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The phenotypic spectrum of COX20-associated mitochondrial disorder.
Ban R, Kopajtich R, Lv J, Stenton SL, Shimura M, Wang Z, Yuan Y, Wang J, Han X, Liu Z, Shi Q, Pu C, Prokisch H, Fang F, Elstner M. Ban R, et al. Among authors: lv j. Brain. 2022 Dec 19;145(12):e125-e127. doi: 10.1093/brain/awac344. Brain. 2022. PMID: 36136859 No abstract available.
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: lv j. Mitochondrion. 2021 Mar;57:222-229. doi: 10.1016/j.mito.2020.12.014. Epub 2021 Jan 2. Mitochondrion. 2021. PMID: 33401012 Free article.
Age-dependent characteristics and prognostic factors of pediatric anti-N-methyl-d-aspartate receptor encephalitis in a Chinese single-center study.
Zhang W, Ren C, Wang X, Li J, Ding C, Han T, Lv J, Chen C, Gong S, Xiuwei Z, Dai L, Feng W, Yang X, Zhang S, Zhou J, Ren H, Guan H, Ren X, Fang F. Zhang W, et al. Among authors: lv j. Eur J Paediatr Neurol. 2021 Sep;34:67-73. doi: 10.1016/j.ejpn.2021.07.004. Epub 2021 Jul 9. Eur J Paediatr Neurol. 2021. PMID: 34399369
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: lv jl. Ann Neurol. 2022 Apr;91(4):466-482. doi: 10.1002/ana.26313. Epub 2022 Mar 6. Ann Neurol. 2022. PMID: 35094435
7,458 results