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Loss of FBXO7 (PARK15) leads to disturbances in proteasomal function and models parkinsonism-like and pyramidal symptoms in mice
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Loss of heart rate variability in ALS: Time and frequency domain assessment
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Lovastatin protects neurite degeneration in LRRK2-G2019S parkinsonism through activating the Akt/Nrf pathway and inhibiting GSK3beta activity
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Low cerebrospinal fluid 3,4-dihydroxyphenylacetic acid and 3,4-dihydroxyphenylglycol levels are biomarkers of Parkinsonian disorders, including PSP
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Lower levels of uric acid and striatal dopamine in non-tremor dominant Parkinson’s disease subtype
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Lrrk2 alleles modify host response to microbial infections
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LRRK2 G2019S mutation carrier with an unusual phenotype: Progressive logopenic aphasia
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LRRK2, MAPT and HTRA2 mutations in the pedigree of familial neurodegenerative parkinsonism with cognitive deterioration spanning five generations in a genetically isolated population of south-eastern Moravia, Czech Republic
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LSVT-BIG© case studies: A snapshot of observations
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Lymphocytes have a detrimental effect on motor behavior in the AAV1/2 A53T α-synuclein mouse model of Parkinson’s disease
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