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abducens nerve paralysis
acoustic nerve
acquired immunodeficiency syndrome
acquired immunodeficiency syndrome, medical precautions with
adolescent medicine
akinetic mute
alcohol intolerance
algorithm
alkylating agents
alpha-fetoprotein
altered states of consciousness
alternating rapid movement, impaired
amphiphysin antibodies
anemia
ankle edema
anti Yo antibody
antimetabolite
apraxia of eye movements
areflexia
arthralgia
arthritis
ascites
asparginase
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxia, sensory
ataxia, truncal
ataxic gait
atonic bladder
atypical
autoantibodies
autoimmune cerebellar ataxia
autoimmune disease
autonomic dysfunction
autonomic neuropathy
Babinski sign
blindness
blood dyscrasias, neurologic findings with
brachial plexus neuropathy
bradykinesia
callosal angle
cane
carcinoembryonic antigen
carcinoma
carcinoma of breast
carcinoma of lung
carcinoma of ovary
cardiomyopathy
cataracts
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar atrophy, primary
cerebellar degeneration
cerebellar lesion
cerebral cortex
cerebral venous thrombosis
cerebrospinal fluid, abnormal
cerebrospinal fluid, drainage of
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, oligoclonal IgG in
cerebrospinal fluid, pressure low
cerebrovascular accident
cerebrovascular accident, recurrent
cerebrovascular disease
ceruloplasmin, serum
chairbound
Charcot-Marie-Tooth
chemotherapy, CNS treatment and complications with
children
chorea
choreoathetosis
chromosomal abnormality
chromosome 11
chromosome 9
cisternogram, radionuclide
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
cognition
cognition, slowed
collapsin response mediator protein 5 IgG
complications
consanguinity
contactin associated protein like 2 antibodies
cranial neuropathy
cranial neuropathy, multiple
Creutzfeldt-Jakob disease, genetic
deep gray nuclei
deep tendon reflexes
degenerative diseases of CNS
dementia
dementia, childhood
dementia, familial
dementia, rapidly progressive
dementia, reversible
depression
dermatitis
dermatomyositis
dexterity, impaired
diabetes mellitus
diagnostic criteria
diarrhea
diarrhea, bloody
diet
differential diagnosis
difficulty climbing stairs
diplopia
dizziness
dopa responsive dystonia
drooling
dysarthria
dysdiadochokinesia
dyskinesia
dysmetria
dysmorphic
dysphagia
dystonia
edema, pedal
efficacy
electromyogram
emotional lability
encephalitis, autoimmune
encephalitis, brainstem
encephalitis, paraneoplastic
encephalomyelitis
encephalopathy
esophageal varices
executive dysfunction
external lumbar drainage
eye movement, disorders of
facial expression abnormality
facial nerve palsy
facial nerve palsy, bilateral
facial nerve palsy, recurrent
facial pain
falling
familial
fever
finger nose finger test
fluorouracil
flush syndrome
foot drop
frataxin
Friedreich's ataxia
frontal lobe, pathologic signs of
gait disorder
gait, magnetic
gaze palsy, horizontal
gene
gene mutation
genetic counselling
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
Gerstmann-Straussler-Scheinker disease
glutamic acid decarboxylase, antibody
growth retardation
Guillain Barre syndrome
hallucination
handwriting
headache
hearing loss
heel-knee-shin test
hepatic encephalopathy
hepatic failure
hepatolenticular degeneration(Wilson's disease)
hepatolenticular degeneration(Wilson's disease), presymptomatic
heralding manifestation
high altitude sickness
human immunodeficiency virus type 1
hydrocephalus
hydrocephalus, normal pressure
hydrocephalus, normal pressure, etiology
hydrocephalus, treatment of
hyperreflexia
hypoalbuminemia
hyponatremia
hypotonia
imbalance
immunodeficiency
immunologic disease
immunology and the nervous system
immunosuppression
immunotherapy
impotence
inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with
inclusion bodies, intranuclear
intellectual deficit
intellectual deterioration
isoniazid
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
jaw pain
Kayser-Fleischer ring
Korsakoff's psychosis
L-dopa
leg weakness, bilateral
leucine rich glioma inactivated 1 antibodies
leukemia
leukemia, neurologic findings assoc.with
leukopenia
limbic encephalitis
liver function enzymes
lumbar drain
lumbar puncture, repeated
lymphoma
malignancy screen
malignancy, occult
masked facies
Melkersson's syndrome
memory, impairment of
meningismus
meningitis
meningitis, neurologic aspects and complications of
meningoencephalopathy
mental retardation
mental status, abnormal
methotrexate
methylhydrazine derivatives
mimics
misdiagnosis
molecular genetics
monoamine oxidase inhibitors
monoclonal antibodies
monoclonal gammopathy
mononeuritis multiplex
mood change
mortality
motor neuron disease
mountain climbing
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, brachial plexus
MRI, diffusion weighted
MRI, flow void, CSF
MRI, high signal foci on
MRI, negative
MRI, periventricular hyperintensity
MRI, punctate pattern
multiple sclerosis
multiple system atrophy
muscle biopsy
muscle pain
muscle weakness
muscle weakness, proximal
myasthenia gravis
myasthenia gravis, paraneoplastic
myasthenic syndrome
myelopathy
myelopathy, chronic progressive
myopathy
myopathy, vacuolar
myositis
myositis, ocular
nausea and vomiting
nemaline rod myopathy
neuroaxonal dystrophy
neuroaxonal dystrophy, infantile
neurocutaneous disease
neuroendocrinology
neurologic complications of, surgery
neurologic complications of, systemic cancer
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic disease, multifocal
neurologic signs
neuromuscular junction
neuronal cell surface antigen
neuronal intranuclear inclusion disease
neuronopathy, sensory
neuropathology
neuropathy
neuropathy, ataxic
neuropathy, painful
neuropathy, paraneoplastic
neuropathy, peripheral
neuropathy, sensory
neurotoxin
next-generation sequencing
nitrogen mustard
NMDA antagonists
nystagmus
ocular motility, disorders of
onconeural antibodies
ophthalmoplegia, progressive external
opsoclonus-myoclonus syndrome
optic atrophy
optic neuritis
orthostatic hypotension
pain
pain, abdominal
paraneoplastic cerebellar degeneration
paraparesis
paraparesis, familial spastic
paraparesis, familial spastic, classification
paraparesis, spastic
paresthesias
Parkinson disease, dystonia with
Parkinson disease, juvenile
Parkinsonism syndrome
pathology
penicillamine
peripheral nerve, lesion of
personality change
pes cavus
picking at skin
pleocytosis of cerebrospinal fluid
POLG1 gene
polyclonal gammopathy
polymyositis
polyneuropathy
polyneuropathy, chronic idiopathic
polyneuropathy, chronic idiopathic, ataxic
polyneuropathy, chronic inflammatory demyelinating
postural abnormality
practice guidelines
pregnancy, neurologic complications in
prion disease
prion protein gene
PRKN gene
procarbazine
progeria
prognosis
progressive neurologic disorder
proprioception, abnormal
protein 14-3-3, cerebrospinal fluid
psychiatric disorder
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis
ptosis
ptosis, bilateral
quadriplegia
radiation hypersensitivity
real-time quaking-induced conversion
Red flags
regional enteritis
remote effect of cancer on the nervous system
renal stones
retinopathy
reversible neurologic disorder
review article
rigidity
scoliosis
screening
sedimentation rate, elevated
seizure
sensorineural hearing loss
sensory polyneuropathy
serologic testing
short steps
shunt procedure, lumboperitoneal
shunt procedure, ventricular
shunt procedure, ventricular-complications of
sinemet
skin, biopsy
skin, lesions in neurologic disorders
slit lamp examination
spastic ataxia
spasticity
spinal muscular atrophy
splenomegaly
startle myoclonus
subarachnoid hemorrhage
tandem gait, ataxic
telangiectases
thrombocytopenia
tinnitus
tonic foot response
transient ischemic attack
treatment of neurologic disorder
tremor
tremor, postural
trientine dihydrochloride
trinucleotide repeats
ulcerative colitis
upgaze, paralysis of
urinary incontinence
ventricular enlargement
ventriculostomy
vinblastine
vincristine neurotoxicity
vision, failure of in childhood
visual evoked response
visual impairment
visual loss
vocal cord paralysis
walking frame
walking, difficulty with
weakness
weakness, progressive
weakness, proximal
weight loss
wheelchair
wide based gait
workup
wrist drop
zinc
Showing articles 1550 to 1600 of 6232 << Previous Next >>

Evaluation of CSF Leaks:High-Resolution CT Compared with Contrast-Enhanced CT and Radionuclide Cisternography
AJNR 20:706-712, Stone,J.A.,et al, 1999

Proton Magnetic Resonance Spectroscopy Pattern of Progressive Multifocal Leukoencephalopathy in AIDS
JNNP 66:520-523, Iranzo,A.,et al, 1999

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

Cat-Scratch Disease Encephalopathy:A Cause of Status Epilepticus in School-Aged Children
J Pediatrics 134:635-638, Armengol,C.E.&Hendley,J.O., 1999

Outcome in Severe Pediatric Guillain-Barre Syndrome after Immunotherapy or Supportive Care
Neurol 52:1494-1497, Graf,W.D.,et al, 1999

Phenotypic Variability in Rippling Muscle Disease
Neurol 52:1453-1459, Vorgerd,M.,et al, 1999

Diagnosis and Treatment of Ischemic Stroke
Am J Med 106:211-221, Alberts,M.J., 1999

Neurologic Manifestations of AIDS in Older Adults
Infect Dis Clin Practice 8:179-185, Finelli,P.F.,et al, 1999

Fibromyalgia Syndrome a Decade Later
Arch Int Med 159:777-785, Goldenberg,D.L., 1999

Physician Assistants in Neurology Practice
Neurol 52:1513, Taft,J.M.&Hooker,R.S., 1999

Neurology and the Skin
JNNP 66:417-430, Hurko,O.&Provost,T.T., 1999

Paraneoplastic Syndromes
Arch Neurol 56:405-408, Dalmau,J.O.&Posner,J.B., 1999

Axillary Neuropathy, In Entrapment Neuropathies, Chp 13 p 346 Lippincott-Raven (Third Ed), Phila
, , 1999

Diagnosis of Viral Infections of the Central Nervous System
NEJM 340:483-484, Huang,C.,et al, 1999

The Exercise Test in Andersen Syndrome
Arch Neurol 56:352-356, Katz,J.S.,et al, 1999

Progressive Multifocal Leukoencephalopathy and Human Immunodeficiency Virus-associated White Matter Lesions in AIDS:Magnetization Transfer MR Imaging
Radiology 210:539-543, Ernst,T.,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

Fatal Guillain-Barre Syndrome
Neurol 52:635-638, Lawn,N.D.&Wijdicks,E.F.M., 1999

Clinical and Neuroradiological Features of Intracranial Vertebrobasilar Artery Dissection
Stroke 30:1083-1090, Hosoya,T.,et al, 1999

Diagnosis, Management, and Treatment of Alzheimer Disease, A Guide for the Internist
Arch Int Med 159:789-798, Richards,S.S.&Hendrie,H.C., 1999

Problems in the Management of Attention-Deficit-Hyperactivity Disorder
NEJM 340:40-46, Zametkin,A.J.&Ernst,M., 1999

Value of Combined Approach with Thallium-201 Single-Proton Emission Computed Tomography and Epstein-Barr Virus DNA Polymerase Chain Reaction in CSF for the Diagnosis of AIDS-Related Primary CNS Lympho
J Clin Oncol 17:554-560, Antinori,A.,et al, 1999

Diagnostic Criteria for Parkinson Disease
Arch Neurol 56:33-39, Gelb,D.J.,et al, 1999

Magnetic Resonance Imaging-Based Volumetry Differentiates Idiopathic Parkinson's Syndrome from Multiple System Atrophy and Progressive Supranuclear Palsy
Ann Neurol 45:65-74, Schulz,J.B.,et al, 1999

Brainstem Tuberculoma Mimicking Glioma:The Role of Antituberculous Drugs as a Diagnostic Tool
Neurol 52:210-211, DelBrutto,O.H.&Mosquera,A., 1999

Use of Diffusion-Weighted MR Imaging in Differential Diagnosis Between Intracerebral Necrotic Tumors and Cerebral Abscesses
AJNR 20:1252-1257, Desprechins,B.,et al, 1999

Ramsay Hunt Syndrome Associated with Brain Stem Enhancement
AJNR 20:278-280, Sartoretti-Schefer,S.,et al, 1999

Neurological Manifestations of Chronic Hepatitis C
J Neurol 246:486-491, Heckmann, J.G.,et al, 1999

Cerebral Toxoplasmosis and Lymphoma in AIDS: Perfusion MR Imaging Experience in 13 Patients
Radiology 208:663-669, Ernst,T.M.,et al, 1998

Diagnosis of Cerebral Venous Thrombosis with Routine Magnetic Resonance: An Update
Eur Neurol 40:179-190, Bianchi,D.,et al, 1998

Cerebellar Degeneration Associated With Human Immunodeficiency Virus Infection
Neurol 50:244-251, Tagliati,M.,et al, 1998

MR Angiography in Internal Carotid Artery Dissection:Improvement of Diagnosis by Selective Demonstration of the Intramural Haematoma
Neuroradiology 40:704-709, Kirsch,E.,et al, 1998

Minimal Number of Plasma Exchanges Needed to Reduce Immunoglobulin in Guillain-Barre Syndrome
Neurol 51:875-877, Yuki,N.,et al, 1998

A 55-Year-Old Man with Attention-Deficit/Hyperactivity Disorder
JAMA 280:1086-1092, Biederman,J., 1998

Alcohol-Related Acute Axonal Polyneuropathy,A Differential Diagnosis of Guillain-Barre Syndrome
Arch Neurol 55:1329-1334, Wohrle,J.C.,et al, 1998

Incidence of Dominant Spinocerebellar and Friedreich Triplet Repeats Among 361 Ataxic Families
Neurol 51:1666-1671, Moseley,M.L.,et al, 1998

The Value of Interphase Cytogenetics in Cytology for the Diagnosis of Leptomeningeal Metastases
Neurol 51:906-908, Van Oostengrugge,R.J.,et al, 1998

Cerebral Amyloid Angiopathy:Propsects for Clinical Diagnosis and Treatment
Neurol 52:690-694, Greenberg,S.M., 1998

Genetic Analysis Enables Definite and Rapid Diagnosis of Cerebrotendinous Xanthomatosis
Neurol 51:865-867, Chen,W.,et al, 1998

New Neuropathological Criteria for Alzheimer Disease
Arch Neurol 55:1174-1176, Hyman,B.T., 1998

Attention-Deficit Hyperactivity Disorder and Hyperkinetic Disorder
Lancet 351:429-433, 3871998., Swanson,J.M.,et al, 1998

Clinical Usefulness of Magnetic Resonance Imaging in Multiple System Atrophy
JNNP 65:65-71, Schrag,A.,et al, 1998

Comparison of Single-and Triple-Dose Contract Material in the MR Screening of Brain Metastases
AJNR 19:821-828, Sze,G.,et al, 1998

Electrophysiological Aids in Distinguishing Organic from Psychogenic Tremor
neurol 50:1882-1884, McAuley,J.H.,et al, 1998

Spinal Epidural Abscess:The Importance of Early Diagnosis and Treatment
JNNP 65:209-212, Mackenzie,A.R.,et al, 1998

Clinicopath Conf
Chronic Inflammatory Demyelinating Polyneuropathy, Case 13-1998, NEJM 338:1212-1219998., , 1998

Patients with Features Similar to Huntington's Disease, Without CAG Expansion in Huntingtin
Neurol 51:215-220, Rosenblatt,A.,et al, 1998

Small-Fiber Sensory Neuropathies:Clinical Course and Neuropathology of Idiopathic Cases
Ann Neurol 44:47-59, Holland,N.R.,et al, 1998

Idiopathic Intracranial Hypertension Without Papilledema, A Case-Control Study in Headache Center
Neurol 51:245-249, Wang,S-J.,et al, 1998



Showing articles 1550 to 1600 of 6232 << Previous Next >>