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advances in neurology
agnosia
agnosia, visual
akinetic mute
alexia
algorithm
alternating rapid movement, impaired
Alzheimer's disease
Alzheimer's disease, rapidly progressive
Alzheimer's disease, rate of clinical decline
Alzheimer's disease, visual variant
AMPA receptor antibodies
amyloid angiopathy, cerebral
amyloid plaques
amyotrophic lateral sclerosis
angiitis, isolated of CNS
animal exposure
anorexia
anxiety
aphasia, transcortical
aphasia, transcortical-sensory
asymptomatic
ataxia
ataxia, cerebellar
ataxia, progressive
ataxia, truncal
ataxic gait
atypical
autoantibodies
autoimmune disease
axonal degeneration
Balint's syndrome
basal ganglia
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavioral disorder
biologic markers
blood transfusion
bovine spongiform encephalopathy
brain biopsy
brain biopsy, complications of
brain biopsy, indication
brain biopsy, negative
carcinoma
CAT scan, abnormal
CAT scan, emission, abnormal
caudate nucleus, lesion of
caudate nucleus, lesion of, bilateral
central nervous system, infection of
cerebellar lesion
cerebellum, disease of
cerebral cortex
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, enzymes in
cerebrospinal fluid, protein of
cerebrovascular accident, mimics
cerebrovascular accident, misdiagnosis
Charles Bonnet's syndrome
children
choreoathetosis
chromosome 20
cingulate gyrus
Clinical Pathologic Conference(C.P.C.)
cognition, slowed
comorbidities
complications
concentration, impaired
confusion
contactin associated protein like 2 antibodies
controversies in neurology
cortical blindness
Creutzfeldt-Jakob disease, genetic
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
delirium
delusion
dementia
dementia, diagnostic evaluation of
dementia, familial
dementia, frontotemporal
dementia, prevention of
dementia, rapidly progressive
dementia, reversible
dementia, screening for
dementia, transmissible
dementia, treatment of
denial of blindness(Antons syndrome)
depression
diabetes mellitus
diagnostic criteria
diet
differential diagnosis
difficulty climbing stairs
diplopia
dizziness
drug withdrawal
dural graft, cadaveric
dysarthria
dysdiadochokinesia
dysmetria
efficacy
electroencephalogram
electroencephalogram, abnormalities of
electroencephalogram, periodic complexes
electron microscopy
electrophoretic pattern, CSF
electrophoretic pattern, serum
encephalitis
encephalitis, autoimmune
encephalitis, paraneoplastic
encephalitis, viral
encephalopathy
encephalopathy, Hashimoto's
encephalopathy, metabolic
endoscopy
enolase
epidemic
epidemiology of neurology
epilepsia partialis continua
episodic disorders
executive dysfunction
eye movement, disorders of
falling
false negative
false positive
familial
farmer
fatal familial insomnia
finger nose finger test
frontal lobe, anatomy and physiology
gait disorder
gait, apraxic
gamma amino butyric acid receptor antibody
gene mutation
genetic counselling
genetic neurologic disorders
genetic testing
Gerstmann syndrome
Gerstmann-Straussler-Scheinker disease
gliosis
glycine receptor antibodies
grasp reflex
growth hormone
hallucination
hallucination, visual
hallucination, visual, benign
handwriting
headache
headache, episodic
heel-knee-shin test
hemianopia, homonymous
hemiparesis
heralding manifestation
hockey stick sign
Huntington's chorea
hyperosmia
hypogeusia
hypophonia
iatrogenic neurologic disorders
imbalance
immunocompetent
immunodeficiency
immunohistochemistry
immunologic disease
immunosuppressive agents
incidence
incoordination
incubation period
insomnia
insular cortex
intellectual deterioration
irritability
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
Jakob-Creutzfeldt disease, Heidenhain variant
Jakob-Creutzfeldt disease, medical precaution with
Jakob-Creutzfeldt disease, variant
Jakob-Creutzfeldt disease, young adult
kuru
kuru plaques
leg numbness
leucine rich glioma inactivated 1 antibodies
Lewy body disease, diffuse
life expectancy
limbic encephalitis
lobar atrophy
lymphoma
lymphoma involving CNS
lymphoma, primary of CNS
malignancy screen
memory, defect of recent
memory, impairment of
mental status, abnormal
migraine
mimics
Mini Mental Status Examination
misdiagnosis
molecular genetics
monoparesis
mortality
Morvan's fibrillary chorea
movement disorder
MRI
MRI pattern
MRI, abnormal
MRI, ADC maps
MRI, diffusion weighted
MRI, diffusion weighted, pattern
MRI, false negative
MRI, false positive
MRI, FLAIR
MRI, functional
MRI, high signal foci on
MRI, high signal intensity of basal ganglia
MRI, indications for
MRI, negative
MRI, proton density
MRI, punctate pattern
MRI, serial
multiple sclerosis
multiple system atrophy
mutism
myoclonic jerks
myoclonus
nasal brushings
negative
neoplasm, primary of CNS
neurologic complications of, surgery
neurologic disease
neurologic disease, diagnoses of
neurologic examination, focal
neurologic signs
neurologic testing
neuron specific enolase
neuronal cell surface antigen
neuropathology
neuropathology, brain
neuropathy
NMDA antagonists
normal
nystagmus
occipital cortex
occipital lobe
occipital lobe, lesion of
occupational neurologic disorders
old age, neurology of
olfactory biopsy
olfactory bulb
olfactory cortex
olfactory mucosa
olfactory pathway
olfactory tract
pain
pain, leg
palmomental response
Parkinson disease
Parkinsonism plus syndrome
Parkinsonism syndrome
pathognomonic
pathologic reflex
peduncular hallucinosis
personality change
pituitary, hormones of
posterior cortical atrophy
posterior leukoencephalopathy syndrome
potassium channel antibodies
practice guidelines
preclinical
prevention of neurologic disorders
prion disease
prognosis
progressive neurologic disorder
protein 14-3-3, cerebrospinal fluid
protein 14-3-3, cerebrospinal fluid, false negative
protein 14-3-3, cerebrospinal fluid, false positive
psychiatric disorder
psychiatric problems in neurologic disorders
psychosis
pulvinar sign
pursuit eye movements, abnormal
putamen, lesion of
putamen, lesion of, bilateral
rapidly progressing neurologic illness
real-time quaking-induced conversion
release phenomena
remote effect of cancer on the nervous system
reversible cerebral vasoconstrictive syndromes
review article
risk factors
risk-benefit assessment
Romberg's sign
rooting reflex
saccadic eye movements, abnormal
sarcoidosis, CNS
scrapie
screening
seizure
senile plaques
sensory symptoms
serum S100 protein
simultanagnosia
single photon emission computed tomography
skin, biopsy
smell
snout reflex
spongy degeneration of brain
square wave jerks
startle myoclonus
startle reaction
stiff legs
striatum, lesion of
striatum, lesion of, bilateral
symmetric brain lesions
tandem gait, ataxic
taste
tau protein
tauopathy
thalamus, lesion of
thalamus, lesion of-bilateral
thyroiditis
tone, muscle
tonsil biopsy
toxic encephalopathy
treatment of neurologic disorder
tremor, intention
vasculitides
vertigo
vertigo, episodic
viral infection, CNS
vision, blurred
visual cortex
visual impairment
visual loss
visual loss, progressive
walking frame
walking, difficulty with
weight loss
West Nile fever
Western immunoblot test
wheelchair
wide based gait
workup
Showing articles 100 to 150 of 1974 << Previous Next >>

A New Variant of Creutzfeldt-Jakob Disease in the UK
Lancet 347:921-925, 915, 916, 91796., Will,R.G.,et al, 1996

Creutzfeldt-Jakob Disease and Bovine Spongiform Encephalopathy:Any Connection?
BMJ 311:1415-1421, Almond,J.W., 1995

Cerebrospinal Fluid Concentration of Neuron-specific Enolase in Diagnosis of Creutzfeldt-Jakob Disease
Lancet 345:1609-1610, Zerr,I.,et al, 1995

Posterior Cortical Atrophy:Neuropathologic Correlations
Arch Neurol 51:269-274, Victoroff,J.,et al, 1994

Human Prion Diseases
Ann Neurol 35:385-395, Prusiner,S.B.&Hsiao,K.K., 1994

The Spongiform Encephalopathies, Editorial
JNNP 54:761-763, Will,R.G., 1991

Ataxic Creutzfeldt-Jakob Disease:Diagnostic Techniques & Neuropathologic Observations in Early Disease
Neurol 35:254-257, Jones,H.R.,et al, 1985

Clin. Path. Conference
Creutzfeldt-Jakob Disease, Ataxic Type, with Kuru Plaques, Case Record 45-1980, NEJM 303:1162-11710., , 1980

Creutzfeldt-Jakob Disease in a 20-year-old Woman
Neurol 30:492-496, Packer,R.J.,et al, 1980

Punctate Diffuse Cortex Signals in Creutzfeldt-Jakob Disease
JAMA Neurol 81:291-292, Chen,Z.,et al, 2024

Roving Eye and Head in a Patient with Genetic Creutzfeldt-Jakob Disease
Neurol 102:e209385, Nishida,K.,, 2024

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Bilateral Thalamic Lesions
AJR 192:W53-W62, Smith,A.B.,et al, 2009

MRI Lesion Profiles in Sporadic Creutzfeldt-Jakob Disease
Neurol 72:1994-2001, Meissner,B.,et al, 2009

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

Isolated Cortical Signal Increase on MR Imaging as a Frequent Lesion Pattern in Sporadic Creutzfeldt-Jakob Disease
AJNR 29:1519-1524, Meissner,B.,et al., 2008

Sporadic Creutzfeldt-Jakob Disease in Two Adolescents
JNNP 79:14-18, Murray,K.,et al, 2008

Transmissible Spongiform Encephalopathy in the 21st Century: Neuroscience for the Clinical Neurologist
Neurol 70:713-722, Brown,P., 2008

Voltage-Gated Potassium Channel Autoimmunity Mimicking Creutzfeldt-Jakob Disease
Arch Neurol 65:1341-1346, Geschwind,M.D.,et al, 2008

Differential Diagnosis of Restricted Diffusion Confined to the Cerebral Cortex
Clin Radiol 63:1245-1253, Sheerin,F.,et al, 2008

CSF Analysis in Patients With Sporadic CJD and Other Transmissible Spongiform Encephalopathies
Eur J Neurol 14:121-124, Green,A.,et al, 2007

Pyramidal Tract Degeneration in Sporadic Creutzfeldt-Jakob Disease
Neuropathology 27:434-441, Iwasaki,Y.,et al, 2007

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

First Symptom in Sporadic Creutzfeldt-Jakob Disease
Neurol 66:286-287, Rabinovici,G.D.,et al, 2006

Onset of Creutzfeldt-Jakob Disease Mimicking an Acute Cerebrovascular Event
Neurol 67:538-539, Hohler,A.D. &Flynn,F.G., 2006

Iatrogenic Creutzfeldt-Jakob Disease: The Waning of an Era
Neurol 67:389-393, Brown,P.,et al, 2006

Sleep-wake Disturbances in Sporadic Creutzfeldt-Jakob Disease
Neurol 66:1418-1424, Landolt,H.-P.,et al, 2006

Creutzfeldt-Jakob Disease Mimicking Radiologic Posterior Reversible Leukoencephalopathy
Neurol 65:329, Sibon,I.,et al, 2005

Carbamazepine Encephalopathy Masquerading as Creutzfeldt-Jakob Disease
Neurol 65:650-651, Horvath,J.,et al, 2005



Showing articles 100 to 150 of 1974 << Previous Next >>