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acrocyanosis
adrenoleukodystrophy
adrenoleukodystrophy, adult onset
adult-onset leukodystrophy, with neuroaxonal spheroids
advances in neurology
adverse drug reaction
affect, flat
agitation
algorithm
Alzheimer's disease
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, preclinical
Alzheimer's disease, treatment of
amyloid angiopathy, cerebral
amyloid beta protein
amyloid plaques
amyloid-related imaging abnormalities
amyotrophic lateral sclerosis
angiitis, granulomatous of CNS
angiography, cerebral
anomic aphasia
anticoagulant, treatment
antiphospholipid antibody syndrome
aphasia
aphasia, logopenic, progressive
aphasia, progressive
aphasia, progressive, non-fluent
aphasia, progressive, primary
apolipoprotein E
APP
APP gene
apraxia
arteritides
ataxia
ataxic gait
autoimmune disease
axonal spheroid
B 12 deficiency
B12
Balint's syndrome
basal ganglia, calcification of
behavioral disorder
biologic markers
bone biopsy
bone survey
bradykinesia
brain atrophy
brain biopsy
brain biopsy, negative
C0ORF72
calcification, intracranial
CAT scan
CAT scan, abnormal
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, abnormal
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
corneal dystrophy
corpus callosum
corpus callosum, lesion of
corpus callosum, thinning
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, familial
dementia, frontal lobe type
dementia, frontotemporal
dementia, presenile
dementia, rapidly progressive
dementia, reversible
dementia, subcortical
dementia, transmissible
dementia, treatment of
depression
diagnostic criteria
differential diagnosis
disorientation
dizziness
dysdiadochokinesia
dysphagia
dystonia
echolalia
electroencephalogram
electroencephalogram, abnormalities of
electroencephalogram, focal delta activity
electromyogram
electron microscopy
encephalopathy
encephalopathy, progressive
enzyme, defect
epidemiology of neurology
executive dysfunction
exome sequencing
Fabry's disease
falling
false negative
familial
fasciculation
fever
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 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
Hodgkin's disease
human immunodeficiency virus type 1
Huntington's chorea
hydrocephalus
hydrocephalus, exvacuo
hydrocephalus, normal pressure
hyperreflexia
hypersomnia
hypertension
hypoglycorrhachia
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
lecanemab
leg weakness, bilateral
lethargy
leukodystrophy
leukoencephalopathy
leukoencephalopathy, adult onset, sporadic
Lewy body
lipomembranous polycystic osteodysplasia
livedo reticularis
lobar atrophy
logopenia
loss of sympathy
lupus anticoagulant
manganese intoxication
memory, defect of recent
memory, impairment of
memory, impairment of, subjective
mental status, abnormal
microangiopathy, brain
microhemorrhage, intracerebral
mild cognitive impairment
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
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 signs
neuropathology
neuropathology, brain
neurosyphilis
nutritional deficiency
nystagmus
obsessive-compulsive disorder
pain, increased response
paranoia
paraparesis, spastic
paraphasias
paratonia
Parkinson disease
Parkinsonism syndrome
PAS positive
PAS positive material in the brain
pathologic reflex
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
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
psychomotor retardation
psychosis
radiation therapy, CNS treatment and complications with
rapidly progressing neurologic illness
real-time quaking-induced conversion
Red flags
release phenomena
reticulum antibodies
review article
roaming behavior
safety
schizophrenia
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
Sneddon's syndrome
spasticity
speech disorder
spongy degeneration of brain
startle myoclonus
stereotyped behavior
steroid therapy, CNS treatment and complications with
stuttering
stuttering following CVA
symmetric brain lesions
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
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
Showing articles 900 to 950 of 2238 << Previous Next >>

Current Clinical Diagnosis in Creutzfeldt-Jakob Disease; Identification of Uncommon Variants
Ann Neurol 48:323-329, Zerr,I. et al, 2000

Leigh Syndrome: Serial MR Imaging and Clinical Follow-Up
AJNR 21:1502-1509, Arii,J. & Tanabe,Y., 2000

Analysis of EEG and CSF 14-3-3 proteins as adis to the diagnosis of Creutzfeldt-Jakob Disease
Neurol 55:811-815, Zerr,I. et al, 2000

Immunization for Alzheimer's Disease: A Shot in the Arm or a Whiff?
Ann Neurol 48:553-555, Levey,A.I., 2000

Hashimoto's Encephalitis as a Differential Diagnosis of Creutzfeldt-Jakob Disease
JNNP 66:172-176, Seipelt,M.,et al, 1999

Dementia and Snoring
Lancet 353:204, Steiner,M.C.,et al, 1999

Progressive Multifocal Leukoencephalopathy and Human Immunodeficiency Virus-associated White Matter Lesions in AIDS:Magnetization Transfer MR Imaging
Radiology 210:539-543, Ernst,T.,et al,, 1999

The Heidenhain Variant of Creutzfeldt-Jakob Disease
Arch Neurol 56:55-61, Kropp,S.,et al, 1999

Diffusion-Weighted MRI in Sporadic Creutzfeldt-Jakob Disease
Neurol 52:205-208, Demaerel,P.,et al, 1999

Investigation of Variant Creutzfeldt-Jakob Disease and Other Human Prion Diseases with Tonsil Biopsy Samples
Lancet 353:183-189,163, Hill,A.F.,et al, 1999

Surgical Treatment and Risk of Sporadic Creutzfeldt-Jakob Disease:A Case-Control Study
Lancet 353:693-697, Collins,S.,et al, 1999

Adult-Onset MELAS Presenting as Herpes Encephalitis
Arch Neurol 56:241-243, Sharfstein,S.R.,et al, 1999

Current and Remote Blood Pressure and Cognitive Decline
JAMA 281:438-445, Glynn,R.J.,et al, 1999

Spatz-Lindenberg Disease,A Rare Cause of Vascular Dementia
Stroke 30:687-689, Larner,A.J.,et al, 1999

Diagnostic Criteria for Parkinson Disease
Arch Neurol 56:33-39, Gelb,D.J.,et al, 1999

Spastic Paraparesis after Anaesthesia
Lancet 353:554, Lee,P.,et al, 1999

Efficacy and Safety of Rivastigmine in Patients with Alzheimer's Disease:International Randomised Controlled
BMJ 318:633-640, 615, Rosler,M.,et al, 1999

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

Diagnosis, Management, and Treatment of Alzheimer Disease, A Guide for the Internist
Arch Int Med 159:789-798, Richards,S.S.&Hendrie,H.C., 1999

High Monounsaturated Fatty Acids Intake Protects Against Age-Related Cognitive Decline
Neurol 52:1563-1569, Solfrizzi,V.,et al, 1999

Cost-Effectiveness of Donepezil in the Treatment of Mild or Moderate Alzheimer's Disease
Neurol 52:1138-1145,1115, Neumann,P,J.,et al, 1999

Rapidly Progressive Dementia
Lancet 353:1150, Bornke,C.,et al, 1999

Clinicopath Conf:Multisystem Neurodegenerative Disease with Dementia Pugilistica
NEJM 340:1269-1277, Case 12-1999, 1999

Abnormal Diffusion-Weighted Magnetic Resonance Images in Creutzfeldt-Jakob Disease
Arch Neurol 56:577-583, Bahn,M.M.,&Parchi,P., 1999

Mortality from Dementia in Occupations at Risk of Exposure to Bovine Spongiform EncephalopathyAnalysis of Death Registrations
BMJ 318:1044-1045, Aylin,P.,et al, 1999

Prevalence and Clinical Correlates of Psychotic Symptoms in parkinson Disease
Arch Neurol 56:595-601, Aarsland,D.,et al, 1999

Infantile Neuroaxonal Dystrophy,Clinical Spectrum and Diagnostic Criteria
Neurol 52:1472-1478, Nardocci,N.,et al, 1999

Medial Temporal Lobe Atrophy on MRI in Dementia with Lewy Bodies
Neurol 52:1153-1158, Barber,R.,et al, 1999

Clinicopath Conf:Lymphoplasmocytic Lymphoma with Motor Neuronopathy,Waldenstrom's Macroglobulinemia
NEJM 340:1661-1669, , 1999

Prion Protein Conformation in a Patient with Sporadic Fatal Insomnia
NEJM 340:1630-1638,1675, Mastrianni,J.A.,et al, 1999

Do We Have Drugs for Dementia? No
Arch Neurol 56:735-737, Pryse-Phillips,W., 1999

Do We Have a Treatment for Alzheimer Disease? Yes
Arch Neurol 56:738-739,735, Gauthier,S., 1999

Low-Density Lipoprotein Cholesterol and the Risk of Dementia with Stroke
JAMA 282:254-260, Moroney,J.T.,et al, 1999

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

Variability in Annual Mini-Mental State Examination Score in Patients with Probable Alzheimer Disease
Arch Neurol 56:857-862, Clark,C.M.,et al, 1999

Molecular Basis of the Neurodegenerative Disorders
NEJM 340:1970-1980, Martin,J.B., 1999

Risk of Transmission of Bovine Spongiform Encephalopathy to Humans in the United States, Report of the Council on Scientific Affairs
JAMA 281:2330-2339, Tan,L.,et al, 1999

Variant Creutzfeldt-Jakob Disease
Lancet 354:317-323, Collinge,J., 1999

Recent Advances, Neurology
BMJ 319:362-366, Larner,A.J.&Farmer,S.F., 1999

Highly Active Antiretroviral Therapy Reverses Brain Metabolite Abnormalities in Mild HIV Dementia
Neurol 53:782-789, Chang,L.,et al, 1999

A Randomized Trial of Risperidone,Placebo,and Haloperidol for Behavioral Symptoms of Dementia
Neurol 53:946-955,899, DeDeyn,P.P.,et al, 1999

Clinicopath Conf, Creutzfeldt-Jakob Disease,Case 28-1999
NEJM 341:901-908, , 1999

Seizures and Creutzfeldt-Jakob Disease
NCMJ 60:108-109, Cokgor,I.,et al, 1999

Creutzfeldt-Jakob Disease Presenting as Complex Partial Status Epilepticus: A Report of Two Cases
JNNP 66:406-407, Rees,J.H.,et al, 1999

Clinical Benefits of Donepezil:Results from a Long-Term Phase III Extension Trial
Neurol 52:A174, Doody,R.S.,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

Diagnosing Dementia with Lewy Bodies
Lancet 354:1227-1228, McKeith,I.G.,et al, 1999

Tube Feeding in Patients with Advanced Dementia,A Review of the Evidence
JAMA 282:1365-1370, Finucane,T.E.,et al, 1999

Nuclear Medicine in Neurology and Psychiatry
Lancet 354:1107-1111, Costa,D.C.,et al, 1999

Dementia as the Most Common Presentation of Cortical-Basal Ganglionic Degeneration
Neurol 53:1969-1974, Grimes,D.A.,et al, 1999



Showing articles 900 to 950 of 2238 << Previous Next >>