Lin Y - Search Results

1

Mitochondrial myopathy without extraocular muscle involvement: a unique clinicopathologic profile.

Lin Y, Wang J, Ren H, Ma X, Wang W, Zhao Y, Xu Z, Liu S, Wang W, Xu X, Wang B, Zhao D, Wang D, Li W, Liu F, Zhao Y, Lu J, Yan C, Ji K. Lin Y, et al. J Neurol. 2024 Feb;271(2):864-876. doi: 10.1007/s00415-023-12005-5. Epub 2023 Oct 17. J Neurol. 2024. PMID: 37847292

2

A different pattern of clinical, muscle pathology and brain MRI findings in MELAS with mt-ND variants.

Wang W, Zhao Y, Xu X, Ma X, Sun Y, Lin Y, Zhao Y, Xu Z, Wang J, Ren H, Wang B, Zhao D, Wang D, Liu F, Li W, Yan C, Ji K. Wang W, et al. Among authors: lin y. Ann Clin Transl Neurol. 2023 Jun;10(6):1035-1045. doi: 10.1002/acn3.51787. Epub 2023 May 23. Ann Clin Transl Neurol. 2023. PMID: 37221696 Free PMC article.

3

A Missense Variant in AIFM1 Caused Mitochondrial Dysfunction and Intolerance to Riboflavin Deficiency.

Zhao Y, Lin Y, Wang B, Liu F, Zhao D, Wang W, Ren H, Wang J, Xu Z, Yan C, Ji K. Zhao Y, et al. Among authors: lin y. Neuromolecular Med. 2023 Dec;25(4):489-500. doi: 10.1007/s12017-023-08750-5. Epub 2023 Aug 21. Neuromolecular Med. 2023. PMID: 37603145

4

Mitochondrial Dysfunction due to Novel COQ8A Variation with Poor Response to CoQ10 Treatment: A Comprehensive Study and Review of Literatures.

Wang J, Lin Y, Xu Z, Yan C, Zhao Y, Ji K. Wang J, et al. Among authors: lin y. Cerebellum. 2024 Oct;23(5):1824-1838. doi: 10.1007/s12311-024-01671-4. Epub 2024 Mar 2. Cerebellum. 2024. PMID: 38429489 Review.

5

HiFi long-read amplicon sequencing for full-spectrum variants of human mtDNA.

Lin Y, Wang J, Xu R, Xu Z, Wang Y, Pan S, Zhang Y, Tao Q, Zhao Y, Yan C, Cao Z, Ji K. Lin Y, et al. BMC Genomics. 2024 May 31;25(1):538. doi: 10.1186/s12864-024-10433-9. BMC Genomics. 2024. PMID: 38822239 Free PMC article.

6

Targeting DRP1 with Mdivi-1 to correct mitochondrial abnormalities in ADOA+ syndrome.

Lin Y, Wang D, Li B, Wang J, Xu L, Sun X, Ji K, Yan C, Liu F, Zhao Y. Lin Y, et al. JCI Insight. 2024 Jun 25;9(15):e180582. doi: 10.1172/jci.insight.180582. JCI Insight. 2024. PMID: 38916953 Free PMC article.

7

Correction: HiFi long-read amplicon sequencing for full-spectrum variants of human mtDNA.

Lin Y, Wang J, Xu R, Xu Z, Wang Y, Pan S, Zhang Y, Tao Q, Zhao Y, Yan C, Cao Z, Ji K. Lin Y, et al. BMC Genomics. 2024 Jul 30;25(1):745. doi: 10.1186/s12864-024-10660-0. BMC Genomics. 2024. PMID: 39080517 Free PMC article. No abstract available.

8

Queuine ameliorates impaired mitochondrial function caused by mt-tRNA^Asn variants.

Lin Y, Wang J, Zhuang X, Zhao Y, Wang W, Wang D, Zhao Y, Yan C, Ji K. Lin Y, et al. J Transl Med. 2024 Aug 22;22(1):780. doi: 10.1186/s12967-024-05574-0. J Transl Med. 2024. PMID: 39175050 Free PMC article.

9

Clinical and Imaging Prognosis in Patients with Delayed Encephalopathy after Acute Carbon Monoxide Poisoning.

Liu J, Si Z, Liu J, Lin Y, Yuan J, Xu S, He Y, Zhang T, Wang A. Liu J, et al. Among authors: lin y. Behav Neurol. 2020 Dec 7;2020:1719360. doi: 10.1155/2020/1719360. eCollection 2020. Behav Neurol. 2020. PMID: 33376556 Free PMC article.

10

An incomplete LEOPARD syndrome presented with generalized lentigines.

Wang T, Lin Y, Sun L, Mao L, Gao X, Liu X, Liu H. Wang T, et al. Among authors: lin y. J Cosmet Dermatol. 2024 Feb;23(2):711-713. doi: 10.1111/jocd.15991. Epub 2023 Sep 16. J Cosmet Dermatol. 2024. PMID: 37715542 No abstract available.

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