Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Zong-Zhi Jiang"'
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:
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
Publikováno v:
Shanghai Jiaotong Daxue xuebao, Vol 57, Iss 11, Pp 1410-1420 (2023)
The slamming process of two-dimensional structures under free fall condition with arbitrary symmetrical shapes is investigated by combining various analytical models for slamming and the precise integration method in the time domain. By closely analy
Externí odkaz:
https://doaj.org/article/e1d1c6307984474cb4154daa2ce3ae38
Publikováno v:
World Journal of Clinical Cases
Background Neuronal intranuclear inclusion disease (NIID) is an unusual autosomal dominant, chronic progressive neurodegenerative disease. The clinical manifestations of NIID are complex and varied, complicating its clinical diagnosis. To the best of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d05facea8946093af314cf52a3ed95d
https://doi.org/10.12998/wjcc.v8.i23.6115
https://doi.org/10.12998/wjcc.v8.i23.6115
Publikováno v:
Multiple Sclerosis and Related Disorders. 46:102491
Anti-synthetase syndrome (ASS) is a rare autoimmune disorder characterized by the presence of antibodies against aminoacyl-transfer RNA synthetase commonly associated inflammatory myopathy. In this case report, we describe an adult female with NMOSD
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::584799bada3a6f6f3371aa8b7ef94fae
https://doi.org/10.1016/j.msard.2020.102491
https://doi.org/10.1016/j.msard.2020.102491