Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain
the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in
Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles
and JavaScript.
Huntington disease (HD)-like 2 (HDL2) is a rare HD phenocopy that seems to be confined to people with African ancestry. This Review summarizes our current knowledge of HDL2 and highlights the need for further studies of neurodegenerative diseases on the African continent.
Schizophrenia is a leading cause of global disability but lacks therapies that target all aspects of the disease. This Review summarizes our current understanding of the pathophysiological mechanisms underlying the disease, highlighting potential targets for new drug development.
Using integrative multiomics, a new study has shed light on the aetiology of ischaemic stroke. By probing the mechanisms underlying stroke, such approaches could aid the development of therapies and improve risk prediction and stratification, with the ultimate aim of developing personalized preventive and therapeutic strategies.
This Perspective proposes a tripartite model involving the amygdala, hippocampus and striatum as key structures underlying cognitive dysfunction in Parkinson disease. The authors explore the anatomical and functional relationships of the structures and summarize evidence of their involvement in the cognitive aspects of the disease.
New research indicates that in a mouse model of Parkinson disease, α-synuclein is trafficked from the brain to the gut by CD11c-expressing macrophages.
Clinical boundaries between neurology and psychiatry hamper understanding of disorders with phenotypes that span these disciplines. In this Review, Peall et al. discuss rare genetic brain disorders with neurological and psychiatric phenotypes, and consider common underlying mechanisms that could be therapeutic targets.
A new study indicates that African American people with multiple sclerosis have higher markers of humoral disease pathology than white people with multiple sclerosis. However, apparent differences in pathophysiology between ethnic groups cannot be fully interpreted without more comprehensive studies that examine the effects of social inequality on disease.
Vascular cognitive impairment and dementia is the second most common cause of dementia after Alzheimer disease. In this Review, the authors examine the potential of key molecules in the pathophysiology as biomarkers of vascular cognitive impairment and dementia and consider the challenges of clinical translation.
The incidence of idiopathic intracranial hypertension is rapidly rising in line with global obesity rates. This Review summarizes evidence suggesting that the condition is not idiopathic but is instead related to systemic metabolic and hormonal perturbations and should thus be considered a metabolic disease.
This Review describes the emerging landscape of diagnostic, categorical and pharmacodynamic biomarkers for amyotrophic lateral sclerosis and considers the role of these biomarkers in the rapidly evolving landscape of new therapeutics for this condition.