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abscess, intracerebral

acquired immunodeficiency syndrome

adenine arabinoside

advances in neurology

adverse drug reaction

agnosia, visual

albumin transfusion

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

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

angiitis, isolated of CNS

animal exposure

anticonvulsants

anticonvulsants, untoward effects of

antithyroid antibodies

antiviral agents

aphasia, progressive

aphasia, transcortical

aphasia, transcortical-sensory

apolipoprotein E

apraxia, dressing

ataxia, cerebellar

ataxia, progressive

ataxia, truncal

autoimmune disease

autonomic dysfunction

axonal degeneration

bacterial infection

Balint's syndrome

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basilar artery occlusion

behavioral disorder

Behcet's syndrome

biologic markers

blood transfusion

bovine spongiform encephalopathy

brain biopsy, complications of

brain biopsy, false negative

brain biopsy, indication

brain biopsy, negative

carbamazepine, toxicity

carbon monoxide poisoning

carcinoma of breast

cardiac transplantation

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

choreoathetosis

chromosomal abnormality

cingulate gyrus

Clinical Pathologic Conference(C.P.C.)

cognition, slowed

cogwheel rigidty

color vision, impaired

concentration, impaired

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

delay in diagnosis

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)

diabetes mellitus

diagnostic criteria

differential diagnosis

difficulty climbing stairs

dissociated sensory loss

drug induced neurologic disorders

drug withdrawal

dural graft, cadaveric

dyschromatopsia

dysdiadochokinesia

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, complications with

electroencephalogram, depth electrode

electroencephalogram, focal delta activity

electroencephalogram, periodic complexes

electroencephalogram, triphasic delta waves

electron microscopy

electrophoretic pattern, CSF

electrophoretic pattern, serum

emotional lability

encephalitis, autoimmune

encephalitis, bornavirus

encephalitis, Japanese

encephalitis, paraneoplastic

encephalitis, viral

encephalomyelitis, postinfectious

encephalopathy, carcinomatous

encephalopathy, Hashimoto's

encephalopathy, metabolic

epidemiology of neurology

epilepsia partialis continua

episodic disorders

executive dysfunction

experimental allergic encephalitis

eye movement, disorders of

Fabry's disease

faciobrachial dystonic seizure

fatal familial insomnia

finger nose finger test

flu-like illness

follicle stimulating hormone

frontal lobe, anatomy and physiology

frontal lobe, pathologic signs of

gamma amino butyric acid receptor antibody

gaze palsy, supranuclear

gaze palsy, vertical

genetic counselling

genetic linkage

genetic neurologic disorders

genetic testing

Gerstmann syndrome

Gerstmann-Straussler-Scheinker disease

glycine receptor antibodies

gyrus, abnormal

Hallervorden Spatz disease

hallucination, visual

hallucination, visual, benign

headache, episodic

heel-knee-shin test

hemianopia, homonymous

hepatolenticular degeneration(Wilson's disease)

heralding manifestation

herpes simplex encephalitis

herpes simplex virus

herpes virus infection

hockey stick sign

hot cross bun sign

human immunodeficiency virus type 1

Huntington's chorea

hydrocephalus, normal pressure

hyperthyroidism

hypoxic encephalopathy

iatrogenic neurologic disorders

immunocompetent

immunodeficiency

immunohistochemistry

immunologic disease

immunosuppressive agents

incubation period

intellectual deterioration

interobserver agreement

intracerebral hemorrhage

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

laminar necrosis, cortical

laughing, pathologic

Leigh's disease

leucine rich glioma inactivated 1 antibodies

leukoencephalitis, acute necrotizing hemorrhagic

Lewy body disease, diffuse

life expectancy

limbic encephalitis

lipid storage disorder of CNS

liver transplantation

lymphoma involving CNS

lymphoma, primary of CNS

lysosomes, abnoral

malignancy screen

memory, defect of recent

memory, impairment of

meningoencephalitis

mental status, abnormal

Mini Mental Status Examination

mitochondrial disease

molecular genetics

Morvan's fibrillary chorea

motor neuron disease

movement disorder

movement disorder, drug induced

movement disorder, extrapyramidal

MRI, abnormal, seizure causing

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, false negative

MRI, false positive

MRI, functional

MRI, high signal foci on

MRI, high signal intensity of basal ganglia

MRI, indications for

MRI, lesion burden

MRI, proton density

MRI, punctate pattern

MRI, spinal cord

MRI, susceptibility weighted

MRI, T1 weighted high signal foci

multiple sclerosis

multiple system atrophy

muscle twitching

myelitis, longitudinal

myelitis, transverse

myoclonic jerks

myoclonus, action

myoclonus, cortical

myoclonus, differential diagnosis of

myoclonus, stimulus sensitive

nasal brushings

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, brain

Niemann-Pick disease

NMDA antagonists

nucleus basalis of Meynert

nystagmus, periodic alternating

occipital cortex

occipital lobe, lesion of

occupational neurologic disorders

ocular motility, disorders of

old age, neurology of

olfactory biopsy

olfactory cortex

olfactory mucosa

olfactory pathway

olfactory tract

organ transplantation

osmotic demyelination syndrome

palmomental response

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 material in the brain

pathologic reflex

peduncular hallucinosis

personality change

pituitary, hormones of

PLEDs, bilateral independent

pleocytosis of cerebrospinal fluid

polymerase chain reaction

polyneuropathy, chronic inflammatory demyelinating

pons, lesion of

posterior cortical atrophy

posterior leukoencephalopathy syndrome

postictal encephalopathy

potassium channel antibodies

practice guidelines

pregnancy, neurologic complications in

prevention of neurologic disorders

progressive infantile poliodystrophy

progressive multifocal leucoencephalopathy

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

psychomotor retardation

psychotic behavior

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

risk-benefit assessment

roving eye movements

saccadic eye movements, abnormal

sarcoidosis, CNS

seizure, nonconvulsive

sensory symptoms

serum S100 protein

simultanagnosia

single photon emission computed tomography

sleep pathology and physiology

slow virus infection of CNS

speech, pressured

spinal cord, lesion of

spongy degeneration of brain

square wave jerks

startle myoclonus

startle reaction

status epilepticus

status epilepticus, nonconvulsive

steroid therapy, CNS treatment and complications with

striatum, lesion of

striatum, lesion of, bilateral

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

symmetric brain lesions

tandem gait, ataxic

temporal lobe, status

thalamic tumors

thalamic tumors, bilateral

thalamus, infarction of

thalamus, infarction, bilateral

thalamus, lesion of

thalamus, lesion of-bilateral

toxic encephalopathy

treatment of neurologic disorder

tremor, intention

tuberous sclerosis

twitching, face

upgaze, paralysis of

urinary incontinence

vertigo, episodic

vibratory sensation

viral infection

viral infection, CNS

vision, blurred

visual acuity, decreased

visual distortions

visual field defect

visual impairment

visual loss, progressive

walking, difficulty with

Wallerian degeneration

weakness, acute

weakness, focal

Wernicke's aphasia

Wernicke's encephalopathy

West Nile fever

Western immunoblot test

white matter disease

wide based gait

Showing articles 200 to 250 of 292 << Previous Next >>

Creutzfeldt-Jakob Disease and Blood Transfusion
lancet 341:205-207, Esmonde,T.F.G.,et al, 1993

Clinicopath Conf
Spongiform Encephalopathy (Creutzfeldt-Jakob Disease) , with Amyloid (KURU) Plaques, Case 17-1993, N, JM 328:66,1993., 1993

Abnormal Eye Movements in Creutzfeldt-Jakob Disease
Ann Neurol 34:192-197, Grant,M.P.,et al, 1993

Familial Creutzfeldt-Jakob Disease (Codon 200 Mutation) with Supranuclear Palsy
Bertoni. J. M. , et al, JAMA 268:2413-2415., , 1992

Evaluation of Cerebral Biopsies for the Diagnosis of Dementia
Arch Neurol 49:28-31, Hulette,C.M.,et al, 1992

Creutzfeldt-Jakob Disease in a Pathologist
Neurol 42:463, Gorman,D.G.,et al, 1992

Protein Processing in Lysosomes:The New Therapeutic Target in Neurodegenerative Disease
Lancet 340:156-159, Mayer,R.J.,et al, 1992

Demonstration of the Transmissible Agent in Tissue From a Pregnant Woman with Creutzfeldt-Jakob Disease
NEJM 327:649, Tamai,Y.,et al, 1992

"Friendly Fire"in Medicine:Hormones, Homografts, and Creutzfeldt-Jakob Disease
Lancet 340:24-27, Brown,P.,et al, 1992

Drug Induced Creutzfeldt-Jakob Like Syndrome
J Psychiatr Neurosci 17:103-105, Finelli,P.F., 1992

Creutzfeldt-Jakob Disease in a Recipient of Human Pituitary-Derived Gonadotrophin:A Second Case
JNNP 55:1094-1095, Cochius,J.I.,et al, 1992

Serial MR Imaging in Creutzfeldt-Jakob Disease
Neuroradiology 33:364-367, Uchino,A.,et al, 1991

Genetic Predisposition to Iatrogenic Creutzfeldt-Jakob Disease
Lancet 337:1441-1442, Collinge,J.,et al, 1991

Creutzfeldt-Jakob Disease in a Patient with a Cadaveric Dural Graft
Neurol 41:940-941, Miyashita,K.,et al, 1991

Mortality, Neoplasia, & Creutzfeldt-Jakob Disease in Patients Treated with Human Pituitary Growth Hormone in the UK
BMJ 302:824-828, Buchanan,C.R.,et al, 1991

The Spongiform Encephalopathies, Editorial
JNNP 54:761-763, Will,R.G., 1991

Creutzfeldt-Jakob Disease and Other Transmissible Spongiform Encephalopathies
Ed, F. O. Bastian, Mosby Year Book, St. Louis 9:153, Maertens,P.&Quindlen,E.A., 1991

CT Appearance of Panencephalopathic and Ataxic Type of Creutzfeldt-Jakob Disease
J Comput Assist Tomogr 15:3332-3344, Berciano,J.,et al, 1991

Magnetic Resonance Imaging of Creutzfeldt-Jakob Disease
Ann Neurol 29:438-440, Milton,W.J.,et al, 1991

Dementia Presenting with Aphasia:Clinical Characteristics
JNNP 54:542-545, Mendez,M.F.&Zander,B.A., 1991

Creutzfeldt-Jakob Disease in Pituitary Growth Hormone Recipients in the United States
JAMA 265:880-884, Fradkin,J.E.,et al, 1991

Mutation of the Prion Protein in Libyan Jews with Creutzfeldt-Jakob Disease
NEJM 324:1091-1097, Hsiao,K.,et al, 1991

Familial Creutzfeldt-Jakob Disease without Periodic EEG Activity
Ann Neurol 28:585-588, Tietjen,G.E.&Drury,I., 1990

Rapid Detection of Creutzfeldt-Jakob Disease and Scrapie Prion Porteins
Neurol 40:110-117, Serban,D.,et al, 1990

A Simple & Effective Method for Inactivating Virus Infectivity from Patients with Creutzfeldt-Jakob Disease
Neurol 40:887-890, Brown,P.,et al, 1990

Positron Emission Tomography in Creutzfeldt-Jakob Disease
Arch Neurol 47:1035-1038, Holthodd,V.A.,et al, 1990

Inherited Human Prion Diseases
Neurol 40:1820-1827, Hsiao,K.&Prusiner,S.B., 1990

The Nucleus Basalis of Meynert in 20 Definite Cases of Creutzfeldt-Jakob Disease
JNNP 52:304-309, Cartier,L.,et al, 1989

Creutzfeldt-Jakob Disease Presenting as Isolated Aphasia
Neurol 39:55-58, Mandell,A.M.,et al, 1989

Transplanted Infections:Donor-To-Host Transmission with the Allograft
Ann Int Med 110:1001-1016, Gottesdiener,K.M., 1989

Transmission of Alpers'Disease (Chr Prog Encephalopathy) Produces Exper Creutzfeldt-Jakob Disease in Hamsters
Neurol 39:615-621, Manuelidis,E.E.,et al, 1989

Creutzfeldt-Jakob Disease without Periodic Sharp Wave Complexes:A Clinical, EEG, and Path Study
Neurol 38:1056-1060, Zochodne,D.W.,et al, 1988

A Creutzfeldt-Jakob Like Syndrome Due to Lithium Toxicity
JNNP 51:120-123, Smith,S.J.M.&Kocen,R.S., 1988

Human Growth Hormone Therapy & Creutzfeldt-Jakob Disease:A Drama in Three Acts
Pediatrics 81:85-92, Brown,P., 1988

Routine Use of Phenolized Formalin in Fixation of Autopsy Brain Tissue to Reduce Risk of Inadvert Trans of Creutzfeldt-Jakob Dis
NEJM 319:654, Brumback,R.A., 1988

Creutzfeldt-Jakob Disease:Correlation of MRI & Neuropathologic Findings
Neurol 38:1481-1482, Gertz,H.J.,et al, 1988

The Decline and Fall of Creutzfeldt-Jakob Disease Associated with Human Growth Hormone Therapy
Neurol 38:1135-1137, Brown,P., 1988

Creutzfeldt-Jakob Disease Following Pituitary-Derived Human Growth Hormone Therapy:A New American Case
Neurol 38:1131-1133, Marzewski,D.J.,et al, 1988

Rapidly Progressive Dementia Caused by Spongiform Encephalopathy
West J Med 148:313-319, Enos,B.E.&Vinters,H.V., 1988

The Epidemiology of Creutzfeldt-Jakob Disease:Conclusion of a 15-year Investigation in France & Review of the Literature
Neurol 37:895-904, Brown,P.,et al, 1987

Iatrogenic Creutzfeldt-Jakob Disease
Neurol 37:1520-1522, Rappaport,E.B., 1987

Prions & Neurodegenerative Diseases
NEJM 317:1571-1581, 15971987., Prusiner,S.B., 1987

Abnormal Proteins in the Cerebrospinal Fluid of Patients with Creutzfeldt-Jakob Disease
NEJM 315:279-283, Harrington,M.G.,et al, 1986

Unilateral Creutzfeldt-Jakob Disease
Neurol 36:1517-1520, Yamanouchi,H.,et al, 1986

Creutzfeldt-Jakob Disease:Clinical Analysis of a Consecutive Series of 230 Neuropathologically Verified Cases
Ann Neurol 20:597-602, Brown,P.,et al, 1986

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

Diagnosis of Creutzfeldt-Jakob Disease by Western Blot Identification of Marker Protein in Human Brain Tissue
NEJM 314:547-551, Brown,P.,et al, 1986

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

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

Creutzfeldt-Jakob Disease Prion Proteins in Human Brains
NEJM 312:73-78, Bockman,J.M.,et al, 1985

Showing articles 200 to 250 of 292 << Previous Next >>