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Guidelines for the use and interpretation of assays for monitoring autophagyGuidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)Genome-wide association study reveals genetic risk underlying Parkinson's diseaseAiming for Study Comparability in Parkinson's Disease: Proposal for a Modular Set of Biomarker Assessments to be Used in Longitudinal StudiesProdromal Markers in Parkinson's Disease: Limitations in Longitudinal Studies and Lessons LearnedKnockdown of Hsc70-5/mortalin induces loss of synaptic mitochondria in a Drosophila Parkinson's disease modelIdentification and functional characterization of a novel R621C mutation in the synphilin-1 gene in Parkinson's diseaseMutation analysis of the neurofilament M gene in Parkinson's diseaseLoss of function mutations in the gene encoding Omi/HtrA2 in Parkinson's diseaseThe role of synphilin-1 in synaptic function and protein degradationReduced basal autophagy and impaired mitochondrial dynamics due to loss of Parkinson's disease-associated protein DJ-1Effects of subthalamic nucleus stimulation on emotional prosody comprehension in Parkinson's disease.Lack of replication of thirteen single-nucleotide polymorphisms implicated in Parkinson's disease: a large-scale international study.Therapeutic strategies for Parkinson's disease based on data derived from genetic research.[Somatoform disorder or neurological syndrome? Complex mental and movement disorder and autonomic dysfunction in a 65-year-old patient - Case 1/2011].LRRK2 in Parkinson's disease - drawing the curtain of penetrance: a commentary.Single-cell expression profiling of dopaminergic neurons combined with association analysis identifies pyridoxal kinase as Parkinson's disease gene.Population-specific frequencies for LRRK2 susceptibility variants in the Genetic Epidemiology of Parkinson's Disease (GEO-PD) Consortium.Subthalamic nucleus stimulation restores the efferent cortical drive to muscle in parallel to functional motor improvement.Alpha-synuclein repeat variants and survival in Parkinson's diseaseGlobal investigation and meta-analysis of the C9orf72 (G4C2)n repeat in Parkinson diseaseParkinson's disease: one biochemical pathway to fit all genes?Modulation of mitochondrial function and morphology by interaction of Omi/HtrA2 with the mitochondrial fusion factor OPA1.Nigral stimulation for resistant axial motor impairment in Parkinson's disease? A randomized controlled trial.Independent and joint effects of the MAPT and SNCA genes in Parkinson disease.Spectrum of phenotypes and genotypes in Parkinson's disease.Combined STN/SNr-DBS for the treatment of refractory gait disturbances in Parkinson's disease: study protocol for a randomized controlled trial.Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case-control study.TREM2 R47H variant and risk of essential tremor: a cross-sectional international multicenter study.Neuromuscular correlates of subthalamic stimulation and upper limb freezing in Parkinson's disease.The NG2 Proteoglycan Protects Oligodendrocyte Precursor Cells against Oxidative Stress via Interaction with OMI/HtrA2Dissecting the role of the mitochondrial chaperone mortalin in Parkinson's disease: functional impact of disease-related variants on mitochondrial homeostasis.Cortical correlates of susceptibility to upper limb freezing in Parkinson's disease.Genes in familial parkinsonism and their role in sporadic Parkinson's disease.New developments in diagnosis and treatment of Parkinson's disease--from basic science to clinical applications.Large-scale replication and heterogeneity in Parkinson disease genetic loci.Large-scale assessment of polyglutamine repeat expansions in Parkinson diseaseA multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants.The use of primary human fibroblasts for monitoring mitochondrial phenotypes in the field of Parkinson's disease.A large-scale genetic association study to evaluate the contribution of Omi/HtrA2 (PARK13) to Parkinson's disease.
P50
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P50
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hulumtues
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հետազոտող
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Rejko Krüger
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Rejko Krüger
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Rejko Krüger
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Rejko Krüger
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Rejko Krüger
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Rejko Krüger
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Rejko Krüger
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