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amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, atypical

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amyotrophic lateral sclerosis, diagnosis of

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, epidemiology of

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amyotrophic lateral sclerosis, familial

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amyotrophic lateral sclerosis, prognosis

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anterior horn cell disease

anti Hu antibody

anticonvulsants

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arrhythmia, cardiac

asthma, poliomyelitis-like syndrome with

ataxia, progressive

behavioral disorder

bulbar palsy, progressive

carbon monoxide poisoning

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CAT scan, abnormal

CAT scan, emission, abnormal

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cerebellar atrophy, primary

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Clinical Pathologic Conference(C.P.C.)

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developmental retardation

dexterity, impaired

diabetes mellitus

diagnostic criteria

diaphragmatic paralysis

differential diagnosis

diplegia, brachial

disability rating scale, neurological

distal muscle atrophy

distal muscle weakness

emotional lability

encephalitis, central European

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enterovirus infection of CNS

epidemiology of neurology

ethics in neurology

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hypotonia, infants

hypoxic encephalopathy

immunohistochemistry

immunosuppression

inclusion body myositis

inflexibility, mental

intellectual deficit

intermittent positive pressure breathing

internal capsule

intrinsic hand muscles, wasting of

jaw jerk, abnormal

Kugelberg-Welander syndrome

kyphoscoliosis, neurologic causes of

laminectomy, cervical

laughing, pathologic

leg weakness, bilateral

leg weakness, unilateral

leukemia, neurologic findings assoc.with

leukoencephalopathy

lid closure, weakness of

life expectancy

life support, withdrawal of

life sustaining treatment

limbic encephalitis

locked-in syndrome

medical-legal aspects of neurology

mental status, abnormal

minimally conscious state

molecular genetics

monomelic amyotrophy

motor neuron disease

motor neuron disease, spontaneous recovery

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

muscle atrophy, progressive

muscle wasting, diffuse

muscle weakness

muscle weakness, insidious onset of

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muscular dystrophy

myelitis, longitudinal

myelitis, transverse

myelopathy, ischemic

myeloradiculitis

myocardial infarction

narcotic analgesics

nausea and vomiting

nerve conduction studies

neurologic complications

neurologic complications of, surgery

neurologic disease

neurologic disease, diagnoses of

neurologic symptoms

neuronal degeneration

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neuropathology, brain

neuroprotective agents

next-generation sequencing

old age, neurology of

owl's eye sign of spinal cord

pain, increased response

pain, management of chronic

palliative care

paralysis, acute

paralysis, acute areflexic

paraneoplastic ganglionopathy

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, flaccid

paraparesis, spastic

paraspinal muscle

Parkinsonism syndrome

Parkinsonism-dementia complex

patient information and support

persistent vegetative state

personality change

phrenic nerve pacemaker

physician assisted suicide

pleocytosis of cerebrospinal fluid

pneumoencephalogram(PEG)

poliomyelitis-like illness

polymerase chain reaction

positive sharp waves

practice guidelines

pregnancy, neurologic complications in

primary lateral sclerosis

progressive neurologic disorder

progressive spinal muscular atrophy

proximal muscle atrophy

pseudobulbar palsy

psychiatric problems in neurologic disorders

psychomotor retardation

pulmonary embolism

pulmonary function tests

pyramidal tract

pyramidal tract dysfunction

quality of life

rapidly progressing neurologic illness

release phenomena

remote effect of cancer on the nervous system

repetitive nerve stimulation

respiratory arrest

respiratory failure

respiratory tract infection

salivation, excessive

scoliosis, neurologic association with

sensory symptoms

serologic testing, false negative

single photon emission computed tomography

sleep pathology and physiology

speech disorder

spinal cord degeneration

spinal cord, compression of

spinal cord, injury of

spinal cord, injury, management of

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

stereotyped behavior

superoxide dismutase

survival motor neuron gene

thalamus, lesion of

tick-borne encephalitis

tongue, atrophy

tongue, fasciculations of

treatment of neurologic disorder

unconsciousness

viral infection

viral infection, CNS

walking, difficulty with

weakness, generalized

weakness, progressive

weaning from respirator, failure to

Werdnig-Hoffman disease

West Nile fever

word-finding difficulty

Showing articles 300 to 350 of 6941 << Previous Next >>

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

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

Severe Neurological Disease Associated with Hyperparathyroidism
Ann Neurol 15:453-456, Patten,B.M.,et al, 1984

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

Mercury Intoxication Simulating Amyotrophic Lateral Sclerosis
JAMA 250:642-643, Adams,C.R.,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

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

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

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

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

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

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

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

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

Alzheimer Neurofibrillary Tangles in Diseases Other Than Senile & Presenile Dementia
Ann Neurol 5:288-294, Wisniewski,K.,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

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

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

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

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

Cervical Spondylotic Myelopathy with Reversible Fasciculations in the Lower Extremities
Arch Neurol 34:774, Kasdon,D., 1977

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

Clinical Correlations of Periodic Lateralized Epileptiform Discharges
Clin Electroenceph 8:191-202, Porecha,H.P.&Reilly,E.L., 1977

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

Showing articles 300 to 350 of 6941 << Previous Next >>