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Beyond ALS and FTD: the phenotypic spectrum of TBK1 mutations includes PSP-like and cerebellar phenotypes
British Library Online Contents | 2018| -
Beyond ALS and FTD: the phenotypic spectrum of TBK1 mutations includes PSP-like and cerebellar phenotypes
British Library Online Contents | 2018| -
Decreased retinal sensitivity and loss of retinal nerve fibers in multiple system atrophy
Online Contents | 2012| -
Effects of Levodopa on quality of sleep and nocturnal movements in Parkinson’s Disease
Free accessOnline Contents | 2021| -
Characteristics of serum neurofilament light chain as a biomarker in hereditary spastic paraplegia type 4
Free accessWiley | 2022| -
Pilot whole-exome sequencing of a German early-onset Alzheimer's disease cohort reveals a substantial frequency of PSEN2 variants
British Library Online Contents | 2016| -
Pilot whole-exome sequencing of a German early-onset Alzheimer's disease cohort reveals a substantial frequency of PSEN2 variants
British Library Online Contents | 2016| -
Towards a common framework of grounded action cognition: Relating motor control, perception and cognition
Online Contents | 2016|Contributors: Synofzik, Matthis -
Lack of enzyme activity in GBA2 mutants associated with hereditary spastic paraplegia/cerebellar ataxia (SPG46)
Online Contents | 2015|Contributors: Synofzik, Matthis -
PolyQ-expanded ataxin-3 protein levels in peripheral blood mononuclear cells correlate with clinical parameters in SCA3: a pilot study
Free accessOnline Contents | 2020| -
Serum Levels of Progranulin Do Not Reflect Cerebrospinal Fluid Levels in Neurodegenerative Disease
Bentham Science Publishers | 2016|
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