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Differential
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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
dementia, frontotemporal
dementia, presenile
dementia, rapidly progressive
dementia, screening for
dementia, transmissible
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 550 to 600 of 2374 << Previous Next >>

Donepezil for the Treatment of Agitation in Alzheimers Disease
NEJM 357:1382-1392,1441, Howard,R.J.,et al, 2007

Clinical Update:Diagnosis and Treatment of Essential Tremor
Lancet 369:1152-1154, Benito-Leon,J&Louis,E.D., 2007

Pulmonary Arteriovenous Malformations in Hereditary Hemorrhagic Telangiectasia: A Series of 126 Patients
Medicine 86:1-7, Cottin,V.,et al, 2007

Wilson Disease: Description of 282 Patients Evaluated Over 3 Decades
Medicine 86:112-121, Taly,A.B., et al, 2007

Driving and Dementia
BMJ 334:1365-1369, Breen,D.A.,et al, 2007

Neuroimaging Findings in Human Prion Disease
JNNP 78:664-670, Macfarlane,R.G.,et al, 2007

Amyotrophic Lateral Sclerosis
Lancet 369:2031-2041, Mitchell,J.D. & Borasio,G.D., 2007

Paroxysmal Extreme Pain Disorder (Previously Familial Rectal Pain Syndrome)
Neurol 69:586-595, Fertleman,C.R.,et al, 2007

The Neuroprotective Effects of Caffeine: A Prospective Population Study (the Three City Study)
Neurol 69:536-545, Ritchie,K.,et al, 2007

Multiple Sclerosis in Twins From Continental Italy and Sardinia: A Nationwide Study
Ann Neurol 59:27-34, Ristori,G.,et al, 2006

Familial Dopa-Responsive Cervical Dystonia
Neurol 66:599-601, Schneider,S.A.,et al, 2006

Metabolic Disease and Stroke: MELAS
emedicine.com, Mandava,P.,et al, 2006

Topiramate in Essential Tremor, A Double-Blind, Placebo-Controlled Trial
Neurol 66:672-677, Ondo,W.G.,et al, 2006

Benign Tremulous Parkinsonism
Arch Neurol 63:354-357,321, Josephs,K.A.,et al, 2006

Effect of Enhanced Psychosocial Care on Antipsychotic Use in Nursing Home Residents with Severe Dementia; Cluster Randomised Trial
BMJ 332:756-758,741, Fossey,J.,et al, 2006

Donepezil in Patients with Severe Alzheimers Disease: Double-Blind, Parallel-Group, Placebo-Controlled Study
Lancet 367:1057-1065,1031, Winblad,B.,et al, 2006

Mild Cognitive Impairment
Lancet 367:1262-1270, Gauthier,S.,et al, 2006

Neuropathologic Features of Amnestic Mild Cognitive Impairment
Arch Neurol 63:665-672,645, Petersen,R.C.,et al, 2006

The Woman Who Needed a Pet
Surv Ophthalmol 51:592-595, Atchison,M.,et al, 2006

Glycogen-Storage Disease Type II
eMedicine, May 2, Ibrahim,J. &McGovern,M., 2006

Dopamine-Responsive Dystonia
eMedicine (Apr), Nikhar,N.K., 2006

Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies
Epilepsy Res 70S:S223-S230, Fujiwara,T., 2006

Epilepsy Syndromes in Infancy
Pediatr Neurol 34:253-263, Korff,C.M. &Nordii,D.R.,Jr., 2006

Young-Onset Dementia, A Practical Approach to Diagnosis
The Neurologist 12:2-13, Ridha,B. &Josephs,K.A., 2006

Coxibs and Alzheimers Disease: Should They Stay or Should They Go?
Ann Neurol 59:219-228, Firuzi,O. &Pratico,D., 2006

Mild Cognitive Impariment is Early-Stage Alzheimer Disease
Arch Neurol 63:15-16, Morris,J.C., 2006

A 24-Week Open-Label Extension Study of Memantine in Moderate to Severe Alzheimer Disease
Arch Neurol 63:49-54, Reisberg,B.,et al, 2006

Prevalence of Fabry Disease in Patients with Cryptogenic Stroke: A Prospective Study
Lancet 366:1794-1796,1754, Rolfs,A.,et al, 2006

Clinicopath Conf, Charcot-Marie-Tooth Disease Type 2, with Aides Pupil and a Mutation in MPZ Gene
NEJM 354:2584-2592, Case 18-2006, 2006

Finding the Causes of Inherited Neuropathies
Arch Neurol 63:812-816, Scherer,S.S., 2006

Frontotemporal Dementia: Clinicopathological Correlations
Ann Neurol 59:952-962, Forman,M.S.,et al, 2006

Behavioral Effects of Memantine in Alzheimer Disease Patients Receiving Donepezil Treatment
Neurol 67:57-63, Cummings,J.L.,et al, 2006

GAMT Deficiency: Features, Treatment, and Outcome in an Inborn Error of Creatine Synthesis
Neurol 67:480-484, Mercimek-Mahmutoglu,S.,et al, 2006

Late-Onset Metachromatic Leukodystrophy: Genotype Strongly Influences Phenotype
Neurol 67:859-863, Rauschka,H.,et al, 2006

Clinicopath Conf, Dopamine-Responsive-Dystonia Caused by a Mutation in the GCH1 Gene
NEJM 355:831-839, Case 26-2006, 2006

Dystonia
NEJM 355:818-829, Tarsy,D. &Simon,D.K., 2006

Fragile X Premutation With Atypical Symptoms at Onset
Arch Neurol 63:1135-1138, Cellini,E.,et al, 2006

Common Misdiagnosis of a Common Neurological Disorder: How Are We Misdiagnosing Essential Tremor?
Arch Neurol 63:1100-1104, Jain,S.,et al, 2006

Restless Legs Syndrome: Is Treatable But Under-Recognised
BMJ 333:457-458, Medcalf,P. &Bhatia,K.P., 2006

Parkinsons Disease and Genetics
The Neurologist 12:240-244, Lester,J.&Otero-Siliceo,E., 2006

The Tuberous Sclerosis Complex
NEJM 355:1345-1356, Crino,P.B.,et al, 2006

Familial Cervical Artery Dissections: Clinical, Morphologic, and Genetic Studies
Stroke 37:2924-2929, Martin,J.J.,et al, 2006

Genetics of Parkinsons Disease and Parkinsonism
Ann Neurol 60:389-398, Hardy,J.,et al, 2006

Prognosis of Migraine Headaches in Adolescents: A 10-Year Follow-Up Study
Neurol 67:1353-1356, Monastero,R.,et al, 2006

Effectiveness of Atypical Antipsychotic Drugs in Patients with Alzheimers Disease
NEJM 355:1525-1538,1604, Schneider,L.S.,et al, 2006

PET of Brain Amyloid and Tau in Mild Cognitive Impairment
NEJM 355:2652-2663, Small,G.W.,et al, 2006

CNS Involvement in Hereditary Neuropathy With Pressure Palsies (HNPP)
Neurol 67:2250-2252, Tackenberg,B.,et al, 2006

Phenotypic Spectrum Associated with Mutations of the Mitochondrial Polymerase y Gene
Brain 129:1674-1684, Horvath, R.,et al, 2006

Mitochondrial DNA Polymerase-y and Human Disease
Hum Mol Genet 15:R244-R252, Hudson, G.,et al, 2006

The Clinical Spectrum of Neuralgic Amyotrophy in 246 cases
Brain 129:438-450, Alfen, N.V. & Baziel, G.M., 2006



Showing articles 550 to 600 of 2374 << Previous Next >>