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abstract reasoning
acrocyanosis
activities of daily living scale
adrenoleukodystrophy
adrenoleukodystrophy, adult onset
adult-onset leukodystrophy, with neuroaxonal spheroids
advances in neurology
adverse drug reaction
affect, flat
age associated memory impairment
agitation
algorithm
alpha-synuclein
Alzheimer's disease
Alzheimer's disease, age of onset
Alzheimer's disease, diagnosis of
Alzheimer's disease, driving with
Alzheimer's disease, early onset
Alzheimer's disease, early symptoms
Alzheimer's disease, familial
Alzheimer's disease, familial, late onset
Alzheimer's disease, heterogeneity of
Alzheimer's disease, noncognitive symptoms
Alzheimer's disease, pathogenesis
Alzheimer's disease, preclinical
Alzheimer's disease, risk factors in
Alzheimer's disease, staging
Alzheimer's disease, treatment of
amyloid
amyloid angiopathy, cerebral
amyloid beta protein
amyloid deposition
amyloid imaging
amyloid plaques
amyloid-related imaging abnormalities
amyotrophic lateral sclerosis
aneurysm, intracranial, familial
angiitis, granulomatous of CNS
angiography, cerebral
anomic aphasia
anosmia
anticholinesterase
anticoagulant, treatment
antiphospholipid antibody syndrome
anxiety
aphasia
aphasia, logopenic, progressive
aphasia, progressive
aphasia, progressive, non-fluent
aphasia, progressive, primary
apolipoprotein E
apoliprotein E, plasma level
APP
APP gene
apraxia
arteritides
asymptomatic
ataxia
ataxic gait
autoimmune disease
autonomic dysfunction
axonal spheroid
B 12 deficiency
B12
Balint's syndrome
basal ganglia, calcification of
behavioral disorder
biologic markers
bladder dysfunction
bone biopsy
bone survey
bradykinesia
brain atrophy
brain biopsy
brain biopsy, negative
brain volume
C0ORF72
calcification, intracranial
caregiver
CAT scan
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
CAT scan, false negative
caudate nucleus, lesion of, bilateral
celiac disease, adult
central nervous system, infection of
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar plaques, amyloid
cerebral cortex
cerebral cortical atrophy
cerebral embolism
cerebral embolism, cardiac origin
cerebroretinal microangiopathy with calcifications and cysts
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, biochemical markers of CNS disease
cerebrospinal fluid, oligoclonal IgG in
cerebrovascular accident
cerebrovascular accident, young adult
chorea
choreoathetosis
chromosomal abnormality
chromosome 1
chromosome 14
chromosome 17
chromosome 20
chromosome 21
clindamycin
Clinical Pathologic Conference(C.P.C.)
cognition
comorbidities
compulsivity
confusion
constipation
controversies in neurology
corneal dystrophy
corpus callosum
corpus callosum, lesion of
corpus callosum, thinning
cost
coumarin
COVID-19
crying, pathologic
cyst, bone
degenerative diseases of CNS
delusion
dementia
dementia, age at onset
dementia, cerebrovascular disease causing
dementia, clinical diagnosis
dementia, diagnostic evaluation of
dementia, differential diagnosis of
dementia, early detection
dementia, familial
dementia, frontal lobe type
dementia, frontotemporal
dementia, presenile
dementia, prevention of
dementia, rapidly progressive
dementia, reversible
dementia, screening for
dementia, subcortical
dementia, transmissible
dementia, treatment of
depression
diagnostic criteria
differential diagnosis
disorientation
dizziness
donepezil
dopamine agonist
driving
dysdiadochokinesia
dyskinesia
dysphagia
dystonia
echolalia
electroencephalogram
electroencephalogram, abnormalities of
electroencephalogram, focal delta activity
electromyogram
electron microscopy
encephalopathy
encephalopathy, progressive
enzyme, defect
epidemiology of neurology
ethics in neurology
evidence-based research
executive dysfunction
exercise
exome sequencing
Fabry's disease
falling
false negative
familial
fasciculation
fever
florbetapir
fluency
fracture, pathologic
frontal lobe, anatomy and physiology
frontal lobe, atrophy
frontal lobe, lesion of
frontal lobe, pathologic signs of
frontotemporal dementia, behavioral variant
gait disorder
gaze palsy
gaze palsy, horizontal
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
genetic counselling
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
genu of corpus callosum
Gerstmann-Straussler-Scheinker disease
gliadin antibodies
gliosis
grasp reflex
grasping
hallucination
hallucination, visual
handedness
head injury
headache
hearing loss
hemosiderosis of CNS, superficial
heralding manifestation
hippocampal atrophy
hippocampus
Hodgkin's disease
human immunodeficiency virus type 1
Huntington's chorea
hydrocephalus
hydrocephalus, exvacuo
hydrocephalus, normal pressure
hyperreflexia
hypersomnia
hypertension
hypoglycorrhachia
hyposmia
hypotension, systemic
imbalance
impulsivity
inappropriate behavior
inclusion bodies
inclusion bodies, intracytopasmic
inclusion bodies, intranuclear
incoordination
inflexibility, mental
intellectual deficit
intellectual deterioration
intestinal biopsy
intracerebral hemorrhage
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, young adult
Kluver-Bucy syndrome
Lafora body
Lafora's disease
language disorder in adults
laughing, pathologic
L-dopa
L-dopa, drug interactions with and side effects of
lecanemab
leg weakness, bilateral
lethargy
leukodystrophy
leukoencephalopathy
leukoencephalopathy, adult onset, sporadic
Lewy body
Lewy body disease, diffuse
life expectancy
lipomembranous polycystic osteodysplasia
livedo reticularis
lobar atrophy
logopenia
loss of sympathy
lupus anticoagulant
manganese intoxication
memory
Memory Impairment Screen
memory, defect of recent
memory, evaluation of
memory, impairment of
memory, impairment of, subjective
mental status, abnormal
microangiopathy, brain
microhemorrhage, intracerebral
mild cognitive impairment
mild cognitive impairment converting to Alzheimer's disease
mimics
Mini Mental Status Examination
misdiagnosis
molecular genetics
monoclonal antibodies
mood change
mortality
motor neuron disease
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, contrast enhanced
MRI, diffusion weighted
MRI, false negative
MRI, functional
MRI, linear enhancement
MRI, serial
MRI, T1 weighted high signal foci
MRI, volumetry
multiple sclerosis, differential diagnosis of
muscle atrophy, progressive
mutism
myoclonic jerks
myoclonus
neologism
neuroaxonal dystrophy
neuroaxonal leukodystrophy
neurocutaneous disease
neurocutaneous melanosis
neurofibrillary degeneration
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic evaluation
neurologic signs
neuropathology
neuropathology, brain
neuroprotective agents
neurosyphilis
nonsteroidal anti-inflammatory drug
normal
nutritional deficiency
nystagmus
obsessive-compulsive disorder
old age, neurology of
orthostatic hypotension
pain, increased response
paranoia
paraparesis, spastic
paraphasias
paratonia
Parkinson disease
Parkinson disease, dementia with
Parkinson disease, diagnosis
Parkinson disease, early symptoms
Parkinson disease, familial
Parkinson disease, fluctuations in
Parkinson disease, nonmotor problems of
Parkinson disease, presymptomatic detection
Parkinson disease, rapid progression
Parkinson disease, surgical treatment of
Parkinson disease, treatment of
Parkinson disease, young onset
Parkinsonism syndrome
Parkinsonism-dementia complex
PAS positive
PAS positive material in the brain
pathologic reflex
patient information and support
pergolide
perseveration
personality change
Pick bodies
Pick's disease
Pittsburgh Compound B
pleocytosis of cerebrospinal fluid
polycystic lipomembranous osteodysplasia
polymerase chain reaction
posterior cortical atrophy
practice guidelines
preclinical
presenilin-1 gene
presenilin-2 gene
prevention of neurologic disorders
prion disease
prognosis
progressive myoclonic epilepsy
progressive neurologic disorder
progressive subcortical gliosis
protein 14-3-3, cerebrospinal fluid
psychiatric disorder
psychiatric problems in neurologic disorders
psychological testing
psychomotor retardation
psychosis
radiation therapy, CNS treatment and complications with
rapidly progressing neurologic illness
real-time quaking-induced conversion
Red flags
release phenomena
REM sleep
REM sleep behavior disorder
reticulum antibodies
review article
risk factors
risk factors, modification
roaming behavior
safety
schizophrenia
screening
seizure
seizure, children
seizure, diagnosis of
seizure, intractable
seizure, teenager
semantic dementia
senile plaques
serologic testing
single photon emission computed tomography
skin, biopsy
skin, lesions in neurologic disorders
sleep pathology and physiology
smell
Smell Identification Test
Sneddon's syndrome
spasticity
speech disorder
spongy degeneration of brain
startle myoclonus
stereotyped behavior
steroid therapy, CNS treatment and complications with
stimulation, deep brain
stuttering
stuttering following CVA
symmetric brain lesions
syncope
synucleinopathy
syphilis, diagnosis and treatment
syphilis, neurologic complications with
systemic illness
tau protein
tauopathy
temporal lobe, atrophy
thalamus, lesion of
thalamus, lesion of-bilateral
tinnitus
tissue plasminogen activator, intravenous
tongue, fasciculations of
transient neurologic deficit
treatment of neurologic disorder
tremor, thalamic stimulation for suppression of
uremia
urinary incontinence
vanishing white matter
vasculopathy
vegetarianism
vertigo
vertigo, episodic
vitamin deficiency
weight loss
wheelchair
Whipple's disease
white matter disease
word-finding difficulty
workup
Showing articles 50 to 100 of 3694 << Previous Next >>

Preclinical Alzheimer Disease
Neurol 63:2341-2347, Saxton,J.,et al, 2004

Neuroimaging and Early Diagnosis of Alzheimer Disease: A Look to the Future
Radiology 226:315-336, Petrella,J.R.,et al, 2003

Early Alzheimer's Disease
NEJM 349:1056-1063, Kawas,C.H., 2003

Identification of New Presenilin Gene Mutations in Early-Onset Familial Alzheimer Disease
Arch Neurol 60:1541-1544,1521, Tedde,A.,et al, 2003

Functional Deficits in Patients with Mild Cognitive Impairment
Neurol 58:758-764, Tabert,M.H.,et al, 2002

Incidence and Outcome of Mild Cognitive Impairment in a Population-Based Prospective Cohort
Neurol 59;1594-1599, Larrieu,S.,et al, 2002

Adult-Onset Leukoencephalopathy with Vanishing White Matter Presenting with Dementia
Ann Neurol 50:665-668, Prass,K.,et al, 2001

Nonsteroidal Antiinflammatory Drugs and the Risk of Alzheimer's Disease
NEJM 345:1515-1521,1567, in 'T Veld,B.A.,et al, 2001

Early Detection of Dementia: Mild Cognitive Impairment (an Evidence-based Review)
Neurol 56:1133-1142, 1131, Petersen,R.C.,et al, 2001

The Preclinical Phase of Alzheimer Disease
Arch Neurol 57:808-813, Elias,M.F.,et al, 2000

The Value of Informant Versus Individual's Complaints of Memory Impairment in Early Dementia
Neurol 55:1724-1726, Carr,D.B.,et al, 2000

Might Olfactory Dysfunction be a Marker of Early Alzheimer's Disease?
Lancet 355:84-85, Burns,A., 2000

Patterns of Brain Activation in People at Risk for Alzheimer's Disease
NEJM 343:450-456,502, Bookheimer,S.Y. et al, 2000

A Case of Sporadic Pick Disease With Onset at 27 Years
Arch Neurol 56:1289-1291, Jacob,J.,et al, 1999

Functional Magnetic Resonance Imaging in Neuropsychiatry
BMJ 319:1551-1554, Longworth,C.,et al, 1999

Screening for Dementia with the Memory Impairment Screen
Neurol 52:231-238,224, Buschke,H.,et al, 1999

Progressive Aphasia with Rapidly Progressive Dementia in a 49 Year Old Woman
JNNP 66:238-243, Greene,J.D.W.,et al,, 1999

Mild Cognitive Impairment, Clinical Characterization and Outcome
Arch Neurol 56:303-308, Petersen,R.C.,et al, 1999

Serial Magnetic Resonance Imaging of Cerebral Atrophy in Preclinical Alzheimer's Disease
Lancet 353:2125, Fox,N.C.,et al, 1999

Altered Brain Activation in Cognitively Intact Individuals at High Risk for Alzheimer's Disease
Neurol 53:1391-1396, Smith,C.D.,et al, 1999

Familial Aggregation in Frontotemporal Dementia
Neurol 50:1541-1545, Stevens,M.,et al, 1998

Hereditary Form of Parkinsonism-Dementia
Ann Neurol 43:768-781, Muenter,M.D.,et al, 1998

Preclinical Prediction of Alzheimer's Disease Using SPECT
Neurol 50:1563-1571, Johnson,K.A.,et al, 1998

The Genetics of Alzheimer Disease, Current Status and Future Prospects
Arch Neurol 55:294-296, Blacker,D.&Tanzi,R.E., 1998

Clinical Characteristics of a Chromosome 17-Linked Rapidly Progressive Familial Frontotemporal Dementia
Arch Neurol 54:539-544, Basun,H.,et al, 1997

The Clinical Introduction of Genetic Testing for Alzheimer Disease, An Ethical Perspective
JAMA 277:832-836, Post,S.G.,et al, 1997

Clin Features of Early-Onset Alzheimer Disease in Large Kindred with an E280A Presenilin-1 Mutation
JAMA 277:793-799, Lopera,F.,et al, 1997

Hereditary Frontotemporal Dementia is Linked to Chromosome 17q21-q22:Genetic & Clinicopath Study of 3 Dutch Families
Ann Neurol 41:150-159, Heutnik,P.,et al, 1997

Creutzfeldt-Jakob Disease in a Young Woman
Lancet 347:945-948, Tabrizi,S.J.,et al, 1996

Preclinical Evidence of Alzheimer's Disease in Persons Homozygous for the e4Allele for Apolipoprotein E
NEJM 334:752-758, 7911996., Reiman,E.M.,et al, 1996

High Apolipoprotein E e4 Allele Frequency in Age-Related Memory Decline
Ann Neurol 39:548-551, Blesa,R.,et al, 1996

Reversible Dementia and Chorea in a Young Woman with the Lupus Anticoagulant
Neurol 46:1599-1603, Van Horn,G.,et al, 1996

A Low, "Normal"Score on the Mini-Mental State Exam Predicts Development of Dementia after Three Years
JAGS 43:656-661, Braekhus,A.,et al, 1995

Neuropsychological Detection and Characterization of Preclinical Alzheimer's Disease
Neurol 45:957-962, Jacobs,D.M.,et al, 1995

Sneddon's Syndrome is a Thrombotic Vasculopathy:Neuropathologic and Neuroradiologic Evidence
Neurol 45:557-560, Geschwind,D.H.,et al, 1995

Statement of Use of Apolipoprotein E Testing for Alzheimer Disease
JAMA 274:1627-1629, Farrer,L.A.,et al, 1995

Familial Alzheimer's Disease
Ann Neurol 36:335-336, Bird,T.D., 1994

Phenotype of Chromosome 14-Linked Familial Alzheimer's Disease in a Large Kindred
Ann Neurol 36:368-378, Lampe,T.H.,et al, 1994

Chromosome 14-Encoded Alzheimer's Disease:Genetic and Clinicopathological Description
Ann Neurol 36:362-367, Haltia,M.,et al, 1994

Familial Progressive Subcortical Gliosis
Neurol 44:1633-1643, Lanska,D.J.,et al, 1994

Parkinson's Disease
JNNP 57:672-681, Marsden,C.D., 1994

Electroencephalography as an Aid in the Exclusion of Alzheimer's Disease
Arch Neurol 51:280-284, Robinson,D.J.,et al, 1994

Clinicopath Conf
Spongiform Encephalopathy (Creutzfeldt-Jakob Disease) , with Amyloid (KURU) Plaques, Case 17-1993, N, JM 328:66,1993., 1993

Pick's Disease Versus Alzheimer's Disease:A Comparison of Clinical Characteristics
Neurol 43:289-292, Mendez,M.F.,et al, 1993

Inherited Prion Disease (PrP lysine 200) in Britain:Two Case Reports
BMJ 306:301-302, 2881993., Collinge,J.,et al, 1993

Presenile-Onset Cerebral Adrenoleukodystrophy Presenting as Balint's Syndrome and Dementia
Neurol 43:1249-1251, Uyama,E.,et al, 1993

Epidemiology of Human Immunodeficincy Virus Encephalopathy in the United States
Neurol 42:1472-1476, Janssen,R.S.,et al, 1992

Celiac Disease, Brain Atrophy, and Dementia
Neurol 41:372-375, Collin,P.,et al, 1991

Membranous Lipodystrophy:MR Imaging Appearance of the Brain
Radiology 180:793-797, Araki,T.,et al, 1991

Early-Onset Dementia & Extrapyramidal Disease:Clinicopath Variant of Gerstmann-Straussler-Scheinker or Alzheimer's Disease?
JNNP 53:932-934, Hart,J.Jr.&Gordon,B., 1990



Showing articles 50 to 100 of 3694 << Previous Next >>