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NEK1 mutations in familial amyotrophic lateral sclerosis
Brenner, David et al. (2016)
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Amyotrophic lateral sclerosis. Multisystem degeneration
Huebers, Annemarie et al. (2016)
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Age-dependent defects of alpha-synuclein oligomer uptake in microglia and monocytes
Bliederhaeuser, Corinna et al. (2016)
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Comment on "Cutting Edge: Inhibiting TBK1 by Compound II Ameliorates Autoimmune Disease in Mice"
Brenner, David et al. (2016)
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Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis
van Rheenen, Wouter et al. (2016)
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LRRK2 contributes to monocyte dysregulation in Parkinson's disease
Bliederhaeuser, Corinna et al. (2016)
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Neurofilament Levels as Biomarkers in Asymptomatic and Symptomatic Familial Amyotrophic Lateral Sclerosis
Weydt, Patrick et al. (2016)
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Rare Variants in MME, Encoding Metalloprotease Neprilysin, Are Linked to Late-Onset Autosomal-Dominant Axonal Polyneuropathies
Auer-Grumbach, Michaela et al. (2016)
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NEK1 variants confer susceptibility to amyotrophic lateral sclerosis
Kenna, Kevin P. et al. (2016)
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Peripheral monocytes are functionally altered and invade the CNS in ALS patients
Zondler, Lisa et al. (2016)
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