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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 150 to 200 of 1974 << Previous Next >>

Clinicopath Conf, Prion Disease (Sporadic Creutzfeldt-Jakob Disease)
NEJM 353:1042-1050, Case 27-2005, 2005

Psychiatric Manifestations of Creutzfeldt-Jakob Disease: A 25-Year Analysis
J Neuropsychiatry Clin Neurosci 17:489-495, Wall,C.A.,et al, 2005

False-Positive Pulvinar Sign on MRI in Sporadic Creutzfeldt-Jakob Disease
Neurol 62:1235-1236, Petzold,G.C.,et al, 2004

White Matter Lesions in Panencephalopathic Type of Creutzfeldt-Jakob Disease: MR Imaging and Pathologic Correlation
AJNR 25:910-918,905, Matsusue,E.,et al, 2004

Sporadic Creutzfeldt-Jakob Disease
Neurol 63:450-456,410, Meissner,B.,et al, 2004

CJD--A Case of Mistaken Identity
Lancet 364:2068, Campbell,S.,et al, 2004

14-3-3 Protein in the CSF of Patients with Rapidly Progressive Dementia
Neurol 61:354-357, Huang,N.,et al, 2003

Thalamic Involvement in Sporadic Creutzfeldt-Jakob Disease: A Diffusion-Weighted MR Imaging Study
AJNR 24:908-915, Tschampa,H.J.,et al, 2003

Antivonvulsants for Creutzfeldt-Jakob Disease?
Lancet 361:224, Fioel,A.,et al, 2003

Extraneural Pathologic Prion Protein in Sporadic Creutzfeldt-Jakob Disease
NEJM 349:1812-1820, Glatzel,M.,et al, 2003

Generalized Convulsive Status Epilepticus in Creutzfeldt-Jakob Disease
Seizure 12:403-406, Neufeld,M.Y.,et al, 2003

Correlation of Diffusion-Weighted Magnetic Resonance Imaging With Neuropathology in Creutzfeldt-Jakob Disease
Arch Neurol 59:128-134, Mittal,S.,et al, 2002

Sporadic Creutzfeldt-Jakob Disease and Surgery
Neurol 59:543-548, Ward,H.J.T.,et al, 2002

Sporadic CJD Clinically Mimicking Variant CJD With Bilateral Increased Signal in the Pulvinar
Neurol 58:148-149, Haik,S.,et al, 2002

Emerging Patterns of Diffusion-Weighted MR Imaging in Creutzfeldt-Jakob Disease: Case Report and Review of the Literature
AJNR 23:550-556, Mao-Draayer,Y.,et al, 2002

Creutzfeldt-Jakob Disease: Serial Changes on Diffusion-Weighted MRI
J Comput Assist Tomogr 25:274-277, Matoba,M.,et al, 2001

14-3-3 Protein Cerebrspinal Fluid Detection in Human Growth Hormone-Treated Creutzfeldt-Jakob Disease Patients
Ann Neurol 49:257-260, Brandel,J.,et al, 2001

Diffusion-Weighted MR Imaging of the Brain
Radiology 217:331-345, Schaefer,P.W.,et al, 2000

Magnetic Resonance Imaging in the Clinical Diagnosis of Creutzfeldt-Jakob Disease
Arch Neurol 57:1751-1757, Schroter,A.,et al, 2000

Iatrogenic Creutzfeldt-Jakob Disease at the Millenium
Neurol 55:1075-1081, Brown,P.,et al, 2000

Misleading Results With the 14-3-3 Assay for the Diagnosis of Creutzfeldt-Jakob Disease
Neurol 55:1396-1397, Chapman,T.,et al, 2000

Risk of Acquiring Creutzfeldt-Jakob Disease from Blood Transfusions: Systematic Review of Case-Control Studies
BMJ 321:17-19, Wilson,K. et al, 2000

FLAIR MRI in sporadic Creutzfeldt-Jakob Disease
Neurol 55:147-148, Vrancken,A.F.J.E. et al, 2000

Alien Hand Sign in Creutzfeldt-Jakob Disease
JNNP 68:103-104, Inzelberg,R.,et al, 2000

Seizures and Creutzfeldt-Jakob Disease
NCMJ 60:108-109, Cokgor,I.,et al, 1999

Creutzfeldt-Jakob Disease Presenting as Complex Partial Status Epilepticus: A Report of Two Cases
JNNP 66:406-407, Rees,J.H.,et al, 1999

Hashimoto's Encephalitis as a Differential Diagnosis of Creutzfeldt-Jakob Disease
JNNP 66:172-176, Seipelt,M.,et al, 1999

Surgical Treatment and Risk of Sporadic Creutzfeldt-Jakob Disease:A Case-Control Study
Lancet 353:693-697, Collins,S.,et al, 1999

Progressive Aphasia with Rapidly Progressive Dementia in a 49 Year Old Woman
JNNP 66:238-243, Greene,J.D.W.,et al,, 1999

Case-Control Study of Risk Factors of Creutzfeldt-Jacob Disease in Europe During 1993-95
Lancet 351:1081-1085, Van Duijn,C.M.,et al, 1998

Creutzfeldt-Jakob Disease (CJD) after Blood Product Transfusion From a Donor with CJD
Neurol 50:1872-1873, Patryk,D.,et al, 1998

Creutzfeldt-Jacob Disease in a Husband and Wife
Neurol 50:684-688, Brown,P.,et al, 1998

Transmission ofr Creutzfeldt-Jakob Disease in Corneal Grafts, Exclusion Criteria Ensure Risk is Small
BMJ 315:1553-1554, Allan,B.&Tuft,S., 1997

Peripheral NEuropathy in Creutzfeldt-Jakob Disease
Neurol 48:784, Esiri,M.M.,et al, 1997

Rapid Spongiform Degeneration of the Cerebrum and Cerebellum in Creutzfeldt-Jakob Encephalitis:Serial MR Findings
AJNR 18:583-586, Tzeng,B-C.,et al, 1997

Creutzfeldt-Jakob Disease after Extracranial Dura Mater Embolization for a Nasopharyngeal Angiofibroma
Neurol 48:1451-1453, Antoine,J.C.,et al, 1997

Creutzfeldt-Jakob Dis after Embolization of Intercostal Arteries with Cadaveric Dura Suggest a Syst Trans of Prion Agent
Neurol 48:1470-1471, Defebvre,L.,et al, 1997

Pruritus in Creutzfeldt-Jakob Disease
Neurol 46:940-941, Shabtai,H.,et al, 1996

Risk Factors for Creutzfeldt-Jakob Disease:A Reanalysis of Case-Control Studies
Neurol 46:1287-1291, Wientjens,D.P.W.M.,et al, 1996

MR Imaging of Creutzfeldt-Jakob Disease
Radiology 199:793-798, Finkenstaedt,M.,et al, 1996

Fatal Insomnia in a Case of Familial Creutzfeldt-Jakob Disease with the Codon 200Lys Mutation
Neurol 46:758-761, Chapman,J.,et al, 1996

Accuracy and Reliability of Periodic Sharp Wave Complexes in Creutzfeldt-Jakob Disease
Arch Neurol 53:162-166, Steinhoff,B.J.,et al, 1996

Creutzfeldt-Jakob Disease in a Young Woman
Lancet 347:945-948, Tabrizi,S.J.,et al, 1996

Creutzfeldt-Jakob Disease from Contaminated Growth Hormone Extracts in France
Neurol 47:690-695, Billette de Villemeur,T.,et al, 1996

Apolipoprotein E Phenotype Freq & CSF Concentra are not Assoc with Creutzfeldt-Jakob Disease
Arch Neurol 53:1233-1238, Zerr,I.,et al, 1996

A Case of Creutzfeldt-Jakob Disease (CJD) Started with Monoparesis of the Left Arm
Rinshi Shinkeigaku 36:1245-1248, Obi, T.,et al, 1996

MRI of Creutzfeldt-Jakob Disease:Asymmetric High Signal Intensity of the Basal Ganglia
Neurol 45:1932-1933, Yoon,S.S.,et al, 1995

Creutzfeldt-Jakob Disease after Liver Transplantation
Ann Neurol 38:269-272, Creange,A.,et al, 1995

Human Spongiform Encephalopathy:The NIH Series of 300 Cases of Experimentally Transmitted Disease
Ann Neurol 35:513-529, Brown,P.,et al, 1994

The Apolipoprotein E Alleles as Major Susceptibility Factors for Creutzfeldt-Jakob Disease
Lancet 344:1315-1318, 13101994., Amouyel,P.,et al, 1994



Showing articles 150 to 200 of 1974 << Previous Next >>