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Research Articles
Open Access
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Early life metal dysregulation in amyotrophic lateral sclerosis
- Pages: 872-882
- First Published: 21 May 2020
Open Access
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Abolishing spontaneous epileptiform activity in human brain tissue through AMPA receptor inhibition
- Pages: 883-890
- First Published: 19 May 2020
Open Access
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Automated cot-side tracking of functional brain age in preterm infants
- Pages: 891-902
- First Published: 05 May 2020
Open Access
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Serum neurofilament light chain in FTLD: association with C9orf72, clinical phenotype, and prognosis
- Pages: 903-910
- First Published: 22 May 2020
Open Access
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Clinical and genetic characteristics of type I sialidosis patients in mainland China
- Pages: 911-923
- First Published: 29 May 2020
Open Access
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CSF and serum ferritin levels in narcolepsy type 1 comorbid with restless legs syndrome
- Pages: 924-931
- First Published: 20 May 2020
Open Access
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Transmission of CJD from nasal brushings but not spinal fluid or RT-QuIC product
- Pages: 932-944
- First Published: 15 June 2020
Open Access
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Temporal association of sNfL and gad-enhancing lesions in multiple sclerosis
- Pages: 945-955
- First Published: 25 May 2020
Open Access
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Mutated RAP1GDS1 causes a new syndrome of dysmorphic feature, intellectual disability & speech delay
- Pages: 956-964
- First Published: 19 May 2020
Open Access
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Hand-onset weakness is a common feature of ALS patients with a NEK1 loss-of-function variant
- Pages: 965-971
- First Published: 27 May 2020
Open Access
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Remote ischemic conditioning combined with intravenous thrombolysis for acute ischemic stroke
- Pages: 972-979
- First Published: 29 May 2020
Open Access
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Mitochondrial encephalopathy Due to a Novel Pathogenic Mitochondrial tRNAGln m.4349C>T Variant
- Pages: 980-991
- First Published: 26 June 2020
Open Access
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Clinical implication of serum biomarkers and patient age in inflammatory demyelinating diseases
- Pages: 992-1001
- First Published: 04 June 2020
Open Access
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Demographic characteristics and neuropsychological assessments of subjective cognitive decline (SCD) (plus)
- Pages: 1002-1012
- First Published: 26 June 2020
Open Access
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Expanding the clinical and phenotypic heterogeneity associated with biallelic variants in ACO2
- Pages: 1013-1028
- First Published: 09 June 2020
Open Access
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Urate is closely linked to white matter integrity in multiple system atrophy
- Pages: 1029-1039
- First Published: 26 June 2020
Open Access
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Fc-gamma IIIa-V158F receptor polymorphism contributes to the severity of Guillain-Barré syndrome
- Pages: 1040-1049
- First Published: 02 June 2020
Brief Communication
Open Access
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Cerebellar cognitive disorder parallels cerebellar motor symptoms in Friedreich ataxia
- Pages: 1050-1054
- First Published: 08 June 2020
Case Study
Open Access
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In vivo evolution of biopsy-proven inflammatory demyelination quantified by R2t* mapping
- Pages: 1055-1060
- First Published: 04 May 2020
Open Access
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Longitudinal study on nerve ultrasound and corneal confocal microscopy in NF155 paranodopathy
- Pages: 1061-1068
- First Published: 20 May 2020