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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
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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
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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
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dementia, prevention of
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demyelinating disease
differential diagnosis
electroencephalogram
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electrophoretic pattern, CSF
encephalitis
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endemic area
endoscopy
epidemic
epidemiology of neurology
experimental allergic encephalitis
eye movement, disorders of
Fabry's disease
familial
fatal familial insomnia
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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
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headache
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hemiparesis
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herpes simplex virus
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human immunodeficiency virus type 1
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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
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MRI, artifacts
MRI, cerebrovascular disease
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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
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MRI, negative
MRI, T1 weighted high signal foci
multiple sclerosis
mutism
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myoclonic jerks
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myoclonus, stimulus sensitive
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neurofibrillary degeneration
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neurologic disease, diagnoses of
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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
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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 350 to 400 of 4355 << Previous Next >>

MR Diagnosis of Creutzfeldt-Jakob Disease:Significance of High Signal Intensity of the Basal Ganglia
AJR 162:137-140, Barboriak,D.P.,et al, 1994

Iatrogenic Creutzfeldt-Jakob Disease:An Example of the Interplay Between Ancient Genes and Modern Medicine
Neurol 44:291-293, Brown,P.,et al, 1994

MRI Abnormalities in Creutzfeldt-Jakob Disease
Neuroradiology 35:584-585, DiRocco,A.,et al, 1993

The Mutations at nt 8993 of Mitochondrial DNA is a Common Cause of Leigh's Syndrome
Ann Neurol 34:827-834, Santorelli,F.M.,et al, 1993

TORCH Infections in the Newborn
Semin Neurol 13:106-115, Donley,D.K., 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

Molecular Genetic Characterization of an X-Linked Form of Leigh's Syndrome
Ann Neurol 33:652-655, Matthews,P.M.,et al, 1993

Positron Emission Tomographjy and Histopathology in Creutzfeldt-Jakob Disease
Neurol 43:1828-1830, Goldman,S.,et al, 1993

Real and Imagined Clinicopathological Limits of"Prior Dementia"
Lancet 341:127-129, Brown,P.,et al, 1993

Ziduvudine Treatment of the AIDS Dementia Complex:Results of a Placebo-Controlled Trial
Ann Neurol 33:343-349, Sidtis,J.J.,et al, 1993

Creutzfeldt-Jakob Disease in a Physician:A Review of the Disorder in Health Care Workers
Neurol 43:205-206, Berger,J.R.&David,N.J., 1993

Inherited Prion Disease (PrP lysine 200) in Britain:Two Case Reports
BMJ 306:301-302, 2881993., Collinge,J.,et al, 1993

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

Gerstmann-Straussler-Schneinker Syndrome:MR Findings
J Comput Assist Tomogr 17:326-327, Wimberger,D.,et al, 1993

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

Analysis of the Prion Protein Gene in Thalamic Dementia
Neurol 42:1859-1863, Petersen,R.B.,et al, 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

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

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

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

Shunting Normal-Pressure Hydrocephalus:Do the Benefits Outweigh the Risks? A Multicenter Study and Literatire Review
Neurol 42:54-59, Vanneste,J.,et al, 1992

Prion Disease
NEJM 326:486-487, Johnson,R.T., 1992

Spinal Cord Syphilis Associated with Human Immunodeficiency Virus Infection:A Treatable Myelopathy
Am J Med 91:101-103, Berger,J.R., 1992

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

Clinicopath Conf
Infantile Striatonigral Regeneration, with Cerebellar Degeneration, Familial, Case 30-1992, NEJM 327, 261-1992., 1992

Progressive Language Disorder Due to Lobar Atrophy
Ann Neurol 31:174-183, Snowden,J.S.,et al, 1992

Fatal Familial Insomnia, A Prion Disease with a Mutation at Codon 178 of the Prion Protein Gene
NEJM 326:444-449, Medori,R.,et al, 1992

Fatal Familial Insomnia:Clinical and Pathologic Study of Five New Cases
Neurol 42:312-319, Manetto,V.,et al, 1992

Fatal Familial Insomnia:A Second Kindred with Mutation of Prion Protein Gene at Codon 178
Neurol 42:669-670, 1992, Medori,R.,et al, 1992

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

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

Use of CT, MRI, & Localized 1H MR Spectroscopy in Canavan's Disease:A Case Report
Ann Neurol 30:106-110, Marks,H.G.,et al, 1991

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

Clinicopath Conf
Tertiary Neurosyphilis, Case 32-1991, NEJM 325:414-422991., , 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

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

Neurodegenerative Diseases of Childhood:MR and CT Evaluation
J Comput Assist Tomogr 15:210-222, Mirowitz,S.A.,et al, 1991

Infantile CNS Spongy Degeneration-14 Cases:Clinical Update
Neurol 40:1876-1882, Gascon,G.G.,et al, 1990

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

Neurologic Manifestations of Giant Cell Arteritis
Am J Med 89:67-72, Reich,K.A.,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

Progressive Rubella Panencephalitis
In Handbk of Clin Neurol, Vinken & Bruyn, Ed, N Holland Publ Co, 56:405-416, Wolinsky,J.S., 1990

MR Findings in Patients with Subacute Necrotizing Encephalomyelopathy (Leigh Syndrome)
AJR 154:1269-1274, Medina,L.,et al, 1990

Clinicopath Conf
Primary (Granulomatous) Angiitis of Central Nervous System, Case Record 8-1989, NEJM 320:514-5249., , 1989



Showing articles 350 to 400 of 4355 << Previous Next >>