NeuralCipher Open access
Apolipoprotein E Alleles and Motor Signs in Older Adults with Alzheimer's Dementia.
DOI: 10.3390/ijms26178562PMID: 40943487
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190.749 articles found
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Relationship Between Each of the Four Major Motor Symptoms and At-Home Physical Activity in Individuals with Parkinson's Disease: A Cross-Sectional Study.
DOI: 10.3390/neurolint17090139PMID: 41002927
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
Open access
The Evolution of Functional Amyloids and Their Impact on Host-Microbe Interactions.
DOI: 10.1002/advs.202510109PMID: 40899597
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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Stress-induced nuclear GAPDH: Scientific update and clinical application.
DOI: 10.1016/j.neurot.2025.e00725PMID: 40903341
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From adaptive deep brain stimulation to adaptive circuit targeting.
DOI: 10.1038/s41582-025-01131-5PMID: 40903613
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Altered Cortical Gyrification, Functional Connections, and Underlying Neurotransmitter Information in Patients with Parkinson's Disease with Levodopa-Induced Dyskinesia.
DOI: 10.1007/s40120-025-00823-wPMID: 40903696
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Dynamic cortical inhibition imbalance as a biomarker of clinical progression in early Parkinson's disease.
DOI: 10.1016/j.nbd.2025.107083PMID: 40912410
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Allosteric regulation of the Golgi-localized PPM1H phosphatase by Rab GTPases modulates LRRK2 substrate dephosphorylation in Parkinson's disease.
DOI: 10.1016/j.jbc.2025.110679PMID: 40912655
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Enzyme Activity-Based Genome-wide Screening for Modifiers of Lysosomal Glucocerebrosidase Uncovers Candidate Risk Factors for Parkinson's Disease.
DOI: 10.1021/acscentsci.5c00240PMID: 41142333
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Transcutaneous Spinal Magnetic Stimulation Affects Subthalamic Activity in Parkinson's Disease.
DOI: 10.1002/mds.70035PMID: 40899224
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Frailty in Patients With Parkinson's Disease in Community and Clinical Settings: A Scoping Review.
DOI: 10.1177/01939459251365725PMID: 40899376
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Faster disease progression in Parkinson's disease with glucocerebrosidase genotype: But not apparent immediate from diagnosis.
DOI: 10.1177/1877718x251361507PMID: 40899843
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