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Differential
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abscess, intracerebral
acquired immunodeficiency syndrome
adenine arabinoside
advances in neurology
agitation
agnosia, visual
Alzheimer's disease
Alzheimer's disease, familial
amyloid
amyloid angiopathy, cerebral
amyloid beta protein
amyloid plaques
amyotrophic lateral sclerosis, guamian type of
aneuploidy
angiitis, isolated of CNS
animal exposure
anomic aphasia
antithyroid antibodies
antiviral agents
areflexia
asymptomatic
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxic gait
autoantibodies
autoimmune disease
Babinski sign
bacterial infection
basal ganglia
basal ganglia, lesion of
basal ganglia, lesion, bilateral
basilar artery occlusion
blindness
blood transfusion
bovine spongiform encephalopathy
brain biopsy
cardiac transplantation
CAT scan, abnormal
central nervous system, infection of
central pontine myelinolysis
cerebellar plaques, amyloid
cerebellum, disease of
cerebral cortex
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, oligoclonal IgG in
cerebrospinal fluid, protein of
cerebrovascular accident
chromosomal abnormality
Clinical Pathologic Conference(C.P.C.)
coma
concentration, impaired
confusion
corneal transplant
cortical blindness
cortical infarction
Creutzfeldt-Jakob disease, genetic
deep gray nuclei
degenerative diseases of CNS
dementia
dementia, differential diagnosis of
dementia, familial
dementia, presenile
dementia, prevention of
dementia, rapidly progressive
dementia, screening for
dementia, transmissible
dementia, treatment of
demyelinating disease
differential diagnosis
electroencephalogram
electroencephalogram, abnormalities of
electroencephalogram, periodic complexes
electroencephalogram, triphasic delta waves
electromyogram
electrophoretic pattern, CSF
encephalitis
encephalitis, bornavirus
encephalitis, viral
encephalomyelitis, postinfectious
encephalopathy
encephalopathy, Hashimoto's
encephalopathy, metabolic
endemic area
endoscopy
epidemic
epidemiology of neurology
experimental allergic encephalitis
eye movement, disorders of
Fabry's disease
familial
fatal familial insomnia
fever
flu-like illness
frontal lobe, pathologic signs of
gait disorder
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
genetic counselling
genetic linkage
genetic neurologic disorders
Gerstmann-Straussler-Scheinker disease
glioma
growth hormone
gyrus, abnormal
Hallervorden Spatz disease
hallucination
head injury
headache
hemianopia, homonymous
hemiparesis
hepatolenticular degeneration(Wilson's disease)
herpes simplex encephalitis
herpes simplex virus
herpes virus infection
hockey stick sign
human immunodeficiency virus type 1
hyperthyroidism
hypothyroidism
hypoxic encephalopathy
iatrogenic neurologic disorders
imbalance
immunohistochemistry
incubation period
intellectual deterioration
interferon
intracerebral hemorrhage
intracerebral hemorrhage, multiple
intracerebral hemorrhage, recurrent
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
Jakob-Creutzfeldt disease, medical precaution with
Jakob-Creutzfeldt disease, variant
kuru
kuru plaques
lead poisoning
Leigh's disease
leukoencephalitis, acute necrotizing hemorrhagic
lymphoma involving CNS
memory, impairment of
meningitis
meningoencephalitis
mimics
misdiagnosis
mitochondrial disease
molecular genetics
mongolism
movement disorder
MRI
MRI, abnormal
MRI, abnormal, seizure causing
MRI, ADC maps
MRI, artifacts
MRI, cerebrovascular disease
MRI, demyelinating disease
MRI, diffusion weighted
MRI, early changes in CVA
MRI, false negative
MRI, FLAIR
MRI, high signal foci on
MRI, high signal intensity of basal ganglia
MRI, lesion burden
MRI, negative
MRI, T1 weighted high signal foci
multiple sclerosis
mutism
myelin
myoclonic jerks
myoclonus
myoclonus, stimulus sensitive
neoplasm, intracranial
neoplasm, primary intracerebral
neoplasm, primary of CNS
neurofibrillary degeneration
neurologic complications of, surgery
neurologic disease, diagnoses of
neurologic signs
neuronal ceroid-lipofuscinosis
neuropathology
neuropathology, brain
nystagmus
olfactory biopsy
olfactory bulb
olfactory cortex
olfactory mucosa
olfactory pathway
olfactory tract
organ donor
organ transplantation
osmotic demyelination syndrome
pain, leg
Parkinson disease
Parkinson disease, postencephalitic
PAS positive
PAS positive material in the brain
personality change
pituitary, hormones of
pleocytosis of cerebrospinal fluid
polymerase chain reaction
pons, lesion of
postictal encephalopathy
preclinical
pregnancy, neurologic complications in
prevention of neurologic disorders
prion disease
prognosis
progressive infantile poliodystrophy
progressive multifocal leucoencephalopathy
progressive neurologic disorder
protein 14-3-3, cerebrospinal fluid
psychiatric problems in neurologic disorders
psychosis
pulvinar sign
rapidly fatal neurologic illness
rapidly progressing neurologic illness
remote effect of cancer on the nervous system
review article
risk factors
sarcoidosis, CNS
scrapie
seizure
senile plaques
slow virus infection of CNS
spongy degeneration of brain
startle myoclonus
startle reaction
steroid
steroid therapy, CNS treatment and complications with
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
symmetric brain lesions
thalamic tumors
thalamic tumors, bilateral
thalamus
thalamus, infarction of
thalamus, infarction, bilateral
thalamus, lesion of
thalamus, lesion of-bilateral
thyroiditis
tonsil biopsy
toxic encephalopathy
trauma
treatment of neurologic disorder
tremor
tremor, intention
tuberous sclerosis
upgaze, paralysis of
urinary incontinence
viral infection
viral infection, CNS
virus, slow
vision, blurred
visual acuity, decreased
visual field defect
visual impairment
visual loss
walking, difficulty with
Wernicke's encephalopathy
West Nile fever
Western immunoblot test
Showing articles 450 to 500 of 4355 << Previous Next >>

Precautions in Handling Tissues
Fluids, & Other Contam Materials from Patients with Documented or Suspected Creutzfeldt-Jakob Diseas, , Aeurol 19:75-77,1986., 1986

Neurologic Abnormalities in Lyme Disease without Erythema Chronicum Migrans
Am J Med 81:73-78, Beik,L.,et al, 1986

Meningovascular Syphilis: CT and MR Findings
Radiology 158:439-442, Holland,B.A.,et al, 1986

Neurological Complications in Infants & Children with Acquired Immune Deficiency Syndrome
Ann Neurol 18:560-566, Belman,A.L.,et al, 1985

Similarity of Brain CT Appearance in Spongy Degeneration to That of Subacute Necrotizing Encephalomyelopathy
Ann Neurol 18:352-354, Lo,W.D.,et al, 1985

Isolation of HTLV-III from CSF & Neural Tissues of Patients with Neurologic Syndromes Related to AIDS
NEJM 313:1493-1497, 15381985., Ho,D.D.,et al, 1985

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

Cerebral MR & CT Imaging in Creutzfeldt-Jakob Disease
J Comput Assist Tomogr 9:125-128, Kovanen,J.,et al, 1985

Potential Epidemic of Creutzfeldt-Jakob Disease from Human Growth Hormone Therapy
NEJM 313:728-731, Brown,P.,et al, 1985

Progressive Encephalopathy in Children with Acquired Immune Deficiency Syndrome
Ann Neurol 17:488-496, Epstein,L.G.,et al, 1985

Computed Tomography During Creutzfeldt-Jakob Disease
Neuroradiology 27:362-364, Westphal,K.P.&Schachenmayr,W., 1985

Creutzfeldt-Jakob Disease after Administration of Human Growth Hormone
Lancet 2:244-246, Powell-Jackson,J.,et al, 1985

Human Growth Hormone & Creutzfeldt-Jakob Disease
Ann Int Med 103:288-289, Raiti,S., 1985

Creutzfeldt-Jakob Disease in a Young Adult with Idiopathic Hypopituitarism, Relation to Growth Hormone
NEJM 313:731-733, Koch,T.K.,et al, 1985

Clinical & Path Features & Lab Confirmation of Creutzfeldt-Jakob Disease with Pituitary Derived Human Growth Hormone
NEJM 313:734-738, Gibbs,C.J.,et al, 1985

Subacute Spongiform Encephalopathy (Creutzfeldt-Jakob Disease) with Amyloid Angiopathy
JNNP 48:1175-1178, Keohane,C.,et al, 1985

Cysticercosis-Review of 230 Patients
Bull Clin Neurosci 50:76-101, McCormick.G.F., 1985

Bitemporal Hypometabolism in Creutzfeldt-Jakob Disease Measured by Positron Emission Tomography
J Comput Assist Tomogr 8:978-981, Friedland,R.P.,et al, 1984

Sodium Hydroxide Decontamination of Creutzfeldt-Jacob Disease Virus
NEJM 310:727, Brown,P.,et al, 1984

Creutzfeldt-Jakob Disease:A Case of 16 Years Duration
Ann Neurol 15:107-110, Cutler,N.R.,et al, 1984

Clinicopathological Conference
Case 49-1983, Creutzfeldt-Jakob, NEJM 309:1440-1449983., , 1983

The Effect of Amantadine on Arousal & EEG Patterns of Creutzfeldt-Jakob Disease
Arch Neurol 40:555-559, Terzano,M.G.,et al, 1983

Limbic Encephalopathy as a Nonmetastatic Complication of Oat Cell Lung Cancer
Am J Med 75:518-520, Brennan,L.V.,et al, 1983

Chemical Disinfection Of Creutzfeldt-Jakob Disease Virus
NEJM 306:1279-1282, Brown,P.,et al, 1982

Leukoencephalopathy After Inhaling"Heroin"Pyrolysate
Lancet 2:1233-1237, Wolters,E.C.,et al, 1982

Autonomic Dysfunction in Subacute Spongiform Encephalopathy
Arch Neurol 38:114-117, Khurana,R.K.,et al, 1981

Abrupt Neurological Deterioration in Children With Kearns-Sayre Syndrome
Arch Neurol 38:247-250, Coulter,D.L.,et al, 1981

Ophthalmoplegia-Plus
Arch Neurol 38:423-426, Okamoto,T.,et al, 1981

Computed Tomography in the Diagnosis of Canavan's Disease
Ann Neurol 10:57-60, Rushton,A.R.,et al, 1981

Computerized Tomography in Subacute Necrotizing Encephalomyelopathy (Leigh Disease)
Ann Neurol 10:268-271, Schwartz,W.J.,et al, 1981

Biologic Distinction Between Sporadic & Familial Alzheimer Disease by an in vitro Cell Fusion Test
Neurol 31:323-325, Dubois-Moreau,M.C.,et al, 1981

Amyotrophic Lateral Sclerosis & its Association with Dementia, Parkinsonism & Other Neurological Disorders:A Review
Brain 104:217-247, Hudson,A.J., 1981

Hyper-Endorphin Syndrome in a Child With Necrotizing Encephalomyelopathy
NEJM 303:914-916, Brandt,N.J.,et al, 1980

Serial EEG Findings in 27 Cases of Creutzfeldt-Jakob Disease
Arch Neurol 37:143-145, Chiofalo,N.,et al, 1980

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

Periodic Lateralized Epileptiform Complexes (PLEDs) in Creutzfeldt-Jakob Disease
Neurol 30:611-617, Au,W.J.,et al, 1980

Familial Subacute Necrotizing Encephalomyelopathy of the Adult Form (Adult Leigh Syndrome)
Ann Neurol 6:200-206, Kalimo,H.,et al, 1979

Clinical Similarity of Alzheimer & Creutzfeldt-Jakob Disease
Ann Neurol 6:368-369, Watson,C.P., 1979

Neurology:An Annotated Bibliography of Recent Literature
Ann Int Med 91:658-663, , 1979

Creutzfeldt-Jakob Disease Treated with Amantadine
JNNP 42:960-961, Sanders,W.L., 1979

Leigh's Disease in an Adult with Evidence of"Inhibitor Factor"in Family Members
Ann Neurol 3:519, Whetsell,W.O.,et al, 1978

Kearns-Sayre Syndrome with Hypoparathyroidism
Ann Neurol 3:513, Horwitz,S.J.,et al, 1978

Bilateral Oculomotor Paralysis Due to Neurosyphilis
Ann Neurol 3:90, Jordan,K.,et al, 1978

Computerized Cranial Tomography in Cerebral Diseases of White Matter
Neurol 28:534, Lane,B.,et al, 1978

CT Scan Appearances in Leigh's Disease (Subacute Necrotizing Encephalomyelopathy)
Neuroradiology 16:48-50, Hall,K.,et al, 1978

Computed Tomography in the Diagnosis of Creutzfeldt-Jakob Disease
J Comput Assist Tomogr 1:211-215, Krishna,C.V.G.,et al, 1977

Creutzfeldt-Jakob Disease:Possible Association with Eating Brains
NEJM 296:820, 1977. (Letter), Alter,M.,et al, 1977

Whipple's Disease Confined to the Brain:A Case Studied Clinically & Pathologically
JNNP 40:901, Romanul,F.C.A.,et al, 1977

Neuro-Behcet Disease:Two Cases & Neuroradiologic Findings
Neurol 27:1148, Kozin,F.,et al, 1977

Whipple's Disease with Predominating Neuro-ophthalmic Manifestations
Ann Neurol 1:247-252, Finelli,P.F.,et al, 1977



Showing articles 450 to 500 of 4355 << Previous Next >>