Neudle.com: paraplegia progressive

Differential
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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

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

adult polyglucosan body disease

advances in neurology

adverse drug reaction

alcohol, neurologic complications with

alcoholism

Alexanders disease

Alexanders disease, adult onset

amphiphysin antibodies

amyloidosis

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

ANA

anemia

anemia, megaloblastic

anesthesia, general

angiitis

angiitis, granulomatous of CNS

angiitis, isolated of CNS

angiography, cerebral

angiography, neurologic complications with

angiography, spinal

ankle edema

ankle reflex, absent

ankylosing spondylitis

anterior horn cell disease

anterior spinal artery

anterior spinal artery infarction

antibiotics

anticoagulant, complications of

anticoagulant, treatment

anticonvulsants

anticonvulsants, untoward effects of

antiganglioside antibodies

antineutrophil cytoplasmic autoantibodies

arteriovenous malformation

asterixis, unilateral

asthma

asthma, poliomyelitis-like syndrome with

atherosclerosis, premature

atlanto-axial subluxation

atrial fibrillation

atrioventricular block

auditory evoked brainstem potentials

autoantibodies

autoimmune disease

autonomic dysfunction

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

bacterial infection, CNS

Barkhof MR criteria for MS

basal ganglia

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavioral disorder

behavioral disorder, acute

blood dyscrasias, neurologic findings with

blood transfusion

bone marrow transplantation

botulism

bowel urgency

brachial amyotrophic diplegia

brachial plexus neuropathy

bradyphrenia

brain atrophy

brain biopsy

brain biopsy, stereotaxic

brainstem, atrophy

brainstem, dysfunction

brainstem, lesion of

breast feeding

Brown Sequard syndrome

brucellosis

brucellosis, nervous system involvement with

bulbar palsy, progressive

C9orf72

camptocormia

campylobacter infection

cancer, unknown origin

carcinoma of unknown origin

carnitine deficiency myopathy

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

cataracts

cauda equina

cauda equina, enhancement

cauda equina, lesion of

caudate nucleus, lesion of

cavernous hemangioma

CD4 counts

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 edema

cerebral palsy

cerebral palsy, associated problems with

cerebral peduncle

cerebral venous thrombosis

cerebritis

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

cervical spine cyst

cervical spine injury, compression

cervical spondylosis

channelopathy

Charcot-Marie-Tooth

chemotherapy, CNS treatment and complications with

chenodeoxycholic acid

children

Chinese paralytic syndrome

cholestanol

choreoathetosis

chromosomal abnormality

chronic progressive external ophthalmoplegia

cirrhosis

Clinical Pathologic Conference(C.P.C.)

clostridium perfringens

clubfoot as related to neurologic disease

cognition

coinfection

colchicine

color vision, impaired

conus medullaris, lesion of

copper deficiency

cornea, opacity of

corpus callosum

corpus callosum, atrophy of

corpus callosum, thinning

cranial neuropathy, multiple

cranio-cervical junction

creatine phosphokinase isoenzyme elevation

creatine phosphokinase(CPK)elevated

crossed adductor reflex

crying, pathologic

cryptococcal meningitis

cultured skin fibroblasts

cytomegalovirus infection

DARS

deafness

deafness, bilateral progressive vs.unilateral acute

deafness, unilateral

decerebrate posture

decompressive spinal cord surgery

deep gray nuclei

deep tendon reflexes

degenerative diseases of CNS

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

developmental milestones, loss of

developmental retardation

differential diagnosis

difficulty climbing stairs

diffuse idiopathic skeletal hyperostosis

digital subtraction angiography

disability rating scale, neurological

disability, neurological

dissociated sensory loss

distal muscle atrophy

distal muscle weakness

drug abuse, inhalation

drug abuse, neurologic complications of

drug abuse, toxic screen In

drug induced neurologic disorders

drug overdose

dysarthria

dysarthria-clumsy hand syndrome

dystonia musculorum deformens

dystonia, cervical

dystrophic calcification

ears of the Lynx MR sign

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

electromyogram

ELISA

embolization, therapeutic

emergencies, neurologic

emergencies, neurosurgical

encephalitis, human immunodeficiency virus type 1

encephalitis, recurrent

encephalitis, viral

encephalopathy

encephalopathy, metabolic

endemic area

endovascular therapy

enterovirus

enterovirus infection of CNS

enzyme, defect

enzyme, muscle disease

enzyme, serum

epicanthal folds

epidemiology of neurology

epileptic encephalopathy

episodic disorders

episodic neurologic deficits

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

fatty acid, elevated plasma content

fetus

fever

fibrillations

fine motor function, impaired

finger nose finger test

Fisher's syndrome

fistula, arterio-venous

fistula, arterio-venous, dural

fistula, arterio-venous, dural, spinal

fluorescent treponema antibody absorption(FTA-ABS)

fluorosis

folic acid deficiency

frontal lobe, atrophy

frontotemporal dementia, behavioral variant

gadolinium

gag reflex, depressed

gait disorder

gait, spastic

galactocerebrosidase

gamma amino butyric acid-mimetic drug

gammaglobulin therapy, intravenous

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

Gerstmann-Straussler-Scheinker disease

girdle sensation

glioblastoma multiforme(astrocytoma Gr.III)

glioma

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glutamic acid decarboxylase, antibody

glutamine

gout

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

heart block, complete

heat intolerance

hemangioma

hemangioma, vertebral

hematoma, epidural-spinal

hematopoietic tissue, extramedullary

hematuria, microscopic

hemianopia

hemiparesis

hemoglobin abnormality, neurologic complications of

hemophagocytosis

hepatic encephalopathy

hepatic failure

hepatitis

hepatolenticular degeneration, non-Wilsonian

herniated disc

herniated disc, cervical

herniated disc, thoracic

herpes virus

herpes virus infection

high arched feet

highly active antiretroviral therapy

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

hydrocephalus, congenital

hydrocephalus, fetal

hydrocephalus, intrauterine

hydrophobia

hyperammonemic encephalopathy

hypercalcemia

hypercapnia

hyperparathyroidism

hyperpigmentation of skin

hypokalemic periodic paralysis

hypomyelination

hypophosphatemia

hypopigmentation of skin

hyporeflexia

hypotension, systemic

hypothalamus, disturbance of

hypothermia

hypothermia, causes of

hypothyroidism

hypotonia

hypoxia

iatrogenic neurologic disorders

imbalance

immunologic disease

immunology and the nervous system

immunosuppression

immunosuppressive agents

immunotherapy

impotence

impulsivity

inability to stand on tiptoes

inborn errors of metabolism

inclusion bodies

inclusion bodies, intranuclear

intellectual deficit, treatable causes of

intellectual deterioration

intelligence quotient

internal capsule

intracerebral hemorrhage

intrathecal antispasticity drugs

intrathecal chemotherapy

intrinsic hand muscles, wasting of

iron, brain

Jamaica ginger paralysis

Kugelberg-Welander syndrome

kyphoscoliosis, neurologic causes of

lactate

lactic dehydrogenase(LDH)

lathyrism

laughing, pathologic

leg numbness

leg weakness, bilateral

leg weakness, unilateral

Leigh's disease

Leigh's disease, adult variety

lenticular nucleus, lesion of, bilateral

lethargy

leukemia

leukemia, neurologic findings assoc.with

leukocyte enzyme abnormality

leukocytosis

leukodystrophy

leukoencephalopathy

leukoencephalopathy, differential diagnosis

leukopenia

level of consciousness, decreased

Lhermitte's sign

lid closure, weakness of

life expectancy

limbic encephalitis

liver disease

liver function enzymes

lumbosacral radiculopathy

Lyme disease

lymph node biopsy

lymphadenopathy

lymphadenopathy, axillary

lymphadenopathy, hilar

lymphocytic pneumonitis

lymphoma

lymphoma involving CNS

lymphoma, primary of CNS

lymphomatoid granulomatosis

Madonna facies

Maghreb

malabsorption

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, 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

methotrexate

methyl benzene

methylmalonic acidemia

methylmalonic aciduria

microcephaly

microdontia

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

mononeuropathy multiplex

movement disorder, extrapyramidal

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, emergent

MRI, false negative

MRI, flow void, blood

MRI, high signal foci on

MRI, high signal intensity of basal ganglia

MRI, negative

MRI, nodular enhancement

MRI, ring sign

MRI, serial

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRI, spine

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 wasting, diffuse

muscle weakness

muscle weakness, proximal

muscle weakness, sudden onset of

muscular dystrophy

muscular dystrophy, classification

muscular dystrophy, distal, Miyoshi

mutism

myasthenia gravis

myasthenia gravis, presenting manifestations

myasthenic syndrome

myelin basic protein

myelitis

myelitis, longitudinal

myelopathy, ascending

myelopathy, chronic progressive

myelopathy, hepatic

myelopathy, necrotizing

myelopathy, radiation induced

myelopathy, tract-specific

myelopathy, transverse

myelopathy, vacuolar

myelopathy, venous hypertensive

myopathy, distal, vacuolar

myopathy, drug-induced

myopathy, inclusion body

myopathy, inclusion body, hereditary

myopathy, metabolic

myopathy, necrotizing

neoplasm, primary of CNS

neoplastic angioendotheliosis

nerve biopsy

nerve conduction studies

nerve conduction studies, motor

nerve culture

nerve root biopsy

nerve root enhancement

nerve root hypertrophy

neuritis, causes of

neurocutaneous disease

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

neuropathology, brain

neuropathy

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

neurosyphilis

neurotoxic

neurotoxin

next-generation sequencing

night blindness

nitrous oxide

numb clumsy hands syndrome

numbness, ascending

numbness, extremity

nutritional deficiency

nystagmus

nystagmus, dissociated

nystagmus, vertical

occupational neurologic disorders

ochronosis

oculodentodigital dysplasia

odontoid process

odynophagia

old age, neurology of

ophthalmoplegia

ophthalmoplegia, painful

ophthalmoplegia, progressive external

opiate

opportunistic infection

optic ataxia

optic atrophy

optic atrophy, hereditary

optic chiasm

optic nerve, lesion of

orthostatic hypotension

owl's eye sign of spinal cord

paralysis, acute areflexic

paraparesis

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

paraplegia, acute

paraplegia, progressive

paraplegia, recurrent

paraplegin

paraspinal muscle

paraspinal muscle weakness

paresthesias, generalized

paresthesias, hands

Parkinson disease

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

perineum, numbness of

periodic paralysis

periodic paralysis, thyrotoxic

peripheral blood smear, abnormal

pernicious anemia

peroneal nerve palsy

peroneal nerve, lesion of

phenylketonuria, adult onset

pleocytosis of cerebrospinal fluid

pleocytosis of cerebrospinal fluid, neutrophilic

POEMS syndrome

poison, organophosphate

poliomyelitis

poliomyelitis-like illness

polycythemia, primary

polyglucosan body

polyglucosan body disease

polymerase chain reaction

polymyositis

polyneuropathy

polyneuropathy, chronic inflammatory demyelinating

pons, lesion of

portal caval shunt

positive sharp waves

posterior column disease

posterior longitudinal ligament, ossification of

potassium

precipitating factors

precocious puberty

prenatal diagnosis by amniocentesis

primary lateral sclerosis

prion disease

prisoners of war, neurologic complications in

progeria

prognosis

progressive multifocal leucoencephalopathy

progressive neurologic disorder

progressive spinal muscular atrophy

proprioception, abnormal

proteinuria

pruritus

pseudobulbar palsy

pseudomonas aeruginosa

pseudomyotonia

psychiatric problems in neurologic disorders

psychological testing

psychological testing, neurologic problems

psychomotor retardation

psychosis

ptosis

ptosis, bilateral

pulmonary infiltrates

pyramidal

pyramidal tract

pyramidal tract dysfunction

Q fever

quadriparesis

quadriparesis, acute

quadriparesis, progressive

quadriplegia

quadriplegia, transient

quality of life

rabies, nervous system involvement with

radiation encephalopathy, delayed

radiation therapy, CNS treatment and complications with

radicular pain

radiculopathy

Rankin score

rapidly progressing neurologic illness

rash

Raynaud's phenomenon

rectal sphincter tone, decreased

recurrent

reflex, brainstem

reflex, brainstem, absent

regional enteritis

release phenomena

remote effect of cancer on the nervous system

renal failure

renal stones

repetitive nerve stimulation

respirator

respiratory failure

respiratory tract infection

reticulum cell sarcoma

retinitis pigmentosa

retrovirus

reversible neurologic disorder

review article

rhabdomyolysis

rheumatoid arthritis

rheumatoid arthritis, neurologic complications of

rubella encephalitis, progressive

saccadic eye movements, abnormal

sclerae, hyperpigmented

scleroderma

scleroderma, neurologic involvement with

screening

scurvy

sea-blue histiocytes

sedimentation rate, elevated

seizure

seizure, children

sensorineural hearing loss

sensory level

sensory loss

serologic testing

serologic testing of cerebrospinal fluid

single photon emission computed tomography

single-fiber electromyography

Sjogren-Larsson syndrome

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skin, biopsy

skin, darkening of

skin, lesions in neurologic disorders

somatosensory evoked potentials

spartin

spastic ataxia

spastic diplegia

spastic paraplegia, type 11

spastic paraplegia, type 15

spastic paraplegia, type 7

spasticity

spasticity, treatment of

spastin

speech disorder

speech disorder, childhood

speech, loss of

spinal cord

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

spongy degeneration of brain

standing difficulty

statin therapy

stem cell transplantation

steppage gait

steroid

steroid therapy, CNS treatment and complications with

stiff legs

stiff man syndrome

strokelike episodes

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

subarachnoid hemorrhage

subcortical U fibers

substantia nigra

sweating

symmetric brain lesions

syndactyly

syphilis, diagnosis and treatment

syphilis, meningomyelitis

syphilis, neurologic complications with

systemic illness

tachycardia

teeth, abnormal

temporal lobe, atrophy

tendon, enlarged

tensilon test, false positive

thyroid function tests

tongue, fasciculations of

tongue, impaired movements of

tongue, weakness

tooth loss

toxins, nervous system

toxoplasmosis, CNS

transient ischemic attack

transposition of the great vessels

trauma

treatment of neurologic disorder

ultrasonography, spinal

upward deviation of eyes

urine test in toxic screen

urine, dark

vaccine

valsalva maneuver

vascular endothelial growth factor

vasculitides

venous engorgement

vertigo

vibratory sensation, abnormal

visual acuity, decreased

visual evoked response

visual loss

vitamin deficiency

vitamin supplementation

vitamin, multiple

walking frame

walking, difficulty with

weakness, generalized

weakness, progressive

weakness, proximal

weakness, rapidly progressive

weight loss

Werdnig-Hoffman disease

Werner's syndrome

West disease

Western immunoblot test

x-linked hydrocephalus

x-ray, spine

zinc

Showing articles 1650 to 1700 of 2444 << Previous Next >>

Mosaic Express of Dystrophin in Carriers of Becker's Muscular Dyst & X-Linked Synd of Myalgia & Cramps
NEJM 327:1100, Minetti,C.&Bonilla,E., 1992

Upper Gastrointestinal Tract Motility in Children with Progressive Muscular Dystrophy
J Pediatr 121:720-724, Staiano,A.,et al, 1992

Lupus-Related Myelopathy:Report of Three Cases and Review of the Literature
JNNP 55:830-835, Provenzale,J.&Bouldin,T.W., 1992

Neurologic Manifestations of Progressive Systemic Sclerosis
Arch Neurol 49:1292-1295, Averbuch-Heller,L.,et al, 1992

Prolonged Weakness after Long-Term Infusion of Vecuronium Bromide
Ann Int Med 117:484-486, Kupfer,Y.,et al, 1992

The Role of Transeophageal Echocardiography in the Acute Onset of Paraplegia
Stroke 23:1660-1661, Walsh,D.V.,et al, 1992

Back Pain and Paraplegia in a Fifteen-Year-Old Boy
J Pediatr 121:652-658, Malik,R.K.,et al, 1992

Decreased Glutamate Transport by the Brain and Spinal Cord in Amyotrophic Lateral Sclerosis
NEJM 326:1464-1468, 14931992., Rothstein,J.D.,et al, 1992

Intrafamilial Heterogeneity in Hereditary Motor Neuron Disease
Neurol 42:1488-1492, Applebaum,J.S.,et al, 1992

Amyotrophic Lateral Sclerosis and Lymphoma:Bone Marroe Examination and Other Diagnostic Tests
Neurol 42:1101-1102, Rowland,L.P.,et al, 1992

Werdnig-Hoffman Disease & Chronic Distal Spinal Muscular Atrophy with Apparent Autosomal Dom Inherit
Ann Neurol 32:404-407, Boylan,K.B.&Cornblath,D.R., 1992

Aluminium Intoxication in Undialysed Adults with Chronic Renal Failure
JNNP 55:697-700, Russo,L.S.,et al, 1992

Delayed Encephalopathy after Acute Carbon Monoxide Intoxication:MR Imaging Features & Cerebral White Matter Lesions
Radiology 184:117-122, Chang,K.H.,et al, 1992

Anti-Hu-Associated Pareneoplastic Encephalomyelitis/Sensory Neuronopathy
Medicine 71:59-72, Dalmau,J.,et al, 1992

Leksell's Posteroventral Pallidotomy in the Treatment of Parkinson's Disease
J Neurosurg 76:53-61, Laitinen,L.V.,et al, 1992

Subacute Idiopathic Demyelinating Polyradiculoneuropathy
Arch Neurol 49:612-616, Hughes,R.,et al, 1992

Thoracic Aortic Aneurysm Presenting as Paraparesis:A Case Report
Neurol 42:1419-1421, Fong,K.Y.,et al, 1992

Spinal Cord Toxoplasma Lesion in AIDS:MR Findings
J Comput Assist Tomogr 16:817-819, Poon,T.P.,et al, 1992

Spinal epidural Abscess, Early Detection with Gadolinium Magnetic Resonance Imaging
Arch Neurol 49:743-746, Teman,A.J., 1992

The Role of Stereotactic Biopsy in the Management of HIV-Related Focal Brain lesions
Neurosurgery 30:825-829, Chappell,E.T.,et al, 1992

Progressive Language Disorder Due to Lobar Atrophy
Ann Neurol 31:174-183, Snowden,J.S.,et al, 1992

Nicotine-Sensitive Paresis
Neurol 42:382-388, Yokota,T.,et al, 1992

Polymyalgia Rheumatica and Mitochondrial Myopathy:Clinicopathologic and Biochemical Studies in Five Cases
Am J Med 92:167-172, Harle,J.,et al, 1992

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

GM-1 Ganglioside for Spinal-Cord Injury
NEJM 326:493, Schonhofer,P.S., 1992

Cardioskeletal Mitochondrial Myopathy Associated with Chronic Magnesium Deficiency
Neurol 42:128-130, Riggs,J.E.,et al, 1992

Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes (MELAS) :Clin Features & DNA Mutation
Neurol 42:545-550, Goto,Y.,et al, 1992

The Neuropsychological Features of Mitochondrial Myopathies and Encephalomyopathies
Arch Neurol 49:158-160, Kartsounis,L.D.,et al, 1992

Motor Neurone Disease
BMJ 304:459-460, Norris,F.H., 1992

Motor Neurone Disease:A Hospice Perspective
BMJ 304:471-473, O'Brien,T.,et al, 1992

Physical Manoeuvres for Combating Orthostatis Dizziness in Autonomic Failure
Lancet 339:897-898, VanLieshout,J.J.,et al, 1992

Adult-Onset Metachromatic Leukodystrophy Presenting as Isolated Peripheral Neuropathy
Neurol 42:1396-1398, Fressinaud,C.,et al, 1992

Occult Epidural Chloroma Complicated by Acute Paraplegia Following Lumbar Puncture
Ann Neurol 31:110-112, Wong,M.C.,et al, 1992

Risk Factors for the Neurologic Complications Associated with Aortic Aneurysms
Arch Neurol 49:284-285, Lynch,D.R.,et al, 1992

Surgical Treatment of Cervical Spondylotic Myelopathy:Time for a Controlled Trial
Neurol 42:5-13, Rowland,L.P., 1992

ELISA Quantitation of Dystrophin for the Diagnosis of Duchenne and Becker Muscular Dystrophies
Neurol 42:570-576, Byers,T.J.,et al, 1992

The Heart in Myotonic Dystrophy
Editorial, Lancet 339:528-5291992., , 1992

Striatal D2 Receptor Status in Patients with Parkinson's Disease, Striatonigral Degeneration, and PSP, (PET)
Ann Neurol 31:184-192, Brooks,D.J.,et al, 1992

Multifocal Demyelinating Motor Neuropathy:Cranial Nerve Involvement and Immunoglobulin Therapy
Neurol 42:506-509, Kaji,R.,et al, 1992

Multifocal Motor Neuropathy with Conduction Block:Is It a Distinct Clinical Entity?
Neurol 42:497-505, Lange,D.J.,et al, 1992

Subacute Necrotizing Myelopathy:MR Imaging in Four Pathologically Proved Cases
AJR 158:163-169, 1701992., Mirich,D.R.,et al, 1992

Dystrophinopathy in Isolated Cases of Myopathy in Females
Neurol 42:967-975, Hoffman,E.P.,et al, 1992

Diagnosis of Duchenne & Becker Muscular Dystrophies by Polymerase Chain Reaction
Multicenter Study Group, JAMA 267:2609-26151992., , 1992

Familial Inclusion Body Myositis:Evidence for Autosomal Dominant Inheritance
Neurol 42:897-902, Nevile,H.E.,et al, 1992

Clinicopath Conf
Emery-Dreifus Muscular Dystrophy, NEJM 327:548-5571992., , 1992

Detection of JC Virus DNA in Peripherl Lymphocytes from PTs with & Without Progressive Multifocal Leukoencephalopathy
Ann Neurol 31:454-462, Tornatore,C.,et al, 1992

The Guillain-Barre Syndrome
NEJM 326:1130-1136, Ropper,A.H., 1992

Schistosomal Granuloma of the Spinal Cord:Evaluation with MR Imaging & Intraoperative Sonography
AJR 158:1351-1353, Silbergleit,R.&Silbergleit,R., 1992

Generalized Myositis in Behcet Disease:TReatment with Cyclosporine
Ann Int Med 116:651-653, Lingenfelser,T.,et al, 1992

Clinicopath Conf
Churg-Strauss Syndrome, Case 18-1992, NEJM 326:1204-1212992., , 1992

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