Annals of Clinical and Translational Neurology: Vol 7, No 5

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Annals of Clinical and Translational Neurology

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Annals of Clinical and Translational Neurology: Volume 7, Issue 5

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Research Articles

Biallelic GRM7 variants cause epilepsy, microcephaly, and cerebral atrophy

Impact of simultaneous subthalamic and nigral stimulation on dysphagia in Parkinson’s disease

Vorinostat in the acute neuroinflammatory form of X-linked adrenoleukodystrophy

Electrophysiological properties and seizure networks in hypothalamic hamartoma

Heritability of alpha and sensorimotor network changes in temporal lobe epilepsy

Analysis of factors associated with brittle response in patients with Parkinson’s disease

Developmental regression and mitochondrial function in children with autism

Deep learning with diffusion basis spectrum imaging for classification of multiple sclerosis lesions

MRI and flortaucipir relationships in Alzheimer's phenotypes are heterogeneous

Evolution of white matter damage in amyotrophic lateral sclerosis

Cortical hyperexcitability evolves with disease progression in ALS

Neuroprotective effects of FK866 against traumatic brain injury: Involvement of p38/ERK pathway

Global FKRP Registry: observations in more than 300 patients with Limb Girdle Muscular Dystrophy R9

Neurotoxicity after hematopoietic stem cell transplant in multiple sclerosis

The A4 study: β-amyloid and cognition in 4432 cognitively unimpaired adults

Genetic modifiers of respiratory function in Duchenne muscular dystrophy

Magnetization transfer ratio quantifies polyneuropathy in hereditary transthyretin amyloidosis

VRK1 (Y213H) homozygous mutant impairs Cajal bodies in a hereditary case of distal motor neuropathy

Immune-mediated axonal dysfunction in seropositive and seronegative primary Sjögren’s syndrome

Reversing 21 years of chronic paralysis via non-invasive spinal cord neuromodulation: a case study

Brief Communication

Dystonia-ataxia syndrome with permanent torsional nystagmus caused by ECHS1 deficiency

A new congenital multicore titinopathy associated with fast myosin heavy chain deficiency

A familial t(4;8) translocation segregates with epilepsy and migraine with aura

A novel de novo RNF216 mutation associated with autosomal recessive Huntington-like disorder

Case Study

Optic nerve sheath diameter ultrasonography for elevated intracranial pressure detection

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