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Differential
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abscess, intracerebral
acquired immunodeficiency syndrome
addiction, heroin
addiction, heroin-neurologic complications with
adenine arabinoside
adrenoleukodystrophy
advances in neurology
adverse drug reaction
affect, flat
aggression
agitation
agnosia
agnosia, visual
akinetic mute
albumin transfusion
Alexanders disease
alexia
algorithm
Alice in Wonderland syndrome
alien hand syndrome
alternating rapid movement, impaired
Alzheimer's disease
Alzheimer's disease, familial
Alzheimer's disease, rapidly progressive
Alzheimer's disease, rate of clinical decline
Alzheimer's disease, visual variant
amantadine
aminoacidurias
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, progressive, primary
aphasia, transcortical
aphasia, transcortical-sensory
apolipoprotein E
apraxia
apraxia, dressing
areflexia
arm weakness
Arnold Chiari malformation
aspartocyclase
asterixis
asymptomatic
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxia, truncal
ataxic gait
atypical
autoantibodies
autoimmune disease
autonomic dysfunction
axonal degeneration
Babinski sign
bacterial infection
Balint's syndrome
basal ganglia
basal ganglia, calcification of
basal ganglia, degeneration
basal ganglia, lesion of
basal ganglia, lesion, bilateral
basilar artery occlusion
bedridden
behavioral disorder
Behcet's syndrome
beriberi
beriberi, infantile
biologic markers
blindness
blood dyscrasias, neurologic findings with
blood transfusion
bovine spongiform encephalopathy
bradykinesia
bradyphrenia
brain atrophy
brain biopsy
brain biopsy, complications of
brain biopsy, false negative
brain biopsy, indication
brain biopsy, negative
brain scan
brainstem
brainstem, lesion of
bulimia
burning paresthesia
cachexia
calcification, intracranial
Canavan's disease
carbamazepine
carbamazepine, toxicity
carbon monoxide poisoning
carcinoma
carcinoma of breast
cardiac transplantation
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, contrast enhanced
CAT scan, demyelinating disease
CAT scan, emission
CAT scan, emission, abnormal
CAT scan, false negative
cataracts
caudate nucleus
caudate nucleus, lesion of
caudate nucleus, lesion of, bilateral
cell fusion test
central nervous system, infection of
central pontine myelinolysis
cerebellar ataxia, children
cerebellar ataxia, children, differential diagnosis of
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar lesion
cerebellar plaques, amyloid
cerebellum, disease of
cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy
cerebral cortex
cerebral cortical atrophy
cerebral glucose metabolism
cerebral infarction
cerebral venous infarction
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, lactic acid concentration
cerebrospinal fluid, oligoclonal IgG in
cerebrospinal fluid, protein of
cerebrovascular accident
cerebrovascular accident, mimics
cerebrovascular accident, misdiagnosis
cerebrovascular accident, nonvascular territory
cerebrovascular accident, young adult
Charles Bonnet's syndrome
chemotherapy, CNS treatment and complications with
children
chorea
choreoathetosis
chromosomal abnormality
chromosome 20
chronic progressive external ophthalmoplegia
cingulate gyrus
Clinical Pathologic Conference(C.P.C.)
coenzyme Q10 deficiency
cognition
cognition, slowed
cogwheel rigidty
color vision, impaired
coma
comorbidities
complications
concentration, impaired
confusion
consanguinity
contactin associated protein like 2 antibodies
controversies in neurology
corneal transplant
cortical blindness
cortical infarction
cortical-basal ganglionic degeneration
Creutzfeldt-Jakob disease, genetic
crying
cultured skin fibroblasts
cytochrome c oxidase
cytochrome c oxidase, deficiency
deafness
deafness, congenital
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)
dentate nuclei
dentate nuclei, lesion of
depression
developmental milestones
developmental milestones, loss of
developmental retardation
dexterity, impaired
diabetes mellitus
diagnostic criteria
diet
differential diagnosis
difficulty climbing stairs
diplopia
disorientation
dissociated sensory loss
dizziness
driving
drug abuse
drug abuse, neurologic complications of
drug induced neurologic disorders
drug withdrawal
dural graft, cadaveric
dysarthria
dyschromatopsia
dysdiadochokinesia
dysmetria
dysphagia
dyspraxia
dystonia
echolalia
efficacy
electroencephalogram
electroencephalogram, abnormalities of
electroencephalogram, complications with
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
encephalopathy, neonatal
endemic area
endoscopy
enkephalins
enolase
enzyme, defect
epidemic
epidemiology of neurology
epilepsia partialis continua
episodic disorders
evoked potentials
executive dysfunction
experimental allergic encephalitis
extrapyramidal
eye movement, disorders of
Fabry's disease
faciobrachial dystonic seizure
Fahr disease
failure to thrive
falling
false negative
false positive
familial
farmer
fasciculation
fatal familial insomnia
fatigue
feeding disorder
fever
fibrillations
finger nose finger test
Fisher C.M.
flavivirus
flu-like illness
follicle stimulating hormone
fontanel, bulging
Friedreich's ataxia
frontal lobe, anatomy and physiology
frontal lobe, pathologic signs of
gadolinium
gait disorder
gait, apraxic
gamma amino butyric acid receptor antibody
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic testing
Gerstmann syndrome
Gerstmann-Straussler-Scheinker disease
glioma
gliosis
glutaric acidemia
glycine receptor antibodies
grandiosity
grasp reflex
grasping
gray matter
growth hormone
gyrus, abnormal
Hallervorden Spatz disease
hallucination
hallucination, visual
hallucination, visual, benign
hand weakness
handwriting
head circumference
head injury
head lag
head turning
headache
headache, episodic
hearing loss
heart block
heel-knee-shin test
hemianopia, homonymous
hemiparesis
hepatolenticular degeneration(Wilson's disease)
hepatomegaly
heralding manifestation
herpes simplex encephalitis
herpes simplex virus
herpes virus infection
hiccoughs
histochemistry
histochemistry of muscle
hockey stick sign
homograft
hot cross bun sign
human immunodeficiency virus type 1
Huntington's chorea
hydrocephalus
hydrocephalus, normal pressure
hyperglycemia
hyperosmia
hyperphagia
hyperreflexia
hyperthyroidism
hypogeusia
hypoglycemia
hypomagnesemia
hyponatremia
hypoparathyroidism
hypophonia
hyporeflexia
hypothermia
hypothyroidism
hypotonia
hypotonia, infants
hypoxic encephalopathy
iatrogenic neurologic disorders
imbalance
immunocompetent
immunodeficiency
immunohistochemistry
immunologic disease
immunosuppressive agents
inattention
inborn errors of metabolism
incidence
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
incoordination
incubation period
infant and newborn with distress, neurologic prognosis in
infant, evaluation of
insomnia
insular cortex
intellectual deterioration
interferon
internuclear ophthalmoplegia
internuclear ophthalmoplegia, unilateral
interobserver agreement
intestinal pseudoobstruction
intracerebral hemorrhage
intrathecal chemotherapy
intraventricular hemorrhage
iron, brain
irritability
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
Kearns-Sayre syndrome
Krabbe's disease
kuru
kuru plaques
lactic acidemia
laminar necrosis, cortical
language disorder in adults
laughing, pathologic
lead poisoning
Leber's hereditary optic neuropathy
leg numbness
leg weakness, bilateral
Leigh's disease
Leigh's disease, adult variety
lenticular nucleus, lesion of
lenticular nucleus, lesion of, bilateral
lethargy
leucine rich glioma inactivated 1 antibodies
leukemia, neurologic findings assoc.with
leukocyte enzyme abnormality
leukodystrophy
leukoencephalitis, acute necrotizing hemorrhagic
leukoencephalopathy
leukoencephalopathy, differential diagnosis
Lewy body
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
macrocephaly
macropsia
magnetic susceptibility
malignancy screen
mania
maple syrup urine disease
Marinesco-Sjogren syndrome
masked facies
megalencephaly
MELAS syndrome
memory, defect of recent
memory, impairment of
meningitis
meningoencephalitis
mental retardation
mental status, abnormal
MERRF syndrome
metabolic disorder, primary
metabolic disorder, primary-screening tests
metachromatic leukodystrophy
metamorphopsia
methotrexate
metronidazole
micrographia
microhemorrhage, intracerebral
micropsia
midbrain, lesion of
migraine
mimics
Mini Mental Status Examination
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
mitochondrial recessive ataxic syndrome
MNGIE syndrome
molecular genetics
mongolism
monoparesis
mortality
Morvan's fibrillary chorea
motor cortex
motor neuron disease
movement disorder
movement disorder, drug induced
movement disorder, extrapyramidal
MRI
MRI pattern
MRI, abnormal
MRI, abnormal, seizure causing
MRI, ADC maps
MRI, artifacts
MRI, CAT scan compared to
MRI, cerebrovascular disease
MRI, complications with
MRI, contrast enhanced
MRI, demyelinating disease
MRI, diffusion tensor
MRI, diffusion weighted
MRI, diffusion weighted, pattern
MRI, early changes in CVA
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, lesion burden
MRI, negative
MRI, paramagnetic effect
MRI, proton density
MRI, punctate pattern
MRI, serial
MRI, spinal cord
MRI, susceptibility weighted
MRI, T1 weighted high signal foci
MRI, target sign
MRS
multiple sclerosis
multiple sclerosis, differential diagnosis of
multiple sclerosis, familial
multiple system atrophy
muscle biopsy
muscle pain
muscle twitching
mutism
myelin
myelitis
myelitis, longitudinal
myelitis, transverse
myelopathy
myoclonic jerks
myoclonus
myoclonus, action
myoclonus, cortical
myoclonus, differential diagnosis of
myoclonus, epilepsy
myoclonus, stimulus sensitive
myopathy
myopathy, mitochondrial
nasal brushings
negative
neoplasm, intracranial
neoplasm, metastatic to CNS
neoplasm, pituitary
neoplasm, primary intracerebral
neoplasm, primary of CNS
nerve conduction studies
neuroendocrinology
neurofibrillary degeneration
neurofibromatosis 1
neurologic complications of, surgery
neurologic complications of, systemic cancer
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
neuropathy, ataxia, retinitis pigmentosa
neuropathy, peripheral
neurotoxic
neurotoxin
Niemann-Pick disease
NMDA antagonists
normal
nortriptyline
nucleus basalis of Meynert
nutritional deficiency
nystagmus
nystagmus, periodic alternating
nystagmus, rotary
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
ophthalmoplegia
ophthalmoplegia, plus syndrome
ophthalmoplegia, progressive external
optic atrophy
optic atrophy, hereditary
optic neuropathy
organ donor
organ transplantation
orthostatic hypotension
osmotic demyelination syndrome
overlap syndrome
owl's eye sign of spinal cord
pain
pain, leg
palmomental response
pancytopenia
paranoia
paraparesis, spastic
paresthesias
parietal lobe, lesion of
parietal lobe, syndromes of
Parkinson disease
Parkinson disease, misdiagnosis
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
Pelizaeus Merzbacher
perseveration
personality change
pes cavus
Pick bodies
Pick's disease
pigmentary retinopathy
pituitary, hormones of
PLEDs
PLEDs, bilateral independent
pleocytosis of cerebrospinal fluid
POLG1 gene
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
prenatal diagnosis by amniocentesis
prevention of neurologic disorders
prion disease
prion protein gene
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
ptosis
pulvinar sign
pursuit eye movements, abnormal
putamen, lesion of
putamen, lesion of, bilateral
pyramidal tract
pyramidal tract dysfunction
pyrimethamine
pyruvate dehydrogenase deficiency
pyruvate metabolism, abnormality of
quadriparesis
quadriplegia
radiation therapy, CNS treatment and complications with
ragged-red fibers
rapidly fatal neurologic illness
rapidly progressing neurologic illness
real-time quaking-induced conversion
release phenomena
remote effect of cancer on the nervous system
respiratory failure
restless leg syndrome
retinal degeneration
retinopathy
reversible cerebral vasoconstrictive syndromes
reversible neurologic disorder
review article
rigidity
risk factors
risk-benefit assessment
Romberg's sign
rooting reflex
roving eye movements
saccadic eye movements, abnormal
sarcoidosis, CNS
scrapie
screening
seizure
seizure, children
seizure, focal
seizure, nonconvulsive
senile plaques
sensorineural hearing loss
sensory loss
sensory symptoms
serum S100 protein
short stature
simultanagnosia
single photon emission computed tomography
skin, biopsy
sleep
sleep pathology and physiology
slow virus infection of CNS
smell
snout reflex
somnolence
spastic diplegia
spasticity
speech, loss of
speech, pressured
spinal cord
spinal cord, lesion of
spinocerebellar degeneration
spongy degeneration of brain
spongy degeneration of brain, differential diagnosis of
square wave jerks
startle myoclonus
startle reaction
status epilepticus
status epilepticus, nonconvulsive
steroid
steroid therapy, CNS treatment and complications with
stiff legs
striatonigral degeneration
striatonigral degeneration, infantile
striatum, lesion of
striatum, lesion of, bilateral
strokelike episodes
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
substantia nigra
suck, poor
sudden death
symmetric brain lesions
tandem gait, ataxic
taste
tau protein
tauopathy
temporal lobe, status
term infant
thalamic tumors
thalamic tumors, bilateral
thalamus
thalamus, infarction of
thalamus, infarction, bilateral
thalamus, lesion of
thalamus, lesion of-bilateral
thiamine deficiency
thyroiditis
titubation
tone, muscle
tonic spasms
tonsil biopsy
toxic encephalopathy
trauma
treatment of neurologic disorder
tremor
tremor, intention
tuberous sclerosis
twitching, face
upgaze, paralysis of
urinary incontinence
urine test for metabolic disorders
vasculitides
vertigo
vertigo, episodic
vibratory sensation
viral infection
viral infection, CNS
virus, slow
vision, blurred
visual acuity, decreased
visual cortex
visual distortions
visual evoked response
visual field defect
visual impairment
visual loss
visual loss, progressive
vitamin deficiency
Von Hippel Lindau
walking frame
walking, difficulty with
Wallerian degeneration
weakness
weakness, acute
weakness, focal
weakness, progressive
weight loss
Wernicke's aphasia
Wernicke's encephalopathy
West Nile fever
Western immunoblot test
wheelchair
white matter disease
white matter disease, periventricular
wide based gait
workup
Showing articles 100 to 150 of 16034 << Previous Next >>

Bovine Spongiform Encephalopathy in the United States - An Epidemiologist's View
NEJM 350:539-542, Donnelly,C.A., 2004

Recipients of Blood or Blood Products "at vCJD risk"
BMJ 328:118-119, Bird,S.M., 2004

Prion Deposition in Olfactory Biopsy of Sporadic Creutzfeldt-Jakob Disease
Ann Neurol 55:294-296, Tabaton,M.,et al, 2004

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

Familial Multiple Sclerosis and Other Inherited Disorders of the White Matter
The Neurologist 10:201-215, Kalman,B. &Leist,T.P., 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

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

Diffusion-Weighted MRI Abnormalities as an Early Diagnostic Marker for Creutzfeldt-Jakob Disease
Neurol 63:443-449,410, Shiga,Y.,et al, 2004

Sensitivity of 14-3-3 Protein Test Varies in Subtypes of Sporadic Creutzfeldt-Jakob Disease
Neurol 63:436-442,410, Castellani,R.J.,et al, 2004

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

Novel Methods for Disinfection of Prion-Contaminated Medical Devices
Lancet 364:521-526, Fichet,G.,et al, 2004

Preclinical vCJD After Blood Transfusion in a PRNP Codon 129 Heterozygous Patient
Lancet 364:527-529, Peden,A.H.,et al, 2004

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

Antivonvulsants for Creutzfeldt-Jakob Disease?
Lancet 361:224, Fioel,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

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

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

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

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

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

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

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

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

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

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

The Incidence of Mitochondrial Encephalomyopathies in Childhood: Clinical Features and Morphological, Biochemical, and DNA Abnormalities
Ann Neurol 49:377-383, Darin,N.,et al, 2001

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

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

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

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

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

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

Leigh Syndrome: Serial MR Imaging and Clinical Follow-Up
AJNR 21:1502-1509, Arii,J. & Tanabe,Y., 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

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

Heroin-Induced Spongiform Leukoencephalopathy: Value of Diffusion MF Imaging
J Comput Assist Tomog 24:735-737, Chen,C.,et al, 2000

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



Showing articles 100 to 150 of 16034 << Previous Next >>