Publication Venue For
Optimizing Patient Selection for Endovascular Treatment in Acute Ischemic Stroke (SELECT): A Prospective, Multicenter Cohort Study of Imaging Selection.
Using global team science to identify genetic parkinson's disease worldwide.
Gender Inequities in the Multiple Sclerosis Community: A Call for Action.
N-acetylcysteine targets 5 lipoxygenase-derived, toxic lipids and can synergize with prostaglandin E2 to inhibit ferroptosis and improve outcomes following hemorrhagic stroke in mice.
NBEA: Developmental disease gene with early generalized epilepsy phenotypes.
18F-flortaucipir tau positron emission tomography distinguishes established progressive supranuclear palsy from controls and Parkinson disease: A multicenter study.
Dendritic spines provide cognitive resilience against Alzheimer's disease.
Incidence and impact of subclinical epileptiform activity in Alzheimer's disease.
Glucocerebrosidase, Parkinson disease, and the “senses and intellect”.
Long-term evolution of multiple sclerosis disability in the treatment era.
Alzheimer's disease pathology is attenuated in a CD38-deficient mouse model.
Apraxia in anti-glutamic acid decarboxylase-associated stiff person syndrome: Link to corticobasal degeneration?.
Gene delivery of neurturin to putamen and substantia nigra in Parkinson disease: A double-blind, randomized, controlled trial.
Training for a neurology career in a rare disease: The role of cyberconsults.
A fatal case of JC virus meningitis presenting with hydrocephalus in a human immunodeficiency virus-seronegative patient..
Hyperintense cortical signal on magnetic resonance imaging reflects focal leukocortical encephalitis and seizure risk in progressive multifocal leukoencephalopathy..
The α2B-adrenergic receptor is mutant in cortical myoclonus and epilepsy.
UBQLN2 mutation causing heterogeneous X-linked dominant neurodegeneration.
Randomized study combining interferon and glatiramer acetate in multiple sclerosis.
Reply to Dr Ismailov.
Short- and long-term sunlight radiation and stroke incidence.
Mouse models of frontotemporal dementia.
Laminin alpha 2 enables glioblastoma stem cell growth.
Meta-analysis of Parkinson's Disease: Identification of a novel locus, RIT2.
Incident cognitive impairment is elevated in the stroke belt: The REGARDS Study.
Disparities in stroke incidence contributing to disparities in stroke mortality.
Exome sequencing allows for rapid gene identification in a Charcot-Marie-Tooth family.
Lipids and stroke: Looking for risk in all the wrong places?.
Comparative analysis of therapeutic options used for myasthenia gravis.
Rett syndrome diagnostic criteria: Lessons from the Natural History Study.
Rett syndrome: Revised diagnostic criteria and nomenclature.
Longitudinal study of vision and retinal nerve fiber layer thickness in multiple sclerosis.
Beyond diagnosis: What biomarkers are teaching us about the "bio"logy of Alzheimer disease.
Considerations on discontinuing natalizumab for the treatment of multiple sclerosis.
Outcome of Optic Neuritis in Pediatric Demyelinating Disease.
Effect of epilepsy magnetic source imaging on intracranial electrode placement.
Early imaging correlates of subsequent motor recovery after stroke.
Magnetic resonance imaging as a potential surrogate for relapses in multiple sclerosis: A meta-analytic approach.
Reperfusion normalizes motor activation patterns in Large-Vessel disease.
Estimated 10-year stroke risk by region and race in the United States: Geographic and racial differences in stroke risk.
Functional imaging: I. Relative predictive value of intracranial electroencephalography.
Functional imaging: II. Prediction of epilepsy surgery outcome.
Care seeking after stroke symptoms.
Association analysis of MAPT H1 haplotype and subhaplotypes in Parkinson's disease.
DBH -1021C→T does not modify risk or age at onset in Parkinson's disease.
National Institutes of Health: The lottery.
Interferon-β for multiple sclerosis: Long-term benefits?.
A second major histocompatibility complex susceptibility locus for multiple sclerosis.
Glatiramer acetate in primary progressive multiple sclerosis: Results of a multinational, multicenter, double-blind, placebo-controlled trial.
Heterozygous parkin point mutations are as common in control subjects as in Parkinson's patients.
Localization of LRRK2 to membranous and vesicular structures in mammalian brain.
Platform Session 4 (36-43).
A longitudinal functional magnetic resonance imaging study of language development in children 5 to 11 years old.
Magnetic source imaging versus intracranial electroencephalogram in epilepsy surgery: A prospective study.
A locus for generalized tonic-clonic seizure susceptibility maps to chromosome 10q25-q26.
False-positive SCA8 gene test in a patient with pathologically proven multiple system atrophy .
Glial fibrillary acidic protein mutations in infantile, juvenile, and adult forms of Alexander disease.
Unusual variants of Alexander's disease.
Hypoperfusion without stroke alters motor activation in the opposite hemisphere.
Slower progression of Parkinson's disease with ropinirole versus levodopa: The REAL-PET study.
Altered hippocampal muscarinic receptors in acetylcholinesterase-deficient mice.
Parkin mutations and susceptibility alleles in late-onset Parkinson's disease.
Quantitative neuropathological changes in presymptomatic Huntington's disease.
Decreased cerebrospinal fluid levels of β-phenylethylamine in patients with Rett syndrome.
Influence of mutation type and X chromosome inactivation on Rett syndrome phenotypes.
Distribution of the mRNAs encoding torsinA and torsinB in the normal adult human brain.
Distribution of the mRNAs encoding torsinA and torsinB in the normal adult human brain.
The hereditary dystonias: An emerging story with a twist.
Dystonia with motor delay in compound heterozygotes for GTP- cyclohydrolase I gene mutations.
Expression of the early onset torsion dystonia gene (DYT1) in human brain.
Apolipoprotein E genotypes and age at onset of Parkinson's disease  (multiple letters).
On the pathological progression of Huntington's disease  (multiple letters).
Decreased cerebrospinal fluid levels of substance P in patients with Rett syndrome.
Modulation of the age at onset of Parkinson's disease by apolipoprotein E genotypes.
Accumulation of β-amyloid precursor protein in HIV encephalitis: Relationship with neuropsychological abnormalities.
Intrinsic epileptogenesis of hypothalamic hamartomas in gelastic epilepsy.
CAG repeat number governs the development rate of pathology in huntington's disease.
Recommendations from the national multiple sclerosis society clinical outcomes assessment task force.
Opportunities and challenges in academic neurology: Report of the long range planning committee of the American Neurological Association.
Developmental dyslexia: A motor-articulatory feedback hypothesis.
Clinical outcomes assessment in multiple sclerosis.
Clinical outcomes and documentation of partial beneficial effects of immunotherapy for multiple sclerosis.
Huntington's disease gene: Regional and cellular expression in brain of normal and affected individuals.
Increased Risk of Parkinson's Disease in Relatives of Patients.
Increased risk of Parkinson's disease in parents and siblings of patients.
Neuronal migration disorders: Positron emission tomography correlations.
Predictive value of induction of psychogenic seizures by suggestion.
Rett syndrome: Controlled study of an oral opiate antagonist, naltrexone.
Visual grasp in corticobasal degeneration.
VISUAL PHENOMENA LIMITED TO THE HEMIANOPIC FIELD IN LESIONS OF THE CENTRAL VISUAL PATHWAYS.
Correlation of myelin basic protein‐like material in cerebrospinal fluid of multiple sclerosis patients with their response to glucocorticoid treatment.
Retinal ganglion cells in Alzheimer's disease and aging.
Mitochondrial oxidative phosphorylation defects in Parkinson's disease.
Preferential loss of striato‐external pallidal projection neurons in presymptomatic Huntington's disease.
Cerebral amyloid angiopathy without and with cerebral hemorrhages: A comparative histological study.
Excitatory amino acid binding sites in the caudate nucleus and frontal cortex of huntington's disease.
Mitochondrial oxidative phosphorylation defects in parkinson's disease.
Sleep-related focal motor seizures in bilateral central macrogyria..
Estimation of familial risk in Alzheimer's disease.
Phosphorus magnetic resonance spectroscopy of patients with mitochondrial cytopathies demonstrates decreased levels of brain phosphocreatine.
Positron emission tomography in manganese intoxication..
Assessment of genetic risk for alzheimer's disease among first‐degree relatives.
Cerebrospinal fluid biogenic amines and biopterin in rett syndrome.
Ideational apraxia: A deficit in tool selection and use.
An isoelectric focusing study in herpes simplex virus encephalitis.
Rett's syndrome: Characterization of respiratory patterns and sleep.
Bilateral lucency of the globus pallidus complicating methylmalonic acidemia.
Facioscapulohumeral dystrophy presenting in infancy with facial diplegia and sensorineural deafness.
The role of plasma lipids in carotid bifurcation atherosclerosis.
Acquired immune deficiency syndrome and multiple tract degeneration in a homosexual man.
Mechanisms of acute carotid stroke.
Mechanisms underlying hemispatial neglect.