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abdominal contractions

abducens nerve paralysis

acid maltase deficiency

acoustic neurinoma

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome, heralded by neurologic invol

ACTH, ectopic syndrome of

adult polyglucosan body disease

advance directives

advances in neurology

adverse drug reaction

Aicardi-Goutieres syndrome

alcohol intolerance

alcoholic polyneuropathy

alien hand syndrome

alkylating agents

alpha-fetoprotein

altered states of consciousness

alveolar hypoventilation

Alzheimer's disease

amphiphysin antibodies

amyloid angiopathy, cerebral

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, bulbar

amyotrophic lateral sclerosis, atypical

amyotrophic lateral sclerosis, childhood

amyotrophic lateral sclerosis, cluster

amyotrophic lateral sclerosis, complications with

amyotrophic lateral sclerosis, conjugal

amyotrophic lateral sclerosis, diagnosis of

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, epidemiology of

amyotrophic lateral sclerosis, etiology of

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, guamian type of

amyotrophic lateral sclerosis, hospitalization

amyotrophic lateral sclerosis, juvenile

amyotrophic lateral sclerosis, misdiagnosis

amyotrophic lateral sclerosis, myasthenic syndrome with

amyotrophic lateral sclerosis, Parkinson-dementia-complex

amyotrophic lateral sclerosis, post-encephalitic

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, sensory symptoms in

amyotrophic lateral sclerosis, treatment of

amyotrophic lateral sclerosis, work up

amyotrophic lateral sclerosis-like syndrome

aneurysm, cavernous sinus

aneurysm, internal carotid artery

angiography, cerebral, beaded vessels

angiography, cerebral, false negative

angiography, cerebral, negative

angiotensin-converting enzyme

animal exposure

ankylosing spondylitis

anterior horn cell disease

anterior interosseous neuropathy

anterior tibial muscle weakness

anti Hu antibody

antibodies to voltage-gated calcium channels

antiviral agents

aphasia, progressive, primary

apraxia of eye movements

aqueduct of Sylvius, obstruction

arrhythmia, cardiac

arthrogryposis multiplex

ataxia telangiectasia

ataxia, cerebellar

ataxia, sensory

ataxia, truncal

atlanto axial dislocation, congenital

atrioventricular block

autoimmune disease

autonomic dysfunction

autonomic neuropathy

B 12 deficiency

bacterial infection

Barkhof MR criteria for MS

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavioral disorder

Bence Jones protein

benign congenital hypotonia

biologic markers

bladder dysfunction

blood dyscrasias, neurologic findings with

bone marrow biopsy

Borrelia burgdorferi infection

botulinum toxin

botulinum toxin, complications of

brachial neuritis

brain biopsy, negative

brainstem, infarction of

brainstem, lesion of

bright tongue sign

Brown Sequard syndrome

Brueghel's syndrome

Brugada syndrome

bulbar palsy, acute

bulbar palsy, progressive

burning paresthesia

calcification, intracranial

calcium channel dysfunction

calf hypertrophy

carbon monoxide poisoning

carcinoembryonic antigen

carcinoma of breast

carcinoma of lung

carcinoma of ovary

cardiovascular disease

CAT scan, abnormal

CAT scan, disappearing lesion on

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, orbits

CAT scan, pelvis

CAT scan, serial

CAT scan, spine

cauda equina, lesion of

cavernous sinus

cavernous sinus, lesion of

cavernous sinus, syndrome

central core disease

central nervous system, infection of

central pontine myelinolysis

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar vermis

cerebellum, neoplasms of

cerebral cortex

cerebral cortical atrophy

cerebral embolism

cerebral peduncle

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, cell count

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, pressure low

cerebrospinal fluid, protein of

cerebrovascular accident

cerebrovascular accident, mimics

cerebrovascular accident, women

cerebrovascular accident, young adult

cervical myelopathy

cervical osteoarthritis

cervical osteophyte

cervical spine injury

cervical spine injury, treatment of

cervical spondylosis

cervical spondylosis, differential diagnosis of

cervical spondylosis, misdiagnosis

Charcot-Marie-Tooth

chemotherapy, CNS treatment and complications with

chest x-ray, abnormal

chewing, impaired

chilbran skin lesions

chorea, Sydenham's

choreoathetosis

chromosomal abnormality

chronic polyneuritis, children

chronic progressive external ophthalmoplegia

cigarette smoking

Clinical Pathologic Conference(C.P.C.)

cluster, geographic

collapsin response mediator protein 5 IgG

compression neuropathy

conduction block

congenital heart disease

congenital myopathy

congestive heart failure

contactin associated protein like 2 antibodies

contractures, joint

controversies in neurology

corpus callosum

corpus callosum, lesion of

corpus callosum, thinning

cortical-basal ganglionic degeneration

cost effectiveness

coxsackievirus, myopathy with

cranial nerve enlargement

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

crying, pathologic

cycad seed flour

cyclophosphamide

cyst, cortical parenchyma

cyst, parenchymal

cyst, ventricular

cysticercosis, cerebral

cysticercosis, intraventricular

cysticercosis, subarachnoid

deafness, bilateral

deafness, sudden

degenerative diseases of CNS

Dejerine-Sottas syndrome

delay in diagnosis

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

demyelinating disease

denervation of muscle

denervation potentials

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

dermatomyositis

developmental milestones

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetes insipidus

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diabetic mononeuropathy

diagnostic criteria

diaphragmatic paralysis

diaphragmatic paralysis, causes of

differential diagnosis

difficulty climbing stairs

diffuse idiopathic skeletal hyperostosis

diplegia, atonic

disability rating scale, neurological

disability, neurological

distal muscle atrophy

distal muscle weakness

down-beat nystagmus

down-beat nystagmus, primary position of gaze

dropped head syndrome

drug interactions

dysthyroid ocularmyopathy

dystonia, children

dystrophic calcification

ears of the Lynx MR sign

electrical injury of nervous system

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electromyogram, decremental response

electron microscopy

electrophoretic pattern, serum

emotional lability

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, paraneoplastic

encephalitis, recurrent

encephalomyelitis

encephalopathy, anoxic

encephalopathy, neonatal

encephalopathy, post anoxic

endocarditis, subacute bacterial

enterovirus infection of CNS

entrapment neuropathy

enzyme, muscle disease

epidemiology of neurology

episodic neurologic deficits

erythema migrans

ethics in neurology

evidence-based research

evoked potentials

exome sequencing

extraocular muscle enlargement

eye movement, disorders of

face, numbness of

facial nerve palsy

facial nerve palsy, bilateral

facial weakness, bilateral

facioscapulohumeral syndrome

failed medical management

fatigable chewing

Fazio-Londe's disease

feeding disorder

finger weakness

flail arm syndrome

football neurologic injuries

fourth ventricle, cyst

fragile-X syndrome

Friedreich's ataxia

frontal behavioral spatial syndrome

frontal lobe, atrophy

frontotemporal dementia, behavioral variant

fundus, abnormality of

funduscopic exam

gag reflex, depressed

gammaglobulin therapy, intravenous

gastrostomy, percutaneous endoscopic

gaze palsy, horizontal

gaze palsy, supranuclear

genetic counselling

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

girdle sensation

GM1 ganglioside antibodies

granulomatous disease

Graves ophthalmopathy

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Gulf War syndrome

handlebar palsy

headache, progressive

headache, severe

health insurance

hearing loss, bilateral

hearing loss, sudden, bilateral

heavy metal intoxication

helminthic infection of CNS

hemianopia, homonymous

hemiplegia, progressive

heralding manifestation

herpes simplex encephalitis

herpes simplex encephalitis, diagnosis of

highly active antiretroviral therapy

history of neurology

Hodgkin's disease

Hodgkin's disease, neurologic involvement with

human immunodeficiency virus type 1

Huntington's chorea

hydrocephalus, non-communicating(obstructive)

hydrocephalus, transient

hyperparathyroidism

hyperpyrexia, CNS disorder causing

hypersegmented polys

hyperthyroidism

hypertrophic intracranial pachymeningitis

hypoglycemic coma

hypoglycorrhachia

hypokalemic alkalosis

hypothalamus, disturbance of

hypotonia, infants

hypoxic encephalopathy

iatrogenic neurologic disorders

imbalance, postural

immune complexes

immunodeficiency

immunoelectrophoresis, serum

immunologic disease

immunology and the nervous system

immunosuppression

immunosuppressive agents

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

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, ubiquitin

inclusion body myositis

incontinence, fecal

infant, evaluation of

infantile tremor syndrome

intellectual deficit

interferon alpha

intermittent positive pressure breathing

internal capsule

intestinal pseudoobstruction

intracranial hypertension, benign

intracranial pressure, increased

intranasal medication

intrinsic hand muscles, wasting of

Isaacs syndrome

Jackson's syndrome

Jakob-Creutzfeldt disease

jaw closure weakness

jaw jerk, abnormal

Kearns-Sayre syndrome

klippel feil syndrome

Korsakoff's psychosis

Kugelberg-Welander syndrome

laminectomy, cervical

laughing, pathologic

lead and the nervous system

Leber's hereditary optic neuropathy

leg weakness, bilateral

leg weakness, unilateral

Leigh's disease

lenticular nucleus, lesion of, bilateral

leucine rich glioma inactivated 1 antibodies

leukemia, neurologic findings assoc.with

leukoencephalopathy

level of consciousness, decreased

Lewy body disease, diffuse

lid closure, weakness of

life expectancy

life support, withdrawal of

life support, withholding of

life sustaining treatment

limbic encephalitis

locked-in syndrome

lumbar puncture

lymphadenopathy

lymphadenopathy, hilar

lymphocytic meningoradiculitis

lymphoma involving CNS

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

malignancy screen

malignancy, occult

masseter muscle weakness

median neuropathy

medical-legal aspects of neurology

memory, defect of recent

memory, impairment of

meningeal enhancement

meningitis, aseptic

meningitis, basilar

meningitis, chronic

meningitis, cysticercosis

meningitis, eosinophilic

meningitis, fungal

meningitis, fungal-negative CSF culture

meningitis, leptospira

meningitis, recurrent

meningoencephalitis

meningoencephalopathy

meningomyelitis

mental retardation

mental status, abnormal

methylhydrazine derivatives

microangiopathy, brain

microangiopathy, retina

Millard Gubler syndrome

minimally conscious state

mitochondrial disease

mitochondrial encephalomyopathy

molecular genetics

monoamine oxidase inhibitors

monoclonal antibodies

monoclonal gammopathy

monoclonal gammopathy of uncertain significance

monomelic amyotrophy

mononeuritis multiplex

mononeuropathy multiplex

mononeuropathy, motor

Motor Band Sign

motor neuron disease

motor neuron disease, juvenile form

motor neuron disease, spontaneous recovery

movement disorder

movement disorder, extrapyramidal

MRI, contrast enhanced

MRI, cranial nerves

MRI, diffusion weighted

MRI, functional

MRI, gradient-echo

MRI, high signal foci on

MRI, paramagnetic effect

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRI, susceptibility weighted

multiple myeloma

multiple sclerosis

multiple sclerosis, diagnosis of

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple sclerosis, treatment of

multiple system atrophy

muscle atrophy, progressive

muscle atrophy, static

muscle diseases, characteristics of

muscle hypertrophy

muscle relaxant

muscle stiffness

muscle strength, testing

muscle tenderness

muscle twitching

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

muscle, metabolic disorders of

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, Becker, carrier

muscular dystrophy, cardiovascular changes with

muscular dystrophy, differential diagnosis of

muscular dystrophy, Duchenne

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

myasthenia gravis

myasthenia gravis, distal weakness

myasthenia gravis, drug induced

myasthenia gravis, limb-girdle

myasthenia gravis, paraneoplastic

myasthenia gravis, treatment of

myasthenic crisis

myasthenic syndrome

myelinolysis, extrapontine

myelitis, longitudinal

myelogram, cervical

myeloneuropathy

myelopathy, ischemic

myelopathy, carcinomatous

myelopathy, chronic progressive

myocardial infarction

myocardial injury

myoclonus, abdominal

myoclonus, segmental

myopathy, carcinomatous

myopathy, centronuclear

myopathy, distal

myopathy, mitochondrial

myopathy, proximal

myopathy, quadriceps

myopathy, thyroid disease causing

myotonia congenita

myotonia dystrophica

N-acetyl-L-aspartic acid

narcotic analgesics

nausea and vomiting

nemaline rod myopathy

nemaline rod myopathy, adult onset

neoplasm, hormone producing

neoplasm, hormone producing, ectopic

neoplasm, primary intracerebral

neoplasm, primary intracranial

neoplasm, primary of CNS

nerve conduction studies

nerve conduction studies, motor

nerve growth factor

nerve hypertrophy

nerve root enhancement

nerve root hypertrophy

neuritis, causes of

neurocutaneous disease

neuroendocrinology

neurofibrillary degeneration

neurogenic bladder

neurogenic vs.myopathic atrophy

neurologic complications

neurologic complications of, surgery

neurologic complications of, systemic cancer

neurologic consultation

neurologic disease

neurologic disease, diagnoses of

neurologic disease, incurable

neurologic disease, multifocal

neurologic disease, tempo

neurologic evaluation

neurologic examination

neurologic signs

neurologic symptoms

neuromuscular blockade

neuromuscular junction

neuromuscular junction, abnormality of

neuronal cell surface antigen

neuronal degeneration

neuronal migration disorder

neuronopathy, sensory

neuroophthalmology

neuropathology, brain

neuropathy, bicycle

neuropathy, diabetic

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, motor, multifocal

neuropathy, painful

neuropathy, paraneoplastic

neuropathy, peripheral

neuropathy, peripheral, treatment

neuropathy, sensory

neuropathy, vasculitic, systemic

neuroprotective agents

neurotransmitter

newborn, evaluation of

next-generation sequencing

nitrogen mustard

NMDA antagonists

nystagmus, primary position of gaze

nystagmus, rotary

occupational neurologic disorders

ocular motility, disorders of

old age, neurology of

olivary degeneration, hypertrophic

onconeural antibodies

Onufrowicz nucleus

ophthalmoplegia

ophthalmoplegia, painful

ophthalmoplegia, progressive external

Oppenheim muscular dystrophy

opsoclonus-myoclonus syndrome

optic disc edema

optic neuropathy

orbit, lesions of

orthostatic hypotension

osmotic demyelination syndrome

owl's eye sign of spinal cord

pain, abdominal

pain, management of chronic

palatal myoclonus

palliative care

paraneoplastic cerebellar degeneration

paraparesis, familial spastic

paraparesis, spastic

paraproteinemia

parasitic infection, CNS

paraspinal muscle

parathyroid adenoma

paresthesias, hands

Parkinson disease

Parkinson disease, L-dopa nonresponsive

Parkinson disease, motor neuron disease with

Parkinson disease, treatment of

Parkinsonism syndrome

Parkinsonism-dementia complex

patient information and support

periodic paralysis

periodic paralysis, thyrotoxic

peripheral nerve, lesion of

pernicious anemia

persistent vegetative state

personality change

phrenic nerve pacemaker

physical activity

physical therapy

physician assisted suicide

pigmentary retinopathy

plasma cell dyscrasia

pleocytosis of cerebrospinal fluid

pneumoencephalogram(PEG)

poison, mercury

poison, neurologic problems with

polyclonal gammopathy

polyglucosan body

polyglucosan body disease

polymerase chain reaction

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, chronic inflammatory demyelinating, variant form

polyneuropathy, chronic inflammatory demyelinating-pure motor syn

polyneuropathy, chronic inflammatory demyelinating-sens atax var

polyneuropathy, chronic inflammatory demyelinating-variant forms

positive sharp waves

post polio syndrome

posterior fossa, differential diagnosis of lesions of

posterior inferior cerebellar artery syndrome

posterior interosseous neuropathy

posterior longitudinal ligament, ossification of

practice guidelines

pregnancy, neurologic complications in

prevention of neurologic disorders

primary lateral sclerosis

progressive multifocal leucoencephalopathy

progressive muscular dystrophy

progressive neurologic disorder

progressive spinal muscular atrophy

progressive supranuclear palsy

proprioception, abnormal

proximal muscle atrophy

pseudobulbar palsy

pseudohypertrophy

psychiatric disorder

psychiatric problems in neurologic disorders

psychomotor retardation

ptosis, bilateral

pulmonary embolism

pulmonary function tests

pyramidal tract

pyramidal tract dysfunction

quadriceps atrophy

quadriceps weakness

quality of life

radiation hypersensitivity

radiation therapy, CNS treatment and complications with

radiation therapy, salivary gland

ragged-red fibers

Raynaud's phenomenon

release phenomena

remote effect of cancer on the nervous system

renal transplantation

repetitive nerve stimulation

respiratory depression

respiratory failure

retinal artery occlusion

retinal branch artery occlusion

retinal infarction

rheumatoid arthritis

risk-benefit assessment

saccadic eye movements, abnormal

salivation, excessive

sarcoidosis, CNS

scleroderma, neurologic involvement with

scoliosis, neurologic association with

seizure, children

seizure, treatment of

sensorineural hearing loss

sensory ganglia

sensory ganglia, abnormal

sensory loss, cutaneous

sensory symptoms

sensory testing

serologic testing

serologic testing of cerebrospinal fluid

serum alanine aminotransferase

shoulder, subluxation

shunt procedure, ventricular

single photon emission computed tomography

sinuses, diseases of

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skin, lesions in neurologic disorders

sleep pathology and physiology

Smell Identification Test

somatosensory evoked potentials

somatosensory evoked potentials, dermatomal

spastic paraplegia, type 11

spastic paraplegia, type 7

speech disorder

speech disorder, childhood

spinal cord degeneration

spinal cord, biopsy

spinal cord, cervical

spinal cord, compression of

spinal cord, enlargement

spinal cord, injury of

spinal cord, injury, management of

spinal cord, lesion of

spinal cord, neoplasm

spinal cord, neoplasm, extramedullary

spinal cord, neoplasm, intramedullary

spinal cord, pathologic exam of

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinal muscular atrophy, classification

spinal muscular atrophy, intermediate form

spinal stenosis

spinal stenosis, cervical canal

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar degeneration

spirochete infection

standing difficulty

startle reaction

status epilepticus

stem cell tourism

stem cell transplantation

sternocleidomastoid muscle

steroid therapy, CNS treatment and complications with

stiff man syndrome

strokelike episodes

subacute myelo-opticoneuropathy(S.M.O.N.)complex

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

subarachnoid hemorrhage

subdural hematoma

superoxide dismutase

suprasellar lesion

survival motor neuron gene

Susac's syndrome

tandem gait, ataxic

temporal lobe, atrophy

temporalis muscle wasting

tensilon test, false positive

testicular atrophy

thalamus, lesion of

thalamus, lesion of-bilateral

thoracic outlet syndromes

thrombocytopenia

thrombophlebitis

thyrotropin-releasing hormone

Tolosa Hunt syndrome

tongue, atrophy

tongue, enlarged

tongue, fasciculations of

tongue, weakness

travel, foreign

treatment of neurologic disorder

tremor, postural

triangle of Guillain and Mollaret

tricresylphosphate

trigeminal nerve

trigeminal nerve, hypertrophy

trinucleotide repeats

tumor necrosis factor inhibitor

ulcers, fingertip

ulnar nerve, deep palmar branch of

ulnar neuropathy

unconsciousness

upgaze, paralysis of

urinary incontinence

urinary urgency

venous thrombosis, non-cerebral

vertigo, positional

vibratory sensation, abnormal

vincristine neurotoxicity

viral infection

viral infection, CNS

visual acuity, decreased

vitamin deficiency

vocal cord paralysis

Waldenstrom's macroglobulinemia

walking, difficulty with

weakness, fatiguable

weakness, generalized

weakness, infant

weakness, progressive

weaning from respirator, failure to

Weber's syndrome

Werdnig-Hoffman disease

Whipple's disease

whistle, inability to

white matter disease

wide based gait

winging of scapula

X-linked bulbospinal neuronopathy

Showing articles 250 to 300 of 9573 << Previous Next >>

Amytrophic Lateral Sclerosis:Part 2, Etiopathogenesis
Ann Neurol 18:419-431, Tandan,R.,et al, 1985

Isolation of LAV/HTLV-III From a Patient with Amyotrophic Lateral Sclerosis
NEJM 313:324-325, Hoffman,P.M.,et al, 1985

ALS & Pet Exposure
Neurol 35:717-720, Tarras,S.,et al, 1985

Pathological Laughter & Crying
In Frederiks, J. A. M. (Ed) Handbook of Clinical Neurology, Elsevier Science Publ, 45:219, Poeck,K., 1985

Cysticercosis-Review of 230 Patients
Bull Clin Neurosci 50:76-101, McCormick.G.F., 1985

Amyotrophic Lateral Sclerosis:A Double-Blind Crossover Trial of Thyrotropin-Releasing Hormone
JNNP 47:1332-1334, Imoto,K.,et al, 1984

Nystagmus in Motor Neuron Disease:Clinicopathological Study of Two Cases
Ann Neurol 16:71-77, Kushner,M.J.,et al, 1984

Inhibition of Terminal Axonal Sprouting by Serum From Patients with Amyotrophic Lateral Sclerosis
NEJM 311:933-939, Gurney,M.E.,et al, 1984

Familial Occurrence of Amyotrophic Lateral Sclerosis, Parkinsonism, & Dementia
Ann Neurol 16:642-648, Schmitt,H.P.,et al, 1984

Benign Focal Amyotrophy
Arch Neurol 41:678-679, Riggs,J.E.,et al, 1984

Conjugal Amyotrophic Lateral Sclerosis
Ann Neurol 14:699, Paolino,E.,et al, 1983

Oligoclonal IgG Bands in Cerebrospinal Fluid in Various Neurological Diseases
Ann Neurol 13:434-439, Chu,A.B.,et al, 1983

Amyotrophic Lateral Sclerosis & Pet Exposure
NEJM 309:244-245, Schenkman,M.,et al, 1983

Acute Respiratory Failure in Motor Neuron Disease
Arch Neurol 40:30-32, Hill,R.,et al, 1983

Effect on Weakness & Spasticity in Amyotrophic Lateral Sclerosis of Thyrotropin-Releasing Hormone
Lancet 2:73-75, Engel,W.K.,et al, 1983

Syndromes of Amytrophic Lateral Sclerosis & Dementia:Relation to Transmissible Creutzfeldt-Jakob Disease
Ann Neurol 14:17-26, Salazar,A.M.,et al, 1983

Enigmatic Dyspnoea:An Unusual Presentation of Motor-Neuron Disease
Lancet 1:933-935, Nightingale,S.,et al, 1982

Long-Term Management of Respiratory Failure in Amyotrophic Lateral Sclerosis
Ann Neurol 12:18-23, Sivak,E.,et al, 1982

Benign Familial Spinal Muscular Atrophy With Hypertrophy of the Calves
Arch Neurol 39:657-660, D'Alessandro,R.,et al, 1982

Amyotrophic Lateral Sclerosis & Paraproteinemia
Neurol 32:896-898, Krieger,C.,et al, 1982

Classic Amyotrophic Lateral Sclerosis With Dementia
Arch Neurol 39:681-683, Wilkstrom,J.,et al, 1982

Nonfamilial Amyotrophy with Dementia, etc
Advances in Neurology, Human Motor Neuron Diseases, Ed. Rowland, Raven Press, NY 1982 vol 36, p 173., Tyler,H.R., 1982

Circulating Immune Complexes in Neurologic Disease
Neurol 31:1402-1407, Noronha,A.B.C.,et al, 1981

Amyotrophic Lateral Sclerosis & its Association with Dementia, Parkinsonism & Other Neurological Disorders:A Review
Brain 104:217-247, Hudson,A.J., 1981

Motor Neuron Disease:Decremental Responses to Repetitive Nerve Stimulation
Neurol 31:202-204, Bernstein,L.P.,et al, 1981

Management of Hypoventilation in Motor Neuron Disease Presenting with Respiratory Insufficiency
Ann Neurol 7:188-191, Sivak,E.D.,et al, 1980

Use of the ECG in the Diagnosis of Childhood Spinal Muscular Atrophy
Arch Neurol 36:317-318, Russman,B.S.,et al, 1979

Spirometry in Amyotrophic Lateral Sclerosis
Arch Neurol 36:74-80, Fallat,R.J.,et al, 1979

Age & Cerebrospinal-Fluid Protein in Motor-Neuron Disease
NEJM 300:437-438, Guiloff,R.J.,et al, 1979

Double-Blind Study of Modified Neurotoxin in Motor Neuron Disease
Neurol 29:77-81, Tyler,H.R., 1979

Presenile Dementia With Motor Neuron Disease in Japan, A New Entity
Arch Neurol 36:592-593, Mitsuyama,Y.,et al, 1979

Amyotrophic Lateral Sclerosis With Ophthalmoplegia; A Cliniocopathologic Study
Arch Neurol 36:615-617, Harvey,D.G.,et al, 1979

Clinical Pathological Conference
Amyotrophic Lateral Sclerosis, Case Record 46-1979, NEJM 301:1104-1111979., , 1979

Autosomal Dominant System Degeneration in Portugese Families of the Azores Islands
Neurol 28:703, Coutinho,P.,et al, 1978

Diaphragmatic Paralysis in Motor Neuron Disease
Neurol 28:18, Parhad,I.M.,et al, 1978

Free Amino Acid Levels in Amyotrophic Lateral Sclerosis
Ann Neurol 3:305, Patten,B.M.,et al, 1978

Distal Chronic Spinal Muscular Atrophy Involving the Hands
JNNP 41:653-658, O'Sullivan,D.J.,et al, 1978

Amyotrophic Lateral Sclerosis
Arch Neurol 35:638-642, Rosen,A.D., 1978

Cellular Immunity In Guamanians with Amyotrophic Lateral Sclerosis & Parkinsonism-Dementia
NEJM 299:680-685, Hoffman,P.M.,et al, 1978

Sparing of the Onufrowicz Nucleus in Sacral Anterior Horn Lesions
Ann Neurol 4:245-249, Iwata,M.,et al, 1978

Viruslike Particles in Amytrophic Lateral Sclerosis:Electron Microscopical Study of a Case
Ann Neurol 1:290, Pena,C.E., 1977

Chronic Neurogenic Quadriceps Amyotrophy
Ann Neurol 2:528, Furukawa,T.,et al, 1977

Control of Emotional Expression in Pseudobulbar Palsy
Arch Neurol 34:717, Lieberman,A.,et al, 1977

Antibody Titers to Coxsackieviruses in Amyotrophic Lateral Sclerosis
NEJM 295:107, Cremer,N.E.,et al, 1976

Frequency of Nerve Fiber Degeneration of Peripheral Motor & Sensory Neurons in Amyotrophic Lateral Sclerosis
Neurol 25:781, Dyck,P.J.,et al, 1975

Mononeuropathy of the Deep Palmar Branch of the Ulnar Nerve in a Diabetic
Arch Neurol 32:564, Finelli,P.F., 1975

Quadriceps Myopathy-Entity or Syndrome
Arch Neurol 31:60, Boddie,H.,et al, 1974

Neurotoxicity of Commonly Used Antineoplastic Agents
NEJM 291:75, 1271974., Weiss,H.,et al, 1974

Neuromuscular Disease in Primary Hyperparathyroidism
Ann Int Med 80:182, Patten,B.M.,et al, 1974

Epidemiology of Motor-Neuron Diseases
NEJM 288:1047, Bobwick,A.R.,et al, 1973

Showing articles 250 to 300 of 9573 << Previous Next >>