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Differential
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acquired immunodeficiency syndrome
acquired immunodeficiency syndrome dementia complex
acquired immunodeficiency syndrome, congenital
acquired immunodeficiency syndrome, infants and children
acromicria
advances in neurology
Aicardi-Goutieres syndrome
Alexanders disease
anemia
aneurysm
aneurysm, asymptomatic
aneurysm, intracranial
anorexia
apraxia of eye movements
aqueduct of Sylvius, stenosis
arm swing, reduced
arthritis
aspartocyclase
aspiration
aspirin
ataxia
ataxia, truncal
ataxic gait
attention span
autoimmune epilepsy
B 12 deficiency
B 12 deficiency, infants
Babinski sign
basal ganglia, calcification of
basal ganglia, lesion of
basal ganglia, lesion, bilateral
biologic markers
blindness
blood transfusion
bone marrow biopsy
bradykinesia
brain atrophy
brain biopsy
breast feeding
Brown-Vialetto-Van Laere syndrome
cachexia
calcification, gyral
calcification, intracranial
Canavan's disease
CAT scan
CAT scan, abnormal
cataplexy
cerebellar lesion
cerebral cortical atrophy
cerebral palsy
cerebral vasculature
cerebral venous infarction
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, lactic acid concentration
cerebrospinal fluid, proteincytologic dissociation
cerebrovascular accident
cerebrovascular disease
cherry red spot
cherry red spot-myoclonus syndrome
children
chorea
choreoathetosis
chromosomal abnormality
chromosome 3
Clinical Pathologic Conference(C.P.C.)
cold hands sign
complications
consanguinity
contractures, joint
controversies in neurology
corpus callosum, atrophy of
corpus callosum, thinning
cough
cranial nerve enhancement
cranial nerve enlargement
cranial neuropathy
cranial neuropathy, multiple
crawl regression
cry, abnormal
crying
cultured skin fibroblasts
cyst
cyst, parenchymal
D-dimer
decision analysis
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, childhood
demyelinating disease
dentate nuclei
dentate nuclei, lesion of
developmental milestones
developmental milestones, loss of
developmental retardation
diagnostic criteria
differential diagnosis
difficulty climbing stairs
diplopia
dopa responsive dystonia
drooling
dropped head syndrome
dysarthria
dysmetria
dysphagia
dysphonia
dystonia
dystonia, children
electroencephalogram, abnormalities of
encephalitis
encephalitis, autoimmune
encephalopathy
encephalopathy, neonatal
encephalopathy, progressive
endoscopic surgery
endoscopy
enzyme, defect
epileptic encephalopathy
episodic disorders
evoked potentials
eye movement, disorders of
facial weakness
facial weakness, bilateral
failure to thrive
falling
familial
FARS2 deficiency
feeding disorder
fever
fine motor function, impaired
finger tapping
foam cells
fontanel, bulging
frontal bossing
fundus, abnormality of
gait disorder
galactorrhea
gangliosidosis GM2
Gaucher's disease
gaze palsy
gaze palsy, supranuclear
gender
gene
gene mutation
genetic counselling
genetic neurologic disorders
genetic testing
glaucoma
globoid cells
glucocerebrosidase
glutamic acid decarboxylase, antibody
granular osmiphilic material
growth retardation
Hallervorden Spatz disease
hand deformity
hands, fisted
head circumference
head lag
headache
hearing loss
hepatic failure
hepatitis
hepatomegaly
hepatosplenomegaly
hexosaminidase-A
human immunodeficiency virus type 1
human immunodeficiency virus type 1, infants and children
hydrocephalus
hydrocephalus, complications with
hydrocephalus, etiology
hydrocephalus, fetal
hydrocephalus, non-communicating(obstructive)
hydrocephalus, treatment of
hyperhomocysteinemia
hyperpigmentation of skin
hyperreflexia
hypertonia
hypomyelination
hyporeflexia
hypothermia
hypotonia
hypotonia, infants
immunomodulation
inattention
inborn errors of metabolism
incoordination
infant, evaluation of
infantile tremor syndrome
intellectual deficit
intellectual deterioration
interferon alpha
intracranial pressure, increased
introverted
iron, brain
irritability
jaundice
Jewish
Krabbe's disease
lactic acidemia
L-dopa
Leigh's disease
lethargy
leukocyte enzyme abnormality
leukocytosis
leukodystrophy
leukoencephalopathy
leukoencephalopathy, differential diagnosis
life expectancy
lipid storage disorder of CNS
liver disease
liver function enzymes
lymphadenopathy
lymphadenopathy, axillary
lymphadenopathy, paraaortic
lysosomal storage disease
macrocephaly
malformation, vascular
masked facies
meconium staining
memory, impairment of
meningeal enhancement
meningitis, CSF cell count-normal
mental retardation
metabolic disorder, primary
metabolic disorder, primary-screening tests
metachromatic leukodystrophy
metachromatic leukodystrophy, late-infantile
microcephaly
midbrain, lesion of
misdiagnosis
mitochondrial disease
monoclonal antibodies
mortality
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, angiography
MRI, contrast enhanced
MRI, diffusion weighted
MRI, hypointense signal foci on
MRI, paramagnetic effect
MRS
mucopolysaccharidoses
muscle biopsy
muscle spasm
myasthenia gravis
myasthenia gravis, infantile and juvenile
myelination of nervous system
myoclonus
myoclonus, epilepsy
nasal speech
nausea and vomiting
neck trauma
nerve conduction studies
neuroaxonal dystrophy
neurocutaneous disease
neurofibrillary degeneration
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic disease, tempo
neurologic examination
neurologic signs
neuronal ceroid-lipofuscinosis
neuroophthalmology
neuropathology
neuropathology, brain
neuropathy
Niemann-Pick disease
nystagmus
nystagmus, rotary
ophthalmoplegia
opisthotonus
opportunistic infection
opportunistic infection, CNS
optic atrophy
optic chiasm, enlarged
optic nerve
optic nerve, enlarged
pain
PANK2 mutation
papilledema
paraparesis, familial spastic
paraparesis, spastic
PAS positive material in the brain
pediatric neurology
pleocytosis of cerebrospinal fluid
port wine nevus
postural abnormality
prognosis
progressive myoclonic epilepsy
progressive neurologic disorder
prolactin, elevated
psychological testing
psychomotor retardation
psychosis
ptosis
pulmonary infiltrates
pyramidal tract
pyramidal tract dysfunction
pyruvate dehydrogenase deficiency
pyruvate metabolism, abnormality of
quadriparesis
quadriplegia
rash
rectal biopsy
renal tubular acidosis
retinal degeneration
retinitis pigmentosa
retropulsion
Rett's syndrome
reversible neurologic disorder
review article
riboflavin transporter deficiency
rigidity
rituximab
Rosenthal fibers
running
scoliosis
scoliosis, neurologic association with
screening
sedimentation rate, elevated
seizure
seizure, children
seizure, drug resistance
seizure, intractable
serositis
short stature
shunt procedure, ventricular
shunt procedure, ventricular-complications of
skin, lesions in neurologic disorders
slurred speech
somnolence
spastic diplegia
spasticity
speech disorder
speech disorder, childhood
speech, loss of
splenomegaly
spongy degeneration of brain
spontaneous remission
startle reaction
status epilepticus
stereotyped behavior
stiff joints
strabismus
striatonigral degeneration
striatonigral degeneration, infantile
strokelike episodes
Sturge-Weber syndrome
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
substantia nigra
suck, poor
symmetric brain lesions
systemic illness
systemic juvenile idiopathic arthritis
Tay-Sachs disease
thalamus, lesion of
thalamus, lesion of-bilateral
thrombocytosis
titubation
toe walking
tone, muscle, increased
toxoplasmosis, CNS
transient neurologic deficit
treatment of neurologic disorder
tremor
tremor, intention
trichopoliodystrophy
tuberous sclerosis
tumor necrosis factor
tyrosine hydroxylase deficiency
vasculopathy
vegetarianism
ventricular enlargement
ventriculostomy
ventriculostomy, endoscopic
visual acuity, decreased
visual evoked response
visual field defect
visual fields, constricted
visual impairment
visual loss
vitamin deficiency
vomiting, episodic
vomiting, recurrent
walking, difficulty with
weakness
weakness, generalized
weakness, progressive
Werdnig-Hoffman disease
West disease
wheelchair
white hair
white matter disease
wide based gait
workup
wrist drop
x-linked hydrocephalus
Showing articles 1450 to 1500 of 2279 << Previous Next >>

Confusion & Memory Loss from Capsular Genu Infarction:A Thalamocortical Disconnection Syndrome?
Neurol 42:1966-1979, Tatemichi,T.K.,et al, 1992

Twinning and Neurologic Morbisity
Am J Dis Child 146:1110-1113, Scheller,J.M.&Nelson,K.B., 1992

Coma Assoc with Bursts of Abnor Movements & Cognitive Disturb:Acute Encephalopathy of Obscure Origin
J Pediatr 121:845-851, Sebire,G.,et al, 1992

Gray Matter Heterotopias:MR Characteristics & Correlation with Develop & Neurologic Manifest
Radiology 182:493-499, Barkovich,A.J.&Kjos,B.O., 1992

Is Aluminium a Dementing Ion?
Editorial, Lancet 339:713-7141992., , 1992

Neurologic Syndrome in 25 Workers from an Aluminim Smelting Plant
Arch Int Med 152:1443-1448, White,D.M.,et al, 1992

Periodic Alternating Gaze Deviation in Infancy
Neurol 42:1740-1743, Legge,R.H.,et al, 1992

Levodopa-Nonresponsive Lewy Body Parkinsonism:Clinicopathologic Study of Two Cases
Neurol 42:1323-1327, Mark,M.H.,et al, 1992

Value of Cranial Untrasound and MRI in Predicting Neurodevelopmental Outcome in Preterm Infants
Pediatrics 90:196-199, vandeBor,M.,et al, 1992

Effects of Intravent Hemorrhage & Socioecon Status on NEur Status of Low Birth Weight Inf at 5 yrs of age
J Pediatr 121:280-285, Vohr,B.,et al, 1992

The Changing Epidemiology of Neural Tube Defects, United STates, 1968-1989
Am J Dis Child 146:857-861, Yen,I.H.,et al, 1992

Matrnal Heat Exposure and Neural Tube Defects
JAMA 268:882-885, Milunsky,A.,et al, 1992

Causal Heterogeneity in Isolated Lissencephaly
Neurol 42:1375-1388, Dobyns,W.B.,et al, 1992

Clinical and NEuroradiol Findings of Congen Hydroceph in Infant Born to Mother with HTLV-I-Assoc Myelopathy
Neurol 42:1406-1408, Tohyama,J.,et al, 1992

Fecal Incontinence
NEJM 326:1002-1007, Madoff,R.D.,et al, 1992

Violence, The Neurologic Contribution:An Overview
Arch Neurol 49:595-603, Elliott,F.A., 1992

Cerebromeningeal Haemophagocytic Lymphohistiocytosis
Lancet 239:104-107, Henter,J.&Elinder,G., 1992

A Correlative Triad of Gadolinium-DTPA MRI, EDSS, & CSF-MBP in Relapsing MS Treated with High-Dose Intravenous Methylprednisolone
Neurol 42:63-67, Barkhof,F.,et al, 1992

A Quantitative MRI Study of Vascular Dementia
Neurol 42:138-142, Liu,C.K.,et al, 1992

Sleep in Alzheimer's Disease and the Sundown Syndrome
Neurol 42:83-94, Vitiello,M.V.,et al, 1992

Does Computed Tomographic Brain Imaging Have a Place in the Diagnosis of Dementia
Arch Int Med 152:1437-1440, Engel,P.A.&Gelber,J., 1992

Cranial Computed Tomographic Ovservations in Multi-Infarct Dementia
Stroke 23:804-811, Gorelick,P.B.,et al, 1992

Preventable Senility:A Call for Action Against the Vascular Dementias
Lancet 340:645-648, Hachinski,V., 1992

Dementia After Stroke:Baseline Frequency, Risks, and Clinical Features in a Hospitalized Cohort
Neurol 42:1185-1193, 1992. a, Tatemichi,T.K.,et al, 1992

The Older Driver, Clinical Assessment and Injury Prevention
Arch Int Med 152:735-740, Underwood,M., 1992

A Prospective Study of Cognitive Funct Following Low-Dose Cranial Radiation for Bone Marrow Trnsplant
Pediatrics 90:447-450, Kramer,J.H.,et al, 1992

The Diagnostic Utility of Elevation in Cerebrospinal Fluid B2-Microglobulin in HIV-1 Dementia
Neurol 42:1707-1712, McArthur,J.C.,et al, 1992

Plasma Vitamin B12 Level as a Potential Cofactor in Studies of HIV Type 1-Related Cognitive Changes
Arch Neurol 49:501-506, Beach,R.S.,et al, 1992

Epidemiology of Human Immunodeficincy Virus Encephalopathy in the United States
Neurol 42:1472-1476, Janssen,R.S.,et al, 1992

A Synd of Autosomal Dominant Alternating Hemiplegia:Mimicking Intractable Epilepsy; Chromosomal Studies; Physiol Investig
Neurol 42:2251-2257, Mikati,M.A.,et al, 1992

Population Study of Incidence, complexity, and Severity of Neuro Disabil Among Survivors Weighing 500-1250 Grams
Pediatrics 90:750-755, Robertson,C.M.T.,et al, 1992

Prevention of First Occur of Neural-Tube Defects by Periconceptional Vitamin Suppl
NEJM 327:1832-1835, 18751992., Czeizel,A.E.&Dudas,I., 1992

Neuroleptic Sensitivity in Patients with Senile Dementia of Lewy Body Type
BMJ 305:673-678, McKeith,J.,et al, 1992

Familial Creutzfeldt-Jakob Disease (Codon 200 Mutation) with Supranuclear Palsy
Bertoni. J. M. , et al, JAMA 268:2413-2415., , 1992

Outlook for the Child with a Cephalocele
Pediatrics 90:914-919, Brown,M.S.,et al, 1992

Clinical Outcome in Aggressively Treated Meningeal Gliomatosis
Neurol 42:252-254, Grant,R.,et al, 1992

Clinicopath Conf
Pick's Diseae, Case 6-1992, NEJM 326:397-405992., , 1992

Brain MRI and Electrophysiologic Abnormalities in Preclinical and Clinical Adrenomyeloneuropathy
Neurol 42:85-91, Aubourg,P.,et al, 1992

MR Imaging of the Spinal Cord in 23 Subjects with ALD-AMN Complex
AJR 158:413-416, Snyder,R.D.,et al, 1992

Clinicopath Conf
Huntington's Diseae, Case2-1992, NEJM 326:117-125992., , 1992

Multiple Sclerosis Dementia
Neurol 42:696, Mendez,M.D.&Frey,W.F., 1992

Event-Related Potential P300 in MS, Relation to Magnetic Resonance Imaging and Cognitive Impairment
Arch Neurol 49:44-50, Honig,L.S.,et al, 1992

Mental Development of 2-Year-Old Children Exposed to Alcohol in Utero
J Pediatr 120:740-746, Autti-Ramo,I.,et al, 1992

Criteria for the Diagnosis of Ischemic Vascular Dementia Proposed by St of CA Alzheimer's Disease Diag Treat Ctrs
Neurol 42:473-480, Chui,H.C.,et al, 1992

Physicians, Elderly Drivers, and Dementia
Lancet 339:41-43, O'Neill,D., 1992

Congenital Central Hypoventilation Syndrome:Diagnosis, Management, and Long-Term Outcome in Thirty-Two Children
J Pediatr 120:381-387, Weese-Mayer,D.E.,et al, 1992

Neuropsychological Abnormalities in Children with Congenital Central Hypoventilation Syndrome
J Pediatr 120:388-393, Silvestri,J.M.,et al, 1992

Factors Impairing Daytime Performance in Patients with Sleep Apnea/Hypopnea Syndrome
Arch Int Med 152:538-541, Cheshire,K.,et al, 1992

Evaluation of Cerebral Biopsies for the Diagnosis of Dementia
Arch Neurol 49:28-31, Hulette,C.M.,et al, 1992

Neurological and Neuropsychological Performance in HIV Seropositive Men Without Symptoms
JNNP 55:143-148, McAllister,R.H.,et al, 1992



Showing articles 1450 to 1500 of 2279 << Previous Next >>