Genetic Variant and Phenotypic Heterogeneity
Category
Research Highlights
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Better understanding of RLS and narcolepsy neurobiology
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Progress in understanding the genetics of epilepsies
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Neural basis of impulse control behaviours in Parkinson’s disease
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Nodding syndrome proved to be a tauopathy
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Recommendations of the International Society of Intraoperative Neurophysiology for intraoperative somatosensory evoked potentials
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The electrodiagnosis of Guillain-Barré syndrome subtypes: Where do we stand?
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Critical review of pure autonomic failure raises awareness for early signs of Parkinson’s disease, Lewy body dementia, and Multiple System Atrophy Pure autonomic failure (PAF) is both, a rare condition and a pathogenetic mystery, first described by Bradbury and Eggleston… Continue Reading
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Progress in understanding the genetics of epilepsies Epilepsies affect around 65 million people worldwide and are clinically a heterogeneous group of neurological disorders. Despite strong evidence for heritability, genome-wide association studies have had little success in identification of risk loci… Continue Reading
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Postconcussion symptoms and health-related quality of life in patients with mild traumatic brain injury A subset of mild traumatic brain injury (mTBI) patients experience post-concussion symptoms. When a cluster of post-concussion symptoms persists for over three months, it is referred… Continue Reading
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Decision-making processes of tracheostomy-assisted ventilation in amyotrophic lateral sclerosis
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