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Differential
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abdominal distention

advances in neurology

alcohol intoxication

alcoholic withdrawal states, DT's, convulsions, etc.

aminoacidopathies

aminoacylase 1 deficiency

anesthesia, general

anticoagulant, treatment

aphasia, children

aphasia, global

apraxia, speech

arrhythmia, cardiac

ascending paralysis

ataxia, cerebellar

attention deficit disorder with hyperactivity

autonomic dysfunction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basophilic stippling of red blood cells

bath salts, psychoactive

behavior, combative

behavioral disorder

behavioral disorder, acute

Benedict's solution test

biotin deficiency

biotinidase deficiency

bone marrow suppression

calcification, intracranial

calcium oxalate crystals

Canavan's disease

carnitine deficiency myopathy

CAT scan, abnormal

CAT scan, muscle

cerebral cortical atrophy

cerebral palsy, associated problems with

cerebral palsy, pure ataxic

cerebral venous thrombosis

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, glycine

ceruloplasmin, serum

cervical spondylosis

cherry red spot

chromosomal abnormality

cirrhosis, infancy

Clinical Pathologic Conference(C.P.C.)

clubbing of fingers

coenzyme Q10 deficiency

cogwheel rigidty

congenital deformities

congenital myopathy

cornea, abnormal

cortical vein thrombosis

cranial nerve palsies

creatine phosphokinase(CPK)elevated

creatinine, elevated

cultured skin fibroblasts

deafness, bilateral

demyelinating disease

developmental evaluation

developmental milestones, loss of

developmental retardation

diabetes insipidus

dinitrophenylhydrazine(D.N.P.H.)reaction

diplegia, atonic

diplegia, spastic cerebral

distal muscle weakness

drug abuse, neurologic complications of

drug abuse, toxic screen In

drug induced neurologic disorders

dural sinus thrombosis

dysplasia of C.N.S.

electrocardiogram, abnormal

electroconvulsive therapy

electroencephalogram

encephalomyopathy

encephalopathy, acute

encephalopathy, metabolic

encephalopathy, neonatal

enzyme, muscle disease

ethylene glycol

exercise intolerance

eye movement, disorders of

Fabry's disease

facial nerve palsy, bilateral

failure to thrive

feeding disorder

ferric chloride test

fingernails, abnormal

fracture, long bone

fragile-X syndrome

gangliosidosis GM1

gangliosidosis GM2

gastroenteritis

gastrointestinal bleeding

genetic diagnosis, prenatal

genetic neurologic disorders

genetic screening

genetic testing

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glycogen storage disease

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

hallucination, auditory

hearing problems in children

heavy metal intoxication

hepatic failure

hepatolenticular degeneration(Wilson's disease)

hepatosplenomegaly

hyperammonemic encephalopathy

hyperamylasemia

hyperbilirubinemia

hyperglycinemia

hyperhomocysteinemia

hypotonia, infants

inborn errors of metabolism

inclusion body myositis

intellectual deficit

intellectual deficit, treatable causes of

intellectual deterioration

intelligence quotient

internuclear ophthalmoplegia, bilateral

ischemic exercise test

isopropyl alcohol

jaw contractures

Kayser-Fleischer ring

klippel feil syndrome

lactic acidemia

lactic dehydrogenase(LDH)

language disorders in children

leg weakness, bilateral

Leigh's disease

lens, dislocation of

leukocyte enzyme abnormality

leukoencephalopathy

leukoencephalopathy, toxic

level of consciousness, decreased

level of consciousness, decreased acute

lipid storage disorder of CNS

liver function enzymes

liver transplantation

Lowe's syndrome

lysosomal storage disease

malignant hyperpyrexia

maple syrup urine disease

marfanoid skeletal abnormalities

McArdle's disease

meningitis, aseptic

mental retardation

mental status, abnormal

mental status, abnormal, acute

metabolic acidosis

metabolic disorder, primary

metabolic disorder, primary-screening tests

metachromatic leukodystrophy

midline defect in children

mitochondrial disease

molecular genetics

movement disorder

movement disorder, extrapyramidal

MRI, contrast enhanced

MRI, demyelinating disease

MRI, diffusion weighted

MRI, venography

mucopolysaccharidoses

muscle atrophy, progressive

muscle atrophy, static

muscle phosphofructokinase deficiency

muscle phosphorylase deficiency

muscle stiffness

muscle weakness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, Duchenne

myoclonic jerks

myopathy, drug-induced

myopathy, metabolic

myopathy, mitochondrial

myotonia dystrophica

nausea and vomiting

nephrotic syndrome

nerve conduction studies

neuritis, heavy metals causing

neurologic complications of, surgery

neurologic disease, diagnoses of

neurologic examination, focal

neurologic signs

neurologic testing

neuromuscular disease, electrodiagnosis of

neuropathy, peripheral

neuropathy, toxic

neurotransmitter

ophthalmoplegia

ophthalmoplegia, neonatal

ornithine transcarbamylase deficiency

palatopharyngeal incompetence

paraparesis, spastic

paresthesias, feet

paresthesias, hands

Parkinsonism syndrome

pectus excavatum

pericardial effusion

periodic paralysis

peripheral blood smear

peripheral blood smear, abnormal

personality change

phenylketonuria

phenylketonuria, adult onset

phosphorylase b kinase deficiency

pleocytosis of cerebrospinal fluid

pleural effusion

position sensation, abnormal

practice guidelines

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

progressive neurologic disorder

proprioception, abnormal

proximal muscle atrophy

psychiatric problems in neurologic disorders

psychological testing, neurologic problems

psychomotor retardation

psychosis, childhood

psychosocial aspects

psychotic behavior

pyridoxine deficiency

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

renal failure, acute

respiratory failure

Rett's syndrome

Sandhoff's disease

sclerae, hyperpigmented

second wind phenomena

seizure, advice to parents and teachers regarding

seizure, children

seizure, neonatal

seizure, psychosocial aspects of

seizure, pyridoxine dependent

seizure, treatment of

self-mutilation

semialdehyde dehydrogenase deficiency

sensorineural hearing loss

skin, lesions in neurologic disorders

speech disorder, childhood

spongy degeneration of brain

steroid therapy, CNS treatment and complications with

stimulant drugs

stool, guaiac positive

subdural hematoma

sweating, abnormality of

sympathomimetic drugs

thrombocytopenia

toxic encephalopathy

toxins, nervous system

treatment of neurologic disorder

urea-cycle enzymopathies

urinalysis, abnormal

urinary incontinence

urine test for metabolic disorders

urine test in toxic screen

violent behavior

vitamin deficiency

weakness, generalized

weakness, progressive

white matter disease

x-linked mental retardation

Showing articles 650 to 700 of 17368 << Previous Next >>

Nerve Conduction Study of Human Tetrodotoxication
Neurol 39:743-745, Oda,K.,et al, 1989

Mitochondrial Encephalomyopathy with Associated Aminoacidopathy in a Male Sibship
J Pediatr 115:81-88, Sooth,F.A.,et al, 1989

Opsoclonus in Organophosphate Poisoning
Arch Neurol 46:704-705, Pullicino,P.&Aquilina,J., 1989

Chemotherapy for Malignant Gliomas? Committee on Health Care Issues
American Neurologic Association, Ann Neurol 25:88-891989., , 1989

Mitochondrial DNA and Genetic Disease
Editorial, Lancet 1:250-2511989., , 1989

Spasm of the Near Reflex Associated with Metabolic Encephalopathy
Neurol 39:150, Moster,M.L.&Hoenig,E.M., 1989

Sulfite Oxidase Deficiency:Clinical, Neuroradiologic, and Biochemical Features in Two New Patients
Neurol 39:252-257, Brown,G.K.,et al, 1989

Acute Profound Dystonia in Infants with Glutaric Acidemia
Pediatrics 83:228-234, Bergman,I.,et al, 1989

Motoneuron Disease:A Disorder Secondary to Solvent Exposure?
Lancet 1:73-76, 82-831989., Hawkes,C.H.,et al, 1989

Hemorrhagic Shock and Encephalopathy:Clinical, Pathologic, and Biochemical Features
J Pediatr 114:194-203, Levin,M.,et al, 1989

Agenesis of the Corpus Callosum:A Marker for Inherited Metabolic Disease
Neurol 39:847-848, Kolodny,E.H., 1989

Agenesis of the Corpus Callosum and Gyral Malformations are Frequent Manifestations of Nonketotic Hyperglycinemia
Neurol 39:817-820, Dobyns,W.B., 1989

Randomised Double Blind Controlled Trial of Cyclosporin in Multiple Sclerosis
JNNP 52:559-565, Rudge,P.,et al, 1989

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

Improved Diagnosis of Becker Muscular Dystrophy by Dystrophin Testing
Neurol 39:1011-1017, Hoffman,E.P.,et al, 1989

Cholesterol Embolism:Experience with 22 Histologically Proven Cases
Surgery 105:737-746, Dahlberg,P.J.,et al, 1989

Busulphan and Phenytoin
Ann Int Med 111:1049-1050, Grigg,A.P.,et al, 1989

Hypothyroidism
In Neurologic Clinics, W. B. Saunders Co, Phila, 7:492-493., Kaminski,H.J.&Ruff,R.L., 1989

Cyclosporin Neurotoxicity in Cardiac Transplant Recipients
JNNP 51:1434-1437, Lane,R.J.M.,et al, 1988

The Reversible Dementias:Do They Reverse?
Ann Int Med 109:476-486, Clarfield,A.M., 1988

An Adolescent with Intermittent Headache, Transient Hemiparesis, and Urinary Abnormalities
J Pediatr 113:769-776, Gruskin,A.B.&Chang,C., 1988

Inborn Errors of Metabolism in Children Referred with Reye's Syndrome, A Changing Pattern
JAMA 260:3167-3170, 3178-31801988., Rowe,P.C.,et al, 1988

Brain Metabolism in Mitochondrial Encephalomyopathy:A PET Study
J Comput Assist Tomogr 12:854-857, DeVolder,A.,et al, 1988

Acute Extrapyramidal Syndrome in Methylmalonic Acidemia:"Metabolic Stroke"Involving the Globus Pallidus
J Pediatr 113:1022-1027, Heidenreich,R.,et al, 1988

Extrapyramidal and Other Neurologic Manifestations Associated with Carbon Disulfide Fumigant Exposure
Arch Neurol 45:537-540, Peters,H.A.,et al, 1988

MELAS Syndrome:Characteristic Migrainous & Epileptic Features and Maternal Transmission
Neurol 38:751-754, Montagne,P.,et al, 1988

Treatment Response in Malignant Optic Glioma of Adulthood
Neurol 38:1071-1074, Albers,G.W.,et al, 1988

Cerebrovascular Complications of L-Asparaginase Therapy
Neurol 38:127-133, Feinberg,W.M.&Swenson,M.R., 1988

Visual System Toxicity Following Intra-arterial Chemotherapy
Neurol 38:284-289, Kupersmith,M.J.,et al, 1988

Treatment of Chiasmatic/Hypothalamic Gliomas of Childhood with Chemotherapy:An Update
Ann Neurol 23:79-85, Packer,R.J.,et al, 1988

Amaurotic Family Idiocy
Am J Dis Child 142:53-56, Abt,I.A., 1988

Orofacial Dyskinesia in Stupor and Coma
Neurol 38:1331-1332, Noda,S.,et al, 1988

Dangers from Methylprednisolone Acetate Therapy by Intraspinal Injection
Arch Neurol 45:804-806, Nelson,D.A., 1988

Treatment of Epidural Cord Compressions from Hodgkin's Disease with Chemotherapy
Am J Med 84:555-558, Burch,P.A.&Grossman,S.A., 1988

Central Nervous System Metastases from Non-Hodgkin's Lymphoma:Treatment & Prophylaxis
Am J Med 84:425-435, Recht,L.,et al, 1988

Facioscapulohumeral Muscular Dystrophy, in Neuromuscular Disease
Springer-Verlag, NY, p289988., Swash,M.&Schwartz,M.S., 1988

Neurologic Complications of Bone marrow Transplantation
In Neurol Complic of Transplants, Neurologic Clinics, 6:377-378988., Davis,D.G.&Patchell,R.A., 1988

A Creutzfeldt-Jakob Like Syndrome Due to Lithium Toxicity
JNNP 51:120-123, Smith,S.J.M.&Kocen,R.S., 1988

Retinitis Pigmentosa
Surv Ophthalmol 33:137-177, Pagon,R.A., 1988

Serial Studies of Auditory Neurotoxicity in Patients Receiving Deferoxamine Therapy
Am J Med 83:1085-1090, Gallant,T.,et al, 1987

Neurological Complications Following Liver Transplantation
Lancet 1:949-951, Adams,D.H.,et al, 1987

Acute Sensory Neuropathy-Neuronopathy from Pyridoxine Overdose
Neurol 37:1729-1732, Albin,R.L.,et al, 1987

Clinical Spectrum of Hereditary Hemorrhagic Telangiectasia (Osler-Wever-Rendu Disease)
Am J Med 82:989-997, Perry,W.H., 1987

Neurologic Manifestations of AIDS
Medicine 66:407-437, McArthur,J.C., 1987

MELAS Syndrome Involving a Mother & Two Children
Arch Neurol 44:971-973, Driscoll,P.F.,et al, 1987

Evidence of Neurologic Dysfunction Related to Long-Term Ethylene Oxide Exposure
Arch Neurol 44:1283-1286, Estrin,W.J.,et al, 1987

Cytochrome c Oxidase Deficiency in Leigh Syndrome
Ann Neurol 22:498-506, DiMauro,S.,et al, 1987

Acute Trimethyltin Limbic-Cerebellar Syndrome
Neurol 37:945-950, Besser,R.,et al, 1987

Clinicopath Conf
Kearns-Sayre Syndrome (Oculocraniosomatic Neuromuscular Disease with Mitochondrial Myopathy) , Case, 4-1,NEJM 317:493-501,1987., 1987

Adrenoleukodystrophy:Dietary Oleic Acid Lowers Hexacosanoate Levels
Ann Neurol 21:230-231, 232-2391987., Rizzo,W.B.,et al, 1987

Showing articles 650 to 700 of 17368 << Previous Next >>