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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 0 to 50 of 2164 Next >>

More Than a Little Unsteady
NEJM 387:e9, Kraft, A.W.,et al, 2022

Clinicopathologic Conference, Normal Pressure Hydrocephalus
NEJM 384:1350-1358, Case 10-2021, 2021

Sporadic Creutzfeldt-Jakob Disease in a Very Young Person
Neurol 97:813-816,801, Appleby, B.S.,et al, 2021

Rapidly Progressive Thalamic Dementia
Neurol 96:e809-e813, Rizzo, A.C.,et al, 2021

Homonymous Hemianopia with Normal Magnetic Resonance Imaging
JAMA Ophthalmol doi:10.1001/JAMAOphthalmol.2020.0447, Cai, S.,et al, 2020

Pantothenate Kinase - Associated Neurodegeneration (PKAN)
Emedicine.Medscape Sept, Hanna, P.A. & Benbadis, S.R., 2018

Selenium Toxicity Associated with Reversible Leukoencephalopathy and Cortical Blindness
JAMA Neurol 75:1282-1283, Rae, W.,et al, 2018

Neurologic Signs and Symptoms Frequently Manifest in Acute HIV Infection
Neurol 87:148-154, Hellmuth, J.,et al, 2016

Clinicopathologic Conference, Primary Central Nervous System Diffuse Large B-cell Lymphoma
NEJM 373:367-377, Case 23-2015, 2015

A 64-year-old Woman with Subacute Encephalopathy
Neurol 85:e64-e65, Bhai, S.,et al, 2015

Degenerative Diseases of the Nervous System, Parkinson Disease
Adams & Victors Principles of Neurology, Chp 39, pg 1082, Ropper, A.H.,et al, 2014

Clinical Reasoning: A Woman with Rapidly Progressive Apraxia
Neurol 80:e162-e165, Pressman, P.,et al, 2013

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

A 23-Year-Old Man With Seizures and Visual Deficit
Neurol 70:73-78, Boustany,R.-M.,et al, 2008

Clinicopath conf., Human Prion Disease, Sporadic CJD
Neurol 69:1881-1887, Geschwind,M.D., et al, 2007

Clinicopath Conf, Multiple-System Atrophy
NEJM 351:912-921, Case 27-2004, 2004

Subacute Sclerosing Panencephalitis
Postgrad Med J 78:63-70, Garg, R.K.,et al, 2002

Diagnostic Criteria for Parkinson Disease
Arch Neurol 56:33-39, Gelb,D.J.,et al, 1999

Clinical Presentation and Pharmacological Therapy in Corticobasal Degeneration
Arch Neurol 55:957-961, Kompoliti,K.,et al, 1998

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

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

Cortical-Basal Ganglionic Degeneration
Neurol 40:1203-1212, Riley,D.E.,et al, 1990

Progressive Rubella Panencephalitis
In Handbk of Clin Neurol, Vinken & Bruyn, Ed, N Holland Publ Co, 56:405-416, Wolinsky,J.S., 1990

Clinical & PET Studies in the'Extrapyramidal Syndrome'of Dementia of the Alzheimer Type
Arch Neurol 47:1318-1323, Tyrrell,P.J.,et al, 1990

Update on Parkinson Disease
NY State J Med, 87:147-1531987., Lieberman,A.N., 1987

Prions & Neurodegenerative Diseases
NEJM 317:1571-1581, 15971987., Prusiner,S.B., 1987

Creutzfeldt-Jakob Disease:Patterns of Worldwide Occurrence & the Significance of Familial & Sporadic Clustering
Ann Neurol 5:177-188, Masters,C.L.,et al, 1979

Pseudoxanthoma Elasticum:A Review of Neurological Complications
Ann Neurol 4:18, Iqbal,A.,et al, 1978

Precautions in Familial Transmissible Dementia
Arch Neurol 35:697-698, Cook,R.,et al, 1978

Subacute Spongiform Encephalopathy (Creutzfeldt-Jakob Disease)
Brain 101:333-344, Masters,C.L.,et al, 1978

Precautions in Medical Care Handling Matrl. of Patients with Transmissible Virus Dementia (Creutzfeldt-Jakob Disease)
NEJM 297:1253, Gajdusek,C.,et al, 1977

Clinical Pathologic Conference, Creutzfeldt-Jakob Disease, (Case record 43-1977)
NEJM 297:930, Scully,R.E.,et al, 1977

Chronic Progressive Panencephalitis due to Rubella Virus Simulating Subacute Sclerosing Panencephalitis
NEJM 292:994-998,1023, Weil, M.L.,et al, 1975

Corticodentatonigral Degeneration with Neuronal Achromasia
Arch Neurol 18:20-33, Rebeiz,J.J.,et al, 1968

Parkinson's Disease
In Handbk of Clinical Neurology, Vinken, P. J. & Bruyn, G. W. , Ed, North-Holland Publ Co, Amsterdam, 6:173, 1968. Selby, G., 1968

Reversible Cortical and Basal Ganglia Lesions in Late-Onset Methylmalonic Aciduria
JAMA Neurol 81:1-82, Chu,X.C.,et al, 2024

A 30-Year-Old Woman Presenting with Rapidly Progressive Dementia and Extreme Hypoglycorrhachia
Neurol 102:e209188, Bai,X.,et al, 2024

Ischemic Retinopathy from Prolonged Orbital Compression
NEJM 390::e14, Chen,Y-K and Chen C-L, 2024

A 51-Year-Old Woman with Abnormal Corups Callosum Signal
JAMA Neurol 81:192-193, Xie,N. & Sun, Q, 2024

A 24-Year-Old Man with Gait Impairment, Hearing Loss, and Recurrent Fever
Neurol 102:e209358, Barbosa,A.R.,et al, 2024

Clinicopatholigic Conference, Rheumatoid Arthritis with Vasculitis Causing A Confluent Mononeuritis Multiplex
NEJM 390:1312-1322, Case 11-2024, 2024

Eye Toward Stroke Prevention:Central Retinal Artery Occlusion and Tandem Internal Carotid Artery Occlusion
Stroke 55:e165-e168, Cheronis,C.,et al, 2024

Vitamin B12 Deficiency:NICE Guideline Summary
BMJ 385:q1019, q1262, Sands,T.,et al, 2024

MR Imaging Findings in Anti-Leucine-Rich Glioma Inactivated Protein 1 Encephalitis:A Systematic Review and Meta-Analysis
AJNR 45:977-986, Almeida,F.C.,et al, 2024

Clinicopathologic Conference, Paraneoplastic Encephalomyelitis Due to Small-Cell Lung Carcinoma and Concurrent Cerebral Amyloid Angiopathy
NEJM< 391357-369, Case 23-2024, 2024

Parkinsons Disease
NEJM 391:442-452, Tanner,C.M. & Ostrem,J.L., 2024

Clinicopathologic Conference, Myeloperoxidase antineutrophil cytoplasmic antibody-associated vasculitis
NEJM 390:843-851, Case 7-2024, 2024

Tau Positron Emission Tomography for Predicting Dementia in Individuals with Mild Cognitive Impairment
JAMA Neurol 81:845-856, Groot,C.,et al, 2024

Clinicopathologic Conference, Nutritional Optic Neuropathy Due to Multiple Nutritional Deficits, Including Vitamin A, Copper, and Zinc Deficiencies
NEJM 391:641-650, Gaier,E.D.,et al, 2024



Showing articles 0 to 50 of 2164 Next >>