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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

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

angiotensin-converting enzyme

anorexia nervosa

anterior horn cell disease

anticonvulsants

anticonvulsants, untoward effects of

apraxia of eye movements

aromatic amino acid decarboxylase deficiency

arthropathy, neuropathic

arylsulfatase A

aspartate aminotransferase

ataxia, cerebellar

autonomic dysfunction

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavioral disorder

biotin deficiency

biotinidase deficiency

blood dyscrasias, neurologic findings with

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

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, 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

choline acetyltransferase

choline chloride

choreoathetosis

chromosomal abnormality

cirrhosis, infancy

Clinical Pathologic Conference(C.P.C.)

codfish vertebrae

coenzyme Q10 deficiency

compression fracture

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

deep gray nuclei

deficiency of ADA2

degenerative diseases of CNS

dementia, presenile

demyelinating disease

dentate nuclei, lesion of

developmental milestones, loss of

developmental retardation

diaphragmatic paralysis

distal muscle atrophy

distal muscle weakness

dopa responsive dystonia

dropped head syndrome

dysostosis multiplex

dystonia, children

dystonic reaction, acute

electrocardiogram, abnormal

electron microscopy

emergencies, neurologic

encephalopathy, neonatal

encephalopathy, progressive

enzyme treatment

enzyme, muscle disease

epidemiology of neurology

exercise intolerance

eye movement, disorders of

Fabry's disease

facial anomalies

facial appearance, abnormal

facial hypoplasia

facial weakness

failure to thrive

Farber's disease

fatty acid, elevated plasma content

feeding disorder

flow study, carotid artery

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 failure

hepatosplenomegaly

heralding manifestation

herniated disc, thoracic

hexosaminidase-A

hexosaminidase-A and B

histochemistry of muscle

Hurler's syndrome

hydrocephalus, normal pressure

hydroxytryptophan L-5(L-5 HTP)

hyperammonemic encephalopathy

hyperbilirubinemia

hyperglycinemia

hyperhomocysteinemia

hypogammaglobulinemia

hypomyelination

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

ischemic exercise test

Kearns-Sayre syndrome

Korsakoff's psychosis

Krabbe's disease

kyphoscoliosis, neurologic causes of

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

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

microspherophakia

mitochondrial disease

mitochondrial encephalomyopathy

molecular genetics

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 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, metabolic

myopathy, mitochondrial

myopathy, necrotizing

myopathy, vacuolar

nausea and vomiting

neonatal screening, genetic neurologic disorders

nerve conduction studies

neuraminidase deficiency

neurologic disease, diagnoses of

neurologic examination

neurologic signs

neuropathy, ataxia, retinitis pigmentosa

neuropathy, painful

neuropathy, peripheral

neurotransmitter

oculogyric crisis

ophthalmoplegia

ophthalmoplegia, progressive external

optic chiasm, enlarged

optic nerve, enlarged

ornithine transcarbamylase deficiency

paraparesis, spastic

paraspinal muscle

paraspinal muscle weakness

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

PAS positive material in the brain

pectus excavatum

pediatric neurology

peroxisomal disease

phenylketonuria

phosphorylase b kinase deficiency

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

polymerase chain reaction

Pompe's disease of glycogen storage

postpartum coma

postural abnormality

precipitating factors

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

progressive neurologic disorder

prolactin, elevated

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychomotor retardation

putamen, lesion of

pyramidal tract

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, psychomotor-temporal lobe

self-mutilation

semialdehyde dehydrogenase deficiency

skin, lesions in neurologic disorders

small vessel disease

sodium valproate

sodium valproate, toxicity

speech disorder

speech disorder, childhood

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

tone, muscle, increased

tongue, enlarged

tongue, weakness

treatment of neurologic disorder

tyrosine hydroxylase deficiency

umbilical-cord blood transplantation

urea-cycle enzymopathies

urinary incontinence

urine test for metabolic disorders

vertebral-basilar insufficiency

vertigo, episodic

vitamin deficiency

weakness, progressive

weakness, proximal

Wernicke's encephalopathy

white matter disease

winging of scapula

Showing articles 400 to 450 of 524 << Previous Next >>

Rapid Diagnosis of Tuberculous Meningitis by Polymerase Chain Reaction
Lancet 337:5-7, Shankar,P.,et al, 1991

Clinicopath Conf
Hepatic Encephalopathy in a 40-Year-Old Woman, Am J Med 90:374-3801991., , 1991

Glucosephosphate Isomerase as a CSF Marker for Leptomeningeal Metastasis
Neurol 41:395-398, Newton,H.B.,et al, 1991

The Evaluation of Patients with Human Immunodeficiency Virus-Related Disorders and Brain Mass Lesions
Arch Int Med 151:1381-1384, Cimino,C.,et al, 1991

Clinicopath Conf
Thrombotic Thrombocytopenic Purpura, Case 30-1991, NEJM 325:265-273991., , 1991

Clinicopath Conf
CA of Lung, DIC, Marantic Endocarditis, Multiple CVA's, Case 36-1991, NEJM 325:714-726., , 1991

Conjugal Multiple Sclerosis:A Clinical and Laboratory Study
Neurol 41:1320-1321, Finelli,P.F., 1991

Tacrine in Alzheimer's Disease
Lancet 337:989-992, Eagger,S.A.,et al, 1991

Sarcoidosis of the Nervous System, A Clinical Approach
Arch Int Med 151:1317-1321, Sharma,Om.P.&Sharma,A.D., 1991

Lyme Neuroborreliosis:Diagnostic Assay for Intrathecal Synthesis of Borrelia Burgdorferi-Specific IgG, A, and M
Ann Neurol 30:197-205, Hansen,K.&Lebech,A., 1991

Clinical Follow-Up and Immunogenetic Studies of 32 Patients with Eosinophilia-Myalgia Syndrome
Lancet 337:1071-1074, Kaufman,L.D.,et al, 1991

Clinical & Laboratory Findings in the Oculocerebrorenal Syndrome of Lowe, with Special Ref to Growth & Renal Function
NEJM 324:1318-1325, Charnas,L.R.,et al, 1991

A Case of Herpes Zoster Myelitis:Positive Magnetic Resonance Imaging Finding
Eur Neurol 31:164-167, Hwang,Y.M.,et al, 1991

Neurosarcoidosis:Signs, Course and Treatment in 35 Confirmed Cases
Medicine 69:261-276, Chapelon,C.,et al, 1990

Risk Factors for Multiple Sclerosis:Race or Place? Editorial
JNNP 53:821-823, 903, 906990., Compston,A., 1990

Extraneural Manifestations of Chronic Inflammatory Demyelinating Polyradiculoneuropathy
Am J Med 89:531-534, Romanick-Schmiedl,S.,et al, 1990

New Uses and Old for Carbamazepine
Patient Care 24:48-81, Browne,T.R.,et al, 1990

A Long-Term Prospective Study of Optic Neuritis:Evaluation of Risk Factors
Ann Neurol 27:386-393, Sandberg-Wollheim,M.,et al, 1990

Dantrolene Sodium and Hepatic Injury
Neurol 40:1427-1432, Chan,C.H., 1990

Narcolspey
NEJM 323:389-394, Aldrich,M.S., 1990

The Widening Spectrum of Infectious Neurological Disease
JNNP 53:629-632, Kennedy,P.G., 1990

Association of the Eosinophilia-Myalgia Syndrome with the Ingestion of Tryptophan
NEJM 322:869-873, 9261990., Hertzman,P.A.,et al, 1990

Cerebrospinal Fluid Lactate Dehydrogenase Levels in Early Stroke and Transient Ischemic Attacks
Stroke 21:854-857, Lampl,Y.,et al, 1990

Clinicopath Conf
Malignant Angioendotheliomatosis, Am J Med 88:522-5281990., , 1990

Clinicopath Conf
Sarcoidosis of CNS and Mediastinal Lymph Nodes, Case Record 6-1990, NEJM 322:388-397990., , 1990

Characteristics of Narcolepsy in Preteenaged Children
Pediatrics 85:205-209, Kotalgal,S.,et al, 1990

Familial Patterns of Narcolepsy
lancet 2:1376-1379, Guilleminault,C.,et al, 1989

Narcolepsy Associated with Lesions of the Diencephalon
Neurol 39:1505-1508, Aldrich,M.S.&Naylor,M.W., 1989

Human Ehrlichiosis Associated with Cerebrospinal Fluid Pleocytosis:A Case Presentation
Am J Med 87:677-678, Dimmitt,D.C.,et al, 1989

Selegiline Use to Prevent Progression of Parkinson's Disease
Arch Neurol 46:1275-1279, Elizan,T.S.,et al, 1989

Abnormal Blood Clotting after Head Injury
Editorial, Lancet 2:957-9581989., , 1989

Lyme Disease:Of Ticks and Titers
J Pediatr 114:328-333, Eichenfield,A.H.&Athreya,B.H., 1989

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

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

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

Clinicopath Conf
HTLV-I Infection, with Adult T-Cell Lymphoma and Tropical Spastic Paraparesis, Case 36-2989, NEJM 32, :6675,1989., 1989

Lyme Disease
NEJM 321:586-596, Steere,A.C., 1989

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

Human Leptospirosis-A Review of 50 Cases
Infection 17:10-14, Lecour,H.,et al, 1989

Hypoparathyroidism
Cecil Textbook of Medicine 18th Ed, W B Saunders Co, Phila, p149688., Arnaud,C.D., 1988

Reduced Felodipine Bioavailability in Pts Taking Anticonvulsants
Lancet 2:480-482, Capewell,S.,et al, 1988

Gene Studies in Newborn Males with Duchenne Muscular Dystrophy Detected by Neonatal Screening
Lancet 2:425-427, Greenberg,C.R.,et al, 1988

Clinicopath Conf
Lyme Disease, Case Record 51-1988, NEJM 319:1654-1662988., , 1988

Genetic Factors in Myasthenia Gravis:A Family Study
Neurol 38:38-42, Kerzin-Storrar,L.,et al, 1988

Lyme Disease, A Neuro-Ophthalmologic View
J Clin Neuro-ophthalmol 7:185-190, MacDonald,A.B., 1987

Carbamazepine Side Effects in Children and Adults
Pellock. J. M. , Epilepsia 28:S64-S707., , 1987

Cholesterol Crystal Embolization:A Review of 221 Cases in the English Literature
Angiology 38:769-784, Fine,M.J.,et al, 1987

Acute Arsenic Intoxication Presenting as Guillain-Barre-Like Syndrome:Donofrio
P. D. , et al, Muscle & Nerve 10:114-120, , 1987

Clinicopath Conf
Malignant Lymphoma, Intravascular, Large-Cell, Immunoblastic type (Malignant Angioendotheliomatosis), , Case86,NEJM 315:874-885,1986., 1986

Temporal Arteritis After Normalization of Erythrocyte Sedimentation Rate in Polymyalgia Rheumatica
Arch Int Med 146:2283-2284, Papadakis,M.A.&Schwartz,N.D., 1986

Showing articles 400 to 450 of 524 << Previous Next >>