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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 100 to 150 of 2172 << Previous Next >>

Sudden Loss of Vision at the Gym
BMJ 375:e067964, Ng, J.K.Y.,et al, 2021

Spontaneous Intracranial Hypotension
NEJM 385:2173-2178, Schievink, W.I., 2021

National Institute of Neurological Disorders and Stroke Consensus Diagnostic Criteria for Traumatic Encephalopathy Syndrome
Neurol 96:848-863, Katz, D.I.,et al, 2021

Clinicopathologic Conference, Systemic Primary Amyloidosis
NEJM 384:363-372, Case 3-2021, 2021

Sport Associated Dementia
BMJ 372:N168, Stewart, W., 2021

Congenital Cytomegalovirus Infection
BMJ 373:m1212, Pesch, M.H.,et al, 2021

A Middle-aged Woman with Severe Scoliosis and Encephalopathy
JAMA Neurol 78:251-252, Mohan, G.,et al, 2021

Clinicopathologic Conference, Lympohplasmic Lymphoma of the CNS (Bing-Neel Syndrome)
NEJM 384:745-753, Case 6-2021, 2021

CLOVES Syndrome
Neurol 96:e1487-e1488, Collins, M.,et al, 2021

A Triad of Tremor, Ataxia, and Cognitive Impairment
Neurol 96:e1802-e1803, Au, L.W.C.,et al, 2021

Decreased Visual Acuity After a Cat Scratch
BMJ 372:n552, Zhou, L. & Kong, X., 2021

Adults with Cerebral Palsy Require Ongoing Neurologic Care
Ann Neurol 89:860-871, Smith, S.E.,et al, 2021

Wilson Disease Presenting with Catatonia
Neurol 96:e2781-e2782, Patel, R.A. & Bailey, M., 2021

Complete Evaluation of Dementia: PET and MRI Correlation and Diagnosis for the Neuroradiologist
AJNR 42:998-1007, Oldan, J.D.,et al, 2021

Clinicopathologic Conference, Delayed Postthypoxic Leukoencephalopathy
NEJM 384:2438-2445, Case 19-2021, 2021

Why cant I see in the dark?
BMJ 373:m1573, Khan, S.,et al, 2021

Clinicopathologic Conference, Cerebral Amyloid Angiopatny-Related Inflammation
NEJM 385:358-368, Case 22-2021, 2021

Vitamin B12 Deficiency in a 29-Year-Old Woman
Neurol 97:e643-e646, Huddar, A.,et al, 2021

Chronic Meningitis
NEJM 385:930-936, Aksamit, A.J., 2021

Dural Arteriovenous Fistula Presenting with Reversible Dementia
Ann Neurol 90:512-513, Yoon, J.Y.,et al, 2021

Frequency and Characterization of Movement Disorders in Anti-IgLON5 Disease
Neurol 97:e1367-e1381, Gaig, C.,et al, 2021

Looking Beyond the Usual
Delhi J Ophthal doi:7869/djo.555, Shakrawal, J.,et al, 2020

Dressing Apraxia as Initial Manifestation of Creutzfeldt-Jakob Disease
Tremor and Other Hyperkinetic Movements 10:1-3, Heckmann, J.G.,et al, 2020

A 73-Year-Old Man with Recurrent Aphasia, Headaches, and Confusion
Neurol 95:e2595-e2599, Bose, G.,et al, 2020

Clinicopathologic Conference,Aceruloplasminemia, Hereditary
NEJM 383:1974-1983, Case 35-2020, 2020

A 72-year-old Man with a Progressive Cognitive and Cerebellar Syndrome
Neurol 95:e2707-e2710, Lad, M. & Griffiths, T.D., 2020

Bithalamic Lesions
Stroke 51:e355-e358, Chen, P.M.,et al, 2020

Clinicopathologic conference, Frontotemporal Lobar Degeneration with tau-positive inclusions consistent with Picks disease
NEJM 383:2666-2675, Case 41-2020, 2020

Rapid Progression of Prion Disease Associated with Transverse Myelitis
Neurol 94:e1670-e1672, Hussein, O.,et al, 2020

Clinicopathologic Conference, AA Amyloidosis, Complicated by Cerebral Mucormycosis
NEJM 382:1457-1466, Case 11-2020, 2020

A 22-Year-Old Man with Progressive Bilateral Visual Loss
Neurol 94:625-630, Yang, S.L.,et al, 2020

A 45-Year-Old Man with Progressive Insomia and Psychiatric and Motor Symptoms
Neurol 94:e1213-e1218, Lima, J.E.E.,et al, 2020

A 42-year-old Woman with Progressive Cognitive Difficulties and Gait Imbalance
Neurol 94:e1219-e1226, Slama, M.C.C.,et al, 2020

Neurologic Features in Severe SARS-CoV-2 Infection
NEJM 382:2268-2270, e110, , 2020

Ears of the Lynx Magnetic Resonance Imaging Sign
Ann Neurol 88:16-17, Baghbanian, S.M.,et al, 2020

Long Survival Sporadic Creutzfeldt-Jakob Disease
Neurol 95:87-88, Liu, X.Y.,et al, 2020

A Woman with Monocular Vision Loss
Neurol 95:e1105-e1109, Danish, H.,et al, 2020

Telemedicine in Neurology
Neurol 94:30-38,16, Hatcher-Martin, J.M.,et al, 2020

Immunocompetent Patient with Multiple Cranial Nerve Palsies, Ataxia, and Cognitive Decline
Neurol 94:e225-e229, Nigam, M.,et al, 2020

A Rare Presentation of Whipple Disease
Neurol 94:e758-e761, Koek, A.T.,et al, 2020

Epilepsy in Older People
Lancet 395:735-748, Sen, A.,et al, 2020

GGC Repeat Expansion of NOTCH2NLC in Adult Patients with Leukoencephalopathy
Ann Neurol 86:962-968,809, Okubo, M.,et al, 2019

Limbic-Predominant Age-Related TDP-43 Encephalopathy (LATE): Consensus Working Group Report
Brain DOI: 10.1093/brain/awz099, Nelson, P.T.,et al, 2019

A 47-year-old Man with Diffuse White Matter Disease and Rapidly Progressive Dementia
Neurol 92:e2832-e2837, Di Luca, D.G.,et al, 2019

Clinicopathologic Conference, Lebers Hereditary Optic Neuropathy
NEJM 381:164-172, Case 21-2019, 2019

A 68-year-old Man with Rapid Cognitive Decline
Neurol 93:315-318, Berth, S.H.,et al, 2019

Case 27-2019:A 16-Year-Old Girl with Head Trauma During a Sailboat Race
CPC,Concussion,Benign Paroxysmal Positional Vertigo, Case 27-2019, NEJM 381:863-871, Iaccarino,M.A.,et al, 2019

Debate Sparks Over LATE, a Recently Recognized Dementia
JAMA 322:914-916, Abbasi, J., 2019

A 58-year-old Man with Hand Tremor and Episodes of Neck Pain
Neurol 93:557-561, Urso, D.,et al, 2019

Rapidly Progressive Vision Loss in a Patient with Breast Cancer
JAMA 322:1098-1099, Izzo, M.C.,et al, 2019



Showing articles 100 to 150 of 2172 << Previous Next >>