Neurology Specific Literature Search   
 
[home][thesaurus]
    

Differential
(Click to cross reference)
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 1050 to 1100 of 2238 << Previous Next >>

The 14-3-3 Brain Protein and Transmissible Spongiform Encephalopathy
NEJM 336:873-875, Moussavian,M.,et al, 1997

Seizures and Epilepsy in the Elderly
Arch Int Med 157:605-617, Thomas,R.J., 1997

Widespread Dilatation of Perivascular Spaces:A Leukoencephalopathy Causing Dementia
Neurol 48:1310-1313, Vital,C.&Julien,J., 1997

Chronic Encephalitis and Epilepsy in Adults and Adolescents:A Variant of Rasmussen's Syndrome
Neurol 48:418-424, Hart,Y.M.,et al, 1997

Familial Idiopathic Brain Calcification with Autosomal Dominant Inheritance
Neurol 48:645-649, Kobari,M.,et al, 1997

Telling Patients They Have Alzheimer's Disease
BMJ 314:321-322, 375-3761997., Rice,K.,et al, 1997

Criteria for Alzheimer's Disease and the Nosology of Dementia with Lewy Bodies
Neurol 48:126-132, Hansen,L.A.&Samuel,W., 1997

Comparison of Extrapyramidal Features in 31 Path Cases of Diffuse Lewy Body Disease & 34 Cases of Parkinson's
Neurol 48:376-380, Louis,E.D.,et al, 1997

A Prospective Study of Estrogen Replacement Therapy and the Risk of Developing Alzheimer's Disease
Neurol 48:1517-1521, Kawas,C.,et al, 1997

Unusual Causes of Headache
Neurol 48:1494-1499, Ramadan,N.M., 1997

Rapid Spongiform Degeneration of the Cerebrum and Cerebellum in Creutzfeldt-Jakob Encephalitis:Serial MR Findings
AJNR 18:583-586, Tzeng,B-C.,et al, 1997

The Risk of Bovine Spongiform Encephalopathy ('Mad Cow Disease') to Human Health
JAMA 278:1008-1011, Brown,P., 1997

Detection of 14-3-3 Protein in the CSF of Genetic Creutzfeldt-Jakob Disease
Neurol 49:593-595, Rosemann,H.,et al, 1997

Creutzfeldt-Jakob Disease after Extracranial Dura Mater Embolization for a Nasopharyngeal Angiofibroma
Neurol 48:1451-1453, Antoine,J.C.,et al, 1997

Creutzfeldt-Jakob Dis after Embolization of Intercostal Arteries with Cadaveric Dura Suggest a Syst Trans of Prion Agent
Neurol 48:1470-1471, Defebvre,L.,et al, 1997

Progressivge Multifocal Leukoencephalopathy Presenting as Human Immunodeficiency Virus Type 1 (HIV) -Assoc Dementia
Neurol 49:263-265, Zunt,J.R.,et al, 1997

Effects of Human Immunodeficiency Virus Infection on the Manifestations of Neurosyphillis
Neurol 49:893-894, deSouze,M.C.&Nitrini,R., 1997

Familial Nature and Continuing Morbidity of the Amyotrophic Lateral Sclerosis-Parkinsonism Dementia Complex of Guam
Neurol 49:400-409, McGeer,P.L.,et al, 1997

Clinicopath Conf
Hodgkin's Disease, Paraneoplastic Cerebellar Degeneration, Case 21-1997, NEJM 337:115-12297., , 1997

Assessment of Digital EEG, Quantitative EEG, and EEG Brain Mapping
Neurol 49:277-292, Nuwer,M., 1997

Measurement of Acetylcholinesterase by PET in the Brains of Healthy Controls & Pts with Alzheimer's Disease
Lancet 349:1805-1809, Iyo,M.,et al, 1997

Seizures, Epilepsy, and Functional Recovery after Traumatic Brain Injury
Neurol 48:803-806, Hernandez,T.D.&Naritoku,D.K., 1997

New Variant Creutzfeldt-Jakob Disease:Neurological Features and Diagnostic Tests
Lancet 350:903-907, Zeidler,M.,et al, 1997

New Variant Creutzfeldt-Jakob Disease:Psychiatric Features
Lancet 350:908-910, Zeidler,M.,et al, 1997

Frontotemporal Dementia is on the MAP
Ann Neurol 41:139-140, Wilhelmsen,K.C., 1997

Alteration of White Matter MR Signal Intensity in Frontotemporal Dementia
AJNR 18:367-378, Kitagaki,H.,et al, 1997

Collection and Normal Levels of the Amyloid Precursor Protein in Plasma
Ann Neurol 41:121-124, Whyte,S.,et al, 1997

Assessment of CSF Levels of Tau Protein in Mildly Demented Patients with Alzheimer's Disese
Neurol 48:632-635, Galasko,D.,et al, 1997

Correlation of MRI and Neuropathology in AIDS
JNNP 62:92-95, Everall,I.P.,et al, 1997

Peripheral NEuropathy in Creutzfeldt-Jakob Disease
Neurol 48:784, Esiri,M.M.,et al, 1997

Bovine Spongiform Encephalopathy and a New Variant of Creutzfeldt-Jakob Disease
Neurol 48:569-571, Epstein,L.G.&Brown,P., 1997

Diagnosis of New Variant Creutzfeldt-Jakob Disease by Tonsil Biopsy
Lancet 349:99-100, Hill,A.F.,et al, 1997

Apolipoprotein E Genotypes in Primary Progressive Aphasia
Neurol 49:51-55, Mesulam,M.M.,et al, 1997

What Are the Obstacles for an Accurate Clinical Diagnosis of Pick's Disease
Neurol 49:62-69, Litvan,I.,et al, 1997

X Linked Adrenoleukodystrophy:Clinical Presentation, Diagnosis, and Therapy
JNNP 63:4-14, vanGeel,B.M.,et al, 1997

Clinicopath Conf
Progressive Supranuclear Palsy, Case 26, 1997, NEJM 337:549-55697., , 1997

Serial Neuropsychological Assess & Magnetic Resonance Imagingf Analysis in Multiple Sclerosis
Arch Neurol 54:1018-1025, Hohol,M.J.,et al, 1997

Tremor and Other Movement Disorders after Whiplash Type Injuries
JNNP 63:110-112, Ellis,S.J., 1997

Donepezil (Aricept) for Alzheimer's Disease
The Medical Letter 39:53-54, , 1997

Prevalence and Severity of Cognitive Impairment with and without Dementia in an Elderly Population
Lancet 349:1793-1796, Graham,J.E.,et al, 1997

Increased Risk of Mortality in Alzheimer's Disease Patients with Higher Education
Neurol 49:798-802, Geerlings,M.I.,et al, 1997

Pupil Dilation to Tropicamide is not Specific for Alzheimer Disease
Arch Neurol 54:841-844, Growdon,J.H.,et al, 1997

A Controlled Trial of Selegiline, Alpha-Tocopherol, or Both as Treatment for Alzheimer's Disease
NEJM 336:1216-1222, 12451997., Sano,M.,et al, 1997

Antioxidants and Dementia
Lancet 349:1189-1190, Lethem,R.&Orrell,M., 1997

Clinical Features and Pharmacologic Treatment of Behavioral Symptoms of Alzheimer's Disease
Neurol 48 (Suppl 6) :S17-S24997., Borson,S.&Raskind,M.A., 1997

Reliability of Wash Univ Road Test:A Performance-Based Assess for Drivers with Dementia of Alzheimer Type
Arch Neurol 54:707-712, Hunt,L.A.,et al, 1997

Midline Cerebral Morphometry Distinguishes Frontotemporal Dementia and Alzheimer's Disease
Neurol 48:978-985, Kaufer,D.I.,et al, 1997

Simulated Car Crashes and Crash Predictors in Drivers with Alzheimer Disease
Arch Neurol 54:545-551, Rizzo,M.,et al, 1997

The Family Caregiver's Role in Alzheimer's Disease
Neurol 48 (Suppl 6) :S25-S29997., Haley,W.E., 1997

Predictors of Time to Institutionalization of Patients with Alzheimer's Disease:The CERAD Experience, Part XVII
Neurol 48:1304-1309, Heyman,A.,et al, 1997



Showing articles 1050 to 1100 of 2238 << Previous Next >>