This Viewpoint discusses new areas of focus in multiple sclerosis, including progressive multiple sclerosis, contributors to multiple sclerosis, and learning from the real world.
This Viewpoint explores the challenges and potential disparities of the lesbian, gay, bisexual, and trangender community in neurological care.
This Viewpoint discusses different techniques for estimating the heritability of amyotrophic lateral sclerosis.
This cohort study, using a data-driven cluster analysis on a broad spectrum of motor and nonmotor features, found 3 distinct phenotypes of Parkinson disease consisting of mainly motor/slow progression, intermediate, and diffuse/malignant subtypes.
This case series study describes the clinical and immunological features of patients with paraneoplastic neurological syndromes and glutamic acid decarboxylase antibodies.
This cohort study uses positron emission tomography to determine whether patients with temporal lobe epilepsy have increased neuroinflammation as shown by translocator protein expression.
This study characterized the clinical, structural, electrophysiologic, and genetic features of a congenital myasthenic syndrome, identified the disease gene and mutation, confirmed pathogenicity of the mutation by expression studies, and instituted optimal pharmacotherapy.
This observational study investigates the associations between multiple sclerosis disability and disease type with lower thoracic cord gray matter and white matter areas using phase sensitive inversion recovery magnetic resonance imaging at 3T, as well as compares these relationships with those obtained at upper cervical levels.
This population-based case-control study investigates the risk of amyotrophic lateral sclerosis associated with diabetes and obesity among Danish individuals.
This cross-sectional study reports that children at genetic risk for autosomal dominant Alzheimer disease have functional and structural brain changes and abnormal levels of plasma amyloid-β 1-42.
This study reports that ApoE4, TREM2 R47H, and rare variants in other genes, such as UNC5C D353N, are likely responsible for the notable occurrence of Alzheimer disease in a large family with late-onset disease.
This review traces the development of intravenous thrombolysis to date, considers the shortcomings of alteplase, and examines alternative thrombolytic approaches currently in the pipeline, including the role of neuroimaging and the possibility of combination therapies.
This case report describes a man in his 30s who developed a progressive gait disorder in his mid-20s.
This case report describes a woman in her 70s experiencing right-sided temporal pain and jaw claudication.
This case report describes a man in his 60s who presented with a 10-month history of rapidly progressive motor impairment.
Create a personal account or sign in to: