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 350 to 400 of 524 << Previous Next >>

Angiotensin-Converting Enzyme Gene Deletion Polymorphism, Risk Factor for Lacune, not Carotid Atheroma
Stroke 26:1329-1333, Markus,H.S.,et al, 1995

Kayser-Fleischer Ring:Hepatolenticular Degeneration (Wilson's Disease)
Neurol 45:1261-1262, Finelli,P.F., 1995

Cerebrospinal Fluid Concentration of Neuron-specific Enolase in Diagnosis of Creutzfeldt-Jakob Disease
Lancet 345:1609-1610, Zerr,I.,et al, 1995

Neurologic manifestations of intravascular lymphomatosis
Acta Neurol Scand 91:494-499, Chapin, J.E.,et al, 1995

Pharmacogenetics and Drug Metabolism of Newer Antidepressant Agents
J Clin Psychiatry 55:38-45, DeVane,C.L., 1994

Clinicopath Conf
Primary Malignant Lymphoma of CNS, Diffuse, Large-Cell]B-Cell Type, Case 36-1994, NEJM 331:861-8684., , 1994

Cerebral Paragonimiasis in Early Active Stage:CT and MR Features
AJR 162:141-145, Cha,S.H.,et al, 1994

Hyperthermia and Heatstroke
Hospital Practice 29:65-68, 73, 78-80994., Simon,H.B., 1994

Neuron-Specific Enolase & Myelin Basic Protein:Relation of CSF Concentr to Neuro Cond of Asphyx Full-Term Infants
Pediatrics 93:234-240, Garcia-Alix,A.,et al, 1994

Hepatotoxic Effects of Tacrine Administration in Patients with Alzheimer's Disease
JAMA 271:992-998, Watkins,P.B.,et al, 1994

30-Week Randomized Controlled Trial of High-Dose Tacrine in Patients with Alzheimer's Disease
JAMA 271:985-991, 10231994., Knapp,M.J.,et al, 1994

Albendazole in Single CT Ring Lesions in Epilepsy
Neurol 44:1344-1346, Padma,M.V.,et al, 1994

Osteomalacic Myopathy
Muscle & Nerve 17:578-580994., Russell,J.A., 1994

Clinicopath Conf
Polyarteritis Nodosa, with Neuropathy, Case 40-1994, NEJM 331:1293-130094., , 1994

Practice Parameter for Diagnosis and Evaluation of Dementia (Summary Statement) Alter
M. , et al, Neurol 44:2203-220694., , 1994

Molecular Genetic Heterogeneity of Myophosphorylase Deficiency (McArdle's Disease)
NEJM 329:241-245, Tsujino,S.,et al, 1993

Epilepsy and Pregnancy
BMJ 307:492-495, O'Brien,M.D.&Gilmour-White,S., 1993

Diag of Occult Muscular Dystrophy:"Chance"Finding of Elevated Serum Aminotransferase Act
J Pediatr 122:254-256, Morse,R.P.&Rosman,N.P., 1993

Hyperintense Globus Pallidus on T1-Weighted MRI in Cirrhotic Pts is Associated with Severity of Liver Failure
Neurol 43:65-69, Pujol,A.,et al, 1993

Effects of Tocopherol and Deprenyl on the Progression of Disability in Early Parkinson's Disease
The Parkinson Study Group, NEJM 328:176-1831993., , 1993

Human Leukocyte Antigens in Fisher's Syndrome
Ann Neurol 33:655-657, Yuki,N.,et al, 1993

Detection of Borrelia Burgdorferi Antigens in Cerebrospinal Fluid
Neurol 43:1093-1097, Coyle,P.K.,et al, 1993

Clinicopath Conf
Cysticercosis Involving Basal Cisterns of Brain, Case 8-1993, NEJM 328:566-573993., , 1993

MR and CT Findings in Cerebral Sparganosis
J Comput Assist Tomogr 17:989-990, Kradel,J.,et al, 1993

Neurosarcoidosis:Progress and Clinical Aspects
Neurol 43:8-12, Scott,T.F., 1993

Skeletal Muscle Toxoplasmosis in Patients with Acquired Immunodeficiency Syndrome:A Clinicopath Study
Ann Neurol 32:535-542, Gherardi,R.,et al, 1992

A Controlled Trial of Tacrine in Alzheimer's Disease
JAMA 268:2523-2529, 25641992., Farlow,M.,et al, 1992

Recurrent Transverse Myelitis, Myasthenia Gravis, and Autoantibodies
Ann Neurol 32:407-409, Lindsey,J.W.,et al, 1992

Absence of Cyme Borreliosis Among Patients with Presumed Bell's Palsy
Arch Neurol 49:940-943, Kuiper,H.,et al, 1992

Complications of Acute Stroke
Lancet 339:721-724, Oppenheimer,S.&Hachinski,V., 1992

Immunodiagnosis of Neurocysticercosis
Arch Neurol 49:633-636, Ramos-Kuri,M.,et al, 1992

Release of Superoxide Dismutase Into CSF as a Marker of Brain Lesion in Acute Cerebral Infarction
Stroke 23:515-518, Strand,T.&Marklund,S.L., 1992

Idiopathic Childhoos Stroke is Associated with Human Leukocyte Antigen (HLA) -B51
Ann Neurol 31:675-677, Mintz,M.,et al, 1992

Polymorphonuclear Leukocytes and Monocytes/Macrophages in the Pathogenesis of Cerebral Ischemia and Stroke
Stroke 23:1367-1379, Kochanek,P.M.&Hallenbeck,J.M., 1992

Wilson Disease
Medicine 71:139-164, Brewer,G.J.&Yuzbasiyan-Gurkan,V., 1992

Myelopathy Associated with Human T Cell Lymphotropic Virus Type 1 in a White European Native to England
BMJ 305:453, Ali,A.&Rudge,P., 1992

Deprenyl Effects of Levodopa Pharmacodynamics, Mood, and Free Radical Scavenging
Neurol 42:541-544, Baronti,F.,et al, 1992

Phenytoin and Carbamazepine Decrease Oral Bioavailability of Praziquantel
Neurol 42:492-496, Bittencourt,P.R.M.,et al, 1992

ELISA Quantitation of Dystrophin for the Diagnosis of Duchenne and Becker Muscular Dystrophies
Neurol 42:570-576, Byers,T.J.,et al, 1992

Conjugal Multiple Sclerosis:Immunogenetic Characterization and Analysis of T-and B-Cell Reactivity to Myelin Proteins
Neurol 42:577-582, Frederickson,S.,et al, 1992

Nervous System Lyme Borreliosis-Revisited
Arch Neurol 49:102-107, Finkel,M.J.&Halperin,J.J., 1992

Central Nervous System Abnormalities in Lyme Neuroborreliosis
Neurol 41:1571-1582, Halperin,J.J.,et al, 1991

Central-Nervous-System Demyelination after Immunisation with Recombinant Hepatitis B Vaccine
Lancet 338:1174-1175, Herroelen,L.,et al, 1991

Wilson Disease:Clinical Presentation, Treatment, and Survival
Ann Int Med 115:720-726, Stremmel,W.,et al, 1991

Eosinophilia-Myalgia Syndrome, A Clinical Case Series of 21 Patients
Arch Int Med 151:533-537, Philen,R.M.,et al, 1991

Polymyositis, Dermatomyositis, and Inclusion-Body Myositis
NEJM 325:1487-1498, Dalakas,M.C., 1991

Localization of Idiopathic Generalized Epilepsy on Chromosome 6p in Families of Juvenile Myoclonic epilepsy patients
Neurol 41:1651-1655, Durner,M.,et al, 1991

Clinicopath Conf
Renal Cholesterol Embolism (after CABG) , Case 2-1991, NEJM 324:113-1201., , 1991

Anomalous Molecular Form of Acetylcholinesterase in CSF in Histologically Diagnosed Alzheimer's Disease
Lancet 337:447-450, Navaratnam,D.S.,et al, 1991

Ticlopidine
Editorial, Lancet 337:459-4601991., , 1991

Showing articles 350 to 400 of 524 << Previous Next >>