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activated protein C resistance
advances in neurology
agitation
agnosia
algorithm
aluminum
Alzheimer's disease
Alzheimer's disease, age of onset
Alzheimer's disease, conjugal
Alzheimer's disease, diagnosis of
Alzheimer's disease, early onset
Alzheimer's disease, familial
Alzheimer's disease, familial, late onset
Alzheimer's disease, heterogeneity of
Alzheimer's disease, incidence
Alzheimer's disease, pathogenesis
Alzheimer's disease, preclinical
Alzheimer's disease, risk factors in
Alzheimer's disease, treatment of
amnesia
amyloid angiopathy, cerebral
amyloid beta protein
amyloid imaging
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, guamian type of
aneuploidy
aneurysm, intracranial, familial
anomic aphasia
anticholinesterase
antiphospholipid antibodies
antithrombin III deficiency
aphasia
aphasia, progressive
aphasia, progressive, primary
apolipoprotein E
APP
APP gene
apraxia
apraxia, constructional
arthrogryposis multiplex
aspiration
asymptomatic
ataxia
attention span
behavioral disorder
benign essential tremor
biologic markers
blood dyscrasias, neurologic findings with
blood transfusion
brain transplantation
CAT scan
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
cataplexy
cell fusion test
central core disease
central nervous system, infection of
cerebellar plaques, amyloid
cerebral cortical atrophy
cerebral edema, vasogenic
cerebral glucose metabolism
cerebral infarction
cerebral venous thrombosis
cerebral venous thrombosis, etiology
cerebrospinal fluid, biochemical markers of CNS disease
cerebrovascular accident
cerebrovascular accident, familial occurrence
cerebrovascular accident, infancy and childhood
cerebrovascular accident, recurrent
cerebrovascular accident, women
cerebrovascular accident, work up for
cerebrovascular accident, young adult
cerebrovascular disease, risk factors in
Charcot-Marie-Tooth
children
choline acetyltransferase
chromosomal abnormality
chromosome 1
chromosome 12
chromosome 14
chromosome 21
chromosome 9
cigarette smoking
clindamycin
coagulopathy
cognition
cost
crying, pathologic
cultured skin fibroblasts
D-dimer
degenerative diseases of CNS
delusion
dementia
dementia, age at onset
dementia, differential diagnosis of
dementia, familial
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dementia, rapidly progressive
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depression
developmental milestones, loss of
diagnostic criteria
differential diagnosis
DNA probes
donepezil
dural sinus thrombosis
dysarthria
dysnomia
dysphagia
dystonia
echolalia
epidemiology of neurology
ethics in neurology
executive dysfunction
Factor V Leiden
false negative
familial
Fazio-Londe's disease
fluency
foam cells
Friedreich's ataxia
frontotemporal dementia, behavioral variant
gaze palsy
gaze palsy, supranuclear
gene
gene mutation
genetic counselling
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
Gilles de la Tourette syndrome
hallucination
head injury
headache
headache, persistent
headache, severe
heavy metal intoxication
hemiparesis
hemoglobin abnormality, neurologic complications of
hepatic failure
hepatosplenomegaly
hippocampus
human genome
Huntington's chorea
hyperpyrexia, CNS disorder causing
hyperreflexia
inattention
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
incoordination
infantile hemiplegia
inflexibility, mental
intellectual deficit
intracerebral hemorrhage
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, medical precaution with
jaundice
Kugelberg-Welander syndrome
language disorder in adults
lipid storage disorder of CNS
lobar atrophy
lupus anticoagulant
lymphoma involving CNS
manic-depressive
medical-legal aspects of neurology
memory, impairment of
middle cerebral artery territory infarction
middle cerebral artery, occlusion of
mild cognitive impairment
misdiagnosis
molecular genetics
mongolism
mortality
motor neuron disease
MRI
MRI, abnormal
MRI, false negative
MRI, functional
MRI, negative
MRI, serial
muscular dystrophy
muscular dystrophy, Duchenne
mutism
myasthenia gravis
myoclonic jerks
myoclonus
myotonia dystrophica
nausea and vomiting
neurofibrillary degeneration
neurofibromatosis 1
neurofibromatosis 2
neurologic disease, diagnoses of
neurologic signs
neuropathology
neuropathology, brain
neuropathy, amyloid
neurotransmitter
nicotine
Niemann-Pick disease
obsessive-compulsive disorder
pain, increased response
paranoia
paraparesis, spastic
paratonia
Parkinson disease
Parkinson disease, familial
Parkinson disease, surgical treatment of
Parkinson disease, treatment of
Parkinsonism syndrome
PAS positive material in the brain
personality change
Pittsburgh Compound B
poison, mercury
poison, neurologic problems with
practice guidelines
preclinical
presenilin-1 gene
presenilin-2 gene
prethrombotic state
prognosis
progressive neurologic disorder
protein C deficiency
protein S deficiency
psychiatric problems in neurologic disorders
psychological testing
psychomotor retardation
psychosis
pulmonary embolism
recombinant DNA
release phenomena
research
review article
RFLPs
risk factors
seizure
senile plaques
single photon emission computed tomography
slow virus infection of CNS
spinal muscular atrophy
spinocerebellar ataxia
splenomegaly
spongy degeneration of brain
stereotyped behavior
stimulation, deep brain
straight sinus
subarachnoid hemorrhage
subdural hematoma
superior sagittal sinus thrombosis
tau protein
thrombophlebitis
treatment of neurologic disorder
tremor
tricresylphosphate
trinucleotide repeats
twins
ubiquilin 1
viral infection, CNS
visuospatial disturbance
Werdnig-Hoffman disease
Wernicke's aphasia
word-finding difficulty
Showing articles 450 to 500 of 2374 << Previous Next >>

Fully-Automated Quantification of Regional Brain Volumes for Improved Detection of Focal Atrophy in Alzheimers Disease
AJNR 30:578-580, Brewer, J.B.,et al, 2009

The Expanding Phenotype of GLUT1-Deficiency Syndrome
Brain & Dev 31:545-552, Brockmann,K., 2009

Pittsburg Compound B Imaging and Prediction of Progression From Cognitive Normality to Symptomatic Alzheimer Disease
Arch Neurol 66:1469-1475, Morris,J.,et al, 2009

Conventional MRI and NOTCH3 Gene Screening in Sporadic CADASIL
Neurol 72:469-471, Liguori,M.,et al, 2009

Predictors of Driving Safety in Early Alzheimer Disease
Neurol 72:521-527, Dawson,J.D.,et al, 2009

Rapidly Progressive Neurodegenerative Dementias
Arch Neurol 66:201-207, Josephs,K.A.,et al, 2009

Autism
Lancet 374:1627-1638, Levy,S.,et al, 2009

Aicardi-Gouti�res Syndrome: Neuroradiologic Findings and Follow-up
AJNR 30:1971-1976, Uggetti,C.,et al, 2009

Clinical Syndromes Associated with Posterior Atrophy: Early Age at Onset AD Spectrum
Neurol 73:1571-1578, Migliaccio,R.,et al, 2009

Leukodystrophies: Classification, Diagnosis, and Treatment
Neurologist 15:319-328, Costello,D.,et al, 2009

CNS Complications of Radiotherapy and Chemotherapy
Lancet 374:1639-1651, Soussain,C.,et al, 2009

Predicting the Time of Conversion to MCI in the Elderly: Role of Verbal Expression and Learning
Neurol 73:1436-1442, 1432, Oulhaj,A.,et al, 2009

Alzheimers Disease
BMJ 338:467-471, Burns,A. &Iliffe,S., 2009

In Vivo Mapping of Amyloid Toxicity in Alzheimer Disease
Neurol 72:1504-1511, Frisoni,B.G.,et al, 2009

Association of HTRA1 Mutations and Familial Ischemic Cerebral Small-Vessel Disease
NEJM 360:1729-1739, Hara,K.,et al, 2009

Genomewide Association Studies of Stroke
NEJM 360:1718-1728, Ikram,M.A.,et al, 2009

Clinicopath Conf, Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL)
NEJM 360:1656-1665, Case 12-2009, 2009

A 63-Year-Old Woman with Urinary Incontinence and Progressive Gait Disorder
Neurol 72:1607-1613, Lossos,A.,et al, 2009

Donepezil Treatment of Patients with MCI: A 48-Week Randomized, Placebo-Controlled Trial
Neurol 72:1555-1561, Doody,R.S.,et al, 2009

Epilepsy, Ataxia, Sensorineural Deafness, Tubulopathy, and KCNJ10 Mutations
NEJM 360:1960-1970, Bockenhauer,D.,et al, 2009

Long-Term Effects of the Concomitant Use of Memantine with Cholinesterase Inhibition in Alzheimer Disease
JNNP 80:600-607, Lopez,O.L.,et al, 2009

Age, Neuropathology, and Dementia
NEJM 360:2302-2309, Savva,G.M.,et al, 2009

CSF Biomarkers and Incipient Alzheimer Disease in Patients with Mild Cognitive Impairment
JAMA 302:385-393,436,452, Mattsson,N.,et al, 2009

Association Between Mid-Life Martial Status and Cognitive Function in Later Life: Population Based Cohort Study
BMJ 339:99,57, H�kansson,K.,et al, 2009

Disclosure of APOE Genotype for Risk of Alzheimers Disease
NEJM 361:245-254,298, Green,R.C.,et al, 2009

Diagnosis and New Treatments in Muscular Dystrophies
JNNP 80:706-714, Manzur,A.Y. &Muntoni,F., 2009

Positron Emission Tomography in Diagnosis of Visual Variant Alzheimer Disease
J Neuro-Ophthalmol 29:149-150, Finelli,P.F., 2009

Neurofibromatosis Type 2
Lancet 373:1974-1986, Astagiri,A.R.,et al, 2009

Risk of Dementia and AD with Prior Exposure to NSAIDs in an Elderly Community-Based Cohort
Neurol 72:1899-1905,1884, Breitner,J.C.S.,et al, 2009

Seizures in Alzheimer Disease: Who, When, and How Common?
Arch Neurol 66:992-997, Scarmeas,N.,et al, 2009

Family History of Melanoma and Parkinson Disease Risk
Neurol 73:1286-1291, Gao,X.,et al, 2009

The Clinical Course of Advanced Dementia
NEJM 361:1529-1538, 1595, Mitchell,S.,et al, 2009

Screening for Intracranial Aneurysms in ADPKD: A More Accurate Risk Assignment Model Is Needed
BMJ 339:706-707, Ong,A., 2009

Practice Parameter: Evaluation of the Child with Microcephaly (An Evidence-Based Review): Report of the Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society
Neurol 73:887-897, Ashwal,S.,et al, 2009

Diagnosis and Therapy in Neuromuscular Disorders: Diagnosis and New Treatments in Mitochondrial Diseases
JNNP 80:943-953, Rahman,S. &Hanna,M.G., 2009

Conversion of Amyloid Positive and Negative MCI to AD over 3 Years: An 11C-PIB PET Study
Neurol 73:754-760, 744, Okello,A.,et al, 2009

Akinetopsia in the Posterior Cortical Variant of Alzheimer Disease
Neurol 73:731-732, Tsai,P. &Mendez,M.F., 2009

DNA �-Amyloid1-42 Trimer Immunization for Alzheimer Disease in a Wild-Type Mouse Model
JAMA 302:1796-1802, Lambracht-Washington,D.,et al, 2009

Association of Plasma Leptin Levels With Incident Alzheimer Disease and MRI Measures of Brain Aging
JAMA 302:2565-2572, 2593, Lieb,W.,et al, 2009

Aicardi-Gouti�res Syndrome
Br Med Bull 89:183-201, Orcesi, S.,et al, 2009

The Hot Cross Bun Sign in the Patients with Spinocerebellar Ataxia
Eur J Neurol 16:513-516, Lee, Y.-C.,et al, 2009

Clinicopath Conf., Adult Cerebral Form of X-Linked Adrenoleukodystrophy
NEJM 360:171-181, Case 1-2009, 2009

Prodromal Alzheimers Disease: Successive Emergence of the Clinical Symptoms
Ann Neurol 64:492-498,479, Amieva,H.,et al, 2008

Memory Problems in an Older Person
BMJ 337:1235-1236, Suresh,K.,et al, 2008

Fragile X-Associated Tremor/Ataxia Syndrome: An Aging Face of the Fragile X Gene
Arch Neurol 65:19-25, Amiri,K.,et al, 2008

Foreign Accent Syndrome as the Initial Sign of Primary Progressive Aphasia
JNNP 79:79-81, Luzzi,S.,et al, 2008

Risperidone, Haloperidol, and Placebo in the Treatment of Aggressive Challenging Behaviour in Patients With Intellectual Disability: A Randomised Controlled Trial
Lancet 371:57-63,9, Tyrer,P.,et al, 2008

Genetics of Familial Amyotrophic Lateral Sclerosis
Neurol 70:144-152, Valdmanis,P.N. &Rouleau,G.A., 2008

NSAID Use and Dementia Risk in the Cardiovascular Health Study: Role of APOE and NSAID Type
Neurol 70:17-24, Szekely,C.A.,et al, 2008

Joint Effect of Stroke and APOE 4 on Dementia Risk: The Canadian Study of Health and Aging
Neurol 70:9-16,5, Jin,Y.P.,et al, 2008



Showing articles 450 to 500 of 2374 << Previous Next >>