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The human hippocampus contributes to short-term memory
doi : 10.1093/brain/awae194
Volume 147, Issue 8, August 2024
Clinical genetic testing in Parkinson’s disease should become part of routine patient care
doi : 10.1093/brain/awae181
Autoimmune ‘secondary synaptopathies’: do NMDAR antibodies cause a primary extra-synaptopathy?
doi : 10.1093/brain/awae236
Disentangling genetic risks for development and progression of Alzheimer’s disease
doi : 10.1093/brain/awae237
Failure of C9orf72 sense repeat-targeting antisense oligonucleotides: lessons learned and the path forward
doi : 10.1093/brain/awae168
The lysosomal β-glucocerebrosidase strikes mitochondria: implications for Parkinson’s therapeutics
doi : 10.1093/brain/awae070
Predictors of cognition after glioma surgery: connectotomy, structure-function phenotype, plasticity
doi : 10.1093/brain/awae093
Peripherally-derived LGI1-reactive monoclonal antibodies cause epileptic seizures in vivo
doi : 10.1093/brain/awae129
Relevance of genetic testing in the gene-targeted trial era: the Rostock Parkinson’s disease study
doi : 10.1093/brain/awae188
Parkinson’s disease variant detection and disclosure: PD GENEration, a North American study
doi : 10.1093/brain/awae142
Neuronal A2A receptor exacerbates synapse loss and memory deficits in APP/PS1 mice
doi : 10.1093/brain/awae113
Leptin receptor reactivation restores brain function in early-life Lepr-deficient mice
doi : 10.1093/brain/awae127
Multivariate mapping of low-resilient neurocognitive systems within and around low-grade gliomas
doi : 10.1093/brain/awae130
De novo variants in ATXN7L3 lead to developmental delay, hypotonia and distinctive facial features
doi : 10.1093/brain/awae160
NMDA receptor autoantibodies primarily impair the extrasynaptic compartment
doi : 10.1093/brain/awae163
Expanded clinical phenotype spectrum correlates with variant function in SCN2A-related disorders
doi : 10.1093/brain/awae125
The clinical and genetic spectrum of inherited glycosylphosphatidylinositol deficiency disorders
doi : 10.1093/brain/awae056
Long-term neuropsychological trajectories in children with epilepsy: does surgery halt decline?
doi : 10.1093/brain/awae121
Thalamic epileptic spikes disrupt sleep spindles in patients with epileptic encephalopathy
doi : 10.1093/brain/awae119
Identifying novel risk genes in intracranial aneurysm by integrating human proteomes and genetics
doi : 10.1093/brain/awae111
Spatial enrichment and genomic analyses reveal the link of NOMO1 with amyotrophic lateral sclerosis
doi : 10.1093/brain/awae123
Revisiting distinct nerve excitability patterns in patients with amyotrophic lateral sclerosis
doi : 10.1093/brain/awae131
Different learning aberrations relate to delusion-like beliefs with different contents
doi : 10.1093/brain/awae122
Biallelic variants in SNUPN cause a limb girdle muscular dystrophy with myofibrillar-like features
doi : 10.1093/brain/awae046
Novel insight into atogepant mechanisms of action in migraine prevention
doi : 10.1093/brain/awae062
Reply: The challenge of assessing invasive biomarkers for epilepsy surgery and To plan efficacious epilepsy surgery
doi : 10.1093/brain/awae165
Correction to: Microbiota from Alzheimer's patients induce deficits in cognition and hippocampal neurogenesis
doi : 10.1093/brain/awae208
Correction to: INPP5K and SIL1 associated pathologies with overlapping clinical phenotypes converge through dysregulation of PHGDH
doi : 10.1093/brain/awae239
