Yo-Tsen Liu
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Explore the profile of Yo-Tsen Liu including associated specialties, affiliations and a list of published articles.
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Articles
46
Citations
762
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0
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Recent Articles
1.
Feng Y, Agrawal S, Yang C, Chang H, Kuo L, Yu W, et al.
Chem Asian J
. 2024 Dec;
20(4):e202401438.
PMID: 39668552
Transthyretin (TTR), a homo-tetrameric protein encoded by the TTR gene, can lead to amyloid diseases when destabilized by mutations. The TTR-Ala97Ser (A97S) mutation is the predominant pathogenic variant found in...
2.
Tsai L, Ting C, Liu Y, Hsiao C, Weng W
Acta Neurol Taiwan
. 2024 Oct;
33(3):81-88.
PMID: 39363429
Spinal muscular atrophy (SMA) is an autosomal recessive motor neuron disease characterized by progressive weakness and atrophy of skeletal muscles. With homozygous survival motor neuron 1 (SMN1) gene mutation, all...
3.
Zhou J, Wang R, Liu Y, Cheng S, Liu H, Yang Y
J Neurol Phys Ther
. 2024 Aug;
48(4):188-197.
PMID: 39164804
Background And Purpose: Dual-task walking is challenging for people with Parkinson disease (PD). Gait performance worsens while executing dual tasks, possibly due to a decline in executive function (EF). This...
4.
Lin J, Lu C, Hu Y, Yang H, Liu Y, Loo J, et al.
Eur Radiol
. 2023 Aug;
34(1):588-599.
PMID: 37553487
Objectives: Angioarchitectural analysis of brain arteriovenous malformations (BAVMs) is qualitative and subject to interpretation. This study quantified the morphology of and signal changes in the nidal and perinidal areas by...
5.
Chang L, Chi N, Chen C, Lin Y, Hsu S, Tsai J, et al.
Cell Mol Neurobiol
. 2022 Dec;
43(6):2769-2783.
PMID: 36580209
Whole exome sequencing (WES) has been used to detect rare causative variants in neurological diseases. However, the efficacy of WES in genetic diagnosis of clinically heterogeneous familial stroke remains inconclusive....
6.
Liu Y, Lee C, Lin C, Wu H, Guo W, Yang H, et al.
Mol Neurobiol
. 2022 Jul;
59(10):5925-5934.
PMID: 35831556
Both angiogenesis and inflammation contribute to activation of matrix metalloproeteinase-9 (MMP-9), which dissolves the extracellular matrix, disrupts the blood-brain barrier, and plays an important role in the pathogenesis of brain...
7.
Lu Y, Hsu C, Liu Y, Chan C, Chuang Y, Lin C, et al.
Biomed J
. 2022 Jun;
45(3):542-548.
PMID: 35660364
Background: Periventricular nodular heterotopia (PVNH) is caused by abnormal neuronal migration, resulting in the neurons accumulate as nodules along the surface of the lateral ventricles. PVNH often cause epilepsy, psychomotor...
8.
Shih Y, Chou C, Peng S, Yu H, Hsu S, Lin C, et al.
Epilepsia
. 2022 May;
63(8):2056-2067.
PMID: 35593439
Objective: Cerebral cavernous malformations (CCMs) present variably, and epileptic seizures are the most common symptom. The factors contributing to cavernoma-related epilepsy (CRE) and drug resistance remain inconclusive. The outcomes of...
9.
Lin J, Cheng J, Liu Y, Hsu T, Lin K, Chen C, et al.
Epilepsia
. 2022 Feb;
63(5):1253-1265.
PMID: 35213059
Objective: Pathogenic variants in DCX on the X chromosome lead to lissencephaly and subcortical band heterotopia (SBH), brain malformations caused by neuronal migration defects. Its product doublecortin (DCX) binds to...
10.
Chou C, Lin P, Yen D, Yu H, Kwan S, Chen C, et al.
Epilepsy Behav
. 2021 Feb;
117:107846.
PMID: 33626492
Introduction: Acute withdrawal of antiepileptic drugs (AEDs) is a safe and effective approach to provoking seizures in order to complete video-electroencephalogram (V-EEG) studies in a timely manner. Previous studies have...