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Differential
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abducens nerve paralysis

abortion, spontaneous

abscess, intracerebral

abscess, intracranial

acoustic neurinoma

Addison's disease

adrenoleukodystrophy

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

advances in neurology

adverse drug reaction

agenesis of corpus callosum

Aicardi's syndrome

alcohol intolerance

alcohol, neurologic complications with

Alexanders disease

Alexanders disease, adult onset

alkylating agents

altered states of consciousness

alternating hemiplegia

alternating hemiplegia of childhood

alternating rapid movement

Alzheimer's disease

Alzheimer's disease, early onset

Alzheimer's disease, familial

Alzheimer's disease, pathogenesis

Alzheimer's disease, treatment of

aminoacidopathies

amyloid angiopathy, cerebral

amyloid angiopathy, hereditary cystatin C

amyloid beta protein

amyloid imaging

amyloidosis, oculoleptomeningeal, familial

amyotrophic chorea-acanthocytosis

anesthesia, general

aneurysm, intracranial, screening for

Angelman syndrome

angiofibroma, facial

angiography, cerebral

angiomyolipomas

animal exposure

anterior horn cell disease

antibiotic prophylaxis

antibodies to voltage-gated calcium channels

anticholinesterase

anticonvulsants

anticonvulsants, discontinuation in seizure-free epileptics

anticonvulsants, effectiveness

anticonvulsants, hypersensitivity syndrome

anticonvulsants, selection of

anticonvulsants, teratogenicity of

anticonvulsants, untoward effects of

antiphospholipid antibodies

aphasia, progressive

apnea, primary central

apolipoprotein E

apraxia, constructional

arrhythmia, cardiac

arteriovenous malformation

arteriovenous malformation, cerebral

arteritis, temporal

arylsulfatase A

ataxia, cerebellar

ataxia, hereditary

ataxia, paroxysmal

ataxia, progressive

ataxia, truncal

attention deficit disorder with hyperactivity

auditory and vestibular pathways

autistic behavior

autonomic dysfunction

autosomal dominant nocturnal frontal lobe epilepsy

axonal spheroid

basal cell carcinoma

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

Bassen-Kornzweig syndrome

behavior modification

behavior, combative

behavioral disorder

benign essential tremor

benign familial neonatal convulsions

beta adrenergic blocker

bilateral periventricular nodular heterotopia

biologic markers

biotin deficiency

biotin deficiency, juvenile form

biotinidase deficiency

biotin-responsive basal ganglia disease

blindness, congenital

blood dyscrasias, neurologic findings with

blue rubber bleb nevus syndrome

bone marrow biopsy

bone marrow transplantation

botulinum toxin

bovine spongiform encephalopathy

brain scan, abnormal

brainstem, atrophy

brainstem, lesion of

brainstem, neoplasms of

brainstem, vascular malformation of

burst suppression pattern, electroencephalogram

cafe au lait spots

calcification, gyral

calcification, intracranial

calcium channel dysfunction

Canavan's disease

capillary blush

carotid artery occlusion, bilateral

CAT scan, abnormal

CAT scan, abscess, cerebral

CAT scan, chest

CAT scan, contrast enhanced

CAT scan, demyelinating disease

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, isodense lesion with acute hemorrhage

cataracts, congenital

caudate nucleus, atrophy

cavernous hemangioma

central core disease

central nervous system, infection of

cerebellar ataxia, children

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar hemangioma

cerebellar hemorrhage

cerebellar lesion

cerebellar plaques, amyloid

cerebellar vermis

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 infarction

cerebral infarction, subcortical

cerebral ischemia

cerebral peduncle

cerebral vasculature

cerebral vasculature, calcification

cerebral venous thrombosis

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, culture of, viral

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, pressure low

cerebrospinal fluid, protein of

cerebrospinal fluid, red cells in

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, familial occurrence

cerebrovascular accident, infancy and childhood

cerebrovascular accident, mimics

cerebrovascular accident, multiple

cerebrovascular accident, neonatal

cerebrovascular accident, non atherosclerotic cause of

cerebrovascular accident, nonarterial territory

cerebrovascular accident, recurrent

cerebrovascular accident, work up for

cerebrovascular accident, young adult

cerebrovascular disease

cerebrovascular disease, surgical treatment of

ceruloplasmin, serum

Charcot-Marie-Tooth

chemotherapy, CNS treatment and complications with

cherry red spot

cherry red spot-myoclonus syndrome

chewing movements

chewing, impaired

chloride channel dysfunction

chorea, familial

chorea, treatment of

choreoathetosis

choreoathetosis, paroxysmal

chromosomal abnormality

chromosome 20 ring

chronic progressive external ophthalmoplegia

cisterna magna, enlarged

Clinical Pathologic Conference(C.P.C.)

clubbing of fingers

cobalamin C deficiency

Cockayne's syndrome

codfish vertebrae

cogwheel rigidty

coin lesion on chest X-ray

cold hands sign

color vision, impaired

compression fracture

compression neuropathy

congenital heart disease

congenital heart disease, CNS complications with

congenital infection, CNS

congenital infection, viral

congenital malformation

congenital malformation, non CNS

congestive heart failure

conjunctival biopsy

contractures, joint

controversies in neurology

copper metabolism, abnormal

cornea, abnormal

corpus callosum

corpus callosum, atrophy of

corpus callosum, hypoplastic

corpus callosum, lesion of

corpus callosum, thinning

cortical blindness

cortical blindness, transient

cortical infarction

cranial nerve enhancement

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

craniopharyngioma

creatine phosphokinase(CPK)elevated

Creutzfeldt-Jakob disease, genetic

crying, pathologic

cultured skin fibroblasts

cyst, peritumoral

cyst, epidermoid of CNS

cyst, neoplastic cerebellum

cyst, parenchymal

cyst, porencephalic

cyst, ventricular

cytomegalovirus infection

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

dementia, cerebrovascular disease causing

dementia, childhood

dementia, differential diagnosis of

dementia, familial

dementia, presenile

dementia, rapidly progressive

dementia, thalamic

dementia, transmissible

demyelinating disease

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

dermatoglyphics

developmental abnormality of brain

developmental disability

developmental evaluation

developmental milestones

developmental milestones, loss of

developmental retardation

developmental venous anomalies

diabetes insipidus

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diagnostic criteria

differential diagnosis

dilantin, hypersensitivity to

dilantin, toxicity

disability, neurological

disease modifying agents

distal muscle atrophy

distal muscle weakness

down-beat nystagmus

Dravet syndrome

dural sinus thrombosis

Durett hemorrhages

dysostosis multiplex

dyssynergia cerebellaris myoclonica

dystonia, painful

dystonia, treatment of

early draining vein

eating disorder

edema, periorbital

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, monitoring, continuous

electroencephalogram, periodic complexes

electroencephalogram, video monitoring with

electron microscopy

electroretinograph

embolism, paradoxical

embolism, septic

emotional lability

encephalitis, viral

encephalomalacia

encephalopathy, acute necrotizing

encephalopathy, acute necrotizing of childhood

encephalopathy, metabolic

encephalopathy, neonatal

encephalopathy, progressive

endovascular therapy

entrapment neuropathy

epicanthal folds

epidemiology of neurology

epileptic encephalopathy

episodic disorders

episodic neurologic deficits

epsilon sarcoglycan gene

esophageal varices

evoked potentials

executive dysfunction

exercise intolerance

exome sequencing

eye movement, disorders of

Fabry's disease

facial anomalies

facial appearance, abnormal

facial expression abnormality

facial hypoplasia

facial nerve palsy

facial nerve palsy, bilateral

failure to thrive

familial adult myoclonic epilepsy

familial hemiplegic migraine

familial rectal pain

FARS2 deficiency

fatal familial insomnia

fatty acid, elevated plasma content

feeding disorder

fibroma, ungual

fine motor function, impaired

finger nose finger test

fingerprint bodies

fingers, abnormal

fistula, arterio-venous

fistula, arterio-venous, dural

fistula, arterio-venous, pulmonary

fluorescene in situ hybridization

fracture, pathologic

fragile-X syndrome

French-Canadian

Friedreich's ataxia

frontal bossing

frontal lobe, behavior with disease of

fundus, abnormality of

funduscopic exam

gamma amino butyric acid

gamma knife therapy

gangliosidosis GM2

gastrointestinal bleeding

Gaucher's disease

Gaucher's disease, adult onset

gaze palsy, supranuclear

gaze palsy, vertical

genetic counselling

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

glioblastoma multiforme(astrocytoma Gr.III)

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

GLUT1 deficiency syndrome

granular osmiphilic material

granulomatosis with polyangiitis

growth hormone deficiency

growth retardation

guanidinoacetate methyltransferase deficiency

gyrus, abnormal

Hallervorden Spatz disease

Hallgren's syndrome

hallucination, visual

head circumference

headache, positional

hearing loss, bilateral

hearing problems in children

heel-knee-shin test

hemangioblastoma

hemangioma, brainstem

hemangioma, facial

hemangioma, internal organs

hemangioma, leptomeningeal

hemangioma, skin

hematuria, gross

hematuria, microscopic

hemihypertrophy, congenital

hemophagocytic lymphohistiocytosis

hemophagocytic lymphohistiocytosis, cerebromeningeal

hemophagocytosis

hemorrhagic diathesis

hepatic encephalopathy

hepatic failure

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), screening for

hepatosplenomegaly

heralding manifestation

hereditary hemorrhagic telangiectasia(HHT)

herpes simplex encephalitis

herpes simplex encephalitis, differential diagnosis of

heterochromia iridis

hexosaminidase-A

hippocampal atrophy

holoprosencephaly

Horner's syndrome

human immunodeficiency virus type 1

Huntington's chorea

Huntington's disease, children

Hurler's syndrome

hydrocephalus, communicating

hyperglycinemia

hyperglycinemia, nonketotic

hyperhomocysteinemia

hyperpigmentation of skin

hypersensitivity reaction

hypertriglyceridemia

hypertrophic cardiomyopathy

hypofibrinogenemia

hypoglycorrhachia

hypomelanosis of Ito

hypomyelination

hypoparathyroidism

hypopigmentation of skin

hypotonia, infants

hypoxic-ischemic leukoencephalopathy

iatrogenic neurologic disorders

ileus, paralytic

immunofluorescence

immunologic disease

inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with

inappropriate behavior

inborn errors of metabolism

inborn errors of metabolism, screening

incidental finding

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, intracytopasmic

incontinentia pigmenti

infantile bilateral striatal necrosis

infantile spasm

infection, recurrent

influenza, avian

insulin resistance

intellectual deficit

intellectual deficit, treatable causes of

intellectual deterioration

intelligence quotient

intestinal pseudoobstruction

intracerebral hemorrhage

intracerebral hemorrhage, familial

intracerebral hemorrhage, lobar

intracerebral hemorrhage, recurrent

intracranial pressure, increased

intrathecal chemotherapy

intrauterine infection

intraventricular hemorrhage

islet cell tumor

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, variant

Jakob-Creutzfeldt disease, young adult

Jervell Lange-Neilson syndrome

joint hypermobility

juvenile myoclonus epilepsy

Kayser-Fleischer ring

KCNQ2 encephalopathy

Kearns-Sayre syndrome

Korsakoff's psychosis

Krabbe's disease

kyphoscoliosis, neurologic causes of

lactic acidemia

lacunar infarction

Lafora's disease

laughing, pathologic

Laurence-Moon-Bardet-Biedl syndrome

learning disability, in children

Leber's hereditary optic neuropathy

Leigh's disease

Leigh's disease, adult variety

lens, dislocation of

lenticular nucleus, lesion of, bilateral

leukemia, neurologic findings assoc.with

leukoencephalopathy

leukoencephalopathy with calcification and cysts

leukoencephalopathy, differential diagnosis

leukoencephalopathy, hereditary diffuse

level of consciousness, decreased

Lhermitte-Duclos disease

Lhermitte's sign

lid abnormalities

life expectancy

lipid storage disorder of CNS

lipomembranous polycystic osteodysplasia

livedo reticularis

liver function enzymes

liver transplantation

long bone lesion

long QT syndrome

low birth weight

lumbar puncture

lymphadenopathy

lymphangiomyomatosis

lymphoma, primary of CNS

lysosomal storage disease

macular degeneration

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

malformation, vascular, familial

malformation, vascular, screening for

malformation, vascular, treatment of

malformation, Vein of Galen

malignant hyperpyrexia

marche a petits pas

medulloblastoma

melanomatosis, primary malignant

memory, defect of recent

memory, impairment of

meningeal enhancement

meningitis, carcinomatous

meningitis, CSF cell count-normal

meningoencephalopathy

mental retardation

mental retardation, etiology of

mental retardation, familial

mesial temporal lobe

mesial temporal lobe epilepsy

mesial temporal sclerosis

metabolic acidosis

metabolic disorder, primary

metabolic disorder, primary-screening tests

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

metachromatic leukodystrophy, juvenile

methylhydrazine derivatives

methylmalonic acidemia

methylmalonic aciduria

microangiopathy, brain

microhemorrhage, intracerebral

microspherophakia

midbrain, lesion of

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

middle cerebral artery territory infarction

middle cerebral artery, occlusion of

migraine, aura of

migraine, without headache

migratory lesion pattern

mild cognitive impairment

Minamata disease

Mini Mental Status Examination

mitochondrial disease

mitochondrial disease, pathogenesis

mitochondrial encephalomyopathy

molecular genetics

molybdenum cofactor deficiency

monoamine oxidase inhibitors

mononeuropathy multiplex

motor neuron disease

movement disorder

movement disorder, extrapyramidal

movement disorder, hyperkinetic

movement disorder, paroxysmal

movement disorder, treatment of

moyamoya, adult

MRI, angiography

MRI, blooming effect

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, cranial nerves

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, gradient-echo

MRI, incidental finding

MRI, spinal cord

MRI, susceptibility weighted

mucopolysaccharidoses

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple system atrophy

muscle hypertrophy

muscle stiffness

muscle tenderness

muscle weakness

muscle weakness, proximal

myasthenia gravis, differential diagnosis

myasthenia gravis, misdiagnosis of

myelination of nervous system

myelopathy, chronic progressive

myoclonic dystonia

myoclonic jerks

myoclonus, action

myoclonus, cortical

myoclonus, epilepsy

myoclonus, essential

myoclonus, stimulus sensitive

myopathy, mitochondrial

myotonia congenita

N-acetylcysteine

nasal bridge, wide

nausea and vomiting

neonatal epilepsy syndromes

neonatal epileptic encephalopathy

neoplasm, intracranial

neoplasm, intracranial-incidence and epidemiology of

neoplasm, metastatic to CNS

neoplasm, metastatic to CNS-treatment of

neoplasm, primary intracerebral

neoplasm, primary intracerebral, reoperation

neoplasm, primary intracranial

neoplasm, primary intracranial-treatment of

neoplasm, primary of CNS

neoplasm, primary of CNS-children

neoplasm, primary of CNS-familial occurrence

neoplasm, primary of CNS-incidence of

neoplasm, primary of CNS-surgical treatment of

neoplasm, primary of CNS-treatment of

nerve conduction studies

neuraminidase deficiency

neuroaxonal dystrophy

neuroaxonal dystrophy, infantile

neuroaxonal dystrophy, juvenile

neuroaxonal leukodystrophy

neurocutaneous disease

neuroendocrinology

neurofibromatosis 1

neuroichthyosis

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic examination, focal

neurologic signs

neurologic symptoms

neurologic testing

neuronal ceroid-lipofuscinosis

neuronal migration disorder

neuroophthalmology

neuropathology, brain

neuropathy, hereditary peripheral

neuropathy, peripheral

neuropathy, vasculitic, systemic

neuropsychiatry

neurotransmitter

nevoid basal cell carcinoma syndrome

next-generation sequencing

Niemann-Pick disease

nitrogen mustard

Noonan Syndrome

nystagmus, monocular

nystagmus, rotary

nystagmus, vertical

occipital lobe, lesion of

ocular myopathy

oculodentodigital dysplasia

oligodendroglioma

ophthalmoplegia

ophthalmoplegia, progressive external

optic atrophy, hereditary

optic nerve, enlarged

optic nerve, hypoplasia of

optic nerve, lesion of

optic neuropathy

optokinetic nystagmus, abnormal

orbit, lesions of

orthostatic hypotension

pain, abdominal

palatal myoclonus

paramyotonia congenita

paraparesis, familial spastic

paraparesis, spastic

paraparesis, spastic, tropical

Parkinson disease

Parkinson disease, dystonia with

Parkinson disease, surgical treatment of

Parkinson disease, treatment of

Parkinsonism syndrome

paroxysmal dystonic choreoathetosis

paroxysmal extreme pain disorder

paroxysmal hemiplegia

paroxysmal kinesigenic dyskinesia

paroxysmal neurologic deficits

PAS positive material in the brain

patient information and support

pectus excavatum

percussion induced muscle contraction

periodic paralysis

periventricular leukomalacia

peroxisomal disease

personality change

phenylketonuria

pheochromocytoma

philtrum, tented

pigmentary retinopathy

Pittsburgh Compound B

pituitary, adenoma

pituitary, hormones of

pleocytosis of cerebrospinal fluid

poison, mercury

poison, neurologic problems with

polycystic kidneys

polycythemia, secondary

polymerase chain reaction

polyps, gastrointestinal tract

pons, lesion of

pontocerebellar atrophy

port wine nevus

portal caval shunt

postural abnormality

potassium channel antibodies

potassium channel dysfunction

practice guidelines

Prader-Labhart-Willi syndrome

precipitating factors

pregnancy, anticonvulsants during

pregnancy, neurologic complications in

premature infant

prenatal diagnosis by amniocentesis

pretectal syndrome

prethrombotic state

primary episodic ataxia

primary familial brain calcification

progressive infantile poliodystrophy

progressive myoclonic epilepsy

progressive neurologic disorder

progressive pallidum atrophy

prolactin, elevated

protein 14-3-3, cerebrospinal fluid

protein C deficiency

protein S deficiency

pseudobulbar palsy

pseudohypoparathyroidism

pseudoretinitis pigmentosa

pseudoxanthoma elasticum

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

psychosis, acute

PTEN hamartoma tumor syndrome

ptosis, bilateral

pulmonary embolism

pulmonary infiltrates

pulmonary stenosis

pupil, dilated, bilateral

pupil, dilated, episodic

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

pyridoxine deficiency

pyruvate metabolism, abnormality of

radiation therapy, CNS treatment and complications with

radiation therapy, stereotactic

ragged-red fibers

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

reading problem, causes of

real-time quaking-induced conversion

respiratory failure

respiratory tract infection

retina, abnormal

retinal degeneration

retinal hamartoma

retinal hemangioma

retinitis pigmentosa

Rett's syndrome

reversible neurologic disorder

rhabdomyoma, cardiac

rhabdomyosarcoma of heart

risk factors, modification

Romano-Ward syndrome

rubella syndrome

salivation, excessive

Schilder's disease

scoliosis, neurologic association with

sea-blue histiocytes

seizure, bathing induced

seizure, cardiac arrhythmia causing

seizure, children

seizure, classification of

seizure, complications following

seizure, crying as manifestation of

seizure, diagnosis of

seizure, differential diagnosis of

seizure, drug resistance

seizure, etiology of

seizure, familial

seizure, febrile

seizure, hereditary

seizure, incidence of

seizure, injury following

seizure, intractable

seizure, laughing as manifestation

seizure, maternal

seizure, neonatal

seizure, nocturnal

seizure, nonepileptic

seizure, paradoxical

seizure, photosensitive

seizure, precipitating factors

seizure, prevalence of

seizure, prognosis in adults

seizure, prognosis in childhood

seizure, psychomotor-temporal lobe

seizure, psychosocial aspects of

seizure, pyridoxine dependent

seizure, risk factors for

seizure, stimulus sensitive

seizure, surgical treatment of

seizure, teenager

seizure, tonic-clonic

seizure, treatment of

seizure, workup of

self-mutilation

semialdehyde dehydrogenase deficiency

sensorineural hearing loss

single photon emission computed tomography

Sjogren-Larsson syndrome

skin, darkening of

skin, lesions in neurologic disorders

skull x-ray, abnormal

sleep pathology and physiology

small vessel disease

small vessel disease, cerebral

Sneddon's syndrome

sodium channel dysfunction

sodium valproate

spastic diplegia

spastic dysphonia

speech disorder

speech disorder, childhood

speech, absence of

speech, delayed development of

speech, loss of

sphingolipodoses

Spielmeyer Vogt syndrome

spinal cord, lesion of

spinal cord, neoplasm

spinal cord, vascular malformation of

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 10

spinocerebellar ataxia type 16

spinocerebellar ataxia type 6

spinocerebellar ataxia type 7

spongy degeneration of brain

startle myoclonus

startle reaction

status epilepticus

stereotaxic surgery

stereotyped behavior

steroid therapy, CNS treatment and complications with

stimulant drugs

stimulation, deep brain

storage disease of CNS

striatonigral degeneration

striatonigral degeneration, infantile

striatum, lesion of

striatum, lesion of, bilateral

striopallidodentate calcifications, familial idiopathic

strokelike episodes

Sturge-Weber syndrome

subarachnoid hemorrhage

subcortical U fibers

subdural hematoma

subependymal nodules

substantia nigra

sulfite oxidase deficiency

superior sagittal sinus thrombosis

symmetric brain lesions

syncope, triggers of

systemic illness

tandem gait, ataxic

tapetoretinal degeneration

Tay-Sachs disease

teeth, abnormal

teeth, wide-spaced

telangiectases, retinal

temper tantrums

temporal lobe, lesion

teratogenic drugs

testicular atrophy

testicular biopsy

testicular enlargement

thalamotuberal artery

thalamus, atrophy of

thalamus, lesion of

thalamus, lesion of-bilateral

thromboangiitis obliterans cerebri

thrombocytopenia

thrombophlebitis

tongue, enlarged

tongue, protrusion of

tonic foot response

torsades de points

toxins, nervous system

transient ischemic attack

transient ischemic attack, recurrent

transient neurologic deficit

treatment of neurologic disorder

tremor, intention

tremor, surgical treatment of

tremor, treatment of

trichopoliodystrophy

trinucleotide repeats

tuber, cortical

tuberous sclerosis

tuberous sclerosis, screening for

unconsciousness

unconsciousness, transient

Unverricht-Lundborg disease

upgaze, paralysis of

urea-cycle enzymopathies

urinalysis, abnormal

urinary incontinence

urine test for metabolic disorders

Usher's syndrome

venous hemangioma

venous thrombosis, non-cerebral

ventricular enlargement

ventricular tachycardia

very long chain fatty acids

vincristine neurotoxicity

violent behavior

viral infection

viral infection, CNS

viral isolation

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

visuospatial disturbance

vitreous opacities

vocal cord paralysis

vomiting, recurrent

Von Hippel Lindau

walking, difficulty with

weakness, acute

weakness, focal

white matter disease

white matter disease, subcortical

whole genome sequencing

wide based gait

Wolff-Parkinson-White syndrome

Wolfram syndrome

X-linked lissencephaly

x-linked mental retardation

Showing articles 2500 to 2550 of 5526 << Previous Next >>

Neurodevelopmental Dysfunction Among Nonreferred Children with Idiopathic Megalencephaly
J Pediatr 131:320-324, Sandler,A.D.,et al, 1997

Maternal Infection and Cerebral Palsy in Infants of Normal Birth Weight
JAMA 278:207-211, 2471997., Grether,J.K.&Nelson,K.B., 1997

Clinicopath Conf
Placental Vascular Thrombosis Due to Listeria Infection, Cerebral Embolism and Infarction, Case 15-1, 97EJM 336:1439-1446,1997., 1997

Assessment of Digital EEG, Quantitative EEG, and EEG Brain Mapping
Neurol 49:277-292, Nuwer,M., 1997

Preliminary Results of Linear Accelerator Radiosurgery for Acoustic Schwannomas
J Neurosurg 85:1013-1019, Mendenhall,W.M.,et al, 1997

Adult-Onset Krabbe's Disease in Siblings with Novel Mutations in the Galactocerebrosidase Gene
Ann Neurol 41:111-114, Bernardini,G.L.,et al, 1997

Retrospective of Concussive Convulsions in Elite Australian Rules & Rugby League Footballers
BMJ 314:171-174, 1581997., McCrory,P.R.,et al, 1997

Clinical Course of Untreated Tonic-Clonic Seizures in Childhood:Prospective, Hospital Based Study
BMJ 314:401-404, 3911997., vanDonselaar,C.A.,et al, 1997

Severe Persistent Visual Field Constriction Associated with Vigabatrin
BMJ 14:180-181, Eke,T.,et al, 1997

Long-Term Psychosocial Outcome in Typical Absence Epilepsy
Arch Pediatr Adolesc Med 151:152, 1581997., Wirrell,E.C.,et al, 1997

Painful Generalised Clonic and Tonic-Clonic Seizures with Retained Consciousness
JNNP 63:792-795, Bell,W.L.,et al, 1997

Reversible MRI Lesions After Seizures
Seizure 6:237-239, Aykut-Bingol,C.,et al, 1997

Mutations in the Sarcoglycan Genes in Patients with Myopathy
NEJM 336:618-624, Duggan,D.J.,et al, 1997

X-Linked Vacuolated Myopathy:Membrane Attack Complex Depos on Muscle Fiber Membr with Calcium Accumul on Sarcolemma
Ann Neurol 41:117-120, Louboutin,J.P.,et al, 1997

Prognosis in Familial ALS:Progr & Surv in Pts with glu100gly & ala4val Mutations in Cu, Zn Superoxide Dismutase
Neurol 48:55-57, Juneja,T.,et al, 1997

Familial Idiopathic Brain Calcification with Autosomal Dominant Inheritance
Neurol 48:645-649, Kobari,M.,et al, 1997

Drugs and Myasthenia Gravis, An Update
Arch Int Med 157:399-408, Wittbrodt,E.T., 1997

Surgery for Parkinson's Disease
JNNP 62:2-8, Obeso,J.A.,et al, 1997

Comparison of Extrapyramidal Features in 31 Path Cases of Diffuse Lewy Body Disease & 34 Cases of Parkinson's
Neurol 48:376-380, Louis,E.D.,et al, 1997

Gabapentin for Parkinsonism:A Double-Blind Placebo-Controlled, Crossover Trial
Am J med 102:60-66, Olson,W.L.,et al, 1997

Gamma Knife Radiosurgery for Treatment of Trigeminal Neuralgia
Neurol 48:608-614, 5651997., Young,R.F.,et al, 1997

Acute Bacterial Meningitis in Adults, A 20-Yr Overview
Arch Int Med 157:425-430, Sigurdardottir,B.,et al, 1997

Chronic Encephalitis and Epilepsy in Adults and Adolescents:A Variant of Rasmussen's Syndrome
Neurol 48:418-424, Hart,Y.M.,et al, 1997

HTLV-Associated Myelopathy in a Cohort of HTLV-I and HTLV-II Infected Blood Donors
neurol 48:315-320, Murphy,E.L.,et al, 1997

Proximal Myotonic Myopathy with MRI White Matter Abnormalities of the Brain
Neurol 48:33-37, Hund,E.,et al, 1997

Successful Treatment of Persistent Migraine Aura with Divalproex Sodium
Neurol 48:261-262, Rothrock,J.F., 1997

Adult-Onset Temporal Lobe Epilepsy Associated with Smoldering Herpes Simplex 2 Infection
Neurol 48:425-430, Cornford,M.E.&McCormick,G.F., 1997

Alcohol Use is a Risk Factor for a First Generalized Tonic-Clonic Seizure
Neurol 48:614-620, Leone,M.,et al, 1997

Thrombotic Thrombocytopenic Purpura:A Treatable Cause of Childhood Encephalopathy
J Pediatr 130:313-316, Lawlor,E.R.,et al, 1997

Linkiage of Locus for Cerebral Cavernous Hemagiomas to Chromosome 7q in 4 Families of Mexican-American Descent
Neurol 48:752-757, Polymeropoulos,M.H.,et al, 1997

Familial Intracranial Aneurysms
Lancet 349:380-384, Ronkainen,A.,et al, 1997

Epidemiology, Pathophysiology, & Management of Hyponatremic Encephalopathy
Am J Med 102:67-77, Fraser,C.L.,et al, 1997

Machado-Joseph Disease in 4 Chinese Pedigrees:Molecular Analysis of 15 Pts
Neurol 48:482-485, Zhou,Y.X.,et al, 1997

Familial episodic Ataxia:Clinical Heterogeneity in Four Families Linked to Chromosome 19p
Ann Neurol 41:8-16, 41997., Baloh,R.W.,et al, 1997

The Clinical Introduction of Genetic Testing for Alzheimer Disease, An Ethical Perspective
JAMA 277:832-836, Post,S.G.,et al, 1997

Accuracy of the Clinical Diagnosis of Corticobasal Degeneration:A clinicopathologic Study
Neurol 48:119-125, Litvan,I.,et al, 1997

Hereditary Frontotemporal Dementia is Linked to Chromosome 17q21-q22:Genetic & Clinicopath Study of 3 Dutch Families
Ann Neurol 41:150-159, Heutnik,P.,et al, 1997

Frontotemporal Dementia is on the MAP
Ann Neurol 41:139-140, Wilhelmsen,K.C., 1997

Clin Features of Early-Onset Alzheimer Disease in Large Kindred with an E280A Presenilin-1 Mutation
JAMA 277:793-799, Lopera,F.,et al, 1997

Cerebral Microsporidiosis Due to Encephalitozoon Cuniculi in a Patient With Human Immunodeficiency Virus Infection
NEJM 336:474-478, Weber,R.,et al, 1997

Adult-Onset Subacute Sclerosing Panecephalitis:Case Reports and Review of the Literature
Mov Dis 12:342-353, Singer,C.,et al, 1997

AIDS Dementia Complex with Generalized Myoclonus
Mov Disord 12:593-597, Maher,J.,et al, 1997

Increased Writing Activity in Neurological Conditions:A Review and Clinical Study
JNNP 61:510-514, vanVugt,P.,et al, 1996

Genetic Factors in Alzheimer's Disease:A Review of Recent Advances
Ann Neurol 40:829-840, Levy-Lahad,E.&Bird,T.D., 1996

Immunosuppression-Induced Leukoencephalopathy from Tacrolimus (FK506)
Ann Neurol 40:575-580, Small,S.L.,et al, 1996

Restless Legs Syndrome:Clinicoetiologic Correlates
Neurol 47:1435-1441, Ondo,W.&Jankovic,J., 1996

Exceptional Multiplicity of Cerebral AVMs Assoc with Hereditary Hemorrhagic Telangiectasia (Osler-Weber-Rendu Syndrome)
AJNR 17:1733-1742, Putman,C.M.,et al, 1996

Isolated Vitamin E Deficiency
Muscle & Nerve 19:1161-1165996., Jackson,C.E.,et al, 1996

Practice Parameter:Genetic Testing Alert
Pract Comm Genet Testing Task Force AAN, Neurol 47:1343-13441996., , 1996

Unusual Clinical Presentations of Cortical-Basal Ganglionic Degeneration
Ann Neurol 40:893-900, Bergeron,C.,et al, 1996

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