Zobrazeno 1 - 10
of 70
pro vyhledávání: '"Jingzhe Han"'
Publikováno v:
BMC Neurology, Vol 24, Iss 1, Pp 1-11 (2024)
Abstract Background Identifying the responsible pathogen is crucial for precision medicine in intracranial infections, and Cerebrospinal Fluid (CSF) Metagenomic Next-Generation Sequencing (mNGS) is a reliable method for this detection. However, the i
Externí odkaz:
https://doaj.org/article/7d8a473d9580451f9bc2617e2719ee38
Autor:
Pingping Fang, Jingzhe Han, Di An, Yi Bu, Guang Ji, Mingjuan Liu, Jinliang Deng, Moran Guo, Xu Han, Hongran Wu, Shaojuan Ma, Xueqin Song
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
AimsThe aim of this study was to conduct a bibliometric analysis of the relevant literature on Duchenne muscular dystrophy (DMD) to ascertain its current status, identify key areas of research and demonstrate the evolution of the field.MethodsThe ana
Externí odkaz:
https://doaj.org/article/d24169a9e84e4b208db03d657a266699
Publikováno v:
Journal of International Medical Research, Vol 52 (2024)
Myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) constitutes a group of autoimmune neuroinflammatory conditions that are characterized by positive serum MOG-immunoglobulin G antibodies. The relationship between MOGAD and immune
Externí odkaz:
https://doaj.org/article/6a1a110d6cb444d9b6394c4eafa5649e
Autor:
Xu Han, Guang Ji, Ning Wang, Le Yi, Yafei Mao, Jinliang Deng, Hongran Wu, Shaojuan Ma, Jingzhe Han, Yi Bu, Pingping Fang, Juyi Liu, Fanzhe Sun, Xueqin Song
Publikováno v:
Journal of Translational Medicine, Vol 21, Iss 1, Pp 1-17 (2023)
Abstract Background Duchenne muscular dystrophy (DMD) is an X-linked, incurable, degenerative neuromuscular disease that is exacerbated by secondary inflammation. N6-methyladenosine (m6A), the most common base modification of RNA, has pleiotropic imm
Externí odkaz:
https://doaj.org/article/0a56394f2b394f1cbc07699231e316dd
Publikováno v:
BMC Neurology, Vol 22, Iss 1, Pp 1-4 (2022)
Abstract Background Meningoencephalocele is a rare malformation caused by congenital and acquired lesions. The association between recurrent bacterial meningitis and meningoencephaloceles with cerebrospinal fluid (CSF) leak is reported in the literat
Externí odkaz:
https://doaj.org/article/d9f40e97f3a1471fb75e1ee3ee9a2b24
Autor:
Ning Wang, Xu Han, Shengpu Hao, Jingzhe Han, Xiaomeng Zhou, Shuyan Sun, Jin Tang, Yanpeng Lu, Hongran Wu, Shaojuan Ma, Xueqin Song, Guang Ji
Publikováno v:
BMC Neurology, Vol 22, Iss 1, Pp 1-11 (2022)
Abstract Background Dysferlinopathy is an autosomal recessive muscular dystrophy caused by pathogenic variants in the dysferlin (DYSF) gene. This disease shows heterogeneous clinical phenotypes and genetic characteristics. Methods We reviewed the cli
Externí odkaz:
https://doaj.org/article/b97d9b8897ed4ec1814afd8e66cd1d4c
Publikováno v:
Journal of International Medical Research, Vol 51 (2023)
With the advancement of magnetic resonance imaging (MRI) techniques, general radiographic methods are no longer sufficient for accurately displaying the structure and pathway of cranial nerves. Various sequences, including 3-dimensional sampling perf
Externí odkaz:
https://doaj.org/article/f3c85ff7f0e34f92ac11956579fb16a9
Publikováno v:
Balkan Medical Journal, Vol 39, Iss 4, Pp 290-296 (2022)
Aims: To evaluate the clinical, pathological, and genetic features of patients with riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency (RR-MADD). Methods: Thirty-one patients with RR-MADD admitted to our hospital from January 2005 to N
Externí odkaz:
https://doaj.org/article/47ad360f2b9544d98d50ece04243221c
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
Neuromyelitis optica spectrum disease (NMOSD) is a debilitating autoimmune inflammatory demyelinating disease of the central nervous system. The relationship between harboring an infection and NMOSD is currently unclear and needs further investigatio
Externí odkaz:
https://doaj.org/article/8b931a943aa54909a163b4045c334d70
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
This study reported a case of a Rhino-Orbital-Cerebral Mycosis (ROCM) patient with multiple groups of cranial nerve damage as the primary clinical manifestation, confirmed by histopathology and cerebrospinal fluid metagenomic next-generation sequenci
Externí odkaz:
https://doaj.org/article/5a2be93d0f05459c90685791d3f61d20