Zhang W - Search Results

1

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: zhang w. Ann Neurol. 2022 Apr;91(4):466-482. doi: 10.1002/ana.26313. Epub 2022 Mar 6. Ann Neurol. 2022. PMID: 35094435

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: zhang w. Zhonghua Er Ke Za Zhi. 2015 Oct;53(10):747-53. Zhonghua Er Ke Za Zhi. 2015. PMID: 26758110 Chinese.

3

A Centralized Report on Pediatric Japanese Encephalitis Cases from Beijing Children's Hospital, 2013.

Li JW, Gao XY, Wu Y, Fu SH, Tan XJ, Cao YX, Zhang WH, Yin ZD, He Y, Li YX, Liang GD, Xu WB, Fang F, Wang HY. Li JW, et al. Biomed Environ Sci. 2016 Dec;29(12):902-908. doi: 10.3967/bes2016.121. Biomed Environ Sci. 2016. PMID: 28081752 Free article.

4

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: zhang l, zhang w. Front Pharmacol. 2019 Mar 12;10:259. doi: 10.3389/fphar.2019.00259. eCollection 2019. Front Pharmacol. 2019. PMID: 30914958 Free PMC article.

5

Next-Generation Sequencing Analysis Reveals Novel Pathogenic Variants in Four Chinese Siblings With Late-Infantile Neuronal Ceroid Lipofuscinosis.

Ren XT, Wang XH, Ding CH, Shen X, Zhang H, Zhang WH, Li JW, Ren CH, Fang F. Ren XT, et al. Front Genet. 2019 Apr 25;10:370. doi: 10.3389/fgene.2019.00370. eCollection 2019. Front Genet. 2019. PMID: 31105743 Free PMC article.

6

Long-term efficacy of mycophenolate mofetil in myelin oligodendrocyte glycoprotein antibody-associated disorders: A prospective study.

Li S, Ren H, Xu Y, Xu T, Zhang Y, Yin H, Zhang W, Li J, Ren X, Fang F, Li W, Zhu Y, Peng B, Wang J, Zhong Y, Cui L. Li S, et al. Among authors: zhang w, zhang y. Neurol Neuroimmunol Neuroinflamm. 2020 Mar 13;7(3):e705. doi: 10.1212/NXI.0000000000000705. Print 2020 May. Neurol Neuroimmunol Neuroinflamm. 2020. PMID: 32170045 Free PMC article.

7

Neurologic Manifestations as Initial Clinical Presentation of Familial Hemophagocytic Lymphohistiocytosis Type2 Due to PRF1 Mutation in Chinese Pediatric Patients.

Feng WX, Yang XY, Li JW, Gong S, Wu Y, Zhang WH, Han TL, Zhuo XW, Ding CH, Fang F. Feng WX, et al. Front Genet. 2020 Mar 4;11:126. doi: 10.3389/fgene.2020.00126. eCollection 2020. Front Genet. 2020. PMID: 32194620 Free PMC article.

8

Clinical phenotypes, genotypes and treatment in Chinese dystonia patients with KMT2B variants.

Li XY, Dai LF, Wan XH, Guo Y, Dai Y, Li SL, Fang F, Wang XH, Zhang WH, Liu TH, Xie ZH, Fang T, Wang L, Ding CH. Li XY, et al. Parkinsonism Relat Disord. 2020 Aug;77:76-82. doi: 10.1016/j.parkreldis.2020.06.002. Epub 2020 Jun 9. Parkinsonism Relat Disord. 2020. PMID: 32634684

9

[Clinical effect of tacrolimus in the treatment of myasthenia gravis in children].

Li JW, Fang F, Ren XT, Zhang WH, Yang XY, Ren CH, Gong S, Lyu JL, Wang XH, Wang X, Wu HS, Ding CH. Li JW, et al. Zhongguo Dang Dai Er Ke Za Zhi. 2020 Sep;22(9):964-969. doi: 10.7499/j.issn.1008-8830.2004215. Zhongguo Dang Dai Er Ke Za Zhi. 2020. PMID: 32933627 Free PMC article. Chinese.

10

Whole exome sequencing identifies a novel homozygous MECR mutation in a Chinese patient with childhood-onset dystonia and basal ganglia abnormalities, without optic atrophy.

Liu Z, Shimura M, Zhang L, Zhang W, Wang J, Ogawa-Tominaga M, Wang J, Wang X, Lv J, Shi W, Zhang VW, Murayama K, Fang F. Liu Z, et al. Among authors: zhang l, zhang w, zhang vw. Mitochondrion. 2021 Mar;57:222-229. doi: 10.1016/j.mito.2020.12.014. Epub 2021 Jan 2. Mitochondrion. 2021. PMID: 33401012 Free article.

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