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Differential
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abdominal muscle paralysis

acetylcholine in CNS

acid maltase deficiency

acid maltase deficiency, adult

acral sensory symptoms

activities of daily living scale

acyl CoA dehydrogenase deficiency

adenosine deaminase deficiency

adrenoleukodystrophy

adrenomyeloneuropathy

advances in neurology

adverse drug reaction

agalsidase alfa

alpha galactosidase A deficiency

alpha glucosidase

Alzheimer's disease

aminoacidopathies

aminoacylase 1 deficiency

anemia, hemolytic

anemia, megaloblastic

angiotensin-converting enzyme

anorexia nervosa

anterior horn cell disease

anticonvulsants

anticonvulsants, blood level determination of

anticonvulsants, untoward effects of

antiviral agents

apraxia of eye movements

aromatic amino acid decarboxylase deficiency

arthropathy, neuropathic

arylsulfatase A

aspartate aminotransferase

ataxia, cerebellar

autonomic dysfunction

B 12 deficiency

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavioral disorder

biotin deficiency

biotinidase deficiency

blood dyscrasias, neurologic findings with

bone demineralization

bone marrow transplantation

brainstem, infarction of

brainstem, lesion of

burning feet, differential diagnosis of

burning paresthesia

calcification, intracranial

calf hypertrophy

Canavan's disease

carbamyl phosphate synthetase-I deficiency

carbonic anhydrase II deficiency

cardiac surgery, neurologic complications with

cardiopulmonary bypass

carnitine deficiency myopathy

CAT scan, abnormal

CAT scan, false negative

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

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, enzymes in

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

ceruloplasmin, serum

cherry red spot

cherry red spot-myoclonus syndrome

chest x-ray, abnormal

choline acetyltransferase

choline chloride

choreoathetosis

chorioretinitis

chromosomal abnormality

cirrhosis, infancy

Clinical Pathologic Conference(C.P.C.)

codfish vertebrae

coenzyme Q10 deficiency

compression fracture

congenital infection, CNS

congenital infection, viral

congestive heart failure

contractures, joint

cornea, opacification in infancy-causes of

cornea, opacity of

corneal dystrophy

cranial nerve enlargement

cranial nerve palsies

creatine phosphokinase(CPK)elevated

creatinine, elevated

cultured skin fibroblasts

cytochrome c oxidase

cytochrome c oxidase, deficiency

cytomegalic inclusion disease

cytomegalovirus infection

cytomegalovirus infection, congenital

deep gray nuclei

deficiency of ADA2

degenerative diseases of CNS

delay in diagnosis

dementia, diagnostic evaluation of

dementia, differential diagnosis of

dementia, presenile

demyelinating disease

dentate nuclei, lesion of

developmental disability

developmental milestones, loss of

developmental retardation

dexterity, impaired

diaphragmatic paralysis

differential diagnosis

difficulty climbing stairs

distal muscle atrophy

distal muscle weakness

dopa responsive dystonia

dropped head syndrome

dysdiadochokinesia

dysostosis multiplex

dystonia, children

dystonic reaction, acute

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

electron microscopy

emergencies, neurologic

emotional lability

encephalopathy, neonatal

encephalopathy, progressive

enzyme inhibition

enzyme treatment

enzyme, induction

enzyme, muscle disease

epidemiology of neurology

esophageal varices

exercise intolerance

eye movement, disorders of

Fabry's disease

facial anomalies

facial appearance, abnormal

facial expression abnormality

facial hypoplasia

facial weakness

failure to thrive

Farber's disease

fatty acid, elevated plasma content

feeding disorder

femoral neuropathy

flow study, carotid artery

fontanel, bulging

fornix, lesion of

fracture, pathologic

frontal bossing

frontal lobe, behavior with disease of

frontal lobe, lesion of

fundus, abnormality of

galactocerebrosidase

gangliosidosis GM1

gangliosidosis GM2

gangliosidosis GM2-AB variant

Gaucher's disease

genetic counselling

genetic diagnosis, prenatal

genetic neurologic disorders

genetic screening

genetic testing

Gilles de la Tourette syndrome

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glucocerebrosidase

glutamate dehydrogenase deficiency

glutaric acidemia

glutaric aciduria

glycogen debranching enzyme deficiency

glycogen storage disease

growth retardation

Hallervorden Spatz disease

Hallervorden Spatz disease, late onset

hallucination, auditory

headache, progressive

headache, thunderclap

hematopoietic tissue, extramedullary

hemianopia, homonymous

hepatic encephalopathy

hepatic failure

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), presymptomatic

hepatosplenomegaly

heralding manifestation

herniated disc, thoracic

hexosaminidase-A

hexosaminidase-A and B

hip flexor weakness

histochemistry of muscle

Hurler's syndrome

hydrocephalus, normal pressure

hydroxytryptophan L-5(L-5 HTP)

hyperammonemic encephalopathy

hyperbilirubinemia

hyperglycinemia

hyperhomocysteinemia

hyperphosphatasia

hypersegmented polys

hypoalbuminemia

hypogammaglobulinemia

hypomyelination

hypoparathyroidism

hypoparathyroidism, idiopathic

hypophosphatemia

hypotonia, infants

ileus, paralytic

immunosuppression

inborn errors of metabolism

inborn errors of metabolism, screening

inclusion bodies, intracytopasmic

infection, recurrent

insulin resistance

intellectual deficit

intellectual deterioration

intelligence quotient

internal capsule

internuclear ophthalmoplegia

internuclear ophthalmoplegia, unilateral

intracranial pressure, increased

intrauterine infection

intrauterine infection, viral

ischemic exercise test

Kayser-Fleischer ring

Kearns-Sayre syndrome

Korsakoff's psychosis

Krabbe's disease

kyphoscoliosis, neurologic causes of

lactic dehydrogenase(LDH)

lacunar infarction

Leber's hereditary optic neuropathy

leg weakness, bilateral

Leigh's disease

Leigh's disease, adult variety

lens, dislocation of

Lesch-Nyhan syndrome

leukocyte enzyme abnormality

life expectancy

lipid storage disorder of CNS

livedo reticularis

liver function enzymes

long bone lesion

lysosomal storage disease

lysosomes, abnoral

McArdle's disease

meconium staining

melanomatosis, primary malignant

memory, defect of recent

mental retardation

mental status, abnormal

mesial temporal lobe

metabolic acidosis

metabolic disorder, primary

metabolic disorder, primary-screening tests

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

methylmalonic acid, serum

methylmalonic acidemia

microspherophakia

migraine, seizures in

mitochondrial disease

mitochondrial encephalomyopathy

molecular genetics

monoamine oxidase inhibitors

motor neuron disease

movement disorder

movement disorder, extrapyramidal

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

mucopolysaccharidoses

multiple sclerosis, differential diagnosis of

multiple system atrophy

muscle atrophy, progressive

muscle hypertrophy

muscle phosphofructokinase deficiency

muscle phosphorylase deficiency

muscle stiffness

muscle strength, testing

muscle wasting, diffuse

muscle weakness

muscle weakness, insidious onset of

muscle weakness, proximal

muscular dystrophy, Duchenne

muscular dystrophy, Duchenne, neonatal screening

myoclonic jerks

myopathy, distal, vacuolar

myopathy, genetic

myopathy, metabolic

myopathy, mitochondrial

myopathy, necrotizing

myopathy, vacuolar

myotonic discharges

nausea and vomiting

neonatal infection, viral

neonatal screening, genetic neurologic disorders

nerve conduction studies

neuraminidase deficiency

neuroendocrinology

neurologic complications of, surgery

neurologic disease

neurologic disease, diagnoses of

neurologic evaluation

neurologic examination

neurologic signs

neuropathy, ataxia, retinitis pigmentosa

neuropathy, iatrogenic

neuropathy, painful

neuropathy, peripheral

neuropathy, sensory

neurotransmitter

nutritional deficiency

oculogyric crisis

ophthalmoplegia

ophthalmoplegia, progressive external

optic chiasm, enlarged

optic nerve, enlarged

ornithine transcarbamylase deficiency

pain, abdominal

paraparesis, spastic

paraspinal muscle

paraspinal muscle weakness

paresthesias, hands

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

PAS positive material in the brain

patient in waiting

pectus excavatum

pediatric neurology

peripheral blood smear, abnormal

pernicious anemia

peroxisomal disease

personality change

phenylketonuria

phosphorylase b kinase deficiency

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

polymerase chain reaction

Pompe's disease of glycogen storage

postpartum coma

postural abnormality

practice guidelines

precipitating factors

pregnancy, anticonvulsants during

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

progressive neurologic disorder

prolactin, elevated

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychomotor retardation

psychotic behavior

pulmonary function tests

pulmonary hypertension

putamen, lesion of

pyramidal tract

pyridoxine deficiency

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

pyruvate-kinase deficiency anemia

renal tubular acidosis

respiratory failure

respiratory tract infection

retinal degeneration

reversible cerebral vasoconstrictive syndromes

reversible neurologic disorder

Reye's syndrome

Sandhoff's disease

Sanfilippo syndrome

scoliosis, neurologic association with

second wind phenomena

seizure, children

seizure, neonatal

seizure, pregnancy

seizure, psychomotor-temporal lobe

self-mutilation

semialdehyde dehydrogenase deficiency

sensorineural hearing loss

serum alanine aminotransferase

skin, lesions in neurologic disorders

slit lamp examination

small for dates infant, problems in

small vessel disease

sodium valproate

sodium valproate, toxicity

speech disorder

speech disorder, childhood

speech, pressured

sphingolipodoses

spinal cord, compression of

spinal cord, lesion of

spinocerebellar ataxia type 1

spinocerebellar degeneration

spongy degeneration of brain

startle reaction

stem cell transplantation

striatum, lesion of

subarachnoid hemorrhage

subarachnoid hemorrhage, cerebral convexity

substantia nigra

symmetric brain lesions

systemic illness

Tay-Sachs disease

temporal lobe, lesion

tetrahydrobiopterin

thalamus, lesion of

thalamus, lesion of-bilateral

thrombocytopenia

thyroid function tests

tone, muscle, increased

tongue, enlarged

tongue, swelling

tongue, weakness

treatment of neurologic disorder

trientine dihydrochloride

type 2 muscle fiber

tyrosine hydroxylase deficiency

ultrasonography, head

umbilical-cord blood transplantation

urea-cycle enzymopathies

urinary incontinence

urine test for metabolic disorders

vertebral-basilar insufficiency

vertigo, episodic

visual impairment

vitamin D deficiency

vitamin deficiency

vitamin, multiple

walking, difficulty with

weakness, progressive

weakness, proximal

Wernicke's encephalopathy

white matter disease

winging of scapula

Showing articles 1150 to 1200 of 1593 << Previous Next >>

Human Leptospirosis-A Review of 50 Cases
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Follow-up and Diagnostic Reappraisal of 75 Patients with Leber's Congenital Amaurosis
Am J Ophthalmol 107:624-631, Lambert,S.R.,et al, 1989

Low Prevalence of Neurological and Neuropsych Abn in Healthy HIV-1-Infected Indiv
Ann Neurol 26:601-611, McArthur,J.C.,et al, 1989

Neurological and Neuropsych Manif of HIV-1:Assoc with ARC not Aympto HIV-1 Infection
Ann Neurol 26:592-600, Janssen,R.S.,et al, 1989

Neuropathology of HIV Infection in Haemophiliacs:Comparative Necropsy Study
BMJ 299:1312-1315, Esiri,M.M.,et al, 1989

Pergolide and Selegiline for Parkinson's Disease
The Medical Letter, 31:81-841989., , 1989

Dopa Responsive Dystonia:A Treatable Condition Misdiagnosed as Cerebral Palsy
BMJ 298:1019-1020, Boyd,K.&Patterson,V., 1989

Cognitive Impairments Associated with Early Parkinson's Disease
Neurol 39:557-561, Levin,B.E.,et al, 1989

Long-Term Efficacy and Safety of Deprenyl (Selegiline) in Advanced Parkinson's Disease
Neurol 39:1109-1111, Golbe,L.I.,et al, 1989

Clinical-Pathologic Correlation in Huntington's Disease:A Neuropsychological and Computed Tomography Study
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Neonatal Seizures
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Bilateral Central Macrogyria:Epilepsy, Pseudobulbar Palsy, and Mental Retardation-A Migration Disorder
Ann Neurol 25:547-554, Kuzniecky,R.,et al, 1989

Brain Damage and Open-Heart Surgery
Editorial, Lancet 2:364-3661989., , 1989

AIDS and the Nervous System
JAMA 261:2396-2399, Dalakas,M.,et al, 1989

The Acquired Immunodeficiency Syndrome (AIDS) Dementia Complex
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Clinicopath Conf
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Lyme Disease
NEJM 321:586-596, Steere,A.C., 1989

Diagnosis of Lyme Disease
Editorial, Lancet 2:198-1991989., , 1989

Magnetic Resonance Imaging and Clinical Correlates of Intellectual Impairment in Myotonic Dystrophy
Arch Neurol 46:536-540, Huber,S.J.,et al, 1989

Congenital Muscular Dystrophy
J Pediatr 115:214-221, Leyten,Q.H.,et al, 1989

Cognitive Loss in Multiple Sclerosis
Arch Neurol 46:162-167, Franklin,G.M.,et al, 1989

Magnetic Resonance Imaging in Pathologically Proven Hallervorden-Spatz Disease
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The Olfactory and Cognitive Deficits of Parkinson's Disease:Evidence for Independence
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Neuropsychological Test Findings in Subjects with Leukoaraiosis
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Ethanol and the Nervous System
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Maternal Alcohol Use During Breast-Feeding and Infant Mental and Motor Development at One Year
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Neurological Outcome after Out-of-Hospital Cardiac Arrest, Prediction by Cerebrospinal Fluid Enzyme Analysis
Arch Neurol 46:753-756, Roine,R.O.,et al, 1989

Neurofibromatosis Type 1 (Recklinghausen's Disease) , Neurologic and Cognitive Assessment
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Persistent Cognitive Impairment in Climbers after Repeated Exposure to Extreme Altitude
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Human Immunodeficiency Virus (HIV) Infection and the Nervous System:Report from The American Academy of Neurology AIDS Task Force
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Selegiline Use to Prevent Progression of Parkinson's Disease
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Neurologic Status and Intracranial Hemorrhage in Very-Low-Birth Weight Preterm Infants
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Abnormal Blood Clotting after Head Injury
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Congenital AIDS:Review of Neurological Problems
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Sulfite Oxidase Deficiency:Clinical, Neuroradiologic, and Biochemical Features in Two New Patients
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Retinitis Pigmentosa
Surv Ophthalmol 33:137-177, Pagon,R.A., 1988

Emery-Dreifuss Muscular Dystrophy:Disease Spectrum and Differential Diagnosis
Neuropediatrics 19:62-71, Voit,T.,et al, 1988

The Peroxisome:Nervous System Role of a Previously Underrated Organelle, The 1987 Robert Wartenberg Lecture
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Dementia and Cognitive Impairment in Parkinson's Disease
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Clinicopath Conf
Lyme Disease, Case Record 51-1988, NEJM 319:1654-1662988., , 1988

Outcome of Neonatal Strokes
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Cyclosporin Neurotoxicity in Cardiac Transplant Recipients
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Internuclear Ophthalmoplegia in Pernicious Anaemia
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Effect of Vitamin E Deficiency on Neurologic Function in Patients with Cystic Fibrosis
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Pediatric Acquired Immunodefieiency Syndrome
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Showing articles 1150 to 1200 of 1593 << Previous Next >>