Annals of Clinical and Translational Neurology: Vol 7, No 12

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Annals of Clinical and Translational Neurology

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Annals of Clinical and Translational Neurology: Volume 7, Issue 12

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Issue Information

Research Articles

Tau pathology associates with in vivo cortical thinning in Lewy body disorders

Electrical stimulation of the endopiriform nucleus attenuates epilepsy in rats by network modulation

Habitual sleep disturbances and migraine: a Mendelian randomization study

Identification and functional characterization of novel GDAP1 variants in Chinese patients with Charcot–Marie–Tooth disease

Viltolarsen in Japanese Duchenne muscular dystrophy patients: A phase 1/2 study

Corpus callosum integrity loss predicts cognitive impairment in Leukoaraiosis

Motor beta cortical oscillations are related with the gait kinematics of youth with cerebral palsy

Elevated levels of extracellular vesicles in progranulin-deficient mice and FTD-GRN Patients

Cardioselective peripheral noradrenergic deficiency in Lewy body synucleinopathies

Brief Communications

Plasma lipidomics of monozygotic twins discordant for multiple sclerosis

Anakinra usage in febrile infection related epilepsy syndrome: an international cohort

Ante- and postmortem tau in autosomal dominant and late-onset Alzheimer’s disease

Case Study

Nusinersen in type 0 spinal muscular atrophy: should we treat?

Pregnancy in MNGIE: a clinical and metabolic honeymoon

Reviews

Altered mental status in “Guillain-Barré syndrome” –a noteworthy clinical clue

Blood neurofilament light: a critical review of its application to neurologic disease

The role of bioactive lipids in attenuating the neuroinflammatory cascade in traumatic brain injury

interACTN Case Summary

The case of a 30-year-old man with subacute gait instability, weakness, and muscle spasms

Letter

Autosomal dominant segregation of CAPN3 c.598_612del15 associated with a mild form of calpainopathy

Reply To Letter

Reply: Autosomal dominant segregation of CAPN3 c.598_612del15 associated with a mild form of calpainopathy

Letter

No evidence supports the genetic heterogeneity of Neuronal intranuclear inclusion disease

Reply To Letter

Reply to: No evidence supports genetic heterogeneity of neuronal intranuclear inclusion disease

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