Neurology Specific Literature Search   
 
[home][thesaurus]
    

Differential
(Click to cross reference)
abducens nerve paralysis
abscess, intracerebral
abscess, intracerebral, treatment of
abscess, intracranial
abscess, intracranial-fungal
acoustic nerve
acquired immunodeficiency syndrome
acquired immunodeficiency syndrome dementia complex
acute cerebellar ataxia
acute necrotizing encephalitis
addiction, heroin
advances in neurology
adverse drug reaction
akinetic mute
algorithm
altered states of consciousness
alternating rapid movement, impaired
Alzheimer's disease
Alzheimer's disease, rapidly progressive
Alzheimer's disease, rate of clinical decline
AMPA receptor antibodies
amyloid angiopathy, cerebral
amyloid plaques
amyotrophic lateral sclerosis
anemia
anemia, iron deficiency
anemia, megaloblastic
aneurysm
aneurysm, intracranial
aneurysm, intracranial, treatment of
angiitis, isolated of CNS
angiography, cerebral, beaded vessels
angiography, cerebral
angiotensin-converting enzyme
animal exposure
anorexia
antibiotic prophylaxis
antibiotics
antibodies to measles
antiviral agents
aortic valve, lesion of
aortic valve, stenosis
aqueduct of Sylvius, obstruction
arachnoiditis
areflexia
arsenic
arteriopathy
arteritides
arthralgia
arthritis
aspergillosis
asymptomatic
ataxia
ataxia, cerebellar
ataxia, progressive
ataxic gait
atypical
autoantibodies
autoimmune disease
autoimmune meningitis
autonomic dysfunction
B 12 deficiency
B12
Babinski sign
bacteremia
bacterial endocarditis, neurologic manifestations of
bacterial infection
basal cistern
basal ganglia
basal ganglia, lesion of
basal ganglia, lesion, bilateral
bedridden
behavioral disorder
biologic markers
blood cultures
blood transfusion
bone marrow biopsy
bone scanning
Borrelia burgdorferi infection
bovine spongiform encephalopathy
brain biopsy
brain biopsy, complications of
brain biopsy, false negative
brain biopsy, indication
brain biopsy, negative
brain biopsy, stereotaxic
brain fog
brain scan
brainstem, lesion of
brucellosis
brucellosis, nervous system involvement with
burning feet
burning feet, differential diagnosis of
burning paresthesia
calcification, intracranial
Canavan's disease
cancer associated hypercoagulation
cancer, cerebrovascular accident complicating patients with
carcinoma
carcinoma of lung
cardiac implantable electronic devices
cardiac surgery
caries
CAT scan
CAT scan, abnormal
CAT scan, cardiac, ultrafast
CAT scan, disappearing lesion on
CAT scan, false negative
CAT scan, serial
CAT scan, spine
cataracts, congenital
cauda equina
cauda equina, lesion of
caudate nucleus, lesion of
caudate nucleus, lesion of, bilateral
celiac disease, adult
central nervous system, infection of
central venous catheter
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar lesion
cerebral cortex
cerebral cortical atrophy
cerebral embolism
cerebral embolism, multiple
cerebral infarction, septic
cerebral ischemia
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, beta-D-glucan
cerebrospinal fluid, culture negative
cerebrospinal fluid, cytology
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, enzymes in
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, oligoclonal IgG in
cerebrospinal fluid, protein of
cerebrospinal fluid, xanthochromia of
cerebrovascular accident
cerebrovascular accident, mimics
cerebrovascular accident, misdiagnosis
cerebrovascular accident, multiple
cerebrovascular disease
cervical spine
chemical meningitis
children
chills
chorea
chorioretinitis
chromosome 20
cingulate gyrus
cisterna magna
Clinical Pathologic Conference(C.P.C.)
coenzyme Q10 deficiency
cognition
cognition, slowed
coinfection
colchicine
coma
comorbidities
complications
computers, handheld
computers, medicine and
computers, neurologic diagnosis and
concentration, impaired
conduction block
confusion
congenital heart disease
congestive heart failure
contactin associated protein like 2 antibodies
controversies in neurology
cortical blindness
cranial nerve palsies
cranial neuropathy
cranial neuropathy, multiple
craniotomy
C-reactive protein, elevated
Creutzfeldt-Jakob disease, genetic
cryptococcal meningitis
cyst, cortical parenchyma
cyst, porencephalic
cyst, ventricular
cysticercosis
cysticercosis, cerebral
cysticercosis, intraventricular
cysticercosis, subarachnoid
cytomegalic inclusion disease
cytomegalovirus infection
cytosine arabinoside
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
delirium
dementia
dementia, clinical diagnosis
dementia, diagnostic evaluation of
dementia, familial
dementia, frontotemporal
dementia, rapidly progressive
dementia, reversible
dementia, screening for
dementia, transmissible
dementia, treatment of
dental infection
dental procedure, neurologic complications with
dentate nuclei
dentate nuclei, lesion of
depression
depression, psychotic
diabetes insipidus
diabetes mellitus
diagnostic criteria
differential diagnosis
difficulty climbing stairs
diplopia
disability, neurological
disorientation
dissociated sensory loss
dizziness
drug abuse
drug induced neurologic disorders
dural graft, cadaveric
dysarthria
dysdiadochokinesia
dysmetria
dyspnea
dystonia
echocardiogram
echocardiogram, transesophageal
echocardiogram, transesophageal, false negative
echocardiogram, transthoracic, false negative
efficacy
ejection fraction, abnormal
electrocardiogram, abnormal
electroencephalogram
electroencephalogram, abnormalities of
electroencephalogram, periodic complexes
electron microscopy
electrophoretic pattern, CSF
electrophoretic pattern, serum
embolism
embolism, fat
embolism, septic
embolism, systemic
empyema, epidural-spinal
encephalitis
encephalitis, autoimmune
encephalitis, brainstem
encephalitis, human immunodeficiency virus type 1
encephalitis, paraneoplastic
encephalitis, viral
encephalopathy
encephalopathy, Hashimoto's
encephalopathy, metabolic
endemic area
endocarditis
endocarditis, acute bacterial
endocarditis, infectious
endocarditis, native-valve
endocarditis, prophylaxis
endocarditis, subacute bacterial
endocarditis, treatment of
endovascular therapy
enolase
enzyme, defect
epidemiology of neurology
epilepsia partialis continua
episodic neurologic deficits
Epstein-Barr virus
ergotism
erythema migrans
evidence-based research
eye movement, disorders of
face, numbness of
facial nerve palsy
facial nerve palsy, bilateral
facial weakness, bilateral
Fahr disease
falling
false negative
false positive
familial
fatal familial insomnia
fatigue
fever
fibrillations
finger nose finger test
fourth ventricle, cyst
fracture, long bone
frontal lobe, anatomy and physiology
fungal infection
fungal infection, CNS
gadolinium
gait disorder
gallium scan
gamma amino butyric acid receptor antibody
gammaglobulin therapy, intravenous
ganglionitis
gastric partitioning
gastric surgery
gastrointestinal disease, neurologic complications
gene mutation
gene therapy
genetic counselling
genetic neurologic disorders
genetic testing
Gerstmann-Straussler-Scheinker disease
glioblastoma multiforme(astrocytoma Gr.III)
gliosis
glossitis
glutaric acidemia
gluten-free diet
glycine receptor antibodies
GM antigen test
granulomatous disease
gray matter
growth hormone
Guillain Barre syndrome
Guillain Barre syndrome, variant forms of
handwriting
headache
headache, frontal
headache, severe
hearing loss
heart block
heart murmur
heart valve surgery
heart valve, prosthetic
heel-knee-shin test
helminthic infection of CNS
hematuria, microscopic
hemianopia, homonymous
hemiparesis
heralding manifestation
herniation syndromes, intracranial
herpes labialis
herpes simplex encephalitis
herpes simplex encephalitis, differential diagnosis of
herpes simplex encephalitis, recurrent
herpes simplex encephalitis, treatment of
herpes simplex myelitis
herpes simplex virus
herpes simplex virus infection, immunosuppressed patient
herpes simplex virus, human nervous system and
herpes simplex virus, localization of
herpes simplex virus, malignancy with
herpes simplex virus, pathogenesis of
herpes simplex virus, pathology of
herpes simplex, neurocutaneous lesions in
herpes virus
herpes virus infection
herpes zoster
herpes, genital
Hispanics
histamine-2 receptor blockers
hockey stick sign
hot cross bun sign
human immunodeficiency virus type 1
Huntington's chorea
hydrocephalus
hydrocephalus, non-communicating(obstructive)
hydrocephalus, transient
hypercalcemia
hyperesthesia
hypersegmented polys
hypertrophic intracranial pachymeningitis
hypoglycorrhachia
hyporeflexia
iatrogenic neurologic disorders
imbalance
immunocompetent
immunodeficiency
immunofluorescent exam of CSF cells
immunohistochemistry
immunologic disease
immunosuppression
immunosuppressive agents
implantable cardioverter defibrillator
impotence
incidence
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion bodies, eosinophilic intranuclear
inclusion bodies, intranuclear
incontinence, fecal
infection
infectious mononucleosis
infectious mononucleosis, neurologic findings with
insular cortex
intellectual deficit
intellectual deterioration
interferon
interferon inducer
intestinal biopsy
intracardiac device
intracardiac devices
intracerebral hemorrhage
intracranial hypertension, benign
intracranial pressure, increased
intrauterine infection, viral
intrauterine infection, viral of CNS
intravenous drug abuse
intravenous line
iododeoxyuridine
iritis
iron, brain
iron, serum, low
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
Jakob-Creutzfeldt disease, medical precaution with
Jakob-Creutzfeldt disease, variant
Jakob-Creutzfeldt disease, young adult
Janeway spots
Kearns-Sayre syndrome
kuru
Leber's hereditary optic neuropathy
leg numbness
leg weakness, bilateral
Leigh's disease
lesions too numerous to count
leucine rich glioma inactivated 1 antibodies
leukocyte enzyme abnormality
level of consciousness, decreased
Lewy body disease, diffuse
life expectancy
limbic encephalitis
limbic system
Lyme disease
lymphadenopathy, hilar
lymphocytic meningoradiculitis
lymphoma
lymphoma involving CNS
lymphoma, primary of CNS
magnetic susceptibility
malabsorption
malabsorption syndrome
malformation, CNS, congenital
malignancy screen
maple syrup urine disease
MELAS syndrome
memory, defect of recent
memory, impairment of
meningeal enhancement
meningismus
meningitis
meningitis, aseptic
meningitis, aspergillus
meningitis, bacterial
meningitis, basilar
meningitis, candida
meningitis, carcinomatous
meningitis, chronic
meningitis, cysticercosis
meningitis, eosinophilic
meningitis, fungal
meningitis, fungal-negative CSF culture
meningitis, granulomatous
meningitis, helminthic
meningitis, neutrophilic
meningitis, neutrophilic, persistent
meningitis, noninfectious
meningitis, parameningeal
meningitis, parasitic
meningitis, recurrent
meningitis, spinal fluid smear and culture-negative
meningitis, TB
meningitis, treatment of
meningitis, treatment of, empirical
meningitis, viral etiology in
meningitis-encephalitis PCR panel
meningoencephalitis
meningomyelitis
mental status, abnormal
MERRF syndrome
metformin
methicillin resistant staphylococcus aureus
methylmalonic acid, serum
metronidazole
Mexican
Mexico
microcephaly
microhemorrhage, intracerebral
micropthalmia
mimics
Mini Mental Status Examination
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
mitochondrial recessive ataxic syndrome
mitral valve lesion
mitral valve vegetation
MNGIE syndrome
molecular genetics
monoamines
monoamines, brain
mononeuritis multiplex
mononeuropathy
mononeuropathy multiplex
monoparesis
mortality
Morvan's fibrillary chorea
motor neuron disease
movement disorder
MRI
MRI pattern
MRI, abnormal
MRI, ADC maps
MRI, complications with
MRI, contrast enhanced
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, paramagnetic effect
MRI, proton density
MRI, punctate pattern
MRI, serial
MRI, spine
MRI, T1 weighted high signal foci
multiple myeloma
multiple sclerosis
multiple system atrophy
muscle atrophy, progressive
muscle pain
muscle weakness
myasthenic syndrome
mycotic aneurysm
myelitis
myelitis, longitudinal
myelopathy
myelopathy, necrotizing
myelopathy, vacuolar
myoclonus
myopathy
myopathy, mitochondrial
myositis
nasal brushings
nausea and vomiting
negative
neoplasm, metastatic to CNS
neoplasm, primary intracerebral
neoplasm, primary of CNS
neoplastic angioendotheliosis
nephritis
nerve biopsy
nerve conduction studies
neuritis
neurofibrillary degeneration
neurologic complications of, surgery
neurologic complications of, systemic cancer
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic examination
neurologic examination, focal
neurologic signs
neurologic symptoms
neurologic testing
neuron specific enolase
neuronal cell surface antigen
neuronopathy, sensory
neuropathology
neuropathology, brain
neuropathy
neuropathy, ataxia, retinitis pigmentosa
neuropathy, peripheral
neuropathy, sensory
neuropathy, vasculitic, systemic
neuropathy, work up for
next-generation sequencing
night sweats
NMDA antagonists
normal
nystagmus
old age, neurology of
olfactory biopsy
olfactory bulb
olfactory cortex
olfactory mucosa
olfactory pathway
olfactory tract
ophthalmoplegia
ophthalmoplegia, progressive external
opportunistic infection
opportunistic infection, CNS
optic atrophy
optic neuropathy
orthostatic hypotension
Osler's nodes
osteomyelitis
osteomyelitis, spinal
pacemaker, cardiac-transvenous
pain
pain, abdominal
pain, back
pain, leg
papilledema
paraparesis
paraproteinemia
parasitic infection, CNS
paresthesias
paresthesias, feet
Parkinson disease
pathognomonic
peripheral blood smear
pernicious anemia
persistent vegetative state
personality change
pes cavus
petechiae
pitfalls
pituitary, hormones of
plasma cell dyscrasia
pleocytosis of cerebrospinal fluid
polyinosinic cytidic acid(poly IC)
polymerase chain reaction
polyneuropathy
polyneuropathy, chronic inflammatory demyelinating
polyneuropathy, subacute idiopathic demyelinating
polyradiculoneuropathy
positive sharp waves
posterior tibial nerve
posterior tibial nerve compression
potassium channel antibodies
practice guidelines
preclinical
pregnancy, neurologic complications in
prion disease
prognosis
progressive multifocal leucoencephalopathy
progressive neurologic disorder
proprioception
proprioception, abnormal
protein 14-3-3, cerebrospinal fluid
protein 14-3-3, cerebrospinal fluid, false negative
protein 14-3-3, cerebrospinal fluid, false positive
proton pump inhibitors
psychiatric disorder
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis
psychotic behavior
pulvinar sign
putamen, lesion of
putamen, lesion of, bilateral
pyramidal tract
pyramidal tract dysfunction
quadriplegia
radiculitis
rapidly fatal neurologic illness
rapidly progressing neurologic illness
rash
real-time quaking-induced conversion
recurrent
Red flags
release phenomena
remote effect of cancer on the nervous system
respirations in CNS disease
respiratory failure
retrovirus
reversible neurologic disorder
review article
rheumatoid arthritis factor(R.A.factor)
risk factors
risk-benefit assessment
Romberg's sign
Roth spots
rubella virus
rubeola virus
sarcoidosis
sarcoidosis, CNS
screening
sedimentation rate, elevated
seizure
seizure, focal
seizure, psychomotor-temporal lobe
sensory loss
sensory loss, cutaneous
sensory symptoms
serologic testing
serologic testing of cerebrospinal fluid
serum S100 protein
shunt procedure, ventricular
single photon emission computed tomography
skin, biopsy
skin, lesions in neurologic disorders
slow virus infection of CNS
spasticity
spinal cord, compression, epidural abscess causing
spirochete infection
splinter hemorrhages
spongy degeneration of brain
staphylococcus aureus
startle myoclonus
steroid
steroid therapy, CNS treatment and complications with
striatum, lesion of
striatum, lesion of, bilateral
strokelike episodes
subacute myelo-opticoneuropathy(S.M.O.N.)complex
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
subacute sclerosing panencephalitis, adult onset
subconjunctival hemorrhage
subtemporal decompression
symmetric brain lesions
syphilis, diagnosis and treatment
systemic illness
tachycardia
talk
tandem gait, ataxic
tarsal tunnel syndrome
tau protein
thalamus, lesion of
thalamus, lesion of-bilateral
third nerve palsy
thrombocytopenia
thyroid function tests
thyroiditis
tick bite
tonsil biopsy
tonsillar herniation of cerebellum
toxic encephalopathy
toxoplasmosis, acquired
toxoplasmosis, CNS
transglutaminase antibodies
transient ischemic attack
transplacental virus infections
treatment of neurologic disorder
treatment, empirical
trigeminal neuralgia
trigeminal neuropathy
trigeminal neuropathy, sensory
Trousseau's syndrome
tumor necrosis factor inhibitor
uncal herniation
urinary incontinence
uveitis
valvulopathy
vasculitides
vasculopathy
vertigo
vibratory sensation
vibratory sensation, abnormal
viral infection
viral infection, CNS
virus, slow
visual loss
visuospatial disturbance
vitamin D deficiency
vitamin deficiency
voriconazole
walking frame
walking, difficulty with
weakness
weakness, generalized
weakness, progressive
weight loss
West Nile fever
Western immunoblot test
white matter disease
white matter disease, subcortical
wide based gait
workup
xerostomia
x-ray, spine
Showing articles 50 to 100 of 4260 << Previous Next >>

Clinical Presentation and Pre-Mortem Diagnosis of Variant Creutzfeldt-Jakob Disease Associated With Blood Transfusion: A Case Report
Lancet 368:2061-2067, Wroe,S.J.,et al, 2006

Diffusion-Weighted and Fluid-Attenuated Inversion Recovery Imaging in Creutzfeldt-Jakob Disease:High Sensitivity and Specificity for Diagnosis
AJNR 26:1551-1562, Young,G.S.,et al, 2005

Neurological presentation of intravascular lymphoma: report of two cases and discussion of diagnostic challenges
Eur J Neurol 12:710-714, Lozsadi, D.A.,et al, 2005

Prion Deposition in Olfactory Biopsy of Sporadic Creutzfeldt-Jakob Disease
Ann Neurol 55:294-296, Tabaton,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

Subacute Inflammatory Demyelinating Polyneuropathy
Neurol 61:1507-1512, Oh,S.J.,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

Challenges in the Identification of Cobalamin-Deficiency Polyneuropathy
Arch Neurol 60:1296-1301, Saperstein,D.S.,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

Subacute Sclerosing Panencephalitis
Postgrad Med J 78:63-70, Garg, R.K.,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

Practice Parameter: Diagnosis of Dementia (an Evidence-Based Review)
Neurol 56:1143-1153, Knopman,D.S.,et al, 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

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

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

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

Clinicopath Conf
Subacute Sclerosing Panencephalitis, Case 15-1998, NEJM 338:1448-1456998., , 1998

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

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

Detection of 14-3-3 Protein in the CSF of Genetic Creutzfeldt-Jakob Disease
Neurol 49:593-595, Rosemann,H.,et al, 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

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

Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities
Ann Neurol 39:343-351, Rahman,S.,et al, 1996

Bovine Spongiform Encephalopathy and Creutzfeldt-Jakob Disease
BMJ 312:790-791, Brown,P., 1996

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

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

Clinicopath Conf
Axonal Polyneuritis Assoc with IgA Lambda Multiple Myeloma, Case 21-1993, NEJM 328:1550-1558993., , 1993

Recurrent Aseptic Meningitis Complicating Intravenous Immunoglobulin Therapy for CIDP
Neurol 42:1636-1637, Vera-Ramirez,M.,et al, 1992

Subacute Idiopathic Demyelinating Polyradiculoneuropathy
Arch Neurol 49:612-616, Hughes,R.,et al, 1992

Neurologic Aspects of Cobalamin Deficiency
Medicine 70:229-245, Healton,E.B.,et al, 1991

The Remote Effects of Cancer on the Nervous System
in Neurol Manif of Systemic Dis, W. B. Saunders, Co, Phila, Neurologic Clinics 7:579-603, Dropcho,E.J., 1989



Showing articles 50 to 100 of 4260 << Previous Next >>