Hasil Pencarian - Xue‐Fan Yu

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  1. 1
    Inflammatory checkpoints in amyotrophic lateral sclerosis: From biomarkers to therapeutic targets

    Inflammatory checkpoints in amyotrophic lateral sclerosis: From biomarkers to therapeutic targets oleh Zongzhi Jiang, Ziyi Wang, Xiaojing Wei, Xue-Fan Yu

    Diterbitkan 2022-12-01
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  2. 2
    The pathogenesis of anti-signal recognition particle necrotizing myopathy: A Review

    The pathogenesis of anti-signal recognition particle necrotizing myopathy: A Review oleh Ruqing Qiu, Ziyi Wang, Xiaojing Wei, Hui Sui, Zongzhi Jiang, Xue-fan Yu

    Diterbitkan 2022-12-01
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  3. 3
    Let-7a gene knockdown protects against cerebral ischemia/reperfusion injury

    Let-7a gene knockdown protects against cerebral ischemia/reperfusion injury oleh Zhong-kun Wang, Fang-fang Liu, Yu Wang, Xin-mei Jiang, Xue-fan Yu

    Diterbitkan 2016-01-01
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  4. 4
    CD163+ macrophage density in perimysial connective tissue associated with prognosis in IMNM

    CD163+ macrophage density in perimysial connective tissue associated with prognosis in IMNM oleh Hui Sun, Zi‐Yi Wang, Ye Han, Xiao‐Jing Wei, Yong‐Chun Wang, Xue‐Fan Yu

    Diterbitkan 2024-05-01
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  5. 5
    A case report: a heterozygous deletion (2791_2805 del) in exon 18 of the filamin C gene causing filamin C-related myofibrillar myopathies in a Chinese family

    A case report: a heterozygous deletion (2791_2805 del) in exon 18 of the filamin C gene causing filamin C-related myofibrillar myopathies in a Chinese family oleh Jing Miao, Fei-fei Su, Xue-mei Liu, Xiao-jing Wei, Yun Yuan, Xue-fan Yu

    Diterbitkan 2018-06-01
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  6. 6
    Case report: A patient with brachio-cervical inflammatory myopathy was misdiagnosed as flail arm syndrome

    Case report: A patient with brachio-cervical inflammatory myopathy was misdiagnosed as flail arm syndrome oleh Hui Sun, Xiao-Jing Wei, Ye Han, Yong-Chun Wang, Zi-Yi Wang, Xue-Fan Yu

    Diterbitkan 2024-07-01
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  7. 7
    A case report: autosomal recessive Myotonia congenita caused by a novel splice mutation (c.1401 + 1G > A) in CLCN1 gene of a Chinese Han patient

    A case report: autosomal recessive Myotonia congenita caused by a novel splice mutation (c.1401 + 1G > A) in CLCN1 gene of a Chinese Han patient oleh Jing Miao, Xiao-jing Wei, Xue-mei Liu, Zhi-xia Kang, Yan-lu Gao, Xue-fan Yu

    Diterbitkan 2018-09-01
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  8. 8
    Next-Generation Sequencing Technologies and Neurogenetic Diseases

    Next-Generation Sequencing Technologies and Neurogenetic Diseases oleh Hui Sun, Xiao-Rong Shen, Zi-Bing Fang, Zong-Zhi Jiang, Xiao-Jing Wei, Zi-Yi Wang, Xue-Fan Yu

    Diterbitkan 2021-04-01
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  9. 9
    Clinical-pathological features and muscle imaging findings in 36 Chinese patients with rimmed vacuolar myopathies: case series study and review of literature

    Clinical-pathological features and muscle imaging findings in 36 Chinese patients with rimmed vacuolar myopathies: case series study and review of literature oleh Xiao-jing Wei, Hui Sun, Jing Miao, Ru-qing Qiu, Zong-zhi Jiang, Zhen-wei Ma, Wei Sun, Xue-fan Yu

    Diterbitkan 2023-04-01
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