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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 150 to 200 of 4355 << Previous Next >>

Limbic Encephalitis as the Presenting Feature of Sj�gren Syndrome
Neurol Clin Pract 3:165-167, Finelli, P. & Inoa, V., 2013

Clinicopathologic Conferences, Celiac Disease, Addisons Disease, and Major Depression Disorder
NEJM 368:2015-2024, Case 16-2013, 2013

Clinicopathologic Conference, Blind and Confused, Neuromyelitis Optica Spectrum Disorder
JAMA Neurol 70:932-936, Sharma, V.,et al, 2013

Subacute Sclerosing Panencephalitis
www.MedLink.com, February, Auwaeter,P.G.&Johnson,R.T., 2013

Aspergillus Meningitis: A Rare Clinical Manifestation of Central Nervous System Aspergillosis
J Infect 66:218-238, Antinori, S.,et al, 2013

Meningoencephalitis from Borrelia Miyamotoi in an Immunocompromised Patient
NEJM 368:240-245, Gugliotta, J.L.,et al, 2013

Sporadic Creutzfeldt-Jakob Disease with Focal Findings: Caveats to Current Diagnostic Criteria
Neurol Internat 5:1-5, Mader, E.C.,et al, 2013

Cerebral White Matter Disruption in Creutzfeldt-Jakob Disease
AJNR 33:1945-1950, Lee,H.,et al, 2012

Cerebral Syphilitic Gumma: A Case Report and Review of the Literature
Neurol Sci 33:1179-1181, Li, J.C.,et al, 2012

Neurological Disorders in Primary Sjogrens Syndrome
Autoimmune Dis: DOI: ID.1152012/645967, Tobon, G.J.,et al, 2012

Neurosyphilis Versus Herpes Encephalitis in a Patient with Confusion, Memory Loss, and T2-Weighted Mesiotemporal Hyperintensity
Case Rep Infect Dis 2012:154863, Vedes,E.,et al, 2012

Evidence-based Guideline: Diagnostic accuracy of CSF 14-3-3 Protein in Sporadic Creutzfeldt-Jakob Disease
Neurol 79:1499-1506, Muayqil, T.,et al, 2012

Differential Diagnosis of Jakob-Creutzfeldt Disease
Arch Neurol 69:1578-1582,1554, Paterson, R.,et al, 2012

A Comparison of Tau and 14-3-3 Protein in the Diagosis of Creutzfeldt-Jakob Disease
Neurol 79:547-552, Hamlin, C.,et al, 2012

Cortical Restricted Diffusion as the Predominant MRI Finding in Sporadic Creutzfeldt-Jakob Disease
Acta Radiologica 52:336-339, Talbott,S.D.,et al, 2011

Differential Diagnosis of Bilateral Abnormalities of the Basal Ganglia and Thalamus
RadioGraphics 31:5-30, Hegde,A.N.,et al, 2011

Encephalitis and antibodies to synaptic and neuronal cell surface proteins
Neurol 77:179-189, Lancaster, E.,et al, 2011

Rapidly Progressive Alzheimer Disease
Arch Neurol 68:1124-1130, Schmidt, C.,et al, 2011

Treatable Neurological Disorders Misdiagnosed as Creutzfeldt-Jakob Disease
Ann Neurol 70:437-444, Chitravas, N.,et al, 2011

Cerebral Amyloid Angiopathy Related Inflammation: Three Case Reports and a Review
JNNP 82:20-26, Chung,K.K.,et al, 2011

Fulminant Encephalopathy With Basal Ganglia Hyperintensities in HIV-Infected Drug Users
Neurol 76:787-794, Newsome,S.D.,et al, 2011

The Evaluation of Rapidly Progressive Dementia
The Neurologist 17:67-74, Rosenbloom,M.H. &Atri,A., 2011

Diffusion-weighted MRI hyperintensity patterns differentiate CJD from other rapid dementias
Neurol 76:1711-1719, Vitali, P.,et al, 2011

Diagnosing variant Creutzfeldt-Jakob disease: a retrospective analysis of the first 150 cases in the UK
JNNP 82:646-651, Heath, C.A.,et al, 2011

Rapidly Progressive Corticobasal Degeneration Syndrome
Case Rep Neurol 3:185-190, Herrero Valverde, A.,et al, 2011

Brain Biopsy in Children With Primary Small-Vessel Central Nervous System Vasculitis
Ann Neurol 68:602-610, 573, Elbers,J.,et al, 2010

Clinicopath Conference: Secondary Syphilis Involving Skin and Optic Nerve (Neurosyphilis)
NEJM 363:865-874, Case 26: 2010, 2010

Atypical Dementia
Lancet 376:656, Cohen-Bittan,J. et al, 2010

Is the Diagnosis at Hand?
The Lancet 375:1134, Holmes,M.V., et al, 2010

Open Biopsy in Patients With Acute Progressive Neurologic Decline and Absence of Mass Lesion
Neurol 75:419-424, Schuette,A.J., et al, 2010

Sporadic Creutzfeldt-Jakob Disease Mimicking Nonconvulsive Status Epilepticus
Neurol 74:1995-1999, Lapergue,B., et al, 2010

The Use of Neuroimaging in the Diagnosis of Mitochondrial Disease
Dev Disabil Res Rev 16:129-135, Friedman, S.D.,et al, 2010

Subacute sclerosing panencephalitis: An Update
Dev Med Child Neurol 52:901-907, Guitierrez, J.,et al, 2010

Rapidly Progressive Neurodegenerative Dementias
Arch Neurol 66:201-207, Josephs,K.A.,et al, 2009

Pathologic Correlates of Diffusion MRI Changes in Creutzfeldt-Jakob Disease
Neurol 72:1425-1431, Manners,D.N.,et al, 2009

A 41-Year-Old Woman with Progressive Leg Weakness and Numbness, Dizziness, and Myalgia
Neurol 72:1262-1276, DiMauro,S.,et al, 2009

MRI Lesion Profiles in Sporadic Creutzfeldt-Jakob Disease
Neurol 72:1994-2001, Meissner,B.,et al, 2009

Diagnosis and Therapy in Neuromuscular Disorders: Diagnosis and New Treatments in Mitochondrial Diseases
JNNP 80:943-953, Rahman,S. &Hanna,M.G., 2009

Clinicopath Conf, Neuro-Behcets Disease
NEJM 360:2341-2351, Case 17-2009, 2009

Clinicopath Conf., Leighs syndrome, Intraventricular Hemorrhage and Periventricular Leukomalacia
NEJM 359:1156-1166, Case 28-2008, 2008

MR Imaging of Familial Creutzfeldt-Jakob Disease: A Blinded and Controlled Study
AJNR 29:1638-1643, Fulbright,R.K.,et al, 2008

Isolated Cortical Signal Increase on MR Imaging as a Frequent Lesion Pattern in Sporadic Creutzfeldt-Jakob Disease
AJNR 29:1519-1524, Meissner,B.,et al., 2008

Voltage-Gated Potassium Channel Autoimmunity Mimicking Creutzfeldt-Jakob Disease
Arch Neurol 65:1341-1346, Geschwind,M.D.,et al, 2008

Sporadic Creutzfeldt-Jakob Disease in Two Adolescents
JNNP 79:14-18, Murray,K.,et al, 2008

Systematic Review of Therapeutic Intervention in Human Prion Disease
Neurol 70:1272-1281, Stewart,L.A.,et al, 2008

Changes in the Incidence and Predictors of Human Immunodeficiency Virus-Associated Dementia in the Era of Highly Active Antiretroviral Therapy
Ann Neurol 63:213-221, Bhaskaran,K.,et al, 2008

Transmissible Spongiform Encephalopathy in the 21st Century: Neuroscience for the Clinical Neurologist
Neurol 70:713-722, Brown,P., 2008

Primary Central Nervous System Vasculitis with Prominent Leptomeningeal Enhancement
Arthritis Rheum:58:595-603, Salvarani, C.,et al, 2008

Differential Diagnosis of Bilateral Thalamic Lesions
Clin Neuroradiol 17:3-22, Linn,J.,et al, 2007

Whipples Disease
NEJM 356:55-66, Fenollar,F.,et al, 2007



Showing articles 150 to 200 of 4355 << Previous Next >>