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Differential
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acetazolamide
adverse drug reaction
agnosia, color
akathisia
akinesia of eyelid function
alexia without agraphia
algorithm
alien hand syndrome
alpha-fetoprotein
Alzheimer's disease
amnesic stroke
anatomy of
anemia
ankle edema
anti IgLON5
anticholinergic drugs
anticholinesterase
anxiety
aphasia
aphasia, progressive, primary
aphonia
applause sign
apraxia
apraxia of eye movements
apraxia of eyelid opening
arm swing, reduced
arylsulfatase A
ascites
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, hereditary
ataxia, paroxysmal
ataxia, progressive
ataxia, truncal
athetosis
autoantibodies
Babinski sign
basal ganglia
basal ganglia, degeneration
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavioral disorder
bent spine syndrome
biologic markers
biopterin deficiency
biotin
biotin deficiency
biotin deficiency, juvenile form
biotin-responsive basal ganglia disease
blepharospasm
botulinum toxin
bradykinesia
brain biopsy
brain damage
brainstem, dysfunction
brainstem, lesion of
bruxism
bulbar dysfunction
bulbar palsy
CAG repeats
calcification, intracranial
camptocormia
carbamazepine
carcinoembryonic antigen
carcinoma
CAT scan
CAT scan, abnormal
CAT scan, false negative
CAT scan, muscle
cataracts
caudate nucleus, atrophy
central hypoventilation
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar degeneration
cerebellar pontine angle
cerebellar pontine angle tumor
cerebral cortex
cerebral cortical atrophy
cerebral embolism
cerebral embolism, cardiac origin
cerebral palsy
cerebral palsy, associated problems with
cerebral peduncle
cerebrovascular accident
ceruloplasmin, serum
channelopathy
Charcot's sign
children
chorea
choreoathetosis
chromosomal abnormality
chromosome 11
chromosome 14
chromosome 20
cirrhosis
cisterna magna
Clinical Pathologic Conference(C.P.C.)
cognition
cogwheel rigidty
cold intolerance
coma
coma, episodic
comorbidities
complications
conjugate gaze, forced
consanguinity
conversion reaction
cortical-basal ganglionic degeneration
cranial nerve palsies
creatine phosphokinase(CPK)elevated
crying, pathologic
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
dementia
depression
dexterity, impaired
diabetes mellitus
diagnostic criteria
diet
differential diagnosis
diplopia
diurnal variation
donepezil
dopa responsive dystonia
down-beat nystagmus
downward gaze
drooling
drug induced neurologic disorders
dying
dysarthria
dysarthria-clumsy hand syndrome
dysdiadochokinesia
dyskinesia
dyskinesia, buccal lingual facial
dyskinesia, facial
dysmetria
dysphagia
dysphasia
dyspraxia
dystonia
dystonia musculorum deformens
dystonia, cervical
dystonia, classification
dystonia, drug induced
dystonia, etiology of
dystonia, evaluation of
dystonia, face
dystonia, focal
dystonia, painful
dystonia, post traumatic
dystonia, treatment of
dystonia, truncal
dystonic reaction, acute
DYT1 mutation
edema, pedal
electromyogram
emotional lability
employment
encephalitis, autoimmune
enzyme, defect
ependymoma
episodic disorders
episodic neurologic deficits
equinovarus
esophageal varices
ethics in neurology
exercise
exercise-induced neurologic dysfunction
extrapyramidal movement disorder, progressive
eye movement, disorders of
facial expression abnormality
falling
familial
fever
fine motor function, impaired
fluctuate
foot deformity
fourth ventricle, enlargement of
fourth ventricle, neoplasm of
frontal behavioral spatial syndrome
gait disorder
gait, apraxic
gangliosidosis GM1
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic testing
gests antagoniste
glabellar sign
globus pallidus
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
globus pallidus, stimulation
grasp reflex
grimacing
growth retardation
Hallervorden Spatz disease
Hallervorden Spatz disease, late onset
hand weakness
hands, fisted
head nodding
headache
health insurance
hearing loss
hemiakathisia
hemianopia
hemianopia, homonymous
hemichorea
hemidystonia
hemifacial spasm
hemiplegia
hepatic encephalopathy
hepatic failure
hepatolenticular degeneration(Wilson's disease)
hepatolenticular degeneration(Wilson's disease), presymptomatic
heralding manifestation
HLA
hoarseness
Huntington's chorea
Huntington's chorea, genetic counselling
Huntington's disease, children
hyperreflexia
hypoalbuminemia
hypometric saccades
hypophonia
hypotonia
iatrogenic neurologic disorders
ideomotor apraxia
imbalance
imbalance, postural
immunodeficiency
immunosuppression
immunotherapy
inattention
incontinence, fecal
incoordination
insomnia
intellectual deficit
intellectual deterioration
internet
intracranial pressure, increased
iron, brain
Jakob-Creutzfeldt disease
jaw jerk, abnormal
Kayser-Fleischer ring
kyphosis
laughing, pathologic
L-dopa
leg spasms
leg spasms, painful
leg weakness, bilateral
lenticular nucleus, lesion of, bilateral
leukemia
leukodystrophy
leukopenia
levitation
lithium
liver disease
liver function enzymes
low back pain
lymphoma
lysosomal storage disease
manganese intoxication
masked facies
memory, defect of recent
memory, impairment of
meningismus
meningitis
mental retardation
metabolic disorder, primary
metachromatic leukodystrophy
metachromatic leukodystrophy, adult onset
midbrain
midbrain, atrophy
midbrain, infarction of
migraine
misdiagnosis
molecular genetics
mortality
movement disorder
movement disorder, drug induced
movement disorder, extrapyramidal
movement disorder, extrapyramidal-treatment of
movement disorder, psychogenic
movement disorder, treatment of
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, eye of tiger sign
MRI, high signal foci on
MRI, high signal intensity of basal ganglia
MRI, mouse ears
MRI, negative
MRI, paramagnetic effect
MRI, spine
MRI, T1 weighted high signal foci
MRS
multiple sclerosis, differential diagnosis of
multiple sclerosis, misdiagnosis
multiple system atrophy
muscle biopsy
muscle hypertrophy
muscle spasm, face
muscle weakness
muscular dystrophy
myasthenia gravis
myelopathy
myelopathy, chronic progressive
myoclonic jerks
myoclonus
myokymia
myopathy
myopathy, metabolic
myorhythmia
neoplasm, posterior fossa
neoplasm, primary of CNS
neoplasm, primary of CNS-children
neurocutaneous disease
neuroendocrinology
neuroleptic
neuroleptic, atypical
neurologic disease, diagnoses of
neurologic disease, diagnoses of, clinical bedside
neurologic disease, tempo
neurologic evaluation
neurologic examination
neurologic signs
neurologic symptoms
neuromyotonia
neuroophthalmology
neuropathology
neuropathy
numb clumsy hands syndrome
nystagmus
nystagmus, vertical
obsessive-compulsive disorder
ocular motility, disorders of
ocular myopathy
ocular myopathy, differential diagnosis
old age, neurology of
opened mouth
ophthalmoplegia
optic atrophy
pain
palilalia
palinopsia
PANK2 mutation
paraparesis
parasomnia
paraspinal muscle
paraspinal muscle weakness
parkin gene
Parkinson disease
Parkinson disease, axial symptoms
Parkinson disease, differential diagnosis of
Parkinson disease, juvenile
Parkinson disease, L-dopa nonresponsive
Parkinson disease, treatment of
Parkinson disease, tremor, absence of
Parkinsonism syndrome
pathology
penguin silhouette sign
penicillamine
personality change
pigmentary retinopathy
Pisa syndrome
pitfalls
pleocytosis of cerebrospinal fluid
polycythemia, secondary
posterior cerebral artery
posterior cerebral artery embolism
posterior cerebral artery territory infarction
postural abnormality
precipitating factors
pregnancy, neurologic complications in
primary episodic ataxia
procyclidine
progeria
prognosis
progressive neurologic disorder
progressive supranuclear palsy
pseudobulbar palsy
psychiatric disorder
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis
ptosis
pull test
pure sensory stroke
pyramidal tract
pyramidal tract dysfunction
radiation hypersensitivity
rapid onset dystonia parkinsonism
rapidly progressing neurologic illness
Red flags
release phenomena
renal stones
respirations in CNS disease
retinal degeneration
retinitis pigmentosa
retinopathy
retrocollis
retropulsion
Rett's syndrome
reversible neurologic disorder
review article
rigidity
rigidity, axial
risk factors
running
saccadic eye movements, abnormal
salivation, excessive
Saudi Arabia
screening
sea-blue histiocytes
seizure
sensorineural hearing loss
sensory loss
sensory loss, cortical
sensory tricks
sequencing difficulty
short stature
shoulder, elevation
sinemet
single photon emission computed tomography
skin, lesions in neurologic disorders
sleep apnea, obstructive
sleep pathology and physiology
slit lamp examination
somnolence
spasticity
speech disorder
speech disorder, childhood
spinal cord
spinal cord, lesion of
spinal muscular atrophy
splenomegaly
stare
stem cell transplantation
stimulation, deep brain
stimulation, deep brain, bilateral
stooped posture
striatum, lesion of
striatum, lesion of, bilateral
substantia nigra
suck reflex
suicide
swallow evaluation
symmetric brain lesions
tardive dystonia
tau protein
tauopathy
telangiectases
tetrahydrobiopterin
thalamus, infarction of
thrombocytopenia
toe walking
tonic foot response
torticollis
trauma
treatment of neurologic disorder
treatment, empirical
tremor
tremor, intention
tremor, jaw
tremor, postural
tricyclic antidepressant
trientine dihydrochloride
trinucleotide repeats
tripping
upgaze
upgaze, paralysis of
urinary incontinence
urinary sulfatidase excretion
vision, blurred
visual evoked response
visual field defect
visual symptoms
vocal cord paralysis
walking
walking frame
walking, difficulty with
weakness, progressive
weight loss
wheelchair
Whipple's disease
white matter disease
wide based gait
zinc
Showing articles 850 to 900 of 1183 << Previous Next >>

Hysterical Gait Disorders:60 Cases
Neurol 39:586-589, Keane,J.R., 1989

Clinicopath Conf
Chronic Osteomyelitis of Spine, with Intervertebral Diskitis (T3-T4) & Epidural Abscess (Staph Aureu, ) , Cas9,NEJM 320:1610-1618,1989., 1989

Cerebellopontine Angle Epidermoid Cysts:A Report on 30 Cases
JNNP 52:986-990, deSouza,C.E.,et al, 1989

Continuous Levodopa Infusions to Treat Complex Dystonia in Parkinson's Disease
Neurol 39:888-891, Sage,J.I.,et al, 1989

Diabetic Truncal Neuropathy:Topography of the Sensory Deficit
Ann Neurol 25:233-238, Stewart,J.D., 1989

Medical Problems of Musicians
NEJM 320:221-227, 246-2481989., Lockwood,A.H., 1989

Acute Profound Dystonia in Infants with Glutaric Acidemia
Pediatrics 83:228-234, Bergman,I.,et al, 1989

Dystonic Posturing in Complex Partial Seizures of Temporal Lobe Onset:A New Lateralizing Sign
Neurol 39:196-201, Kotagal,P.,et al, 1989

Clinicopath Conf
Subacute Cerebellar Degeneration, Cystadenocarcinoma of Ovary, (with Paraneoplastic Syndrome) , Case, 34-1EJM 321:524-535,1989., 1989

Adrenoleukodystrophy
JAMA 262:1504-1506, Ladenson,P.W., 1989

Risk Factors for Recurrent Nonsyncopal Falls, A Prospective Study
JAMA 261:2663-2668, Nevitt,M.C.,et al, 1989

Prevention of Falls Among the Elderly
NEJM 320:1055-1059, Tinetti,M.E.&Speechley,M., 1989

Hemifacial Spasm Associated with Epidermoid Tumors of the Cerebellopontine Angle
Neurol 39:577-580, Auger,R.G.&Piepgras,D.G., 1989

The Acquired Immunodeficiency Syndrome (AIDS) Dementia Complex
Ann Int Med 111:400-410, Ho,D.D.,et al, 1989

Clinicopath Conf
HTLV-I Infection, with Adult T-Cell Lymphoma and Tropical Spastic Paraparesis, Case 36-2989, NEJM 32, :6675,1989., 1989

Human T-Lymphotropic Virus Type I-Associated Myelopathy Presenting as Spinocerebellar Syndrome
Ann Neurol 25:419-420, Iwasaki,Y.,et al, 1989

Falling and Postural Deficits Due to Acute Unilateral Basal Ganglia Lesions
Arch Neurol 46:492-496, Labadie,E.L.,et al, 1989

Guillain-Barre Syndrome Presenting as High-Altitude Cerebral Edema
NEJM 321:545, Shlim,D.R.&Cohen,M.T., 1989

Usefulness of a Writing Aid in Writer's Cramp
Neurol 39:149-150, Koller,W.C.&Vetere-Overfield,B., 1989

The"Yips":A Focal Dystonia of Golfers
Neurol 39:192-195, McDaniels,K.D.,et al, 1989

Treatment of Focal Dystonias of the Hand with Botulism Toxin Injections
JNNP 52:355-363, Cohen,L.G.,et al, 1989

Clinicopath Conf
Primary (Granulomatous) Angiitis of Central Nervous System, Case Record 8-1989, NEJM 320:514-5249., , 1989

Diabetic Truncal Neuropathy Presenting as Abdominal Hernia
Neurol 39:1488-1490, Parry,G.J.&Floberg,J., 1989

Post-Traumatic Torticollis
Neurol 39:1642-1643, Isaac,K.&Cohen,J.A., 1989

Cerebral Palsy Diplegia:Improvements for Walking
BMJ 299:1115-1116, Patrick,J., 1989

Demyelinating Diseases
In Rowlands Merritt's Textbk of Neurology, Lea & Febiger, Phila, 8th Ed, p. 749, Sibley,W.A.,et al, 1989

Refsum Disease
In Rowland's Merritt's Textbk of Neurology, Lea & Febiger, Phila, 8thEd, p. 509, Menkes,J.H., 1989

Magnetic Resonance Imaging in Pathologically Proven Hallervorden-Spatz Disease
Neurol 39:440-442, Schaffert,D.A.,et al, 1989

Brain White-Matter Changes in the Elderly Prone to Falling
Arch Neurol 46:1292-1296, Masdeu,J.C.,et al, 1989

Hypothyroidism
In Neurologic Clinics, W. B. Saunders Co, Phila, 7:492-493., Kaminski,H.J.&Ruff,R.L., 1989

Diphenhydramine-Induced Dystonia
Clin Pharmacy 8:471, Santora,J.,et al, 1989

Friedreich Ataxia
In Rowland, L. P. Merritt's Textbook of Neurology, 8th Ed, Lea & Febiger, Phila, Ch 13, p627, Rosenberg,R.N., 1989

Life-Threatening Cranial Dystonia Following Trihexyphenidyl Withdrawal
Movement Disorders 4:349-353, Gimenez-Roldan,S.,et al, 1989

Antecollis in Parkinsonism
Lancet 1:1320-1321, Jorens,P.G.,et al, 1989

Cervical Myelopathy Secondary to Movement Disorders:Case Report
Neurosurgery 24:902-905, El-Mallakh,R.S.,et al, 1989

Paroxysmal Cerebellar Ataxia
Aust NZ J Med 19:113-117, Feeney,G.F.&Boyle,R.S., 1989

Hemifacial Spasm, In Movement Disorders, A Comprehensive Survey
Futura Publ., NY. Ch. 9 p.510, Weiner,W.J. &LangA.E., 1989

Transient Paroxysmal Dystonia in Infancy
Neuropediatr 19:171-174, Angelini,L.,et al, 1988

Chronic Progressive Spinobulbar Spasticity, A Rare Form of Primary Lateral Sclerosis
Arch Neurol 45:509-513, Gastaut,J.L.,et al, 1988

Rapidly Progressive Dementia Caused by Spongiform Encephalopathy
West J Med 148:313-319, Enos,B.E.&Vinters,H.V., 1988

Brain Metabolism in Mitochondrial Encephalomyopathy:A PET Study
J Comput Assist Tomogr 12:854-857, DeVolder,A.,et al, 1988

Primary Lateral Sclerosis, A Clinical Diagnosis Reemerges
Arch Neurol 45:1304-1307, Younger,D.S.,et al, 1988

Idiopathic Hypoparathyroidism and Paroxysmal Dystonic Choreoathetosis
Ann Neurol 24:585, Barabas,G.&Tucker,S.M., 1988

Dystonic-Parkinsonian Syndrome after Cyanide Poisoning:Clinical and MRI Findings
JNNP 51:1345-1348, Carella,F.,et al, 1988

Acute Extrapyramidal Syndrome in Methylmalonic Acidemia:"Metabolic Stroke"Involving the Globus Pallidus
J Pediatr 113:1022-1027, Heidenreich,R.,et al, 1988

Blepharospasm
Editorial, Lancet 2:10591988., , 1988

Hyperthyroidism Presenting as Pyramidal Tract Disease
BMJ 297:1395-1396, Shaw,P.J.,et al, 1988

Clinicopath Conf
Paraneoplastic Encephalitis (Limbic and Brain-Stem Encephalitis) , Case Record 39-1988, NEJM 319:849, 860,, 1988

Dystonia and Tremor Induced by Peripheral Trauma:Predisposing Factors
JNNP 51:1512-1519, Jankovic,J.&VanDer Linden,C., 1988

Diagnostic Criteria for Rett Syndrome
The Rett Syndrome Diagnostic Criteria Work Group, Ann Neurol 23:425-4281988., , 1988



Showing articles 850 to 900 of 1183 << Previous Next >>