Neudle.com: leukocyte enzyme abnormality

Differential
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abdominal muscle paralysis

acetylcholine

acetylcholine in CNS

acid maltase deficiency

acid maltase deficiency, adult

acral sensory symptoms

acyl CoA dehydrogenase deficiency

adenosine deaminase deficiency

adrenoleukodystrophy

adrenomyeloneuropathy

advances in neurology

adverse drug reaction

agalsidase alfa

alopecia

alpha galactosidase A deficiency

aminoacylase 1 deficiency

angiotensin-converting enzyme

anorexia nervosa

anterior horn cell disease

anticonvulsants

anticonvulsants, untoward effects of

apraxia

apraxia of eye movements

aromatic amino acid decarboxylase deficiency

arthropathy

arthropathy, neuropathic

arylsulfatase A

aspartate aminotransferase

autonomic dysfunction

Babinski sign

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavioral disorder

biotin deficiency

biotinidase deficiency

blindness

blood dyscrasias, neurologic findings with

bone marrow transplantation

brainstem, infarction of

brainstem, lesion of

burning feet

burning feet, differential diagnosis of

burning hands

burning paresthesia

calcification, intracranial

calf hypertrophy

Canavan's disease

carbamyl phosphate synthetase-I deficiency

carbidopa

carbonic anhydrase II deficiency

CAT scan, false negative

cataracts

caudate nucleus, lesion of

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar hemorrhage

cerebellar infarction

cerebellar lesion

cerebellar vermis

cerebral cortical atrophy

cerebral infarction, hemorrhagic

cerebral ischemia

cerebral palsy

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, glycine

cerebrospinal fluid, protein of

cerebrospinal fluid, proteincytologic dissociation

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, cryptogenic

cerebrovascular accident, familial occurrence

cerebrovascular accident, infancy and childhood

cerebrovascular accident, non atherosclerotic cause of

cerebrovascular accident, recurrent

cerebrovascular accident, young adult

cerebrovascular disease

cherry red spot

cherry red spot-myoclonus syndrome

children

cholesterol

choline acetyltransferase

choline chloride

choreoathetosis

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

codfish vertebrae

coenzyme Q10 deficiency

coma

compression fracture

confusion

congestive heart failure

cornea, opacification in infancy-causes of

cornea, opacity of

corneal dystrophy

cranial nerve enlargement

cranial nerve palsies

creatine phosphokinase(CPK)elevated

creatinine, elevated

cry, abnormal

crying

cultured skin fibroblasts

cystinuria

cytochrome c oxidase

cytochrome c oxidase, deficiency

deep gray nuclei

deficiency of ADA2

degenerative diseases of CNS

dementia

dementia, presenile

demyelinating disease

dentate nuclei

dentate nuclei, lesion of

developmental milestones, loss of

developmental retardation

diaphragmatic paralysis

diet

distal muscle atrophy

distal muscle weakness

dopa responsive dystonia

dopamine

drooling

dropped head syndrome

dystonic reaction, acute

echolalia

efficacy

electrocardiogram, abnormal

electromyogram

electron microscopy

emergencies, neurologic

encephalopathy

encephalopathy, neonatal

encephalopathy, progressive

enzyme treatment

enzyme, defect

enzyme, muscle disease

epidemiology of neurology

exercise

exercise intolerance

eye movement, disorders of

Fabry's disease

facial anomalies

facial appearance, abnormal

fatty acid, elevated plasma content

feeding disorder

fever

floppy infant

flow study, carotid artery

fornix, lesion of

fracture, pathologic

frontal bossing

frontal lobe, behavior with disease of

frontal lobe, lesion of

fucosidosis

fundus, abnormality of

gangliosidosis GM2-AB variant

genetic diagnosis, prenatal

genetic neurologic disorders

genetic screening

genetic testing

Gilles de la Tourette syndrome

globoid cells

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glucocerebrosidase

glutamate dehydrogenase deficiency

glutaric acidemia

glutaric aciduria

glycine

glycogen debranching enzyme deficiency

glycogen storage disease

glycoprotein

growth retardation

Hallervorden Spatz disease

Hallervorden Spatz disease, late onset

hallucination

hallucination, auditory

headache, progressive

headache, thunderclap

headbanging

hearing loss

heart murmur

hematopoietic tissue, extramedullary

hemianopia, homonymous

hepatic failure

hepatomegaly

hepatosplenomegaly

heralding manifestation

herniated disc, thoracic

hexosaminidase-A

hexosaminidase-A and B

histochemistry

histochemistry of muscle

homocystinuria

Hurler's syndrome

hydrocephalus

hydrocephalus, normal pressure

hydroxytryptophan L-5(L-5 HTP)

hyperammonemic encephalopathy

hypogammaglobulinemia

inborn errors of metabolism

inborn errors of metabolism, screening

inclusion bodies, intracytopasmic

intellectual deterioration

intelligence quotient

internal capsule

internuclear ophthalmoplegia

internuclear ophthalmoplegia, unilateral

intrauterine

iron, brain

irritability

ischemic exercise test

jaundice

Jewish

Kearns-Sayre syndrome

Korsakoff's psychosis

Krabbe's disease

kyphoscoliosis, neurologic causes of

lactate

lacunar infarction

L-dopa

Leber's hereditary optic neuropathy

leg weakness, bilateral

Leigh's disease

Leigh's disease, adult variety

leukocyte enzyme abnormality

leukodystrophy

life expectancy

lipid storage disorder of CNS

livedo reticularis

liver disease

lysosomal storage disease

melanomatosis, primary malignant

MELAS syndrome

memory, defect of recent

mental retardation

mental status, abnormal

MERRF syndrome

mesial temporal lobe

metabolic acidosis

metabolic disorder, primary

metabolic disorder, primary-screening tests

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

microspherophakia

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, CAT scan compared to

MRI, demyelinating disease

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, eye of tiger sign

MRI, hypointense signal foci on

MRI, paramagnetic effect

MRI, vessel wall

MRI, vessel wall enhancement

MRS

mucopolysaccharidoses

multiple sclerosis, differential diagnosis of

multiple system atrophy

muscle atrophy, progressive

muscle phosphofructokinase deficiency

muscle phosphorylase deficiency

muscle spasm

muscle stiffness

muscle wasting, diffuse

muscle weakness

muscle weakness, insidious onset of

muscle weakness, proximal

muscular dystrophy, Duchenne

muscular dystrophy, Duchenne, neonatal screening

myopathy, distal, vacuolar

myopathy, metabolic

myopathy, mitochondrial

myopathy, necrotizing

neonatal screening, genetic neurologic disorders

nerve biopsy

nerve conduction studies

neuraminidase deficiency

neurologic disease, diagnoses of

neurologic examination

neurologic signs

neuropathology

neuropathy

neuropathy, ataxia, retinitis pigmentosa

neuropathy, painful

neuropathy, peripheral

ophthalmoplegia, progressive external

opisthotonus

optic atrophy

optic chiasm, enlarged

optic nerve

optic nerve, enlarged

ornithine transcarbamylase deficiency

paraspinal muscle weakness

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

PAS positive

PAS positive material in the brain

phosphorylase b kinase deficiency

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

polymerase chain reaction

polyneuropathy

Pompe's disease of glycogen storage

precipitating factors

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

prognathism

prognosis

progressive neurologic disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychomotor retardation

psychosis

putamen, lesion of

pyramidal tract

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

pyruvate-kinase deficiency anemia

rash

recurrent

renal failure

renal tubular acidosis

respiratory failure

respiratory tract infection

retinal degeneration

retinopathy

reversible cerebral vasoconstrictive syndromes

reversible neurologic disorder

scoliosis, neurologic association with

screaming

screening

second wind phenomena

seizure

seizure, children

seizure, neonatal

seizure, psychomotor-temporal lobe

self-mutilation

semialdehyde dehydrogenase deficiency

short stature

skin, biopsy

skin, lesions in neurologic disorders

small vessel disease

sodium valproate

sodium valproate, toxicity

somnolence

spasticity

speech disorder

speech disorder, childhood

sphingolipodoses

spinal cord

spinal cord, compression of

spinal cord, lesion of

spinocerebellar ataxia type 1

spinocerebellar degeneration

splenomegaly

spongy degeneration of brain

startle reaction

stem cell transplantation

subarachnoid hemorrhage

subarachnoid hemorrhage, cerebral convexity

substantia nigra

suck, poor

symmetric brain lesions

systemic illness

Tay-Sachs disease

temporal lobe, lesion

term infant

tetrahydrobiopterin

thalamus, lesion of

thalamus, lesion of-bilateral

thiamine

tinnitus

tone, muscle, increased

tongue, enlarged

tongue, weakness

transketolase

treatment of neurologic disorder

tyrosine

tyrosine hydroxylase deficiency

tyrosinemia

umbilical-cord blood transplantation

urea

urea-cycle enzymopathies

uremia

urinary incontinence

urine test for metabolic disorders

urine, dark

vasculitides

vasculopathy

vertebral-basilar insufficiency

weakness, progressive

weakness, proximal

Wernicke's encephalopathy

wheelchair

white matter disease

winging of scapula

Showing articles 450 to 500 of 524 << Previous Next >>

MPTP:A Neurotoxin Relevant to the Pathophysiology of Parkinson's Disease, The 1985 George Cotzias Lecture
Neurol 36:250-258, Snyder,S.H.&D'Amato,R.J., 1986

Narcolepsy & Immunity
BMJ 292:359-360, Parkes,J.D.,et al, 1986

Cerebrospinal Fluid Acetylcholinesterase Activity in Senile Dementia of the Alzheimer Type
Ann Neurol 17:46-48, Tune,L.,et al, 1985

Myocardial Damage from Acute Cerebral Lesions
Stroke 15:990-993, Kolin,A.,et al, 1984

Chediak-Higashi Syndrome
Arch Neurol 41:1001-1002, Pettit,R.E.,et al, 1984

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

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

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

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

Creatine Kinase BB Isoenzyme in CSF in Neurologic Diseases
Arch Neurol 40:169-172, Pfeiffer,F.E.,et al, 1983

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

Multiple Sclerosis, (First of Two Parts)
NEJM 307:1183-1188, 1982, McFarlin,D.E.,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

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

Diagnostic Delay in Duchenne's Muscular Dystrophy
JAMA 247:478-480, Crisp,D.E.,et al, 1982

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

The Genetics of Susceptibility to Multiple Sclerosis
Epidemiol Rev 4:45-65, Spielman,R.S.&Nathanson,N., 1982

Diagnosis & Treatment of Reye's Syndrome
JAMA 246:2441-2444, Dodge,P.R.,et al, 1981

Phenytoin-Induced Methadone Withdrawal
Ann Int Med 94:349-351, Tong,T.G.,et al, 1981

Deprenyl in Parkinson Disease
Neurol 31:19-23, Eisler,T.,et al, 1981

Infection of Collagenase in the Treatment of Herniated Lumbar Disk
JAMA 245:730-732, Sussman,B.J.,et al, 1981

Interaction Between Estrogen & Dilantin In A Menopausal Woman
NEJM 304:788-789, Notelovitz,M.,et al, 1981

Peripheral Source of MB Band of Creatine Kinase in Alcoholic Rhabdomyolysis
JAMA 244:580-582, Siegel,A.J., 1980

Interaction Between Carbamazepine & Warfarin
BMJ 280:1415-1416, Ross,J.R.Y.,et al, 1980

A Family with Hereditary Ataxia:HLA Typing
Neurol 30:12-20, Nino,H.E.,et al, 1980

Hypoparathyroidism & Elevated Muscle Enzymes
Neurol 30:192-195, Shane,E.,et al, 1980

Sensory Neuropathy Associated with Primary Biliary Cirrhosis, Histologic & Morphometric Studies
Arch Neurol 37:84-87, Charron,L.,et al, 1980

Efficacy of Radionuclide Scanning in Patients with Lung Cancer
JAMA 242:2855-2857, Kelly,R.J.,et al, 1979

Valproic Acid, Review of a New Antiepileptic Drug
Arch Neurol 36:393-398, Bruni,J.,et al, 1979

Serum LDH-5 in Carriers of Duchenne Muscular Dystrophy
Neurol 29:239-241, Burt,D.,et al, 1979

Elevated Skeletal-Muscle Enzymes During Quinidine Therapy
NEJM 300:1218, Weiss,M.,et al, 1979

Enzyme Treatment of Spinal Cord Transected Rats
Ann Neurol 5:203-206, Feringa,E.R.,et al, 1979

Acute Hepatic Failure Associated with the Use of Sodium Valproate
NEJM 300:962-966, Suchy,F.J.,et al, 1979

Haemophilic Neuromyopathy
JNNP 42:600-605, Defaria,C.R.,et al, 1979

Insulin-Induced Weakness in Hypokalemic Myopathy
Ann Neurol 6:139-140, Ruff,R.L., 1979

Idiopathic Hypoparathyroidism:A Cause of Fits in the Elderly
BMJ l:1460, Graham,K.,et al, 1979

Creatine Phosphokinase MB Band In Oculopharyngeal Muscular Dystrophy
(Letter) NEJM 301:270979., Diskin,C.J., 1979

Reye's Syndrome in the Adult Patient
Am J Med 67:672-678, Atkins,J.N.,et al, 1979

Lidase Treatment of Spinal Cord Transected Rats
Ann Neurol 6:78-79, Kowalski,T.F.,et al, 1979

Effect of Valproic Acid on Hepatic Function
Neurol 28:961-964, Willmore,L.J.,et al, 1978

HLA & Cogan's Syndrome
NEJM 298:1094, Kaiser-Kuper,M.I.,et al, 1978

Diagnostic Significance of Myeloperoxidase Assay in Neuronal Ceroidlipofuscinoses (Batten-Vogt Syndrome)
Neurol 28:924-927, Pilz,H.,et al, 1978

HLA Antigens in the Landry-Guillain-Barre Syndrome & Chronic Relapsing Polyneuritis
Ann Neurol 4:285-289, Stewart,G.J.,et al, 1978

Cellular Immunity In Guamanians with Amyotrophic Lateral Sclerosis & Parkinsonism-Dementia
NEJM 299:680-685, Hoffman,P.M.,et al, 1978

HLA & Neurologic Fisease
Neurol 28:413, Compston,A., 1978

HLA-B8 in Polymyositis
NEJM 298:1260, Behan,W.M.H.,et al, 1978

Creatine Kinase BB Isoenzyme Levels by Radioimmunoassay in Patients with Neurolological Disease
Ann Neurol 3:52, Bell,R.D.,et al, 1978

Electrocardiographic Changes & Myocardial Damage in Patients with Acute Cerebrovascular Accidents
Stroke 8:448, Dimant,J.,et al, 1977

Cyclic AMP in CSF of Patients with Neurologic Disease
NEJM 296:691, Vapaatalo,H.,et al, 1977

Spinocerebellar Ataxia & HLA Linkage:Risk Prediction by HLA Typing
NEJM 296:1138, Jackson,J.F.,et al, 1977

Showing articles 450 to 500 of 524 << Previous Next >>