Showing 1 - 9 results of 9 for search 'Yaye Wang', query time: 0.03s Refine Results
  1. 1
    MORC2 p.R252W Mutant Axonal Charcot–Marie–Tooth Disease Causes Peripheral Neuropathies and Pathological Myofiber Destruction

    MORC2 p.R252W Mutant Axonal Charcot–Marie–Tooth Disease Causes Peripheral Neuropathies and Pathological Myofiber Destruction by Yaye Wang, Jingzhe Han, Jinru Zhang, Yue Wu, Xueqin Song

    Published 2022-05-01
    Get full text
    Article
  2. 2
    Case report: Meningoencephalocele and recurrent bacterial meningitis in chronic idiopathic intracranial hypertension

    Case report: Meningoencephalocele and recurrent bacterial meningitis in chronic idiopathic intracranial hypertension by Jinru Zhang, Jianchao Wu, Yue Wu, Yaye Wang, Jingzhe Han

    Published 2022-11-01
    Get full text
    Article
  3. 3
    A family with riboflavin-reactive lipid deposition myopathy caused by a novel compound heterozygous mutation in the electron transfer flavoprotein dehydrogenase gene

    A family with riboflavin-reactive lipid deposition myopathy caused by a novel compound heterozygous mutation in the electron transfer flavoprotein dehydrogenase gene by Yue Wu, Jingzhe Han, Yaye Wang, Jinru Zhang, Xueqin Song, Guang Ji

    Published 2020-11-01
    Get full text
    Article
  4. 4
    A case of reversible splenial lesion syndrome secondary to Fanconi syndrome with white matter swelling as the main manifestation

    A case of reversible splenial lesion syndrome secondary to Fanconi syndrome with white matter swelling as the main manifestation by Jingzhe Han, Yaye Wang, Yue Wu, Jinru Zhang, Xueqin Song, Guang Ji

    Published 2021-01-01
    Get full text
    Article
  5. 5
    Formation of chlorate and perchlorate during electrochemical oxidation by Magnéli phase Ti4O7 anode: inhibitory effects of coexisting constituents

    Formation of chlorate and perchlorate during electrochemical oxidation by Magnéli phase Ti4O7 anode: inhibitory effects of coexisting constituents by Lu Wang, Yaye Wang, Yufei Sui, Junhe Lu, Baowei Hu, Qingguo Huang

    Published 2022-09-01
    Get full text
    Article
  6. 6
    A novel splice‐site mutation in CHMP2B associated with frontotemporal dementia: The first report from China and literature review

    A novel splice‐site mutation in CHMP2B associated with frontotemporal dementia: The first report from China and literature review by Chang Li, Ya Wen, Mengqiu Zhao, Yaye Wang, Ping Li, Liang Wang, Shan Wang

    Published 2023-08-01
    Get full text
    Article
  7. 7
    Characterization of 31 Patients with Riboflavin-Responsive Multiple acyl-CoA Dehydrogenase Deficiency

    Characterization of 31 Patients with Riboflavin-Responsive Multiple acyl-CoA Dehydrogenase Deficiency by Jinru Zhang, Jingzhe Han, Yaye Wang, Yue Wu, Lixia Ma, Xueqin Song, Guang Ji

    Published 2022-07-01
    Get full text
    Article
  8. 8
    A novel compound heterozygous SPG7 variant is associated with progressive spastic ataxia and persecutory delusions found in Chinese patients: two case reports

    A novel compound heterozygous SPG7 variant is associated with progressive spastic ataxia and persecutory delusions found in Chinese patients: two case reports by Shan Wang, Yaye Wang, Yue Wu, Jinru Zhang, Weilin Zhang, Chang Li, Xueqin Song

    Published 2022-05-01
    Get full text
    Article
  9. 9
    Case Report: A Novel Splice-Site Mutation in DNAJB6 Associated With Juvenile-Onset Proximal–Distal Myopathy in a Chinese Patient

    Case Report: A Novel Splice-Site Mutation in DNAJB6 Associated With Juvenile-Onset Proximal–Distal Myopathy in a Chinese Patient by Guang Ji, Guang Ji, Ning Wang, Ning Wang, Xu Han, Xu Han, Yaye Wang, Yaye Wang, Jinru Zhang, Jinru Zhang, Yue Wu, Yue Wu, Hongran Wu, Hongran Wu, Shaojuan Ma, Shaojuan Ma, Xueqin Song, Xueqin Song

    Published 2022-06-01
    Get full text
    Article

Search Tools: