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Differential
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acquired immunodeficiency syndrome

acyl CoA dehydrogenase deficiency

adult polyglucosan body disease

advances in neurology

adverse drug reaction

alcohol, neurologic complications with

arrhythmia, cardiac

atrioventricular block

bladder dysfunction

blood dyscrasias, neurologic findings with

bulimia nervosa

calf hypertrophy

cardiovascular disease

carnitine deficiency myopathy

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

coenzyme Q10 deficiency

congestive heart failure

contractures, joint

creatine kinase

creatine phosphokinase isoenzyme elevation

creatine phosphokinase MB isoenzyme elevation

creatine phosphokinase(CPK)elevated

delay in diagnosis

dermatomyositis

developmental retardation

diagnostic criteria

difficulty climbing stairs

distal muscle atrophy

distal muscle weakness

drug induced neurologic disorders

dystrophic calcification

eating disorder

electrocardiogram, abnormal

enzyme, muscle disease

exercise intolerance

Fabry's disease

femoral neuropathy

fine motor function, impaired

genetic counselling

genetic neurologic disorders

genetic screening

genetic testing

glycogen debranching enzyme deficiency

glycogen storage disease

Gowers maneuver

growth retardation

hip flexor weakness

human immunodeficiency virus type 1

hypoparathyroidism, idiopathic

immunologic disease

immunosuppressive agents

inborn errors of metabolism

inborn errors of metabolism, screening

inclusion bodies

inclusion body myositis

ischemic exercise test

Kearns-Sayre syndrome

Kugelberg-Welander syndrome

lactic dehydrogenase(LDH)

learning disability

learning disability, in children

Leber's hereditary optic neuropathy

leg weakness, bilateral

Leigh's disease

leukocyte enzyme abnormality

leukoencephalopathy

lipid lowering agent

lipid storage disorder of CNS

liver function enzymes

Lowe's syndrome

metachromatic leukodystrophy

mitochondrial disease

mitochondrial encephalomyopathy

motor neuron disease

muscle atrophy, progressive

muscle phosphofructokinase deficiency

muscle phosphorylase deficiency

muscle strength, testing

muscle tenderness

muscle weakness

muscle weakness, causes of

muscle weakness, insidious onset of

muscle weakness, intermediate onset of

muscle weakness, proximal

muscle weakness, sudden onset of

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, central nervous system abnormality

muscular dystrophy, Duchenne

muscular dystrophy, Duchenne, carrier

muscular dystrophy, Duchenne, neonatal screening

muscular dystrophy, Duchenne, presymptomatic detection

myeloneuropathy

myopathy, acute

myopathy, alcoholic

myopathy, distal, vacuolar

myopathy, drug-induced

myopathy, hypokalemic

myopathy, inflammatory

myopathy, metabolic

myopathy, mitochondrial

myopathy, necrotizing

myopathy, vacuolar

neonatal screening, genetic neurologic disorders

nerve conduction studies

neurogenic bladder

neurologic complications of, surgery

neurologic disease, diagnoses of

neuropathy, ataxia, retinitis pigmentosa

neuropathy, sensory

oculopharyngeal muscular dystrophy

ophthalmoplegia, progressive external

paraparesis, spastic

phosphorylase b kinase deficiency

polyglucosan body

polyglucosan body disease

prenatal diagnosis by amniocentesis

progressive neurologic disorder

serum glutamic oxaloacetic transaminase

serum glutamic pyruvic transaminase

skin, lesions in neurologic disorders

speech disorder, childhood

speech, delayed development of

spinal muscular atrophy

spinal muscular atrophy, adult onset

standing difficulty

systemic illness

Tay-Sachs disease

toxoplasma gondii

toxoplasmosis, muscle

treatment of neurologic disorder

type 2 muscle fiber

urinary incontinence

walking, difficulty with

weakness, generalized

weakness, progressive

white matter disease

Showing articles 1100 to 1150 of 1300 << Previous Next >>

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

Small Bowel Resection with Vitamin E Deficiency & Progressive Spinocerebellar Syndrome
Neurol 34:1046-1052, Bertoni,J.M.,et al, 1984

Iatrogenic Causalgia
Arch Neurol 41:821-824, Horowitz,S.H., 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

The Cerebrohepatorenal (Zellweger) Syndrome
NEJM 310:1141-1146, Moser,A.E.,et al, 1984

Neurologic Outcome in Children with Inborn Errors of Urea Synthesis
NEJM 310:1500-1505, Msall,M.,et al, 1984

Treatment of Episodic Hyperammonemia in Children with Inborn Errors of Urea Synthesis
NEJM 310:1630-1634, Brushlow,S.W.,et al, 1984

Neurological Disorders Associated with Deficiency of Glutamate Dehydrogenase
Ann Neurol 15:144-153, Plaitakis,A.,et al, 1984

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

Safe Readministration of Valproate after an Episode of Hepatotoxicity
Ann Neurol 13:688, Ramsay,R.E., 1983

CSF Enzymes in Lacunar & Cortical Stroke
Stroke 14:266-269, Donnan,G.A.,et al, 1983

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

Creatine Kinase BB Isoenzyme in CSF in Neurologic Diseases
Arch Neurol 40:169-172, Pfeiffer,F.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

Phytanic Acid Storage Disease:Hearing Maintained After 15 Years of Dietary Treatment
Neurol 33:237-240, Djupesland,G.,et al, 1983

Reflex Sympathetic Dystrophy (Causalgia) Treatment with Guanethidine
Arch Neurol 40:430-432, Tabira,T.,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

The Early Clinical Manifestations of Lyme Disease
Ann Int Med 99:76-82, Steere,A.C.,et al, 1983

Monocular Polyopia
Arch Neurol 40:756-757, Hirst,L.W.,et al, 1983

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

Pyridoxine Deficiency & Peripheral Neuropathy Associated with Long-Term Phenelzine Therapy
Am J Med 75:887-888, Heller,C.A.,et al, 1983

Clinicopathological Conference
Maroteaux-Lamy Syndrome, Case 44-1983, NEJM 309:1109-1117983., , 1983

Effect of Carbamazepine on Coumadin Metabolism
Ann Neurol 13:691-692, Massey,E.W., 1983

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

Mucopolysaccaridosis IV (Morquio Syndrome) , in The Metabolic Basis of Inherited Disease
(Ed) 5th Ed. , McGraw-Hill, New York, p. 766, Stanbury,J.B., 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

Deprenyl In Parkinson's Disease
Lancet 2:695-696, , 1982

Neuroaxonal Dystrophy in Young Adults:A Clinicopathological Study of Two Unrelated Cases
Ann Neurol 11:335-343, Williamson,K.,et al, 1982

Examination of Dental Pulp to Diagnose Infantile Neuroaxonal Dystrophy
Arch Neurol 39:422-423, Carlo,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

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

Cerebrospinal Fluid:A Selective Review
Ann Neurol 11; 1-101982., Cutler,R.W.P.,et al, 1982

Santavuori Disease:Diagnosis by Leukocyte Ultrastructure
Neurol 32:1277-1281, Baumann,R.J.,et al, 1982

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

Release Of Adenylate Kinase Into CSF During Open-Heart Surgery & Its Relation To Postop. Intellectual Function
Lancet 1:1139-1142, Aberg,T.,et al, 1982

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

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

Heredopathia Atactica Polyneuritiformis
Arch Neurol 38:605-606, Refsum,S., 1981

Diagnosis & Treatment of Reye's Syndrome
JAMA 246:2441-2444, Dodge,P.R.,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

Biochemical Evidence Of Dysfunction Of Brain Neurotransmitters In The Lesch-Nyhan Syndrome
NEJM 305:1106-1111, Lloyd,K.G.,et al, 1981

Showing articles 1100 to 1150 of 1300 << Previous Next >>