Yi-Chu Liao
Overview
Explore the profile of Yi-Chu Liao including associated specialties, affiliations and a list of published articles.
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Snapshot
Articles
172
Citations
2088
Followers
0
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Related Specialties
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Recent Articles
1.
Hsu S, Liao Y, Chung C, Ihara M, Choi J, Tang S, et al.
J Chin Med Assoc
. 2025 Jan;
88(3):189-195.
PMID: 39806999
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is the most common hereditary cerebral small vessel disease caused by mutations in the NOTCH3 gene. This review highlights the...
2.
Liang K, Chen Y, Hsu C, Kao Z, Tsai P, Huang H, et al.
J Chin Med Assoc
. 2024 Dec;
88(3):246-252.
PMID: 39730204
Background: Coronavirus disease 2019 (COVID-19), caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) virus, presents with varying severity among individuals. Both viral and host factors can influence the...
3.
Lee M, Chiu C, Liao Y, Cheng Y, Lee C, Ho C, et al.
Curr Res Food Sci
. 2024 Dec;
9:100917.
PMID: 39628601
For vegetarians or vegan athletes, improving the utilization of plant-based protein and the absorption of amino acids is crucial. This study explored the impact of combining pea protein with TWK10...
4.
Fang S, Hsiao C, Jih K, Tsai Y, Lai K, Chou C, et al.
Ann Clin Transl Neurol
. 2024 Dec;
12(1):158-168.
PMID: 39625954
Objective: The genetic causes of a significant number of patients with cerebellar ataxia remain unsolved. Variations in the ITM2B gene, typically linked to dominantly inherited dementia, can sometimes present with...
5.
Gravesteijn G, Rutten J, Cerfontaine M, Hack R, Liao Y, Jolly A, et al.
JAMA Neurol
. 2024 Nov;
82(1):49-60.
PMID: 39610302
Importance: Typical cysteine-altering NOTCH3 (NOTCH3cys) variants are highly prevalent (approximately 1 in 300 individuals) and are associated with a broad spectrum of small vessel disease (SVD), ranging from early-onset stroke...
6.
Liu Y, Lee C, Liao Y, Huang J, Kuo H, Jih K, et al.
Neurobiol Dis
. 2024 Nov;
202:106715.
PMID: 39490684
Hypermetabolism is a prominent characteristic of ALS patients. Aberrant activation of AMPK, an energy sensor regulated by adiponectin, is known to cause TDP-43 mislocalization, an early event in ALS pathogenesis....
7.
Chen C, Saito S, Lee Y, Kim J, Cheng Y, Liao Y, et al.
Stroke
. 2024 Oct;
55(12):e321-e322.
PMID: 39474712
No abstract available.
8.
Hsiao C, Liao Y, Lee Y
Mov Disord
. 2024 Oct;
39(9):1658-1659.
PMID: 39441135
No abstract available.
9.
Ou Yang W, Tsai Y, Liu Y, Wang Y, Hsiao C, Lai K, et al.
Mult Scler Relat Disord
. 2024 Oct;
92:105923.
PMID: 39418777
Background: Neuromyelitis optica spectrum disorder (NMOSD) is an autoimmune inflammatory disease of the central nervous system, characterized by pathogenic anti-Aquaporin-4 antibodies (AQP4-Ab). Given that infections can trigger autoimmune responses, we...
10.
Liao Y, Hsu S, Hsiao C, Lee Y
Brain
. 2024 Oct;
148(2):e8-e11.
PMID: 39395184
No abstract available.