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abdominal muscle paralysis

abdominal reflex, absent

abducens nerve paralysis

abscess, spinal cord

achilles tendon, enlarged

acid maltase deficiency

acid maltase deficiency, adult

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

acquired immunodeficiency syndrome myelopathy

addiction, heroin-neurologic complications with

Addison's disease

adrenoleukodystrophy

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

adult polyglucosan body disease

advances in neurology

adverse drug reaction

alcohol injection

alcohol, neurologic complications with

Alexanders disease

Alexanders disease, adult onset

Alzheimer's disease

aminoacidopathies

amphiphysin antibodies

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

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

anterior spinal artery infarction

anticoagulant, complications of

anticoagulant, treatment

anticonvulsants

anticonvulsants, untoward effects of

antiganglioside antibodies

antineutrophil cytoplasmic autoantibodies

antispasticity drugs

antiviral agents

arrhythmia, cardiac

arteriovenous malformation

arteritis, temporal

ascending paralysis

asterixis, causes of

asterixis, unilateral

asthma, poliomyelitis-like syndrome with

ataxia, cerebellar

ataxia, progressive

ataxia, sensory

atherosclerosis, premature

atlanto-axial subluxation

atrial fibrillation

atrioventricular block

auditory evoked brainstem potentials

autoimmune disease

autonomic dysfunction

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

axonal degeneration

azidodeoxythymidine

B 12 deficiency

bacterial infection

bacterial infection, CNS

Barkhof MR criteria for MS

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavioral disorder

behavioral disorder, acute

Behcet's syndrome

bladder dysfunction

blood dyscrasias, neurologic findings with

blood transfusion

bone marrow transplantation

brachial amyotrophic diplegia

brachial plexus neuropathy

brain biopsy, stereotaxic

brainstem, atrophy

brainstem, dysfunction

brainstem, lesion of

Brown Sequard syndrome

brucellosis, nervous system involvement with

bulbar palsy, progressive

campylobacter infection

cancer, unknown origin

carcinoma of breast

carcinoma of lung

carcinoma of unknown origin

carnitine deficiency myopathy

carotid angiogram

CAT scan, abnormal

CAT scan, chest

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

cauda equina, enhancement

cauda equina, lesion of

caudate nucleus, lesion of

cavernous hemangioma

central nervous system, infection of

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar lesion

cerebellar plaques, amyloid

cerebral cortical atrophy

cerebral palsy, associated problems with

cerebral peduncle

cerebral venous thrombosis

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, amonia

cerebrospinal fluid, culture of, viral

cerebrospinal fluid, cytology

cerebrospinal fluid, cytology, false negative

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, glutamine

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, proteincytologic dissociation

cerebrospinal fluid, xanthochromia of

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, mimics

cerebrovascular accident, recurrent

cerebrovascular disease

cervical myelopathy

cervical spine cyst

cervical spine injury, compression

cervical spondylosis

Charcot-Marie-Tooth

chemotherapy, CNS treatment and complications with

chenodeoxycholic acid

Chinese paralytic syndrome

choreoathetosis

chromosomal abnormality

chronic progressive external ophthalmoplegia

Clinical Pathologic Conference(C.P.C.)

clostridium perfringens

clubfoot as related to neurologic disease

color vision, impaired

compression fracture

conduction block

conus medullaris, lesion of

copper deficiency

cornea, opacity of

corpus callosum

corpus callosum, atrophy of

corpus callosum, thinning

cortical blindness

Coxiella burnetti

cranial neuropathy

cranial neuropathy, multiple

cranio-cervical junction

creatine phosphokinase isoenzyme elevation

creatine phosphokinase(CPK)elevated

crossed adductor reflex

crying, pathologic

cryptococcal meningitis

cultured skin fibroblasts

cyclophosphamide

cytomegalovirus infection

deafness, bilateral progressive vs.unilateral acute

deafness, unilateral

decerebrate posture

decompressive spinal cord surgery

deep gray nuclei

deep tendon reflexes

degenerative diseases of CNS

delay in diagnosis

dementia, childhood

dementia, familial

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

dementia, subcortical

dementia, thalamic

demyelinating disease

denervation of muscle

denervation potentials

dental prostheses

dentate nuclei, lesion of

dermatomyositis

descending paralysis

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetes mellitus

diarrhea, bloody

differential diagnosis

difficulty climbing stairs

diffuse idiopathic skeletal hyperostosis

digital subtraction angiography

digits, abnormal

diplegia, atonic

diplegia, brachial

disability rating scale, neurological

disability, neurological

dissociated sensory loss

distal muscle atrophy

distal muscle weakness

drop metastasis

drug abuse, inhalation

drug abuse, neurologic complications of

drug abuse, toxic screen In

drug induced neurologic disorders

dysarthria-clumsy hand syndrome

dystonia musculorum deformens

dystonia, cervical

dystrophic calcification

ears of the Lynx MR sign

electrical sensation

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

embolization, therapeutic

emergencies, neurologic

emergencies, neurosurgical

emotional lability

encephalitis, focal

encephalitis, human immunodeficiency virus type 1

encephalitis, recurrent

encephalitis, viral

encephalopathy, metabolic

endovascular therapy

enterovirus infection of CNS

enzyme, muscle disease

epicanthal folds

epidemiology of neurology

epileptic encephalopathy

episodic disorders

episodic neurologic deficits

Epstein-Barr virus

erectile dysfunction

erythema migrans

evoked potentials

exercise intolerance

exome sequencing

eye movement, disorders of

facial appearance, abnormal

facial nerve palsy

facial nerve palsy, bilateral

facial nerve palsy, recurrent

facial weakness

facial weakness, bilateral

failed medical management

failure to thrive

FARS2 deficiency

fatty acid, elevated plasma content

fine motor function, impaired

finger nose finger test

Fisher's syndrome

fistula, arterio-venous

fistula, arterio-venous, dural

fistula, arterio-venous, dural, spinal

flaccid paralysis

flail arm syndrome

flu-like illness

fluorescent treponema antibody absorption(FTA-ABS)

folic acid deficiency

foot drop, bilateral

frontal lobe, atrophy

frontotemporal dementia, behavioral variant

gag reflex, depressed

galactocerebrosidase

gamma amino butyric acid-mimetic drug

gammaglobulin therapy, intravenous

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)

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glutamic acid decarboxylase, antibody

gram negative rod

granulomatosis with polyangiitis

granulomatous disease

Guillain Barre syndrome

Guillain Barre syndrome, axonal form

Guillain Barre syndrome, complications

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, etiology of

Guillain Barre syndrome, infantile and childhood form

Guillain Barre syndrome, prognosis of

Guillain Barre syndrome, variant forms of

Hallervorden Spatz disease

hearing loss, bilateral

hearing loss, sudden, bilateral

hearing problems in children

heart block, complete

heat intolerance

hemangioma, vertebral

hematoma, epidural-spinal

hematopoietic tissue, extramedullary

hematuria, microscopic

hemoglobin abnormality, neurologic complications of

hemophagocytosis

hepatic encephalopathy

hepatic failure

hepatolenticular degeneration, non-Wilsonian

herniated disc, cervical

herniated disc, thoracic

herpes virus infection

high arched feet

highly active antiretroviral therapy

hip flexor weakness

Horner's syndrome

H-reflex testing

human diploid cell rabies vaccine

human herpesvirus 6

human immunodeficiency virus type 1

human immunodeficiency virus type 1, pathogenesis

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

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

hydrocephalus, congenital

hydrocephalus, fetal

hydrocephalus, intrauterine

hyperammonemic encephalopathy

hyperparathyroidism

hyperpigmentation of skin

hyperthyroidism

hypoglycorrhachia

hypokalemic periodic paralysis

hypomyelination

hypophosphatemia

hypopigmentation of skin

hypotension, systemic

hypothalamus, disturbance of

hypothermia, causes of

iatrogenic neurologic disorders

immunologic disease

immunology and the nervous system

immunosuppression

immunosuppressive agents

inability to stand on tiptoes

inborn errors of metabolism

inclusion bodies

inclusion bodies, intranuclear

incontinence, fecal

intellectual deficit

intellectual deficit, treatable causes of

intellectual deterioration

intelligence quotient

internal capsule

intracerebral hemorrhage

intrathecal antispasticity drugs

intrathecal chemotherapy

intrinsic hand muscles, wasting of

Jamaica ginger paralysis

jaw jerk, abnormal

Krabbe's disease

Kugelberg-Welander syndrome

kyphoscoliosis, neurologic causes of

lactic dehydrogenase(LDH)

laughing, pathologic

leg weakness, bilateral

leg weakness, unilateral

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

level of consciousness, decreased

Lhermitte's sign

lid closure, weakness of

life expectancy

limbic encephalitis

liver function enzymes

locked-in syndrome

lumbosacral radiculopathy

lymph node biopsy

lymphadenopathy

lymphadenopathy, axillary

lymphadenopathy, hilar

lymphocytic pneumonitis

lymphoma involving CNS

lymphoma, primary of CNS

lymphomatoid granulomatosis

malabsorption syndrome

malformation, vascular

malformation, vascular, dural

malformation, vascular, treatment of

Man-In-The-Barrel syndrome

Marburg's disease

mediastinum, mass of

medulla oblongata, lesion of

melanocytoma, meningeal

Melkersson's syndrome

memory, impairment of

meningeal biopsy

meningeal biopsy, false negative

meningeal enhancement

meningeal sarcomatosis

meningitis, aseptic

meningitis, brucellosis

meningitis, CSF cell count-normal

meningitis, lymphomatous

meningoencephalitis

meningomyelitis

meningovascular syphilis

mental retardation

mental status, abnormal

metabolic acidosis

metabolic disorder, primary

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

methylmalonic acidemia

methylmalonic aciduria

midbrain, lesion of

middle cerebellar peduncle

middle cerebellar peduncle, lesion, bilateral

mitochondrial disease

mitochondrial encephalomyopathy

mitochondrial recessive ataxic syndrome

molecular genetics

monoclonal gammopathy

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 weighted

MRI, disappearing lesion on

MRI, false negative

MRI, flow void, blood

MRI, high signal foci on

MRI, high signal intensity of basal ganglia

MRI, nodular enhancement

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRI, T1 weighted high signal foci

MRI, target sign

mucopolysaccharidoses

multiple sclerosis

multiple sclerosis, acute

multiple sclerosis, chronic progressive

multiple sclerosis, diagnosis of

multiple sclerosis, differential diagnosis of

multiple sclerosis, late-onset

multiple sclerosis, misdiagnosis

multiple sclerosis, prognosis

multiple sclerosis, spinal form

multiple sclerosis, treatment of

multiple system atrophy

muscle atrophy, progressive

muscle stiffness

muscle twitching

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

muscle weakness, sudden onset of

muscular dystrophy

muscular dystrophy, classification

muscular dystrophy, distal, Miyoshi

myasthenia gravis

myasthenia gravis, presenting manifestations

myasthenic syndrome

myelin basic protein

myelitis, longitudinal

myelitis, transverse

myelogram, thoracic

myeloneuropathy

myelopathy, ischemic

myelopathy, ascending

myelopathy, chronic progressive

myelopathy, hepatic

myelopathy, necrotizing

myelopathy, radiation induced

myelopathy, tract-specific

myelopathy, transverse

myelopathy, vacuolar

myelopathy, venous hypertensive

myeloradiculopathy

myoclonic jerks

myopathy, acute

myopathy, distal

myopathy, distal, vacuolar

myopathy, drug-induced

myopathy, inclusion body

myopathy, inclusion body, hereditary

myopathy, metabolic

myopathy, necrotizing

myopathy, toxic

myopathy, vacuolar

myositis, ocular

myotonic discharges

Native Americans

nausea and vomiting

neoplasm, primary of CNS

neoplastic angioendotheliosis

nerve conduction studies

nerve conduction studies, motor

nerve root biopsy

nerve root enhancement

nerve root hypertrophy

neuritis, causes of

neurocutaneous disease

neuroendocrinology

neurofibromatosis 1

neurogenic bladder

neuroichthyosis

neurologic complications of, surgery

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic examination

neurologic examination, focal

neurologic signs

neurolymphomatosis

neuromuscular disease, electrodiagnosis of

neuromuscular junction, abnormality of

neuronal ceroid-lipofuscinosis

neuropathology, brain

neuropathy, acute

neuropathy, amyloid

neuropathy, demyelinating

neuropathy, medication induced

neuropathy, motor

neuropathy, motor, multifocal

neuropathy, painful

neuropathy, peripheral

neuropathy, sensory

neuropathy, vasculitic, systemic

neuroradiology, interventional

next-generation sequencing

night blindness

numb clumsy hands syndrome

numbness, ascending

numbness, extremity

nutritional deficiency

nystagmus, dissociated

nystagmus, vertical

occupational neurologic disorders

oculodentodigital dysplasia

odontoid process

old age, neurology of

ophthalmoplegia

ophthalmoplegia, painful

ophthalmoplegia, progressive external

opportunistic infection

optic atrophy, hereditary

optic nerve, lesion of

optic neuropathy

oral ulcerations

orthostatic hypotension

owl's eye sign of spinal cord

pain, abdominal

pain, interscapular

pain, total body

palatal myoclonus

paralysis, acute

paralysis, acute areflexic

paraparesis, acute

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, familial spastic, variants

paraparesis, flaccid

paraparesis, painful

paraparesis, spastic

paraparesis, spastic, tropical

paraparesis, transient

paraplegia, acute

paraplegia, progressive

paraplegia, recurrent

paraspinal muscle

paraspinal muscle weakness

parathyroid adenoma

paresthesias, feet

paresthesias, generalized

paresthesias, hands

Parkinson disease

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

Pelizaeus Merzbacher

perineum, numbness of

periodic paralysis

periodic paralysis, thyrotoxic

peripheral blood smear, abnormal

pernicious anemia

peroneal nerve palsy

peroneal nerve, lesion of

peroxisomal disease

personality change

phenylketonuria

phenylketonuria, adult onset

physical activity

pleocytosis of cerebrospinal fluid

pleocytosis of cerebrospinal fluid, neutrophilic

poison, organophosphate

poliomyelitis-like illness

polycythemia, primary

polyglucosan body

polyglucosan body disease

polymerase chain reaction

polyneuropathy, chronic inflammatory demyelinating

pons, lesion of

portal caval shunt

positive sharp waves

posterior column disease

posterior longitudinal ligament, ossification of

precipitating factors

precocious puberty

prenatal diagnosis by amniocentesis

primary lateral sclerosis

prisoners of war, neurologic complications in

progressive multifocal leucoencephalopathy

progressive neurologic disorder

progressive spinal muscular atrophy

proprioception, abnormal

pseudobulbar palsy

pseudomonas aeruginosa

psychiatric problems in neurologic disorders

psychological testing

psychological testing, neurologic problems

psychomotor retardation

ptosis, bilateral

pulmonary infiltrates

pyramidal tract

pyramidal tract dysfunction

quadriparesis, acute

quadriparesis, progressive

quadriplegia, transient

quality of life

rabies, nervous system involvement with

radiation encephalopathy, delayed

radiation therapy, CNS treatment and complications with

rapidly progressing neurologic illness

Raynaud's phenomenon

rectal sphincter tone, decreased

reflex, brainstem

reflex, brainstem, absent

regional enteritis

release phenomena

remote effect of cancer on the nervous system

repetitive nerve stimulation

respiratory failure

respiratory tract infection

reticulum cell sarcoma

retinitis pigmentosa

reversible neurologic disorder

rheumatoid arthritis

rheumatoid arthritis, neurologic complications of

rickettsial organism

root lesion, nerve

Rosenthal fibers

rubella encephalitis, progressive

saccadic eye movements, abnormal

saddle anesthesia

sarcoidosis, CNS

Schilder's disease

Schmidt syndrome

sclerae, hyperpigmented

scleroderma, neurologic involvement with

sea-blue histiocytes

sedimentation rate, elevated

seizure, children

sensorineural hearing loss

serologic testing

serologic testing of cerebrospinal fluid

sickle cell disease

single photon emission computed tomography

single-fiber electromyography

Sjogren-Larsson syndrome

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skin, darkening of

skin, lesions in neurologic disorders

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 muscular atrophy

spinal stenosis

spinal stenosis, cervical canal

spinal xanthomatosis

spinocerebellar ataxia type 3/Machado Joseph disease

spirochete infection

spongy degeneration of brain

standing difficulty

stem cell transplantation

steroid therapy, CNS treatment and complications with

stiff man syndrome

strokelike episodes

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

subarachnoid hemorrhage

subcortical U fibers

substantia nigra

symmetric brain lesions

syphilis, diagnosis and treatment

syphilis, meningomyelitis

syphilis, neurologic complications with

systemic illness

teeth, abnormal

temporal lobe, atrophy

tendon, enlarged

tensilon test, false positive

testicular atrophy

thalamus, lesion of

thrombocytopenia

thrombophlebitis

thyroid function tests

tinnitus, pulsatile

tongue, atrophy

tongue, enlarged

tongue, fasciculations of

tongue, impaired movements of

tongue, weakness

toxins, nervous system

toxoplasmosis, CNS

transient ischemic attack

transposition of the great vessels

treatment of neurologic disorder

treatment, empirical

tremor, intention

tuberculoma of CNS

tuberculosis, spinal

tuberous sclerosis

ulcerative colitis

ulcers, fingertip

ultrasonography, spinal

upward deviation of eyes

urinary frequency

urinary incontinence

urinary retention

urinary urgency

urine test in toxic screen

valsalva maneuver

vascular endothelial growth factor

venous engorgement

vibratory sensation, abnormal

viral infection

viral infection, CNS

viral isolation

vision, blurred

visual acuity, decreased

visual evoked response

vitamin deficiency

vitamin supplementation

vitamin, multiple

walking, difficulty with

weakness, acute

weakness, episodic

weakness, generalized

weakness, progressive

weakness, proximal

weakness, rapidly progressive

Werdnig-Hoffman disease

Werner's syndrome

Western immunoblot test

white matter disease

whole body imaging

wide based gait

winging of scapula

xanthoma, tendon

x-linked hydrocephalus

Showing articles 1950 to 2000 of 2444 << Previous Next >>

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

Retinitis Pigmentosa
Surv Ophthalmol 33:137-177, Pagon,R.A., 1988

Serum Antibodies to GM1 Ganglioside in Amytrophic Lateral Sclerosis
Neurol 38:1457-1461, Pestronk,A.,et al, 1988

Emery-Dreifuss Muscular Dystrophy:Disease Spectrum and Differential Diagnosis
Neuropediatrics 19:62-71, Voit,T.,et al, 1988

Facioscapulohumeral Muscular Dystrophy, in Neuromuscular Disease
Springer-Verlag, NY, p289988., Swash,M.&Schwartz,M.S., 1988

Rapidly Progressive Dementia Caused by Spongiform Encephalopathy
West J Med 148:313-319, Enos,B.E.&Vinters,H.V., 1988

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

Paraneoplastic Syndromes Involving the Eyes
In Walsh & Hoyt's Clin Neuro-ophthal, 4th ed, Williams & Wilkins, Vol 3, p 1735-1746, Miller,N.R., 1988

Iodinated Contrast Agents in Myasthenia Gravis
Neurol 37:1400-1402, Frank,J.H.,et al, 1987

Carbon Monoxide Toxicity:MR Imaging in the Brain
Radiology 162:787-788, Horowitz,A.L.,et al, 1987

Life Spans of Duchenne Muscular Dystrophy Patients in the Hospital Care Program in Japan
J Neurol Sci 81:155-158, Mukoyama,M.,et al, 1987

Hysterical Paraplegia
JNNP 50:375-382, Baker,J.H.E.&Silver,J.R., 1987

Pretended Paralysis Requiring Artificial Ventilation
BMJ 294:961-962, Hopkins,A.&Clarke,C., 1987

Infarction of the Conus Medullaris
Ann Neurol 21:470-474, Anderson,N.E.,et al, 1987

Nontraumatic Spinal Epidural & Subdural Hematomas
Neurol 37:1351-1356, Mattle,H.,et al, 1987

Spinal Injuries & BMX Bicycles
BMJ 294:1259-1260, Johnson,S.R.&Rairclough,J.A., 1987

Progressive Supranuclear Palsy & a Multi-Infarct State
Neurol 37:570-576, Dubinsky,R.M.&Jankovic,J., 1987

Cervical Cord Compression Due to Extension of a Papillary Thyroid Carcinoma
Am J Med 82:156-158, Ginsberg,J.,et al, 1987

MR Imaging in a Case of Hallervorden-Spatz Disease
J Comput Assist Tomogr 11:1057-1058, Tanfani,G.,et al, 1987

Cyclophosphamide"Pulses"in Chronic Progressive Multiple Sclerosis, A Preliminary Clinical Trial
Arch Neurol 44:828-832, Myers,L.W.,et al, 1987

Cyclophosphamide in Chronic Progressive Multiple Sclerosis, Maintenance vs Nonmaintenance Therapy
Arch Neurol 44:823-827, Goodkin,D.E.,et al, 1987

The Neurologic Presentation of Vasculitic & Rheumatologic Syndromes, A Review
Medicine 66:157-180, Sigal,L.H., 1987

Neurologic Manifestations of AIDS
Medicine 66:407-437, McArthur,J.C., 1987

Neurologic Disease as the Presenting Manifestation of Acquired Immunodefieicney Syndrome
South Med J 80:683-686, Berger,J.R.,et al, 1987

Acute Paraparesis Secondary to Arnold-Chiari Type I Malformation & Neck Hyperflexion
Ann Neurol 21:100-101, Vlcek,B.W.&Ito,B., 1987

Disorders of the Autonomic Nervous System:Part 1. Pathophysiology & Clinical Features
Ann Neurol 21:419-430, McLeod,J.G.&Tuck,R.R., 1987

Progressive Aphasia without Dementia:Two Cases with Focal Spongiform Degeneration
Ann Neurol 22:527-532, Kirshner,H.S.,et al, 1987

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

Clinicopath Conference
Adenocarcinoma of Lung, with Metastases to Leptomeninges, Medulla Oblongata, Spinal Cord, & Liver, C, se 32-JM 317:366-375,1987., 1987

Aortic Dissection
NEJM 317:1060-1067, DeSanctis,R.W.,et al, 1987

Limb Dystonia in Progressive Supranuclear Palsy
Neurol 37:1546-1549, Rafal,R.D.&Friedman,J.H., 1987

Neurological Clues from Environmental Neurotoxins
BMJ 295:346-347, Martyn,C.N., 1987

Explanation & Management of Neurological Disability
BMJ 294:1203-1205, Critchley,E.M.R.&Mitchell,J.D., 1987

Progressive Multifocal Leukoencephalopathy Associated with Human Immunodeficiency Virus Infection
Ann Int Med 107:78-87, Berger,J.R., 1987

Chronic Muscle Weakness Caused by Borrelia Burgdorferi Meningoradiculitis
Ann Neurol 22:389-392, Wokke,J.H.J.,et al, 1987

Unusual Manifestations of Nervous System Borrelia Burgdorferi Infection
Arch Neurol 44:781-783, Midgard,R.&Hofstad,H., 1987

Prednisone Treatment in Duchenne Muscular Dystrophy, Long-Term Benefit
Arch Neurol 44:818-822, DeSilva,S.,et al, 1987

Practical Problems in the Respiratory Care of Patients with Muscular Dystrophy
NEJM 316:1197-1205, Smith,P.E.M.,et al, 1987

Frequency of Cerebral Infarction in Patients with Inherited Neuromuscular Disease
Stroke 18:805-807, Biller,J.,et al, 1987

MELAS Syndrome Involving a Mother & Two Children
Arch Neurol 44:971-973, Driscoll,P.F.,et al, 1987

Spectrum of Inclusion Body Myositis
Arch Neurol 44:1154-1157, Ringel,S.P.,et al, 1987

Current Status of Thyrotropin-Releasing Hormone Therapy in Amyotrophic Lateral Sclerosis
Comm. on Health Care Issues, Amer Neuro Assoc, Ann Neurol 22:541-54387., , 1987

A Rating Scale for Amyotrophic Lateral Sclerosis:Description & Preliminary Experience
Ann Neurol 22:328-333, Appel,V.,et al, 1987

Late Denervation in Patients with Antecedent Paralytic Poliomyelitis
NEJM 317:7-12, Cashman,N.R.,et al, 1987

Motor Neuron Disease in the US, 1971 & 1973-1978:Patterns of Mortality & Associated Conditions at Time of Death
Neurol 37:1339-1343, Leone,M.,et al, 1987

Clinincopath Conf
Progressive Muscular Atrophy & Diabetic Neuromuscular Disease, Case 21-1987, NEJM 316:1326-13357., , 1987

Computed Tomography Abnormalities in Hanging
Neuroradiology 29:297-298, Bianco,F.&Floris,R., 1987

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

Clinicopath Conf
Kearns-Sayre Syndrome (Oculocraniosomatic Neuromuscular Disease with Mitochondrial Myopathy) , Case, 4-1,NEJM 317:493-501,1987., 1987

Miliary Metastasis to the Brain:Clinical & Radiologic Features
Neurol 37:1817-1818, Floeter,M.K.,et al, 1987

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