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amyotrophic lateral sclerosis, epidemiology of

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, guamian type of

anterior horn cell disease

anterior tibial muscle weakness

apraxia of eye movements

arthrogryposis multiplex

ataxia telangiectasia

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ataxia, truncal

benign congenital hypotonia

Brugada syndrome

bulbar palsy, progressive

calf hypertrophy

carcinoembryonic antigen

central core disease

cerebellar ataxia, children

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cerebellar degeneration

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choreoathetosis

chromosomal abnormality

chronic polyneuritis, children

Clinical Pathologic Conference(C.P.C.)

congenital heart disease

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congestive heart failure

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Dejerine-Sottas syndrome

denervation of muscle

denervation potentials

dermatomyositis

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes mellitus

diaphragmatic paralysis

differential diagnosis

distal muscle atrophy

distal muscle weakness

electrocardiogram, abnormal

encephalopathy, anoxic

encephalopathy, neonatal

enzyme, muscle disease

epidemiology of neurology

eye movement, disorders of

facial weakness, bilateral

facioscapulohumeral syndrome

Fazio-Londe's disease

Friedreich's ataxia

genetic counselling

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genetic linkage

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genetic screening

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growth retardation

Guillain Barre syndrome

heavy metal intoxication

history of neurology

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

Huntington's chorea

hypoglycemic coma

hypotonia, infants

hypoxic encephalopathy

immunodeficiency

immunosuppression

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

infant, evaluation of

intestinal pseudoobstruction

intrinsic hand muscles, wasting of

Isaacs syndrome

klippel feil syndrome

Kugelberg-Welander syndrome

leg weakness, bilateral

leg weakness, unilateral

lid closure, weakness of

life expectancy

mental retardation

molecular genetics

motor neuron disease

movement disorder

movement disorder, extrapyramidal

MRI, spinal cord

multiple system atrophy

muscle atrophy, progressive

muscle diseases, characteristics of

muscle hypertrophy

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, limb-girdle

myasthenic crisis

myelopathy, chronic progressive

myocardial injury

myopathy, carcinomatous

myopathy, centronuclear

myopathy, mitochondrial

myopathy, thyroid disease causing

myotonia congenita

myotonia dystrophica

nemaline rod myopathy

nerve conduction studies

neuritis, causes of

neurocutaneous disease

neuroendocrinology

neurofibrillary degeneration

neurologic disease, diagnoses of

neurologic evaluation

neuronal ceroid-lipofuscinosis

neuronal degeneration

neuropathy, diabetic

neuropathy, hereditary peripheral

newborn, evaluation of

ocular motility, disorders of

Onufrowicz nucleus

Oppenheim muscular dystrophy

paraparesis, familial spastic

Parkinson disease

patient information and support

peroneal muscle atrophy, causes of

poison, mercury

poison, neurologic problems with

post polio syndrome

pregnancy, neurologic complications in

primary lateral sclerosis

progressive muscular dystrophy

progressive neurologic disorder

progressive spinal muscular atrophy

proximal muscle atrophy

radiation hypersensitivity

Refsum's disease

respiratory failure

risk-benefit assessment

Roussy Levy syndrome

scoliosis, neurologic association with

skin, lesions in neurologic disorders

spinal cord degeneration

spinal cord, lesion of

spinal cord, pathologic exam of

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinal muscular atrophy, classification

spinal muscular atrophy, intermediate form

spinocerebellar ataxia

stiff man syndrome

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

survival motor neuron gene

tongue, fasciculations of

treatment of neurologic disorder

tricresylphosphate

trinucleotide repeats

tuberous sclerosis

viral infection

vitamin E deficiency

walking, difficulty with

weakness, generalized

weakness, infant

weakness, progressive

weaning from respirator, failure to

Werdnig-Hoffman disease

whistle, inability to

winging of scapula

X-linked bulbospinal neuronopathy

Showing articles 450 to 500 of 7279 << Previous Next >>

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

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

Exacerbation of Charcot-Marie-Tooth Disease in Pregnancy
Neurol 32:1311-1314, Pollock,M.,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

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

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

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

Primary Lateral Sclerosis
Arch Neurol 38:630-633, Beal,M.F.,et al, 1981

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

Pattern Reversal Visual Evoked Potentials
Arch Neurol 38:739-741, Bird,T.D.,et al, 1981

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

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

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

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

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

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

Central Vestibular Involvement in Peroneal Muscle Atrophy:A Preliminary Report
Ann Neurol 5:118-120, Melgaard,B.,et al, 1979

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

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

Haemophilic Neuromyopathy
JNNP 42:600-605, Defaria,C.R.,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

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

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

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

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

Lower Motor Neuron Disease with Spinocerebellar Degeneration
Ann Neurol 2:524, Page,R.W.,et al, 1977

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

Postradiation Motor Neuron Syndrome
Arch Neurol 33:786, Sadowsky,C.H.,et al, 1976

Charcot-Marie-Tooth Disease Associated With"Essential Tremor"
Neurol Sciences 28:17-40, Salisachs,P.J., 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

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

Poliomyelitis-A Persistent Problem
NEJM 288:370, Weinstein,L., 1973

Neuropathy in Thyrotoxicosis-Correspondence-NEJM 289:219
1973., , 1973

Possible Neurogenic Factor in Muscular Dystrophy:Its Similarity to Denervation Atrophy
JNNP 36:399-410, Dastur,D.K.,et al, 1973

Reversible Forms of Motor Neuron-Disease:Lead"Neuropathy"
Neurol 22:446, Boothby,J., 1972

Amyotrophic Lateral Sclerosis
Richard Kisonak, Associated Press, Boston Globe Apr 30972., , 1972

Neurological Problems in Endocrine Diseases
Med Clin North Am 56:1029, Dale,A., 1972

Neurological Disorders in Patients Following Surgery for Peptic Ulcer
Neurol 22:450, Hoffman,P., 1972

Showing articles 450 to 500 of 7279 << Previous Next >>