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acid maltase deficiency

acid maltase deficiency, adult

acoustic neurinoma

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome, heralded by neurologic invol

ACTH, ectopic syndrome of

acute intermittant porphyria

Addison's disease

adult polyglucosan body disease

advance directives

advances in neurology

adverse drug reaction

alcohol, neurologic complications with

alcoholic polyneuropathy

alien hand syndrome

alpha glucosidase

alpha-fetoprotein

alveolar hypoventilation

Alzheimer's disease

aminoacidopathies

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

ankle reflex, preserved

ankylosing spondylitis

anterior horn cell disease

anterior interosseous neuropathy

anterior spinal artery infarction

anterior tibial muscle weakness

anti citrullinated antibody

anti Hu antibody

antibodies to voltage-gated calcium channels

anticonvulsants

antiviral agents

aphasia, progressive, primary

apraxia of eye movements

arm swing, reduced

arrhythmia, cardiac

arterial dissection

arterial dissection, aorta

arterial dissection, vertebral

arthrogryposis multiplex

ascending paralysis

aspartate aminotransferase

asthma, poliomyelitis-like syndrome with

ataxia telangiectasia

ataxia, cerebellar

ataxia, hereditary

ataxia, progressive

ataxia, truncal

athetosis, causes of

atlanto axial dislocation, congenital

autoimmune disease

automatic behavior

automobile accidents

autonomic dysfunction

axonal degeneration

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basophilic stippling of red blood cells

behavioral disorder

Behcet's syndrome

Bence Jones protein

benign congenital hypotonia

biologic markers

bitemporal visual field defect

bladder dysfunction

blood transfusion

bone marrow biopsy

botulinum toxin

botulinum toxin, complications of

brachial amyotrophic diplegia

brachial neuritis

brainstem, infarction of

brainstem, lesion of

bright tongue sign

Brown Sequard syndrome

Brugada syndrome

bulbar palsy, acute

bulbar palsy, childhood

bulbar palsy, progressive

calcification, intracranial

calcium channel dysfunction

calf hypertrophy

Canavan's disease

carbon monoxide poisoning

carcinoembryonic antigen

carcinoma of breast

carcinoma of lung

carpo-pedal spasm

CAT scan, abnormal

CAT scan, emission

CAT scan, emission, abnormal

cauda equina, enhancement

cavernous sinus, syndrome

central core disease

central nervous system, infection of

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar lesion

cerebellar vermis

cerebellum, neoplasms of

cerebral cortex

cerebral cortical atrophy

cerebral embolism

cerebral peduncle

cerebral venous thrombosis

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, cell count

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, enzymes in

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, oligoclonal IgM in

cerebrospinal fluid, protein of

cerebrospinal fluid, proteincytologic dissociation

cerebrovascular accident

cerebrovascular accident, familial occurrence

cerebrovascular accident, young adult

cerebrovascular disease, cardiovascular disease with

cervical collar

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

cherry red spot

cherry red spot-myoclonus syndrome

chest x-ray, abnormal

chewing, impaired

Chinese paralytic syndrome

chondroitin sulfate C

chorea, Sydenham's

choreoathetosis

chromosomal abnormality

chronic polyneuritis, children

ciguatera poisoning

Clinical Pathologic Conference(C.P.C.)

cluster, geographic

cold intolerance

cold temperature

compression neuropathy

conduction block

congenital heart disease

congenital myopathy

congestive heart failure

controversies in neurology

conversion reaction

cortical hand knob

cortical-basal ganglionic degeneration

cost effectiveness

coxsackievirus, myopathy with

cranial nerve enhancement

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

craniopharyngioma

creatine phosphokinase(CPK)elevated

critical care unit

critical illness

crying, pathologic

cultured skin fibroblasts

Cushing's syndrome

cycad seed flour

cyclophosphamide

deep gray nuclei

degenerative diseases of CNS

Dejerine-Sottas syndrome

delay in diagnosis

dementia, age at onset

dementia, cerebrovascular disease causing

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

denervation of muscle

denervation potentials

dentate nuclei, lesion of

dermatomyositis

developmental disability

developmental milestones

developmental milestones, loss of

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

diplegia, brachial

disability rating scale, neurological

disability, neurological

distal muscle atrophy

distal muscle weakness

dropped head syndrome

drug induced neurologic disorders

drug interactions

electrical injury of nervous system

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electromyogram, decremental response

electron microscopy

electrophoretic pattern, serum

embolism, nucleus pulposus

emotional lability

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, central European

encephalitis, Japanese

encephalitis, paraneoplastic

encephalitis, Powassan

encephalitis, viral

encephalomyelitis

encephalomyeloneuritis

encephalopathy, anoxic

encephalopathy, neonatal

encephalopathy, post anoxic

endocarditis, subacute bacterial

enterovirus infection of CNS

entrapment neuropathy

enzyme treatment

enzyme, muscle disease

epidemiology of neurology

episodic disorders

episodic neurologic deficits

episodic unconsciousness

ethics in neurology

evidence-based research

evoked potentials

executive dysfunction

exercise intolerance

extremity, cold

eye movement, disorders of

facial nerve palsy

facial nerve palsy, bilateral

facial nerve palsy, causes of

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

fasciculation, benign

fatigable chewing

Fazio-Londe's disease

feeding disorder

fine motor function, impaired

finger weakness

flaccid paralysis

flail arm syndrome

flu-like illness

football neurologic injuries

Friedreich's ataxia

frontal behavioral spatial syndrome

frontal lobe, atrophy

frontal lobe, behavior with disease of

frontal lobe, lesion of

frontotemporal dementia, behavioral variant

F-wave response

gag reflex, depressed

gamma amino butyric acid

gammaglobulin therapy, intravenous

gangliosidosis GM2

gastrectomy, neurologic complications following

gastroenteritis

gastrostomy, percutaneous endoscopic

gaze palsy, horizontal

gaze palsy, supranuclear

gaze palsy, vertical

genetic counselling

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

genital ulcerations

glycogen storage disease

GM1 ganglioside

GM1 ganglioside antibodies

granular atrophy, cerebral cortex

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, variant forms of

Gulf War syndrome

Hallervorden Spatz disease

hallucination, auditory

handlebar palsy

Hand-Schuller-Christian disease

head circumference

health insurance

heavy metal intoxication

hemifacial atrophy

hemiplegia, progressive

heralding manifestation

herpes simplex encephalitis

herpes simplex encephalitis, diagnosis of

herpes zoster, oticus

heterochromia iridis

highly active antiretroviral therapy

histochemistry of muscle

history of neurology

Hodgkin's disease

Hodgkin's disease, neurologic involvement with

Horner's syndrome

Horner's syndrome, etiologies of

human immunodeficiency virus type 1

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

Huntington's chorea

hyperadrenalism

hyperinsulinism

hyperparathyroidism

hyperpigmentation of skin

hyperthyroidism

hypogammaglobulinemia

hypoglycemic coma

hypokalemic alkalosis

hypokalemic periodic paralysis

hypoparathyroidism

hypotension, systemic

hypothalamus, disturbance of

hypotonia, infants

hypoxia, newborn

hypoxic encephalopathy

iatrogenic neurologic disorders

ideomotor apraxia

ileus, paralytic

imbalance, postural

immune complexes

immunization, neurologic complications with

immunodeficiency

immunoelectrophoresis, serum

immunohistochemistry

immunologic disease

immunosuppression

immunosuppressive agents

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, ubiquitin

inclusion body myositis

incontinentia pigmenti

infant, evaluation of

infantile neuronal degeneration

infantile tremor syndrome

infectious mononucleosis, neurologic findings with

inflexibility, mental

initiative, lack of

injection, intramuscular

intellectual deficit

intellectual deterioration

intermittent positive pressure breathing

internal capsule

intestinal pseudoobstruction

intrinsic hand muscles, wasting of

Isaacs syndrome

islet cell tumor

Jackson's syndrome

Jakob-Creutzfeldt disease

jaw jerk, abnormal

juvenile distal and segmental muscular atrophy

klippel feil syndrome

Kugelberg-Welander syndrome

kyphoscoliosis, neurologic causes of

laboratory values, normal

lactic acidemia

laminectomy, cervical

language disorder in adults

laughing, pathologic

lead and the nervous system

leg weakness, bilateral

leg weakness, unilateral

leukemia, neurologic findings assoc.with

leukoencephalopathy

leukoencephalopathy, differential diagnosis

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

loss of sympathy

lumbar puncture

lumbosacral radiculopathy

lymphadenopathy

lymphadenopathy, hilar

lymphoma involving CNS

lysosomal storage disease

lysosomes, abnoral

macular degeneration

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

Man-In-The-Barrel syndrome

masseter muscle wasting

median neuropathy

medical-legal aspects of neurology

Melkersson's syndrome

memory, defect of recent

memory, impairment of

meningeal enhancement

meningitis, aseptic

meningitis, neutrophilic

meningoencephalitis

mental retardation

mental status, abnormal

metabolic disorder, primary

midbrain, atrophy

midbrain, lesion of

Millard Gubler syndrome

minimally conscious state

mitochondrial disease

mitochondrial encephalomyopathy

mitral valve lesion

Moebius syndrome

molecular genetics

monoclonal antibodies

monoclonal gammopathy

monomelic amyotrophy

mononeuritis multiplex

mononeuropathy, motor

Montreal cognitive assessment

Motor Band Sign

motor neuron disease

motor neuron disease, juvenile form

motor neuron disease, misdiagnosis

motor neuron disease, spontaneous recovery

movement disorder

movement disorder, extrapyramidal

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, functional

MRI, gradient-echo

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 sleep latency test

multiple system atrophy

muscle atrophy, progressive

muscle atrophy, static

muscle diseases, characteristics of

muscle hypertrophy

muscle relaxant

muscle stiffness

muscle twitching

muscle wasting, diffuse

muscle weakness

muscle weakness, causes of

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

muscular dystrophy, neurogenic hypothesis of

myasthenia gravis

myasthenia gravis, diagnosis

myasthenia gravis, differential diagnosis

myasthenia gravis, distal weakness

myasthenia gravis, drug induced

myasthenia gravis, limb-girdle

myasthenia gravis, misdiagnosis of

myasthenia gravis, treatment of

myasthenic crisis

myasthenic syndrome

myelin basic protein

myelitis, longitudinal

myelitis, transverse

myelogram, cervical

myeloneuropathy

myelopathy, ischemic

myelopathy, carcinomatous

myelopathy, chronic progressive

myelopathy, necrotizing

myelopathy, radiation induced

myeloradiculitis

myeloradiculopathy

myocardial infarction

myocardial injury

myoclonic jerks

myopathy, autoimmune

myopathy, carcinomatous

myopathy, centronuclear

myopathy, critically ill

myopathy, distal

myopathy, mitochondrial

myopathy, neurogenic hypothesis of

myopathy, quadriceps

myopathy, steroid responsive

myopathy, thyroid disease causing

myotonia congenita

myotonia dystrophica

myxedema, neurologic manifestations of

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, pituitary

neoplasm, primary intracerebral

neoplasm, primary of CNS

nerve conduction studies

nerve conduction studies, motor

nerve growth factor

nerve root enhancement

neuralgia, intercostal

neuritis, causes of

neurocutaneous disease

neuroendocrinology

neurofibrillary degeneration

neurofibromatosis 1

neurofibromatosis 2

neurogenic bladder

neurogenic vs.myopathic atrophy

neurologic complications

neurologic complications of, surgery

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic consultation

neurologic disease

neurologic disease, diagnoses of

neurologic disease, incurable

neurologic disease, tempo

neurologic evaluation

neurologic signs

neurologic symptoms

neurologic testing

neuromuscular blockade

neuromuscular disease, electrodiagnosis of

neuromuscular junction

neuromuscular junction, abnormality of

neuron specific enolase

neuronal ceroid-lipofuscinosis

neuronal degeneration

neuronal intranuclear inclusion disease

neuronopathy, sensory

neuroophthalmology

neuropathology, brain

neuropathy, acute

neuropathy, amyloid

neuropathy, bicycle

neuropathy, diabetic

neuropathy, diphtheritic

neuropathy, hereditary peripheral

neuropathy, motor

neuropathy, motor, multifocal

neuropathy, multifocal

neuropathy, painful

neuropathy, paraneoplastic

neuropathy, peripheral

neuropathy, peripheral, treatment

neuropathy, short-fiber

neuropathy, toxic

neuroprotective agents

neurotransmitter

newborn, evaluation of

next-generation sequencing

NMDA antagonists

nystagmus, primary position of gaze

nystagmus, rotary

nystagmus, vertical

obsessive-compulsive disorder

occupational neurologic disorders

occupational neuropathies

ocular motility, disorders of

oculogyric crisis

old age, neurology of

olivary degeneration, hypertrophic

Onufrowicz nucleus

ophthalmoplegia

ophthalmoplegia, painful

ophthalmoplegia, progressive external

ophthalmoplegia, total

Oppenheim muscular dystrophy

oral ulcerations

organ transplantation

otitis, neurologic complications with

owl's eye sign of spinal cord

pain, abdominal

pain, increased response

pain, management of chronic

palatal myoclonus

palliative care

palmomental response

paralysis, acute

paralysis, acute areflexic

paralysis, asymmetric

paralysis, use-related

paraneoplastic ganglionopathy

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, flaccid

paraparesis, spastic

paraproteinemia

paraspinal muscle

parathyroid adenoma

paratrigeminal syndrome

Parkinson disease

Parkinson disease, atypical

Parkinson disease, axial symptoms

Parkinson disease, L-dopa nonresponsive

Parkinson disease, motor neuron disease with

Parkinson disease, postencephalitic

Parkinson disease, treatment of

Parkinson disease, tremor, absence of

Parkinsonism syndrome

Parkinsonism-dementia complex

paroxysmal neurologic deficits

pathologic reflex

patient information and support

penguin silhouette sign

periarteritis nodosa

periodic paralysis

periodic paralysis, thyrotoxic

peripheral vascular disease

peroneal muscle atrophy, causes of

peroxisomal disease

persistent vegetative state

personality change

pheochromocytoma

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

poliomyelitis vaccine

poliomyelitis, neonatal

poliomyelitis, provocation

poliomyelitis-like illness

polyclonal gammopathy

polyglucosan body

polyglucosan body disease

polymerase chain reaction

polymerase chain reaction, false negative

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, critically ill

Pompe's disease of glycogen storage

pons, lesion of

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

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

primary aldosteronism

primary lateral sclerosis

progressive muscular dystrophy

progressive neurologic disorder

progressive spinal muscular atrophy

progressive supranuclear palsy

proprioception, abnormal

proximal muscle atrophy

pseudoathetosis

pseudobulbar palsy

pseudohypertrophy

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

pulmonary embolism

pulmonary function tests

pupil, abnormality in neurologic disorders

pyramidal tract

pyramidal tract dysfunction

quadriceps atrophy

quadriceps weakness

quality of life

rabies, nervous system involvement with

radial nerve, palsy of

radiation hypersensitivity

radiation therapy, CNS treatment and complications with

radiation therapy, salivary gland

ragged-red fibers

rapidly progressing neurologic illness

recombinant DNA

Refsum's disease

rehabilitation for neurologic disorders

release phenomena

REM sleep behavior disorder

remote effect of cancer on the nervous system

renal cell carcinoma

repetitive nerve stimulation

respiratory arrest

respiratory depression

respiratory failure

respiratory tract infection

retinal degeneration

retinitis pigmentosa

retrograde axonal flow

reverse split hand sign

rheumatoid arthritis

rheumatoid arthritis, neurologic complications of

rigidity, axial

risk-benefit assessment

root lesion, nerve

Roussy Levy syndrome

rubella encephalitis

rubeola, encephalitis

saccadic eye movements, abnormal

salivation, excessive

scoliosis, neurologic association with

segmental demyelination

seizure, children

seizure, treatment of

semantic dementia

sensorineural hearing loss

sensory ganglia

sensory ganglia, abnormal

sensory symptoms

sensory testing

sequencing difficulty

serologic testing

serologic testing of cerebrospinal fluid

serologic testing, false negative

serum alanine aminotransferase

shell fish poisoning

shoulder, subluxation

single photon emission computed tomography

single-fiber electromyography

skin, lesions in neurologic disorders

sleep apnea, obstructive

sleep offset paralysis

sleep onset paralysis

sleep paralysis

sleep pathology and physiology

Smell Identification Test

somatosensory evoked potentials

somatosensory evoked potentials, dermatomal

spastic diplegia

speech disorder

speech disorder, childhood

speech, loss of

spinal cord degeneration

spinal cord, cervical

spinal cord, compression of

spinal cord, infarction of

spinal cord, injury of

spinal cord, injury, management of

spinal cord, ischemic lesion of

spinal cord, lesion of

spinal cord, neoplasm

spinal cord, neoplasm, extramedullary

spinal cord, neoplasm, infants and children

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 ataxia type 3/Machado Joseph disease

spinocerebellar degeneration

spongy degeneration of brain

sports medicine, neurology of

standing difficulty

stem cell tourism

stem cell transplantation

stereotyped behavior

sternocleidomastoid muscle

stiff man syndrome

stimulant drugs

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

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

subarachnoid hemorrhage

subdural hematoma

substantia nigra

sudden infant death syndrome

superoxide dismutase

survival motor neuron gene

synucleinopathy

syphilis, neurologic complications with

tandem gait, ataxic

temporal lobe, atrophy

temporalis muscle wasting

tensilon test, false positive

thalamus, lesion of

thalamus, lesion of-bilateral

thoracic outlet syndromes

thrombophlebitis

thyrotropin-releasing hormone

tick-borne encephalitis

Tolosa Hunt syndrome

tongue, atrophy

tongue, enlarged

tongue, fasciculations of

tongue, impaired movements of

tongue, weakness

torticollis, infants and children

toxins, nervous system

travel, foreign

treatment of neurologic disorder

tremor, cerebellar

tremor, intention

tremor, postural

triangle of Guillain and Mollaret

tricresylphosphate

trinucleotide repeats

Trousseau's sign

tuberous sclerosis

ulnar nerve, deep palmar branch of

ulnar neuropathy

unconsciousness

unconsciousness, episodic

unconsciousness, transient

upgaze, paralysis of

urea-cycle enzymopathies

urinary incontinence

urinary retention

vaccination, neurologic complications with

venous thrombosis, non-cerebral

ventricular enlargement

vestibular function, tests of

viral infection

viral infection, CNS

viral isolation

vision, blurred

visual acuity, decreased

visual evoked response

visual field defect

visual fields, constricted

visual impairment

visual symptoms

vitamin E deficiency

Waldenstrom's macroglobulinemia

walking, difficulty with

watershed infarcts

weakness, acute

weakness, fatiguable

weakness, focal

weakness, generalized

weakness, infant

weakness, progressive

weakness, proximal

weakness, rapidly progressive

weaning from respirator, failure to

Weber's syndrome

Werdnig-Hoffman disease

West Nile fever

whistle, inability to

white matter disease

wide based gait

winging of scapula

word-finding difficulty

X-linked bulbospinal neuronopathy

Showing articles 350 to 400 of 2918 << Previous Next >>

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

Monomelic Amyotrophy
Arch Neurol 41:388-394, Gourie-Devi,M.,et al, 1984

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

Sudden Infant Death Syndrome Caused by Poliomyelitis
Arch Neurol 41:775-777, Dunne,J.W.,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

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

Adult Polyglucosan Body Disease:Clinical & Nerve Biopsy Findings in Two Cases
Ann Neurol 13:440-444, Vos,A.L.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

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

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

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

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

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

Neurological Complications of Immunization
Ann Neurol 12:119-128, Fenichel,G.M., 1982

Neurogenic Arthrogryposis in One Identical Twin, Sul
Arch Neurol 39:717-718, Yi,C.,et al, 1982

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

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

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

Progressive Pontobulbar Palsy With Deafness
Arch Neurol 38:186-190, Brucher,J.M.,et al, 1981

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

Preservation of the Phrenic Motorneurons in Werdnig-Hoffman Disease
Ann Neurol 9:506-510, Kuzuhara,S.,et al, 1981

Olivopontocerebellar Atrophy in Children:A Report of Seven Cases in Two Families
Ann Neurol 10:355-363, Colan,R.V.,et al, 1981

Vitamin E Deficiency in Werdnig-Hoffmann Disease
Ann Neurol 10:266-268, Shapira,Y.,et al, 1981

Primary Lateral Sclerosis
Arch Neurol 38:630-633, Beal,M.F.,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

Progressive Bulbar Paralysis Associated With Neurgl Deafness, A Nosological Entity
Arch Neurol 37:214-216, Alberica,R.,et al, 1980

Infantile Neuronal Degeneration Masquerading as Werdnig-Hoffmann Disease
Ann Neurol 8:317-324, Steiman,G.S.,et al, 1980

Poliomyelitis Worldwide
Editorial, BMJ 280:1555-15561980., , 1980

Gross Demonstration of Atrophic Cauda Equina Roots in Motor Neuron Disease, An Improved Method
Arch Neurol 37:394, Meneses,A., 1980

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

Remission of a Syndrome Indistinguishable from Motor Neuron Disease after Resection of Bronchial Carcinoma
BMJ 2:176-177, , 1979

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

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

Subacute Motor Neuronopathy:A Remote Effect of Lymphoma
Ann Neurol 5:271-287, Schold,S.C.,et al, 1979

Clinical Symposia, Scoliosis
CIBA, 30:21978., Keim,H.A., 1978

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

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