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Differential
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abdominal reflex, absent

abducens nerve paralysis

abducens nerve paralysis, bilateral

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

acquired immunodeficiency syndrome, congenital

acquired immunodeficiency syndrome, infants and children

Addison's disease

adolescent medicine

adrenal crisis, acute

adrenoleukodystrophy

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

advances in neurology

adverse drug reaction

affect, inappropriate

agnosia, visual

alcohol intolerance

alternating hemiplegia

alternating rapid movement

Alzheimer's disease

Alzheimer's disease, driving with

Alzheimer's disease, visual variant

amaurosis fugax

AMPA receptor antibodies

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, childhood

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, Parkinson-dementia-complex

amyotrophic lateral sclerosis, post-encephalitic

ANA-negative systemic lupus erythematosus

anemia, megaloblastic

anesthesia, general

angiitis, isolated of CNS

angiitis, isolated of CNS, tumefactive

angiography, cerebral, beaded vessels

angiography, cerebral

angiography, cerebral, false negative

angiography, cerebral, negative

ankle, swelling of

antibiotics, neurologic complications with

antibodies to measles

anticardiolipin antibodies

anticoagulant, treatment

anticonvulsants, selection of

antiphospholipid antibodies

antiviral agents

aqueduct of Sylvius, obstruction

arylsulfatase A

ataxia, cerebellar

ataxia, truncal

auditory evoked brainstem potentials

autoimmune basal ganglia encephalitis

autoimmune disease

automobile accidents

autonomic dysfunction

axonal spheroid

azidodeoxythymidine

B 12 deficiency

bacterial infection, CNS

basal ganglia, calcification of

basal ganglia, infarction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavioral disorder

behavioral disorder, acute

Behcet's syndrome

bicycle injuries

blind spot, enlarged

blindness, sudden

blood brain barrier

blood transfusion

bone marrow biopsy

bone marrow transplantation

brain scan, abnormal

brainstem, lesion of

burning feet, differential diagnosis of

burning paresthesia

calcification, intracranial

carcinoma of breast

carcinoma of lung

carcinoma of pancreas

carcinoma of stomach

carotid artery occlusion, neck

carotid artery stenosis

carpo-pedal spasm

CAT scan, abnormal

CAT scan, disappearing lesion on

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, serial

cauda equina, enhancement

celiac disease, childhood

central nervous system, infection of

central pontine myelinolysis

cerebellar atrophy, primary

cerebellar degeneration

cerebellar infarction

cerebellar lesion

cerebellum, disease of

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortex

cerebral cortical atrophy

cerebral embolism

cerebral embolism, cardiac origin

cerebral infarction

cerebral infarction, hemorrhagic

cerebral infarction, subcortical

cerebral ischemia

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, cytology

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, pressure increased

cerebrovascular accident

cerebrovascular accident, atrial myxoma

cerebrovascular accident, bilateral

cerebrovascular accident, familial occurrence

cerebrovascular accident, infancy and childhood

cerebrovascular accident, multiple

cerebrovascular accident, neonatal

cerebrovascular accident, non atherosclerotic cause of

cerebrovascular accident, nonvascular territory

cerebrovascular accident, recurrent

cerebrovascular accident, three territory involvement

cerebrovascular accident, topographic pattern

cerebrovascular accident, women

cerebrovascular accident, work up for

cerebrovascular accident, young adult

cerebrovascular disease

cerebrovascular disease, cardiovascular disease with

ceruloplasmin, serum

chemotherapy, CNS treatment and complications with

cherry red spot

cherry red spot-myoclonus syndrome

choreoathetosis

chorioretinitis

chromosomal abnormality

chronic progressive external ophthalmoplegia

Clinical Pathologic Conference(C.P.C.)

clubbing of fingers

cogwheel rigidty

collapsin response mediator protein 5 IgG

concentration, impaired

congenital infection, CNS

congenital infection, viral

conjunctival biopsy

contactin associated protein like 2 antibodies

corneal dystrophy

cortical blindness

cortical blindness, transient

cortical infarction

cortical infarction, small

cranial nerve enhancement

cranial nerve palsies

cranial nerve palsies, bilateral

cranial neuropathy, multiple

C-reactive protein, elevated

crying, pathologic

cryptococcal meningitis

cultured skin fibroblasts

cyst, cortical parenchyma

cyst, ventricular

cysticercosis, cerebral

cysticercosis, intraventricular

cysticercosis, subarachnoid

cytomegalic inclusion disease

cytomegalovirus infection

deafness, congenital

decerebrate posture

decision analysis

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

dementia, cerebrovascular disease causing

dementia, childhood

dementia, presenile

dementia, rapidly progressive

dementia, reversible

dementia, subcortical

dementia, transmissible

dementia, treatment of

demyelinating disease

depth perception, impaired

developmental evaluation

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes mellitus

diagnostic criteria

dialysis dementia

differential diagnosis

difficulty climbing stairs

disability rating scale, neurological

DPPX, antibodies, encephalitis

dysequilibrium syndrome

dyskinesia, facial

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, pediatric patients

electroencephalogram, periodic complexes

electroencephalogram, video monitoring with

electron microscopy

electroretinograph

encephalitis, autoimmune

encephalitis, etiology

encephalitis, human immunodeficiency virus type 1

encephalitis, paraneoplastic

encephalitis, viral

encephalomyelitis

encephalopathy, metabolic

encephalopathy, neonatal

encephalopathy, post traumatic

encephalopathy, progressive

epidemiology of neurology

epilepsia partialis continua

episodic neurologic deficits

ethics in neurology

evoked potentials

exercise intolerance

eye movement, disorders of

Fabry's disease

facial weakness

faciobrachial dystonic seizure

failure to thrive

familial hemiplegic migraine

fatty acid, elevated plasma content

finger nose finger test

fingerprint bodies

fontanel, bulging

fourth ventricle, cyst

fracture, long bone

frontal lobe, pathologic signs of

fundus, abnormality of

fungal infection, CNS

gamma amino butyric acid receptor antibody

gangliosidosis GM2

gastrointestinal disease, neurologic complications

gaze palsy, supranuclear

gaze palsy, vertical

genetic counselling

genetic diagnosis, prenatal

genetic neurologic disorders

genetic screening

genetic testing

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glutamic acid decarboxylase, antibody

glycine receptor antibodies

granular atrophy, cerebral cortex

growth retardation

gyrus, abnormal

Hallervorden Spatz disease

hallucination, visual

head injury, pediatric

head injury, prognosis in

headache, severe

headache, vascular

health insurance

hearing loss, bilateral

hearing problems in children

heel-knee-shin test

helminthic infection of CNS

hemianopia, homonymous

hemiparesis, recurrent

hemiparesis, transient

hepatic failure

hepatolenticular degeneration(Wilson's disease)

hepatosplenomegaly

heralding manifestation

herpes simplex encephalitis

hexosaminidase-A

Hodgkin's disease, neurologic involvement with

human immunodeficiency virus type 1

human immunodeficiency virus type 1, acute infection

human immunodeficiency virus type 1, infants and children

human T-lymphotropic virus type I(HTLV-I)

Huntington's chorea

Huntington's chorea, genetic counselling

Huntington's disease, children

hydrocephalus, non-communicating(obstructive)

hydrocephalus, transient

hyperpigmentation of skin

hypoglycorrhachia

hypotension, systemic

hypotonia, infants

iatrogenic neurologic disorders

immunofluorescence

immunologic disease

immunosuppression

immunosuppressive agents

impaired vigilance

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

infant and newborn with distress, neurologic prognosis in

infant, evaluation of

infantile spasm

intellectual deficit

intellectual deficit, treatable causes of

intellectual deterioration

intelligence quotient

intestinal pseudoobstruction

intracerebral hemorrhage

intracranial hypertension, benign

intracranial pressure, increased

intrathecal chemotherapy

intrauterine infection

intrauterine infection, viral

intrauterine infection, viral of CNS

intraventricular hemorrhage

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, variant

jaw contractures

Kayser-Fleischer ring

Kearns-Sayre syndrome

lactic acidemia

lacunar infarction

Lafora's disease

language disorders in children

Leber's hereditary optic neuropathy

leg weakness, bilateral

Leigh's disease

Leigh's disease, adult variety

lenticular nucleus, lesion of, bilateral

leucine rich glioma inactivated 1 antibodies

leukoencephalopathy

level of consciousness, decreased

life expectancy

limbic encephalitis

lipid storage disorder of CNS

livedo reticularis

liver transplantation

lupus anticoagulant

lymphadenopathy

lymphoma involving CNS

lymphoma, primary of CNS

lysosomal storage disease

malignancy screen

manic-depressive

marche a petits pas

medical-legal aspects of neurology

melanoma, malignant

memory, defect of recent

memory, impairment of

meningeal enhancement

meningitis, aseptic

meningitis, carcinomatous

meningitis, chronic

meningitis, cysticercosis

meningitis, eosinophilic

meningitis, lymphomatous

meningitis, noninfectious

meningovascular syphilis

mental retardation

mental status, abnormal

mesial temporal lobe

metabolic disorder, primary

metabolic disorder, primary-screening tests

metachromatic leukodystrophy

metachromatic leukodystrophy, juvenile

microangiopathy, brain

microangiopathy, retina

middle cerebral artery, occlusion of

middle cerebral artery, stenosis of

migraine, hemiplegic

mitochondrial disease

mitochondrial encephalomyopathy

mitral valve lesion

molecular genetics

monoclonal antibodies

Morvan's fibrillary chorea

motor neuron disease

movement disorder

movement disorder, extrapyramidal

moyamoya, adult

MRI, angiography

MRI, angiography, false negative

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, diffusion weighted

MRI, false negative

MRI, high signal foci on

MRI, paramagnetic effect

MRI, punctate pattern

MRI, ring sign, open

MRI, spinal cord

MRI, target sign

multinucleated giant cell

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

muscle stiffness

muscle weakness

muscle weakness, proximal

myasthenia gravis, differential diagnosis

myasthenia gravis, misdiagnosis of

myelitis, longitudinal

myelitis, transverse, recurrent

myelopathy, vacuolar

myocardial infarction

myoclonic jerks

myoclonus, epilepsy

myopathy, mitochondrial

nausea and vomiting

neoplasm, intracranial, differential diagnosis of

neoplasm, metastatic

neoplasm, metastatic to eye

nerve conduction studies

neurexin-3 alpha antibodies

neuroaxonal dystrophy

neuroaxonal dystrophy, infantile

neuroaxonal dystrophy, juvenile

neuroendocrinology

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic disease, multifocal

neurologic evaluation

neurologic examination, focal

neurologic signs

neuronal cell surface antigen

neuronal ceroid-lipofuscinosis

neuroophthalmology

neuropathology, brain

neuropathy, peripheral

neuropathy, peripheral, treatment

newborn, evaluation of

Niemann-Pick disease

NMDA antagonists

occipital lobe, lesion of

old age, driving and

old age, neurology of

ophthalmoplegia

opportunistic infection

opportunistic infection, CNS

optic neuritis, bilateral

optic neuropathy

orthostatic hypotension

overlap syndrome

owl's eye sign of spinal cord

pain, abdominal

palmomental response

paraparesis, familial spastic

paraparesis, spastic

parasitic infection, CNS

Parkinson disease

Parkinsonism syndrome

PAS positive material in the brain

peripheral vascular disease

peroxisomal disease

persistent vegetative state

personality change

phenylketonuria

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

pleocytosis of cerebrospinal fluid, neutrophilic

pneumoencephalogram(PEG)

polymerase chain reaction

polyneuropathy, uremic

potassium channel antibodies

precipitating factors

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

progressive infantile poliodystrophy

progressive myoclonic epilepsy

progressive neurologic disorder

pseudobulbar palsy

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

ptosis, bilateral

pulmonary infiltrates

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

ragged-red fibers

rapidly progressing neurologic illness

reading disorder, acquired

reading problem, causes of

release phenomena

remote effect of cancer on the nervous system

renal transplantation

respirations in CNS disease

respiratory tract infection

restless leg syndrome

reticulum cell sarcoma

retina, abnormal

retinal branch artery occlusion

retinal degeneration

retinal hemorrhages

retinal infarction

retinitis pigmentosa

Rett's syndrome

reversible neurologic disorder

root lesion, nerve

rubella encephalitis, progressive

rubella syndrome

Schilder's disease

sea-blue histiocytes

sedimentation rate, elevated

seizure, children

seizure, intractable

seizure, neonatal

seizure, prognosis in childhood

seizure, treatment of

sensorineural hearing loss

serologic testing

serologic testing of cerebrospinal fluid

serologic testing, false negative

shunt procedure, ventricular

simultanagnosia

skateboard injuries

skin, darkening of

skin, lesions in neurologic disorders

skull x-ray, abnormal

slow virus infection of CNS

small vessel disease

small vessel vasculitis

Sneddon's syndrome

somatosensory evoked potentials

spastic diplegia

speech disorder

speech disorder, childhood

speech disorder, non aphasic

spinal cord, embolism of

spinal cord, infarction of

spinal cord, lesion of

spinal cord, pathologic exam of

spinocerebellar ataxia

spinocerebellar ataxia type 7

spongy degeneration of brain

standing difficulty

startle reaction

status epilepticus

status epilepticus, intractable

steroid therapy, CNS treatment and complications with

striatal encephalitis

striatum, lesion of

striatum, lesion of, bilateral

strokelike episodes

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

subarachnoid hemorrhage

subarachnoid hemorrhage, cerebral convexity

subdural hematoma

substantia nigra

Susac's syndrome

symmetric brain lesions

syphilis, congenital

syphilis, diagnosis and treatment

syphilis, neurologic complications with

systemic lupus erythematosus

tapetoretinal degeneration

Tay-Sachs disease

temporal lobe, lesion

temporal lobe, lesion, bilateral

teratoma, ovarian

testicular atrophy

thalamus, lesion of

thalamus, lesion of-bilateral

third nerve palsy

Three territory sign

thromboangiitis obliterans cerebri

thrombophlebitis

toxoplasmosis, acquired

toxoplasmosis, CNS

transient ischemic attack

transient ischemic attack, recurrent

transient neurologic deficit

transport of patient

treatment of neurologic disorder

trinucleotide repeats

Trousseau's sign

tuberous sclerosis

tumor necrosis factor

ulcerative colitis

upgaze, paralysis of

uremic encephalopathy

uremic twitching

urinary incontinence

urine test for metabolic disorders

ventricular enlargement

vertigo, episodic

very long chain fatty acids

viral infection

viral infection, CNS

vision, blurred

vision, failure of in childhood

visual acuity, decreased

visual evoked response

visual field defect

visual fields, constricted

visual impairment

visual loss, progressive

visual loss, slow

visual symptoms

visuospatial disturbance

walking, difficulty with

Wernicke's encephalopathy

Whipple's disease

white matter disease

white matter disease, periventricular

white matter disease, subcortical

wide based gait

Showing articles 50 to 100 of 4089 << Previous Next >>

Whipple Disease Confined to the Central Nervous System in Childhood
AJNR 17:1589-1591, Duprez,T.P.J.,et al, 1996

Sneddon's Syndrome is a Thrombotic Vasculopathy:Neuropathologic and Neuroradiologic Evidence
Neurol 45:557-560, Geschwind,D.H.,et al, 1995

Encephalopathy in Children with Perinatally Acquired Immunodeficiency Virus Infection
J Pediatr 126:710-715, Lobato,M.N.,et al, 1995

Mitochondrial DNA and Disease
NEJM 333:638-644, Johns,D.R., 1995

Familial Hemiplegic Migraine and Autosomal Dominant Arteriopathy with Leukoencephalopathy (CADASIL)
Ann Neurol 38:817-824, Hutchinson,M.,et al, 1995

Clinical Spectrum of CADASIL:A Study of 7 Families
Lancet 346:934-939, Chabriat,H.,et al, 1995

Niemann-Pick Disease Type C:Diagnosis and Outcome in Children, with Particular Reference to Liver disease
J Pediatr 123:242-247, Kelly,D.A.,et al, 1993

Small Infarctions of Cochlear, Retinal, and Encephalic Tissue in Young Women
Stroke 23:903-907, Schwitter,J.,et al, 1992

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

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

Reversal of a Neurologic Paraneoplastic Syndrome with Octreotide (Sandostatin) in a Pt with Glucagonoma
Am J Med 91:434-436, Holmes,A.,et al, 1991

Hallervorden-Spatz Syndrome and Brain Iron Metabolism
Arch Neurol 48:1285-1293, Swaiman,K.F., 1991

Creutzfeldt-Jakob Disease and Other Transmissible Spongiform Encephalopathies
Ed, F. O. Bastian, Mosby Year Book, St. Louis 9:153, Maertens,P.&Quindlen,E.A., 1991

A Follow-up Study of Intractable Seizures in Childhood
Ann Neurol 28:699-705, Huttenlocher,P.R.&Hapke,R.J., 1990

Brain Injuries Among Infants, Children, Adolescents, and Young Adults
Am J Dis Child 144:684-691, Kraus,J.F.,et al, 1990

Cerebrovascular Disease & Antiphospholipis Antibodies in SLE, Lupus-Like Dis, & Primary Antiphospholipid Synd
Am J Med 86:391-399, Asherson,R.A.,et al, 1989

Elevated Serum Levels of Tumor Necrosis Factor are Associated with Prog Encephalopathy in Children with AIDS
Am J Dis Child 143:771-774, Mintz,M.,et al, 1989

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

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

MR Imaging of a Group I Case of Hallervorden-Spatz Disease
J Comput Assist Tomogr 12:851-853, Mutoh,K.,et al, 1988

Retroviruses in the Nervous System:Neurological Involv in AIDS
Neurological Disorders Assoc with HTLV-I, NIH Symposium (Suppl) , Ann Neurol 23:S1-S2178., , 1988

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

Risk Factors for Falls Among Elderly Persons Living in the Community
NEJM 319:1701-1707, Tinetti,M.E.,et al, 1988

Mineralization of the Basal Ganglia Detected by CT in Hallervorden-Spatz Syndrome
Neurol 38:154-155, Tennison,M.B.,et al, 1988

Neurological Manifestations in Three German Children with AIDS
Neuropediatrics 18:99-106, Biggemann,B.,et al, 1987

Rett's Syndrome, Correlation of Electroencephalogram Characteristics with Clinical Staging
Arch Neurol 44:1053-1056, Glaze,D.G.,et al, 1987

ABC of AIDS, Neurological Manifestations
BMJ 294:1399-1401, Carne,C.A., 1987

Neurologic Manifestations of Infection with Human Immunodeficiency Virus, Clinical Features & Pathogenesis
Ann Int Med 107:383-391, Gabuzda,D.H.,et al, 1987

Neurological Complications in Infants & Children with Acquired Immune Deficiency Syndrome
Ann Neurol 18:560-566, Belman,A.L.,et al, 1985

Progressive Dementia, Visual Deficits, Amyotrophy, & Microinfarcts
Neurol 35:789-796, Kaplan,J.G.,et al, 1985

Creutzfeldt-Jakob Disease after Administration of Human Growth Hormone
Lancet 2:244-246, Powell-Jackson,J.,et al, 1985

Cysticercosis-Review of 230 Patients
Bull Clin Neurosci 50:76-101, McCormick.G.F., 1985

Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, & Strokelike Episodes:A Distinctive Clinical Syndrome
Ann Neurol 16:481-488, Pavlakis,S.G.,et al, 1984

Clinicopathological Conference Metachromatic Leukodystrophy (juvenile type)
Case 7-1984, NEJM 310:445-4551984., , 1984

A Progressive Syndrome of Autism, Dementia, Ataxia, & Loss of Purposeful Hand Use in Girls:Rett's Syndrome
Ann Neurol 14:471-491, Hagberg,B., 1983

Livedo Reticularis & Cerebrovascular Lesions (Sneddon's Syndrome) , Clin, Radiolog & Path Features in Eight Cases
Brain 106:965-979, Rebollo,M.,et al, 1983

Clin. Path. Conference
Adrenoleukodystrophy, with Peripheral Neuropathy, Case Record 5-1982, NEJM 306:286-29382., , 1982

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

Atrial Myxoma with Intellectual Decline & Cerebral Growths on CT Scan
Ann Neurol 5:396-400, Frank,R.A.,et al, 1979

Ocular Involvement in Whipple's Disease
Arch Ophthalmol 96:1431-1436, Font,R.L.,et al, 1978

Clinical & Extraneural Histologic Diagnosis of Neuronal Ceroidlipofuscinosis
Neurol 28:1008-1012, Miley,C.E.III.,et al, 1978

Neurological Manifestations of Fabry Disease in Female Carriers
Ann Neurol 4:537-540, Bird,T.D.,et al, 1978

Leigh's Disease in an Adult with Evidence of"Inhibitor Factor"in Family Members
Ann Neurol 3:519, Whetsell,W.O.,et al, 1978

Neuro-Behcet Disease:Two Cases & Neuroradiologic Findings
Neurol 27:1148, Kozin,F.,et al, 1977

Whipple's Disease with Predominating Neuro-ophthalmic Manifestations
Ann Neurol 1:247-252, Finelli,P.F.,et al, 1977

A Fatal Encephalopathy in Chronic Haemodialysis Patients
Lancet 764, Burks,J.S.,et al, 1976

Neurologic Disorders in Renal Failure (1st of Two Parts)
NEJM 294:143, Raskin,N.H.,et al, 1976

Chronic Progressive Panencephalitis due to Rubella Virus Simulating Subacute Sclerosing Panencephalitis
NEJM 292:994-998,1023, Weil, M.L.,et al, 1975

Progressive Rubella Panencephalitis
NEJM 292:990-993,1023, Townsend,J.,et al, 1975

Infiltration of the Leptomeninges by Systemic Cancer:a Clinical & Pathologic Study
Arch Neurol 30:122, Olson,M.E.,et al, 1974

Showing articles 50 to 100 of 4089 << Previous Next >>