Ma1, a novel neuron- and testis-specific protein, is recognized by the serum of patients with paraneoplastic neurological disordersA new case of complete primary cerebellar agenesis: clinical and imaging findings in a living patientWeighing brain activity with the balance: a contemporary replication of Angelo Mosso's historical experimentA TWO-ROUTE MODEL OF SPEECH PRODUCTIONWeighing brain activity with the balance: Angelo Mosso's original manuscripts come to lightImmunotherapy for Guillain-Barre syndrome: a systematic reviewImpoverishment of spontaneous language and the prediction of Alzheimer's diseaseThe effects of very early Alzheimer's disease on the characteristics of writing by a renowned authorInflammatory brain changes in Lyme borreliosisThe spectrum of disease in chronic traumatic encephalopathyAutomated MRI measures identify individuals with mild cognitive impairment and Alzheimer's diseaseTherapeutic approaches to Alzheimer's diseasePlasticity in the human central nervous systemC9orf72 repeat expansions are a rare genetic cause of parkinsonismPerceptual differentiation and category effects in normal object recognition: a PET studyNeuroeconomic dissociation of semantic dementia and behavioural variant frontotemporal dementiaMRI analysis of an inherited speech and language disorder: structural brain abnormalitiesModelling paraneoplastic CNS disease: T-cells specific for the onconeuronal antigen PNMA1 mediate autoimmune encephalomyelitis in the ratA mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvementThe expression of DJ-1 (PARK7) in normal human CNS and idiopathic Parkinson's diseaseThe myopathic form of coenzyme Q10 deficiency is caused by mutations in the electron-transferring-flavoprotein dehydrogenase (ETFDH) geneSenataxin modulates neurite growth through fibroblast growth factor 8 signallingOPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypesCharcot-Marie-Tooth disease type 2E, a disorder of the cytoskeletonKIAA1797/FOCAD encodes a novel focal adhesion protein with tumour suppressor function in gliomasDirect visualization of alpha-synuclein oligomers reveals previously undetected pathology in Parkinson's disease brainThe first ALS2 missense mutation associated with JPLS reveals new aspects of alsin biological functionARNT2 mutation causes hypopituitarism, post-natal microcephaly, visual and renal anomaliesReduced glucocerebrosidase is associated with increased α-synuclein in sporadic Parkinson's diseasePINK1 protein in normal human brain and Parkinson's diseaseAutosomal recessive cortical myoclonic tremor and epilepsy: association with a mutation in the potassium channel associated gene CNTN2Glucocerebrosidase is shaking up the synucleinopathiesNeuroprotection by PlGF gene-modified human mesenchymal stem cells after cerebral ischaemiaFibulin-5 mutations link inherited neuropathies, age-related macular degeneration and hyperelastic skinThe cerebral cortex of Albert Einstein: a description and preliminary analysis of unpublished photographsHypokinesia without decrement distinguishes progressive supranuclear palsy from Parkinson's diseaseTau elevations in the brain extracellular space correlate with reduced amyloid-β levels and predict adverse clinical outcomes after severe traumatic brain injurySensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementiaDelirium is a strong risk factor for dementia in the oldest-old: a population-based cohort studyInhibition of rho kinase enhances survival of dopaminergic neurons and attenuates axonal loss in a mouse model of Parkinson's disease
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