Fang F - 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: fang h. 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

[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: fang f. Zhonghua Er Ke Za Zhi. 2015 Oct;53(10):747-53. Zhonghua Er Ke Za Zhi. 2015. PMID: 26758110 Chinese.

3

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: fang h. Sci China Life Sci. 2018 Dec;61(12):1606. doi: 10.1007/s11427-017-9130-4. Sci China Life Sci. 2018. PMID: 28730341

4

[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. 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.

5

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

6

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

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

7

Phenotypes and genotypes of mitochondrial diseases with mtDNA variations in Chinese children: A multi-center study.

Shi Y, Chen G, Sun D, Hu C, Liu Z, Shen D, Wang J, Song T, Zhang W, Li J, Ren X, Han T, Ding C, Wang Y, Fang F. Shi Y, et al. Among authors: fang f. Mitochondrion. 2022 Jan;62:139-150. doi: 10.1016/j.mito.2021.11.006. Epub 2021 Nov 17. Mitochondrion. 2022. PMID: 34800692

8

Leigh Syndrome: A Study of 209 Patients at the Beijing Children's Hospital.

Stenton SL, Zou Y, Cheng H, Liu Z, Wang J, Shen D, Jin H, Ding C, Tang X, Sun S, Han H, Ma Y, Zhang W, Jin R, Wang H, Sun D, Lv JL, Prokisch H, Fang F. Stenton SL, et al. Among authors: fang f. Ann Neurol. 2022 Apr;91(4):466-482. doi: 10.1002/ana.26313. Epub 2022 Mar 6. Ann Neurol. 2022. PMID: 35094435

9

Clinical and genetic spectrum of hereditary spastic paraplegia in Chinese children.

Wang J, Fang F, Ding C, Li J, Wu Y, Zhang W, Bao X, Lv J, Wang X, Ren X; Paediatric Neurology Study Group. Wang J, et al. Among authors: fang f. Dev Med Child Neurol. 2023 Mar;65(3):416-423. doi: 10.1111/dmcn.15385. Epub 2022 Sep 15. Dev Med Child Neurol. 2023. PMID: 36109173 Free article.

10

[Progressive cavitating leukoencephalopathy: four cases and literatures review].

Ren CH, Fang F, Cheng H, Ding CH, Chen CH, Zhang YJ, Shen DM. Ren CH, et al. Among authors: fang f. Zhonghua Er Ke Za Zhi. 2017 Apr 2;55(4):283-287. doi: 10.3760/cma.j.issn.0578-1310.2017.04.010. Zhonghua Er Ke Za Zhi. 2017. PMID: 28441825 Review. Chinese.

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