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http://medilib.ir
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If patients only knew how bureaucracy obstructs their involvement in research and clinical trials
doi : 10.1093/brain/awaf309
Volume 148, Issue 10, October 2025
The duality of disease: the Alzheimer’s disease dilemma through the lens of nosos and asthenia
doi : 10.1093/brain/awaf239
Stem cell-derived dopamine cell therapies for Parkinson’s disease: what have the first trials shown?
doi : 10.1093/brain/awaf322
Unpacking the relationship between exercise and amyotrophic lateral sclerosis
doi : 10.1093/brain/awaf310
Transforming tissue transcriptomes, delivering on the promise of machine learning
doi : 10.1093/brain/awaf323
The miracle dilemma: demystifying a common challenge in neuroprognostication
doi : 10.1093/brain/awaf245
Mental health research delivery: what can the National Health Service learn from the private sector?
doi : 10.1093/brain/awaf257
Neurological complications of Orthopoxvirus infections: neurotropism and neurovirulence
doi : 10.1093/brain/awaf181
Filamin A in focus: unravelling the multifaceted roles of filamin A in neurodevelopment and neurological disorders
doi : 10.1093/brain/awaf180
Remyelination of chronic demyelinated lesions with directly induced neural stem cells
doi : 10.1093/brain/awaf208
Biallelic LGI1 and ADAM23 variants cause hippocampal epileptic encephalopathy via the LGI1–ADAM22/23 pathway
doi : 10.1093/brain/awaf202
Stimulants for disorders of consciousness in the intensive care unit: a randomized, placebo-controlled trial
doi : 10.1093/brain/awaf228
Ventromedial prefrontal cortex lesions disrupt learning to reward others
doi : 10.1093/brain/awaf056
MRI R2* captures inflammation in disconnected brain structures after stroke: a translational study
doi : 10.1093/brain/awaf082
Dynamic reorganization of task-related network interactions in post-stroke aphasia recovery
doi : 10.1093/brain/awaf036
Functional contribution of astrocytic Kir4.1 channels to spasticity after spinal cord injury
doi : 10.1093/brain/awaf147
Cell-type-specific networks during hippocampal seizures at the micro- and macroscale
doi : 10.1093/brain/awaf024
Parkinson’s disease mutant Miro1 causes mitochondrial dysfunction and dopaminergic neuron loss
doi : 10.1093/brain/awaf051
At-home wearables and machine learning capture motor impairment and progression in adult ataxias
doi : 10.1093/brain/awaf154
Dysregulated cortical excitability and tau phosphorylation in a β3 integrin mouse model of autism
doi : 10.1093/brain/awaf089
Extreme exercise in males is linked to mTOR signalling and onset of amyotrophic lateral sclerosis
doi : 10.1093/brain/awaf235
Deep learning-based cell type profiles reveal signatures of Alzheimer’s disease resilience and resistance
doi : 10.1093/brain/awaf285
Selective vulnerability and resilience to Alzheimer's disease tauopathy as a function of genes and the connectome
doi : 10.1093/brain/awaf179
Neuropsychiatric symptoms and progression to pathologically confirmed Alzheimer’s disease
doi : 10.1093/brain/awaf156
Treatment-resistant recurrent unipolar and bipolar depression: associative learning abnormalities
doi : 10.1093/brain/awaf280
Correction of sodium channel mutations in sensory neurons reverses aberrant properties
doi : 10.1093/brain/awaf155
Effects of atidarsagene autotemcel gene therapy on peripheral nerves in late-infantile metachromatic leukodystrophy
doi : 10.1093/brain/awaf157
Genotype and phenotype spectrum of Charcot-Marie-Tooth disease due to mutations in SORD
doi : 10.1093/brain/awaf021
Brain accumulation of lactosylceramide characterizes GALC deficiency in a zebrafish model of Krabbe disease
doi : 10.1093/brain/awaf150
Astrocyte regeneration via FGF8-DBX1 signalling facilitates recovery in neuromyelitis optica rats
doi : 10.1093/brain/awaf148
Reply: Brainstem cavernous malformations: observation, microsurgical resection or stereotactic radiosurgery
doi : 10.1093/brain/awaf206
Brainstem cavernous malformations: observation, microsurgical resection or stereotactic radiosurgery
doi : 10.1093/brain/awaf205
Correction to: Remyelination of chronic demyelinated lesions with directly induced neural stem cells
doi : 10.1093/brain/awaf274
Correction to: Heterozygous variants in USP25 cause genetic generalized epilepsy
doi : 10.1093/brain/awaf287
