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abscess, intracerebral
acquired immunodeficiency syndrome
adenine arabinoside
advances in neurology
adverse drug reaction
affect, flat
aggression
agitation
agnosia
agnosia, visual
akinetic mute
albumin transfusion
alexia
algorithm
Alice in Wonderland syndrome
alien hand syndrome
alternating rapid movement, impaired
Alzheimer's disease
Alzheimer's disease, familial
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Alzheimer's disease, rate of clinical decline
Alzheimer's disease, visual variant
amantadine
ammonia
AMPA receptor antibodies
amyloid angiopathy, cerebral
amyloid plaques
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, childhood
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, guamian type of
amyotrophic lateral sclerosis, Parkinson-dementia-complex
amyotrophic lateral sclerosis, post-encephalitic
anatomy of
aneuploidy
angiitis, isolated of CNS
animal exposure
anomic aphasia
anorexia
anticonvulsants
anticonvulsants, untoward effects of
antithyroid antibodies
antiviral agents
anxiety
aphasia
aphasia, progressive
aphasia, transcortical
aphasia, transcortical-sensory
apolipoprotein E
apraxia
apraxia, dressing
arm weakness
asterixis
asymptomatic
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ataxia, cerebellar
ataxia, progressive
ataxia, truncal
ataxic gait
atypical
autoantibodies
autoimmune disease
autonomic dysfunction
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bacterial infection
Balint's syndrome
basal ganglia
basal ganglia, lesion of
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basilar artery occlusion
bedridden
behavioral disorder
Behcet's syndrome
biologic markers
blindness
blood transfusion
bovine spongiform encephalopathy
bradykinesia
bradyphrenia
brain biopsy
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brain biopsy, negative
brain scan
carbamazepine
carbamazepine, toxicity
carbon monoxide poisoning
carcinoma
carcinoma of breast
cardiac transplantation
CAT scan
CAT scan, abnormal
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CAT scan, emission, abnormal
CAT scan, false negative
caudate nucleus, lesion of
caudate nucleus, lesion of, bilateral
cell fusion test
central nervous system, infection of
central pontine myelinolysis
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar lesion
cerebellum, disease of
cerebral cortex
cerebral cortical atrophy
cerebral glucose metabolism
cerebral infarction
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cerebral venous thrombosis
cerebral venous thrombosis, deep
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, cell count
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, enzymes in
cerebrospinal fluid, oligoclonal IgG in
cerebrospinal fluid, protein of
cerebrovascular accident
cerebrovascular accident, mimics
cerebrovascular accident, misdiagnosis
Charles Bonnet's syndrome
children
chorea
choreoathetosis
chromosomal abnormality
chromosome 20
cingulate gyrus
Clinical Pathologic Conference(C.P.C.)
cognition
cognition, slowed
cogwheel rigidty
color vision, impaired
coma
comorbidities
complications
concentration, impaired
confusion
contactin associated protein like 2 antibodies
controversies in neurology
corneal transplant
cortical blindness
cortical infarction
cortical-basal ganglionic degeneration
Creutzfeldt-Jakob disease, genetic
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
delirium
delusion
dementia
dementia, childhood
dementia, diagnostic evaluation of
dementia, differential diagnosis of
dementia, familial
dementia, frontotemporal
dementia, presenile
dementia, prevention of
dementia, rapidly progressive
dementia, reversible
dementia, screening for
dementia, transmissible
dementia, treatment of
demyelinating disease
denial of blindness(Antons syndrome)
depression
diabetes mellitus
diagnostic criteria
diet
differential diagnosis
difficulty climbing stairs
diplopia
disorientation
dissociated sensory loss
dizziness
driving
drug induced neurologic disorders
drug withdrawal
dural graft, cadaveric
dysarthria
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dysmetria
dysphagia
dystonia
echolalia
efficacy
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electroencephalogram, abnormalities of
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electroencephalogram, depth electrode
electroencephalogram, focal delta activity
electroencephalogram, periodic complexes
electroencephalogram, triphasic delta waves
electromyogram
electron microscopy
electrophoretic pattern, CSF
electrophoretic pattern, serum
emotional lability
encephalitis
encephalitis, autoimmune
encephalitis, bornavirus
encephalitis, Japanese
encephalitis, paraneoplastic
encephalitis, viral
encephalomyelitis, postinfectious
encephalopathy
encephalopathy, carcinomatous
encephalopathy, Hashimoto's
encephalopathy, metabolic
endemic area
endoscopy
enolase
epidemic
epidemiology of neurology
epilepsia partialis continua
episodic disorders
experimental allergic encephalitis
extrapyramidal
eye movement, disorders of
Fabry's disease
faciobrachial dystonic seizure
Fahr disease
falling
false negative
false positive
familial
farmer
fasciculation
fatal familial insomnia
fatigue
fever
fibrillations
finger nose finger test
Fisher C.M.
flavivirus
flu-like illness
follicle stimulating hormone
frontal lobe, anatomy and physiology
frontal lobe, pathologic signs of
gait disorder
gait, apraxic
gamma amino butyric acid receptor antibody
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
genetic counselling
genetic linkage
genetic neurologic disorders
genetic testing
Gerstmann syndrome
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gliosis
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grandiosity
grasp reflex
grasping
gray matter
growth hormone
gyrus, abnormal
Hallervorden Spatz disease
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hallucination, visual
hallucination, visual, benign
hand weakness
handwriting
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headache
headache, episodic
heel-knee-shin test
hemianopia, homonymous
hemiparesis
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heralding manifestation
herpes simplex encephalitis
herpes simplex virus
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homograft
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human immunodeficiency virus type 1
Huntington's chorea
hydrocephalus
hydrocephalus, normal pressure
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insular cortex
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interobserver agreement
intracerebral hemorrhage
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
Jakob-Creutzfeldt disease, conjugal
Jakob-Creutzfeldt disease, Heidenhain variant
Jakob-Creutzfeldt disease, medical precaution with
Jakob-Creutzfeldt disease, unilateral
Jakob-Creutzfeldt disease, variant
Jakob-Creutzfeldt disease, young adult
jocularity
kuru
kuru plaques
laminar necrosis, cortical
laughing, pathologic
lead poisoning
Leigh's disease
leucine rich glioma inactivated 1 antibodies
leukoencephalitis, acute necrotizing hemorrhagic
Lewy body disease, diffuse
life expectancy
limbic encephalitis
linear lesion
lipid storage disorder of CNS
lithium
liver disease
liver transplantation
lobar atrophy
lymphoma
lymphoma involving CNS
lymphoma, primary of CNS
lysosomes, abnoral
macropsia
malignancy screen
mania
masked facies
memory, defect of recent
memory, impairment of
meningitis
meningoencephalitis
mental status, abnormal
metamorphopsia
micrographia
micropsia
migraine
mimics
Mini Mental Status Examination
misdiagnosis
mitochondrial disease
molecular genetics
mongolism
monoparesis
mortality
Morvan's fibrillary chorea
motor cortex
motor neuron disease
movement disorder
movement disorder, drug induced
movement disorder, extrapyramidal
MRI
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MRI, ADC maps
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MRI, indications for
MRI, lesion burden
MRI, negative
MRI, proton density
MRI, punctate pattern
MRI, serial
MRI, spinal cord
MRI, susceptibility weighted
MRI, T1 weighted high signal foci
multiple sclerosis
multiple system atrophy
muscle twitching
mutism
myelin
myelitis
myelitis, longitudinal
myelitis, transverse
myelopathy
myoclonic jerks
myoclonus
myoclonus, action
myoclonus, cortical
myoclonus, differential diagnosis of
myoclonus, stimulus sensitive
nasal brushings
negative
neoplasm, intracranial
neoplasm, metastatic to CNS
neoplasm, pituitary
neoplasm, primary intracerebral
neoplasm, primary of CNS
nerve conduction studies
neurofibrillary degeneration
neurofibromatosis 1
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neurologic disease
neurologic disease, diagnoses of
neurologic examination, focal
neurologic signs
neurologic testing
neuron specific enolase
neuronal cell surface antigen
neuronal ceroid-lipofuscinosis
neuropathology
neuropathology, brain
neuropathy
neurotoxic
neurotoxin
Niemann-Pick disease
NMDA antagonists
normal
nortriptyline
nucleus basalis of Meynert
nystagmus
nystagmus, periodic alternating
occipital cortex
occipital lobe
occipital lobe, lesion of
occupational neurologic disorders
ocular motility, disorders of
old age, neurology of
olfactory biopsy
olfactory bulb
olfactory cortex
olfactory mucosa
olfactory pathway
olfactory tract
organ donor
organ transplantation
osmotic demyelination syndrome
pain
pain, leg
paranoia
parietal lobe, lesion of
parietal lobe, syndromes of
Parkinson disease
Parkinson disease, motor neuron disease with
Parkinson disease, postencephalitic
Parkinsonism plus syndrome
Parkinsonism syndrome
PAS positive
PAS positive material in the brain
pathognomonic
pathologic reflex
peduncular hallucinosis
perseveration
personality change
pituitary, hormones of
PLEDs
PLEDs, bilateral independent
pleocytosis of cerebrospinal fluid
polymerase chain reaction
polyneuropathy
polyneuropathy, chronic inflammatory demyelinating
polysomnogram
pons, lesion of
posterior cortical atrophy
posterior leukoencephalopathy syndrome
postictal encephalopathy
potassium channel antibodies
practice guidelines
preclinical
pregnancy, neurologic complications in
prevention of neurologic disorders
prion disease
prognosis
progressive infantile poliodystrophy
progressive multifocal leucoencephalopathy
progressive neurologic disorder
proprioception
prosopagnosia
protein 14-3-3, cerebrospinal fluid
protein 14-3-3, cerebrospinal fluid, false negative
protein 14-3-3, cerebrospinal fluid, false positive
pruritus
psychiatric disorder
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis
psychotic behavior
pulvinar sign
pursuit eye movements, abnormal
putamen, lesion of
putamen, lesion of, bilateral
pyramidal tract
pyramidal tract dysfunction
rapidly fatal neurologic illness
rapidly progressing neurologic illness
real-time quaking-induced conversion
release phenomena
remote effect of cancer on the nervous system
reversible cerebral vasoconstrictive syndromes
reversible neurologic disorder
review article
rigidity
risk factors
risk-benefit assessment
Romberg's sign
rooting reflex
saccadic eye movements, abnormal
sarcoidosis, CNS
scrapie
screening
seizure
seizure, focal
seizure, nonconvulsive
senile plaques
sensory symptoms
serum S100 protein
simultanagnosia
single photon emission computed tomography
skin, biopsy
sleep
sleep pathology and physiology
slow virus infection of CNS
smell
snout reflex
somnolence
speech, pressured
spinal cord
spinal cord, lesion of
spongy degeneration of brain
square wave jerks
startle myoclonus
startle reaction
status epilepticus
status epilepticus, nonconvulsive
steroid
steroid therapy, CNS treatment and complications with
striatum, lesion of
striatum, lesion of, bilateral
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
symmetric brain lesions
tandem gait, ataxic
taste
tau protein
tauopathy
temporal lobe, status
thalamic tumors
thalamic tumors, bilateral
thalamus
thalamus, infarction of
thalamus, infarction, bilateral
thalamus, lesion of
thalamus, lesion of-bilateral
thyroiditis
tonsil biopsy
toxic encephalopathy
trauma
treatment of neurologic disorder
tremor
tremor, intention
tuberous sclerosis
twitching, face
upgaze, paralysis of
urinary incontinence
vasculitides
vertigo
vertigo, episodic
vibratory sensation
viral infection
viral infection, CNS
virus, slow
vision, blurred
visual acuity, decreased
visual cortex
visual distortions
visual field defect
visual impairment
visual loss
visual loss, progressive
walking frame
walking, difficulty with
Wallerian degeneration
weakness, acute
weakness, focal
weight loss
Wernicke's aphasia
Wernicke's encephalopathy
West Nile fever
Western immunoblot test
wheelchair
white matter disease
wide based gait
workup
Showing articles 0 to 50 of 290 Next >>

Clinicopathologic Conference, Genetic Creutzfeldt-Jakob Disease
NEJM 386;674-687, Case 5-2022, 2022

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

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

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

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

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

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

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

A 57-Year-Old Woman with Progressive Ataxia and Falls
Neurol 95:650-656, Badahdah, A., 2020

Bornavirus Encephalitis Shows a Characteristic Magnetic Resonance Phenotype in Humans
Ann Neurol 88:723-735, Finck, T.,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

Variant Creutzfeldt-Jakob Disease Diagnosed 7.5 Years after Occupational Exposure
NEJM 383:83-85, Brandel, J.P.,et al, 2020

An Atypical Presentation of Creutzfeldt-Jakob Disease with a Heidenhain Variant and Balints Syndrome
Cureus DOI:10.7759/cureus,8608, Gupta,A. & Dhingra,A., 2020

RT-QuIC: A New Test for Sporadic CJD
Pract Neurol 19:49-55, Green, A.J.E., 2019

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

Cerebellar Ataxia and Hearing Impairment
JAMA Neurol 74:243-244, Lin, C.Y. & Kuo, S.H., 2017

Diagnosis of Human Prion Disease Using Real-Time Quaking-Induced Conversion Testing of Olfactory Mucosa and Cerebrospinal Fluid Samples
JAMA Neurol 74:155-162,144, Bongianni, M.,et al, 2017

Precipitous Deterioration of Motor Function, Cognition, and Behavior
JAMA Neurol 74:591-596, Fernandez-Fournier, M.,et al, 2017

Creutzfeldt-Jakob Disease and Hashimotos Thyroiditis: A Case Report Illustrating Prion-Induced Encephalitis
J Neuroinfect D 7:1-6, Dabul, L.,et al, 2016

Distinguishing Neuroimaging Features in Patients Presenting with Visual Hallucinations
AJNR 37:774-781, Winton-Brown, T.T.,et al, 2016

Cerebrospinal Fluid Real-Time Quaking-Induced Conversion is a Robust and Reliable Test for Sporadic Creutzfeldt-Jakob Disease: An International Study
Ann Neurol 80:160-165, McGuire, L.I.,et al, 2016

Diffusion-Weighted MRI Abnormalities Antedate the Onset of Sporadic Creutzfeldt-Jakob Disease
Neurol 87:843, Suzuki, K.,et al, 2016

Long-Term Preclinical Magnetic Resonance Imaging Alterations in Sporadic Creutzfeldt-Jakob Disease
Ann Neurol 80:629-632, Zanusso, G.,et al, 2016

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

Rapid and Sensitive RT-QuIC Detection of Human Creutzfeldt-Jakob Disease Using Cerebrospinal Fluid
mBio 6:e02451-14, Orru,C.D.,et al, 2015

Unilateral Cortical Hyperintensity in Diffusion-Weighted MRI;New Criteria for Early Sporadic Creutzfeldt-Jakob Disease
Iran J Neurol 14:108-109, Tabrizi,N.,&Abedini,M, 2015

Limbic Encephalitis Associated with Anti-Voltage-Gated Potassium Channel Complex Antibodies Mimicking Creutzfeldt-Jakob Disease
JAMA Neurol 71:79-82, Yoo,J.Y. & Hirsch, L.J., 2014

A Test for Creutzfeldt-Jakob Disease Using Nasal Brushings
NEJM 371:519-529, Orru, C.D.,et al, 2014

Serial Magnetic Resonance Imaging Changes in Sporadic Creutzfeldt-Jakob Disease with Valine Homozygosity at Codon 129 of the Prion Protein Gene
JAMA Neurol 71:1186-1187, Furukawa, F.,et al, 2014

Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Creutzfeldt-Jakob Disease (Subacute Spongiform Encephalopathy)
Adams & Victors Principles of Neurology, Chp 33, pg 769, Ropper, A.H.,et al, 2014

A Creutzfeldt-Jakob Disease Case Presenting with Psychiatric Symptoms
JNBS doi:10.5455/JNBS.1386249156, Aslan,A.A.,et al, 2014

Sporadic Creutzfeldt-Jakob Disease with Focal Findings: Caveats to Current Diagnostic Criteria
Neurol Internat 5:1-5, Mader, E.C.,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

Evidence-based Guideline: Diagnostic accuracy of CSF 14-3-3 Protein in Sporadic Creutzfeldt-Jakob Disease
Neurol 79:1499-1506, Muayqil, T.,et al, 2012

Differential Diagnosis of Jakob-Creutzfeldt Disease
Arch Neurol 69:1578-1582,1554, Paterson, R.,et al, 2012

Cerebral White Matter Disruption in Creutzfeldt-Jakob Disease
AJNR 33:1945-1950, Lee,H.,et al, 2012

Rapidly Progressive Corticobasal Degeneration Syndrome
Case Rep Neurol 3:185-190, Herrero Valverde, A.,et al, 2011

The Evaluation of Rapidly Progressive Dementia
The Neurologist 17:67-74, Rosenbloom,M.H. &Atri,A., 2011

Cortical Restricted Diffusion as the Predominant MRI Finding in Sporadic Creutzfeldt-Jakob Disease
Acta Radiologica 52:336-339, Talbott,S.D.,et al, 2011

Differential Diagnosis of Bilateral Abnormalities of the Basal Ganglia and Thalamus
RadioGraphics 31:5-30, Hegde,A.N.,et al, 2011

Diffusion-weighted MRI hyperintensity patterns differentiate CJD from other rapid dementias
Neurol 76:1711-1719, Vitali, P.,et al, 2011

Diagnosing variant Creutzfeldt-Jakob disease: a retrospective analysis of the first 150 cases in the UK
JNNP 82:646-651, Heath, C.A.,et al, 2011

Encephalitis and antibodies to synaptic and neuronal cell surface proteins
Neurol 77:179-189, Lancaster, E.,et al, 2011

Rapidly Progressive Alzheimer Disease
Arch Neurol 68:1124-1130, Schmidt, C.,et al, 2011

Treatable Neurological Disorders Misdiagnosed as Creutzfeldt-Jakob Disease
Ann Neurol 70:437-444, Chitravas, N.,et al, 2011

Open Biopsy in Patients With Acute Progressive Neurologic Decline and Absence of Mass Lesion
Neurol 75:419-424, Schuette,A.J., et al, 2010

Sporadic Creutzfeldt-Jakob Disease Mimicking Nonconvulsive Status Epilepticus
Neurol 74:1995-1999, Lapergue,B., et al, 2010

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

Pathologic Correlates of Diffusion MRI Changes in Creutzfeldt-Jakob Disease
Neurol 72:1425-1431, Manners,D.N.,et al, 2009



Showing articles 0 to 50 of 290 Next >>