Brain

Recent Papers/Articles

Mitochondrial DNA copy number differentiates the Lebers hereditary optic neuropathy affected individuals from the unaffected mutation carriers

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Volume: 139

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Widespread synaptic loss in multiple sclerosis

Volume: 139

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ALDH18A1 gene mutations cause dominant spastic paraplegia SPG9: loss of function effect and plausibility of a dominant negative mechanism

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Volume: 139

READ
Cerebellar damage limits reinforcement learning

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Volume: 139

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Reply: ALDH18A1 gene mutations cause dominant spastic paraplegia SPG9: loss of function effect and plausibility of a dominant negative mechanism

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Volume: 139

READ
Reply: Skin biopsies in the differential diagnosis of parkinsonism: are we ready for simplified protocols?

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Volume: 139

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What lies beneath grey matter atrophy in multiple sclerosis?

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Volume: 139

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Corrigendum

Volume: 139

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Axial myopathy: an overlooked feature of muscle diseases

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Volume: 139

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Free-thiamine is a potential biomarker of thiamine transporter-2 deficiency: a treatable cause of Leigh syndrome

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Volume: 139

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Reconstruction of single cortical projection neurons reveals primary spine loss in multiple sclerosis

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Volume: 139

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Visual short-term memory deficits in REM sleep behaviour disorder mirror those in Parkinsons disease

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Volume: 139

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Early detection of intentional harm in the human amygdala

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Volume: 139

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Mutations in the MORC2 gene cause axonal Charcot-Marie-Tooth disease

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Volume: 139

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ALS5/SPG11/KIAA1840 mutations cause autosomal recessive axonal Charcot-Marie-Tooth disease

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Volume: 139

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MTHFSD and DDX58 are novel RNA-binding proteins abnormally regulated in amyotrophic lateral sclerosis

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Volume: 139

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