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abdominal reflex, absent

abducens nerve paralysis

abscess, spinal cord

achilles tendon, enlarged

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

acquired immunodeficiency syndrome myelopathy

acquired immunodeficiency syndrome, congenital

acquired immunodeficiency syndrome, infants and children

acquired immunodeficiency syndrome-related complex

addiction, heroin-neurologic complications with

Addison's disease

adrenoleukodystrophy

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

adult polyglucosan body disease

adult T-cell leukemia-lymphoma

advances in neurology

adverse drug reaction

agenesis of corpus callosum

Aicardi-Goutieres syndrome

alcohol injection

alcohol, neurologic complications with

Alexanders disease

Alexanders disease, adult onset

Alzheimer's disease

aminoacidopathies

amyloid plaques

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, bulbar

amyotrophic lateral sclerosis, atypical

amyotrophic lateral sclerosis, diagnosis of

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, etiology of

amyotrophic lateral sclerosis, juvenile

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, treatment of

anemia, megaloblastic

anesthesia, general

aneurysm, vertebral basilar system

angiitis, granulomatous of CNS

angiitis, isolated of CNS

angiography, cerebral

angiography, neurologic complications with

angiography, spinal

ankle reflex, absent

ankylosing spondylitis

anterior horn cell disease

anterior spinal artery

anticonvulsants

anticonvulsants, untoward effects of

antispasticity drugs

aphasia, children

apraxia, speech

arteriovenous malformation

arteritis, temporal

asterixis, causes of

asterixis, unilateral

ataxia, cerebellar

ataxia, hereditary

ataxia, progressive

ataxia, sensory

ataxia, truncal

atherosclerosis, generalized

atherosclerosis, premature

atlanto-axial subluxation

atrioventricular block

attention deficit disorder with hyperactivity

auditory evoked brainstem potentials

autoimmune disease

autonomic dysfunction

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

azidodeoxythymidine

B 12 deficiency

bacterial infection

bacterial infection, CNS

ballismus, bilateral

Barkhof MR criteria for MS

basal ganglia, calcification of

basal ganglia, infarction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavioral disorder

Behcet's syndrome

Benedict's solution test

bladder dysfunction

blood dyscrasias, neurologic findings with

blood transfusion

bone marrow biopsy

bone marrow transplantation

brachial plexus neuropathy

brain biopsy, stereotaxic

brainstem, atrophy

brainstem, dysfunction

brainstem, glioma

brainstem, glioma in children

brainstem, glioma, adult

brainstem, infarction of

brainstem, ischemia

brainstem, lesion of

brainstem, neoplasms of

Brown Sequard syndrome

brucellosis, nervous system involvement with

bulbar palsy, progressive

burning paresthesia

calcification, intracranial

carcinoma of pancreas

cardiac transplantation

carotid angiogram

CAT scan, abdomen

CAT scan, abnormal

CAT scan, demyelinating disease

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, myelogram with

CAT scan, serial

CAT scan, spinal cord

CAT scan, spine

cavernous hemangioma

central nervous system, infection of

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar degeneration

cerebellar hemangioma

cerebellar infarction

cerebellar lesion

cerebellar plaques, amyloid

cerebellar vermis

cerebral cortical atrophy

cerebral embolism

cerebral embolism, cardiac origin

cerebral folate deficiency syndrome

cerebral infarction

cerebral palsy, associated problems with

cerebral palsy, pure ataxic

cerebral peduncle

cerebral venous thrombosis

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, amonia

cerebrospinal fluid, culture of

cerebrospinal fluid, culture of, viral

cerebrospinal fluid, cytology

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, glutamine

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, mimics

cerebrovascular accident, recurrent

cerebrovascular accident, vascular territory involved

cerebrovascular disease

cervical myelopathy

cervical spine cyst

cervical spine injury, compression

cervical spondylosis

Charcot-Marie-Tooth

chilbran skin lesions

chorea, causes of

chorea, familial

choreoathetosis

choroid plexus, tumor of

chromosomal abnormality

chronic progressive external ophthalmoplegia

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

coccidioidomycosis

color vision, impaired

compression fracture

concentration, impaired

congenital bilateral perisylvian syndrome

congenital infection, viral

congenital malformation

congenital malformation, non CNS

controversies in neurology

copper deficiency

cornea, opacity of

coronary artery bypass

corpus callosum

corpus callosum, atrophy of

corpus callosum, lesion of

corpus callosum, thinning

cortical blindness

Coxiella burnetti

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

cranio-cervical junction

crossed adductor reflex

crying, pathologic

cryptococcal meningitis

cultured skin fibroblasts

cyclophosphamide

cyst, epidermoid of CNS

deafness, bilateral progressive vs.unilateral acute

deafness, unilateral

decerebrate posture

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

dementia, childhood

dementia, familial

dementia, presenile

dementia, reversible

dementia, subcortical

dementia, thalamic

dementia, treatment of

demyelinating disease

dental prostheses

dentate nuclei, lesion of

dermatomyositis

developmental abnormality of brain

developmental milestones

developmental milestones, loss of

developmental retardation

dexterity, impaired

diagnostic criteria

diarrhea, bloody

differential diagnosis

diffuse idiopathic skeletal hyperostosis

digital subtraction angiography

digiti quinti sign

digits, abnormal

dinitrophenylhydrazine(D.N.P.H.)reaction

diplegia, atonic

diplegia, spastic cerebral

disability, neurological

distal muscle atrophy

distal muscle weakness

Dravet syndrome

drug abuse, inhalation

drug abuse, neurologic complications of

dysarthria-clumsy hand syndrome

dyskinesia, buccal lingual facial

dysplasia of C.N.S.

dystonia musculorum deformens

dystonia, cervical

dystonia, children

dystrophic calcification

ears of the Lynx MR sign

electrical sensation

electroencephalogram

electroencephalogram, abnormalities of

electron microscopy

embolization, therapeutic

emergencies, neurologic

emotional lability

encephalitis lethargica

encephalitis, recurrent

encephalitis, viral

encephalomyelitis

encephalopathy, metabolic

endovascular therapy

enzyme, muscle disease

epicanthal folds

epidemiology of neurology

epileptic encephalopathy

Epstein-Barr virus

erythema migrans

evoked potentials

exome sequencing

facial anomalies

facial appearance, abnormal

facial nerve palsy

facial nerve palsy, bilateral

facial nerve palsy, recurrent

facial weakness

facial weakness, bilateral

failure to thrive

FARS2 deficiency

fatal familial insomnia

fatty acid, elevated plasma content

feeding disorder

ferric chloride test

fetal alcohol syndrome

fine motor function, impaired

finger nose finger test

fistula, arterio-venous

fistula, arterio-venous, dural

fistula, arterio-venous, dural, spinal

flaccid paralysis

fluorescent treponema antibody absorption(FTA-ABS)

folic acid deficiency

Friedreich's ataxia

frontal lobe, pathologic signs of

gag reflex, depressed

galactocerebrosidase

gamma amino butyric acid-mimetic drug

gastric partitioning

genetic counselling

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

geographic location

Gerstmann-Straussler-Scheinker disease

girdle sensation

glioblastoma multiforme(astrocytoma Gr.III)

glioma, low-grade

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

gram negative rod

granulomatosis with polyangiitis

granulomatous disease

Guillain Barre syndrome

Hallervorden Spatz disease

hearing problems in children

heart block, complete

hemangioma, vertebral

hematoma, epidural-spinal

hematopoietic tissue, extramedullary

hematuria, microscopic

hemoglobin abnormality, neurologic complications of

hemophagocytosis

hemosiderosis of CNS, superficial

hepatic encephalopathy

hepatic failure

hepatolenticular degeneration, non-Wilsonian

hepatosplenomegaly

herniated disc, cervical

herniated disc, thoracic

herpes virus infection

high arched feet

history of neurology

Hodgkin's disease

Horner's syndrome

human herpesvirus 6

human immunodeficiency virus type 1

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

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

hydrocephalus, congenital

hydrocephalus, fetal

hydrocephalus, intrauterine

hydrocephalus, viral induced

hyperammonemic encephalopathy

hyperparathyroidism

hyperpigmentation of skin

hyperpyrexia, CNS disorder causing

hypersegmented polys

hyperthyroidism

hypertrophic intracranial pachymeningitis

hypoglycorrhachia

hypoglycorrhachia, causes of

hypomyelination

hypopigmentation of skin

hypothalamus, disturbance of

hypothermia, causes of

iatrogenic neurologic disorders

immunologic disease

immunology and the nervous system

immunosuppression

immunosuppressive agents

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic intranuclear

incontinence, fecal

intellectual deficit

intellectual deficit, treatable causes of

intellectual deterioration

intelligence quotient

interferon alpha

internal capsule

intracerebral hemorrhage

intracerebral hemorrhage, multiple

intrathecal antispasticity drugs

intrauterine infection

intrauterine infection, viral

intrauterine infection, viral of CNS

intrinsic hand muscles, wasting of

Jakob-Creutzfeldt disease

Jamaica ginger paralysis

jaw jerk, abnormal

klippel feil syndrome

Krabbe's disease

kyphoscoliosis, neurologic causes of

lactic acidemia

lactic dehydrogenase(LDH)

lacunar infarction

language disorders in children

laughing, pathologic

leg weakness, bilateral

Leigh's disease

Leigh's disease, adult variety

lenticular nucleus, lesion of, bilateral

leukemia, neurologic findings assoc.with

leukocyte enzyme abnormality

leukoencephalopathy

leukoencephalopathy, differential diagnosis

Lhermitte's sign

life expectancy

locked-in syndrome

lymphadenopathy

lymphocytic pneumonitis

lymphoma involving CNS

lymphomatoid granulomatosis

magnetic stimulation

magnetic stimulation, brain

malabsorption syndrome

malformation, CNS, congenital

malformation, vascular

malformation, vascular, dural

malformation, vascular, treatment of

maple syrup urine disease

medulla oblongata, lesion of

Melkersson's syndrome

memory, impairment of

meningeal biopsy

meningeal enhancement

meningeal gliomatosis

meningeal sarcomatosis

meningitis, actinomycotic

meningitis, aseptic

meningitis, bacterial

meningitis, blastomyces

meningitis, brucellosis

meningitis, candida

meningitis, carcinomatous

meningitis, chronic

meningitis, chronic benign lymphocytic

meningitis, cladosporium

meningitis, coenurosis

meningitis, CSF cell count-normal

meningitis, cysticercosis

meningitis, echinococcal

meningitis, eosinophilic

meningitis, fungal

meningitis, helminthic

meningitis, histoplasma

meningitis, leptospira

meningitis, lymphomatous

meningitis, Mollaret's

meningitis, nocardia

meningitis, paracoccidioides

meningitis, post myelography

meningitis, recurrent

meningitis, syphilitic

meningitis, toxoplasma

meningoencephalitis

meningoencephalitis, toxoplasma

meningomyelitis

meningovascular syphilis

mental retardation

mental status, abnormal

metabolic acidosis

metabolic disorder, primary

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

metachromatic leukodystrophy, late-infantile

methylmalonic acidemia

methylmalonic aciduria

middle cerebellar peduncle

middle cerebellar peduncle, lesion, bilateral

midline defect in children

mitochondrial disease

molecular genetics

mononeuritis multiplex

mononeuropathy multiplex

Morquio syndrome

motor neuron disease

movement disorder

movement disorder, extrapyramidal

MRI, angiography

MRI, angiography, contrast enhanced

MRI, brachial plexus

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, demyelinating disease

MRI, diffusion tensor

MRI, diffusion weighted

MRI, false negative

MRI, high signal foci on

MRI, high signal intensity of basal ganglia

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRI, T1 weighted high signal foci

MRI, target sign

mucopolysaccharidoses

multinucleated giant cell

multiple sclerosis

multiple sclerosis, chronic progressive

multiple sclerosis, diagnosis of

multiple sclerosis, differential diagnosis of

multiple sclerosis, etiology of

multiple sclerosis, late-onset

multiple sclerosis, misdiagnosis

multiple sclerosis, prognosis

multiple sclerosis, spinal form

multiple sclerosis, treatment of

multiple system atrophy

muscle twitching

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

myasthenia gravis

myelitis, longitudinal

myelitis, transverse

myelogram, thoracic

myeloneuropathy

myelopathy hand

myelopathy, ischemic

myelopathy, ascending

myelopathy, chronic progressive

myelopathy, hepatic

myelopathy, necrotizing

myelopathy, radiation induced

myelopathy, transverse

myelopathy, vacuolar

myelopathy, venous hypertensive

myeloradiculopathy

myoclonic jerks

myoclonus, epilepsy

myopathy, vacuolar

myositis, ocular

Native Americans

nausea and vomiting

neoplasm, primary intracerebral

neoplasm, primary of CNS

neoplasm, primary of CNS-classification

neoplasm, primary of CNS-metastasizing to subarachnoid space

neoplasm, primary of CNS-treatment of

nerve conduction studies

nerve root enhancement

neuritis, causes of

neurocutaneous disease

neuroendocrinology

neurofibromatosis 1

neurogenic bladder

neuroichthyosis

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic examination

neurologic examination, focal

neurologic signs

neurologic symptoms

neuronal ceroid-lipofuscinosis

neuronal intranuclear inclusion disease

neuroophthalmology

neuropathology, brain

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, peripheral

neuropathy, peripheral, treatment

neuropathy, sensory

neuropathy, vasculitic, systemic

neuroradiology, interventional

next-generation sequencing

night blindness

numb clumsy hands syndrome

nutritional deficiency

nystagmus, dissociated

nystagmus, rotary

nystagmus, vertical

occupational neurologic disorders

ocular dysmetria

ocular motility, disorders of

oculodentodigital dysplasia

oculogyric crisis

odontoid process

old age, neurology of

operculum syndrome, bilateral

ophthalmoplegia

ophthalmoplegia, progressive external

opportunistic infection

opportunistic infection, CNS

optic atrophy, hereditary

optic nerve, lesion of

optic neuropathy

oral ulcerations

organ transplantation

orthostatic hypotension

pain, abdominal

palatal myoclonus

palatopharyngeal incompetence

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, familial spastic, variants

paraparesis, painful

paraparesis, spastic

paraparesis, spastic, tropical

parathyroid adenoma

paresthesias, feet

paresthesias, generalized

paresthesias, hands

Parkinson disease

Parkinson disease, arteriosclerotic

Parkinson disease, asymmetric onset

Parkinson disease, L-dopa nonresponsive

Parkinson disease, postencephalitic

Parkinson disease, tremor, absence of

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

Pelizaeus Merzbacher

peripheral blood smear, abnormal

pernicious anemia

peroneal nerve palsy

peroneal nerve, lesion of

peroxisomal disease

personality change

phenylketonuria

phenylketonuria, adult onset

physical activity

platelet transfusion

pleocytosis of cerebrospinal fluid

pleocytosis of cerebrospinal fluid, neutrophilic

poison, organophosphate

polycythemia, primary

polyglucosan body

polyglucosan body disease

polymerase chain reaction

polyneuropathy, familial

pons, lesion of

portal caval shunt

posterior column disease

posterior inferior cerebellar artery syndrome

posterior longitudinal ligament, ossification of

postural abnormality

precocious puberty

prenatal diagnosis by amniocentesis

primary lateral sclerosis

prisoners of war, neurologic complications in

progressive neurologic disorder

proprioception, abnormal

pseudobulbar palsy

pseudomonas aeruginosa

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, neurologic problems

psychomotor retardation

psychosis, childhood

psychosocial aspects

pulmonary embolism

pulmonary infiltrates

pupil, abnormality in neurologic disorders

pure dysarthria

pursuit eye movements, abnormal

pyramidal tract

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

quadriparesis, progressive

radiation encephalopathy, delayed

radiation therapy, CNS treatment and complications with

Raynaud's phenomenon

rectal sphincter tone, decreased

regional enteritis

release phenomena

remote effect of cancer on the nervous system

respiratory dyskinesias

respiratory failure

reticulum cell sarcoma

retinal detachment

retinitis pigmentosa

reversible neurologic disorder

rheumatoid arthritis

rheumatoid arthritis, neurologic complications of

rickettsial organism

Rosenthal fibers

rubella encephalitis, progressive

saccadic eye movements, abnormal

sarcoidosis, CNS

scalp tenderness

Schilder's disease

sclerae, hyperpigmented

scleroderma, neurologic involvement with

sea-blue histiocytes

sedimentation rate, elevated

seizure, advice to parents and teachers regarding

seizure, children

seizure, familial

seizure, febrile

seizure, intractable

seizure, neonatal

seizure, psychosocial aspects of

seizure, tonic-clonic

seizure, treatment of

sensorineural hearing loss

sensory loss, cutaneous

serologic testing

serologic testing of cerebrospinal fluid

Shy-Drager syndrome

sickle cell disease

single photon emission computed tomography

Sjogren-Larsson syndrome

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skin, darkening of

skin, lesions in neurologic disorders

skin, temperature difference

skull x-ray, abnormal

sleep pathology and physiology

sodium channel dysfunction

sodium valproate

solitary scerlosis

somatosensory evoked potentials

spastic diplegia

spastic paraplegia, type 11

spastic paraplegia, type 15

spastic paraplegia, type 7

spasticity, treatment of

speech disorder

speech disorder, childhood

speech, loss of

spinal cord, biopsy

spinal cord, cervical

spinal cord, compression of

spinal cord, enlargement

spinal cord, extramedullary cyst of

spinal cord, herniation

spinal cord, infarction of

spinal cord, injury of

spinal cord, injury, management of

spinal cord, injury, prognosis in

spinal cord, ischemic lesion of

spinal cord, lesion of

spinal cord, neoplasm

spinal cord, neoplasm, extramedullary

spinal cord, neoplasm, extramedullary intradural

spinal cord, neoplasm, intramedullary

spinal cord, neoplasm, meningioma

spinal cord, neoplasm, neurofibroma

spinal cord, pathologic exam of

spinal cord, vascular disorders Affecting

spinal cord, vascular malformation of

spinal epidural arteriovenous malformation

spinal stenosis

spinal stenosis, cervical canal

spinal xanthomatosis

spinocerebellar ataxia type 1

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar degeneration

spirochete infection

spongy degeneration of brain

startle reaction

status epilepticus

steroid therapy, CNS treatment and complications with

striatonigral degeneration

striatonigral degeneration, infantile

striopallidodentate calcifications, familial idiopathic

strokelike episodes

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

subarachnoid hemorrhage

subcortical U fibers

substantia nigra

superior cerebellar artery infarction

symmetric brain lesions

syphilis, diagnosis and treatment

syphilis, meningomyelitis

syphilis, neurologic complications with

systemic illness

teeth, abnormal

tendon, enlarged

testicular atrophy

thalamus, lesion of

thrombocytopenia

tinnitus, pulsatile

tongue, atrophy

tongue, fasciculations of

tongue, impaired movements of

tongue, weakness

toxins, nervous system

toxoplasmosis, acquired

toxoplasmosis, CNS

transient ischemic attack

transposition of the great vessels

treatment of neurologic disorder

treatment, empirical

tremor, cerebellar

tremor, intention

trinucleotide repeats

tuberculoma of CNS

tuberculosis, spinal

tuberous sclerosis

ulcerative colitis

ulcers, fingertip

ultrasonography

ultrasonography, head, fetus-neonate

ultrasonography, spinal

urinary frequency

urinary incontinence

urinary urgency

urine test for metabolic disorders

venous engorgement

vibratory sensation, abnormal

viral infection

viral infection, CNS

viral isolation

visual acuity, decreased

visual evoked response

vitamin deficiency

Vogt-Koyanagi-Harada syndrome

walking, difficulty with

Wallerian degeneration

weakness, generalized

weakness, progressive

weakness, proximal

Werdnig-Hoffman disease

Werner's syndrome

Western immunoblot test

white matter disease

white matter disease, periventricular

wide based gait

xanthoma, tendon

x-linked hydrocephalus

Showing articles 200 to 250 of 715 << Previous Next >>

Intrathecal Baclofen for Severe Spinal Spasticity
NEJM 320:1517-1521, 1553-15551989., Penn,R.D.,et al, 1989

Treatment of Spastic Paresis
NEJM 320:1553-1555, Young,R.R., 1989

Hyperthyroidism Presenting as Pyramidal Tract Disease
BMJ 297:1395-1396, Shaw,P.J.,et al, 1988

Acute Extrapyramidal Syndrome in Methylmalonic Acidemia:"Metabolic Stroke"Involving the Globus Pallidus
J Pediatr 113:1022-1027, Heidenreich,R.,et al, 1988

Elevated Serum Antibody Titers to Epstein-Barr Virus in HTLV-I Associated Myelopathy (HAM)
Neurol 38:1650-1653, Itoyama,Y.,et al, 1988

MR Imaging of the Brain in Myelopathy Associated with Human T-Cell Lymphotropic Virus Type I
J Comput Assist Tomogr 12:750-754, Hara,Y.,et al, 1988

HTLV-I-Associated Myelopathy:Oligoclonal Immunoglobulin G Bands Contain Anti-HTLV-I-p24 Antibody
Ann Neurol 24:727-731, Grimaldi,L.M.E.,et al, 1988

Plasmapheresis in Treatment of Human T-Lymphotropic Virus Type-I Associated Myelopathy
Lancet 2:1109-1113, Matsuo,H.,et al, 1988

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

Pediatric Acquired Immunodefieiency Syndrome
Am J Dis Child 142:29-35, Belman,A.L.,et al, 1988

Detection of HTLV-I DNA & Antigen in Spinal Fluid & Blood of Pts with Chronic Progressive Myelopathy
NEJM 318:1141-1147, 11951988., Bhagavati,S.,et al, 1988

Primary Lateral Sclerosis, A Clinical Diagnosis Reemerges
Arch Neurol 45:1304-1307, Younger,D.S.,et al, 1988

Chronic Progressive Spinobulbar Spasticity, A Rare Form of Primary Lateral Sclerosis
Arch Neurol 45:509-513, Gastaut,J.L.,et al, 1988

Radiculomeningeal Vascular Malformations of the Spine:MR Imaging
Radiology 164:845-849, Nasaryk,T.J.,et al, 1987

The Autosomal Dominant Form of"Pure"Familial Spastic Paraplegia:Clinical Findings & Linkage Analysis of a Pedigree
Neurol 37:910-915, Boustany,R.M.N.,et al, 1987

Cranial Magnetic Resonance Imaging in the Evaluation of Myelopathy of Undetermined Etiology
Neurol 37:840-843, Miska,R.M.,et al, 1987

Retrovirus-Associated Myelopathies
Arch Neurol 44:659-663, Roman,G.C., 1987

Human T-Lymphotropic Virus Type I Antibodies in The Serum of Pts with Tropical Spastic Paraparesis in the Seychelles
Arch Neurol 44:605-607, Roman,G.C.,et al, 1987

Familial Cases of HTLV-I-Associated Myelopathy
Ann Neurol 22:601-605, Miyai,I.,et al, 1987

Tropical Spastic Paraparesis in the Seychelles Islands:A Clinical & Case-Control Neuroepidemiologic Study
Neurol 37:1323-1328, Roman,G.C.,et al, 1987

Myelopathy Hand
Editorial, Lancet 2:721-7221987., , 1987

Magnetic Resonance Imaging in Isolated Noncompressive Spinal Cord Syndromes
Ann Neurol 22:714-723, Miller,D.H.,et al, 1987

Tropical Spastic Paraparesis Associated with Human T Lymphotropic Virus Type I in an East African Naturalised in Sweden
BMJ 295:1380-1381, Ryberg,B.,et al, 1987

Myelopathies & Retroviral Infections
Ann Neurol 21:113-115, Johnson,R.T.&McArthur,J.C., 1987

Tropical Spastic Paraparesis:HTLV-I Antibodies in Patients from the Seychelles
NEJM 316:51, Roman,G.C.,et al, 1987

Endemic Tropical Spastic Paraparesis Associated with HTLV-I:A Clinical & Seroepidem Study of 25 Cases
Ann Neurol 21:123-130, Vernant,J.C.,et al, 1987

Chronic Progressive Myelopathy Associated with Elevated Antibodies to HTLV-I & Adult T-Cell Leukemialike Cells
Ann Neurol 21:117-121, Osame,M.,et al, 1987

Antibody to Human T-Lymphotropic Virus Type I In West-Indian-Born UK Residents with Spastic Paraparesis
Lancet 1:415-416, Newton,M.,et al, 1987

Neurologic Sequelae of Chronic Solvent Vapor Abuse
Neurol 36:698-702, Hormes,J.T.,et al, 1986

Lathyrism:Evidence for Role of the Neuroexcitatory Aminoacid BOAA
Lancet 2:1066-1067, Spencer,P.S.,et al, 1986

Familial Spastic Paraparesis & Deafness, A New X-Linked Neurodegenerative Disorder
Arch Neurol 43:943-946, Wells,C.R.&Jankovic,J., 1986

Association of High Cyanide & Low Sulphur Intake in Cassava-Induced Spastic Paraparesis
Lancet 2:1211-1213, Cliff,J.,et al, 1985

Portal-Systemic Myelopathy after Portacaval Shunt Surgery
Arch Int Med 145:1921-1922, Lebovics,E.,et al, 1985

Vacuolar Myelopathy Pathologically Resembling Subacute Combined Degeneration in Patients with AIDS
NEJM 312:874-879, Petito,C.K.,et al, 1985

Pyramidal Tract Deficits & Polyneuropathy in Hyperthyroidism
Am J Med 78:1041-1044, Fisher,M.,et al, 1985

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

Atypical Alzheimer's Disease with Spastic Paresis & Ataxia
Ann Neurol 17:297-300, Aikawa,H.,et al, 1985

Familial Multisystem Atrophy with Possible Thalamic Dementia
Neurol 34:1213-1217, Katz,D.A.,et al, 1984

Alcoholic Myelopathy without Substantial Liver Disease
Arch Neurol 41:999-1001, Sage,J.I.,et al, 1984

Long-Term Treatment of Cerebrotendinous Xanthomatosis with Chenodeoxycholic Acid
NEJM 311:1649-1652, Berginer,V.M.,et al, 1984

Adrenoleukodystrophy:Clinical & Biochemical Manifestations in Carriers
Neurol 34:798-801, O'Neill,B.P.,et al, 1984

Multiple Sclerosis After Age 50
Neurol 33:1537-1544, Noseworthy,J.,et al, 1983

Myeloneuropathy & Macrocytosis Associated with Nitrous Oxide Abuse
Arch Neurol 40:416-418, Bianco,G.,et al, 1983

Neurodegenerative Disease of Infancy & Childhood
Ann Neurol 13:351-364, Dyken,P.,et al, 1983

Familial Spastic Paraplegia, Mental Retardation, & Precocious Puberty
Arch Neurol 40:809-810, Raphaelson,M.I.,et al, 1983

Multifocal Central Nervous System Damage Caused by Toluene Abuse
Neurol 33:1337-1340, Lazar,R.B.,et al, 1983

Coma & Thyrotoxicosis
Ann Neurol 14:689-690, Newcomer,J.,et al, 1983

Neurologic Complications of Primary Sjogren's Syndrome
Medicine 61:247-257, Alexander,E.L.,et al, 1982

Motor Spastic Paraplegia & Unilateral Infra-nuclear Facial Palsy Complicating Tetanus
BMJ 285:477-478, Jain,M.K.,et al, 1982

Clinical & Electrophysiological Studies in Primary Lateral Sclerosis
Jr. , Arch Neurol 39:662-664982., Russo,L.S., 1982

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