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abscess, intracerebral
abscess, intracranial
abscess, sphenoid sinus
acetazolamide
aciduria
Adies pupil
adolescent medicine
advances in neurology
adverse drug reaction
algorithm
alpha-fetoprotein
altered states of consciousness
alternating hemiplegia
alternating hemiplegia of childhood
AMPA receptor antibodies
amyloidosis
amyotrophic lateral sclerosis
anemia
ankle edema
anti GQ1b IgG antibody
anticholinergic drugs
apraxia of eye movements
areflexia
artane
arthralgia
arthrogryposis multiplex
ascites
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, truncal
ataxic-dystonia syndromes
athetosis
athetosis, causes of
atlanto-axial subluxation
ATP1A3 gene
attention deficit disorder with hyperactivity
autoantibodies
autoimmune basal ganglia encephalitis
autoimmune disease
autonomic dysfunction
autonomic neuropathy
Babinski sign
basal ganglia, calcification of
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavioral disorder
benign essential tremor
biopterin deficiency
bladder dysfunction
blepharospasm
botulinum toxin
bradykinesia
brain atrophy
brainstem, atrophy
brainstem, lesion of
burning skin
calcification, intracranial
camptocormia
carbamazepine
carcinoembryonic antigen
carcinoma
carotid artery disease
carotid artery occlusion, neck
carotid artery stenosis
CAT scan
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
CAT scan, isodense lesion with acute hemorrhage
cataracts
catecholamine
cavernous sinus, syndrome
central nervous system, infection of
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar lesion
cerebellum
cerebral cortical atrophy
cerebral hypoperfusion
cerebral ischemia
cerebral palsy
cerebral palsy, associated problems with
cerebral vasculature, calcification
cerebral venous thrombosis
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gold sol.curve of
cerebrospinal fluid, xanthochromia of
cerebrovascular accident
cerebrovascular accident, infancy and childhood
ceruloplasmin, serum
cervical spine
Charcot-Marie-Tooth
chelation therapy
children
chorea
chorea, causes of
choreoathetosis
choreoathetosis, paroxysmal
chromosomal abnormality
chromosome 11
chromosome 14
chromosome 9
cisternogram, radionuclide
Clinical Pathologic Conference(C.P.C.)
coccidioidomycosis
cognition
cogwheel rigidty
complications
compression fracture
contractures, joint
cornea, opacity of
cranial nerve palsies
cranial neuropathy
cranial neuropathy, multiple
deferiprone
degenerative diseases of CNS
delay in diagnosis
dementia
dental procedure, neurologic complications with
depression
dermatomyositis
developmental milestones, loss of
developmental retardation
dexterity, impaired
diabetes insipidus
diabetes mellitus
diagnostic criteria
diet
differential diagnosis
diphenhydramine
diplopia
diurnal variation
DNA probes
donut sign
dopa responsive dystonia
dopamine
drooling
drop attacks
drug induced neurologic disorders
dural sinus thrombosis
dysarthria
dysarthria-clumsy hand syndrome
dysdiadochokinesia
dyskinesia
dyskinesia, causes of
dyskinesia, drug induced
dysphagia
dysphonia
dyspraxia
dystonia
dystonia musculorum deformens
dystonia musculorum deformens, carrier
dystonia, axial
dystonia, cervical
dystonia, children
dystonia, classification
dystonia, etiology of
dystonia, evaluation of
dystonia, face
dystonia, focal
dystonia, laryngeal
dystonia, painful
dystonia, segmental
dystonia, symptomatic
dystonia, treatment of
DYT1 mutation
edema, pedal
efficacy
empyema, epidural
empyema, subdural
encephalitis
encephalitis, autoimmune
encephalitis, brainstem
encephalitis, focal
encephalitis, paraneoplastic
encephalopathy
encephalopathy, progressive
endarterectomy, carotid
enzyme, defect
episodic neurologic deficits
equinovarus
esophageal varices
exome sequencing
eye movement, disorders of
facial expression abnormality
facial movement disorder
facial nerve palsy
Fahr disease
familial
fatigue
fine motor function, impaired
foot deformity
frontal lobe, pathologic signs of
fungal infection, CNS
gait disorder
galactorrhea
gamma amino butyric acid
gamma amino butyric acid receptor antibody
gammaglobulin therapy, intravenous
gene
gene mutation
genetic counselling
genetic linkage
genetic neurologic disorders
genetic testing
gests antagoniste
Gilles de la Tourette syndrome
globus pallidus
globus pallidus, stimulation
GLUT1 deficiency syndrome
glutamic acid decarboxylase, antibody
granuloma, pulmonary
grasp reflex
growth retardation
Guillain Barre syndrome
hands, fisted
head nodding
headache, positional
hearing loss
heparin, subcutaneous
hepatic encephalopathy
hepatic encephalopathy, treatment of
hepatic failure
hepatolenticular degeneration(Wilson's disease)
hepatolenticular degeneration(Wilson's disease), presymptomatic
Hodgkin's disease
homovanillic acid
hospitalization
Huntington's chorea
hydrocephalus
hydrocephalus, normal pressure
hyperreflexia
hypertonia
hypoalbuminemia
hypocalcemia
hypoglycorrhachia
hypoparathyroidism
hypoparathyroidism, idiopathic
hyporeflexia
hyposmia
hypotonia
iatrogenic neurologic disorders
imbalance
immunodeficiency
immunosuppression
immunotherapy
inborn errors of metabolism
inclusion bodies, intranuclear
intellectual deficit
intellectual deterioration
intracranial hypertension, benign
intracranial pressure, increased
iron, brain
jugular foramen syndrome
Kayser-Fleischer ring
klippel feil syndrome
L-dopa
leg spasms
leg spasms, painful
leg weakness, bilateral
leucine rich glioma inactivated 1 antibodies
leukemia
leukopenia
Lhermitte's sign
limbic encephalitis
lithium
liver function enzymes
lymphoma
masked facies
mastoiditis
memory, impairment of
meningismus
meningitis
meningitis, carcinomatous
meningitis, fungal
meningitis, syphilitic
meningitis, TB
mental retardation
mental status, abnormal
microcephaly
mimics
misdiagnosis
molecular genetics
monoamines
monoclonal antibodies
mononeuropathy
mortality
motor neuron disease
movement disorder
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movement disorder, paroxysmal
movement disorder, treatment of
MRI
MRI pattern
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MRI, eye of tiger sign
MRI, paramagnetic effect
MRI, spinal cord
MRI, spinal cord, increased intramedullary cord signal
MRI, spine
multiple sclerosis
multiple system atrophy
Munchausen syndrome
muscle diseases, characteristics of
muscle pain
muscle weakness, proximal
muscle, metabolic disorders of
muscular dystrophy
muscular dystrophy, Duchenne
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myasthenia gravis
myasthenic crisis
myelitis
myelitis, transverse
myelitis, transverse, idiopathic
myelitis, transverse, prognosis
myelopathy
myelopathy, chronic progressive
myoclonic jerks
myoclonus
myoglobinuria
myopathy
myopathy, carcinomatous
myopathy, thyroid disease causing
myositis
myotonia dystrophica
nasal stuffiness
neck pain
neuritis, causes of
neurochemistry
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neuroendocrinology
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neurologic disease, diagnoses of
neurologic signs
neuronal intranuclear inclusion disease
neuroophthalmology
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neuropathy, diabetic
neuropsychiatry
neurotomy
neurotransmitter
next-generation sequencing
NMDA antagonists
norepinephrine
numb clumsy hands syndrome
nystagmus
nystagmus, monocular
obsessive-compulsive disorder
ocular motility, disorders of
ophelia syndrome
ophthalmoplegia
optic atrophy
optic neuropathy
osteomyelitis
osteomyelitis, skull
otitis, neurologic complications with
pain
pallidotomy
PANK2 mutation
paraparesis
Parkinson disease
Parkinson disease, differential diagnosis of
Parkinson disease, dystonia with
Parkinson disease, juvenile
Parkinsonism syndrome
paroxysmal dystonic choreoathetosis
paroxysmal hemiplegia
paroxysmal neurologic deficits
parsidol
pathology
pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection
penicillamine
personality change
phenylketonuria
pigmentary retinopathy
plasmapheresis
pleocytosis of cerebrospinal fluid
pneumoencephalogram(PEG)
poison, neurologic problems with
poliomyelitis
polymyositis
polyneuropathy
pons, lesion of
porphyria
postural abnormality
potassium channel antibodies
practice guidelines
precipitating factors
pregnancy, neurologic complications in
primary familial brain calcification
PRKN gene
progeria
prognosis
progressive neurologic disorder
prolactin, elevated
pseudohypoparathyroidism
psychiatric disorder
psychiatric problems in neurologic disorders
psychological testing, neurologic problems
psychosis
pupil, abnormality in neurologic disorders
pupil, tonic
quadriparesis
quality of life
radiation hypersensitivity
radiculopathy
rapid onset dystonia parkinsonism
rapidly progressing neurologic illness
recurrent
Red flags
renal stones
respiratory failure
retinopathy
reversible neurologic disorder
review article
RFLPs
rigidity
Riley-Day syndrome
risk factors
rituximab
safety
sarcoidosis
scoliosis
screening
sedimentation rate, elevated
seizure
sensorineural hearing loss
sensory level
sensory tricks
serologic testing
serologic testing, false negative
seronegative
sexual dysfunction in neurologic disease
shaking
short stature
sicca syndrome
sinemet
sinusitis
Sjogren's syndrome
Sjogren's syndrome, neurologic manifestations of
skin, lesions in neurologic disorders
sleep pathology and physiology
slit lamp examination
spastic dysphonia
speech disorder
speech disorder, childhood
speech disorder, non aphasic
spinal cord
spinal cord, lesion of
spinal muscular atrophy
spinocerebellar ataxia
spinocerebellar ataxia type 28
spinocerebellar degeneration
splenomegaly
startle reaction
status epilepticus
stereotaxic surgery
steroid
steroid therapy, CNS treatment and complications with
stiff man syndrome
stimulation, deep brain
stimulation, deep brain, bilateral
striatal encephalitis
striopallidodentate calcifications, familial idiopathic
substantia nigra
symmetric brain lesions
tardive dyskinesia
tardive dystonia
telangiectases
tetrahydrobiopterin
thalamus, lesion of-bilateral
thrombocytopenia
thrombophlebitis
thrombophlebitis, prophylaxis
toe walking
tonic foot response
tonic spasms
torticollis
transient ischemic attack
transient ischemic attack, limb shaking
transient neurologic deficit
trauma
treatment of neurologic disorder
tremor
tremor, postural
trientine dihydrochloride
trigeminal neuralgia
tripping
tyrosine hydroxylase deficiency
unconsciousness
unconsciousness, transient
urinary incontinence
urinary retention
urinary urgency
valium
vasospasm, cerebral
visual loss
walking
walking frame
walking, difficulty with
Werdnig-Hoffman disease
wheelchair
white matter disease
Wolfram syndrome
workup
wrist drop
writers cramp
xerophthalmia
xerostomia
zinc
Showing articles 900 to 950 of 2609 << Previous Next >>

SCA-12: Tremor with Cerebellar and Cortical Atrophy is Associated with a CAG Repeat Expansion
Neruol 56:299-303,287, O'Hearn,E.,et al, 2001

Hypertrophic Chronic Pachymeningitis as a Localized Immune Process in the Craniocervical Region
Neurol 56:107-109, Boller,B.,et al, 2001

Sensory Guillain-Barre Syndrome
Neurol 56:82-86, Oh,S.J.,et al, 2001

Immediate Surgery for Moyomoya Syndrome?
Arch Neurol 58:130-131,132, Roach,E.S., 2001

Surgery for Moyamoya Syndrome?
Arch Neurol 58:128-129,132, Scott,R.M., 2001

A Controlled Study of Intravenous Immunoglobulin Combined with Prednisone in the Treatment of IBM
Neurol 56:323-327, Dalakas,M.C.,et al, 2001

A Painful Hip as a Presentation of Guillain-Barre Syndrome in Children
BMJ 322:149-150, Tang,T. &Noble-Jamieson,C., 2001

Spinal Cord Involvement in Primary Angiitis of the Central Nervous System: A Report of Two Cases
AJNR 22:577-582, Campi,A.,et al, 2001

Sustained Bilateral Hemodynamic Benefit of Contralateral Carotid Endarterectomy in Patients with Symptomatic Internal Carotid Artery Occlusion
Stroke 32:728-734, Rutgers,D.R.,et al, 2001

A Blind Panic
Lancet 357:1262, Ayuk,J.,et al, 2001

Chiropractic Manipulation and Stroke
Stroke 32:1054-1060, Rothwell,D.M.,et al, 2001

Cocaine-Induced Persistent Dyskinesias
Neurol 56:964-965, Weiner,W.J.,et al, 2001

Gluten Sensitivity in Sporadic and Hereditary Cerebellar Ataxia
Ann Neurol 49:540-543, Bushara,K.O.,et al, 2001

Guillain-Barre Syndrome Complicated with Hemolytic Anemia in Association with Antiganglioside GM3 Antibody
Am J Med 110:399-400, Aoyama,K.,et al, 2001

Polymyalgia Rheumatica and Giant Cell Arteritis
Rheum Dis Clin North Amer 26:493-515, Evans,J.M. & Hunder,G.G., 2000

Neurologic Complications of the Reactivation of Varicella-Zoster Virus
NEJM 342:635-645, Gilden,D.H.,et al, 2000

Autoantibodies to Ganglionic Acetylcholine Receptors in Autoimmune Autonomic Neuropathies
NEJM 343:847-855, Verning,S. et al, 2000

Visual Manifestations of Giant Cell Arteritis
Medicine 79:283-292, Gonzalez-Gay,M.A.,et al, 2000

Hemidystonia and Hemichoreoathetosis as an Initial Manifestation of Moyamoya Disease
Arch Neurol 57:1510-1512, Lyoo,C.H.,et al, 2000

Indomethacin Reduces CSF Pressure in Intracranial Hypertension
Neurol 55:1043-1045, Forderreuther,S. & Straube,A., 2000

Effect of Contralateral Occlusion on Long-Term Efficacy of Endarterectomy in the Asymptomatic Carotid Atherosclerosis Study (ACAS)
Stroke 31:2330-2334, Baker,W.H.,et al, 2000

Dilated Stomach and Weak Muscles
Lancet 356:1898, Rigby,S.P.,et al, 2000

Paraneoplastic Cerebellar Ataxia Due to Autoantibodies Against a Glutamate Receptor
NEJM 342:21-27, Smitt,P.S.,et al, 2000

Benign Prognosis of Never-Symptomatic Carotid Occlusion
Neurol 54:878-882, Powers,W.J.,et al, 2000

Short-Term Arteriographic and Clinical Outcome After Cerebral Angioplasty and Stenting for Intracranial Vertebrobasilar and Carotid ATherosclerotic Occlusive Disease
AJNR 21:249-254, Mori,T.,et al, 2000

Uses of Botulinum Toxin Injection in Medicine Today
BMJ 320:161-165, Munchau,A. & Bhatia,K.P., 2000

Rotational Vertebral Artery Occlusion Syndrome with Vertigo Due to "Labyrinthine Excitation"
Neurol 54:1376-1379, Strupp,M.,et al, 2000

Cardiac Dysfunction in Neuromuscular Diseases
The Neurologist 6:67-82, Pourmand,R., 2000

Neurological Manifestations of Dengue Infection
Lancet 355:1053-1059, Solomon,T.,et al, 2000

Long-Term outcome in Patients With Guillain-Barre Syndrome Requiring Mechanical Ventilation
Neurol 54:2311-2315, Fletcher,D.D.,et al, 2000

Thrombotic Thrombocytopenic Purpura Associated with Clopidogrel
NEJM 342:1773-1777,1824, Bennett,C.L.,et al, 2000

Idiopathic Stabbing Headache Associated With Monocular Visual Loss
Arch Neurol 57:745-746, Ammache,Z.,et al, 2000

Deterioration of Giant Cell Arteritis With Corticosteroid Therapy
Arch Neurol 57:581-584, Staunton,H.,et al, 2000

Magnetic Resonance Venography in Idiopathic Pseudotumor Cerebri
J Neuro-Ophthal 20:12-13, Lee,A.G.&Brazis,P.W., 2000

Influenza Vaccine and the Risk of Relapse of Guillain-Barre Syndrome
Neurol 55:452-453, Wijdicks,E.F.M. et al, 2000

Significance of Hyperintense Vessels on FLAIR MRI in Acute Stroke
Neurol 55:265-269, Kamran,S. et al, 2000

Disease Progression in Sporadic Inclusion Body Myositis: Observations in 78 Patients
Neurol 55:296-198, Peng,A. et al, 2000

Inborn Errors of Metabolism as a Cause of Neurological Disease in Adults: An Approach to Investigation
JNNP 69: 5-12, Gray,R.G.F. et al, 2000

Human Immunodeficiency Virus-Associated Pure motor Lumbosacral Polyradiculopathy
Arch Neurol 57:1034-1039, Benatar,M.G. & Eastman,R.W., 2000

Guillain-Barre Syndrome: An Unusual Presentation of West Nile Virus Infection
Neurol 55:144-146, Ahmed,S. et al, 2000

C1/C2 Rotary Subluxation Due to Spasmodic Torticollis
JNNP 69:135-136, Dalvie,S. et al, 2000

Three-year Survival and Functional Outcome of Patients With Idiopathic Adult Hydrocephalus Syndrome
Neurol 55:576-578, Malm,J. et al, 2000

Intrathecal Baclofen for the Treatment of Dystonia in Patients with Reflex Sympathetic Dystrophy
NEJM 343:625-630,654, van Hilten,B.J. et al, 2000

Relation Between Cholinesterase Inhibitor and Pisa Syndrome
Lancet 355:2222, Kwak,Y.T. et al, 2000

Spinocerebellar Ataxia Type 8
Neurol 55:649-657, Day,J.W. et al, 2000

CT Angiography for the Detection and Characterization of Carotid Artery Bifurcation Disease
Stroke 31:2168-2174, Anderson,G.B et al, 2000

Long-Term Clinical and Angiographic Outcomes in Symptomatic Patients with 70% to 99% Carotid Artery Stenosis
Stroke 31:2037-2042, Paciaroni,M. et al, 2000

Dermatomyositis
Lancet 355:53-57, Callen,J.P., 2000

Multifocal Dural Enhancement Associated with Temporal Arteritis
Arch Neurol 57:119-122, Joelson,E.,et al, 2000

A Six-Year-Old Girl with Tick paralysis
NEJM 342:90-94, Felz,M.W.,et al, 2000



Showing articles 900 to 950 of 2609 << Previous Next >>