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adrenal medullary tissue
adverse drug reaction
akinesia
akinesia of eyelid function
akinetic mute
alien hand syndrome
Alzheimer's disease
amitriptyline
amyotrophic lateral sclerosis
anti Hu antibody
anxiety
aphasia
aphasia, progressive, primary
apolipoprotein E
apomorphine
applause sign
apraxia
apraxia of eyelid opening
aqueduct of Sylvius, enlargement
arm swing, reduced
aspiration
ataxia
ataxia, cerebellar
ataxia, progressive
ataxia, truncal
athetosis
atypical
auditory evoked brainstem potentials
autoantibodies
autonomic dysfunction
basal ganglia
basal ganglia, lesion of
behavioral disorder
benign essential tremor
benzodiazepine agonist
bilirubin encephalopathy
biologic markers
blepharospasm
blinking
blinking, reduced
botulinum toxin
bradykinesia
bradykinesia, facial
bradyphrenia
brain atrophy
brain transplantation
brainstem, atrophy
brainstem, lesion of
breast feeding
bromocriptine
carcinoma
carcinoma of lung
CAT scan
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
cataplexy
cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy
cerebral cortical atrophy
cerebral infarction
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrovascular accident
cerebrovascular accident, multiple
Charcot's sign
choline acetyltransferase
chromosomal abnormality
chromosome 20
Clinical Pathologic Conference(C.P.C.)
cogentin
cogwheel rigidty
complications
compulsivity
cortical-basal ganglionic degeneration
cranial neuropathy, multiple
Creutzfeldt-Jakob disease, genetic
cry, abnormal
cry, high-pitched
crying, pathologic
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, frontotemporal
dementia, presenile
dementia, rapidly progressive
dementia, subcortical
dementia, transmissible
depression
diagnostic criteria
differential diagnosis
diplopia
disability, neurological
dizziness
doll's head maneuver
dopamine agonist
dopamine receptor
dopamine receptor, D2
downward gaze
downward gaze, paralysis of
drooling
drug induced neurologic disorders
dysarthria
dysphagia
dystonia
dystonia, cervical
dystonia, face
dystonia, focal
electroencephalogram
emotional lability
encephalitis, brainstem
encephalopathy
enzyme activity
epidemiology of neurology
extrapyramidal movement disorder, progressive
eye movement, disorders of
facial appearance, abnormal
facial expression abnormality
facial nerve palsy
falling
familial
fever
fine motor function, impaired
fracture, long bone
frontal behavioral spatial syndrome
frontal lobe, behavior with disease of
frontal lobe, lesion of
frontal lobe, pathologic signs of
gait disorder
gait, apraxic
gaze palsy
gaze palsy, horizontal
gaze palsy, supranuclear
gaze palsy, vertical
gene
genetic linkage
glabellar sign
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
grasp reflex
groaning
hallucination
handwriting
head injury
hearing loss
hemidystonia
hepatosplenomegaly
heralding manifestation
hip fracture
hummingbird sign
Huntington's chorea
hydrocephalus, normal pressure
hyperbilirubinemia
hyperbilirubinemia, CNS abnormality after
hypertension
hypometric saccades
hypophonia
hyposmia
idazoxan
ideomotor apraxia
imbalance
imbalance, postural
incidence
incontinence, fecal
incoordination
insomnia
intellectual deficit
internuclear ophthalmoplegia
intrathecal medication
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, young adult
jaundice
jaw jerk, abnormal
kernicterus
laughing, pathologic
L-dopa
L-dopa, drug interactions with and side effects of
learning disability, in children
Lewy body
Lewy body disease, diffuse
lid
lid abnormalities
life expectancy
lysosomal storage disease
masked facies
memory, impairment of
meningitis
mental retardation
methysergide
micrographia
midbrain
midbrain, atrophy
misdiagnosis
molecular genetics
morning glory sign
moro reflex
mortality
motor neuron disease
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, diffusion weighted
MRI, high signal foci on
MRI, high signal intensity of basal ganglia
MRI, mouse ears
MRI, volumetry
MRS
multiple system atrophy
myoclonus
neck extension
neurologic disease, diagnoses of
neurologic disease, tempo
neurologic signs
neurologic symptoms
neuroophthalmology
neuropathology
neuropathology, brain
neurotransmitter
Niemann-Pick disease
nystagmus
nystagmus, primary position of gaze
nystagmus, retractorius
nystagmus, rotary
obsessive-compulsive disorder
ocular myopathy
ocular myopathy, differential diagnosis
oculogyric crisis
opened mouth
ophthalmoplegia
ophthalmoplegia, neonatal
ophthalmoplegia, total
opisthotonus
Parkinson disease
Parkinson disease, arteriosclerotic
Parkinson disease, atypical
Parkinson disease, axial symptoms
Parkinson disease, dementia with
Parkinson disease, diagnosis
Parkinson disease, differential diagnosis of
Parkinson disease, drug induced
Parkinson disease, L-dopa nonresponsive
Parkinson disease, misdiagnosis
Parkinson disease, treatment of
Parkinson disease, tremor, absence of
Parkinsonism multiple-system atrophy
Parkinsonism syndrome
pathology
penguin silhouette sign
pergolide
personality change
Pick's disease
polymerase chain reaction
postural abnormality
posturography
preclinical
premature infant
pretectal syndrome
prion disease
procainamide
prognosis
progressive neurologic disorder
progressive supranuclear palsy
progressive supranuclear palsy, natural history
proteinopathy
pseudobulbar palsy
psychiatric problems in neurologic disorders
psychomotor retardation
ptosis
ptosis, bilateral
pure akinesia
quadrigeminal plate
rapidly progressing neurologic illness
reading disorder, acquired
reading problem, causes of
release phenomena
remote effect of cancer on the nervous system
retrocollis
retropulsion
review article
rigidity
rigidity, axial
risk factors
saccadic eye movements
saccadic eye movements, abnormal
safety
seizure
seizure, laughing as manifestation
sensorineural hearing loss
sequencing difficulty
setting sun phenomena
shunt procedure, ventricular
Shy-Drager syndrome
sinemet
single photon emission computed tomography
sleep
sleep pathology and physiology
smell
Smell Identification Test
speech disorder
splenomegaly
stare
striatonigral degeneration
stridor
substantia nigra
suck, poor
superior colliculus
swallowing
synucleinopathy
systemic illness
tau protein
tauopathy
tetanus
thalamus, lesion of
thalamus, lesion of-bilateral
treatment of neurologic disorder
tremor
tricyclic antidepressant
trismus
upgaze
upgaze, paralysis of
urinary incontinence
vertical gaze
vision, blurred
visual symptoms
vocalizations
walking, difficulty with
wheelchair
white matter disease
zolpidem
Showing articles 0 to 50 of 3899 Next >>

Involuntary Groaning Induced by Levodopa Therapy in a Patient With Progressive Supranuclear Palsy
JAMA Neurol 77:1569, Park, J.E., 2020

Atypical Parkinsonian Syndromes: A General Neurologists Perspective
Eur J Neurol 25:41-58, Deutschlander, A.B.,et al, 2018

Advances in Progressive Supranuclear Palsy: New Diagnostic Criteria, Biomarkers, and Therapeutic Approaches
Lancet Neurol 16:552-563, Boxer, A.L.,et al, 2017

Intrathecal 2-hydroxypropyl-�-cyclodextrin Decreases Neurological Disease Progression in Niemann-Pick disease, type C1: a non-randomised, open-label, phase 1-2 trial
Lancet 390:1758-1768, Ory, D.S.,et al, 2017

Progressive Parkinsonism, Balance Difficulties, and Supranuclear Gaze Palsy
JAMA Neurol 71:104-107, Erro, R.,et al, 2014

Degenerative Diseases of the Nervous System, Progressive Supranuclear Palsy
Adams & Victors Principles of Neurology, Chp 39, pg 1096, Ropper, A.H.,et al, 2014

Criteria for the Diagnosis of Corticobasal Degeneration
Neurol 80:496-503, Armstrong, M.J.,et al, 2013

Functional Impairment in Progressive Supranuclear Palsy
Neurol 80:380-384, Duff, K.,et al, 2013

Facial Bradykinesia
JNNP 84:681-685, Bologna, M.,et al, 2013

Incidence and Pathology of Synucleinopathies and Tauopathies Related to Parkinsonism
JAMA Neurol 70:859-866, Savica, R.,et al, 2013

Progressive Supranuclear Palsy: A Current Review
The Neurologist 14:79-88, Lubarsky,M. &Juncos,J.L., 2008

Tau Forms in CSF as a Reliable Biomarker for Progressive Supranuclear Palsy
Neurol 71:1796-1803, Borroni,B.,et al, 2008

New and Reliable MRI Diagnosis for Progressive Supranuclear Palsy
Neurol 64:2050-2055, Oba,H.,et al, 2005

Morning Glory Sign: A Particular MR Finding in Progressive Supranuclear Palsy
Magn Reson Med Sci 3:125-132, Adachi, M., et al, 2004

Clinical Features and Natural Histry of Progressive Supranuclear Palsy, A Clinical Cohort Study
Neurol 60:910-916, Nath,W.,et al, 2003

Diffusion-Weighted Imaging Discriminates Progressive Supranuclear Palsy from PD, But Not From the Parkinson Variant of Multiple System Atrophy
Neurol 60:922-927, Seppi,K.,et al, 2003

Cholinergic Vesicular Transporters in Progressive Supranuclesar Palsy
Neurol 58:1013-1018,997, Suzuki,M.,et al, 2002

Improved Accuracy of Clinical Diagnosis of Lewy Body Parkinson's Disease
Neurol 57:1497-1499, Hughes,A.J.,et al, 2001

Computerized Posturography Analysis of Progressive Suprnuclear Palsy
Arch Neurol 57:1464-1469, Ondo,W.,et al, 2000

Magnetic Resonance Imaging-Based Volumetry Differentiates Idiopathic Parkinson's Syndrome from Multiple System Atrophy and Progressive Supranuclear Palsy
Ann Neurol 45:65-74, Schulz,J.B.,et al, 1999

Zolpidem in Progressive Supranuclear Palsy
NEJM 341:543-544, Daniele,A.,et al, 1999

Prevalence of Progressive Supranuclear Palsy and Multiple System Atrophy:A Cross-Sectional Study
Lancet 354:1771-1775, Schrag,A.,et al, 1999

Progressive Supranuclear Palsy, A Survey of the Disease Course
Neurol 50:1637-1647, Santacruz,P.,et al, 1998

Pharmacological Therapy in Progressie Supranuclear Palsy
Arch Neurol 55:1099-1102, Kompoliti,K.,et al, 1998

What is the Accuracy of the Clinical Diagnosis of Multiple System Atrophy
Arch Neurol 54:937-944, Litvan,I.,et al, 1997

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

Bilirubin Metabolism and Kernicterus
Adv Pediatr 44:173-229, Gourley,G.R., 1997

Neuropsychiatric Aspects of Progressive Supranuclear Palsy
Neurol 47:1184-1189, Litvan,I.,et al, 1996

Natural History of Progressive Supranuclear Palsy & Clin Predictors of Survival:A Clinicopath Study
JNNP 61:615-620, Litvan,I.,et al, 1996

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

Clinicopath Study of Paraneoplastic Brainstem Encephalitis and Ophthalmoparesis
J Neuro-Ophthalmol 16:44-48, Crino,P.B.,et al, 1996

Some Specific Clinical Features Differentiate Multiple System Atrophy (Striatonigral Variety) from Parkinson's Disease
Arch Neurol 52:294-298, Colosimo,C.,et al, 1995

Parkinsonism-Recognition and Differential Diagnosis
BMJ 310:447-452, Quinn,N., 1995

Apolipoprotein E Genotype in Diverse Neurodegenerative Disorders
Ann Neurol 38:131-135, Schneider,J.A.,et al, 1995

Preliminary NINDS Neuropathologic Criteria for Steele-Richardson-Olszewski Syndrome (Progressive Supranuclear Palsy)
Neurol 44:2015-2019, Hauw,J.-J., 1994

Botulinum Toxin-A Improves the Rigidity of Progressive Supranuclear Palsy
Ann Neurol 35:237-239, Polo,K.B.&Jabbari,B., 1994

Progressive Supranuclear Palsy:Neuropathologic and Clinical Heterogeneity
Neurol 44:1015-1024, Gearing,M.,et al, 1994

The Syndrome of'Pure Akinesia'and Its Relationship to Progressive Supranuclear Palsy
Neurol 44:1025-1029, Riley,D.E.,et al, 1994

Eye Movements in Parkinsonian Syndromes:Vidailhet
M. , et al, Neurol 35:420-42694., , 1994

Diff Diag of parkinson's Disease, Multiple Sys Atrophy, & Steele-Richardson-Olszewski Syndrome:Striatal F-Dopa PET Data
JNNP 57:278-284, Burn,D.J.,et al, 1994

Clinicopath Conf
progressive Supranuclear Palsy, Case 46-1993, NEJM 329:1560-1567993., , 1993

Olfactory Testing Differentiates Between Progressive Supranuclear Palsy & Idiopathic Parkinson's Dis
Neurol 43:962-965, Doty,R.L.,et al, 1993

Multiple System Atrophy & Prog Supranuc Palsy, Dimin Striatal D2 Dopamine Receptor Act by SPECT
Arch Neurol 50:513-516, vanRoyen,E.,et al, 1993

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

Striatal D2 Receptor Status in Patients with Parkinson's Disease, Striatonigral Degeneration, and PSP, (PET)
Ann Neurol 31:184-192, Brooks,D.J.,et al, 1992

The Apomorphine Test in Parkinsonian Syndromes
JNNP 54:870-872, D'Costa,D.F.,et al, 1991



Showing articles 0 to 50 of 3899 Next >>