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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
ACTH
advances in neurology
Aicardi-Goutieres syndrome
Alexanders disease
anemia
aneurysm
aneurysm, asymptomatic
aneurysm, intracranial
anorexia
apraxia of eye movements
aqueduct of Sylvius, stenosis
areflexia
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
black toenail sign
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 cortex
cerebral cortical atrophy
cerebral ischemia
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 accident, mimics
cerebrovascular disease
cherry red spot
cherry red spot-myoclonus syndrome
children
chorea
choreoathetosis
chromosomal abnormality
chromosome 3
Clinical Pathologic Conference(C.P.C.)
clinodactyly
cold hands sign
complications
congenital infection, CNS
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
encephalomalacia
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
fetus
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
gyrus, abnormal
Hallervorden Spatz disease
hand deformity
hands, fisted
head bobbing
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
hypsarrhythmia
immunomodulation
inattention
inborn errors of metabolism
incoordination
infant, evaluation of
infantile spasm
infantile tremor syndrome
intellectual deficit
intellectual deterioration
interferon alpha
intracranial pressure, increased
introverted
iron, brain
irritability
jaundice
Jewish
Krabbe's disease
lactic acidemia
laminar necrosis, cortical
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, CNS, congenital
malformation, vascular
masked facies
meconium staining
MELAS syndrome
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
mitochondrial encephalomyopathy
mongolism
monoclonal antibodies
mortality
movement disorder
movement disorder, extrapyramidal
MRI
MRI lesion location
MRI pattern
MRI, abnormal
MRI, angiography
MRI, contrast enhanced
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, gyral swelling
MRI, hypointense signal foci on
MRI, paramagnetic effect
MRI, serial
MRI, T1 weighted high signal foci
MRS
mucopolysaccharidoses
muscle biopsy
muscle spasm
myasthenia gravis
myasthenia gravis, infantile and juvenile
myelination of nervous system
myoclonus
myoclonus, epilepsy
myoclonus, multifocal
myoclonus, treatment of
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
recurrent
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, crying as manifestation of
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
spinal muscular atrophy
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
temporal lobe, lesion, bilateral
thalamus, lesion of
thalamus, lesion of-bilateral
thrombocytosis
titubation
toe walking
tone, muscle, increased
tongue, fasciculations of
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 2100 to 2150 of 2319 << Previous Next >>

Encephalopathy in Infants & Children With Chronic Renal Disease
Arch Neurol 38:656-658, Foley,C.M.,et al, 1981

Progressive Infantile Poliodystrophy, Assoc. With Disturbed Pyruvate Oxidation in Muscle & Liver
Arch Neurol 38:767-772, Prick,M.J.J.,et al, 1981

Biotin-Responsive Carboxylase Deficiency Associated With Subnormal Plasma & Urinary Biotin
NEJM 304:817-820, Thoene,J.,et al, 1981

Cerebral Disorder In Alcoholism, Syndromes Of Impairment
Brain 104:1-20, Lishman,W.A., 1981

Amyotrophic Lateral Sclerosis & its Association with Dementia, Parkinsonism & Other Neurological Disorders:A Review
Brain 104:217-247, Hudson,A.J., 1981

Temporal Arteritis Presenting as Ataxia and Dementia
Post Grad Med 69:246-249, Shenberger,K.N.,et al, 1981

Handedness, Clumsiness & Cognitive Ability
Develop Med Child Neurol 22:569-579, Bishop,D.V.M., 1980

Leukoencephalopathy & Elevated Levels Of Myelin Basic Protein In The CSF Of Patients With Acute Lymphoblastic Leukemia
NEJM 303:19-21, Gangji,D.,et al, 1980

Acquired Aphasia with Convulsive Disorder:Course & Prognosis
Neurol 30:524-529, Mantovani,J.F.,et al, 1980

Human Cerebellar Hypoplasia, A Syndrome of Diverse Causes
Arch Neurol 37:300-305, Sarnatt,H.B.,et al, 1980

Idiopathic Hyperammonemia Associated with Cerebral arteriovenous Malformation
Arch Neurol 37:111-112, Michaelson,P.S., 1980

A Family with Hereditary Ataxia:HLA Typing
Neurol 30:12-20, Nino,H.E.,et al, 1980

Creutzfeldt-Jakob Disease in a 20-year-old Woman
Neurol 30:492-496, Packer,R.J.,et al, 1980

Fetal Methylmercury Poisoning:Clinical & Toxicological Data on 29 Cases
Ann Neurol 7:348-353, Marsh,D.O.,et al, 1980

Parkinson Disease, Dementia, & Alzheimer Disease:Clinicopathological Correlations
Ann Neurol 7:329-335, Boller,F.,et al, 1980

Diagnosis of Infatile Neuroaxonal Dystrophy by Skin Biopsy
Ann Neurol 7:377-379, Wisniewski,K.,et al, 1980

Maternal & Fetal Sequelae of Anticoagulation During Pregnancy
Am J Med 68:122-140, Hall,J.G.,et al, 1980

Hazards of Oral Anticoagulants During Pregnancy
JAMA 243:1549-1551, Stevenson,R.E.,et al, 1980

Cognitive Function in Patients With Multiple Sclerosis
Arch Neurol 37:577-579, Peyser,J.M.,et al, 1980

Lafora Disease:Diagnosis by Liver Biopsy
Ann Neurol 8:409-415, Nishimura,R.N.,et al, 1980

Evidence For & Against the Transmissibility of Alzheimer Disease
Neurol 30:945-950, Goudsmit,J.,et al, 1980

Amygdaloid Changes in Aging & Dementia
Arch Neurol 37:625-629, Herzog,A.G.,et al, 1980

Demonstration of CSF Gamma-globulin Banding in Presenile Dementia
Neurol 30:882-884, Williams,A.,et al, 1980

Decreased Computerized Tomography Numbers in Patients With Presenile Dementia
Arch Neurol 37:401-409, Naeser,M.A.,et al, 1980

Presenile Alzheimer Disease:Amyloid Plaques in the Cerebellum
Neurol 30:820-825, Pro,J.D.,et al, 1980

Dementia From Aluminum Pots
NEJM 303:164, Levick,S.E., 1980

Pathological Verification of Ischemic Score in Differentiation of Dementias
Ann Neurol 7:486-488, Rosen,W.G.,et al, 1980

Reversible Dementia, Illustrative Cases, Definition, & Review
JAMA 243:2434-2439, Cummings,J.,et al, 1980

Alzheimer's Disease
Editorial, BMJ 281:1374-13751980., , 1980

Progressive White Matter Destruction Following Irradiation of an Extracranial Neoplasm
Ann Neurol 8:76-78, Rottenberg,D.A.,et al, 1980

Clin. Path. Conference
Creutzfeldt-Jakob Disease, Ataxic Type, with Kuru Plaques, Case Record 45-1980, NEJM 303:1162-11710., , 1980

Osteopetrosis, Renal Tubular Acidosis & Basal Ganglia Calcification in Three Sisters
Am J Med 69:64-74, Whythe,M.P.,et al, 1980

Amelioration Of Neurologic Abnormalities After"Enzyme Replacement"In Adenosine Deaminase Deficiency
NEJM 303:377-380, Hirschhorn,R.,et al, 1980

Ventriculitis in an Adult Delineated by Radio Nuc. Brain Scan, Asso. with Misleading Findings on CT
Arch Neurol 37:381-383, Singh,R.S.,et al, 1980

Alternating Hemiplegia in Infants:Report of Five Cases
Dev Med Child Neurol 22:784-791, Krageloh,I.&Aicardi,J., 1980

Adult Polysaccharidosis
Arch Neurol 36:840-845, Peress,N.S.,et al, 1979

Clinical Recovery from Schilder Disease
Neurol 29:244-251, Ellison,P.H.,et al, 1979

Congenital Ocular Motor Apraxia
Arch Neurol 36:29-31, Orrison,W.W.,et al, 1979

Primary Glioblastoma of the Pineal Gland
Arch Neurol 36:717-718, Kalyanaraman,U.P., 1979

"Agenesis"of the Temporal Lobe
Arch Neurol 36:590-591, Kansu,T.,et al, 1979

Dementia in Parkinson Disease
Ann Neurol 6:355-359, Lieberman,A.,et al, 1979

Familial Tapetorentinal Degeneration & Epilepsy
Arch Neurol 36:544-546, Cohan,S.L.,et al, 1979

Cockayne Syndrome:Unusual Neuropathological Findings & Review of the Literature
Ann Neurol 6:340-348, 1979, Soffer,D.,et al, 1979

The"Hypernormal"CT Scan in Dementia:Bilateral Isodence Subdural Hematomas
Neurol 29:1522-1524, Jacobson,P.L.,et al, 1979

Pseudodementia
Am J Psychiatry 136:895-900, Wells,C.E., 1979

Multiple Sclerosis Presenting with Acute Remitting Psychiatric Symptoms
JNNP 42:859-863, Matthews,W.B., 1979

Agenesis of the Corpus Callosum:A Study of the Frequency of Associated Malformations
Ann Neurol 6:349-354, Parrish,M.L.,et al, 1979

A Neuropathologic Study of Whipple's Disease
Acta Neuropathol. (Berl. ) 48:223-2269., Powers,J.M.,et al, 1979

Clinicopathologic Studies of Primary Cerebral Amyloid Angiopathy
Mayo Clin Proc 54:22-31, , 1979

Neoplastic Angioendotheliosis
Arch Neurol 36:5-7, Dolman,C.L.,et al, 1979



Showing articles 2100 to 2150 of 2319 << Previous Next >>