ÌÇÐÄvlog

This longitudinal analysis of a French national cohort evaluates the association of migraine and type 2 diabetes in women, including changes in the prevalence of active migraine episodes before and after type 2 diabetes diagnosis.

This cohort study examines whether there are disparities between African American and white individuals in molecular biomarkers for Alzheimer disease.

This cohort study uses propensity score–matching analyses to examine disability progression in matched pairs of patients with secondary progressive multiple sclerosis who were treated with rituximab vs those who were never treated with rituximab.

This systematic review and meta-analysis assesses the rates of procedural complications and fatalities within the 30 days after endovascular or neurosurgical treatment for unruptured intracranial aneurysms.

This cohort study assesses depression and anxiety in adults with cerebral palsy compared with age-, sex-, and practice-matched adults with cerebral palsy.

This study evaluates the clinical, radiologic,al and prognostic features of of myelin oligodendrocyte glycoprotein autoantibody myelitis and compares with myelitis with aquaporin-4–IgG and multiple sclerosis.

This case study investigates the association of regional in vivo retention of the tau positron emission tomography ligand [¹⁸F]flortaucipir with the density of tau neuropathology in the corresponding brain regions in a patient with early-onset Alzheimer disease caused by a PSEN1 mutation.

This case-control study investigates cerebrospinal fluid levels of neurofilament light protein in participants with various forms of dementia, motor neuron disease, and movement disorders and controls, as determined by clinical and autopsy-definite criteria.

This medical record review identifies factors and diagnostic errors that contribute to the initial misdiagnosis of optic nerve sheath meningiomas.

This validation study assesses the ability of a panel of umbilical cord microRNA to evaluate the development and severity of encephalopathy in infants following perinatal asphyxia.

This study uses exome sequencing and genetic evaluation to explain the shared condition of 4 children from 2 unrelated families who were affected by refractory epileptic seizures, respiratory failure, brain abnormalities, and death in the neonatal period.