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Differential
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accommodation
accomodation, abnormal
affect, flat
agitation
algorithm
alien hand syndrome
alternating rapid movement, impaired
Alzheimer's disease
Alzheimer's disease, familial
amyloid plaques
aneurysm
aneurysm, intracranial
angiography, cerebral
angioid streaks
anomic aphasia
antibodies to measles
anticholinergic drugs
aphasia
aphasia, progressive, primary
apraxia
apraxia of eye movements
aspiration
ataxia
ataxia, cerebellar
ataxia, progressive
ataxic gait
atypical
autonomic dysfunction
axonal spheroid
B cell lymphoma
Babinski sign
basal ganglia, degeneration
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavioral disorder
blindness
blinking
blinking, reduced
blood transfusion
bradykinesia
bradyphrenia
brain biopsy
brainstem, lesion of
cachexia
callosal angle
camptocormia
carcinoma
carcinoma of lung
carotid artery occlusion, bilateral
CAT scan, angiography
CAT scan, angiography, false negative
CAT scan, chest
CAT scan, emission
CAT scan, emission, abnormal
CAT scan, venography
caudate nucleus, lesion of, bilateral
cerebellar atrophy, primary
cerebellar lesion
cerebral cortex
cerebral cortical atrophy
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, drainage of
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, oligoclonal IgG in
cerebrovascular accident
chemotherapy, CNS treatment and complications with
children
chorea
choreoathetosis
Clinical Pathologic Conference(C.P.C.)
cognition
cognition, slowed
cogwheel rigidty
coma
confusion
congenital infection, CNS
conjunctival biopsy
contractures, joint
convergence
convergence, impaired
corneal transplant
corpus callosum, lesion of
cortical blindness
cortical-basal ganglionic degeneration
Creutzfeldt-Jakob disease, genetic
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, familial
dementia, presenile
dementia, rapidly progressive
dementia, reversible
dementia, thalamic
dementia, transmissible
depression
developmental milestones, loss of
diabetes mellitus
diagnostic criteria
dietary supplement
differential diagnosis
difficulty climbing stairs
dizziness
dopamine agonist
driving
drooling
dural arteriovenous malformation
dysarthria
dysdiadochokinesia
dyskinesia, buccal lingual facial
dysmetria
dysphagia
dyspraxia
dystonia
electroencephalogram, abnormalities of
electroencephalogram, periodic complexes
electroencephalogram, triphasic delta waves
electron microscopy
encephalitis
encephalitis, viral
encephalopathy
enolase
epidemiology of neurology
executive dysfunction
extrapyramidal movement disorder, progressive
eye movement, disorders of
falling
false negative
familial
fatigue
finger nose finger test
fingerprint bodies
fistula, arterio-venous, dural
frontal behavioral spatial syndrome
frontal lobe, anatomy and physiology
frontal lobe, pathologic signs of
fundus, abnormality of
gait disorder
gait, festinating
gait, magnetic
gait, spastic
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene
genetic neurologic disorders
Gerstmann-Straussler-Scheinker disease
glabellar sign
gray matter
gyrus, abnormal
Hallervorden Spatz disease
handwriting
headache
headache, severe
hearing loss
heel-knee-shin test
hemianopia, homonymous
hemiparesis
hemorrhage, thalamic
hepatosplenomegaly
heralding manifestation
human immunodeficiency virus type 1
human immunodeficiency virus type 1, acute infection
hydrocephalus
hydrocephalus, normal pressure
hyperreflexia
hypersomnia
hypertension
hypometric saccades
hypophonia
imbalance
imbalance, postural
inattention
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion bodies, eosinophilic intranuclear
intellectual deficit
intellectual deterioration
intracerebral hemorrhage
iron, brain
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
Jakob-Creutzfeldt disease, Heidenhain variant
Jakob-Creutzfeldt disease, medical precaution with
Jakob-Creutzfeldt disease, young adult
kinesia paradoxica
kuru
lactic acidemia
lacunar infarction
L-dopa
leg dragging
leukoencephalopathy
leukoencephalopathy, hereditary diffuse
levitation
Lewy body
logopenia
lumbar puncture, complications of
lymphoma
lymphoma, primary of CNS
maculopathy
marche a petits pas
masked facies
memory, defect of recent
memory, impairment of
meningitis
mesial temporal lobe
micrographia
microhemorrhage, intracerebral
midbrain, atrophy
mimics
Mini Mental Status Examination
misdiagnosis
molecular genetics
mood change
mortality
movement disorder
movement disorder, extrapyramidal
MPTP
MRI
MRI, abnormal
MRI, angiography
MRI, angiography, false negative
MRI, contrast enhanced
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, negative
MRI, paramagnetic effect
MRI, punctate pattern
MRI, serial
MRI, venography
multiple system atrophy
myoclonic jerks
myoclonus
myoclonus, epilepsy
neoplasm, primary of CNS-treatment of
neuroaxonal leukodystrophy
neurologic disease, diagnoses of
neurologic disease, tempo
neurologic signs
neurologic symptoms
neuron specific enolase
neuronal ceroid-lipofuscinosis
neuropathology
neuropathology, brain
neuropathy
neurosyphilis
neurotoxic
neurotoxin
nystagmus
occipital cortex
occipital lobe, lesion of
ocular motility, disorders of
orthostatic hypotension
PANK2 mutation
Parkinson disease
Parkinson disease, akinetic form
Parkinson disease, asymmetric onset
Parkinson disease, dementia with
Parkinson disease, diagnosis
Parkinson disease, differential diagnosis of
Parkinson disease, etiology of
Parkinson disease, freezing phenomena in
Parkinson disease, heterogeneity of
Parkinson disease, L-dopa nonresponsive
Parkinson disease, pathogenesis of
Parkinson disease, surgical treatment of
Parkinson disease, treatment of
Parkinson disease, unilateral
Parkinsonism multiple-system atrophy
Parkinsonism syndrome
PAS positive
PAS positive material in the brain
perseveration
persistent vegetative state
personality change
picking at skin
pleocytosis of cerebrospinal fluid
polymerase chain reaction
postural abnormality
prion disease
prognosis
progressive neurologic disorder
progressive supranuclear palsy
protein 14-3-3, cerebrospinal fluid
protein 14-3-3, cerebrospinal fluid, false negative
pseudoxanthoma elasticum
psychiatric problems in neurologic disorders
psychological testing
psychological testing, neurologic problems
psychomotor retardation
putamen, lesion of
putamen, lesion of, bilateral
rapidly progressing neurologic illness
real-time quaking-induced conversion
release phenomena
retina, abnormal
retinal hemorrhages
retinitis pigmentosa
retinopathy
retropulsion
reversible neurologic disorder
review article
rigidity
Romberg's sign
rubella encephalitis
rubella encephalitis, progressive
rubella syndrome
rubella virus
rubeola virus
saccadic eye movements, abnormal
scrapie
seizure
selenium
sensory loss
sensory loss, cortical
seroconversion
serologic testing
serologic testing of cerebrospinal fluid
shunt procedure, lumboperitoneal
shunt procedure, ventricular
sinemet
skin, biopsy
skin, lesions in neurologic disorders
slow virus infection of CNS
spasticity
speech disorder
speech disorder, childhood
speech, slowed
speech, soft
spongy degeneration of brain
stare
startle myoclonus
startle reaction
stem cell rescue
stem cell transplantation
stooped posture
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
subarachnoid hemorrhage
suck reflex
symmetric brain lesions
synucleinopathy
syphilis, diagnosis and treatment
syphilis, neurologic complications with
tandem gait, ataxic
tau protein
tauopathy
temporal lobe
temporal lobe, lesion
temporal lobe, lesion, bilateral
thalamus, lesion of
thalamus, lesion of-bilateral
thyroiditis
toxins, nervous system
trauma
treatment of neurologic disorder
tremor
tremor, intention
tremor, resting
twins
upgaze, paralysis of
urinary incontinence
Venereal Disease Research Laboratory test
venous hypertension
venous ischemia
ventricular enlargement
viral infection
viral infection, CNS
viral isolation
virus, slow
vision, failure of in childhood
visual acuity, decreased
visual impairment
visual loss
visual loss, progressive
visual loss, slow
vitamin E
voice, abnormality of
walking frame
walking, difficulty with
weight loss
wheelchair
white matter disease
white matter disease, subcortical
wide based gait
workup
writing
Showing articles 150 to 200 of 2172 << Previous Next >>

Neurosyphilis
NEJM 381:1358-1363, Ropper, A.H.,et al, 2019

Clinicopathologic Conference, Creutzfeldt-Jakob Disease
NEJM 381:1569-1578, Case 32-2019, 2019

Diagnosis and Management of Dementia
JAMA 322:1589-1599, Arvanitakis, Z.,et al, 2019

Chronic Dengue Virus Panencephalitis in a Patient with Progressive Dementia with Extrapyramidal Features
Ann Neurol 86:695-703, Johnson, T.P.,et al, 2019

Neurodegenerative Disease Mortality Among Former Professional Soccer Players
NEJM 381:1801-1808,1862, Mackay, D.F.,et al, 2019

Prolonged Microgravity Affects Human Brain Structure and Function
AJNR 40:1878-1885, Roberts,D.R.,et al, 2019

Progressive Proximal Weakness in a 56-year-old Man with Bone Pain
Neurol 93:939-944, Torabi,T.,et al, 2019

Challenging Diagnosis of Gerstmann-Straussler-Scheinker Disease
Neurol 92:101-103, Kang, M.J.,et al, 2019

"Ears of the Lynx" MRI Sign is Associated with SPG11 and SPG15 Hereditary Spastic Paraplegia
AJNR 40:199-203, Pascual, B.,et al, 2019

Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
Lancet Neurol 18:1136-1146, Shribman,S.,et al, 2019

Central Nervous System Infections Due to Coccidioidomycosis
J Fungi 5:2-12, Jackson, N.R.,et al, 2019

Rare Presentation of Spontaneous, Direct, Carotid Cavernous Fistula in Late Pregnancy:A Case Report
Ophthalmol Clin Res 2:73-77, Agrawal,N.,et al, 2019

Basa Ganglia Calcifications (Fahrs Syndrome): Related Conditions and Clinical Features
Neurol Sci 40:2251-2263, Donzuso,G.,et al, 2019

Wilson Disease
NIDDK Oct2018, , 2018

Neuronal Intranuclear Inclusion Disease Showing Intranuclear Inclusions in Renal Biopsy 12 Years Earlier
Neurol 91:884-886, Motoki, M.,et al, 2018

Progressive Gait Difficulty and Incontinence in a 40-year-old Man with HIV
Neurol 91:1065-1070, Silverman, A.,et al, 2018

Cerebral Atrophy and Leukoencephalopathy in a Young Man Presenting with Encephalitic Episodes
JAMA Neurol 75:1563-1564, Xiao, F.,et al, 2018

Rapid Progression of Reversible Cognitive Impairment in an 80-year-old Man
Neurol 91:1109-1113, Bouthour, W.,et al, 2018

Practice Guide Update Summary: Mild Cognitive Impairment
Neurol 90:126-135, Petersen, R.C.,et al, 2018

Neurological Manifestations Among US Government Personnel Reporting Directional Audible and Sensory Phenomena in Havana, Cuba
JAMA 319:1125-1133, 1098, 1079, Swanson, R.L.,et al, 2018

Antibody-Mediated Encephalitis
NEJM 378:840-851, Dalmau, J.,et al, 2018

A 75-year-old man with parkinsonism, mood depression, and weight loss
Neurol 90:572-575, Frattini, E.,et al, 2018

Toxidrome Recognition in Chemical - Weapons Attacks
NEJM 378:1611-1620, Ciottone, G.R., 2018

Orbital Apex Syndrome
NEJM 378:18, Sacks. C.A., 2018

Progressive cognitive decline, cerebellar ataxia, recurrent myoclonus, and epilepsy
Neurol 90:e1827-e1831, Xiao, F.,et al, 2018

Diagnosis and Management of the Antiphospholipid Syndrome
NEJM 378:2010-2021, Garcia, D. & Erkan, D., 2018

Clinicopathologic Conference, Poststroke Mania and the Frontal Lobe Syndrome
NEJM 379:182-189, Case 21-2018, 2018

Prodromal Symptoms of Multiple Sclerosis in Primary Care
Ann Neurol 83:1162-1173, Disanto,G.,et al, 2018

Subacute Progressive Ptosis, Ophthalmoplegia, Gait Instability, and Cognitive Changes
JAMA Neurol 75:1284-1285, Lin, J.,et al, 2018

Cognitive Impairment Before Intracerebral Hemorrhage is Associated with Cerebral Amyloid Angiopathy
Stroke 49:40-45, Banerjee, G.,et al, 2018

Huntington Disease: Clinical Features and Diagnosis
UptoDate Dec 2017, Oksana Suchowersky, 2017

Clinicopathologic Conference, Primary Progressive Aphasia, Semantic Variant, due to TAR DNA Binding Protein 43 associated Frontotemporal Lobar Degen
NEJM 376:158-167, Case 1-2017, 2017

Diagnosis and Management of Dementia with Lewy Bodies
Neurol 89:88-100, McKeith, I.G.,et al, 2017

Clinicopathologic Conference, Advanced AIDS Complicated by HSV-1 Encephalopathy. Basal-Cell Carcinoma. Kaposis Sarcoma.
NEJM 376:2580-2589, Case 20-2017, 2017

A 54-year-old woman with Dementia, Myoclonus, and Ataxia
Neurol 89:e7-e12, Ali, F.,et al, 2017

A New Potential Biomarker for Dementia with Lewy Bodies
Neurol 89:318-326, Donadio, V.,et al, 2017

Amyotrophic Lateral Sclerosis
NEJM 377:162-172, Brown, R.H.,et al, 2017

Dentate Update: Imaging Features of Entities that Affect the Dentate Nucleus
AJNR 38:1467-1474, Bond, K.M.,et al, 2017

MRI of the Swallow Tail Sign: A Useful Marker in the Diagnosis of Lewy Body Dementia?
AJNR 38:1737-1741, Shams, S.,et al, 2017

A 57-year-old man with Unilateral Anosmia, Papilledema, and Meningismus
Neurol 89:e86-e90, Bradshaw, M.J.,et al, 2017

Chess Study Revives Debate Over Cognition-Enhancing Drugs
JAMA doi:10.1001/JAMA:2017.8114, Lyon, J., 2017

Sarcoidosis Limbic Encephalitis
Iran J Neurol 16:156-158, Toudou-Daouda, M.,et al, 2017

A 55-year-old Man with Rapidly Progressive Dementia and Parkinsonism
Neurol 89:e182-e187, Tabuas-Pereira, M.,et al, 2017

A Case of Ataxia, Seizure, and Choreoathetosis in a 34-year-old Woman
Neurol 89:e220-e223, Xiao, F. & Wang, X.F., 2017

Myeloperoxidase-Anti-Neutrophil Cytoplasmic Antibody-Positive Hypertrophic Pachymeningitis
Neurol 89:e253-e254, Culbertson, C.J.,et al, 2017

Paraneoplastic and Autoimmune Encephalitis
UptoDate July, Dalmau, J.,et al, 2017

Spontaneous Subarachnoid Haemorrhage
Lancet 389:655-666, Macdonald, R.L. & Schweizer, T.A., 2017

Characteristics in Limbic Encephalitis with Anti-Adenylate Kinase 5 Autoantibodies
Neurol 88:514-524,508, Do, L. & Chanson, E., 2017

Professional Football may be Linked to Brain Injuries Usually Seen in Boxing
BMJ 356:j811, Hawkes, N., 2017

Personality Changes, Executive Dysfunction, and Motor and Memory Impairment
JAMA Neurol 74:245-246, Lopez Chiriboga, A.S.,et al, 2017



Showing articles 150 to 200 of 2172 << Previous Next >>