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Differential
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agraphia
akinesia
akinesia of eyelid function
alexia
alpha-fetoprotein
Alzheimer's disease, visual variant
aminoacidurias
ANA
anomic aphasia
anterior cerebral artery
anterior cerebral artery territory infarction
anterior cerebral artery, occlusion, language disorder with
aphasia
aphasia, children
aphasia, progressive, primary
aphasia, transcortical
aphasia, transcortical-sensory
apraxia
apraxia of eye movements
apraxia of eyelid closure
apraxia of eyelid opening
apraxia, constructional
apraxia, speech
arthritis
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, truncal
attention deficit disorder with hyperactivity
autism
automobile accidents
Benedict's solution test
bifid uvula
blepharospasm
brain biopsy
bruxism
calcification, intracranial
carcinoembryonic antigen
carcinoma
carotid artery disease
carotid artery occlusion, bilateral
carotid artery occlusion, neck
carphology
CAT scan
CAT scan, abnormal
CAT scan, emission, abnormal
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar degeneration
cerebral arteries, territory of
cerebral cortical atrophy
cerebral infarction
cerebral palsy
cerebral palsy, associated problems with
cerebral palsy, pure ataxic
cerebrovascular accident
cerebrovascular accident, bilateral
Charcot's sign
children
chorea
choreoathetosis
chromosomal abnormality
chromosome 11
cleft palate
Clinical Pathologic Conference(C.P.C.)
cogwheel rigidty
confusion
cortical-basal ganglionic degeneration
degenerative diseases of CNS
dementia
dementia, childhood
dementia, frontotemporal
dementia, presenile
diabetes mellitus
dinitrophenylhydrazine(D.N.P.H.)reaction
diplegia, atonic
diplegia, spastic cerebral
drooling
dysarthria
dysphagia
dysplasia of C.N.S.
dystonia
ecchymoses
electroencephalogram
encephalitis
encephalitis, viral
executive dysfunction
extrapyramidal movement disorder, progressive
eye closure
eye movement, disorders of
familial
ferric chloride test
fever
frontal lobe, pathologic signs of
gag reflex, depressed
gait disorder
gait, apraxic
gaze palsy
gaze palsy, vertical
gene
gene mutation
genetic linkage
genetic neurologic disorders
genetic testing
glabellar sign
growth retardation
handwriting
hearing problems in children
hemianopia, homonymous
hemiparesis
hypertension
hypotonia
immunodeficiency
immunosuppression
immunosuppressive agents
in situ hybridization
insular cortex
intellectual deficit
intellectual deficit, treatable causes of
intelligence quotient
jaw jerk, abnormal
karyotyping
klippel feil syndrome
language disorder in adults
language disorders in children
L-dopa
leukemia
lid
lid abnormalities
lobar atrophy
lymphoma
maple syrup urine disease
masked facies
memory, impairment of
mental retardation
microaneurysm, retinal
micrographia
midline defect in children
misdiagnosis
mortality
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, serial
multiple system atrophy
mutism
myelodysplasia
myoclonus
myoclonus, stimulus sensitive
nasal speech
neglect
neurocutaneous disease
neuroendocrinology
neurologic disease, diagnoses of
neurologic examination, focal
neuropathology
neuropathology, brain
neuropathy
ocular motility, disorders of
ocular myopathy
ocular myopathy, differential diagnosis
operculum syndrome
operculum syndrome, bilateral
ophthalmoplegia
palatopharyngeal incompetence
Parkinson disease
Parkinsonism syndrome
pathology
personality change
phenylketonuria
Pick bodies
Pick's disease
pneumonia
polymerase chain reaction
posterior cortical atrophy
progeria
prognosis
progressive multifocal leucoencephalopathy
progressive neurologic disorder
progressive supranuclear palsy
pseudobulbar palsy
psychological testing, neurologic problems
psychomotor retardation
psychosis
psychosis, childhood
psychosocial aspects
ptosis
pure akinesia
radiation hypersensitivity
release phenomena
respirations in CNS disease
retropulsion
Rett's syndrome
review article
rigidity
rocking
scoliosis
seizure
seizure, advice to parents and teachers regarding
seizure, psychosocial aspects of
seizure, treatment of
semantic dementia
simultanagnosia
single photon emission computed tomography
skin, lesions in neurologic disorders
somnolence
speech disorder
speech disorder, childhood
speech, loss of
spina bifida
spinal muscular atrophy
steroid therapy, CNS treatment and complications with
stuttering
systemic lupus erythematosus
tachycardia
tauopathy
telangiectases
temporal lobe, atrophy
thrombocytopenia
urinary incontinence
urine test for metabolic disorders
visual field defect
visuospatial disturbance
walking, difficulty with
wheelchair
white matter disease
word-finding difficulty
Showing articles 500 to 550 of 608 << Previous Next >>

Speech Arrest & Supplementary Motor Area Seizures
Neurol 34:110-111, Peled,R.,et al, 1984

Aphemia Clinical-Anatomic Correlations
Arch Neurol 40:720-727, Schiff,H.B.,et al, 1983

Mutism after Closed Head Injury
Arch Neurol 40:601-606, Levin,H.S.,et al, 1983

Motor Aphasia Unaccompanied by Faciobrachial Weakness
Neurol 33:519-521, Masdeu,J.C.,et al, 1983

Developmental Learning Disabilities of the Right Hemisphere
Arch Neurol 40:463-468, Weintraub,S.,et al, 1983

Blepharospasm & Orofacial-Cervical Dystonia:Clinical & Pharmacological Findings in 100 Patients
Ann Neurol 13:402-411, Jankovic,J.,et al, 1983

Juvenile Progressive Bulbar Palsy
Arch Neurol 40:351-353, Albers,J.W.,et al, 1983

Dialysis Encephalopathy, Clinical, Electroencephalographic & Interventional Aspects
Medicine 62:129-141, O'Hare,J.A., 1983

Delayed Neurologic Sequelae in Carbon Monoxide Intoxication
Arch Neurol 40:433-435, Choi,I.I.S., 1983

Clin. Path. Conference
Multiple-System Atrophy with Parkinsonism, Case 28-13, NEJM 308:1406-1414983., , 1983

Unrecognized Chronic Lithium Neurotoxic Reactions
JAMA 250:2029-2030, Lewis,D.A., 1983

Recognising & Preventing Duchenne Muscular Dystrophy
BMJ 287:1083-1084, Firth,M.A.,et al, 1983

Aphasia With Nonhemorrhagic Lesions in the Basal Ganglia & Internal Capsule
Arch Neurol 39:15-20, Damasio,A.R.,et al, 1982

Global Aphasia Without Hemiparesis:A Sign of Embolic Encephalopathy
Neurol 32:403-406, VanHorn,G.,et al, 1982

Localization in Transcortical Sensory Aphasia
Arch Neurol 39:475-478, Kertesz,A.,et al, 1982

Spinocerebellar Degeneration Secondary to Chronic Intestinal Malabsorption:A Vitamin E Deficiency Syndrome
Ann Neurol 12:419-424, Harding,A.E.,et al, 1982

"Tip-of-the-tongue"Phenomenon in Parkinson Disease
Neurol 32:567-570, Matison,R.,et al, 1982

The Child Who is Slow to Talk
BMJ 285:671-672, Robinson,R.J., 1982

Von Recklinghausen Neurofibromatosis
NEJM 305:1617-1627, Riccardi,V.M., 1981

Pronounced Cerebellar Features in Legionnaires'Disease
BMJ 283:276, Maskill,M.R., 1981

Primary Lateral Sclerosis
Arch Neurol 38:630-633, Beal,M.F.,et al, 1981

Speech Disorders of Parkinsonism:A Review
JNNP 44:751-758, Critchley,E.M.R., 1981

Metastasis to the Base of the Skull:Clinical Findings in 43 Patients
Neurol 31:530-537, Greenberg,H.S.,et al, 1981

Paroxysmal Symptoms as the First Manifestations of Multiple Sclerosis
JNNP 43:296-304, Twomey,J.A.,et al, 1980

The Aphasia Syndrome of Stroke in the Left Anterior Cerebral Artery Territory
Arch Neurol 37:97-l00, Alexander,M.P.,et al, 1980

Imitating Gestures, A Quantitative Approach to Ideomotor Apraxia
Arch Neurol 37:6-10, Renzi,E.De.,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

Juvenile Metachromatic Leukodystrophy
Arch Neurol 37:42-46, Haltia,T.,et al, 1980

"Top of the Basilar"Syndrome
Neurol 30:72-79, 1980, Caplan,L.R., 1980

Ocular Myasthenia:Diagnosis & Therapy
In Neuro-Ophthalmology, Vol X ed. by J. Glaser. CV Mosby Co, St. Louis, Daroff,R., 1980

Sydenham Chorea:An Update
Neurol 30:331-334, Nausieda,P.A.,et al, 1980

Aphasia After Left Hemispheric Intracerebral Hemorrhage
Neurol 30:1193-1202, Alexander,M.P.,et al, 1980

Intracranial Calcification in Hyperparathyroidism Associated with Gait Apraxia & Parkinsonism
Neurol 30:1005-1007, Margolin,D.,et al, 1980

Children's Language Disorders:Recent Research Advances
Ann Neurol 7:497-507, Ludlow,C.L., 1980

Adult Celiac Disease Presenting as Cerebellar Syndrome
Neurol 30:245-249 1980., Finelli,P.F.,et al, 1980

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

Tapia's Syndrome
Arch Neurol 36:257-260, Schoenberg,B.S.,et al, 1979

Language Deficits After Apparent Clinical Recovery from Childhood Aphasia
Ann Neurol 6:405-409, Woods,B.,et al, 1979

Aphemia with Hemiplegic Migraine
Neurol 29:1317-1318, Jenkyn,L.R., 1979

Fusiform Basilar Artery Aneurysm in a Child
Neurol 29:1045-1049, Read,D.,et al, 1979

Dysarthria-Clumsy Hand Syndrome Produced by Capsular Infarct
Ann Neurol 6:263-265, Spertell,R.B.,et al, 1979

Familial Periodic Ataxia
Arch Neurol 36:568-569, Donat,J.R.,et al, 1979

Aphasia Rehabilitation
Arch Neurol 36:187, Benson,D.F., 1979

Aphasia, The Sole Manifestation of Focal Status Epilepticus
Neurol 29:745-748, Hamilton,N.G.,et al, 1979

Self-Limited Granulomatous Angiitis of the Cerebellum
Ann Neurol 5:490-492, Beresford,H.R.,et al, 1979

Hereditary Paroxysmal Ataxia:Response to Acetazolamide
Neurol 28:1259-1264, Griggs,R.C.,et al, 1978

Aphasia Following Infarction of the Left Supplementary Motor Area
Neurol 28:1220-1223, Masdeu,J.C.,et al, 1978

Aphasias & Related Disturbances
Textbook of Medicine. Ed. R. W. Wilkins Little Brown & Co. , Boston, p. 867, Benson,D.F., 1978

Identification of Speech Lateralization by Intracarotid Injection of Methohexital
Ann Neurol 4:86, Willmore,L.J.,et al, 1978



Showing articles 500 to 550 of 608 << Previous Next >>