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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
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
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
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
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
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
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
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
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 50 to 100 of 1913 << Previous Next >>

Balint Syndrome Due to Creutzfeldt-Jakob Disease
Neurol 63:395, Ances,B.M.,et al, 2004

Diagnosing Variant Creutzfeldt-Jakob Disease with the Pulvinar Sign:"MR Imaging Findings in 86 Neuropathologically Confirmed Cases
AJNR 24:1560-1569, Collie,D.A.,et al, 2003

Detection of Pathologic Prion Protein in the Olfactory Epithelium in Sporadic Creutzfeldt-Jakob Disease
NEJM 348:711-719,681, Zanusso,G.,et al, 2003

Challenging the Clinical Utility of the 14-3-3 Protein for the Diagnosis of Sporadic Creutzfeldt-Jakob Disease
Arch Neurol 60:813-816,803, Geschwind,M.D.,et al, 2003

Conspicuity and Evolution of Lesions in Creutzfeldt-Jakob Disease at Diffusion-Weighted Imaging
AJNR 23:1164-1172,1070, Murata,T.,et al, 2002

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

Neurodegenerative Diseases and Prions
NEJM 344:1516-1526,1548, Prusiner,S.B., 2001

CSF Detection of the 14-3-3 Protein in Unselected Patients with Dementia
Neurol 56:1528-1533, Burkhard,P.R.,et al, 2001

Bovine Spongiform Encephalopathy and Variant Creutzfeldt-Jakob Disease
BMJ 322:841-844, Brown,P., 2001

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

New Variant Creutzfeldt-Jakob Disease Presenting with Loss of Taste and Smell
JNNP 71:412-413, Reuber,M.&Al-Din,A.S.N., 2001

Quantitation of 14-3-3 and Neurol-Specific Enolase Proteins in CSF in Creutzfeldt-Jakob Disease
Neurol 57:728-730, Aksamit,A.L.,et al, 2001

The Pulvinar Sign on Magnetic Resonance Imaging in Variant Creutzfeldt-Jakob Disease
Lancet 355:1412-1418,1384, Zeidler,M.,et al, 2000

Diagnosis of New Variant Creutzfeldt-Jakob Disease
Ann Neurol 47:575-582, Will,R.G.,et al, 2000

14-3-3 Testing in Diagnosing Creutzfeldt-Jakob Disease
Neurol 55:514-516, Lemstra,A.W. et al, 2000

Current Clinical Diagnosis in Creutzfeldt-Jakob Disease; Identification of Uncommon Variants
Ann Neurol 48:323-329, Zerr,I. et al, 2000

Analysis of EEG and CSF 14-3-3 proteins as adis to the diagnosis of Creutzfeldt-Jakob Disease
Neurol 55:811-815, Zerr,I. et al, 2000

Dementia with Lewy Bodies in a Neuropathologic Series of Suspected Creutzfeldt-Jakob Disease
Neurol 55:1401-1404, Haik,S.,et al, 2000

Variant Creutzfeldt-Jakob Disease in UK children: A National Surveillance Study
Lancet 356: 1224-1227, Verity,C.M.,et al, 2000

Risk of Transmission of Bovine Spongiform Encephalopathy to Humans in the United States, Report of the Council on Scientific Affairs
JAMA 281:2330-2339, Tan,L.,et al, 1999

Variant Creutzfeldt-Jakob Disease
Lancet 354:317-323, Collinge,J., 1999

Clinicopath Conf, Creutzfeldt-Jakob Disease,Case 28-1999
NEJM 341:901-908, , 1999

The Heidenhain Variant of Creutzfeldt-Jakob Disease
Arch Neurol 56:55-61, Kropp,S.,et al, 1999

Diffusion-Weighted MRI in Sporadic Creutzfeldt-Jakob Disease
Neurol 52:205-208, Demaerel,P.,et al, 1999

Investigation of Variant Creutzfeldt-Jakob Disease and Other Human Prion Diseases with Tonsil Biopsy Samples
Lancet 353:183-189,163, Hill,A.F.,et al, 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

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

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

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

New Variant Creutzfeldt-Jakob Disease:Neurological Features and Diagnostic Tests
Lancet 350:903-907, Zeidler,M.,et al, 1997

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

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

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

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

The 14-3-3 Brain Protein in Cerebrospinal Fluid as a Marker for Transmissible Spongiform Encephalopathies
NEJM 335:924-930, 9631996., Hsich,G.,et al, 1996

Diagnosis of Creutzfeldt-Jakob Disease in Two-Dimensional Gel Electrophoresis of Cerebrospinal Fluid
Lancet 348:846-849, Zerr,I.,et al, 1996

Diagnostic Criteria for Sporadic Creutzfeldt-Jakob Disease
Arch Neurol 53:913-920, Kretzschmar,H.A.,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

BSE Linked to New Variant of CJD in Humans
BMJ 312:795, 791, 843, 85496., , 1996

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



Showing articles 50 to 100 of 1913 << Previous Next >>