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Differential
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abscess, intracerebral

acquired immunodeficiency syndrome

adenine arabinoside

advances in neurology

adverse drug reaction

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

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

anticonvulsants, untoward effects of

antithyroid antibodies

aphasia, transcortical

aphasia, transcortical-sensory

autonomic dysfunction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basilar artery occlusion

bovine spongiform encephalopathy

bradykinesia

bradyphrenia

brain biopsy

brain biopsy, complications of

brain biopsy, false negative

brain biopsy, indication

brain biopsy, negative

brain scan

carbamazepine

carbamazepine, toxicity

carbon monoxide poisoning

carcinoma

carcinoma of breast

cardiac transplantation

CAT scan

CAT scan, abnormal

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

caudate nucleus, lesion of

caudate nucleus, lesion of, bilateral

cell fusion test

central nervous system, infection of

central pontine myelinolysis

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar lesion

cerebellum, disease of

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, oligoclonal IgG in

cerebrospinal fluid, protein of

cerebrovascular accident

cerebrovascular accident, mimics

cerebrovascular accident, misdiagnosis

Charles Bonnet's syndrome

children

chorea

choreoathetosis

chromosomal abnormality

chromosome 20

cingulate gyrus

Clinical Pathologic Conference(C.P.C.)

cognition

cognition, slowed

cogwheel rigidty

color vision, impaired

coma

comorbidities

complications

concentration, impaired

confusion

contactin associated protein like 2 antibodies

controversies in neurology

corneal transplant

cortical blindness

cortical infarction

cortical-basal ganglionic degeneration

Creutzfeldt-Jakob disease, genetic

deep gray nuclei

degenerative diseases of CNS

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)

differential diagnosis

difficulty climbing stairs

diplopia

disorientation

dissociated sensory loss

dizziness

driving

drug induced neurologic disorders

drug withdrawal

dural graft, cadaveric

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

epidemiology of neurology

epilepsia partialis continua

episodic disorders

executive dysfunction

experimental allergic encephalitis

extrapyramidal

eye movement, disorders of

Fabry's disease

faciobrachial dystonic seizure

fatal familial insomnia

fatigue

fever

fibrillations

finger nose finger test

Fisher C.M.

flavivirus

flu-like illness

follicle stimulating hormone

frontal lobe, anatomy and physiology

frontal lobe, pathologic signs of

gait disorder

gait, apraxic

gamma amino butyric acid receptor antibody

gaze palsy

gaze palsy, supranuclear

genetic neurologic disorders

genetic testing

Gerstmann syndrome

Gerstmann-Straussler-Scheinker disease

glioma

gliosis

glycine receptor antibodies

Hallervorden Spatz disease

hallucination

hallucination, visual

hallucination, visual, benign

hemianopia, homonymous

hemiparesis

hepatolenticular degeneration(Wilson's disease)

heralding manifestation

herpes simplex encephalitis

herpes simplex virus

herpes virus infection

hockey stick sign

homograft

hot cross bun sign

human immunodeficiency virus type 1

Huntington's chorea

hydrocephalus

hydrocephalus, normal pressure

hypoxic encephalopathy

iatrogenic neurologic disorders

immunosuppressive agents

intellectual deterioration

interferon

interobserver agreement

intracerebral hemorrhage

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

kuru

kuru plaques

laminar necrosis, cortical

leucine rich glioma inactivated 1 antibodies

leukoencephalitis, acute necrotizing hemorrhagic

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

memory, defect of recent

memory, impairment of

meningitis

meningoencephalitis

mental status, abnormal

Mini Mental Status Examination

misdiagnosis

mitochondrial disease

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, demyelinating disease

MRI, diffusion tensor

MRI, diffusion weighted

MRI, diffusion weighted, pattern

MRI, early changes in CVA

MRI, high signal foci on

MRI, high signal intensity of basal ganglia

MRI, punctate pattern

MRI, serial

MRI, spinal cord

MRI, susceptibility weighted

MRI, T1 weighted high signal foci

multiple sclerosis

multiple system atrophy

myelitis, longitudinal

myoclonus, differential diagnosis of

myoclonus, stimulus sensitive

nasal brushings

negative

neoplasm, intracranial

neoplasm, metastatic to CNS

neoplasm, pituitary

neoplasm, primary intracerebral

neoplasm, primary of CNS

nerve conduction studies

neurofibrillary degeneration

neurofibromatosis 1

neurologic complications of, surgery

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

nucleus basalis of Meynert

nystagmus

nystagmus, periodic alternating

occipital cortex

occipital lobe

occipital lobe, lesion of

occupational neurologic disorders

ocular motility, disorders of

old age, neurology of

organ transplantation

osmotic demyelination syndrome

parietal lobe, lesion of

parietal lobe, syndromes of

Parkinson disease

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

perseveration

personality change

pituitary, hormones of

PLEDs

PLEDs, bilateral independent

pleocytosis of cerebrospinal fluid

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

prevention of neurologic disorders

prion disease

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

pulvinar sign

pursuit eye movements, abnormal

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

rapidly fatal neurologic illness

rapidly progressing neurologic illness

real-time quaking-induced conversion

release phenomena

remote effect of cancer on the nervous system

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

seizure, nonconvulsive

single photon emission computed tomography

skin, biopsy

sleep

sleep pathology and physiology

slow virus infection of CNS

spinal cord, lesion of

spongy degeneration of brain

status epilepticus, nonconvulsive

steroid

steroid therapy, CNS treatment and complications with

stiff legs

striatum, lesion of

striatum, lesion of, bilateral

subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease

symmetric brain lesions

temporal lobe, status

thalamic tumors

thalamic tumors, bilateral

thalamus

thalamus, infarction of

thalamus, infarction, bilateral

thalamus, lesion of

thalamus, lesion of-bilateral

treatment of neurologic disorder

visual acuity, decreased

visual loss, progressive

walking frame

walking, difficulty with

Wallerian degeneration

Wernicke's encephalopathy

West Nile fever

Western immunoblot test

Showing articles 250 to 292 of 292 << Previous

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

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

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

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

Creutzfeldt-Jakob Disease of Long Duration:Clinicopathological Characteristics
Ann Neurol 16:295-304, Brown,P.,et al, 1984

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

Supranuclear Gaze Palsy in Familial Creutzfeldt-Jakob Disease
Arch Neurol 40:618-622, Bertoni,J.M.,et al, 1983

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

Repeated Suppression Of Creutzfeldt-Jakob Disease With Vidarabine
Jr. , et al, Lancet 2:564-56582., Furlow,T.W., 1982

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

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

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

Transissible Dementias:Current Problems in Tissue Handling
Neurol 30:302-303, Baringer,J.R.,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

Evidence For & Against the Transmissibility of Alzheimer Disease
Neurol 30:945-950, Goudsmit,J.,et al, 1980

Clin. Path. Conference
Creutzfeldt-Jakob Disease, Ataxic Type, with Kuru Plaques, Case Record 45-1980, NEJM 303:1162-11710., , 1980

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

Failure of Interferon to Modify Creutzfeldt-Jakob Disease
BMJ 280:902, Kovanen,J.,et al, 1980

Alzheimer Neurofibrillary Tangles in Diseases Other Than Senile & Presenile Dementia
Ann Neurol 5:288-294, Wisniewski,K.,et al, 1979

Creutzfeldt-Jakob Disease:Patterns of Worldwide Occurrence & the Significance of Familial & Sporadic Clustering
Ann Neurol 5:177-188, Masters,C.L.,et al, 1979

Studies in Aging of the Brain:IV. Familial Alzheimer Dis. :Relat. to Transmiss. Demetia, Aneuploidy, & Microtubular Defects
Neurol 29:1402, Book,R.H.,et al, 1979

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

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

Precautions in Familial Transmissible Dementia
Arch Neurol 35:697-698, Cook,R.,et al, 1978

Subacute Spongiform Encephalopathy (Creutzfeldt-Jakob Disease)
Brain 101:333-344, Masters,C.L.,et al, 1978

Precautions in Medical Care Handling Matrl. of Patients with Transmissible Virus Dementia (Creutzfeldt-Jakob Disease)
NEJM 297:1253, Gajdusek,C.,et al, 1977

Clinical Pathologic Conference, Creutzfeldt-Jakob Disease, (Case record 43-1977)
NEJM 297:930, Scully,R.E.,et al, 1977

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

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

Viral Infections & Demylinating Diseases
NEJM 288:1103, Weiner,J.,et al, 1973

The Association of Parkinsonism & Motor Neuron Disease
Neurol 22:443, Brait,K., 1972

Progressive Dementia-"Aspects of Diagnosis"
Hospital Physician, Nov 1970, p. 84., , 1970

Spastic Pseudosclerosis (Creutzfeldt-Jakob Dis) Van Rossum A. , In:Vinken, P. J.
Handbk of Clin Neurol Vol 6 North-Holland Publ. Amster 1968 Ch 28, p 726., Bruyn,G.W., 1968

Neuro CPC of MGH
Jacob-Creutzfeldt Disease, NEJM 264:1359-13641961., , 1961

Clinical Picture in Creutzfeldt-Jakob Disease
Trans of Amer Neuro Assn 5:l47, Fisher,C.M., 1960

Showing articles 250 to 292 of 292 << Previous