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Journal of Advanced Research|December 25, 2025
Parabacteroides goldsteinii mitigates parkinsonism in LRRK2 mutant mice by reducing neuroinflammation through Gut-Brain axisJian-Da Lin, Hsun Li, Chia-Lang Hsu, et al.Journal of Advanced Research|August 15, 2025
Refining antibiotic cocktail regimens for pseudo-germ-free mice and their impact on gut microbiome and pancreatic tumor proteomicsSuraphan Panyod, Wei-Kai Wu, Yen-Peng Lee, et al.Journal of the Formosan Medical Association = Taiwan Yi Zhi|October 28, 2025
Neuronal-specific antibody in patients with multiple system atrophy and progressive supranuclear palsyMimi S Fang, Ming-Chen Tsai, Friederike A Arlt, et al.Movement Disorders : Official Journal of the Movement Disorder Society|March 8, 2025
Update on Treatments for Parkinson's Disease Motor Fluctuations - An International Parkinson and Movement Disorder Society Evidence-Based Medicine ReviewRob M A de Bie, Regina Katzenschlager, Bart E K S Swinnen, et al.Journal of Advanced Research|May 27, 2025
Fibrinogen exacerbates α-synuclein aggregation and mitochondrial dysfunction via alpha5beta3 integrin in Parkinson's diseaseZifeng Huang, Jialing Zheng, Feilan Yuan, et al.Movement Disorders : Official Journal of the Movement Disorder Society|September 27, 2023
Phenotypic Heterogeneity in Patients with Mutations in the Mitochondrial Complex I Assembly Gene NDUFAF5Pin-Shiuan Chen, Ni-Chung Lee, Chieh-Ju Sung, et al.Movement Disorders : Official Journal of the Movement Disorder Society|August 29, 2025
Prevalence of NOTCH2NLC and FMR1 Repeat Expansions in Atypical Parkinsonism Compared to Asymptomatic Elderly IndividualsPin-Shiuan Chen, Yi-Ling Liu, Pu-Tien Chiang, et al.Medrxiv : the Preprint Server for Health Sciences|February 6, 2026
Is <i>SORL1</i> a common genetic target across neurodegenerative diseases?: A multi-ancestry biobank scale assessmentMarzieh Khani, Sheila N Yeboah, Catalina Cerquera-Cleves, et al.Brain : a Journal of Neurology|May 26, 2026
Is SORL1 a common genetic target across neurodegenerative diseases? A multi-ancestry biobank studyMarzieh Khani, Sheila N Yeboah, Catalina Cerquera-Cleves, et al.Brain : a Journal of Neurology|November 3, 2020
Mitochondrial UQCRC1 mutations cause autosomal dominant parkinsonism with polyneuropathyChin-Hsien Lin, Pei-I Tsai, Han-Yi Lin, et al.Pageof 23