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acid maltase deficiency

acoustic neurinoma

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome, heralded by neurologic invol

advance directives

advances in neurology

adverse drug reaction

alcoholic polyneuropathy

alpha-fetoprotein

alveolar hypoventilation

Alzheimer's disease

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

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

apraxia of eye movements

arrhythmia, cardiac

arthrogryposis multiplex

ataxia telangiectasia

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ataxia, truncal

atlanto axial dislocation, congenital

atrioventricular block

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basal ganglia, lesion of

behavioral disorder

Bence Jones protein

benign congenital hypotonia

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botulinum toxin, complications of

brachial neuritis

brainstem, infarction of

brainstem, lesion of

bright tongue sign

Brown Sequard syndrome

Brugada syndrome

bulbar palsy, acute

bulbar palsy, progressive

calcium channel dysfunction

calf hypertrophy

carbon monoxide poisoning

carcinoembryonic antigen

carcinoma of breast

cardiovascular disease

CAT scan, abnormal

CAT scan, emission

CAT scan, emission, abnormal

cavernous sinus, syndrome

central core disease

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar degeneration

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, protein of

cerebrovascular accident

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

chest x-ray, abnormal

chewing, impaired

chorea, Sydenham's

choreoathetosis

chromosomal abnormality

chronic polyneuritis, children

Clinical Pathologic Conference(C.P.C.)

cluster, geographic

compression neuropathy

conduction block

congenital heart disease

congenital myopathy

congestive heart failure

contractures, joint

controversies in neurology

cost effectiveness

coxsackievirus, myopathy with

creatine phosphokinase(CPK)elevated

crying, pathologic

cycad seed flour

degenerative diseases of CNS

delay in diagnosis

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

denervation of muscle

denervation potentials

dentatorubral-pallidoluysian atrophy

dermatomyositis

developmental milestones

developmental retardation

dexterity, impaired

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diabetic mononeuropathy

diagnostic criteria

diaphragmatic paralysis

diaphragmatic paralysis, causes of

differential diagnosis

difficulty climbing stairs

diplegia, atonic

disability rating scale, neurological

disability, neurological

distal muscle atrophy

distal muscle weakness

dropped head syndrome

drug interactions

dystrophic calcification

electrical injury of nervous system

electrocardiogram, abnormal

electromyogram, decremental response

electron microscopy

electrophoretic pattern, serum

emotional lability

encephalopathy, anoxic

encephalopathy, neonatal

encephalopathy, post anoxic

endocarditis, subacute bacterial

enterovirus infection of CNS

entrapment neuropathy

enzyme, muscle disease

epidemiology of neurology

ethics in neurology

evidence-based research

evoked potentials

eye movement, disorders of

facial weakness, bilateral

facioscapulohumeral syndrome

fatigable chewing

Fazio-Londe's disease

finger weakness

flail arm syndrome

football neurologic injuries

fragile-X syndrome

Friedreich's ataxia

frontal lobe, atrophy

frontotemporal dementia, behavioral variant

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

GM1 ganglioside antibodies

growth retardation

Guillain Barre syndrome

Gulf War syndrome

handlebar palsy

health insurance

heavy metal intoxication

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

hyperparathyroidism

hypoglycemic coma

hypotonia, infants

hypoxic encephalopathy

iatrogenic neurologic disorders

immune complexes

immunodeficiency

immunoelectrophoresis, serum

immunologic disease

immunosuppression

immunosuppressive agents

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, ubiquitin

inclusion body myositis

infant, evaluation of

infantile tremor syndrome

intellectual deficit

intermittent positive pressure breathing

internal capsule

intestinal pseudoobstruction

intrinsic hand muscles, wasting of

Isaacs syndrome

Jackson's syndrome

Jakob-Creutzfeldt disease

jaw closure weakness

jaw jerk, abnormal

klippel feil syndrome

Kugelberg-Welander syndrome

laminectomy, cervical

laughing, pathologic

lead and the nervous system

leg weakness, bilateral

leg weakness, unilateral

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

locked-in syndrome

lumbar puncture

lymphadenopathy

lymphoma involving CNS

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

masseter muscle weakness

median neuropathy

medical-legal aspects of neurology

mental retardation

Millard Gubler syndrome

minimally conscious state

molecular genetics

monoclonal antibodies

monoclonal gammopathy

monomelic amyotrophy

mononeuropathy, motor

Motor Band Sign

motor neuron disease

motor neuron disease, juvenile form

motor neuron disease, spontaneous recovery

movement disorder

movement disorder, extrapyramidal

MRI, diffusion weighted

MRI, functional

MRI, gradient-echo

MRI, paramagnetic effect

MRI, spinal cord

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, treatment of

myasthenic crisis

myasthenic syndrome

myelogram, cervical

myelopathy, ischemic

myocardial infarction

myocardial injury

myopathy, carcinomatous

myopathy, centronuclear

myopathy, distal

myopathy, mitochondrial

myopathy, quadriceps

myopathy, thyroid disease causing

myotonia congenita

myotonia dystrophica

N-acetyl-L-aspartic acid

narcotic analgesics

nemaline rod myopathy

nemaline rod myopathy, adult onset

neoplasm, primary intracerebral

neoplasm, primary intracranial

neoplasm, primary of CNS

nerve conduction studies

nerve conduction studies, motor

nerve growth factor

neuritis, causes of

neurocutaneous disease

neuroendocrinology

neurofibrillary degeneration

neurogenic vs.myopathic atrophy

neurologic complications

neurologic complications of, surgery

neurologic consultation

neurologic disease

neurologic disease, diagnoses of

neurologic disease, incurable

neurologic evaluation

neurologic signs

neurologic symptoms

neuromuscular blockade

neuromuscular junction

neuromuscular junction, abnormality of

neuronal degeneration

neuronal migration disorder

neuroophthalmology

neuropathology, brain

neuropathy, bicycle

neuropathy, diabetic

neuropathy, hereditary peripheral

neuropathy, motor, multifocal

neuropathy, peripheral

neuropathy, peripheral, treatment

neuroprotective agents

neurotransmitter

newborn, evaluation of

NMDA antagonists

nystagmus, primary position of gaze

nystagmus, rotary

occupational neurologic disorders

ocular motility, disorders of

old age, neurology of

olivary degeneration, hypertrophic

Onufrowicz nucleus

ophthalmoplegia

ophthalmoplegia, painful

ophthalmoplegia, progressive external

Oppenheim muscular dystrophy

owl's eye sign of spinal cord

pain, management of chronic

palatal myoclonus

palliative care

paraparesis, spastic

paraproteinemia

paraspinal muscle

parathyroid adenoma

Parkinson disease

Parkinson disease, motor neuron disease with

Parkinson disease, treatment of

Parkinsonism syndrome

Parkinsonism-dementia complex

patient information and support

periodic paralysis

periodic paralysis, thyrotoxic

persistent vegetative state

personality change

phrenic nerve pacemaker

physical activity

physical therapy

physician assisted suicide

plasma cell dyscrasia

pleocytosis of cerebrospinal fluid

pneumoencephalogram(PEG)

poison, mercury

poison, neurologic problems with

polyclonal gammopathy

polyglucosan body disease

polymerase chain reaction

polyneuropathy, chronic inflammatory demyelinating

positive sharp waves

post polio syndrome

posterior fossa, differential diagnosis of lesions of

posterior inferior cerebellar artery syndrome

posterior interosseous neuropathy

practice guidelines

pregnancy, neurologic complications in

prevention of neurologic disorders

primary lateral sclerosis

progressive muscular dystrophy

progressive neurologic disorder

progressive spinal muscular atrophy

proximal muscle atrophy

pseudobulbar palsy

pseudohypertrophy

psychiatric problems in neurologic disorders

psychomotor retardation

pulmonary embolism

pulmonary function tests

pyramidal tract

pyramidal tract dysfunction

quadriceps atrophy

quadriceps weakness

quality of life

radiation hypersensitivity

radiation therapy, salivary gland

release phenomena

remote effect of cancer on the nervous system

repetitive nerve stimulation

respiratory depression

respiratory failure

risk-benefit assessment

salivation, excessive

scoliosis, neurologic association with

seizure, children

seizure, treatment of

sensory ganglia

sensory ganglia, abnormal

sensory symptoms

sensory testing

serologic testing

serum alanine aminotransferase

shoulder, subluxation

single photon emission computed tomography

skin, lesions in neurologic disorders

sleep pathology and physiology

Smell Identification Test

somatosensory evoked potentials

somatosensory evoked potentials, dermatomal

speech disorder

spinal cord degeneration

spinal cord, compression of

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

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar degeneration

standing difficulty

stem cell tourism

stem cell transplantation

sternocleidomastoid muscle

stiff man syndrome

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

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

subarachnoid hemorrhage

subdural hematoma

superoxide dismutase

survival motor neuron gene

tandem gait, ataxic

temporal lobe, atrophy

temporalis muscle wasting

tensilon test, false positive

testicular atrophy

thoracic outlet syndromes

thrombophlebitis

thyrotropin-releasing hormone

Tolosa Hunt syndrome

tongue, atrophy

tongue, enlarged

tongue, fasciculations of

tongue, weakness

treatment of neurologic disorder

tremor, postural

triangle of Guillain and Mollaret

tricresylphosphate

trinucleotide repeats

ulnar nerve, deep palmar branch of

ulnar neuropathy

unconsciousness

upgaze, paralysis of

urinary incontinence

venous thrombosis, non-cerebral

viral infection

viral infection, CNS

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

whistle, inability to

white matter disease

winging of scapula

X-linked bulbospinal neuronopathy

Showing articles 200 to 250 of 8823 << Previous Next >>

The Natural History of Motoneuron Loss in Amyotrophic Lateral Sclerosis
Neurol 38:409-413, Munsat,T.L.,et al, 1988

Use of Composite Scores (Megascores) to Measure Deficit in Amyotrophic Lateral Sclerosis
Neurol 38:405-408, Andres,P.L.,et al, 1988

Motoneuron Disease and Past Poliomyelitis in England and Wales
Lancet 1:1319-1322, Martyn,C.N.,et al, 1988

Magnetic Resonance Imaging in Amyotrophic Lateral Sclerosis
Ann Neurol 23:418-420, Goodin,D.S.,et al, 1988

A Double-Blind Study of the Effectiveness of Cyclosporine in Amyotrophic Lateral Sclerosis
Arch Neurol 45:381-386, Appel,S.H.,et al, 1988

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

Amyotrophic Lateral Sclerosis Presenting with Sleep Hypopnea Syndrome
Chest 93:1309-1312, Carre,P.C.,et al, 1988

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

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

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

Motor Neuron Disease & Paraproteinemia
Neurol 37:335-337, Rudnicki,S.,et al, 1987

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

Location of the Gene for X-Linked Spinal Muscular Atrophy
Neurol 36:1595-1598, Fischbeck,K.H.,et al, 1986

Motor Neuron Disease & Plasma Cell Dyscrasia
Neurol 36:1429-1436, Shy,M.E.,et al, 1986

A Double-Blind, Placebo-Controlled Trial of TRH in Amyotrophic Lateral Sclerosis
Neurol 36:141-145, Caroscio,J.T.,et al, 1986

Controlled Trial of Thyrotropin Releasing Hormone in Amyotrophic Lateral Sclerosis
Neurol 36:146-151, Brooke,M.H.,et al, 1986

Amyotrophic Lateral Sclerosis:Effects of Administration of Thyrotropin-Releasing Hormone
Neurol 36:152-159, Mitsumoto,H.,et al, 1986

Amyotrophic Lateral Sclerosis, Associated Clinical Disorders & Immunological Evaluations
Arch Neurol 43:234-238, Appel,S.H.,et al, 1986

Familial Adult Motor Neuron Disease:Amyotrophic Lateral Sclerosis
Neurol 36:511-517, Mulder,D.W.,et al, 1986

Post-Polio Syndrome
J Med Assoc Ga 74:510-511, Bailey,A.A., 1985

Amyotrophic Lateral Sclerosis:Part 1. Clinical Features, Pathology, & Ethical Issues in Management
Ann Neurol 18:271-280, Tandan,R.,et al, 1985

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Showing articles 200 to 250 of 8823 << Previous Next >>