This Viewpoint discusses the future of precision medicine in the field of ischemic stroke, first looking at the current status of genetic approaches and then exploring the status of phenotype-based delineations.
This case series describes rebound syndrome in patients with multiple sclerosis after cessation of fingolimod treatment.
This case-control study examines associations between cumulative HLA genetic risk burden and clinical and MRI-based phenotypes in patients with multiple sclerosis.
This case-control study evaluates the association of exposures to environmental toxins with the odds of developing amyotrophic lateral sclerosis.
This genome-wide association study investigates genetic loci associated with survival in an international population of patients with amytrophic lateral sclerosis.
This cohort study examines data on elderly patients with glioblastoma from the National Cancer Database to compare the association of overall survival with combined-modality therapy including radiotherapy and chemotherapy, radiotherapy alone, and chemotherapy alone.
This cohort study aims to determine the prevalence of abnormal blood pressure, blood glucose levels, and temperature in pediatric patients with acute arterial ischemic stroke and to explore any association between these measures and neurological outcome.
This study uses whole-exome and targeted squencing to identify constitutional and mosaic mutations of MTOR associated with focal cortical dysplasia, hemimegalencephaly, and diffuse megalencephaly.
This study of clinical and autopsy data examines the association of memory problems with primary progressive aphasia on the basis of autopsy-confirmed neuropathologic diagnoses of frontotemporal lobar degeneration vs Alzheimer disease.
This cross-sectional study reports the proportion of patients with thymoma who had potentially pathogenic neural synaptic autoantibodies.
This study explores the association between the symptoms of chemotherapy-induced peripheral neuropathy and the risk of falls for patients receiving neurotoxic chemotherapy.
This review presents findings on the genetic mutations associated with Alzheimer disease, polymorphisms increasing risk, and amyloid β protein–reducing therapies.
This review article discusses what is currently known about Zika virus, neuroimmunologic complications, and the impact on global human health.
This case report describes a man with a history of progressive bilateral hearing loss and an acute left homonymous hemianopsia.
This case report describes a woman in her early 40s who presented to the emergency department with multiple scotomas in both eyes and auditory changes in her left ear.
This case report describes a woman in her early 40s with fluctuating neck pain in whom imaging revealed spontaneous cerebrospinal fluid leakage with engorgement of venous plexus.
This case series describes members of the same family with spinocerebellar ataxia type 16 with choreoathetosis, dystonia, and myoclonus.
Create a personal account or sign in to: