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Differential
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abducens nerve paralysis

abortion, spontaneous

abscess, intracerebral

abscess, intracranial

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

advances in neurology

adverse drug reaction

agenesis of corpus callosum

alcohol, neurologic complications with

Alexanders disease

Alexanders disease, adult onset

algorithm

alkylating agents

alopecia

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

amyloid angiopathy, cerebral

amyloid angiopathy, hereditary cystatin C

amyloid beta protein

amyloid imaging

amyloidosis

amyloidosis, oculoleptomeningeal, familial

amyotrophic chorea-acanthocytosis

anemia

anesthesia, general

aneurysm

aneurysm, intracranial, screening for

Angelman syndrome

angiofibroma, facial

angiography, cerebral

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

antimetabolite

antioxidant

antiphospholipid antibodies

apnea, primary central

apolipoprotein E

APP gene

apraxia

apraxia, constructional

arteriovenous malformation

arteriovenous malformation, cerebral

attention deficit disorder with hyperactivity

attention span

atypical

auditory and vestibular pathways

aura

autism

autistic behavior

autonomic dysfunction

autosomal dominant nocturnal frontal lobe epilepsy

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

biotin deficiency

biotin deficiency, juvenile form

biotinidase deficiency

biotin-responsive basal ganglia disease

blindness

blindness, congenital

blood dyscrasias, neurologic findings with

blue rubber bleb nevus syndrome

body odor

bone marrow biopsy

bone marrow transplantation

bone pain

botulinum toxin

bovine spongiform encephalopathy

brainstem, neoplasms of

brainstem, vascular malformation of

bulbar palsy

buphthalmos

burning feet

burst suppression pattern, electroencephalogram

cafe au lait spots

CAG repeats

calcification, gyral

calcification, intracranial

calcium channel dysfunction

carotid artery occlusion, bilateral

CAT scan

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

catalepsy

cataplexy

cataracts

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 edema

cerebral embolism

cerebral infarction

cerebral infarction, subcortical

cerebral vasculature, calcification

cerebral venous thrombosis

cerebritis

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

channelopathy

Charcot-Marie-Tooth

chemotherapy, CNS treatment and complications with

cherry red spot

cherry red spot-myoclonus syndrome

chewing movements

chewing, impaired

children

chloride channel dysfunction

choreoathetosis, paroxysmal

chromosomal abnormality

chronic progressive external ophthalmoplegia

cirrhosis

cisterna magna, enlarged

cleft lip

cleft palate

Clinical Pathologic Conference(C.P.C.)

clonazepam

clonus

clubbing of fingers

cobalamin C deficiency

coin lesion on chest X-ray

cold hands sign

colloid cyst

color vision, impaired

compression neuropathy

confabulation

confusion

congenital heart disease

congenital heart disease, CNS complications with

congenital infection, CNS

congenital infection, viral

congenital malformation

congenital malformation, non CNS

congestive heart failure

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

cultured skin fibroblasts

cyst, epidermoid of CNS

cyst, neoplastic cerebellum

cytomegalovirus infection

degenerative diseases of CNS

delay in diagnosis

dementia

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

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

depression

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

diarrhea

diet

differential diagnosis

dilantin

dilantin, hypersensitivity to

dilantin, toxicity

diplopia

disability, neurological

disease modifying agents

distal muscle atrophy

distal muscle weakness

dural sinus thrombosis

dyssynergia cerebellaris myoclonica

dystonia

dystonia, face

dystonia, painful

dystonia, treatment of

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, monitoring, continuous

electroencephalogram, periodic complexes

electroencephalogram, video monitoring with

electromyogram

electron microscopy

electroretinograph

embolism, paradoxical

encephalopathy, acute necrotizing

encephalopathy, acute necrotizing of childhood

encephalopathy, metabolic

encephalopathy, neonatal

encephalopathy, progressive

endovascular therapy

entrapment neuropathy

enzyme, defect

ependymoma

epicanthal folds

epidemiology of neurology

epidermoid

epileptic encephalopathy

episodic disorders

episodic neurologic deficits

epistaxis

epsilon sarcoglycan gene

esophageal varices

evoked potentials

excitotoxin

executive dysfunction

exercise

exercise intolerance

exome sequencing

eye movement, disorders of

eye, pain in

Fabry's disease

facial anomalies

facial appearance, abnormal

facial expression abnormality

facial hypoplasia

facial nerve palsy

facial nerve palsy, bilateral

familial adult myoclonic epilepsy

familial hemiplegic migraine

familial rectal pain

FARS2 deficiency

fasciculation

fatal familial insomnia

fatigue

fatty acid, elevated plasma content

fine motor function, impaired

finger nose finger test

fistula, arterio-venous

fistula, arterio-venous, dural

fistula, arterio-venous, pulmonary

fluctuate

flunarizine

fluorescene in situ hybridization

frontal lobe, behavior with disease of

fucosidosis

fundus, abnormality of

gamma amino butyric acid

gastrointestinal bleeding

Gaucher's disease

Gaucher's disease, adult onset

gaze palsy

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

glioblastoma multiforme(astrocytoma Gr.III)

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

GLUT1

GLUT1 deficiency syndrome

granular osmiphilic material

granulomatosis with polyangiitis

grasp reflex

grimacing

growth hormone

growth hormone deficiency

growth retardation

guanidinoacetate methyltransferase deficiency

gynecomastia

gyrus, abnormal

Hallervorden Spatz disease

Hallgren's syndrome

hallucination

hallucination, visual

hearing loss, bilateral

hearing problems in children

hemangioma, brainstem

hemangioma, facial

hemangioma, internal organs

hemangioma, leptomeningeal

hemangioma, skin

hematuria, gross

hematuria, microscopic

hemianopia

hemihypertrophy, congenital

hemiparesis

hemiplegia

hemophagocytic lymphohistiocytosis

hemophagocytic lymphohistiocytosis, cerebromeningeal

hemophagocytosis

hemoptysis

hemorrhagic diathesis

hepatic encephalopathy

hepatic failure

hepatitis

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), screening for

hepatomegaly

hepatosplenomegaly

heralding manifestation

hereditary hemorrhagic telangiectasia(HHT)

herpes simplex encephalitis

herpes simplex encephalitis, differential diagnosis of

human immunodeficiency virus type 1

Huntington's chorea

Huntington's disease, children

Hurler's syndrome

hydrocephalus

hydrocephalus, communicating

hyperactivity

hyperekplexia

hyperglycinemia

hyperglycinemia, nonketotic

hyperhidrosis

hyperhomocysteinemia

hyperphagia

hyperpigmentation of skin

hyperreflexia

hypersensitivity reaction

hypertrophic cardiomyopathy

hypopigmentation of skin

hypoxic-ischemic leukoencephalopathy

hypsarrhythmia

iatrogenic neurologic disorders

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

inappropriate behavior

inattention

inborn errors of metabolism

inborn errors of metabolism, screening

incidental finding

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, intracytopasmic

incontinentia pigmenti

incoordination

infantile bilateral striatal necrosis

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

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, variant

Jakob-Creutzfeldt disease, young adult

jaundice

jaw pain

Jervell Lange-Neilson syndrome

Jewish

joint hypermobility

juvenile myoclonus epilepsy

karyotyping

Kayser-Fleischer ring

KCNQ2 encephalopathy

Kearns-Sayre syndrome

keratoconus

ketogenic diet

Korsakoff's psychosis

Krabbe's disease

kyphoscoliosis, neurologic causes of

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

lens, ectopic

lenticular nucleus, lesion of, bilateral

lethargy

leukemia, neurologic findings assoc.with

leukodystrophy

leukoencephalopathy

leukoencephalopathy with calcification and cysts

leukoencephalopathy, differential diagnosis

leukoencephalopathy, hereditary diffuse

level of consciousness, decreased

Lhermitte-Duclos disease

lipid storage disorder of CNS

lipomembranous polycystic osteodysplasia

liver function enzymes

liver transplantation

lymphoma, primary of CNS

lysosomal storage disease

macrocephaly

macrognathia

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

megalencephaly

melanomatosis, primary malignant

MELAS syndrome

memory, defect of recent

memory, impairment of

meningeal enhancement

meningioma

meningismus

meningitis

meningitis, carcinomatous

meningitis, CSF cell count-normal

meningoencephalopathy

mental retardation

mental retardation, etiology of

mental retardation, familial

MERRF syndrome

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

methotrexate

methylhydrazine derivatives

methylmalonic acidemia

methylmalonic aciduria

metoprolol

Mexican

mexiletine

microangiopathy, brain

microcephaly

microdontia

micrognathia

microhemorrhage, intracerebral

microspherophakia

microsurgery

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

miglustat

migraine

migraine, aura of

migraine, without headache

migratory lesion pattern

mild cognitive impairment

mimics

Minamata disease

Mini Mental Status Examination

misdiagnosis

mitochondrial disease

mitochondrial disease, pathogenesis

mitochondrial encephalomyopathy

molecular genetics

molybdenum cofactor deficiency

mongolism

monoamine oxidase inhibitors

mononeuropathy multiplex

movement disorder, extrapyramidal

movement disorder, hyperkinetic

movement disorder, paroxysmal

movement disorder, treatment of

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, cranial nerves

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, fetal

MRI, FLAIR

MRI, gradient-echo

MRI, incidental finding

MRI, susceptibility weighted

MRS

mucopolysaccharidoses

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple system atrophy

muscle weakness, proximal

mutism

myasthenia gravis, differential diagnosis

myasthenia gravis, misdiagnosis of

myelination of nervous system

myelomalacia

myelopathy

myelopathy, chronic progressive

myoclonus, stimulus sensitive

myokymia

myopathy

myopathy, mitochondrial

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 biopsy

nerve conduction studies

neuraminidase deficiency

neuritis

neuroaxonal dystrophy

neuroaxonal dystrophy, infantile

neuroaxonal dystrophy, juvenile

neuroaxonal leukodystrophy

neurocutaneous disease

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic examination, focal

neuronal ceroid-lipofuscinosis

neuronal migration disorder

neurons

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, hereditary peripheral

neuropathy, peripheral

neuropathy, vasculitic, systemic

nevoid basal cell carcinoma syndrome

nevus

next-generation sequencing

occipital lobe, lesion of

ocular myopathy

oculodentodigital dysplasia

oligodendroglioma

ophthalmoplegia

ophthalmoplegia, progressive external

opisthotonus

optic atrophy

optic atrophy, hereditary

optic glioma

optic nerve, enlarged

optic nerve, hypoplasia of

optic nerve, lesion of

optic neuropathy

optokinetic nystagmus, abnormal

orbit

orbit, lesions of

orthostatic hypotension

paramyotonia congenita

paranoia

paraparesis

paraparesis, familial spastic

paraparesis, spastic

paraparesis, spastic, tropical

paratonia

paresthesias

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

PAS positive material in the brain

patient information and support

pectus excavatum

penicillamine

percussion induced muscle contraction

periodic paralysis

periventricular leukomalacia

pigmentary retinopathy

Pittsburgh Compound B

pituitary, adenoma

pituitary, hormones of

pleocytosis of cerebrospinal fluid

poison, mercury

poison, neurologic problems with

POLG1 gene

polycystic kidneys

polycythemia, secondary

polydactyly

polyhydramnios

polymerase chain reaction

polyneuropathy

polyps, gastrointestinal tract

pons, atrophy

pons, lesion of

pontocerebellar atrophy

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

propranolol

protein 14-3-3, cerebrospinal fluid

pseudohypoparathyroidism

pseudoretinitis pigmentosa

pseudoxanthoma elasticum

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

psychosis

psychosis, acute

PTEN hamartoma tumor syndrome

ptosis

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

pyridoxine deficiency

pyruvate metabolism, abnormality of

quadriparesis

quadriplegia

radiation therapy, CNS treatment and complications with

radiation therapy, stereotactic

ragged-red fibers

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

rash

reading problem, causes of

real-time quaking-induced conversion

respiratory tract infection

reversible neurologic disorder

review article

rhabdomyoma, cardiac

rhabdomyosarcoma of heart

rigidity

risk factors

risk factors, modification

salivation, excessive

scoliosis, neurologic association with

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, 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

senile plaques

sensorineural hearing loss

single photon emission computed tomography

Sjogren-Larsson syndrome

skin, biopsy

skin, darkening of

skin, lesions in neurologic disorders

skull x-ray, abnormal

sleep

sleep pathology and physiology

small vessel disease

small vessel disease, cerebral

smiling

Sneddon's syndrome

sodium channel dysfunction

speech disorder, childhood

speech, absence of

speech, delayed development of

speech, loss of

sphingolipodoses

Spielmeyer Vogt syndrome

spinal cord

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

splenomegaly

spondylolysis

spongy degeneration of brain

steroid therapy, CNS treatment and complications with

stimulant drugs

stimulation, deep brain

storage disease of CNS

strabismus

straight sinus

striatonigral degeneration

striatonigral degeneration, infantile

striatum, lesion of

striatum, lesion of, bilateral

striopallidodentate calcifications, familial idiopathic

strokelike episodes

stuporous

Sturge-Weber syndrome

stuttering

subarachnoid hemorrhage

sulfite oxidase deficiency

superior sagittal sinus thrombosis

symmetric brain lesions

tapetoretinal degeneration

telangiectases, retinal

temper tantrums

temporal lobe, lesion

testicular enlargement

thalamotomy

thalamotuberal artery

thalamus, atrophy of

thalamus, lesion of

thalamus, lesion of-bilateral

thromboangiitis obliterans cerebri

tongue, protrusion of

toxins, nervous system

transient ischemic attack

transient ischemic attack, recurrent

transient neurologic deficit

trauma

treatment of neurologic disorder

tremor, surgical treatment of

tremor, treatment of

tremulousness

trichopoliodystrophy

trinucleotide repeats

tuberous sclerosis, screening for

tubulopathy

twins

unconsciousness

unconsciousness, transient

undiagnosed

Unverricht-Lundborg disease

upgaze, paralysis of

urea-cycle enzymopathies

uric acid, low

urinalysis, abnormal

urinary incontinence

urine test for metabolic disorders

venous thrombosis, non-cerebral

ventricular enlargement

ventricular tachycardia

very long chain fatty acids

vinblastine

vincristine neurotoxicity

vision, failure of in childhood

visual acuity, decreased

visual evoked response

visual field defect

visual fields, constricted

visual impairment

visual loss

visual loss, progressive

visual loss, slow

visuospatial disturbance

walking, difficulty with

white matter disease, subcortical

whole genome sequencing

wide based gait

Wolff-Parkinson-White syndrome

X-linked lissencephaly

x-linked mental retardation

Showing articles 150 to 200 of 5526 << Previous Next >>

Reduced GABA Synthesis in Pyridoxine-Dependent Seizures
Lancet 343:1133-1134, Gospe,S.M.,et al, 1994

The Relationship of Essential Tremor to Other Movement Disorders:Report on 678 Patients
Ann Neurol 35, 717-7231994., Koller,W.C.,et al, 1994

Familial Sneddon's Syndrome:Clinical, Hematologic, and Radiographic Findings in Two Brothers
Neurol 44:399-405, Pettee,A.D.,et al, 1994

Periventricular Heterotopia and Epilepsy
Neurol 44:51-55, Huttenlocher,P.R.,et al, 1994

The Nondystrophic Myotonias
In Myology, McGraw-Hill, 2nd Ed, Ch49, p1291-13024., Rudel,R.,et al, 1994

Neurological Involvement in Wegener's Granulomatosis:An Analysis of 324 Consecutive Pts at the Mayo Clin
Neurol 33:4-9, Nishino,H.,et al, 1993

Aicardi's Syndrome:MR Appearance of Unusual Orbital and Ventricular Cystic Lesions
AJR 160:601-603, Mehta,r.C.,et al, 1993

Progr Myoclonus Epilepsy of Unverricht-Lundborg Type:Clin & Molecular Genetic Study from US 4 Affected Sibs
Neurol 43:2284-2286, Lehesjoki,A.E.,et al, 1993

Seizure Characteristics in Chromosome 20 Benign Familial Neonatal Convulsions
Neurol 43:1355-1360, Ronen,G.M.,et al, 1993

Twin Birth is Not a Risk Factor for Seizures
Neurol 43:2515-2519, Berkovic,S.F.,et al, 1993

Delayed Diagnosis of Juvenile Myoclonic Epilepsy
JNNP 55:497-499, Grunewald,R.A.,et al, 1992

Familial Rectal Pain:A Type of Reflex Epilepsy?
Ann Neurol 32:824-826, Schubert,R.&Cracco,J.B., 1992

A Synd of Autosomal Dominant Alternating Hemiplegia:Mimicking Intractable Epilepsy; Chromosomal Studies; Physiol Investig
Neurol 42:2251-2257, Mikati,M.A.,et al, 1992

Juvenile Myoclonic Epilepsy, Underdiagnosed and Treatment May Have to be Life Long
BMJ 305:4-5, Timmings,P.L.&Richens,A., 1992

New Research in Tuberous Sclerosis, Probably More Common with More Adult Complications
BMJ 304:1647-1648, Mitchell,S.&Bradbeer,C., 1992

Wilson's Disease:Current Status
Am J Med 92:643-654, Yarze,J.C.,et al, 1992

Clinicopath Conf
Infantile Striatonigral Regeneration, with Cerebellar Degeneration, Familial, Case 30-1992, NEJM 327, 261-1992., 1992

Effect of Stereotactic Thalamic Lesion on Essential Tremor
Lancet 340:206-207, Lakie,M.,et al, 1992

Causal Heterogeneity in Isolated Lissencephaly
Neurol 42:1375-1388, Dobyns,W.B.,et al, 1992

Twinning and Neurologic Morbisity
Am J Dis Child 146:1110-1113, Scheller,J.M.&Nelson,K.B., 1992

Fatal Familial Insomnia, A Prion Disease with a Mutation at Codon 178 of the Prion Protein Gene
NEJM 326:444-449, Medori,R.,et al, 1992

Fatal Familial Insomnia:Clinical and Pathologic Study of Five New Cases
Neurol 42:312-319, Manetto,V.,et al, 1992

Hypomelanosis of Ito
Editorial, Lancet 339:651-6521992., , 1992

Recurrent Encephalopathy and Seizures in a US Native with HTLV-I-Associated Myelopathy/Tropical Spastic Paraparesis
Neurol 42:658-661, Smith,C.R.,et al, 1992

Cerebromeningeal Haemophagocytic Lymphohistiocytosis
Lancet 239:104-107, Henter,J.&Elinder,G., 1992

Angelman Syndrome: Clinical Profile
J Child Neurol 7:270-280, Zori,R.T.,et al, 1992

A Clinical Study of Noonan Syndrome
Arch Dis Child 67:178-183, Sharland, M.,et al, 1992

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

Localization of Idiopathic Generalized Epilepsy on Chromosome 6p in Families of Juvenile Myoclonic epilepsy patients
Neurol 41:1651-1655, Durner,M.,et al, 1991

Monozygotic Twins with Seizures, Shared Characteristics
Arch Neurol 48:1041-1045, Segal,R.A.,et al, 1991

Benign Familial Neonatal Convulsions:Evidence for Clinical and Genetic Heterogeneity
Ann Neurol 29:469-473, Ryan,S.G.,et al, 1991

MR of Progressive Neurodegenerative Change in Treated Menkes'Kinky Hair Disease
Neuroradiology 33:181-182, Johnsen,D.E.,et al, 1991

Diagnostic Tests for Choreoacanthocytosis
Neurol 41:1000-1006, Feinberg,T.E.,et al, 1991

Brain Tumors
NEJM 324:1471-1476, 1555-15641991., Black,P.McL., 1991

Fucosidosis Revisited:A Review of 77 Patients
Am J Med Genet 38:111-131, Willems,P.J.,et al, 1991

Epilepsy Octet, Epidemiology, Classification, Natural History, and Genetics of Epilepsy
Lancet 336:93-96, Shorvon,S.D., 1990

Stereotactic Gamma Knife Radiosurgery
Arch Neurol 47:169-175, Lunsford,L.D.,et al, 1990

Infantile CNS Spongy Degeneration-14 Cases:Clinical Update
Neurol 40:1876-1882, Gascon,G.G.,et al, 1990

Familial Idiopathic Striopallidodentate Calcifications
Neurol 39:381-385, Ellie,E.,et al, 1989

Neurofibromatosis and Other Disorders Among Children with CNS Tumors and Their Families
Neurol 39:487-492, Baptiste,M.,et al, 1989

Hereditary Long Q-T Syndrome Presenting as Epilepsy:Electroencephalography Laboratory Diagnosis
Ann Neurol 25:514-516, Gospe,S.M.&Choy,M., 1989

Late Onset of Distinct Neurologic Syndromes in Galactosemic Siblings
Neurol 39:741-742, Friedman,J.H.,et al, 1989

Neurological and Developmental Findings in Children with Cataracts
Am J Dis Child 13:706-710, Pike,M.G.,et al, 1989

Juvenile Myoclonic Epilepsy:An Autosomal Recessive Disease
Ann Neurol 25:440-443, Panayiotopoulos,C.P.&Obeid,T., 1989

Familial Alzheimer's Disease with Myoclonus and'Spongy Change'
Arch Neurol 45:1097-1100, Duffy,P.,et al, 1988

Rett Syndrome:Natural History and Management
Pediatrics 82:1-10, Moeschler,J.B.,et al, 1988

Familial Oculoleptomeningeal Amyloidosis, Report of a New Family with Unusual Features
Arch Neurol 45:1118-1122, Uitti,R.J.,et al, 1988

Livedo Reticularis, Porcelain-White Scars, and Cerebral Thromboses
Lancet 1:1263-1265, Burton,J.L., 1988

Cerebral Cavernous Malformations:Incidence and Familial Occurrence
NEJM 319:343-347, Rigamonti,D.,et al, 1988

Hereditary Dentatorubral-Pallidoluysian Atrophy:Clinical and Pathologic Variants in a Family
Neurol 38:1065-1070, Takahashi,H.,et al, 1988

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