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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

advances in neurology

Aicardi-Goutieres syndrome

Alexanders disease

aneurysm, asymptomatic

aneurysm, intracranial

apraxia of eye movements

aqueduct of Sylvius, stenosis

arm swing, reduced

ataxia, truncal

autoimmune epilepsy

B 12 deficiency

B 12 deficiency, infants

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

biologic markers

black toenail sign

blood transfusion

bone marrow biopsy

Brown-Vialetto-Van Laere syndrome

calcification, gyral

calcification, intracranial

Canavan's disease

CAT scan, abnormal

cerebellar lesion

cerebral cortex

cerebral cortical atrophy

cerebral ischemia

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

choreoathetosis

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

cold hands sign

congenital infection, CNS

contractures, joint

controversies in neurology

corpus callosum, atrophy of

corpus callosum, thinning

cranial nerve enhancement

cranial nerve enlargement

cranial neuropathy

cranial neuropathy, multiple

crawl regression

cultured skin fibroblasts

cyst, parenchymal

decision analysis

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

dementia, childhood

demyelinating disease

dentate nuclei, lesion of

developmental milestones

developmental milestones, loss of

developmental retardation

diagnostic criteria

differential diagnosis

difficulty climbing stairs

dopa responsive dystonia

dropped head syndrome

dystonia, children

electroencephalogram, abnormalities of

encephalitis, autoimmune

encephalomalacia

encephalopathy, neonatal

encephalopathy, progressive

endoscopic surgery

epileptic encephalopathy

episodic disorders

evoked potentials

eye movement, disorders of

facial weakness

facial weakness, bilateral

failure to thrive

FARS2 deficiency

feeding disorder

fine motor function, impaired

fontanel, bulging

frontal bossing

fundus, abnormality of

gangliosidosis GM2

Gaucher's disease

gaze palsy, supranuclear

genetic counselling

genetic neurologic disorders

genetic testing

glucocerebrosidase

glutamic acid decarboxylase, antibody

granular osmiphilic material

growth retardation

gyrus, abnormal

Hallervorden Spatz disease

head circumference

hepatic failure

hepatosplenomegaly

hexosaminidase-A

human immunodeficiency virus type 1

human immunodeficiency virus type 1, infants and children

hydrocephalus, complications with

hydrocephalus, etiology

hydrocephalus, fetal

hydrocephalus, non-communicating(obstructive)

hydrocephalus, treatment of

hyperhomocysteinemia

hyperpigmentation of skin

hypomyelination

hypotonia, infants

immunomodulation

inborn errors of metabolism

infant, evaluation of

infantile spasm

infantile tremor syndrome

intellectual deficit

intellectual deterioration

interferon alpha

intracranial pressure, increased

Krabbe's disease

lactic acidemia

laminar necrosis, cortical

Leigh's disease

leukocyte enzyme abnormality

leukoencephalopathy

leukoencephalopathy, differential diagnosis

life expectancy

lipid storage disorder of CNS

liver function enzymes

lymphadenopathy

lymphadenopathy, axillary

lymphadenopathy, paraaortic

lysosomal storage disease

malformation, CNS, congenital

malformation, vascular

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

midbrain, lesion of

mitochondrial disease

mitochondrial encephalomyopathy

monoclonal antibodies

movement disorder

movement disorder, extrapyramidal

MRI lesion location

MRI, angiography

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, gyral swelling

MRI, hypointense signal foci on

MRI, paramagnetic effect

MRI, T1 weighted high signal foci

mucopolysaccharidoses

myasthenia gravis

myasthenia gravis, infantile and juvenile

myelination of nervous system

myoclonus, epilepsy

myoclonus, multifocal

myoclonus, treatment of

nausea and vomiting

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, brain

Niemann-Pick disease

nystagmus, rotary

ophthalmoplegia

opportunistic infection

opportunistic infection, CNS

optic chiasm, enlarged

optic nerve, enlarged

paraparesis, familial spastic

paraparesis, spastic

PAS positive material in the brain

pediatric neurology

pleocytosis of cerebrospinal fluid

port wine nevus

postural abnormality

progressive myoclonic epilepsy

progressive neurologic disorder

prolactin, elevated

psychological testing

psychomotor retardation

pulmonary infiltrates

pyramidal tract

pyramidal tract dysfunction

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

renal tubular acidosis

retinal degeneration

retinitis pigmentosa

Rett's syndrome

reversible neurologic disorder

riboflavin transporter deficiency

Rosenthal fibers

scoliosis, neurologic association with

sedimentation rate, elevated

seizure, children

seizure, crying as manifestation of

seizure, drug resistance

seizure, intractable

shunt procedure, ventricular

shunt procedure, ventricular-complications of

skin, lesions in neurologic disorders

spastic diplegia

speech disorder

speech disorder, childhood

speech, loss of

spinal muscular atrophy

spongy degeneration of brain

spontaneous remission

startle reaction

status epilepticus

stereotyped behavior

striatonigral degeneration

striatonigral degeneration, infantile

strokelike episodes

Sturge-Weber syndrome

subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease

substantia nigra

symmetric brain lesions

systemic illness

systemic juvenile idiopathic arthritis

Tay-Sachs disease

temporal lobe, lesion, bilateral

thalamus, lesion of

thalamus, lesion of-bilateral

tone, muscle, increased

tongue, fasciculations of

toxoplasmosis, CNS

transient neurologic deficit

treatment of neurologic disorder

tremor, intention

trichopoliodystrophy

tuberous sclerosis

tumor necrosis factor

tyrosine hydroxylase deficiency

ventricular enlargement

ventriculostomy

ventriculostomy, endoscopic

visual acuity, decreased

visual evoked response

visual field defect

visual fields, constricted

visual impairment

vitamin deficiency

vomiting, episodic

vomiting, recurrent

walking, difficulty with

weakness, generalized

weakness, progressive

Werdnig-Hoffman disease

white matter disease

wide based gait

x-linked hydrocephalus

Showing articles 2300 to 2319 of 2319 << Previous

Dementia in Cerebral Vascular Disease
Cerebral Vascular Diseases, Grunne & Stratton, Inc. , pp 232-236 (Edited by Toole & others), Fisher,C.M., 1968

"Estimation of Gestational Age by Neuro. Assess. in First Week of Life"
Arch Dis Child 43:353, Farr,V., 1968

Spastic Pseudosclerosis (Creutzfeldt-Jakob Dis) Van Rossum A. , In:Vinken, P. J.
Handbk of Clin Neurol Vol 6 North-Holland Publ. Amster 1968 Ch 28, p 726., Bruyn,G.W., 1968

Corticodentatonigral Degeneration with Neuronal Achromasia
Arch Neurol 18:20-33, Rebeiz,J.J.,et al, 1968

Huntington's Chorea
Bruyn, G. W. In Vinken & Bruyn, Handbk of Clin Neurol, North-Holland Publ Co, Amsterdam, 6:298, , 1968

Parkinson's Disease
In Handbk of Clinical Neurology, Vinken, P. J. & Bruyn, G. W. , Ed, North-Holland Publ Co, Amsterdam, 6:173, 1968. Selby, G., 1968

The Neuro-Psychiatric Syndr. Assoc. with Chronic Liver Disease & an Extensive Portal-Systemic Collat. Circul
Quart J Med 36:135, 1967 Jan., Read,A.E.,et al, 1967

Dementia & Folate Deficiency
Quart J Med 36:, 1967 Apr., Strachan,R.,et al, 1967

The Brain in Multiple Neurofibromatosis:A Suggested Neuropathological Basis for the Assoc. Mental Defect
Brain 90:829, Rosman,N.P.,et al, 1967

Thalamic Tumors
J Neurosurg 24:505, Cheek,W.R.,et al, 1966

Mental Deficiency Associated with Muscular Dystrophy
Brain 89:769, Rosman,N.P.,et al, 1966

Diagnostic Significance of Median Facial Anomalies for Holoprosencephaly
Pediatr 256, 1964 Aug., DeMeyer,W.,et al, 1964

Encephalopathy in Whipple's Disease
Neurol 12:65, Lampert,P.,et al, 1962

Neuro CPC of MGH
Jacob-Creutzfeldt Disease, NEJM 264:1359-13641961., , 1961

Clinical Picture in Creutzfeldt-Jakob Disease
Trans of Amer Neuro Assn 5:l47, Fisher,C.M., 1960

Paraplegia In Flexion of Cerebral Origin
J Neuropath Exper Neuro 13:267, Yakovlev,P., 1954

Triethylene Melamine in the Treatment of Neoplastic Disease
Arch Int Med 87:477-516, Karnofsky,D.A.,et al, 1951

Denver Developmental Screening Test-Testing Materials
, , 1850

Goodenough Draw-A-Person Test-Handout.
, , 1850

Clinical Study of Nine Patients with ReNU Syndrome
, Okamoto,N.,et al,

Showing articles 2300 to 2319 of 2319 << Previous