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Differential
(Click to cross reference)
amphiphysin antibodies
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, atypical
ANA
aneurysm, abdominal aortic
aneurysm, aortic arch
animal exposure
anterior horn cell disease
anterior spinal artery
anterior spinal artery infarction
arachnoiditis
arbovirus
arm atrophy
arm weakness
arterial dissection, aorta
arterial dissection, vertebral
autoantibodies
Bagel sign
basal ganglia, lesion, bilateral
Behcet's syndrome
bladder dysfunction
brainstem, lesion of
burning paresthesia
buttock numbness
carcinoma
carcinoma of breast
carcinoma of lung
CAT scan, myelogram with
cauda equina
cauda equina, blood supply of
cauda equina, enhancement
cauda equina, lesion of
central cord syndrome
cerebellar lesion
cerebral cortex
cerebral venous thrombosis
cerebrospinal fluid, lactic acid concentration
cerebrovascular accident
children
cluster, geographic
complications
constipation
conus medullaris, lesion of
cranial nerve enhancement
cranial nerve palsies
cranial neuropathy
deep gray nuclei
dentate nuclei
dentate nuclei, lesion of
Desproges-Gotteron syndrome
diagnostic criteria
differential diagnosis
diplegia, brachial
disability, neurological
embolism
embolism, nucleus pulposus
encephalitis
encephalitis, Powassan
encephalitis, viral
endemic area
enterovirus
enterovirus infection of CNS
epidemiology of neurology
erectile dysfunction
Europe
facial nerve palsy, bilateral
familial
farmer
fasciculation
fever
fibrillations
flaccid paralysis
flail arm syndrome
flavivirus
gadolinium
gene mutation
genetic neurologic disorders
genital ulcerations
geographic location
gyrus, abnormal
headache
herniated disc
herniated disc, lumbar
herniation syndromes, intracranial
incontinence, fecal
Leber's hereditary optic neuropathy
leg weakness, bilateral
Leigh's disease
Man-In-The-Barrel syndrome
MELAS syndrome
meningeal enhancement
meningitis
meningitis, late neurologic sequelae in
meningitis, neurologic aspects and complications of
meningitis, neutrophilic
midbrain, lesion of
misdiagnosis
mitochondrial disease
molecular genetics
mortality
motor neuron disease
MRI
MRI pattern
MRI, abnormal
MRI, contrast enhanced
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, false negative
MRI, mass effect on
MRI, negative
MRI, ring sign
MRI, spinal cord
MRI, spinal cord, increased intramedullary cord signal
MRI, spine
MRI, target sign
myelitis
myelitis, autoimmune
myelitis, longitudinal
myelitis, transverse
myelopathy
myelopathy, acute
myelopathy, paraneoplastic
neck pain
nerve root enhancement
neurologic disease, diagnoses of
neuromyelitis optica (Devic's disease)
optic neuropathy, hereditary
oral ulcerations
overlap syndrome
owl's eye sign of spinal cord
pain
pain, anal
pain, back
pain, buttock
paralysis, acute
paralysis, acute areflexic
paraparesis
paraparesis, flaccid
paraparesis, progressive
paraplegia
Parkinsonism syndrome
perineum, numbness of
pleocytosis of cerebrospinal fluid
poliomyelitis-like illness
pons, lesion of
positive sharp waves
posterior fossa, lesion of
posterior fossa, mass of
prethrombotic state
prognosis
progressive neurologic disorder
putamen, lesion of, bilateral
quadriplegia
remote effect of cancer on the nervous system
respiratory tract infection
review article
risk factors
season
sensory level
sensory loss
serologic testing
skin, lesions in neurologic disorders
spinal cord
spinal cord, cervical
spinal cord, infarction of
spinal cord, ischemic lesion of
spinal cord, lesion of
spinal cord, vascular disorders Affecting
steroid
steroid therapy, CNS treatment and complications with
substantia nigra
suspended sensory loss
symmetric brain lesions
tethered spinal cord
thalamus, lesion of
thalamus, lesion of-bilateral
tick bite
tick-borne encephalitis
tonsillar herniation of cerebellum
treatment of neurologic disorder
urinary incontinence
urinary retention
uveitis
vertebral infarction
viral infection
viral infection, CNS
walking
weakness
weakness, proximal
West Nile fever
white matter disease
Showing articles 1500 to 1550 of 2488 << Previous Next >>

Acute Disseminated Encephalomyelitis:MR and CT Features
AJNR 17:104-109, Mader,I.,et al, 1996

Cortical Hyperintensity on Proton Density-Weighted Images:An MR Sign of Cyclosporine-Related Encephalopathy
AJNR 17:337-344, Jansen,O.,et al, 1996

Progressive Ataxia, Focal Seizures, and Malabsorption Syndrome in a 41 Year Old Woman
JNNP 60:225-230, Mumford,C.J.,et al, 1996

A Man with Weight Loss, Ataxia, and Confusion for 3 Months
Lancet 347:448, Beversdorf,D.,et al, 1996

Does Cryptic Gluten Sensitivity Play a Part in Neurological Illness?
Lancet 347:369-370, Hadjivassiliou,M.,et al, 1996

Proving the Worth of Neurologists?
Neurol 46:276-277, Hillen,M.E.&Sage,J.I., 1996

Recovery from Primary Deep Cerebral Venous Sinus Thrombosis with Recanalisation
Neuroradiology 37:645-648, Nagatoma,Y.,et al, 1996

The Neuromythology of Silicone Breast Implants
Neurol 46:308-314, Rosenberg,N.L., 1996

The Stroke Syndrome of Cortical Vein Thrombosis
Neurol 47:376-382, Jacobs,K.,et al, 1996

Natural History of Progressive Supranuclear Palsy & Clin Predictors of Survival:A Clinicopath Study
JNNP 61:615-620, Litvan,I.,et al, 1996

Delayed-Onset Cerebellar Syndrome
Arch Neurol 53:450-454, Louis,E.D.,et al, 1996

Evidence-Based Medicine, Critical Pathways, Practice Guidelines, & Managed Care:Prevention & Care of Stroke
Arch Neurol 53:867-871, Ringel,S.P.&Hughes,R.L., 1996

The Ambulatory Workload of Office-Based Neurologists
Arch Neurol 53:379-381, Menken,M., 1996

Assessment of Plasmapheresis
Report of the Therapeutics and Technology Assessment Subcommittee of the AAN, Neurol 47:840-8431996., , 1996

Cost-Effectiveness Analysis:What Is It and How Will It Influence Neurology
Ann Neurol 39:818-823, Holloway,R.G., 1996

The"Gulf War Syndrome"-Is There Evidence of Dysfunction in the Nervous System
JNNP 60:449-451, Jamal,G.A.,et al, 1996

The World-Wide Burden of Neurologic Disease
Neurol 47:21-25, Bergen,D.C., 1996

BSE Linked to New Variant of CJD in Humans
BMJ 312:795, 791, 843, 85496., , 1996

A New Variant of Creutzfeldt-Jakob Disease in the UK
Lancet 347:921-925, 915, 916, 91796., Will,R.G.,et al, 1996

Seven-Year Follow-up of Neurologic Involvement in Behcet Syndrome
Arch Neurol 53:691-694, Akman-Demir,G.,et al, 1996

MR Findings in Listerial Rhombencephalitis
AJNR 17:593-596, Alper,G.,et al, 1996

Brachial Plexopathy Associated with Human Granulocytic Ehrlichiosis
Neurol 46:1026-1029, Horowitz,H.W.,et al, 1996

Neurologic Consequences of HTLV-II Infection in Injection-Drug Users
Neurol 46:1556-1560, Dooneief,G.,et al, 1996

Wolfram Syndrome:Hereditary Diabetes Mellitus with Brainstem and Optic Atrophy
Ann Neurol 39:352-360, Scolding,N.J.,et al, 1996

Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities
Ann Neurol 39:343-351, Rahman,S.,et al, 1996

Niemann-Pick Disease Type C from Bench to Bedside
JAMA 276:561-564, Schiffmann,R., 1996

Neurological Signs, Aging, and the Neurodegenerative Syndromes
Arch Neurol 53:498-502, Waite,L.M.,et al, 1996

Cerebral Infarction Associated with Kearns-Sayre Syndrome-Related Cardiomyopathy
Neurol 46:826-828, Provenzale,J.M.,et al, 1996

Leptomeningeal Carcinomatosis:Presenting Features and Prognostic Factors
Arch Neurol 53:626-632, Balm,M.&Hammack,J., 1996

Opsoclonus
Semin Neurol 16:21-26, Averbuch-Heller,L.&Remler,B., 1996

Diffuse Lewy Body Disease:Clinical Features in Nine Cases without Coexistent Alzheimer's Disease
JNNP 60:531-538, Hely,M.A.,et al, 1996

Early CT Signs in Acute Middle Cerebral Artery Infarction:Predictive Value for Subsequent Infarct Locations and Outcome
Neurol 47:366-375, Moulin,T.,et al, 1996

Assessment:Electronystagmography, Report of the Therapeutics and Technology Assessment Subcommittee
Neurol 46:1763-1766, Ferguson,J.H.,et al, 1996

Profile of a Neurology Residency
Arch Neurol 52:1123-1126, D'Esposito,M., 1995

Clinicopath Conf
Granulomatous Angiitis of CNS, Case 33-1995, NEJM 333:1135-1143995., , 1995

Adult-Onset Spinocerebellar Dysfunction Caused by a Mutation in the Gene for the a-Tocopherol-Transfer Protein
NEJM 333:1313-1318, 13511995., Gotoda,T.,et al, 1995

Mitochondrial DNA and Disease
NEJM 333:638-644, Johns,D.R., 1995

Clinicopathological Study of 35 Cases of Multiple System Atrophy
JNNP 58:160-166, Wenning,G.K.,et al, 1995

Some Specific Clinical Features Differentiate Multiple System Atrophy (Striatonigral Variety) from Parkinson's Disease
Arch Neurol 52:294-298, Colosimo,C.,et al, 1995

Wernicke Encephalopathy with Symmetric Pericentral Involvement:MR Findings
J Comput Assist Tomogr 19:306-308, Yamashita,M.&Yamamoto,T., 1995

Clinical, Neuropath & Genetic Studies of Large Spinocerebellar Ataxia Type 1 (SCA1) Kindred: (CAG) n Early Premonitory Signs & Symp
Neurol 45:24-30, Genis,D.,et al, 1995

Autosomal Dominant Cerebellar Phenotypes:The Genotype has Settled the Issue
Neurol 45:1-5, Rosenberg,R.N., 1995

Exercise-Related Dissection of Craniocervical Arteries:CT, MR and Angiographic Findings
J Comput Assist Tomogr 19:268-276, Provenzale,J.M.,et al, 1995

A Single-Photon Emission Computed Tomographic Study of Anosognosia in Alzheimer's Disease
Arch Neurol 52:415-420, Starkstein,S.E.,et al, 1995

Determining Brain Death in Adults
Neurol 45:1003-1011, Wijdicks,E.F.M., 1995

Practice Parameters for Determining Brain Death in Adults
Neurol 45:1012-1014, Rosenberg,J.H.,et al, 1995

Asymmetrical Skin Temperature in Ischemic Stroke
Stroke 26:1543-1547, Korpelainen,J.T.,et al, 1995

Levorotatory Form of 5-Hydroxytryptophan in Friedreich's Ataxia
Arch Neurol 52:456-460, Trouillas,P.,et al, 1995

Double-Blind Study with Levorotatory form of Hydroxytryptophan in Pts with Degen Cerebellar Dis
Arch Neurol 52:451-455, 4401995., Wessel,K.,et al, 1995

Dentatorubral-Pallidoluysian Atrophy:Clin Features Closely Related to Unstable Expansion of Trinucleotide (CAG) Repeat
Ann Neurol 37:769-775, Ikeuchi,T.,et al, 1995



Showing articles 1500 to 1550 of 2488 << Previous Next >>