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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
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antiviral agents
areflexia
asymptomatic
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ataxia, cerebellar
ataxia, hereditary
ataxic gait
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autoimmune disease
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bacterial infection
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basal ganglia, lesion of
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basilar artery occlusion
blindness
blood transfusion
bovine spongiform encephalopathy
brain biopsy
cardiac transplantation
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central pontine myelinolysis
cerebellar plaques, amyloid
cerebellum, disease of
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cerebral venous thrombosis, deep
cerebrospinal fluid
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cerebrovascular accident
chromosomal abnormality
Clinical Pathologic Conference(C.P.C.)
coma
concentration, impaired
confusion
corneal transplant
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cortical infarction
Creutzfeldt-Jakob disease, genetic
deep gray nuclei
degenerative diseases of CNS
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demyelinating disease
differential diagnosis
electroencephalogram
electroencephalogram, abnormalities of
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electrophoretic pattern, CSF
encephalitis
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epidemiology of neurology
experimental allergic encephalitis
eye movement, disorders of
Fabry's disease
familial
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flu-like illness
frontal lobe, pathologic signs of
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gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
genetic counselling
genetic linkage
genetic neurologic disorders
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glioma
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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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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
MRI, demyelinating disease
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MRI, early changes in CVA
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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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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 250 to 300 of 4355 << Previous Next >>

HIV-associated Neurologic Disease Incidence Changes: Multicenter AIDS Cohort Study, 1990-1998
Neurol 56:257-260, Sacktor,N.,et al, 2001

Bovine Spongiform Encephalopathy and Variant Creutzfeldt-Jakob Disease
BMJ 322:841-844, Brown,P., 2001

The Incidence of Mitochondrial Encephalomyopathies in Childhood: Clinical Features and Morphological, Biochemical, and DNA Abnormalities
Ann Neurol 49:377-383, Darin,N.,et al, 2001

Creutzfeldt-Jakob Disease: Serial Changes on Diffusion-Weighted MRI
J Comput Assist Tomogr 25:274-277, Matoba,M.,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

New Variant Creutzfeldt-Jakob Disease Presenting with Loss of Taste and Smell
JNNP 71:412-413, Reuber,M.&Al-Din,A.S.N., 2001

Dementia with Lewy Bodies in a Neuropathologic Series of Suspected Creutzfeldt-Jakob Disease
Neurol 55:1401-1404, Haik,S.,et al, 2000

Magnetic Resonance Imaging in the Clinical Diagnosis of Creutzfeldt-Jakob Disease
Arch Neurol 57:1751-1757, Schroter,A.,et al, 2000

Clinicopath Conf,Cerebral Amyloid Angiogpathy and Giant-Cell Inflammatory Reaction to Beta 4-Amyloid and Vasculitis, Case 10-2000
NEJM 342:957-965, , 2000

The Pulvinar Sign on Magnetic Resonance Imaging in Variant Creutzfeldt-Jakob Disease
Lancet 355:1412-1418,1384, Zeidler,M.,et al, 2000

Highly Active Antiretroviral Therapy for Patients with AIDS Dementia Complex: Effect on MR Imaging Findings and Clinical Course
AJNR 21:670-678, Thurnher,M.M.,et al, 2000

Diagnosis of New Variant Creutzfeldt-Jakob Disease
Ann Neurol 47:575-582, Will,R.G.,et al, 2000

Risk of Acquiring Creutzfeldt-Jakob Disease from Blood Transfusions: Systematic Review of Case-Control Studies
BMJ 321:17-19, Wilson,K. et al, 2000

FLAIR MRI in sporadic Creutzfeldt-Jakob Disease
Neurol 55:147-148, Vrancken,A.F.J.E. et al, 2000

14-3-3 Testing in Diagnosing Creutzfeldt-Jakob Disease
Neurol 55:514-516, Lemstra,A.W. et al, 2000

Incidence and Prevalence of Neurological Disorders Associated with HIV Since the Introduction of Highly Active Antiretroviral Therapy (HAART)
JNNP 69:376-380, Maschke,M. et al, 2000

Current Clinical Diagnosis in Creutzfeldt-Jakob Disease; Identification of Uncommon Variants
Ann Neurol 48:323-329, Zerr,I. et al, 2000

Leigh Syndrome: Serial MR Imaging and Clinical Follow-Up
AJNR 21:1502-1509, Arii,J. & Tanabe,Y., 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

Misleading Results With the 14-3-3 Assay for the Diagnosis of Creutzfeldt-Jakob Disease
Neurol 55:1396-1397, Chapman,T.,et al, 2000

Heroin-Induced Spongiform Leukoencephalopathy: Value of Diffusion MF Imaging
J Comput Assist Tomog 24:735-737, Chen,C.,et al, 2000

Variant Creutzfeldt-Jakob Disease in UK children: A National Surveillance Study
Lancet 356: 1224-1227, Verity,C.M.,et al, 2000

Iatrogenic Creutzfeldt-Jakob Disease at the Millenium
Neurol 55:1075-1081, Brown,P.,et al, 2000

Alien Hand Sign in Creutzfeldt-Jakob Disease
JNNP 68:103-104, Inzelberg,R.,et al, 2000

Seizures and Creutzfeldt-Jakob Disease
NCMJ 60:108-109, Cokgor,I.,et al, 1999

Creutzfeldt-Jakob Disease Presenting as Complex Partial Status Epilepticus: A Report of Two Cases
JNNP 66:406-407, Rees,J.H.,et al, 1999

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

Surgical Treatment and Risk of Sporadic Creutzfeldt-Jakob Disease:A Case-Control Study
Lancet 353:693-697, Collins,S.,et al, 1999

The Heidenhain Variant of Creutzfeldt-Jakob Disease
Arch Neurol 56:55-61, Kropp,S.,et al, 1999

Progressive Aphasia with Rapidly Progressive Dementia in a 49 Year Old Woman
JNNP 66:238-243, Greene,J.D.W.,et al,, 1999

Highly Active Antiretroviral Therapy Reverses Brain Metabolite Abnormalities in Mild HIV Dementia
Neurol 53:782-789, Chang,L.,et al, 1999

Abnormal Diffusion-Weighted Magnetic Resonance Images in Creutzfeldt-Jakob Disease
Arch Neurol 56:577-583, Bahn,M.M.,&Parchi,P., 1999

Mortality from Dementia in Occupations at Risk of Exposure to Bovine Spongiform EncephalopathyAnalysis of Death Registrations
BMJ 318:1044-1045, Aylin,P.,et al, 1999

Prion Protein Conformation in a Patient with Sporadic Fatal Insomnia
NEJM 340:1630-1638,1675, Mastrianni,J.A.,et al, 1999

Clinicopath Conf, Creutzfeldt-Jakob Disease,Case 28-1999
NEJM 341:901-908, , 1999

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

Creutzfeldt-Jacob Disease in a Husband and Wife
Neurol 50:684-688, Brown,P.,et al, 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

Regress of HIV Enceph & Basal Ganglia Signal Intensity Abnor MRI in AIDS after Protease Inhibitor
Neuroradiology 206:491-498, Filippi,C.G.,et al, 1998

Retinocochleocerebral Vasculopathy
Medicine 77:12-40, Petty,G.W.,et al, 1998

Susac Syndrome
Medicine 77:3-11, Papo,T.,et al, 1998

Imaging the Brain, Part 1 & 2
NEJM 338:812-820, 889-8961998., Gilman,S., 1998

Acute Leukoencephalopathies:Differential Diagnosis and Investigation
The Neurologist 4:148-166, Weinshenker,B.G.,et al, 1998

An Unusual Case of Creutzfeldt-Jakob Disease
Neurol 51:617-619, Vingerhoets,F.J.G.,et al, 1998

Case-Control Study of Risk Factors of Creutzfeldt-Jacob Disease in Europe During 1993-95
Lancet 351:1081-1085, Van Duijn,C.M.,et al, 1998

Creutzfeldt-Jakob Disease (CJD) after Blood Product Transfusion From a Donor with CJD
Neurol 50:1872-1873, Patryk,D.,et al, 1998



Showing articles 250 to 300 of 4355 << Previous Next >>