NeuralCipher Source record
Crystallizing the Parkinson’s Disease Protein LRRK2 Under Microgravity Conditions
DOI: 10.1101/259655
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190.851 articles found
Open access
Antioxidant and Cell-Signaling Functions of Hydrogen Sulfide in the Central Nervous System.
DOI: 10.1155/2018/1873962PMID: 29507650
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
Open access
CLOCK 3111T/C Variant Correlates with Motor Fluctuation and Sleep Disorders in Chinese Patients with Parkinson's Disease.
DOI: 10.1155/2018/4670380PMID: 29535854
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
Open access
Prevalence and Clinical Characteristics of Probable REM Behavior Disorder in Thai Parkinson's Disease Patients.
DOI: 10.1155/2018/7657191PMID: 29535855
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
Open access
Early fine motor impairment and behavioral dysfunction in (Thy-1)-h[A30P] alpha-synuclein mice.
DOI: 10.1002/brb3.915PMID: 29541535
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Carvacrol prevents impairments in motor and neurochemical parameters in a model of progressive parkinsonism induced by reserpine.
DOI: 10.1016/j.brainresbull.2018.01.017PMID: 29378222
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Glucocerebrosidase and Parkinson Disease: Molecular, Clinical, and Therapeutic Implications.
DOI: 10.1177/1073858417748875PMID: 29400127
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FOXO in Neural Cells and Diseases of the Nervous System.
DOI: 10.1016/bs.ctdb.2017.10.002PMID: 29433734
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Surgical treatment of spinal disorders in Parkinson's disease.
DOI: 10.1007/s00586-018-5499-yPMID: 29397444
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Binding of alpha-synuclein to partially oxidized glyceraldehyde-3-phosphate dehydrogenase induces subsequent inactivation of the enzyme.
DOI: 10.1016/j.abb.2018.02.002PMID: 29408361
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Combination of CDNF and Deep Brain Stimulation Decreases Neurological Deficits in Late-stage Model Parkinson's Disease.
DOI: 10.1016/j.neuroscience.2018.01.052PMID: 29408408
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CSF lamp2 concentrations are decreased in female Parkinson's disease patients with LRRK2 mutations.
DOI: 10.1016/j.brainres.2018.01.016PMID: 29456132
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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