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addiction, heroin

addiction, heroin-neurologic complications with

advances in neurology

adverse drug reaction

alcohol, neurologic complications with

arterial dissection

arterial dissection, bilateral

arterial dissection, carotid

arterial dissection, spontaneous

ataxia, cerebellar

ataxia, progressive

auditory evoked brainstem potentials

autoimmune basal ganglia encephalitis

axonal spheroid

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, hemorrhage

basal ganglia, hemorrhage, bilateral

basal ganglia, infarction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavioral disorder

bilirubin encephalopathy

bone marrow transplantation

brainstem, lesion of

calcification, intracranial

carbon monoxide poisoning

carotid artery disease

carotid artery stenosis

carotid artery stenosis, bilateral

CAT scan, abnormal

CAT scan, angiography

CAT scan, contrast enhanced

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

centrum semiovale

cerebellar degeneration

cerebellar infarction

cerebellar infarction, bilateral

cerebellar lesion

cerebellum, disease of

cerebral cortex

cerebral cortical atrophy

cerebral infarction

cerebral infarction, hemorrhagic

cerebrotendinous xanthomatosis

cerebrovascular accident

chemotherapy, CNS treatment and complications with

chorea, familial

choreoathetosis

chromosomal abnormality

congenital malformation

corpus callosum, lesion of

corpus callosum, thinning

cranial neuropathy

Cree leukoencephalopathy

cry, high-pitched

cryoglobulinemia

deep gray nuclei

degenerative diseases of CNS

dementia, childhood

demyelinating disease

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

developmental retardation

disability rating scale, neurological

disseminated intravascular coagulation(DIC)

drug abuse, neurologic complications of

drug induced neurologic disorders

dyssynergia cerebellaris myoclonica

encephalitis, autoimmune

encephalopathy, acute

encephalopathy, delayed

encephalopathy, neonatal

encephalopathy, post anoxic

epidemiology of neurology

frontal lobe, behavior with disease of

gaze palsy, supranuclear

gaze palsy, vertical

genetic neurologic disorders

genetic testing

globus pallidus

globus pallidus focused ultrasound ablation

globus pallidus, hemorrhage

globus pallidus, infarction

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

globus pallidus, swelling

Hallervorden Spatz disease

Hallervorden Spatz disease, late onset

headache, recurrent

hemianopia, homonymous

hepatic encephalopathy

hepatic failure

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration, non-Wilsonian

high altitude sickness

human immunodeficiency virus type 1

hyperalimentation

hyperammonemic encephalopathy

hyperbaric oxygen

hyperbilirubinemia

hyperbilirubinemia, CNS abnormality after

hypotension, systemic

hypoxic encephalopathy

iatrogenic neurologic disorders

immunosuppression

inborn errors of metabolism

industrial neurologic disorders

intellectual deficit

intellectual deterioration

internal capsule

intracerebral hemorrhage

iodine deficiency

lenticular nucleus, lesion of

lenticular nucleus, lesion of, bilateral

leukoencephalopathy

liver function enzymes

liver transplantation

manganese intoxication

maple syrup urine disease

memory, impairment of

mental retardation

metabolic acidosis

metabolic disorder, primary

methanol intoxication

methylmalonic acidemia

methylmalonic aciduria

midbrain, infarction of

midbrain, lesion of

mild cognitive impairment

movement disorder

movement disorder, drug induced

movement disorder, extrapyramidal

MRI, CAT scan compared to

MRI, complications with

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, eye of tiger sign

MRI, false negative

MRI, high signal foci on

MRI, high signal intensity of basal ganglia

MRI, paramagnetic effect

MRI, susceptibility weighted

MRI, T1 weighted fat suppression

MRI, T1 weighted high signal foci

myelinolysis, extrapontine

myelopathy, hepatic

myoclonus, epilepsy

Native Americans

neurofibromatosis 1

neurologic complications

neurologic complications of, surgery

neurologic signs

neuropathology, brain

neurotoxicity, acute

occupational neurologic disorders

oculogyric crisis

ophthalmoplegia

ophthalmoplegia, neonatal

organ transplantation

osmotic demyelination syndrome

paraparesis, spastic

parenteral alimentation

Parkinson disease

Parkinson disease, familial

Parkinson disease, fluctuations in

Parkinson disease, on-off phenomena in

Parkinson disease, surgical treatment of

Parkinson disease, treatment of

Parkinsonism syndrome

personality change

pigmentary retinopathy

poison, neurologic problems with

portal caval shunt

postural abnormality

premature infant

prevention of neurologic disorders

progressive neurologic disorder

progressive pallidum atrophy

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

quality of life

radiation therapy, CNS treatment and complications with

renal failure, acute

retinal degeneration

retinitis pigmentosa

reversible neurologic disorder

sea-blue histiocytes

seizure, children

self-mutilation

semialdehyde dehydrogenase deficiency

sensorineural hearing loss

setting sun phenomena

skin, cherry-red

spastic diplegia

speech disorder

speech disorder, childhood

static encephalopaty of childhood with neurodegeneration in adulthood

stereotaxic surgery

stimulant drugs

striatum, lesion of

substantia nigra

subthalamic nucleus

symmetric brain lesions

systemic illness

thalamus, lesion of

thalamus, lesion of-bilateral

toxic encephalopathy

toxins, nervous system

toxoplasmosis, CNS

treatment of neurologic disorder

upgaze, paralysis of

uremic encephalopathy

urinary incontinence

urine test for metabolic disorders

visual acuity, decreased

visual evoked response

visual field defect

watershed infarcts

white matter disease

white matter disease, periventricular

Showing articles 650 to 700 of 3801 << Previous Next >>

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

Familial Multisystem Atrophy with Possible Thalamic Dementia
Neurol 34:1213-1217, Katz,D.A.,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

Mitochondrial Encephalomyopathy:Fluctuating Symptoms & CT
Neurol 34:1456-1460, Yamamoto,T.,et al, 1984

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

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

Neurological Complications of Acquired Immune Deficiency Syndrome:Analysis of 50 Patients
Ann Neurol 14:403-418, Snider,W.D.,et al, 1983

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

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

Bilateral Optic Neuropathy with Remission in Young Men, Variation on a Theme by Leber
Arch Neurol 40:2-6, Lessell,S.,et al, 1983

Quadriceps Myopathy:A Varient of the Limb-Girdle Dystrophy Syndrome
JNNP 46:355-357, Swash,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

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

Cardiomyopathy Associated with the Syndrome of Amyotrophic Chorea & Acanthocytosis
Ann Int Med 96:616-617, Faillace,R.T.,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

Progressive Hemifacial Atrophy
Arch Neurol 39:44-46, Asher,S.W.,et al, 1982

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

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

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

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

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

Neurological Disease In Ex-Far-East Prisoners Of War
Lancet 2:135-137, Gibberd,F.B.,et al, 1980

Acne Fulminans with Inflammatory Myopathy
Neurol 8:67-69, Noseworthy,J.H.,et al, 1980

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

Leukaemia:Neurological Involvement
in Handbk of Clinical Neurology, Vinkin PJ & Bruyn GW, Ed, North-Holland Publ Co, Amsterdam 39:1, Yuill,G.M., 1980

Myotonic Dystrophy
In Harrison's Principles of Internal Medicine, 9th Ed, McGraw-Hill Book Co, NY 206180., Adams,R.D.,et al, 1980

Basal Ganglia Calcification in Kearns-Sayre Syndrome
Arch Neurol 36:711-713, Robertson,W.C.Jr., 1979

Quadriceps Myopathy in Two Brothers
Rhode Island Med J 62:125, Finelli,P.F., 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

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

Showing articles 650 to 700 of 3801 << Previous Next >>