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Annals of Neurology: Volume 80, Number 4, October 2016
- First Published: 28 September 2016
Issue Information
Review
Research Articles
no
Neuroanatomic Correlates of Female Sexual Dysfunction in Multiple Sclerosis
- Pages: 490-498
- First Published: 27 July 2016
Open Access
oa
Long-term evolution of multiple sclerosis disability in the treatment era
- Pages: 499-510
- First Published: 27 July 2016
no
Infantile spasms in down syndrome: Rescue by knockdown of the GIRK2 channel
- Pages: 511-521
- First Published: 27 July 2016
no
Microdialysis to Optimize Cord Perfusion and Drug Delivery in Spinal Cord Injury
- Pages: 522-531
- First Published: 27 July 2016
no
Statin therapy prevents the onset of Parkinson disease in patients with diabetes
- Pages: 532-540
- First Published: 29 July 2016
no
Bedside quantitative electroencephalography improves assessment of consciousness in comatose subarachnoid hemorrhage patients
- Pages: 541-553
- First Published: 29 July 2016
no
Characteristic microglial features in patients with hereditary diffuse leukoencephalopathy with spheroids
- Pages: 554-565
- First Published: 04 August 2016
no
Mycoplasma pneumoniae triggering the Guillain-Barré syndrome: A case-control study
- Pages: 566-580
- First Published: 04 August 2016
no
A Novel Imaging Marker for Small Vessel Disease Based on Skeletonization of White Matter Tracts and Diffusion Histograms
- Pages: 581-592
- First Published: 12 August 2016
no
Cerebral white matter lesions and post-thrombolytic remote parenchymal hemorrhage
- Pages: 593-599
- First Published: 17 August 2016
no
ATXN2-AS, a gene antisense to ATXN2, is associated with spinocerebellar ataxia type 2 and amyotrophic lateral sclerosis
- Pages: 600-615
- First Published: 17 August 2016
no
Preclinical disease activity in multiple sclerosis: A prospective study of cognitive performance prior to first symptom
- Pages: 616-624
- First Published: 23 August 2016
Brief Communications
no
Multifocal nerve lesions and LZTR1 germline mutations in segmental schwannomatosis
- Pages: 625-628
- First Published: 29 July 2016
no
Long-term preclinical magnetic resonance imaging alterations in sporadic Creutzfeldt–Jakob disease
- Pages: 629-632
- First Published: 08 August 2016
no
KIF5A mutations cause an infantile onset phenotype including severe myoclonus with evidence of mitochondrial dysfunction
- Pages: 633-637
- First Published: 27 July 2016
Open Access
oa
A recurrent mutation in KCNA2 as a novel cause of hereditary spastic paraplegia and ataxia
- First Published: 20 August 2016