zhang L, Shen D, Ding C, Yang X, Zhang W, Li J, Deng J, Gong S, Liu J, Qian S, Fang F. Liu Z, et al. Among authors: liu j. Front Pharmacol. 2019 Mar 12;10:259. doi: 10.3389/fphar.2019.00259. eCollection 2019. Front Pharmacol. 2019. PMID: 30914958 Free PMC article.

10

[Clinical and genetic characteristics of 62 children with mitochondrial epilepsy].

Han XD, Fang F, Li H, Liu ZM, Shi YQ, Wang JL, Ren XT, Ding CH, Chen CH, Li JW, Zhang WH, Deng J. Han XD, et al. Among authors: liu zm. Zhonghua Er Ke Za Zhi. 2019 Nov 2;57(11):844-851. doi: 10.3760/cma.j.issn.0578-1310.2019.11.006. Zhonghua Er Ke Za Zhi. 2019. PMID: 31665838 Chinese.

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