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Differential
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abdominal protrusion
activities of daily living
activities of daily living scale
agnosia
agnosia, visual
agraphia
akinetic mute
alexia
Alzheimer's disease
Alzheimer's disease, diagnosis of
Alzheimer's disease, visual variant
amyloid angiopathy, cerebral
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, diagnosis of
amyotrophic lateral sclerosis, differential diagnosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, etiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, prognosis
amyotrophic lateral sclerosis, treatment of
anomic aphasia
aphasia
aphasia, progressive
aphasia, progressive, non-fluent
aphasia, progressive, primary
aphasia, transcortical
aphasia, transcortical-sensory
apolipoprotein E
apraxia
apraxia, constructional
arthralgia
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxic gait
attention span
automobile accidents
B 12 deficiency
B12
behavioral disorder
binge eating
biologic markers
blepharospasm
bone biopsy
bone pain
bone scanning
brain atrophy
brain biopsy
bruxism
bulimia
C0ORF72
calculations
CAT scan
CAT scan, abnormal
CAT scan, dementia
CAT scan, emission, abnormal
cerebellar atrophy, primary
cerebellar degeneration
cerebellar tonsils
cerebellum, disease of
cerebral cortical atrophy
cerebrospinal fluid, leak
cerebrospinal fluid, pressure low
Charles Bonnet's syndrome
choreoathetosis
chromosomal abnormality
chromosome 17
Clinical Pathologic Conference(C.P.C.)
cognition
coma
comprehension, impaired
compulsivity
confusion
controversies in neurology
corpus callosum
corpus callosum, atrophy of
cortical-basal ganglionic degeneration
crying, pathologic
degenerative diseases of CNS
delirium
delusion
dementia
dementia, age at onset
dementia, clinical diagnosis
dementia, diagnostic classification
dementia, diagnostic evaluation of
dementia, differential diagnosis of
dementia, familial
dementia, frontal lobe type
dementia, frontotemporal
dementia, presenile
dementia, rapidly progressive
dementia, reversible
dementia, treatment of
depression
diagnostic criteria
differential diagnosis
difficulty climbing stairs
disinhibition-dementia-parkinsonism-amyotrophic complex
dizziness
drug withdrawal
dural tear
dysarthria
dysmetria
eating disorder
electromyogram
electron microscopy
emotional lability
epidural blood patch
executive dysfunction
falling
familial
fasciculation
fatigue
fibrillations
finger nose finger test
flail arm syndrome
fluency
foot drop
frontal lobe, atrophy
frontal lobe, behavior with disease of
frontal lobe, pathologic signs of
frontotemporal brain sagging syndrome
frontotemporal dementia, behavioral variant
gait disorder
gait, waddling
gaze palsy, vertical
gene
gene mutation
genetic neurologic disorders
genetic testing
glabellar sign
grasp reflex
hallucination
hallucination, visual
hallucination, visual, benign
head injury
headache
headache, chronic
headache, positional
hearing loss
hemianopia, homonymous
herpes simplex encephalitis
hippocampus
House sign
Huntington's chorea
hyperreflexia
hypersomnia
imbalance
imbalance, postural
impulsivity
inappropriate behavior
inattention
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion bodies, intracytopasmic
inclusion bodies, ubiquitin
inflexibility, mental
initiative, lack of
insomnia
insular cortex
insular cortex, lesion
intellectual deficit
intellectual deterioration
interpeduncular cistern, compressed
irritability
Jakob-Creutzfeldt disease
jaw jerk, abnormal
Kluver-Bucy syndrome
language disorder in adults
laughing, pathologic
leg weakness, bilateral
Lewy body disease, diffuse
lobar atrophy
locked-in syndrome
logopenia
loss of sympathy
memory
memory, defect of recent
memory, impairment of
memory, recent
meningeal enhancement
mental status, abnormal
mesial temporal sclerosis
midbrain, swollen
migraine
mimics
misdiagnosis
Montreal cognitive assessment
mood change
mortality
motor neuron disease
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, functional
MRI, negative
MRI, serial
MRI, spine
MRS
multiple system atrophy
muscle biopsy
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
mutism
myopathy
myopathy, inclusion body
myopathy, inclusion body with Paget's disease
nausea and vomiting
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic examination, focal
neurologic signs
neuropathology
neuropathology, brain
nutritional deficiency
nystagmus
obsessive-compulsive disorder
ophthalmoplegia
ophthalmoplegia, total
Paget's disease
pain, increased response
pallido-ponto-nigral degeneration
palmomental response
paranoia
paraparesis
paraphasias
paraplegia, in flexion
Parkinson disease
Parkinson disease, atypical
Parkinsonism syndrome
pathologic reflex
peduncular hallucinosis
perseveration
personality change
Pick bodies
Pick's disease
pons, flattened
posterior cortical atrophy
posterior leukoencephalopathy syndrome
prepontine cistern, effaced
primary intracranial hypotension
primary lateral sclerosis
prognosis
progranulin
progressive neurologic disorder
progressive subcortical gliosis
progressive supranuclear palsy
pruritus
pseudobulbar palsy
psychiatric problems in neurologic disorders
psychological testing
psychomotor retardation
psychosis
quadriplegia
rapidly progressing neurologic illness
Red flags
release phenomena
repetition, impaired
respiratory failure
respiratory tract infection
reversible cerebral vasoconstrictive syndromes
reversible neurologic disorder
review article
rigidity, axial
risk factors
roaming behavior
rooting reflex
sagging of the brain
sclerosis, bone
seizure
semantic dementia
sexual behavior, disorder of
simultanagnosia
single photon emission computed tomography
single photon emission computed tomography, false negative
sleep pathology and physiology
snout reflex
spasticity
speech disorder
speech, loss of
splenium of corpus callosum
splenium of corpus callosum, displaced
spongy degeneration of brain
stereotyped behavior
suck reflex
synucleinopathy
systemic illness
tangential
tau protein
tauopathy
temporal lobe
temporal lobe, atrophy
temporal lobe, lesion
temporal lobe, lesion, bilateral
tinnitus
tinnitus, pulsatile
tongue, atrophy
tongue, fasciculations of
tonsillar herniation of cerebellum
trauma
treatment of neurologic disorder
ubiquitin
upgaze, paralysis of
urinary incontinence
vegetarianism
visual field defect
visuospatial disturbance
vitamin deficiency
weakness, progressive
wheelchair
white matter disease
wide based gait
Wingspan study
word-finding difficulty
Showing articles 350 to 400 of 3968 << Previous Next >>

Diagnosis, Management, and Treatment of Alzheimer Disease, A Guide for the Internist
Arch Int Med 159:789-798, Richards,S.S.&Hendrie,H.C., 1999

Abnormal Diffusion-Weighted Magnetic Resonance Images in Creutzfeldt-Jakob Disease
Arch Neurol 56:577-583, Bahn,M.M.,&Parchi,P., 1999

Mortality from Dementia in Occupations at Risk of Exposure to Bovine Spongiform EncephalopathyAnalysis of Death Registrations
BMJ 318:1044-1045, Aylin,P.,et al, 1999

Infantile Neuroaxonal Dystrophy,Clinical Spectrum and Diagnostic Criteria
Neurol 52:1472-1478, Nardocci,N.,et al, 1999

Creutzfeldt-Jakob Disease and Related Transmissible Spongiform Encephalopathies
NEJM 339:1994-2004, Johnson,R.T. & Gibbs,Jr.,C.J., 1998

Carbon Monoxide Poisoning
NEJM 339:1603-1608, Ernst,A. & Zibrak,J. D., 1998

New Neuropathological Criteria for Alzheimer Disease
Arch Neurol 55:1174-1176, Hyman,B.T., 1998

Longitudinal Study of CSF Levels of Tau, A beta 1-40, and A beta 1-42 (43) in Alzheimer's Disease
Ann Neurol 44:17-26, 61998., Kanai,M.,et al, 1998

Preclinical Prediction of Alzheimer's Disease Using SPECT
Neurol 50:1563-1571, Johnson,K.A.,et al, 1998

An Unusual Case of Creutzfeldt-Jakob Disease
Neurol 51:617-619, Vingerhoets,F.J.G.,et al, 1998

Prader-Willi and Angelman Syndromes
Medicine 77:140-151, Cassidy,S.B.&Schwartz,S., 1998

MR Differential Diagnosis of Normal-Pressure Hydrocephalus and Alzheimer Disease:Significance of Perihippocampal Fissures
AJNR 19:813-819, Holodny,A.I.,et al, 1998

SPECT in the Identif of New Variant Creutzfeldt-Jakob Disease:Case Reports
BMJ 316:593-594, 5631998., deSilva,R.,et al, 1998

The Role of 99m-Tc HMPAO SPECT in the Diagnosis of Creutzfeldt-Jacob Disease
AJNR 19:454-455, Miller,D.A.,et al, 1998

Detection of 14-3-3 Protein in Cerebrospinal Fluid Supports Dx of Creutzfeldt-Jakob Disease
Ann Neurol 43:32-40, Zerr,I.,et al, 1998

Diagnosis of Creutzfeldt-Jakob Disease by Measurement of S100 Protein in Serum:Case-Control Study
BMJ 316:577-581, 5631998., Otto,M.,et al, 1998

Tourette Syndrome:Update and Review of the Literature
The Neurologist 4:188-195, Feigin,A.&Clarke,H., 1998

Retinocochleocerebral Vasculopathy
Medicine 77:12-40, Petty,G.W.,et al, 1998

Utility of the Apolipoprotein E Genotype in the Diagnosis of Alzheimer's Disease
NEJM 338:506-511, Mayeux,R.,et al, 1998

Alzheimers Disease with Asymmetric Parietal Lobe Atrophy: A Case Report
J Neurol Sci 160:96-99, Kaida,K.-I.,et al, 1998

Subcotical Arteriosclerotic Encephalopathy (Binswangers Disease)
, Ghika,J. &Bogousslavsky, J., 1998

Posterior Cerebral Artery Syndromes
, Caplan,L.R. &Bogousslavsky,J., 1998

The Effect of Different Diagnostic Criteria on the Prevalence of Dementia
NEJM 337:1667-1674, Erkinjuntti,T.,et al, 1997

Genetic Testing for Alzheimer Disease, Practical and Ethical Issues
Arch Neurol 54:1226-1229, Roses,A.D., 1997

New Variant Creutzfeldt-Jakob Disease:Psychiatric Features
Lancet 350:908-910, Zeidler,M.,et al, 1997

Clinical Features and Pharmacologic Treatment of Behavioral Symptoms of Alzheimer's Disease
Neurol 48 (Suppl 6) :S17-S24997., Borson,S.&Raskind,M.A., 1997

The Risk of Bovine Spongiform Encephalopathy ('Mad Cow Disease') to Human Health
JAMA 278:1008-1011, Brown,P., 1997

Detection of 14-3-3 Protein in the CSF of Genetic Creutzfeldt-Jakob Disease
Neurol 49:593-595, Rosemann,H.,et al, 1997

Diffusion-Weighted Magnetic Resonance Imaging in Creutzfeldt-Jakob Disease
Lancet 349:847-848, Demarerel,P.,et al, 1997

The 14-3-3 Brain Protein and Transmissible Spongiform Encephalopathy
NEJM 336:873-875, Moussavian,M.,et al, 1997

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

X Linked Adrenoleukodystrophy:Clinical Presentation, Diagnosis, and Therapy
JNNP 63:4-14, vanGeel,B.M.,et al, 1997

Pupil Dilation to Tropicamide is not Specific for Alzheimer Disease
Arch Neurol 54:841-844, Growdon,J.H.,et al, 1997

Assessment of CSF Levels of Tau Protein in Mildly Demented Patients with Alzheimer's Disese
Neurol 48:632-635, Galasko,D.,et al, 1997

Bovine Spongiform Encephalopathy and a New Variant of Creutzfeldt-Jakob Disease
Neurol 48:569-571, Epstein,L.G.&Brown,P., 1997

Diagnosis of New Variant Creutzfeldt-Jakob Disease by Tonsil Biopsy
Lancet 349:99-100, Hill,A.F.,et al, 1997

Criteria for Alzheimer's Disease and the Nosology of Dementia with Lewy Bodies
Neurol 48:126-132, Hansen,L.A.&Samuel,W., 1997

Transmissible Spongiform Encephalopathies
NEJM 337:1821-1828, Haywood,A.M., 1997

Brain magnetic Resonance Diffusion Abnormalities in Creutzfeldt-Jakob Disease
Arch Neurol 54:1411-1415, Bahn,M.M.,et al, 1997

The Clinical Introduction of Genetic Testing for Alzheimer Disease, An Ethical Perspective
JAMA 277:832-836, Post,S.G.,et al, 1997

Unusual Clinical Presentations of Cortical-Basal Ganglionic Degeneration
Ann Neurol 40:893-900, Bergeron,C.,et al, 1996

Noninvasive Perfusion MRI in Alzheimer's Disease:A Preliminary Report
Neurol 47:1339-1342, Sandson,T.A.,et al, 1996

Dementia with Lewy Bodies:Reliability and Validity of Clinical and Pathologic Criteria
Neurol 47:1403-1409, Mega,M.S.,et al, 1996

Consensus Guidelines for Clin & Path Dx of Dementia with Lewy Bodies (DLB) :Report of DLB Intl Workshop
Neurol 47:1113-1114, 11241996., McKeith,I.G.,et al, 1996

Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities
Ann Neurol 39:343-351, Rahman,S.,et al, 1996

Preclinical Evidence of Alzheimer's Disease in Persons Homozygous for the e4Allele for Apolipoprotein E
NEJM 334:752-758, 7911996., Reiman,E.M.,et al, 1996

Alzheimer Disease and Nonfluent Progressive Aphasia
Arch Neurol 53:1072-1078, Greene,J.D.W.,et al, 1996

Potential Transmission of BSE via Medicinal products
BMJ 312:988-989, Wickham,E.A., 1996

Bovine Spongiform Encephalopathy and Creutzfeldt-Jakob Disease
BMJ 312:790-791, Brown,P., 1996

Diagnosing Motor Neurone Disease
BMJ 312:650-651, Chancellor,A.M., 1996



Showing articles 350 to 400 of 3968 << Previous Next >>