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Plasma Metabolites Link Dietary Patterns to Stroke Risk
. 93:500-510.
2023
Tubers Affecting the Fusiform Face Area Are Associated with Autism Diagnosis
. 93:577-590.
2023
Hydroxychloroquine for Primary Progressive Multiple Sclerosis
. 90:940-948.
2021
Profile of Autism Spectrum Disorder in Tuberous Sclerosis Complex: Results from a Longitudinal, Prospective, Multisite Study
. 90:874-886.
2021
Longitudinal CSF Iron Pathway Proteins in Posthemorrhagic Hydrocephalus: Associations with Ventricle Size and Neurodevelopmental Outcomes
. 90:217-226.
2021
Genomewide Association Studies of LRRK2 Modifiers of Parkinson's Disease
. 90:76-88.
2021
Serum Glial Fibrillary Acidic Protein: A Neuromyelitis Optica Spectrum Disorder Biomarker
. 89:895-910.
2021
Multisite Study of Evoked Potentials in Rett Syndrome
. 89:790-802.
2021
Tuber Locations Associated with Infantile Spasms Map to a Common Brain Network
. 89:726-739.
2021
Correction to: “Optimizing Patient Selection for Endovascular Treatment in Acute Ischemic Stroke (SELECT): A Prospective Multicenter Cohort Study of Imaging Selection” (Annals of Neurology, (2020), 87, 3, (419-433), 10.1002/ana.25669)
. 88:1056-1057.
2020
Comparison of Core Features in Four Developmental Encephalopathies in the Rett Natural History Study
. 88:396-406.
2020
Real-World Effectiveness of Initial Disease-Modifying Therapies in Pediatric Multiple Sclerosis
. 88:42-55.
2020
Optimizing Patient Selection for Endovascular Treatment in Acute Ischemic Stroke (SELECT): A Prospective, Multicenter Cohort Study of Imaging Selection
. 87:419-433.
2020
Using global team science to identify genetic parkinson's disease worldwide
. 86:153-157.
2019
Glial injury in neurotoxicity after pediatric CD19-directed chimeric antigen receptor T cell therapy
. 86:42-54.
2019
Gender Inequities in the Multiple Sclerosis Community: A Call for Action
. 84:958-959.
2018
N-acetylcysteine targets 5 lipoxygenase-derived, toxic lipids and can synergize with prostaglandin E
2
to inhibit ferroptosis and improve outcomes following hemorrhagic stroke in mice
. 84:854-872.
2018
NBEA: Developmental disease gene with early generalized epilepsy phenotypes
. 84:788-795.
2018
18
F-flortaucipir tau positron emission tomography distinguishes established progressive supranuclear palsy from controls and Parkinson disease: A multicenter study
. 82:622-634.
2017
Dendritic spines provide cognitive resilience against Alzheimer's disease
. 82:602-614.
2017
Incidence and impact of subclinical epileptiform activity in Alzheimer's disease
. 80:858-870.
2016
Glucocerebrosidase, Parkinson disease, and the “senses and intellect”
. 80:660-661.
2016
Long-term evolution of multiple sclerosis disability in the treatment era
. 80:499-510.
2016
Gene delivery of neurturin to putamen and substantia nigra in Parkinson disease: A double-blind, randomized, controlled trial
. 78:248-257.
2015
Alzheimer's disease pathology is attenuated in a CD38-deficient mouse model
. 78:88-103.
2015
Training for a neurology career in a rare disease: The role of cyberconsults
. 77:738-740.
2015
A fatal case of JC virus meningitis presenting with hydrocephalus in a human immunodeficiency virus-seronegative patient.
. 76:140-147.
2014
Hyperintense cortical signal on magnetic resonance imaging reflects focal leukocortical encephalitis and seizure risk in progressive multifocal leukoencephalopathy.
. 75:659-669.
2014
UBQLN2 mutation causing heterogeneous X-linked dominant neurodegeneration
. 75:793-798.
2014
Three times weekly glatiramer acetate in relapsing-remitting multiple sclerosis.
. 73:705-713.
2013
Randomized study combining interferon and glatiramer acetate in multiple sclerosis
. 73:327-340.
2013
Reply to Dr Ismailov
. 73:146-147.
2013
Short- and long-term sunlight radiation and stroke incidence
. 73:32-37.
2013
Mouse models of frontotemporal dementia
. 72:837-849.
2012
Laminin alpha 2 enables glioblastoma stem cell growth
. 72:766-778.
2012
Meta-analysis of Parkinson's Disease: Identification of a novel locus, RIT2
. 71:370-384.
2012
Reply
. 70:666-667.
2011
Incident cognitive impairment is elevated in the stroke belt: The REGARDS Study
. 70:229-236.
2011
Got milk?
. 70:3-4.
2011
Disparities in stroke incidence contributing to disparities in stroke mortality
. 69:619-627.
2011
Exome sequencing allows for rapid gene identification in a Charcot-Marie-Tooth family
. 69:464-470.
2011
Lipids and stroke: Looking for risk in all the wrong places?
. 69:597-599.
2011
Comparative analysis of therapeutic options used for myasthenia gravis
. 68:797-805.
2010
Rett syndrome diagnostic criteria: Lessons from the Natural History Study
. 68:951-955.
2010
Rett syndrome: Revised diagnostic criteria and nomenclature
. 68:944-950.
2010
Longitudinal study of vision and retinal nerve fiber layer thickness in multiple sclerosis
. 67:749-760.
2010
Beyond diagnosis: What biomarkers are teaching us about the "bio"logy of Alzheimer disease
. 67:283-285.
2010
Considerations on discontinuing natalizumab for the treatment of multiple sclerosis
. 68:409-411.
2010
Outcome of Optic Neuritis in Pediatric Demyelinating Disease
. 68:S86-S86.
2010
Effect of epilepsy magnetic source imaging on intracranial electrode placement
. 65:716-723.
2009
Early imaging correlates of subsequent motor recovery after stroke
. 65:596-602.
2009
Magnetic resonance imaging as a potential surrogate for relapses in multiple sclerosis: A meta-analytic approach
. 65:268-275.
2009
Reperfusion normalizes motor activation patterns in Large-Vessel disease
. 65:203-208.
2009
Estimated 10-year stroke risk by region and race in the United States: Geographic and racial differences in stroke risk
. 64:507-513.
2008
Functional imaging: I. Relative predictive value of intracranial electroencephalography
. 64:25-34.
2008
Functional imaging: II. Prediction of epilepsy surgery outcome
. 64:35-41.
2008
Care seeking after stroke symptoms
. 63:466-472.
2008
DBH -1021C→T does not modify risk or age at onset in Parkinson's disease
. 62:99-101.
2007
Interferon-β for multiple sclerosis: Long-term benefits?
. 61:283-285.
2007
Association analysis of MAPT H1 haplotype and subhaplotypes in Parkinson's disease
. 62:137-144.
2007
Glatiramer acetate in primary progressive multiple sclerosis: Results of a multinational, multicenter, double-blind, placebo-controlled trial
. 61:14-24.
2007
Heterozygous parkin point mutations are as common in control subjects as in Parkinson's patients
. 61:47-54.
2007
LRRK2 protein is a component of Lewy bodies [3]
. 60:617-618.
2006
Localization of LRRK2 to membranous and vesicular structures in mammalian brain
. 60:557-569.
2006
Platform Session 4 (36–43)
. 60:s139-s141.
2006
A longitudinal functional magnetic resonance imaging study of language development in children 5 to 11 years old
. 59:796-807.
2006
Magnetic source imaging versus intracranial electroencephalogram in epilepsy surgery: A prospective study
. 59:835-842.
2006
Simvastatin enhances learning and memory independent of amyloid load in mice
. 60:729-739.
2006
A locus for generalized tonic-clonic seizure susceptibility maps to chromosome 10q25-q26
. 58:449-458.
2005
Erratum: Unusual variants of Alexander's disease (Annals of Neurology (2005) 57 (327-338))
. 58:172.
2005
Distal spinal and bulbar muscular atrophy caused by dynactin mutation
. 57:687-694.
2005
False-positive SCA8 gene test in a patient with pathologically proven multiple system atrophy [1]
. 57:462-463.
2005
Glial fibrillary acidic protein mutations in infantile, juvenile, and adult forms of Alexander disease
. 57:310-326.
2005
Unusual variants of Alexander's disease
. 57:327-338.
2005
Hypoperfusion without stroke alters motor activation in the opposite hemisphere
. 56:796-802.
2004
Slower progression of Parkinson's disease with ropinirole versus levodopa: The REAL-PET study
. 54:93-101.
2003
Altered hippocampal muscarinic receptors in acetylcholinesterase-deficient mice
. 53:788-796.
2003
Parkin mutations and susceptibility alleles in late-onset Parkinson's disease
. 53:624-629.
2003
No evidence for genetic association or linkage of the cathepsin D (CTSD) exon 2 polymorphism and Alzheimer disease
. 49:114-116.
2001
Quantitative neuropathological changes in presymptomatic Huntington's disease
. 49:29-34.
2001
Survival in a transgenic model of FALS is independent of iNOS expression [1]
. 50:273.
2001
Decreased cerebrospinal fluid levels of β-phenylethylamine in patients with Rett syndrome
. 47:801-803.
2000
Influence of mutation type and X chromosome inactivation on Rett syndrome phenotypes
. 47:670-679.
2000
Distribution of the mRNAs encoding torsinA and torsinB in the normal adult human brain
. 46:761-769.
1999
Distribution of the mRNAs encoding torsinA and torsinB in the normal adult human brain
. 46:761-769.
1999
The hereditary dystonias: An emerging story with a twist
. 44:4-5.
1998
Dystonia with motor delay in compound heterozygotes for GTP- cyclohydrolase I gene mutations
. 44:10-16.
1998
Expression of the early onset torsion dystonia gene (DYT1) in human brain
. 43:669-673.
1998
Apolipoprotein E genotypes and age at onset of Parkinson's disease [4] (multiple letters)
. 44:294-295.
1998
On the pathological progression of Huntington's disease [1] (multiple letters)
. 44:148.
1998
Surgical treatment of hypothalamic hamartoma [3]
. 43:273-274.
1998
Decreased cerebrospinal fluid levels of substance P in patients with Rett syndrome
. 42:978-981.
1997
Modulation of the age at onset of Parkinson's disease by apolipoprotein E genotypes
. 42:655-658.
1997
Accumulation of β-amyloid precursor protein in HIV encephalitis: Relationship with neuropsychological abnormalities
. 42:34-40.
1997
Intrinsic epileptogenesis of hypothalamic hamartomas in gelastic epilepsy
. 42:60-67.
1997
CAG repeat number governs the development rate of pathology in huntington's disease
. 41:689-692.
1997
Recommendations from the national multiple sclerosis society clinical outcomes assessment task force
. 42:379-382.
1997
Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease
. 39:767-778.
1996
Opportunities and challenges in academic neurology: Report of the long range planning committee of the American Neurological Association
. 39:693-699.
1996
Expression of Hel-N1 and Hel-N2 in small-cell lung carcinoma.
. 39:679-681.
1996
Clinical outcomes assessment in multiple sclerosis
. 40:469-479.
1996
Clinical outcomes and documentation of partial beneficial effects of immunotherapy for multiple sclerosis
. 37:5-6.
1995
Huntington's disease gene: Regional and cellular expression in brain of normal and affected individuals
. 37:218-230.
1995
Increased Risk of Parkinson's Disease in Relatives of Patients
. 37:685-685.
1995
Regional distribution of protease‐resistant prion protein in fatal familial insomnia
. 38:21-29.
1995
Reply
. 37:685-685.
1995
Autoantibodies against the Hel‐N1 RNA‐binding protein among patients with lung carcinoma: An association with type I anti–neuronal nuclear antibodies
. 36:200-205.
1994
Concentric sclerosis (Baló): Morphometric and in situ hybridization study of lesions in six patients
. 35:18-30.
1994
Increased risk of Parkinson's disease in parents and siblings of patients
. 36:659-661.
1994
Neuronal migration disorders: Positron emission tomography correlations
. 35:290-297.
1994
Predictive value of induction of psychogenic seizures by suggestion
. 35:359-361.
1994
Rett syndrome: Controlled study of an oral opiate antagonist, naltrexone
. 35:464-470.
1994
VISUAL PHENOMENA LIMITED TO THE HEMIANOPIC FIELD IN LESIONS OF THE CENTRAL VISUAL PATHWAYS
. 34:279-279.
1993
Clinical determinants of dememtia related to stroke
. 33:568-575.
1993
Correlation of myelin basic protein‐like material in cerebrospinal fluid of multiple sclerosis patients with their response to glucocorticoid treatment
. 33:10-17.
1993
Retinal ganglion cells in Alzheimer's disease and aging
. 33:248-257.
1993
Mitochondrial oxidative phosphorylation defects in Parkinson's disease
. 32:113-114.
1992
Preferential loss of striato‐external pallidal projection neurons in presymptomatic Huntington's disease
. 31:425-430.
1992
Reply
. 32:227-227.
1992
Reply
. 32:595-596.
1992
Cerebral amyloid angiopathy without and with cerebral hemorrhages: A comparative histological study
. 30:637-649.
1991
Excitatory amino acid binding sites in the caudate nucleus and frontal cortex of huntington's disease
. 30:785-793.
1991
Mitochondrial oxidative phosphorylation defects in parkinson's disease
. 30:332-339.
1991
Sleep-related focal motor seizures in bilateral central macrogyria.
. 28:840-842.
1990
Estimation of familial risk in Alzheimer's disease
. 27:338-340.
1990
Phosphorus magnetic resonance spectroscopy of patients with mitochondrial cytopathies demonstrates decreased levels of brain phosphocreatine
. 27:626-630.
1990
Reply
. 27:340-341.
1990
Reply
. 28:840-840.
1990
Assessment of genetic risk for alzheimer's disease among first‐degree relatives
. 25:485-493.
1989
Cerebrospinal fluid biogenic amines and biopterin in rett syndrome
. 25:56-60.
1989
Tomaculous neuropathy presenting as acute recurrent polyneuropathy
. 26:98-100.
1989
Diagnostic criteria for Rett syndrome. The Rett Syndrome Diagnostic Criteria Work Group.
. 23:425-428.
1988
An isoelectric focusing study in herpes simplex virus encephalitis
. 24:227-232.
1988
Reply
. 22:96-97.
1987
Rett's syndrome: Characterization of respiratory patterns and sleep
. 21:377-382.
1987
Bilateral lucency of the globus pallidus complicating methylmalonic acidemia
. 20:364-366.
1986
Facioscapulohumeral dystrophy presenting in infancy with facial diplegia and sensorineural deafness
. 17:513-516.
1985
The role of plasma lipids in carotid bifurcation atherosclerosis
. 17:301-303.
1985
Acquired immune deficiency syndrome and multiple tract degeneration in a homosexual man
. 15:502-505.
1984
The comparative effects of organic brain disease on cerebral blood flow and measured intelligeence
. 13:155-159.
1983
Electrophysiological and clinical correlation in myasthenia gravis
. 12:348-354.
1982
Acute autonomic and sensory neuropathy
. 8:441-444.
1980
Sarcoid polyneuropathy: A histologically proved case
. 7:178-181.
1980
Mechanisms of acute carotid stroke
. 6:245-252.
1979
Tarsal tunnel syndrome: Electrophysiological study
. 5:327-330.
1979
Rapid improvement in nerve conduction velocity following renal transplantation
. 4:369-373.
1978
The malignancy of dementias
. 3:559-561.
1978
Botulism: Electrophysiological studies
. 1:481-485.
1977
Identity
International Standard Serial Number (issn)
0364-5134
Electronic International Standard Serial Number (eissn)
1531-8249