Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Yung-Tsai Chu"'
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-9 (2024)
Abstract Polymorphisms in the PSAP gene, which encodes prosaposin and is involved in the lysosomal function, yielded conflicting results regarding the association with Parkinson’s disease (PD). Therefore, this study aims to investigate the role of
Externí odkaz:
https://doaj.org/article/682293816fc8484d81bd86e004fba66d
Publikováno v:
Frontiers in Neurology, Vol 14 (2023)
BackgroundCerebral amyloid angiopathy-related inflammation (CAA-ri) is a clinical syndrome characterized by MRI findings of amyloid-related imaging abnormalities-edema (ARIA-E) suggestive of autoimmune and inflammatory reaction and hemorrhagic eviden
Externí odkaz:
https://doaj.org/article/358e6cb1efed48c3a18fc0a908a49d0e
Publikováno v:
BMC Neurology, Vol 20, Iss 1, Pp 1-10 (2020)
Abstract Background Phospholipase A2 group VI (PLA2G6) mutations associated with neurodegeneration (PLAN) manifest as heterogeneous neurodegenerative disorders with variable ages of onset. The genotype-phenotype correlation is not well-established. W
Externí odkaz:
https://doaj.org/article/d3d809cc09e942bba8c58746441f491a
Autor:
Chih‐Hao Chen, Yung‐Tsai Chu, Ya‐Fang Chen, Tzu‐Yu Ko, Yu‐Wen Cheng, Ming‐Jen Lee, Pei‐Lung Chen, Sung‐Chun Tang, Jiann‐Shing Jeng
Publikováno v:
European journal of neurologyREFERENCES. 29(11)
The NOTCH3 mutation is a common cause of hereditary cerebral small vessel disease (CSVD) and may be a cause of spontaneous intracerebral haemorrhage (ICH). The aim was to investigate the clinical/imaging features for identifying the NOTCH3-mutation-r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5177872c1b103d35968167eee00fa62f
https://pubmed.ncbi.nlm.nih.gov/35781912
https://pubmed.ncbi.nlm.nih.gov/35781912
Publikováno v:
BMC Neurology, Vol 20, Iss 1, Pp 1-10 (2020)
BMC Neurology
BMC Neurology
Background Phospholipase A2 group VI (PLA2G6) mutations associated with neurodegeneration (PLAN) manifest as heterogeneous neurodegenerative disorders with variable ages of onset. The genotype-phenotype correlation is not well-established. We aim to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::128b1a0859be4984241f18b90654409c
http://link.springer.com/article/10.1186/s12883-020-01684-6
http://link.springer.com/article/10.1186/s12883-020-01684-6
Publikováno v:
Acta neurologica Taiwanica. 30
Parkinson' disease (PD) is a common neurodegenerative disease with the pathological hallmark of alpha-synuclein aggregation within dopaminergic neurons. The etiology of PD comes from a complex interplay between genetic and environmental factors. Thou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fca6acabf34291b2093489cc5eeec92e
https://pubmed.ncbi.nlm.nih.gov/34841503
https://pubmed.ncbi.nlm.nih.gov/34841503
Autor:
Kang Po Lee, Pi Shan Sung, Chung-Wei Lee, Chih-Hao Chen, Li-Kai Tsai, Yen-Heng Lin, Jiann-Shing Jeng, Yung Tsai Chu, Sung-Chun Tang
Publikováno v:
Stroke. 51(12)
Background and Purpose: Contrast-induced encephalopathy (CIE) is a rare and underrecognized complication after endovascular thrombectomy (EVT) for acute ischemic stroke. This study investigated the incidence and risk factors of CIE in patients who un
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30a2c6d0e5929310e4419bfea62e09f2
https://pubmed.ncbi.nlm.nih.gov/33121385
https://pubmed.ncbi.nlm.nih.gov/33121385
Additional file 1 Supplementary Table 1. The 40 candidate genes involved in PD and related neurodegenerative disorders that were used for targeted NGS in the study.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::16d21e9270c8e31ee76353616cd10070
