Neudle.com: white blood cell enzyme abnormality

Differential
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abdominal muscle paralysis

acetylcholine

acetylcholine in CNS

acid maltase deficiency

acid maltase deficiency, adult

aciduria

acral sensory symptoms

acyl CoA dehydrogenase deficiency

adenosine deaminase deficiency

adrenoleukodystrophy

adrenomyeloneuropathy

advances in neurology

adverse drug reaction

agalsidase alfa

agranulocytosis

alopecia

alpha galactosidase A deficiency

aminoacylase 1 deficiency

angiography, cerebral, negative

angiography, neurologic complications with

angiokeratoma

angiotensin-converting enzyme

anterior horn cell disease

anticholinergic drugs

anticoagulant, complications of

anticonvulsants

anticonvulsants, hypersensitivity syndrome

anticonvulsants, untoward effects of

antiphospholipid antibodies

anxiety

apraxia

apraxia of eye movements

areflexia

aromatic amino acid decarboxylase deficiency

arthropathy, neuropathic

arylsulfatase A

ascending paralysis

ascites

aspartate aminotransferase

atherosclerosis, generalized

athetosis

autism

autonomic dysfunction

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basophilic stippling of red blood cells

behavioral disorder

biotin deficiency

biotinidase deficiency

blindness

blood dyscrasias, neurologic findings with

bone marrow infarction

bone marrow necrosis

bone marrow suppression

bone marrow transplantation

brain atrophy

brain biopsy

brain biopsy, false negative

brain purpura

brainstem

brainstem, infarction of

burning feet, differential diagnosis of

burning hands

burning paresthesia

cachexia

calcification, intracranial

calf hypertrophy

Canavan's disease

cancer, cerebrovascular accident complicating patients with

carbamazepine

carbamazepine, toxicity

carbamyl phosphate synthetase-I deficiency

carbidopa

carbonic anhydrase II deficiency

carcinoma

carcinoma of lung

cardiac catheterization, neurologic complications

cardiac surgery, neurologic complications with

CAT scan, false negative

cataracts

caudate nucleus, lesion of

CD4 counts

central nervous system, infection of

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar hemorrhage

cerebellar infarction

cerebellar lesion

cerebellar vermis

cerebral cortical atrophy

cerebral embolism

cerebral embolism, cardiac origin

cerebral embolism, multiple

cerebral infarction

cerebral infarction, hemorrhagic

cerebral infarction, subcortical

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

cerebrospinal fluid, xanthochromia of

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, bilateral

cerebrovascular accident, cryptogenic

cerebrovascular accident, familial occurrence

cerebrovascular accident, infancy and childhood

cerebrovascular accident, multiple

cerebrovascular accident, non atherosclerotic cause of

cerebrovascular accident, recurrent

cerebrovascular accident, young adult

cerebrovascular disease

cerebrovascular disease, rapidly progressive

ceruloplasmin, serum

chemotherapy, CNS treatment and complications with

cherry red spot

cherry red spot-myoclonus syndrome

chest pain

chest x-ray, abnormal

children

cholesterol

choline acetyltransferase

choline chloride

chorea

choreoathetosis

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

coagulopathy

codfish vertebrae

coenzyme Q10 deficiency

congestive heart failure

copper metabolism, abnormal

coprolalia

cornea, opacification in infancy-causes of

cornea, opacity of

corneal dystrophy

coronary artery bypass

corpus callosum, infarction of

cortical blindness

cough

cranial nerve enlargement

cranial nerve palsies

crawl regression

C-reactive protein, elevated

creatine phosphokinase isoenzyme elevation

creatine phosphokinase(CPK)elevated

creatinine, elevated

cry, abnormal

crying

cultured skin fibroblasts

cytochrome c oxidase, deficiency

degenerative diseases of CNS

dehydration

dementia

dementia, presenile

demyelinating disease

dentate nuclei

dentate nuclei, lesion of

depression

dermatitis

developmental milestones, loss of

developmental retardation

diaphragmatic paralysis

diarrhea

diet

disorientation

disseminated intravascular coagulation(DIC)

distal muscle atrophy

distal muscle weakness

dopa responsive dystonia

dopamine

doxycycline

drooling

dropped head syndrome

dystonic reaction, acute

ejection fraction, abnormal

electrocardiogram, abnormal

electromyogram

electron microscopy

embolism

embolism, atheromatous

embolism, cholesterol

embolism, fat

embolism, retinal

emergencies, medical

emergencies, neurologic

encephalomyelitis

encephalopathy

encephalopathy, acute

encephalopathy, neonatal

encephalopathy, progressive

endemic area

endocarditis

endocarditis, marantic

enteritis

enzyme treatment

enzyme, defect

enzyme, muscle disease

enzyme, serum

eosinophilia

epidemiology of neurology

epistaxis

Epstein-Barr virus

Epstein-Barr virus, negative

eye movement, disorders of

Fabry's disease

facial anomalies

facial appearance, abnormal

facial expression abnormality

fatty acid, elevated plasma content

feeding disorder

femoral artery catheterization

ferritin, elevated

fever

fibrin split products

fingernails, abnormal

floppy infant

flow study, carotid artery

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

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Hallervorden Spatz disease

Hallervorden Spatz disease, late onset

hallucination

hallucination, auditory

headache, progressive

headache, severe

headache, thunderclap

heavy metal intoxication

hematopoietic tissue, extramedullary

hematuria, microscopic

hemianopia, homonymous

hemiplegia

hemoglobin abnormality, neurologic complications of

hemoglobinuria

hemolytic-uremic syndrome

hepatic encephalopathy

hepatic failure

hepatitis

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), presymptomatic

hepatolenticular degeneration(Wilson's disease), screening for

hepatomegaly

hepatosplenomegaly

heralding manifestation

herniated disc, thoracic

heterophile antibody test

hexosaminidase-A

hexosaminidase-A and B

histochemistry

histochemistry of muscle

homocystinuria

homosexual

human granulocytic anaplasmosis

human immunodeficiency virus type 1

human immunodeficiency virus type 1, acute infection

Hurler's syndrome

hydrocephalus

hydrocephalus, normal pressure

hydroxytryptophan L-5(L-5 HTP)

hyperammonemic encephalopathy

hypersensitivity reaction

hypogammaglobulinemia

hypoglycemia

hypoglycorrhachia

hypokalemia

hypokalemic paralysis

iatrogenic neurologic disorders

ileus, paralytic

imbalance

immunosuppression

immunosuppressive agents

inborn errors of metabolism

inborn errors of metabolism, screening

inclusion bodies, intracytopasmic

incoordination

infection

infection, recurrent

infectious mononucleosis

insulin resistance

intellectual deficit

intellectual deterioration

intelligence quotient

interferon

interferon antibodies

interferon beta 1-a

interferon beta 1-b

internal capsule

internuclear ophthalmoplegia

internuclear ophthalmoplegia, unilateral

intracerebral hemorrhage

intrauterine

iron, brain

irritability

ischemic exercise test

jaundice

jaw pain

Jewish

Kayser-Fleischer ring

Kearns-Sayre syndrome

Korsakoff's psychosis

Krabbe's disease

kyphoscoliosis, neurologic causes of

lactate

lactic dehydrogenase(LDH)

lacunar infarction

lamotrigine

L-dopa

Leber's hereditary optic neuropathy

leg weakness, bilateral

Legionella pneumophilia

Legionnaires'disease

Leigh's disease

Leigh's disease, adult variety

leukemia, neurologic findings assoc.with

leukocyte enzyme abnormality

lipid storage disorder of CNS

livedo reticularis

liver disease

liver function enzymes

liver transplantation

lymph node biopsy

lymphadenopathy

lymphadenopathy, axillary

lymphadenopathy, cervical

lymphadenopathy, paraaortic

lymphocytic choriomeningitis

lymphocytosis

lymphoma

lymphoma involving CNS

lymphopenia

lysosomal storage disease

lysosomes, abnoral

macrocephaly

malaise

malignant hyperpyrexia

melanomatosis, primary malignant

MELAS syndrome

memory, defect of recent

meningitis

meningitis, aseptic

meningitis, plasma cell

menses

menses, irregular

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

microangiopathic hemolytic anemia

microhemorrhage, intracerebral

microspherophakia

mimics

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

mitoxantrone

mitral valve vegetation

movement disorder, drug induced

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, false negative

MRI, gradient-echo

MRI, hypointense signal foci on

MRI, negative

MRI, paramagnetic effect

MRI, spine

MRI, susceptibility weighted

MRI, vessel wall

MRI, vessel wall enhancement

MRS

mucopolysaccharidoses

multiple sclerosis

multiple sclerosis, children

multiple sclerosis, differential diagnosis of

multiple sclerosis, early onset

multiple sclerosis, relapsing

multiple sclerosis, treatment 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

mycoplasma

mycoplasma pneumoniae

myopathy, distal, vacuolar

myopathy, metabolic

myopathy, mitochondrial

myopathy, necrotizing

neonatal screening, genetic neurologic disorders

neoplastic angioendotheliosis

nerve biopsy

nerve conduction studies

neuraminidase deficiency

neuritis, heavy metals causing

neuroleptic

neuroleptic malignant syndrome

neurologic complications

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic examination

neurologic signs

neuromuscular disease, electrodiagnosis of

neuropathology

neuropathy

neuropathy, ataxia, retinitis pigmentosa

neuropathy, painful

neuropathy, peripheral

neuropathy, toxic

neurotransmitter

neutropenia

nonsteroidal anti-inflammatory drug

ophthalmoplegia, progressive external

opisthotonus

opportunistic infection

optic atrophy

optic chiasm, enlarged

optic nerve

optic nerve, enlarged

optic neuritis

organ donor

organ transplantation

ornithine transcarbamylase deficiency

paraspinal muscle weakness

paresthesias, feet

paresthesias, hands

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

PAS positive

PAS positive material in the brain

pathology

patient information and support

peripheral blood smear

peripheral blood smear, abnormal

phosphorylase b kinase deficiency

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

pleural effusion

pneumonia

polymerase chain reaction

polyneuropathy

Pompe's disease of glycogen storage

porphyria

position sensation, abnormal

postpartum

postpartum coma

postural abnormality

precipitating factors

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

prognathism

prognosis

progressive neurologic disorder

prolactin, elevated

proprioception, abnormal

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychomotor retardation

psychosis

pulmonary function tests

pulmonary infiltrates

putamen, lesion of

pyramidal tract

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

pyruvate-kinase deficiency anemia

renal transplantation

renal tubular acidosis

respiratory failure

respiratory tract infection

retinal degeneration

retinal hemorrhages

retinopathy

reversible cerebral vasoconstrictive syndromes

reversible neurologic disorder

salivation, excessive

scoliosis, neurologic association with

screaming

screening

second wind phenomena

sedimentation rate

sedimentation rate, elevated

seizure

seizure, children

seizure, drug-induced

seizure, elderly

seizure, neonatal

seizure, psychomotor-temporal lobe

self-mutilation

semialdehyde dehydrogenase deficiency

serologic testing

serositis

serum alanine aminotransferase

serum glutamic oxaloacetic transaminase

skin, lesions in neurologic disorders

slit lamp examination

small vessel disease

sodium valproate

sodium valproate, toxicity

speech disorder, childhood

sphingolipodoses

spinal cord

spinal cord, compression of

spinal cord, lesion of

spinocerebellar ataxia type 1

spinocerebellar degeneration

splenomegaly

splinter hemorrhages

spongy degeneration of brain

startle reaction

stem cell transplantation

steroid

steroid therapy, CNS treatment and complications with

subarachnoid hemorrhage

subarachnoid hemorrhage, cerebral convexity

subcutaneous nodules

substantia nigra

suck, poor

superior cerebellar artery infarction

sweating

sweating, abnormality of

symmetric brain lesions

systemic illness

systemic juvenile idiopathic arthritis

Tay-Sachs disease

temporal lobe, lesion

term infant

tetrahydrobiopterin

thalamus, lesion of

thalamus, lesion of-bilateral

tone, muscle, increased

tongue, enlarged

tongue, weakness

tranquilizers, neurologic complications with

transketolase

transluminal angioplasty, coronary artery

treatment of neurologic disorder

tremor

trientine dihydrochloride

tyrosine

tyrosine hydroxylase deficiency

tyrosinemia

umbilical-cord blood transplantation

unconsciousness

urea

urea-cycle enzymopathies

uremia

urinary casts

urinary incontinence

urinary tract infection

urine test for metabolic disorders

urine test in toxic screen

vertebral-basilar insufficiency

visual acuity, decreased

visual loss

vital capacity

vitamin deficiency

walking, difficulty with

weakness

weakness, generalized

weakness, progressive

weakness, proximal

weight loss

Wernicke's encephalopathy

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Hematopoietic Stem-Cell Transplantation in Globoid-Cell Leukodystrophy
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Follow-up of Nine Patients with Hurler Syndrome After Bone Marrow Transplantation
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Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities
Ann Neurol 39:343-351, Rahman,S.,et al, 1996

Clinical Variability in Adult-Onset Acid Maltase Deficiency:Report of Affected Sibs and Review of Literature
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Dopamine, Dystonia, and the Deficient Co-Factor
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Clinicopath Conf
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Neurol 44:461-466, Wilkinson,D.A.,et al, 1994

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Wilson Disease
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Clinicopath Conf
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Lancet 1:1101, Wierzbicki,A.S.,et al, 1988

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Cholesterol Crystal Embolization:A Review of 221 Cases in the English Literature
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