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Differential
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adenylate kinase 5 autoantibodies
advances in neurology
agitation
agnosia, visual
akinetic mute
Alice in Wonderland syndrome
alien hand syndrome
alternating rapid movement
aluminum
Alzheimer's disease
Alzheimer's disease, diagnosis of
Alzheimer's disease, familial
Alzheimer's disease, heterogeneity of
Alzheimer's disease, incidence
Alzheimer's disease, pathogenesis
Alzheimer's disease, preclinical
Alzheimer's disease, risk factors in
Alzheimer's disease, treatment of
amnesia
amyloid
amyloid angiopathy, cerebral
amyloid beta protein
amyloid imaging
amyloid plaques
amyloidosis
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, guamian type of
anomic aphasia
anorexia
anti IgLON5
anticholinesterase
anticonvulsants
antiviral agents
aphasia
aphasia, progressive, primary
apolipoprotein E
APP
applause sign
apraxia
apraxia of eyelid opening
apraxia, constructional
areflexia
arm swing, reduced
arthrogryposis multiplex
aspiration
asymptomatic
ataxia
ataxia, cerebellar
ataxia, progressive
ataxia, sensory
ataxia, truncal
ataxic gait
attention span
atypical
autoantibodies
automobile accidents
axonal injury
basal ganglia, lesion, bilateral
behavioral disorder
biologic markers
blast injury
blepharospasm
blinking, reduced
bovine spongiform encephalopathy
boxing
bradykinesia
bradyphrenia
brain atrophy
brain biopsy
brain transplantation
brain weight
bruxism
bulbar palsy
callosal angle
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
cataplexy
cavum septi pellucidi
central core disease
central hypoventilation
cerebellar ataxia, neuropathy and vestibular areflexia syndrome
cerebellar atrophy, secondary
cerebellar plaques, amyloid
cerebellum, disease of
cerebral cortex
cerebral cortical atrophy
cerebral edema, vasogenic
cerebral glucose metabolism
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, biochemical markers of CNS disease
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, oligoclonal IgG in
Charcot-Marie-Tooth
choline acetyltransferase
chorea
choreoathetosis
chorioretinitis
chronic traumatic encephalopathy
cisternogram, radionuclide
Clinical Pathologic Conference(C.P.C.)
cognition
color vision, impaired
complications
compulsivity
concussion
concussion, recurrent
confusion
controversies in neurology
cortical blindness
cortical-basal ganglionic degeneration
cough
cultured skin fibroblasts
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, diagnostic evaluation of
dementia, differential diagnosis of
dementia, frontal lobe type
dementia, frontotemporal
dementia, presenile
dementia, rapidly progressive
dementia, screening for
dementia, subcortical
dementia, transmissible
depression
developmental milestones, loss of
dexterity, impaired
diagnostic criteria
dialysis
diarrhea
diet
differential diagnosis
diplopia
donepezil
downward gaze
dysarthria
dyschromatopsia
dysdiadochokinesia
dysmetria
dysnomia
dysphagia
dystonia
dystonia, focal
echolalia
efficacy
electroencephalogram
electroencephalogram, abnormalities of
encephalitis
encephalitis, autoimmune
encephalitis, viral
encephalopathy
encephalopathy, post traumatic
epidemiology of neurology
executive dysfunction
eye movement, disorders of
falling
familial
Fazio-Londe's disease
fine motor function, impaired
finger nose finger test
flortaucipir
foam cells
football neurologic injuries
frontal behavioral spatial syndrome
frontal lobe, atrophy
frontal lobe, behavior with disease of
frontal lobe, pathologic signs of
frontotemporal dementia, behavioral variant
gait disorder
gait, apraxic
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gender
gene
gene mutation
genetic counselling
genetic neurologic disorders
genetic testing
Gerstmann-Straussler-Scheinker disease
granulovacuolar degeneration
grasp reflex
Hallervorden Spatz disease
handwriting
head injury
head injury, mild
head injury, repetitive
head injury, return to play following
headache
headache, frontal
heavy metal intoxication
heel-knee-shin test
hemianopia, homonymous
hemifacial spasm
hepatic failure
hepatosplenomegaly
heralding manifestation
herpes virus infection
hippocampal atrophy
hippocampus
hippocampus, hyperintense
histochemistry
HLA
hoarseness
hockey
Huntington's chorea
hydrocephalus, normal pressure
hypophonia
ideomotor apraxia
imbalance
imbalance, postural
immunohistochemistry
immunoperoxidase staining
impulsivity
inattention
incidence
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion bodies, intranuclear
inclusion bodies, ubiquitin
incoordination
initiative, lack of
insomnia
intellectual deficit
intellectual deterioration
interferon
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
Jakob-Creutzfeldt disease, variant
Jakob-Creutzfeldt disease, young adult
jaundice
Kluver-Bucy syndrome
Kugelberg-Welander syndrome
language disorder in adults
L-dopa
lead poisoning
Lewy body
Lewy body disease, diffuse
limbic encephalitis
lipid storage disorder of CNS
lobar atrophy
logopenia
loss of sympathy
lymphadenopathy
macropsia
manganese intoxication
masked facies
memory, defect of recent
memory, impairment of
meningitis
mental status, abnormal
mesial temporal lobe
metamorphopsia
micropsia
midbrain
midbrain, atrophy
mild cognitive impairment
Mini Mental Status Examination
misdiagnosis
mitochondrial disease
molecular genetics
mongolism
Montreal cognitive assessment
mood change
mortality
motor neuron disease
movement disorder
movement disorder, extrapyramidal
MRI
MRI pattern
MRI, abnormal
MRI, diffusion weighted
MRI, diffusion weighted, pattern
MRI, false negative
MRI, FLAIR
MRI, negative
MRI, serial
MRI, volumetry
MRI, voxel-based morphometry
multiple system atrophy
muscle spasm, face
mutism
myasthenia gravis
myoclonic jerks
myoclonus
myotonia dystrophica
nerve conduction studies
neurofibrillary degeneration
neurofibrillary degeneration, causes of
neurologic disease, diagnoses of
neurologic disease, tempo
neurologic signs
neurologic symptoms
neurologic testing
neuron specific enolase
neuronal ceroid-lipofuscinosis
neuroophthalmology
neuropathology
neuropathology, brain
neuropathy
neuropathy, sensory
neurotransmitter
Niemann-Pick disease
nucleus basalis of Meynert
obsessive-compulsive disorder
old age, neurology of
olfactory bulb
ophthalmoplegia
ophthalmoplegia, total
optic atrophy
palmomental response
paranoia
parasomnia
Parkinson disease
Parkinson disease, atypical
Parkinson disease, axial symptoms
Parkinson disease, dementia with
Parkinson disease, L-dopa nonresponsive
Parkinson disease, postencephalitic
Parkinson disease, tremor, absence of
Parkinsonism syndrome
PAS positive material in the brain
pathologic reflex
pathology
penguin silhouette sign
perseveration
personality change
Pick bodies
Pick's disease
Pittsburgh Compound B
PLEDs
PLEDs, bilateral independent
pleocytosis of cerebrospinal fluid
pneumoencephalogram(PEG)
poison, mercury
poison, neurologic problems with
positional head-hanging test
preclinical
pregnancy, neurologic complications in
prion disease
prognosis
progressive neurologic disorder
progressive supranuclear palsy
prosopagnosia
protein 14-3-3, cerebrospinal fluid
protein 14-3-3, cerebrospinal fluid, false negative
proteinopathy
pseudobulbar palsy
psychiatric problems in neurologic disorders
psychological testing
psychomotor retardation
psychosis
pugilistic parkinsonism
punch-drunk syndrome
pursuit eye movements, abnormal
rapidly progressing neurologic illness
reading disorder, acquired
reading problem, causes of
real-time quaking-induced conversion
release phenomena
respirations in CNS disease
retrocollis
review article
rheumatoid arthritis
rheumatoid arthritis, neurologic complications of
rigidity
rigidity, axial
risk factors
Romberg's sign
saccadic eye movements
saccadic eye movements, abnormal
salivation, excessive
screening
semantic dementia
senile plaques
sequencing difficulty
serologic testing
serologic testing of cerebrospinal fluid
sinemet
single photon emission computed tomography
sleep apnea, obstructive
sleep pathology and physiology
smell
Smell Identification Test
soccer
speech disorder
speech disorder, non aphasic
splenomegaly
spongy degeneration of brain
sports medicine, neurology of
square wave jerks
staining reactions in neuropathology
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
subacute sclerosing panencephalitis, adult onset
substantia nigra
symmetric brain lesions
synucleinopathy
tandem gait, ataxic
tangential
tau protein
tauopathy
temporal lobe, atrophy
temporal lobe, lesion
temporal lobe, lesion, bilateral
thalamus, lesion of-bilateral
toxoplasmosis, CNS
trauma
treatment of neurologic disorder
tremor
tremor, intention
tremor, jaw
tricresylphosphate
tuberous sclerosis
ubiquitin
vaccine
vasculitides
vasculopathy
vestibulopathy
vibratory sensation, abnormal
viral infection
viral infection, CNS
vision, blurred
visual distortions
visual loss
visual symptoms
visuospatial disturbance
vocal cord paralysis
voice, abnormality of
walking frame
walking, difficulty with
war
weight loss
Werdnig-Hoffman disease
wheelchair
white matter disease
wide based gait
Williams syndrome
word-finding difficulty
Showing articles 0 to 50 of 992 Next >>

Laboratory Diagnosis of Creutzfeldt-Jakob Disease
NEJM 386:1345-1350, Zerr, I., 2022

Alzheimers Disease
Lancet 397:1577-1590, Scheltens, P.,et al, 2021

Clinicopathologic Conference, Cerebellar Ataxia, Neuropathy and Vestibular Areflexia Syndrome
NEJM 385:165-175, Case 20-2021, 2021

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

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

Links in the Chain of Chronic Traumatic Encephalopathy
NEJM 380:1771-1772, Ropper, A.H., 2019

Atypical Parkinsonian Syndromes: A General Neurologists Perspective
Eur J Neurol 25:41-58, Deutschlander, A.B.,et al, 2018

Advances in Progressive Supranuclear Palsy: New Diagnostic Criteria, Biomarkers, and Therapeutic Approaches
Lancet Neurol 16:552-563, Boxer, A.L.,et al, 2017

Acute Plasma Tau relates to Prolonged return to play after concussion
Neurol 88:595-602, Gill, J.,et al, 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

Clinical Manifestations of the anti-IgLON5 Disease
Neurol 88:1736-1743,1688, Gaig, C.,et al, 2017

A 64-year-old Man with Visual Distortions
Neurol 87:e252-e256, McGrath, E.R.,et al, 2016

A Young Man with Progressive Language Difficulty and Early-Onset Dementia
JAMA Neurol 73:595-599, Botha, H.,et al, 2016

Clinicopathologic Conference, Frontotemporal Lobar Degeneration with Tau-positive Inclusions (Picks Disease Subtype) Due to a Gly389Arg MAPT Mutation, Resulting in the Behavioral Variant of Frontotemporal Dementia with Parkinsonism
NEJM 372:1151-1162, Miller, B.L.,et al, 2015

A 56-year-old Man with Cognitive Impairment and Difficulty Tying his Necktie
Neurol 85:e116-e122, Baker, J.M.,et al, 2015

Degenerative Diseases of the Nervous System, Alzheimer Disease
Adams & Victors Principles of Neurology, Chp 39, pg 1063, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Behavioral Variant FTLD
Adams & Victors Principles of Neurology, Chp 39, pg 1074, Ropper, A.H.,et al, 2014

Blood Biomarkers for Brain Injury in Concussed Professional Ice Hockey Players
JAMA Neurol 71:684-692,677, Shahim, P.,et al, 2014

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

Incidence and Pathology of Synucleinopathies and Tauopathies Related to Parkinsonism
JAMA Neurol 70:859-866, Savica, R.,et al, 2013

Clinical Presentation of Chronic Traumatic Encephalopathy
Neurol 81:1122-1129, Stern, R.A.,et al, 2013

A Comparison of Tau and 14-3-3 Protein in the Diagosis of Creutzfeldt-Jakob Disease
Neurol 79:547-552, Hamlin, C.,et al, 2012

Serial MRI and CSF Biomarkers in Normal Aging, MCI, and AD
Neurol 75:143-151, Vemuri,P., et al, 2010

Traumatic Brain Injury - Football, Warfare, and Long-Term Effects
NEJM 363:1293-1296, DeKosky,S.T.,et al, 2010

Alzheimers Disease
NEJM 362:329-344, Querfurth,H.W. &LaFerla,F.M., 2010

Combining MR Imaging, Positron-Emission Tomography, and CSF Biomarkers in the Diagnosis and Prognosis of Alzheimers Disease
AJNR 31:347-354, Walhovd, K.B.,et al, 2010

A 75-Year-Old Woman with Progressive Right-Hand Tremor and Inability to Use Her Right Side
Neurol 73:1399-1405, Kertesz,A.,et al, 2009

Rapidly Progressive Neurodegenerative Dementias
Arch Neurol 66:201-207, Josephs,K.A.,et al, 2009

Age, Neuropathology, and Dementia
NEJM 360:2302-2309, Savva,G.M.,et al, 2009

Chronic Traumatic Encephalopathy in Athletes: Progressive Tauopathy following Repetitive Head Injury
J Neuropathol Exp Neurol 68:709-735, McKee, A.C.,et al, 2009

Tau Forms in CSF as a Reliable Biomarker for Progressive Supranuclear Palsy
Neurol 71:1796-1803, Borroni,B.,et al, 2008

Progressive Supranuclear Palsy: A Current Review
The Neurologist 14:79-88, Lubarsky,M. &Juncos,J.L., 2008

PET of Brain Amyloid and Tau in Mild Cognitive Impairment
NEJM 355:2652-2663, Small,G.W.,et al, 2006

Multiple Diagnostic Tests Are Needed to Assess Multiple Causes of Dementia
Arch Neurol 63:144-146,146, Rikkert,M.G.M.O.,et al, 2006

Neuropathologic Features of Amnestic Mild Cognitive Impairment
Arch Neurol 63:665-672,645, Petersen,R.C.,et al, 2006

Frontotemporal Dementia: Clinicopathological Correlations
Ann Neurol 59:952-962, Forman,M.S.,et al, 2006

Frontotemporal Lobar Degeneration with Motor Neuron Disease
Arch Neurol 63:489-490, Clark,C.M. &Forman,M.S., 2006

CSF Tests in the Differential Diagnosis of Cretuzfeldt-Jakob Disease
Neurol 67:637-643, Sanchez-Juan,P.,et al, 2006

A-beta Vaccination Effects on Plaque Pathology in the Absence of Encephalitis in Alzheimer Disease
Neurol 64:129-131,10, Masliah,E.,et al, 2005

A 10-Item Smell Identification Scale Related to Risk for Alzheimers Disease
Ann Neurol 58:155-160, Taberr,M.H.,et al, 2005

Tau Protein and 14-3-3 Protein in the Differential Diagnosis of Creutzfeldt-Jakob Disease
Neurol 58:192-197, Otto,M.,et al, 2002

Alzheimer Disease
JAMA 287:2335-2338, Cummings,J.L. &Cole,G., 2002

Use of 14-3-3 and Other Brain-specific Proteins in CSF in the Diagnosis of Variant Creutzfeldt-Jakob Disease
JNNP 70:744-748, Green,A.J.E.,et al, 2001

Evaluation of CSf-tau and CSF-AB42 as Diagnostic Markers for Alzheimer Disease in Clinical Practice
Arch Neurol 58:373-379,349, Andreasen,N.,et al, 2001

Clinicopath Conf:Multisystem Neurodegenerative Disease with Dementia Pugilistica
NEJM 340:1269-1277, Case 12-1999, 1999

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

Clinicopath Conf
Subacute Sclerosing Panencephalitis, Case 15-1998, NEJM 338:1448-1456998., , 1998

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



Showing articles 0 to 50 of 992 Next >>