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Differential
(Click to cross reference)
acquired immunodeficiency syndrome
acquired immunodeficiency syndrome dementia complex
acquired immunodeficiency syndrome, congenital
acquired immunodeficiency syndrome, infants and children
acrocyanosis
Addison's disease
adrenal lesion
adrenoleukodystrophy
adrenoleukodystrophy, adult onset
adrenoleukodystrophy, carrier
adrenomyeloneuropathy
adult-onset leukodystrophy, with neuroaxonal spheroids
advances in neurology
adverse drug reaction
affect, flat
agitation
akinetic mute
algorithm
Alzheimer's disease
Alzheimer's disease, diagnosis of
Alzheimer's disease, early onset
Alzheimer's disease, familial
Alzheimer's disease, familial, late onset
Alzheimer's disease, heterogeneity of
Alzheimer's disease, preclinical
Alzheimer's disease, treatment of
amaurosis fugax
amyloid angiopathy, cerebral
amyloid angiopathy, cerebral, Dutch type
amyloid angiopathy, hereditary cystatin C
amyloid beta protein
amyloid plaques
amyloid-related imaging abnormalities
amyotrophic lateral sclerosis
ANA-negative systemic lupus erythematosus
anemia
angiitis
angiitis, granulomatous of CNS
angiitis, isolated of CNS
angiitis, isolated of CNS, tumefactive
angiography, cerebral, beaded vessels
angiography, cerebral
angiography, cerebral, false negative
anomic aphasia
antibodies to measles
anticardiolipin antibodies
anticoagulant, treatment
antiphospholipid antibodies
antiphospholipid antibody syndrome
anxiety
aphasia
aphasia, logopenic, progressive
aphasia, progressive
aphasia, progressive, non-fluent
aphasia, progressive, primary
apolipoprotein E
APP
APP gene
apraxia
arteriopathy
arteritides
arthritis
arylsulfatase A
asymptomatic
ataxia
ataxia, cerebellar
ataxia, truncal
ataxic gait
atrial myxoma
auditory evoked brainstem potentials
autism
autoimmune disease
axonal spheroid
B 12 deficiency
B cell lymphoma
B12
Balint's syndrome
basal ganglia
basal ganglia, calcification of
basal ganglia, infarction
basal ganglia, lesion of
behavioral disorder
Behcet's syndrome
biologic markers
blindness
blindness, sudden
blood transfusion
bone biopsy
bone marrow biopsy
bone marrow transplantation
bone survey
bovine spongiform encephalopathy
bradykinesia
brain atrophy
brain biopsy
brain biopsy, negative
brain scan, abnormal
bruxism
C0ORF72
cachexia
calcification, intracranial
cardiomyopathy
carotid artery occlusion, neck
carotid artery stenosis
case studies
CAT scan
CAT scan, abnormal
CAT scan, emission, abnormal
CAT scan, false negative
cataracts
caudate nucleus, lesion of, bilateral
celiac disease, adult
central nervous system, infection of
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar infarction
cerebellar plaques, amyloid
cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy
cerebral cortex
cerebral cortical atrophy
cerebral embolism
cerebral embolism, cardiac origin
cerebral infarction
cerebral infarction, hemorrhagic
cerebral infarction, small, deep
cerebral infarction, subcortical
cerebral ischemia
cerebroretinal microangiopathy with calcifications and cysts
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, lactic acid concentration
cerebrospinal fluid, oligoclonal IgG in
cerebrovascular accident
cerebrovascular accident, atrial myxoma
cerebrovascular accident, bilateral
cerebrovascular accident, familial occurrence
cerebrovascular accident, infancy and childhood
cerebrovascular accident, multiple
cerebrovascular accident, non atherosclerotic cause of
cerebrovascular accident, recurrent
cerebrovascular accident, three territory involvement
cerebrovascular accident, topographic pattern
cerebrovascular accident, women
cerebrovascular accident, work up for
cerebrovascular accident, young adult
cerebrovascular disease
cerebrovascular disease, cardiovascular disease with
children
chorea
choreoathetosis
chromosomal abnormality
chromosome 1
chromosome 14
chromosome 17
chromosome 19
chromosome 20
chromosome 21
chronic progressive external ophthalmoplegia
clindamycin
Clinical Pathologic Conference(C.P.C.)
cognition
coma
comorbidities
compulsivity
confusion
corneal dystrophy
corpus callosum
corpus callosum, lesion of
corpus callosum, thinning
cortical blindness
cortical blindness, transient
cortical infarction
cortical infarction, small
coumarin
COVID-19
cranial nerve palsies
C-reactive protein, elevated
crying, pathologic
cultured skin fibroblasts
cyst, bone
deafness
degenerative diseases of CNS
delirium
delusion
dementia
dementia, age at onset
dementia, cerebrovascular disease causing
dementia, childhood
dementia, clinical diagnosis
dementia, diagnostic evaluation of
dementia, differential diagnosis of
dementia, familial
dementia, frontal lobe type
dementia, frontotemporal
dementia, presenile
dementia, rapidly progressive
dementia, reversible
dementia, subcortical
dementia, transmissible
dementia, treatment of
demyelinating disease
depression
developmental milestones
developmental milestones, loss of
developmental retardation
diabetes mellitus
diagnostic criteria
diet
differential diagnosis
diplopia
disability rating scale, neurological
disorientation
dizziness
dural graft, cadaveric
dysdiadochokinesia
dysphagia
dystonia
echocardiogram
echolalia
electroencephalogram
electroencephalogram, abnormalities of
electroencephalogram, focal delta activity
electroencephalogram, pediatric patients
electroencephalogram, periodic complexes
electromyogram
electron microscopy
encephalitis
encephalitis, viral
encephalopathy
encephalopathy, metabolic
encephalopathy, progressive
enzyme, defect
epidemic
epidemiology of neurology
evoked potentials
executive dysfunction
exercise intolerance
exome sequencing
Fabry's disease
failure to thrive
falling
false negative
familial
familial hemiplegic migraine
farmer
fasciculation
fatty acid, elevated plasma content
fenfluramine
fever
fluency
fracture, pathologic
frontal lobe, anatomy and physiology
frontal lobe, atrophy
frontal lobe, lesion of
frontal lobe, pathologic signs of
frontotemporal dementia, behavioral variant
gadolinium
gait disorder
gait, apraxic
gaze palsy
gaze palsy, horizontal
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
genu of corpus callosum
Gerstmann-Straussler-Scheinker disease
gliadin antibodies
gliosis
globus pallidus
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
granular atrophy, cerebral cortex
grasp reflex
grasping
growth hormone
growth retardation
gyrus, abnormal
Hallervorden Spatz disease
hallucination
hallucination, visual
handedness
head injury
headache
hearing loss
hearing loss, bilateral
hearing problems in children
heart block
hemiparesis
hemiplegia
hemosiderosis of CNS, superficial
hepatitis
hepatosplenomegaly
heralding manifestation
Hodgkin's disease
human immunodeficiency virus type 1
Huntington's chorea
Huntington's disease, children
hydrocephalus
hydrocephalus, exvacuo
hydrocephalus, normal pressure
hyperreflexia
hypersomnia
hypertension
hypoglycorrhachia
hypogonadism
hypotension, systemic
hypotonia
iatrogenic neurologic disorders
imbalance
immunosuppressive agents
impaired vigilance
impulsivity
inappropriate behavior
inattention
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion bodies, eosinophilic intranuclear
inclusion bodies, intracytopasmic
inclusion bodies, intranuclear
incoordination
infection
inflexibility, mental
intellectual deficit
intellectual deterioration
intestinal biopsy
intestinal pseudoobstruction
intracerebral hemorrhage
intracerebral hemorrhage, familial
intracerebral hemorrhage, lobar
intracerebral hemorrhage, recurrent
intracerebral hemorrhage, young adult
iron, brain
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
Jakob-Creutzfeldt disease, medical precaution with
Jakob-Creutzfeldt disease, variant
Jakob-Creutzfeldt disease, young adult
Kearns-Sayre syndrome
Kluver-Bucy syndrome
lactic acidemia
lacunar infarction
Lafora body
Lafora's disease
language disorder in adults
language disorders in children
laughing, pathologic
Leber's hereditary optic neuropathy
lecanemab
leg weakness, bilateral
Leigh's disease
lethargy
leukodystrophy
leukoencephalopathy
leukoencephalopathy, adult onset, sporadic
level of consciousness, decreased
Lewy body
life expectancy
lipid storage disorder of CNS
lipomembranous polycystic osteodysplasia
livedo reticularis
liver disease
lobar atrophy
logopenia
Lorenzo's oil
loss of sympathy
lupus anticoagulant
lymphadenopathy
lymphoma
lymphoma involving CNS
manganese intoxication
mania
manic-depressive
MELAS syndrome
memory, defect of recent
memory, impairment of
memory, impairment of, subjective
meningeal biopsy
meningeal enhancement
meningovascular syphilis
mental retardation
mental status, abnormal
MERRF syndrome
metabolic disorder, primary
metachromatic leukodystrophy
metachromatic leukodystrophy, juvenile
microangiopathy, brain
microangiopathy, retina
microcephaly
microhemorrhage, intracerebral
microinfarcts
middle cerebral artery, occlusion of
middle cerebral artery, stenosis of
migraine
migraine, hemiplegic
mild cognitive impairment
mimics
Mini Mental Status Examination
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
mitral valve lesion
molecular genetics
monoclonal antibodies
monoparesis
mood change
mortality
motor neuron disease
movement disorder
movement disorder, extrapyramidal
moyamoya
moyamoya, adult
MRI
MRI, abnormal
MRI, angiography
MRI, CAT scan compared to
MRI, contrast enhanced
MRI, diffusion weighted
MRI, false negative
MRI, functional
MRI, gradient-echo
MRI, high signal foci on
MRI, linear enhancement
MRI, punctate pattern
MRI, ring sign, open
MRI, serial
MRI, spinal cord
MRI, susceptibility weighted
MRI, T1 weighted high signal foci
multiple sclerosis
multiple sclerosis, differential diagnosis of
multiple sclerosis, misdiagnosis
muscle atrophy, progressive
muscle biopsy
muscle weakness
muscle weakness, proximal
mutism
myasthenia gravis, differential diagnosis
myasthenia gravis, misdiagnosis of
myelomalacia
myelopathy
myocardial infarction
myoclonic jerks
myoclonus
myopathy
myopathy, mitochondrial
nausea and vomiting
negative
neologism
neoplasm, intracranial, differential diagnosis of
neoplastic angioendotheliosis
nerve biopsy
nerve conduction studies
neuroaxonal dystrophy
neuroaxonal dystrophy, infantile
neuroaxonal leukodystrophy
neurocutaneous disease
neurocutaneous melanosis
neuroendocrinology
neurofibrillary degeneration
neurologic complications of, systemic cancer
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic examination, focal
neurologic signs
neuroophthalmology
neuropathology
neuropathology, brain
neuropathy
neuropathy, peripheral
neurosyphilis
Niemann-Pick disease
normal
Notch3 gene
nutritional deficiency
nystagmus
obsessive-compulsive disorder
occipital lobe, lesion of
occupational neurologic disorders
ophthalmoplegia
opportunistic infection
opportunistic infection, CNS
optic atrophy
optic neuritis
optic neuritis, bilateral
optic neuropathy
pain
pain, increased response
pancytopenia
papilledema
paranoia
paraparesis, familial spastic
paraparesis, spastic
paraphasias
paratonia
Parkinson disease
Parkinson disease, dementia with
Parkinson disease, familial
Parkinson disease, rapid progression
Parkinson disease, young onset
Parkinsonism syndrome
Parkinsonism-dementia complex
PAS positive
PAS positive material in the brain
pathologic reflex
peripheral vascular disease
peroxisomal disease
perseveration
personality change
Pick bodies
Pick's disease
pigmentary retinopathy
Pittsburgh Compound B
pleocytosis of cerebrospinal fluid
pneumoencephalogram(PEG)
polycystic lipomembranous osteodysplasia
polymerase chain reaction
posterior cortical atrophy
practice guidelines
preclinical
prenatal diagnosis by amniocentesis
presenilin-1 gene
presenilin-2 gene
prevention of neurologic disorders
prion disease
prognosis
progressive myoclonic epilepsy
progressive neurologic disorder
progressive subcortical gliosis
protein 14-3-3, cerebrospinal fluid
pseudobulbar palsy
psychiatric disorder
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis
ptosis
pulmonary infiltrates
pyramidal tract dysfunction
quadriparesis
quadriplegia
radiation therapy, CNS treatment and complications with
ragged-red fibers
rapidly progressing neurologic illness
real-time quaking-induced conversion
rectal biopsy
recurrent
Red flags
release phenomena
respirations in CNS disease
reticulum antibodies
retinal branch artery occlusion
retinal infarction
retinal lesion
retinopathy
Rett's syndrome
review article
rigidity
risk factors
roaming behavior
rocking
safety
Schilder's disease
schizophrenia
scoliosis
screening
sedimentation rate, elevated
seizure
seizure, children
seizure, diagnosis of
seizure, intractable
seizure, teenager
semantic dementia
senile plaques
sensorineural hearing loss
sensory symptoms
serologic testing
short stature
single photon emission computed tomography
skin, biopsy
skin, darkening of
skin, lesions in neurologic disorders
small vessel disease
Sneddon's syndrome
somatosensory evoked potentials
spasticity
speech disorder
spinal cord, embolism of
spinal cord, infarction of
spinal cord, lesion of
spinal cord, pathologic exam of
splenomegaly
spongy degeneration of brain
startle myoclonus
status epilepticus
status epilepticus, intractable
stereotyped behavior
steroid therapy, CNS treatment and complications with
strokelike episodes
stuttering
stuttering following CVA
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
subarachnoid hemorrhage
subarachnoid hemorrhage, cerebral convexity
substantia nigra
sural nerve
Susac's syndrome
symmetric brain lesions
syphilis, diagnosis and treatment
syphilis, neurologic complications with
systemic illness
systemic lupus erythematosus
tau protein
tauopathy
temporal lobe, atrophy
testicular atrophy
thalamus, lesion of
thalamus, lesion of-bilateral
Three territory sign
thromboangiitis obliterans cerebri
thrombophlebitis
tinnitus
tissue plasminogen activator, intravenous
titubation
tongue, fasciculations of
toxoplasmosis, CNS
transient ischemic attack
transient ischemic attack, recurrent
transient neurologic deficit
treatment of neurologic disorder
tumor necrosis factor
ulcerative colitis
upgaze, paralysis of
uremia
urinary incontinence
vanishing white matter
vasculitides
vasculopathy
vegetarianism
vertigo
vertigo, episodic
viral infection
viral infection, CNS
vision, failure of in childhood
visual acuity, decreased
visual evoked response
visual field defect
visual impairment
visual loss
vitamin deficiency
weakness
weight loss
wheelchair
Whipple's disease
white matter disease
word-finding difficulty
workup
Showing articles 900 to 950 of 2806 << Previous Next >>

Progressive Posterior Cortical Dysfunction
Neurol 63:1175-1180, Renner,J.A.,et al, 2004

Clinical, Genetic, and Neuropathologic Characteristics of Posterior Cortical Atrophy
Neurol 63:1168-1174, Tang-Wai,D.F.,et al, 2004

Hyperinsulinemia and Risk of Alzheimer Disease
Neurol 63:1187-1192, Luchsinger,J.A.,et al, 2004

Autonomic Failure as the Initial Presentation of Parkinson Disease and Dementia with Lewy Bodies
Neurol 63:1093-1095, Kaufmann,H.,et al, 2004

Neonatal Brain Injury
NEJM 351:1985-1995, Ferriero,D.M., 2004

The Metabolic Syndrome, Inflammation, and Risk of Cognitive Decline
JAMA 292:2237-2242, Yaffe,K.,et al, 2004

Diabetes Mellitus in Midlife and the Risk of Dementia Three Decades Later
Neurol 63:1902-1907, Beeri,M.S.,et al, 2004

Memory Complaints in Nondemented Men Predict Future Pathologic Diagnosis of Alzheimer Disease
Neurol 63:1960-1961, Jorm,A.F.,et al, 2004

CJD--A Case of Mistaken Identity
Lancet 364:2068, Campbell,S.,et al, 2004

Rivastigmine for Dementia Associated with Parkinson's Disease
NEJM 351:2509-2518,2547, Emre,M.,et al, 2004

Neurosyphillis in the Modern Era
JNNP 75:1727-1730, Timmermans,M. &Carr,J., 2004

Mixed Dementia, Emerging Concepts and Therapeutic Implications
JAMA 292:2901-2908, Langa,K.M.,et al, 2004

Reduced Risk of Alzheimer Disease in Users of Antioxidant Vitamin Supplements
Arch Neurol 61:82-88, Zandi,P.P.,et al, 2004

Tissue Distribution of Bovine Spongiform Encephalopathy Agent in Primates after Intravenous or Oral Infection
Lancet 363:422-428,411, Herzog,C.,et al, 2004

Possible Transmission of Variant Creutzfeldt-Jakob Disease by Blood Transfusion
Lancet 363:417-421,411, Llewelyn,C.A.,et al, 2004

Treatment-Induced Leukoencephalopathy in Primary CNS Lymphoma,A Clinical and Autopsy Study
Neurol 62:451-456, Lai,R.,et al, 2004

Bovine Spongiform Encephalopathy in the United States - An Epidemiologist's View
NEJM 350:539-542, Donnelly,C.A., 2004

Memantine Treatment in Patients with Moderate to Severe Alzheimer Disease Already Receiving Donepezil, A Randomized Controlled Trial
JAMA 291:317-324, Tariot,P.N.,et al, 2004

Recipients of Blood or Blood Products "at vCJD risk"
BMJ 328:118-119, Bird,S.M., 2004

Imaging Cerebral Atrophy:Normal Ageing to Alzheimer's Disease
Lancet 363:392-394, Fox,N.C.&Schott,J.M., 2004

Periodontal Disease as a Risk Factor for Ischemic Stroke
Stroke 35:496-501, Crau,A.J.,et al, 2004

Prion Deposition in Olfactory Biopsy of Sporadic Creutzfeldt-Jakob Disease
Ann Neurol 55:294-296, Tabaton,M.,et al, 2004

Whole Brain Diffusion Tensor Imaging in HIV-Associated Cognitive Impairment
AJNR 25:195-200,167, Ragin,A.B.,et al, 2004

Comparison of Different MRI Brain Atrophy Rate Measures with Clinical Disease Progression in AD
Neurol 62:591-600, Jack, Jr.,C.R.,et al, 2004

Susac Syndrome:Report of Four Cases and Review of the Literature
AJNR 25:382-388,351, Do,T.H.,et al, 2004

Diabetes Mellitus and Risk of Alzheimer Disease and Decline in Cognitive Function
Arch Neurol 61:661-666, Arvanitakis,Z.,et al, 2004

Fibromuscular Dysplasia
NEJM 350:1862-1871, Slovut,D.P. &Olin,J.W., 2004

Size of the Treatment Effect on Cognition of Cholinesterase Inhibition in Alzheimer's Disease
JNNP 75:677-685, Rockwood,K., 2004

False-Positive Pulvinar Sign on MRI in Sporadic Creutzfeldt-Jakob Disease
Neurol 62:1235-1236, Petzold,G.C.,et al, 2004

Progressive Binasal Hemianopia
Lancet 363:1606, Pringle,E.,et al, 2004

Estimating Prognosis for Nursing Home Residents with Advanced Dementia
JAMA 291:2734-2740, Mitchell,S.L.,et al, 2004

Neurosyphilis with Complex Partial Status Epilepticus and Mesiotemporal MRI Abnormalities Mimicking herpes Simplex Encephalitis
JNNP 75:833, Marano,E.,et al, 2004

Dementia After Stroke
Stroke 35:1264-1269, Ivan,C.S.,et al, 2004

Folate Intake and Risk of Stroke Among Women
Stroke 35:1259-1263, Al-Delaimy,W.K.,et al, 2004

Preclinical Alzheimer Disease
Neurol 63:2341-2347, Saxton,J.,et al, 2004

Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy (CADASIL)
Pract Neurology 4:50-55, Razvi,S.S.M. &Muir,K.W., 2004

Neuro-Ophthalmic Findings in the Visual Variant of Alzheimers Disease
Ophthalmology 111:376-381, Lee,A.G. &Martin,C.O., 2004

Clinical Manifestations of Cerebral Amyloid Angiopathy-Related Inflammation
Ann Neurol 55:250-256, Eng,J.A.,et al, 2004

A ripping roller coaster ride
Neurol 61:1255, Blacker, D.J. & Wijdicks, E.F.M., 2003

Diagnosis and Complications of Cushings Syndrome: A Consensus Statement
J Clin Endocrinol Metab 88:5593-5602, Arnaldi,G.,et al, 2003

Spontaneous Intracranial Internal Carotid Artery Dissection: 6 Case Report and a Review of 39 Cases in the Literature
Rinsho Shinkeigaku 43:313-321, Nagumo,K.,et al, 2003

The Topography of Metabolic Deficits in Posterior Cortical Atrophy (the Visual Variant of Alzheimers Disease) with FDG-PET
JNNP 74:1521-1529, Nestor,P.J.,et al, 2003

Silent Infarcts Demonstrated by Diffusion-Weighted MRI in CADASIL
Eur Neurol 49: 178-180, Moon,S.Y.,et al, 2003

Loss of Calculation Abilities in Patients with Mild and Moderate Alzheimer Disease
Arch Neurol 60:1585-1589, Martin,R.C.,et al, 2003

Primary Progressive Aphasia--A Language-Based Dementia
NEJM 349:1535-1542, Mesulam,M.-M., 2003

Donepezil is Associated with Delayed Nursing Home Placement in Patients with Alzheimer's Disease
Am Geriatr Soc 51:937-944, Geldmacher,D.S.,et al, 2003

Exercise Plus Behavioral Management in Patients with Alzheimer's Disease
JAMA 290:2015-2022, Teri,L.,et al, 2003

Efficacy and Tolerability of Donepezil in Vascular Dementia
Stroke 34:2323-2332, Black,S.,et al, 2003

Clinical Features and Neuropathology of Autosomal Dominant Spinocerebellar Ataxia (SCA17)
Ann Neurol 43:367-375, Rolfs,A.,et al, 2003

Vascular Syndromes of the Thalamus
Stroke 34:2264-2278, Schumahmann,J.D., 2003



Showing articles 900 to 950 of 2806 << Previous Next >>