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Pei-Shan Wang

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Articles 31
Citations 355
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Recent Articles
1.
Wei Q, Fan W, Li H, Wang P, Wanga P, Xu M, et al.
J Genet Genomics . 2025 Jan; PMID: 39814172
Hereditary spastic paraplegias (HSPs) refer to a genetically and clinically heterogeneous group of neurodegenerative disorders characterized by the degeneration of motor neurons. To date, a significant number of patients still...
2.
Chen L, Zhang M, Xu H, Ye H, Chen D, Wang P, et al.
Research (Wash D C) . 2024 Dec; 7:0548. PMID: 39664295
Disease-associated microglia (DAM) are observed in neurodegenerative diseases, demyelinating disorders, and aging. However, the spatiotemporal dynamics and evolutionary trajectory of DAM during the progression of amyotrophic lateral sclerosis (ALS) remain...
3.
Wang P, Yang X, Wei Q, Lv Y, Wu Z, Li H
Ann Med . 2024 Oct; 56(1):2407522. PMID: 39351695
Objective: In the Asian population, variants are the most common cause of amyotrophic lateral sclerosis (ALS). To date, more than 200 variants have been reported in . This study aimed...
4.
Wei Q, Yu H, Wang P, Xie J, Dong H, Wu Z, et al.
CNS Neurosci Ther . 2023 Nov; 30(4):e14529. PMID: 38013626
Introduction: Hereditary spastic paraplegias (HSPs) comprise a group of neurodegenerative disorders characterized by progressive degeneration of upper motor neurons. Homozygous or compound heterozygous variants in COQ4 have been reported to...
5.
Liu G, Li N, Meng R, Wang P
Zhongguo Zhen Jiu . 2023 Jul; 43(7):743-6. PMID: 37429651
Objective: To observe the effect of buccal acupuncture on pain after lumbar spinal fusion. Methods: Sixty patients undergoing lumbar spinal fusion were randomly divided into an observation group (30 cases,...
6.
Chou F, Chen C, Lee A, Wang P
Front Cell Dev Biol . 2022 Jul; 10:821848. PMID: 35903551
Individuals with intrauterine growth restriction (IUGR) are at an increased risk for neurodevelopmental impairment. Fetal cortical neurogenesis is a time-sensitive process in which fetal neural stem cells (NSCs) follow a...
7.
Wei Q, Wang P, Dong H, Luo W, Wu Z, Li H
Mol Genet Genomic Med . 2022 Mar; 10(5):e1927. PMID: 35347897
No abstract available.
8.
Chen L, Xu H, Wang P, Yang X, Wu Z, Li H
Front Genet . 2021 Nov; 12:746060. PMID: 34721532
Mutations in superoxide dismutase 1 gene () are the most frequent high penetrant genetic cause for amyotrophic lateral sclerosis (ALS) in the Chinese population. A detailed natural history of -mutated...
9.
Wei Q, Luo W, Yu H, Wang P, Dong H, Li H, et al.
J Genet Genomics . 2021 Aug; 48(8):751-754. PMID: 34384721
No abstract available.
10.
Chou F, Newton K, Wang P
Genes (Basel) . 2021 Mar; 12(3). PMID: 33668810
Gestational hypertensive disorders continue to threaten the well-being of pregnant women and their offspring. The only current definitive treatment for gestational hypertensive disorders is delivery of the fetus. The optimal...