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abstract reasoning
abulia
acquired immunodeficiency syndrome
acquired immunodeficiency syndrome dementia complex
acquired immunodeficiency syndrome, infants and children
addiction, heroin
agitation
akinesia
akinesia of eyelid function
alien hand syndrome
alpha-fetoprotein
Alzheimer's disease
antibodies to measles
aphasia
aphasia, progressive, primary
apnea
apolipoprotein E
apomorphine
applause sign
apraxia
apraxia of eye movements
apraxia of eyelid opening
apraxia, constructional
apraxia, speech
areflexia
arm swing, reduced
astasia abasia
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, truncal
ataxic gait
atypical
autism
axonal spheroid
azidodeoxythymidine
basal ganglia, calcification of
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavioral disorder
Binswanger disease
biologic markers
blepharospasm
blinking, reduced
bradykinesia
bradyphrenia
brain biopsy
brainstem, deformity of
brainstem, lesion of
bruxism
calcification, intracranial
carcinoembryonic antigen
carcinoma
carcinoma of lung
CAT scan
CAT scan, abnormal
CAT scan, emission, abnormal
central nervous system, infection of
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar ataxia, primary
cerebellar degeneration
cerebellar infarction
cerebellar lesion
cerebral cortical atrophy
cerebral infarction, subcortical
cerebrospinal fluid, oligoclonal IgG in
cerebrovascular accident
cerebrovascular accident, multiple
cerebrovascular disease
Charcot's sign
chest x-ray, abnormal
children
chorea
chorea, causes of
choreoathetosis
chorioretinitis
chromosomal abnormality
chromosome 11
Clinical Pathologic Conference(C.P.C.)
cogwheel rigidty
complications
concentration, impaired
confusion
corpus callosum
corpus callosum, infarction of
cortical-basal ganglionic degeneration
cyanide poison
cyst
cyst, parenchymal
cyst, subcortical
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, age at onset
dementia, cerebrovascular disease causing
dementia, childhood
dementia, rapidly progressive
dementia, subcortical
demyelinating disease
dentate nuclei
depression
developmental retardation
dexterity, impaired
diabetes mellitus
diagnostic criteria
differential diagnosis
diplopia
disability, neurological
disconnection syndrome
disorientation
downward gaze
drooling
drug abuse
drug abuse, neurologic complications of
dysarthria
dyskinesia, buccal lingual facial
dysphagia
dyspraxia
dystonia
dystonia, focal
electroencephalogram, abnormalities of
electroencephalogram, periodic complexes
emotional lability
encephalitis
encephalitis, brainstem
encephalitis, paraneoplastic
encephalopathy, delayed
enzyme, defect
epidemiology of neurology
exercise
exome sequencing
extrapyramidal movement disorder, progressive
eye movement, disorders of
eyelid opening, difficulty with
facial recognition, impairment
falling
familial
fine motor function, impaired
fracture, long bone
frontal behavioral spatial syndrome
frontal lobe, pathologic signs of
gait disorder
gait, apraxic
galactosemia
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
genetic linkage
genetic neurologic disorders
genetic testing
glabellar sign
grasp reflex
growth retardation
hallucination
hallucination, visual
hand clapping
hand flapping
hand wringing
handwriting
head injury
headache
hemorrhage, thalamic
heralding manifestation
hip fracture
human immunodeficiency virus type 1
Huntington's chorea
Huntington's chorea, late onset
Huntington's chorea, misdiagnosis of
hydrocephalus
hydrocephalus, normal pressure
hyperparathyroidism
hyperreflexia
hypertension
hypophonia
hypotonia
hypotonia, infants
iatrogenic neurologic disorders
ideomotor apraxia
imbalance
imbalance, postural
immunodeficiency
immunosuppression
inborn errors of metabolism
incidence
inclusion bodies
inclusion bodies, eosinophilic intranuclear
incoordination
intellectual deficit
intellectual deterioration
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
jaw jerk, abnormal
jocularity
lacunar infarction
language disorder in adults
language disorders in children
L-dopa
lethargy
leukemia
leuko-araiosis
leukoencephalopathy
leukoencephalopathy, hereditary diffuse
leukoencephalopathy, toxic
levitation
Lewy body
Lewy body disease, diffuse
lid
lid abnormalities
limbic encephalitis
limbic system
lipid storage disorder of CNS
lobar atrophy
lymphoma
lysosomal storage disease
masked facies
memory, defect of recent
memory, impairment of
meningitis
mental retardation
mental status, abnormal
microangiopathy, brain
micrographia
midbrain
midbrain, atrophy
midbrain, compression
miglustat
mild cognitive impairment
misdiagnosis
mortality
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, diffusion weighted
MRI, high signal intensity of basal ganglia
MRI, negative
multinucleated giant cell
multiple system atrophy
myelopathy, vacuolar
myoclonic jerks
myoclonus
myoclonus, stimulus sensitive
myopia
neck extension
neuroaxonal leukodystrophy
neurocutaneous disease
neuroendocrinology
neurologic disease, diagnoses of
neurologic disease, diagnoses of, clinical bedside
neurologic disease, tempo
neurologic signs
neurologic symptoms
neuroophthalmology
neuropathology
neuropathology, brain
neuropathy
Niemann-Pick disease
nystagmus
ocular motility, disorders of
ocular myopathy
ocular myopathy, differential diagnosis
old age, neurology of
ophthalmoplegia
paraparesis
Parkinson disease
Parkinson disease, atypical
Parkinson disease, axial symptoms
Parkinson disease, dementia with
Parkinson disease, L-dopa nonresponsive
Parkinson disease, tremor, absence of
Parkinsonism syndrome
pathologic reflex
pathology
patient information and support
penguin silhouette sign
personality change
pleocytosis of cerebrospinal fluid
Poretti-Boltshauser syndrome
preclinical
pregnancy, neurologic complications in
prion disease
progeria
prognosis
progressive neurologic disorder
progressive supranuclear palsy
pseudobulbar palsy
psychiatric problems in neurologic disorders
psychological testing
psychomotor retardation
psychosis
ptosis
pure akinesia
pyramidal tract dysfunction
radiation hypersensitivity
reading disorder, acquired
reading problem, causes of
release phenomena
REM sleep
remote effect of cancer on the nervous system
renal cell carcinoma
respirations in CNS disease
retinal degeneration
retrocollis
retropulsion
Rett's syndrome
review article
rigidity
rigidity, axial
rocking
rooting reflex
rubeola virus
saccadic eye movements
saccadic eye movements, abnormal
sagging of the brain
salivation, excessive
scoliosis
screaming
seizure
seizure, laughing as manifestation
seizure, psychomotor-temporal lobe
sensory loss
sensory loss, cortical
sequencing difficulty
shunt procedure, lumboperitoneal
shunt procedure, lumboperitoneal-complications of
sinemet
singing
single photon emission computed tomography
skin, lesions in neurologic disorders
small vessel disease
snout reflex
spatial orientation
speech disorder
spinal muscular atrophy
stereotyped behavior
stereotypy
stuttering
stuttering following CVA
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
subcortical U fibers
tau protein
tauopathy
telangiectases
thalamic tumors
thalamus, infarction of
thalamus, lesion of
titubation
tonsillar herniation of cerebellum
toxic encephalopathy
treatment of neurologic disorder
tremor
tremor, intention
upside-down vision
viral infection
viral infection, CNS
vision, blurred
visual symptoms
visuospatial disturbance
walking, difficulty with
wheelchair
white matter disease
white matter disease, periventricular
whole genome sequencing
wide based gait
writing
Showing articles 1200 to 1250 of 2487 << Previous Next >>

Serotonin Syndrome and the Combined Use of Deprenyl and An Antidepressant in Parkinson's Disease
Neurol 48:1070-1077, Richard,I.H.,et al, 1997

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

The Expansion of the CAG Repeat in Ataxin-2 is a Frequent Cause of Autosomal Dominant Spinocerebellar Ataxia
Neurol 49:1009-1013, Lorenzetti,D.,et al, 1997

Spinocerebellar Ataxia Type 6, Molecular & Clin Features of 35 Japanese Pts (1 Homozygous for CAG Repeat Expan)
Neurol 49:1238-1243, 11961997., Matsumura,R.,et al, 1997

Cerebral & Cerebellar Atrophy on Serial MRI in an Initially Symptom Free Subject at Risk of Familial Prion Disease
BMJ 315:856-857, Fox,N.C.,et al, 1997

Cerebral Manifestation of Erdheim-Chester Disease:Clinical and Radiologic Findings
Neurol 49:1702-1705, Bohlega,S.,et al, 1997

Ocular Findings in Ramsay Hunt Syndrome
J Neuro-Ophthalmol 17:199-201, Mansour,A.M.&Bailey,B.J., 1997

Pallidal Stimulation for Parkinson's Disease, Two Targets
Neurol 49:1564-1569, Bejjani,B.,et al, 1997

Frontotemporal Degeneration, Pick Disease, and Corticobasal Degeneration
Arch Neurol 54:1425-1427, 14291997., Neary,D., 1997

Frontotemporal Dementia, Pick Disease, and Corticobasal Degeneration
Arch Neurol 54:1427-1429, Kertesz,A., 1997

CSF Antigliadin Antibodies and the Ramsay Hunt Syndrome
Neurol 49:1131-1133, Chinnery,P.F.,et al, 1997

Unilateral Pallidotomy for Parkinson's Disease:Comparison of Outcome in Yonger Vs Elderly Patients
Neurol 49:1072-1077, Uitti,R.J.,et al, 1997

Posteroventral Medial Pallidotomy in Advanced Parkinson's Disease
NEJM 337:1036-1042, Lang,A.E.,et al, 1997

Chemosensory Event-Related Potentials in Response to Trigeminal & Olfactory Stim in Idio Parkinson's Dis
Neurol 49:1424-1431, Barz,S.,et al, 1997

Olfactory Dysfunction in Familial Parkinsonism
Neurol 49:1262-1267, Markopoulou,K.,et al, 1997

Adult-Onset Subacute Sclerosing Panecephalitis:Case Reports and Review of the Literature
Mov Dis 12:342-353, Singer,C.,et al, 1997

Sympathetic Cardioneuropathy in Dysautonomias
NEJM 336:696-702, 7211997., Goldstein,D.S.,et al, 1997

Localization of Lesion in Denial of Hemiplegia After Acute Stroke
Stroke 28:67-71, Ellis,S.&Small,M., 1997

Identification of Brain Region for Coordianting Speech Articulation
Lancet 394:221-222, Donnan,G.A.,et al, 1997

Parkinsonism Associated with Long-Term Cocaine Abuse
Arch Int Med 157:241, Domingo,P.&Martinez,E., 1997

Is There a Gulf War Syndrome? Searching for Syndromes by Factor Analysis of Symptoms
JAMA 227:215-222, 2591997., Haley,R.W.,et al, 1997

Self-Reported Exposure to Neurotoxic Chemical Combinations in the Gulf War:A Cross-Sectional Epidemiologic Study
JAMA 227:231-237, 2591997., Haley,R.W.&Kurt,T.L., 1997

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

Occupational Exposures to Metals as Risk Factors for Parkinson's Disease
Neurol 48:650-658, Gorell,J.M.,et al, 1997

Cabergoline Treatment of Early Parkinson's Disease:First Yr of Trtm Comparison of Cabergoline & Levodopa
Neurol 48:363-368, Rinne,U.K.,et al, 1997

Proton Magnetic Resonance Spectroscopy in Parkinson's Disease and Progressive Supranuclear Palsy
JNNP 62:239-242, Federico,F.,et al, 1997

Surgery for Parkinson's Disease
JNNP 62:2-8, Obeso,J.A.,et al, 1997

Usefulness of Pallidotomy in Advanced Parkinson's Disease
JNNP 62:125-132, Johansson,F.,et al, 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

Low-Dose Clozapine Improves Dyskinesias in Parkinson's Disease
Neurol 48:658-662, Durif,F.,et al, 1997

Diagnosis of Chronic Manganese Intoxication by Magnetic Resonance Imaging
NEJM 336:965-966, Arjona,A.,et al, 1997

Mortality from Parkinson Disease
Arch Neurol 54:260-264, Louis,E.D.,et al, 1997

P3 Latency Change in Aging and Parkinson Disease
Arch Neurol 54:296-302, Tachibana,H.,et al, 1997

Clinicopath Conf
Nonbact Thrombotic Endocarditis, Aortic Valve, with Cerebral, Renal & Splenic Emboli & Multiple Infa, cts, CA se 28-1997,NEJM 337:770-777,1997., 1997

A 36-Year-Old Woman Recuperating From a Stroke
JAMA 277:1970-1976, Alexander,M., 1997

Pure or Predominant Sensory Stroke Due to Brain Stem Lesion
Stroke 28:1761-1764, Kim,J.S.&Bae,Y.H., 1997

Presymptomatic Hypertension is a Major Feature in the Diagnosis of Progressive Supranuclear Palsy
Arch Neurol 54:1104-1108, Ghika,J.&Bogousslavsky,J., 1997

Characterizing Swallowing Abnormalities in Progressive Supranuclear Palsy
Neurol 48:1654-1662, Litvan,I.,et al, 1997

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

High-Frequency Unilateral Thalamic Stimulation in the Treatment of Essential and Parkinsonian Tremor
Ann Neurol 42:292-299, Koller,W.,et al, 1997

High-Frequency Stimulation of the Globus Pallidus for the Treatment of Parkinson's Disease
Neurol 49:249-253, Pahwa,R.,et al, 1997

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

Balance in the Healthy Elderly
Arch Neurol 54:976-981, Camicioli,R.,et al, 1997

Pain After Thalamic Stroke:Right Diencephalic Predominance and Clinical Features in 180 Patients
Neurol 48:1196-1199, Nasreddine,Z.S.&Saver,J.L., 1997

Gabapentin for Parkinsonism:A Double-Blind Placebo-Controlled, Crossover Trial
Am J med 102:60-66, Olson,W.L.,et al, 1997

Ataxia and Slurred Speech after Artesunate Treatment for Falciparum Malaria
NEJM 336:1328, Miller,L.G.&Panosian,C.B., 1997

Gene Locus for Autosomal Recessive Distal Myopathy with Rimmed Vacuoles Maps to Chromosome 9
Ann Neurol 41:432-437, Ikeuchi,T.,et al, 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

Paraneoplastic Cerebellar Degeneration
Arch Int Med 157:1258-1262, Bolla,L.&Palmer,R.M., 1997



Showing articles 1200 to 1250 of 2487 << Previous Next >>