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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 900 to 950 of 1593 << Previous Next >>

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

Dementia in 2 Histologically Confirmed Cases of MS:One Isolated Dementia & One Assoc with Psychiatric Symptoms
JNNP 57:353-359, Fontaine,B.,et al, 1994

Association of 1800 cGy Cranial Irradiation with Intellectual Function in Children with Acute Lymphoblastic Leukaemia
Lancet 344:224-227, Jankovic,M.,et al, 1994

Mitochondrial Neurogastrointestinal Encephalomyopathy (MMGIE) :Clin Biochem & Genetic Features of Auto Recess Mitochond Disorder
Neurol 44:721-727, Hirano,M.,et al, 1994

Course and Outcome of Acute Cerebellar Ataxia
Ann Neurol 35:673-679, Connolly,A.M.,et al, 1994

Cognitive Effects of Lyme Disease in Children
Pediatr 94:185-189, Adams,W.V.,et al, 1994

Med Trtm of Rasmussen's Syndrome (Chronic Enceph & Epilepsy) :High-Dose Steroids or Immunoglobulins in 19 Pts
Neurol 44:1030-1036, Hart,Y.M.,et al, 1994

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

Motor & Cognitive Devel in Children with Congen Hypothyroidism:A Long-Term Eval of the Effects of Neonatal Treatment
J Pediatr 124:903-909, Kooistra,L.,et al, 1994

Methylmercury Poisoning:Long-Term Clinical, Radiological, Toxicological, and Pathological Studies of an Affected Family
Ann Neurol 35:680-688, Davis,L.E.,et al, 1994

Diagnosis and Management of Pituitary Tumours
BMJ 308:1087-1091, Levy,A.&Lightman,S.L., 1994

Parkinson's Disease
JNNP 57:672-681, Marsden,C.D., 1994

Cystic Periventricular Leukomalacia and Type of Cerebral Palsy in Preterm Infants
J Pediatr 125:S1-S8, Rogers,B.,et al, 1994

Reduced GABA Synthesis in Pyridoxine-Dependent Seizures
Lancet 343:1133-1134, Gospe,S.M.,et al, 1994

Do Young Boys with Fragile X Syndrome have Macroorchidism
Pediatrics 93:992-995, Lachiewicz,A.M.&Dawson,D.V., 1994

MR Imaging of Diseases of the Limbic System
AJR 163:657-665, Tien,R.D.,et al, 1994

Does Carnitine Admin Inprove Symptoms Attributed to Anticonvulsant Meds? Double-Blinded Study
Pediatrics 93:893-895, 8911994., Freeman,J.M.,et al, 1994

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

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

Ganciclovir Therapy for Symptomatic Congenital Cytomegalovirus Infection in Infants:A Two-Regimen Experience
J Pediatr 124:318-322, Nigro,G.,et al, 1994

Prothrombotic States in Young People with Idiopathic Stroke:Prospective Study
Stroke 25:287-290, Baringarrementeria,F., 1994

X1-Antitrypsin Deficiency in Intracranial Aneurysms and Cervical Artery Dissection
Lancet 343, 452-4531994., Schievink,W.I.,et al, 1994

Cerebrotendinous Xanthomatosis:Molecular Diagnosis Enables Presymptomatic Detection of a Treatable Disease
Neurol 44:288-290, Meiner,V.,et al, 1994

Familial Sneddon's Syndrome:Clinical, Hematologic, and Radiographic Findings in Two Brothers
Neurol 44:399-405, Pettee,A.D.,et al, 1994

Congential Deficienty of Factor VII in Subarachnoid Hemorrhage
Stroke 25:508-510, Papa,M.L.,et al, 1994

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

The Neurologic Syndrome of Vitamin E Deficiency:A Significant Cause of Ataxia
Neurol 43:2167-2169, Kayden,H.J., 1993

Serum Folate and Chronic Fatigue Syndrome
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Apathy Following Cerebrovascular Lesions
Stroke 24:1625-1630, Starkstein,S.E.,et al, 1993

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

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

Magnetic Resonance Imaging of Brain and the Neuromotor Disorder in Endemic Cretinism
Ann Neurol 34:91-94, Ma,T.,et al, 1993

Arginase Deficiency Presenting as Cerebral Palsy
Pediatrics 91:995-996, Scheuerle,A.E.,et al, 1993

Neimann-Pick Disease Type C in a Middle-Aged Woman
Neurol 43:1435-1436, Lanska,D.J.&Lanska,M.J., 1993

Functional Abilities at Age 4 Years of Children Born Before 29 Weeks of Gestation
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Neuroleptics, Learning Disability, and the Community:Some History and Mystery
BMJ 307:184-187, Manchester,D., 1993

Alternating Hemiplegia of Childhood
J Pediatr 122:673-679, Bourgeois,M.,et al, 1993

A Predictive Model for Delirium in Hospitalized Elderly Medical Patients Based on Admission Characteristics
Ann Int Med 119:474-481, Inouye,S.K.,et al, 1993

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

Treatment of Convulsive Status Epilepticus
Recommendations of the Epilepsy Foundation of America's Working Group on Status Epilepticus, JAMA 27, :54-859,1993., 1993

Alternating Hemiplegia of Childhood:A Study of 10 Pts & Results of Flunarizine Treatment
Neurol 43:36-41, Silver,K.&Andermann,F., 1993

Effects of Stimulus Intensity & Electrode Placement on Efficacy & Cognition of ECT
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Withdrawal of Antiepileptic Medication in Children-Effects of Congit Funct Multicenter Holmfrid Study
Aldenkamp. A. P. , et al, neurol 43:41-50., , 1993

Fetal Alcohol Syndrome and Fetal Alcohol Effects
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Prenatal Alcohol Exposure and Long-Term Developmental Consequences
Lancet 341:907-910, Spohr,H.,et al, 1993

Population-Based Norms for the Mini-Mental State Examination by Age and Educational Level
JAMA 269:2386-2391, 24201993., Crum,R.M.,et al, 1993

An Unusual Cause of Cerebral Venous Thrombosis in a Four-Year-Old Child
Stroke 24:603-605, Rich,C.,et al, 1993

Abnormal Cranial Magnetic Resonance Imaging Scans in Sickle-Cell Disease
Arch Neurol 50:629-635, Kugler,S.,et al, 1993

Subacute Combined Degen with High Serum Vit B12 Level & Abnormal Vit B12 Binding Protein:New Cause Old Synd
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Cortical Vascular Abnor in Synd of Celiac Disease, Epilepsy, Bilateral Occipital Calc, & Folate Deficiency
Ann Neurol 34:399-403, Bye,A.M.E.,et al, 1993

Showing articles 900 to 950 of 1593 << Previous Next >>