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Differential
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abdominal protrusion
activities of daily living
activities of daily living scale
agnosia
agnosia, visual
agraphia
akinetic mute
alexia
Alzheimer's disease
Alzheimer's disease, diagnosis of
Alzheimer's disease, visual variant
amyloid angiopathy, cerebral
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, diagnosis of
amyotrophic lateral sclerosis, differential diagnosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, etiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, prognosis
amyotrophic lateral sclerosis, treatment of
anomic aphasia
aphasia
aphasia, progressive
aphasia, progressive, non-fluent
aphasia, progressive, primary
aphasia, transcortical
aphasia, transcortical-sensory
apolipoprotein E
apraxia
apraxia, constructional
arthralgia
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxic gait
attention span
atypical
automobile accidents
B 12 deficiency
B12
behavioral disorder
binge eating
biologic markers
blepharospasm
bone biopsy
bone pain
bone scanning
brain atrophy
brain biopsy
bruxism
bulimia
C9orf72
calculations
CAT scan
CAT scan, abnormal
CAT scan, dementia
CAT scan, emission, abnormal
cerebellar atrophy, primary
cerebellar degeneration
cerebellar tonsils
cerebellum, disease of
cerebral cortical atrophy
cerebrospinal fluid, leak
cerebrospinal fluid, pressure low
Charles Bonnet's syndrome
choreoathetosis
chromosomal abnormality
chromosome 17
Clinical Pathologic Conference(C.P.C.)
cognition
coma
comprehension, impaired
compulsivity
confusion
controversies in neurology
corpus callosum
corpus callosum, atrophy of
cortical-basal ganglionic degeneration
crying, pathologic
degenerative diseases of CNS
delirium
delusion
dementia
dementia, age at onset
dementia, clinical diagnosis
dementia, diagnostic classification
dementia, diagnostic evaluation of
dementia, differential diagnosis of
dementia, familial
dementia, frontal lobe type
dementia, frontotemporal
dementia, presenile
dementia, rapidly progressive
dementia, reversible
dementia, treatment of
depression
diagnostic criteria
differential diagnosis
difficulty climbing stairs
disinhibition-dementia-parkinsonism-amyotrophic complex
dizziness
drug withdrawal
dural tear
dysarthria
dysmetria
eating disorder
electromyogram
electron microscopy
emotional lability
epidural blood patch
executive dysfunction
falling
familial
fasciculation
fatigue
fibrillations
finger nose finger test
flail arm syndrome
fluency
foot drop
frontal lobe, atrophy
frontal lobe, behavior with disease of
frontal lobe, pathologic signs of
frontotemporal brain sagging syndrome
frontotemporal dementia, behavioral variant
gait disorder
gait, waddling
gaze palsy, vertical
gene
gene mutation
genetic neurologic disorders
genetic testing
glabellar sign
grasp reflex
hallucination
hallucination, visual
hallucination, visual, benign
head injury
headache
headache, chronic
headache, positional
headache, severe
headache, throbbing
hearing loss
hemianopia, homonymous
herpes simplex encephalitis
hippocampus
House sign
Huntington's chorea
hyperreflexia
hypersomnia
imbalance
imbalance, postural
impulsivity
inappropriate behavior
inattention
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion bodies, intracytopasmic
inclusion bodies, ubiquitin
inflexibility, mental
initiative, lack of
insomnia
insular cortex
insular cortex, lesion
intellectual deficit
intellectual deterioration
interpeduncular cistern, compressed
intracranial hypotension
intrathecal chemotherapy
irritability
Jakob-Creutzfeldt disease
jaw jerk, abnormal
Kluver-Bucy syndrome
language disorder in adults
laughing, pathologic
leg weakness, bilateral
leukemia
level of consciousness, decreased
Lewy body disease, diffuse
lobar atrophy
locked-in syndrome
logopenia
loss of sympathy
lymphoma
lymphoma involving CNS
lymphoma, primary of CNS
memory
memory, defect of recent
memory, impairment of
memory, recent
meningeal enhancement
mental status, abnormal
mesial temporal sclerosis
midbrain, swollen
migraine
mimics
misdiagnosis
Montreal cognitive assessment
mood change
mortality
motor neuron disease
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, functional
MRI, negative
MRI, serial
MRI, spine
MRS
multiple system atrophy
muscle biopsy
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
mutism
myopathy
myopathy, inclusion body
myopathy, inclusion body with Paget's disease
nausea and vomiting
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic examination, focal
neurologic signs
neuropathology
neuropathology, brain
nutritional deficiency
nystagmus
obsessive-compulsive disorder
ophthalmoplegia
ophthalmoplegia, total
Paget's disease
pain, increased response
pallido-ponto-nigral degeneration
palmomental response
paranoia
paraparesis
paraphasias
paraplegia, in flexion
Parkinson disease
Parkinson disease, atypical
Parkinsonism syndrome
pathologic reflex
peduncular hallucinosis
perseveration
personality change
Pick bodies
Pick's disease
pituitary hyperemia
pons, flattened
posterior cortical atrophy
posterior leukoencephalopathy syndrome
prepontine cistern, effaced
primary intracranial hypotension
primary lateral sclerosis
prognosis
progranulin
progressive neurologic disorder
progressive subcortical gliosis
progressive supranuclear palsy
pruritus
pseudobulbar palsy
psychiatric problems in neurologic disorders
psychological testing
psychomotor retardation
psychosis
quadriplegia
radiation therapy, CNS treatment and complications with
rapidly progressing neurologic illness
Red flags
release phenomena
repetition, impaired
respiratory failure
respiratory tract infection
reversible cerebral vasoconstrictive syndromes
reversible neurologic disorder
review article
rigidity, axial
risk factors
roaming behavior
rooting reflex
sagging of the brain
sclerosis, bone
seizure
semantic dementia
sexual behavior, disorder of
simultanagnosia
single photon emission computed tomography
single photon emission computed tomography, false negative
sleep pathology and physiology
snout reflex
spasticity
speech disorder
speech, loss of
splenium of corpus callosum
splenium of corpus callosum, displaced
spongy degeneration of brain
stem cell transplantation
stereotyped behavior
suck reflex
synucleinopathy
systemic illness
tangential
tau protein
tauopathy
temporal lobe
temporal lobe, atrophy
temporal lobe, lesion
temporal lobe, lesion, bilateral
tinnitus
tinnitus, pulsatile
tongue, atrophy
tongue, fasciculations of
tonsillar herniation of cerebellum
trauma
treatment of neurologic disorder
ubiquitin
upgaze, paralysis of
urinary incontinence
vegetarianism
visual field defect
visuospatial disturbance
vitamin deficiency
weakness, progressive
wheelchair
white matter disease
wide based gait
Wingspan study
word-finding difficulty
Showing articles 1400 to 1450 of 2292 << Previous Next >>

Progressive Multifocal Leucoencephalopathy
Brit J Hosp Med 50:187-192, Sweeney,B.J.,et al, 1993

The Mutations at nt 8993 of Mitochondrial DNA is a Common Cause of Leigh's Syndrome
Ann Neurol 34:827-834, Santorelli,F.M.,et al, 1993

Brain Imaging in Late-Onset CM2 Gangliosidosis
Neurol 43:2055-2058, Streifler,J.Y.,et al, 1993

Gene Therapy for Neurologic Disease
Arch Neurol 50:1252-1268, Suhr,S.T.&Gage,F.H., 1993

MRI Abnormalities in Creutzfeldt-Jakob Disease
Neuroradiology 35:584-585, DiRocco,A.,et al, 1993

Driving and Alzheimer's Disease:The Risk of Crashes
Neurol 43:2448-2456, Drachman,D.A.,et al, 1993

End-State Alzheimer's Disease:Glasgow Coma Scale and the Neurologic Examination
Arch Neurol 50:1309-1315, Benesch,C.G.,et al, 1993

Dementia in AIDS Patients:Incidence and Risk Factors
Neurol 43:2245-2252, McArthur,J.C.,et al, 1993

A New Bedside Test of Cognition for Patients with HIV Infection
Ann Int Med 119:1001-1004, Jones,B.N.,et al, 1993

Clinical-Neuropathologic Correlation in HIV-Associated Dementia
Neurol 43:2230-2237, Glass,J.D.,et al, 1993

Alzheimer's Disease
BMJ 307:779-782, Rossor,M., 1993

HIV Encephalopathy and Dementia
Psychiatr Clin North Am 15:455-466, Pajeau,A.K.&Roman,G.C., 1992

Creutzfeldt-Jakob Disease in a Recipient of Human Pituitary-Derived Gonadotrophin:A Second Case
JNNP 55:1094-1095, Cochius,J.I.,et al, 1992

Familial Creutzfeldt-Jakob Disease (Codon 200 Mutation) with Supranuclear Palsy
Bertoni. J. M. , et al, JAMA 268:2413-2415., , 1992

Amyloidoma of the CNS. I. Clinical and Pathologic Study
Neurol 42:2019-2023, Cohen,M.,et al, 1992

Amyloid Angiopathy in Diffuse Lewy Body Disease
Neurol 42:2131-2135, Wu,E.,et al, 1992

Drug Induced Creutzfeldt-Jakob Like Syndrome
J Psychiatr Neurosci 17:103-105, Finelli,P.F., 1992

Neuropsychiatric Systemic Lupus Erythematosus in Elderly People:A Case Series
JNNP 55:1157-1161, Dennis,M.S.,et al, 1992

CT of 338 Active Professional Boxers
Radiology 185:509-512, Jordan,B.D.,et al, 1992

Cerebral Artery Aneurysms in Children Infected with Human Immunodeficiency Virus
J Pediatr 121:927-930, Husson,R.N.,et al, 1992

Cortical Biopsy in Alzheimer's Disease:Dx Accuracy & Neurochem Neuropath, & Cognit Correl
Ann Neurol 32:625-632, Dekosky,S.T.,et al, 1992

A Controlled Trial of Tacrine in Alzheimer's Disease
JAMA 268:2523-2529, 25641992., Farlow,M.,et al, 1992

A Double-Blind, Placebo-Controlled Multicenter Study of Tacrine for Alzheimer's Dissease
NEJM 327:1253-1259, 13061992., Davis,K.L.,et al, 1992

Familial Alzheimer's Disease:Second Gene Locus Located, Markers for Familial Disease May be Available
BMJ 305:1108-1109, Mullan,M., 1992

Confusion & Memory Loss from Capsular Genu Infarction:A Thalamocortical Disconnection Syndrome?
Neurol 42:1966-1979, Tatemichi,T.K.,et al, 1992

The Molecular Pathogenesis of Alzheimer's Disease:Clinical Prospects
Lancet 340:1512-1515, Murphy,M., 1992

Analysis of the Prion Protein Gene in Thalamic Dementia
Neurol 42:1859-1863, Petersen,R.B.,et al, 1992

The Older Driver, Clinical Assessment and Injury Prevention
Arch Int Med 152:735-740, Underwood,M., 1992

Personality Changes in Alzheimer's Disease
Arch Neurol 49:486-491, Chatterjee,A.,et al, 1992

Brain Imaging in Human Immunodeficiency Virus Infection
Semin Neurol 12:57-69, Ketonen,L.&Tuite,M.J., 1992

The Diagnostic Utility of Elevation in Cerebrospinal Fluid B2-Microglobulin in HIV-1 Dementia
Neurol 42:1707-1712, McArthur,J.C.,et al, 1992

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

Aluminium Intoxication in Undialysed Adults with Chronic Renal Failure
JNNP 55:697-700, Russo,L.S.,et al, 1992

Levodopa-Nonresponsive Lewy Body Parkinsonism:Clinicopathologic Study of Two Cases
Neurol 42:1323-1327, Mark,M.H.,et al, 1992

Blinded Clinical Evaluation of Positron Emission Tomography for Diagnosis of Probable Alzheimer's Disease
Neurol 42:765-770, Powers,W.J.,et al, 1992

Comparative Analysis of Computed Tomographic and Magnetic Resonance Imaging Scans in Alzheimer Patients and Controls
Arch Neurol 49:381-384, Sandor,T.,et al, 1992

Cerebral Glucose Metabolism in Parkinson's Disease with and without Dementia
Arch Neurol 49:1262-1268, Peppard,R.F.,et al, 1992

Detection in Life of Confirmed Alzheimer's Disease, Medial Temporal Lobe Atrophy by Computed Tomography
Lancet 340:1179-1183, Jobst,K.A.,et al, 1992

Neuroleptic Sensitivity in Patients with Senile Dementia of Lewy Body Type
BMJ 305:673-678, McKeith,J.,et al, 1992

Central Nervous System Involvement in the Eosinophilia-Myalagia Syndrome
Arch Neurol 49:1082-1085, Lynn,J.,et al, 1992

Intellectual Development at Age 12 Years of Children with Congen Hypothyroidism Diag by Neonatal Scr
J Pediatr 121:581-584, Glorieux,J.,et al, 1992

Bilateral Thalamic Glioma-Review of Eight Cases with Personality Change and Mental Deterioration
AJNR 13:1225-1230, Partlow,G.D.,et al, 1992

Brain MRI and Electrophysiologic Abnormalities in Preclinical and Clinical Adrenomyeloneuropathy
Neurol 42:85-91, Aubourg,P.,et al, 1992

MR Imaging of the Spinal Cord in 23 Subjects with ALD-AMN Complex
AJR 158:413-416, Snyder,R.D.,et al, 1992

Progressive Language Disorder Due to Lobar Atrophy
Ann Neurol 31:174-183, Snowden,J.S.,et al, 1992

Clinicopath Conf
Huntington's Diseae, Case2-1992, NEJM 326:117-125992., , 1992

Fatal Familial Insomnia, A Prion Disease with a Mutation at Codon 178 of the Prion Protein Gene
NEJM 326:444-449, Medori,R.,et al, 1992

Fatal Familial Insomnia:Clinical and Pathologic Study of Five New Cases
Neurol 42:312-319, Manetto,V.,et al, 1992

Fatal Familial Insomnia:A Second Kindred with Mutation of Prion Protein Gene at Codon 178
Neurol 42:669-670, 1992, Medori,R.,et al, 1992

Multiple Sclerosis Dementia
Neurol 42:696, Mendez,M.D.&Frey,W.F., 1992



Showing articles 1400 to 1450 of 2292 << Previous Next >>