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Differential
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abdominal protrusion

abscess, intracerebral

aceruloplasminemia

achilles tendon, enlarged

acid maltase deficiency

acute intermittant porphyria

acyl CoA dehydrogenase deficiency

Addison's disease

adolescent medicine

adrenoleukodystrophy

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

adult polyglucosan body disease

adult-onset leukodystrophy, with neuroaxonal spheroids

advances in neurology

adverse drug reaction

agenesis of corpus callosum

Alexanders disease

alternating hemiplegia

alternating hemiplegia of childhood

alveolar hypoventilation

Alzheimer's disease

Alzheimer's disease, diagnosis of

Alzheimer's disease, early onset

Alzheimer's disease, familial

Alzheimer's disease, preclinical

Alzheimer's disease, risk factors in

Alzheimer's disease, visual variant

aminoacidopathies

aminoacylase 1 deficiency

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, misdiagnosis

anesthesia, general

aneurysm, intracranial

angiofibroma, facial

angiomyolipomas

ankle reflex, absent

ankle, swelling of

anorexia nervosa

anterior horn cell disease

antibiotic prophylaxis

anticonvulsants

anticonvulsants, selection of

antiviral agents

aphasia, progressive, primary

aphasia, transcortical

aphasia, transcortical-sensory

apolipoprotein E

apraxia, constructional

aromatic amino acid decarboxylase deficiency

arrhythmia, cardiac

arteriovenous malformation

arteriovenous malformation, cerebral

arteriovenous malformation, multiple

arteriovenous malformation, pulmonary

asymmetric crying facies

ataxia telangiectasia

ataxia, cerebellar

ataxia, hereditary

ataxia, paroxysmal

ataxia, progressive

ataxia, truncal

ataxic-dystonia syndromes

atrial fibrillation

atrial paralysis

atrioventricular block

attention deficit disorder with hyperactivity

auditory and vestibular pathways

auditory evoked brainstem potentials

autism, screening for

autistic behavior

autoimmune basal ganglia encephalitis

autoimmune disease

automobile accidents

autonomic dysfunction

autonomic nervous system

autosomal dominant leukodystrophy

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

axonal degeneration

axonal spheroid

B 12 deficiency

bacterial infection

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basilar artery stenosis

behavior, combative

behavioral disorder

biologic markers

biotin deficiency

biotin deficiency, juvenile form

bladder dysfunction

bleeding disorder

blood dyscrasias, neurologic findings with

bone marrow transplantation

brachial neuritis

brachial neuritis, acute

brachial neuritis, bilateral

brachial plexus neuropathy

brachial plexus neuropathy, bilateral

brachial plexus neuropathy, familial

brachial plexus neuropathy, recurrent

brain biopsy, negative

brain biopsy, stereotaxic

brainstem, atrophy

brainstem, lesion of

burning paresthesia

calcification, heart

calcification, intracranial

calcification, muscle

calcium oxalate crystals

calf hypertrophy

carbamyl phosphate synthetase-I deficiency

cardiovascular disease

CAT scan, abdomen

CAT scan, abnormal

CAT scan, chest

CAT scan, emission, abnormal

CAT scan, isodense lesion with acute hemorrhage

cataracts, congenital

caudate nucleus, atrophy

caudate nucleus, lesion of

central nervous system, infection of

cerebellar ataxia, autosomal recessive

cerebellar ataxia, hereditary

cerebellar ataxia, neuropathy and vestibular areflexia syndrome

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar hemorrhage

cerebellar lesion

cerebellar vermis

cerebellum, disease of

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortex

cerebral cortical atrophy

cerebral embolism

cerebral embolism, cardiac origin

cerebral embolism, carotid origin

cerebral infarction

cerebral infarction, subcortical

cerebral palsy, etiology

cerebral palsy, work up

cerebral peduncle

cerebral vasculature, calcification

cerebral venous thrombosis

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, enzymes in

cerebrospinal fluid, glycine

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, proteincytologic dissociation

cerebrospinal fluid, red cells in

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, cardiac disease causing

cerebrovascular accident, cryptogenic

cerebrovascular accident, familial occurrence

cerebrovascular accident, infancy and childhood

cerebrovascular accident, mimics

cerebrovascular accident, misdiagnosis

cerebrovascular accident, multiple

cerebrovascular accident, neonatal

cerebrovascular accident, non atherosclerotic cause of

cerebrovascular accident, nonarterial territory

cerebrovascular accident, nonvascular territory

cerebrovascular accident, recurrent

cerebrovascular accident, young adult

cerebrovascular disease

ceruloplasmin, serum

cervical spondylosis

Charcot-Marie-Tooth

chenodeoxycholic acid

cherry red spot

cherry red spot-myoclonus syndrome

chest x-ray, abnormal

choreoathetosis

chromosomal abnormality

cingulate island sign

cirrhosis, infancy

Clinical Pathologic Conference(C.P.C.)

clubbing of fingers

clubfoot as related to neurologic disease

coat-hanger pain

cobalamin C deficiency

codfish vertebrae

cognitive delay

cold hands sign

cold temperature

color vision, impaired

coma, sudden onset

complete blood count

compression fracture

cone-rod dystrophy

confidentiality

congenital birth defects

congenital heart disease

congenital infection, CNS

congenital malformation

congenital myasthenic syndromes

contractures, joint

contraindications

controversies in neurology

copper deficiency

cornea, abnormal

cornea, opacification in infancy-causes of

cornea, opacity of

corneal dystrophy

corpus callosum

corpus callosum, atrophy of

corpus callosum, hypoplastic

corpus callosum, lesion of

corpus callosum, thinning

cortical blindness

cortical blindness, transient

cortical infarction

cortical ribbon sign

cost effectiveness

C-reactive protein, elevated

creatine phosphokinase(CPK)elevated

creatinine, elevated

Cree leukoencephalopathy

Creutzfeldt-Jakob disease, genetic

cryopyrin-associated periodic syndrome

cultured skin fibroblasts

cyst, peritumoral

cyst, benign intracranial

cyst, cortical parenchyma

cyst, neoplastic cerebellum

cyst, parenchymal

cytomegalovirus infection

deep gray nuclei

deep tendon reflexes

degenerative diseases of CNS

Dejerine-Sottas syndrome

delay in diagnosis

delayed dentition

dementia, age at onset

dementia, childhood

dementia, diagnostic evaluation of

dementia, differential diagnosis of

dementia, familial

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

dementia, reversible

dementia, subcortical

dementia, treatment of

demyelinating disease

dental procedure, neurologic complications with

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

descending paralysis

developmental disability

developmental evaluation

developmental milestones

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetes mellitus

diagnostic criteria

diamond on quadriceps

differential diagnosis

difficulty climbing stairs

disability, neurological

disease modifying agents

distal muscle atrophy

distal muscle weakness

diurnal variation

dopa responsive dystonia

down-beat nystagmus

downward deviation of eyes

dropped head syndrome

drug induced neurologic disorders

drug interactions

dyschromatopsia

dysdiadochokinesia

dystonia, cervical

dystonia, children

dystonia, etiology of

dystonia, painful

dystonic reaction, acute

ears of the Lynx MR sign

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, inflammatory disease

electroencephalogram, monitoring, continuous

electroencephalogram, periodic complexes

electroencephalogram, video monitoring with

electron microscopy

electrophoretic pattern, serum

electroretinograph

embolism, paradoxical

emergencies, neurologic

Emery-Dreifuss muscular dystrophy

emotional lability

encephalitis, autoimmune

encephalopathy, acute

encephalopathy, acute necrotizing

encephalopathy, acute necrotizing of childhood

encephalopathy, metabolic

encephalopathy, neonatal

encephalopathy, progressive

endocarditis, prophylaxis

endolymphatic sac tumors

enzyme treatment

enzyme, muscle disease

epicanthal folds

epidemiology of neurology

epileptic encephalopathy

episodic disorders

episodic neurologic deficits

epistaxis, recurrent

erectile dysfunction

erythromelalgia

ethics in neurology

ethylmalonic aciduria

ethylmalonic encephalopathy

evidence-based research

executive dysfunction

exercise intolerance

exome sequencing

eye movement, disorders of

Fabry's disease

face, elongated

facial anomalies

facial appearance, abnormal

facial asymmetry

facial hypoplasia

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

failure to thrive

family planning

FARS2 deficiency

fatal familial insomnia

fatty acid dehydrogenase deficiency

fatty acid, elevated plasma content

feeding disorder

ferritin, elevated

fever, recurrent

fibrinolytic agents, contraindications

fibroma, ungual

fine motor function, impaired

finger nose finger test

fingers, abnormal

fistula, arterio-venous, pulmonary

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

Friedreich's ataxia

Friedreich's ataxia, late onset

frontal balding

frontal bossing

frontotemporal dementia, behavioral variant

fundus, abnormality of

gangliosidosis GM1

gaze palsy, supranuclear

gaze palsy, vertical

genetic counselling

genetic diagnosis

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

geniculate body, lateral

Gerstmann-Straussler-Scheinker disease

globus pallidus

globus pallidus, infarction

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glucose level, serum

glucose tolerance test, abnormal

GLUT1 deficiency syndrome

glutaric acidemia

glutaric aciduria

glycogen storage disease

Gowers maneuver

growth retardation

Hallervorden Spatz disease

hallucination, visual

head circumference

headache, chronic

headache, persistent

headache, positional

headache, severe

health insurance

hearing loss, bilateral

hearing loss, sudden, unilateral

hearing problems in children

hemangioblastoma

hemianopia, homonymous

hemianopia, transient

hemiparesis, transient

hemophagocytic lymphohistiocytosis

hepatic encephalopathy

hepatic failure

hepatolenticular degeneration(Wilson's disease)

hepatosplenomegaly

heralding manifestation

hereditary hemorrhagic telangiectasia(HHT)

high arched feet

high arched palate

Horner's syndrome

Huntington's chorea

Huntington's chorea, genetic counselling

Huntington's chorea, late onset

Huntington's chorea, misdiagnosis of

Huntington's chorea, presymptomatic detection of

Huntington's chorea, sporadic form

Huntington's disease, children

Hurler's syndrome

hydroxyglutaric aciduria

hyperammonemic encephalopathy

hyperamylasemia

hyperbilirubinemia

hyperglycinemia

hyperglycinemia, nonketotic

hyperhomocysteinemia

hyperpigmentation of skin

hypertrophic intracranial pachymeningitis

hypoglycorrhachia

hypogonadism, hypogonadotropic

hypomyelination

hypoparathyroidism

hypopigmentation of skin

hypotension, neurologic causes of

hypotension, systemic

hypotonia, infants

hypoxic-ischemic leukoencephalopathy

iatrogenic neurologic disorders

ileus, paralytic

imbalance, postural

immunomodulation

implantable cardioverter defibrillator

inappropriate behavior

inborn errors of metabolism

inborn errors of metabolism, screening

inclusion bodies

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

inclusion bodies, ubiquitin

infantile spasm

inflexibility, mental

insulin resistance

intellectual deficit

intellectual deterioration

intelligence quotient

internal capsule

internuclear ophthalmoplegia, bilateral

interstitial pulmonary fibrosis

intracerebral hemorrhage

intracranial pressure, increased

intranasal medication

intraventricular hemorrhage

intrinsic hand muscles, wasting of

iron, serum, low

JAK2 V617F mutation

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

jaw closure weakness

joint hypermobility

keratoconjunctivitis

Korsakoff's psychosis

Krabbe's disease

kyphoscoliosis, neurologic causes of

lactic acidemia

lacunar infarction

Lafora's disease

laughing, pathologic

learning disability

learning disability, in children

Leber's hereditary optic neuropathy

leg spasms, painful

leg weakness, bilateral

Legius syndrome

Leigh's disease

Leigh's disease, adult variety

lens, dislocation of

leucine-rich repeat kinase 2 gene

leukocyte enzyme abnormality

leukoencephalopathy

leukoencephalopathy with calcification and cysts

leukoencephalopathy, hereditary diffuse

level of consciousness, decreased

lid abnormalities

lid closure, weakness of

life expectancy

limb-girdle weakness

lipid storage disorder of CNS

livedo reticularis

liver function enzymes

loss of sympathy

lymphangiomyomatosis

lysosomal storage disease

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

manganese intoxication

manic-depressive

maple syrup urine disease

marche a petits pas

Marcus Gunn pupil

masseter muscle weakness

McLeod syndrome

meconium staining

medical-legal aspects of neurology

medulla oblongata

medulla oblongata, atrophy

medulla oblongata, lesion of

medulla oblongata, neoplasm of

melanomatosis, primary malignant

memory, defect of recent

memory, impairment of

meningitis, aseptic

meningitis, basilar

meningitis, carcinomatous

meningitis, CSF cell count-normal

meningitis, leptospira

meningoencephalitis

mental retardation

mental retardation, familial

mental status, abnormal

mesial temporal lobe

metabolic acidosis

metabolic disorder, primary

metabolic disorder, primary-screening tests

metachromatic leukodystrophy

methylglutaconic aciduria

methylmalonic acidemia

microangiopathy, brain

microhemorrhage, intracerebral

microspherophakia

midbrain, infarction of

midbrain, lesion of

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

migratory lesion pattern

mitochondrial disease

mitochondrial encephalomyopathy

mitral valve prolapse

molecular genetics

molybdenum cofactor deficiency

monoclonal antibodies

motor neuron disease

movement disorder

movement disorder, extrapyramidal

movement disorder, hyperkinetic

moyamoya, adult

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, demyelinating disease

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, eye of tiger sign

MRI, false negative

MRI, gradient-echo

MRI, gyral enhancement

MRI, high signal foci on

MRI, high signal intensity of basal ganglia

MRI, hypointense signal foci on

MRI, optic nerve

MRI, paramagnetic effect

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRI, susceptibility weighted

MRI, T1 weighted high signal foci

mucopolysaccharidoses

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple system atrophy

muscle atrophy, focal

muscle atrophy, progressive

muscle phosphofructokinase deficiency

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, cardiovascular changes with

muscular dystrophy, central nervous system abnormality

muscular dystrophy, classification

muscular dystrophy, Duchenne

muscular dystrophy, Duchenne, neonatal screening

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

muscular dystrophy, pattern of muscle involvement

myasthenia gravis

myasthenia gravis, congenital

myasthenia gravis, familial incidence of

myasthenia gravis, misdiagnosis of

myasthenia gravis, seronegative

myasthenia gravis, treatment of

myelin protein zero gene

myeloneuropathy

myelopathy, chronic progressive

myeloproliferative disorder

myoclonic encephalopathy of infancy

myoclonic jerks

myoclonus, cortical

myoclonus, epilepsy

myoclonus, stimulus sensitive

myopathy, drug-induced

myopathy, genetic

myopathy, inclusion body

myopathy, inclusion body with Paget's disease

myopathy, metabolic

myopathy, mitochondrial

myopathy, proximal

myopathy, vacuolar

myotonia dystrophica

myotonia dystrophica, classification

myotonia dystrophica, type 2

myotonic discharges

nasal bridge, wide

Native Americans

nausea and vomiting

neonatal epilepsy syndromes

neonatal epileptic encephalopathy

neonatal screening, genetic neurologic disorders

neoplasm, metastatic to CNS

neoplasm, metastatic to CNS-differential diagnosis of

neoplasm, peripheral nerve

neoplasm, primary intracerebral, presenting as CVA

neoplasm, primary intracranial

neoplasm, primary of CNS

nephrocalcinosis

nerve conduction studies

nerve hypertrophy

nerve root enhancement

nerve root hypertrophy

neuroaxonal leukodystrophy

neurocutaneous disease

neurodegeneration with brain iron accumulation

neuroendocrinology

neurofibromatosis 1

neurogenic bladder

neuroichthyosis

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic disease, tempo

neurologic evaluation

neurologic examination

neurologic examination, focal

neurologic practice

neurologic signs

neurologic testing

neuromuscular junction

neuronal ceroid-lipofuscinosis

neuronal intranuclear inclusion disease

neuronal migration disorder

neuronopathy, sensory

neuroophthalmology

neuropathology, brain

neuropathy, classification of

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, painful

neuropathy, peripheral

neuropathy, sensory

neuropathy, work up for

neurotransmitter

next-generation sequencing

Niemann-Pick disease

night blindness

NMDA antagonists

Notch3 gene, false negative

numbness, extremity

nystagmus, gaze-evoked

nystagmus, monocular

nystagmus, rotary

nystagmus, vertical

obsessive-compulsive disorder

occipital lobe, infarction

occipital lobe, lesion of

ocular dysmetria

ocular motility, disorders of

oculodentodigital dysplasia

oculogyric crisis

old age, neurology of

ophthalmoplegia

ophthalmoplegia, neonatal

ophthalmoplegia, progressive external

optic atrophy, bilateral

optic chiasm, enlarged

optic disc edema

optic nerve, compression of

optic nerve, enhancement

optic nerve, enlarged

optic nerve, lesion of

optic neuritis, bilateral

optic neuropathy

optic neuropathy, bilateral

optic neuropathy, hereditary

optical coherence tomography

ornithine transcarbamylase deficiency

orthostatic hypotension

ovarian dysgenesis

ovarian insufficiency

oxalosis, primary

pacemaker, cardiac-transvenous

Paget's disease

pain, abdominal

pain, increased response

pancreatic cyst

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, spastic

paraspinal muscle

paresthesias, feet

paresthesias, lower extremity

Parkinson disease

Parkinson disease, atypical

Parkinson disease, dystonia with

Parkinson disease, familial

Parkinson disease, juvenile

Parkinsonism syndrome

paroxysmal hemiplegia

paroxysmal neurologic deficits

PAS positive material in the brain

patient in waiting

patient information and support

pectus excavatum

Pelizaeus Merzbacher

percussion induced muscle contraction

peripheral blood smear

peripheral nerve, lesion of

peroxisomal disease

Perrault syndrome

personality change

phenylketonuria

phenylketonuria, adult onset

phenylketonuria, maternal

pheochromocytoma

philtrum, tented

platelet inhibiting drugs

pleocytosis of cerebrospinal fluid

poison, neurologic problems with

polycythemia, primary

polycythemia, secondary

polyglucosan body

polyglucosan body disease

polymerase chain reaction

polymerase chain reaction, false negative

polymerase chain reaction, false positive

Pompe's disease of glycogen storage

pons, lesion of

portal caval shunt

posterior cerebral artery territory infarction

posterior cortical atrophy

posterior fossa, lesion of

posterior leukoencephalopathy syndrome

postpartum coma

postural abnormality

practice guidelines

precipitating factors

pregnancy, neurologic complications in

premature infant

prenatal diagnosis by amniocentesis

presenilin-1 gene

presenilin-2 gene

prevention of neurologic disorders

primary episodic ataxia

primary familial brain calcification

primary thrombocythemia

prion protein gene

progressive myoclonic epilepsy

progressive neurologic disorder

prolactin, elevated

proprioception, abnormal

protein 14-3-3, cerebrospinal fluid

protein S deficiency

proton pump inhibitors

proximal muscle atrophy

proximal myotonic myopathy

pseudobulbar palsy

pseudohypoparathyroidism

pseudoxanthoma elasticum

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychological testing, neurologic problems

psychomotor retardation

psychotic behavior

ptosis, bilateral

pulmonary embolism

pulmonary hypertension

pupil, dilated and fixed, bilateral

pupil, dilated, bilateral

pupil, dilated, episodic

putamen, lesion of

pyramidal tract

pyramidal tract dysfunction

pyridoxine deficiency

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

quadriparesis, progressive

quadriplegia, transient

ragged-red fibers

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

real-time quaking-induced conversion

release phenomena

renal cell carcinoma

respiratory failure

respiratory tract infection

retina, abnormal

retinal degeneration

retinal hamartoma

retinal hemangioma

Rett's syndrome

reversible neurologic disorder

Reye's syndrome

Reye's syndrome, prognosis of

rhabdomyosarcoma of heart

risk-benefit assessment

root lesion, nerve

Rosenthal fibers

saccadic eye movements, abnormal

salivation, excessive

sarcoglycanopathy

Schilder's disease

sclerae, hyperpigmented

sclerosis, bone

scoliosis, neurologic association with

scotoma, central

sedimentation rate, elevated

seizure, children

seizure, complications following

seizure, crying as manifestation of

seizure, diagnosis of

seizure, etiology of

seizure, intractable

seizure, laughing as manifestation

seizure, neonatal

seizure, paradoxical

seizure, psychomotor-temporal lobe

seizure, pyridoxine dependent

seizure, teenager

seizure, treatment of

seizure, workup of

self-mutilation

semialdehyde dehydrogenase deficiency

sensorineural hearing loss

sensory loss, leg

serum lipase, elevated

shoulder, pain in

shoulder-girdle wasting

simultanagnosia

single photon emission computed tomography

Sjogren-Larsson syndrome

skin, darkening of

skin, lesions in neurologic disorders

skull bone, thickening

sleep pathology and physiology

slit lamp examination

small vessel disease

small vessel disease, cerebral

SNCA duplication

Southern immunoblot test

spastic diplegia

spastic paraplegia, type 11

speech disorder

speech disorder, childhood

speech, absence of

speech, delayed development of

speech, loss of

spinal cord, compression of

spinal cord, lesion of

spinal cord, neoplasm

spinal muscular atrophy

spinal muscular atrophy, classification

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 10

spinocerebellar ataxia type 2

spinocerebellar ataxia type 28

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar ataxia type 7

spinocerebellar degeneration

spirochete infection

splenium of corpus callosum

spontaneous remission

SPRED1 mutation

startle reaction

status epilepticus

stem cell transplantation

stereotyped behavior

steroid therapy, CNS treatment and complications with

stress, emotional

striatal encephalitis

striatonigral degeneration

striatonigral degeneration, infantile

striatum, lesion of

striopallidodentate calcifications, familial idiopathic

strokelike episodes

subarachnoid hemorrhage

subcortical U fibers

subdural hematoma

subependymal nodules

substantia nigra

sulfite oxidase deficiency

superior sagittal sinus thrombosis

sweating, abnormality of

symmetric brain lesions

systemic illness

tandem gait, ataxic

teeth, abnormal

teeth, number of in infants

telangiectases, retinal

temporal lobe, atrophy

temporal lobe, lesion

temporal lobe, lesion, bilateral

temporalis muscle wasting

temporalis muscle weakness

temporomandibular joint, dislocation

testicular atrophy

testicular enlargement

tetrahydrobiopterin

thalamus, lesion of

thalamus, lesion of-bilateral

thrombocytopenia

thrombophlebitis

tissue plasminogen activator, intravenous

tongue, enlarged

tongue, fasciculations of

tonic foot response

transient ischemic attack

transient neurologic deficit

transverse smile

travel, foreign

treatment of neurologic disorder

treatment resistant

tremor, cerebellar

tremor, intention

tremor, postural

tremor, resting

tremor, writing

trinucleotide repeats

tuberous sclerosis

tuberous sclerosis, screening for

tumefactive lesion

tumor suppressor gene

tyrosine hydroxylase deficiency

ultrasonography

ultrasonography, nerve

uncal herniation

unconsciousness

unconsciousness, transient

Unverricht-Lundborg disease

upgaze, paralysis of

urea-cycle enzymopathies

urinalysis, abnormal

urinary frequency

urinary incontinence

urine test for metabolic disorders

venous thrombosis, non-cerebral

ventricular garlands

vestibular areflexia

vestibular migraine

vibratory sensation, abnormal

violent behavior

viral infection, CNS

vision loss, sequential

vision, blurred

vision, failure of in childhood

visual acuity, decreased

visual acuity, decreased, monocular

visual field defect

visual impairment

visual loss, progressive

visual loss, slow

visuospatial disturbance

vitamin deficiency

vitamin E deficiency

Von Hippel Lindau

Von Hippel Lindau, screening protocol for

von Hippel-Lindau, screening

walking, difficulty with

walking, difficulty with in dark

weakness, acute

weakness, episodic

weakness, fatiguable

weakness, focal

weakness, generalized

weakness, progressive

weakness, proximal

weakness, rapidly progressive

Wernicke's encephalopathy

whistle, inability to

white matter disease

white matter disease, subcortical

white matter disease, unilateral

whole genome sequencing

wide based gait

winging of scapula

Wolff-Parkinson-White syndrome

word-finding difficulty

xanthoma, tendon

X-linked bulbospinal neuronopathy

x-linked hydrocephalus

x-linked intellectual deficit

x-linked mental retardation

Showing articles 650 to 700 of 797 << Previous Next >>

Wilson's Disease, Development of Neurological Disease after Beginning Penicillamine Therapy
Arch Neurol 47:595-596, Glass,J.D.,et al, 1990

Neurologic & Evoked Potential Abnormalities in Subtle Cobalamin Deficiency States
Arch Neurol 47:1008-1012, Karnaze,D.S.&Carmel,R., 1990

Positron Emission Tomography in Creutzfeldt-Jakob Disease
Arch Neurol 47:1035-1038, Holthodd,V.A.,et al, 1990

Neurologic Sequelae of Domoic Acid Intoxication Due to the Ingestion of Contaminated Mussels
NEJM 322:1781-1787, Teitelbaum,J.S.,et al, 1990

Transplantation of Human Fetal Dopamine Cells for Parkinson's Disease
Arch Neurol 47:505-512, Freed,C.R.,et al, 1990

National Cancer Institute Workshop Statement
Advances in Clinical Imaging Using Positron Emission Tomography, Arch Int Med 150:735-739, 729990., , 1990

Cerebral Metabolic Asymmetries & Assoc Neuro-psych Patterns in Early Dementia of the Alzheimer Type
Arch Neurol 47:753-760, Haxby,J.V., 1990

Infantile Spasms:I. PET Identified Focal Cortical Dysgenesis in Cryptogenic Cases for Surgical Treatment
Ann Neurol 27:406-413, Shields,W.D.,et al, 1990

Slowly Progressive Aphasia:Three Cases with Language, Memory, CT and PET Data
JNNP 53:987-993, Kempler,D.,et al, 1990

Plasticity in the Aging Brain
Arch Neurol 47:1336-1341, Kaye,J.A.,et al, 1990

Caze Distractibility in Wilson's Disease
Ann Neurol 25:415-417, Lennox,G.&Jones,R., 1989

Homing in on Wilson's Disease
Editorial, Lancet 1:822-8231989., , 1989

PET Scanning, Provides Information on Function
BMJ 298:692-694, Frackowiak,R.S.J.&Jones,T., 1989

SPECT and PET in Epilepsy
Editorial, Lancet 1:135-1371989., , 1989

Normal-Pressure Hydrocephalus and the Saga of the Treatable Dementias
JAMA 262:2577-2581, 2592-25931989., Friedland,R.P., 1989

Subacute Combined Degeneration of the Spinal Cord
In Rowland's, Merritt's Textbk of Neurology, Lea & Febiger, Phila, 8th Ed, p. 691, Mancall,E.L., 1989

Cerebral Glucose Metabolism in Wernicke's Broca's, and Conduction Aphasia
Arch Neurol 46:27-34, Metter,E.J.,et al, 1989

Cyanide-Induced Parkinsonism:Clinical, MRI, and 6-Fluorodopa PET Studies
Neurol 39:142-144, Rosenberg,N.L.,et al, 1989

Cerebral Glucose Metabolism in the Course of Subacute Sclerosing Panencephalitis
Arch Neurol 46:97-100, Huber,M.,et al, 1989

Positron Emission Tomography in a Patient with Progressive Multifocal Leukoencephalopathy
Neurol 38:1864-1867, Kiyosawa,M.,et al, 1988

Brain Metabolism in Mitochondrial Encephalomyopathy:A PET Study
J Comput Assist Tomogr 12:854-857, DeVolder,A.,et al, 1988

Internuclear Ophthalmoplegia in Pernicious Anaemia
BMJ 297:1583, Kandler,R.H.&Davies-Jones,G.A.B., 1988

Cerebellar & Brainstem Hypometabolism in Olivo-pontocerebellar Atrophy Detected with Positron Emission Tomography
Ann Neurol 23:223-230, Gilman,S.,et al, 1988

Brain Glucose Metabolism in Thalamic Syndrome
JNNP 51:427-428, Laterre,E.C.,et al, 1988

Cerebral Hypometabolism in Progressive Supranuclear Palsy Studied with Positron Emission Tomography
Ann Neurol 24:399-406, Foster,N.L.,et al, 1988

Diagnosis and Treatment of Presymptomatic Wilson's Disease
Lancet 2:435-437, Walshe,J.M., 1988

Dementia in Down's Syndrome:Cerebral Glucose Utilization, Neuropsychological Assessment, and Neuropathology
Neurol 38:938-942, Schapiro,M.B.,et al, 1988

Neuropsychiatric Disorders Caused by Cobalamin Deficiency in the Absence of Anemia or Macrocytosis
NEJM 318:1720-1728, 1752-17541988., Lindenbaum,J.,et al, 1988

Pernicious Anemia:Report of Pts Without the Expected Findings of Very Low Serum Cobalamine Levels, Anemia, & Macrocytosis
Arch Int Med 148:1712-1714, Carmel,R., 1988

Hereditary Defect of Cobalamin Metabolism (cblG Mutation) Presenting as a Neurologic Disorder in Adulthood
NEJM 318:1738-1741, 1752-17541988., Carmel,R.,et al, 1988

Surgical Treatment of Intractable Neonatal-Onset Seizures:The Role of Positron Emission Tomography
Neurol 38:1178-1188, Chugani,H.T.,et al, 1988

Diagnosis & Treatment of Aphasia, Part I & Part II
JAMA 259:1043-1047, 1205-12101988., Albert,M.L.&Helm-Estabrooks,N., 1988

Disconnection & Cerebral Metabolism, The Case of Conduction Aphasia
Arch Neurol 45:275-279, Kempler,D.,et al, 1988

Improvement of Cerebral CT Abnor Following Liver Transplant in a Patient with Wilson Disease
J Comput Assist Tomogr 12:138-149, Rothfus,W.E.,et al, 1988

Positron Emission Tomography-A New Approach to Brain Chemistry
JAMA 260:2704-2710, Jacobson,H.G., 1988

The Metabolic Pathology of the AIDS Dementia Complex
Ann Neurol 22:700-706, Rottenberg,D.A.,et al, 1987

Normal Caudate Glucose Metabolism in Persons at Risk for Huntington's Disease
Arch Neurol 44:254-257, Young,A.B.,et al, 1987

Reduced Cerebral Glucose Metabolism in Asymptomatic Subjects at Risk for Huntington's Disease
NEJM 316:357-362, Mazziotta,J.C.,et al, 1987

Positron Emission Tomography & Histopathology in Pick's Disease
Neurol 37:439-445, Kamo,H.,et al, 1987

The Lennox-Gastaut Syndrome:Metabolic Subtypes Determined by FDG Positron Emission Tomography
Ann Neurol 21:4-13, Chugani,H.T.,et al, 1987

Cerebral Glucose Metabolism in the Lennox-Gastaut Syndrome
Ann Neurol 21:14-21, Theodore,W.H.,et al, 1987

Primary Progressive Aphasia-Differentiation from Alzheimer's Disease
Ann Neurol 22:533-534, Mesulam,M.M., 1987

The Combined Use of Positron Emission Tomography & DNA Polymorphisms for Preclinical Detection of Huntington's Disease
Neurol 37:1441-1447, Hayden,M.R.,et al, 1987

The Use of Trientine in Preventing the Effects of Interrupting Penicillamine Therapy in Wilson's Disease
NEJM 317:209-213, Scheinberg,I.H.,et al, 1987

Wilson's Disease Studies with FDG & Positron Emission Tomography
Neurol 37:1707-1711, Hawkins,R.A.,et al, 1987

Lesions of the Putamen:Their Relevance to Dystonia
Neurol 37:1125-1129, Fross,R.D.,et al, 1987

Differentiation of Cerebral Radiation Necrosis from Tumor Recurrence by[18F]FDG & 82RB PET Scan
J Comput Assist Tomogr 11:563-570, Doyle,W.K.,et al, 1987

Plasma R Binder Deficiency & Neurologic Disease
NEJM 317:1330-1332, Sigal,S.H.,et al, 1987

Raised Cerebrospinal-Fluid Copper Concentration in Parkinson's Disease
Lancet 2:238-241, Pall,H.E.,et al, 1987

Metabolic & Clinical Correlates of Acute Ischemic Infarction
Neurol 37:1103-1110, Kushner,M.,et al, 1987

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