Zobrazeno 1 - 10
of 127
pro vyhledávání: '"XIAO Jing-wei"'
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 11, Iss 5, Pp 1267-1279 (2024)
Abstract Objective The pathological features of immune‐mediated necrotizing myopathy (IMNM) are dominated by the infiltration of macrophages. We aimed to perform a histopathologic semiquantitative analysis to investigate the relationship between ma
Externí odkaz:
https://doaj.org/article/a95497e58cb44b76b9a911de26a45aa0
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
Brachio-cervical inflammatory myopathy (BCIM) is a rare inflammatory myopathy characterized by dysphagia, bilateral upper limb atrophy, limb-girdle muscle weakness, and myositis-specific antibody (MSA) negativity. BCIM has a low incidence and is comm
Externí odkaz:
https://doaj.org/article/da35c5eade2b46148399dff97aca5b93
Publikováno v:
In Chinese Journal of Traumatology November 2022 25(6):345-352
Autor:
Xiao-jing Wei, Hui Sun, Jing Miao, Ru-qing Qiu, Zong-zhi Jiang, Zhen-wei Ma, Wei Sun, Xue-fan Yu
Publikováno v:
Frontiers in Neurology, Vol 14 (2023)
IntroductionRimmed vacuolar myopathies (RVMs) are a group of genetically heterogeneous diseases that share histopathological characteristics on muscle biopsy, including the aberrant accumulation of autophagic vacuoles. However, the presence of non-co
Externí odkaz:
https://doaj.org/article/d9428fef048a417ea86d172cfb4eab06
Publikováno v:
China Journal of Orthopaedics & Traumatology / Zhongguo Gu Shang; 2024, Vol. 37 Issue 3, p319-326, 8p
Publikováno v:
BMC Neurology, Vol 18, Iss 1, Pp 1-5 (2018)
Abstract Background Filamin C-related myofibrillar myopathies (MFM) are progressive skeletal myopathies with an autosomal dominant inheritance pattern. The conditions are caused by mutations of the filamin C gene (FLNC) located in the chromosome 7q32
Externí odkaz:
https://doaj.org/article/aa6f8e4e8d75445eb91723aa68970d16
Publikováno v:
EXPLORE. 18:608-611
Background Herpes zoster presents as clustered blisters on one side of the body, accompanied by nerve pain. This is caused by reactivation of the varicella zoster virus, and it occurs primarily in people with weakened immunity. Tumor and chemotherapy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2de758e28d959dc696055fabdb385c10
https://doi.org/10.1016/j.explore.2021.08.003
https://doi.org/10.1016/j.explore.2021.08.003
Autor:
Xiao‐Jing Wei, Bingxiang Xue, Jens Handelmann, Zhiyong Hu, Heidar Darmandeh, Viktoria H. Gessner, Lukas J. Gooßen
Publikováno v:
Advanced Synthesis & Catalysis. 364:3336-3341
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e839fd3f7d4147566ab1949160b466a1
https://doi.org/10.1002/adsc.202200321
https://doi.org/10.1002/adsc.202200321
Publikováno v:
BMC Neurology, Vol 18, Iss 1, Pp 1-3 (2018)
Abstract Background Autosomal recessive Myotonia congenita (Becker’s disease) is caused by mutations in the CLCN1 gene. The condition is characterized by muscle stiffness during sustained muscle contraction and variable degree of muscle weakness th
Externí odkaz:
https://doaj.org/article/6c699af1d7d4443784cdba2ecd203953
Publikováno v:
Life, Vol 11, Iss 4, p 361 (2021)
Next-generation sequencing (NGS) technology has led to great advances in understanding the causes of Mendelian and complex neurological diseases. Owing to the complexity of genetic diseases, the genetic factors contributing to many rare and common ne
Externí odkaz:
https://doaj.org/article/9cf695fbc4104b54a92baa974ca1460c