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adolescent medicine

advances in neurology

adverse drug reaction

akathisia

algorithm

alternating hemiplegia

alternating hemiplegia of childhood

AMPA receptor antibodies

amphiphysin antibodies

anti GQ1b IgG antibody

anti IgLON5

anticholinergic drugs

autoimmune basal ganglia encephalitis

autoimmune disease

autonomic dysfunction

basal ganglia

basal ganglia, infarction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

carbon monoxide poisoning

cardiac arrest

cardiac arrest and resuscitation

CAT scan

CAT scan, abnormal

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, muscle

catalepsy

cataplexy

caudate nucleus, atrophy

cerebellar degeneration

cerebral cortical atrophy

cerebral palsy

cerebral venous thrombosis

cerebral venous thrombosis, deep

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrovascular accident

cerebrovascular accident, infancy and childhood

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

clonazepam

clozapine

cognition

collapsin response mediator protein 5 IgG

coma

complications

conversion reaction

creatine phosphokinase(CPK)elevated

cyanide poison

degenerative diseases of CNS

delay in diagnosis

dementia

dementia, presenile

developmental milestones, loss of

developmental retardation

diagnostic criteria

diet

differential diagnosis

disease modifying agents

dopa responsive dystonia

dopamine agonist

dopamine depleting agents

DPPX

DPPX, antibodies

DPPX, antibodies, encephalitis

drug induced neurologic disorders

dysarthria

dyskinesia

dyskinesia, buccal lingual facial

dyskinesia, drug induced

dysphagia

dystonia

dystonia musculorum deformens

dystonia, classification

dystonia, delayed onset

dystonia, drug induced

dystonia, etiology of

dystonia, evaluation of

dystonia, face

dystonia, focal

dystonia, treatment of

dystonia, truncal

dystonic reaction, acute

DYT1 mutation

efficacy

electroencephalogram, abnormalities of

electromyogram

encephalitis

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, paraneoplastic

encephalopathy

encephalopathy, neonatal

encephalopathy, post anoxic

enzyme, defect

executive dysfunction

exome sequencing

eye movement, disorders of

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

gaze palsy, supranuclear

genetic neurologic disorders

genetic testing

gests antagoniste

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

GLUT1

GLUT1 deficiency syndrome

glutamic acid decarboxylase, antibody

glycine receptor antibodies

Hallervorden Spatz disease

Hallervorden Spatz disease, late onset

hepatolenticular degeneration(Wilson's disease)

Huntington's disease, children

hypoxic encephalopathy

iatrogenic neurologic disorders

inborn errors of metabolism

inclusion bodies, intranuclear

intellectual deterioration

internal cerebral vein

L-dopa, delayed treatment in Parkinsonism

L-dopa, drug interactions with and side effects of

left handedness

Leigh's disease

lenticular nucleus, lesion of

lenticular nucleus, lesion of, bilateral

leucine rich glioma inactivated 1 antibodies

leukodystrophy

life expectancy

limbic encephalitis

lipid storage disorder of CNS

low back pain

lumbar puncture

lysosomal storage disease

masked facies

mellaril

memory

memory, impairment of

meningitis, carcinomatous

mental retardation

mental status, abnormal

metabolic disorder, primary

metabolic disorder, primary-screening tests

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

mitochondrial disease

monoclonal antibodies

movement disorder

movement disorder, delayed onset

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, extrapyramidal-treatment of

movement disorder, hyperkinetic

movement disorder, treatment of

MRI

MRI, abnormal

MRI, CAT scan compared to

MRI, eye of tiger sign

MRI, negative

MRI, paramagnetic effect

neuroleptic, atypical

neurologic disease, diagnoses of

neurologic signs

neuronal intranuclear inclusion disease

obsessive-compulsive disorder

oculogyric crisis

old age, neurology of

paraspinal muscle weakness

Parkinson disease

Parkinson disease, drug induced

Parkinson disease, dystonia with

Parkinson disease, fluctuations in

Parkinson disease, freezing phenomena in

Parkinson disease, juvenile

Parkinson disease, L-dopa nonresponsive

Parkinson disease, mode of onset

Parkinson disease, on-off phenomena in

Parkinson disease, prognosis of

Parkinson disease, rapid onset

Parkinson disease, treatment of

Parkinson disease, unilateral

Parkinson disease, young onset

Parkinsonism syndrome

paroxysmal hemiplegia

paroxysmal neurologic deficits

pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection

phenothiazine

phenothiazine, dyskinesia associated with

pigmentary retinopathy

Pisa syndrome

pleocytosis of cerebrospinal fluid

postural abnormality

potassium channel antibodies

practice guidelines

precipitating factors

prevention of neurologic disorders

PRKN gene

prognosis

progressive neurologic disorder

psychiatric disorder

psychiatric problems in neurologic disorders

psychomotor retardation

putamen, lesion of, bilateral

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

quality of life

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

recurrent

remote effect of cancer on the nervous system

reserpine treatment in movement disorder

salivation, excessive

seizure, laughing as manifestation

seizure, neonatal

seizure, unknown origin

sensorineural hearing loss

sensory tricks

serologic testing

serologic testing, false negative

seronegative

sinemet

sleep pathology and physiology

stem cell transplantation

steroid

steroid therapy, CNS treatment and complications with

stimulation, deep brain

stooped posture

streptococcal infection

streptococcus pyogens

striatal encephalitis

tardive dyskinesia, treatment of

tardive dystonia

tardive pain syndrome

tetrabenazine

tetrahydrobiopterin

thalamus, infarction of

thalamus, lesion of-bilateral

tonic foot response

torticollis

torticollis, benign paroxysmal

torticollis, familial

torticollis, infants and children

toxic encephalopathy

toxins, nervous system

treatment of neurologic disorder

tricyclic antidepressant

trinucleotide repeats

urinary sulfatidase excretion

walking, difficulty with

weakness, progressive

white matter disease

whole genome sequencing

wide based gait

workup

writers cramp

Showing articles 1000 to 1050 of 1853 << Previous Next >>

Weekend and Holiday Increase in the Onset of Ischemic Stroke in Young Women
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Factors Delaying Hospital Admission in Acute Stroke:The Copenhagen Stroke Study
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The Syndrome of Posterior Choroidal Artery Territory Infarction
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Neurologic Presentation of Wilson Disease without Kayser-Fleischer Rings
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Delayed-Onset Cerebellar Syndrome
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Antiepileptic Drugs
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Discontinuation of Antiepileptic Drug Treatment after Two Seizure-Free Yrs in Children with Cerebral Palsy
Pediatr 97:192-197, Delgado,M.R.,et al, 1996

High Apolipoprotein E e4 Allele Frequency in Age-Related Memory Decline
Ann Neurol 39:548-551, Blesa,R.,et al, 1996

Botulinum Toxin Versus Trihexphenidyl in Cervical Dystonia:A Prospective, Randomized, Double-Blind Controlled Study
Neurol 46:1066-1072, Brans,J.W.M.,et al, 1996

Dementia and Adult-Onset Unprovoked Seizures
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Celiac Disease with Cerebral Calcium and Silica Deposits:X-ray Spectroscopic Findings, An Autopsy Study
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Reversible Dementia and Chorea in a Young Woman with the Lupus Anticoagulant
Neurol 46:1599-1603, Van Horn,G.,et al, 1996

Cough, Exertional, and Sexual Headaches:An Analysis of 72 Benign and Symptomatic Cases
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Creutzfeldt-Jakob Disease in a Young Woman
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Varicalla-Zoster Virus DNA in CSF & Arteries in Delayed Contralat Hemiplegia:Evid for Viral Invasion of Cerebr Art
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Chorea-Ballismus with Nonketotic Hyperglycemia in Primary Diabetes Mellitus
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Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities
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Niemann-Pick Disease Type C from Bench to Bedside
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Multifocal Motor Neuropathy
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Preclinical Evidence of Alzheimer's Disease in Persons Homozygous for the e4Allele for Apolipoprotein E
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Subcortical Heterotopia:A Distinct Clinicoradiologic Entity
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Discontinuation of Anticonvulsant Therapy in Children Free of Seizures for 1 Year:A Prospective Study
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Simple Partial Status Epilepticus:Causes, Treatment and Outcome in 47 Patients
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Non-Convulsive Status Epilepticus:Causes, Treatment, and Outcome in 65 Patients
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Random Comp Monother Trial of Phenobarb, Phenytoin, Carbamazepine, or Sod Valp for Newly Dx Child Epilep
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Startle Provoked Epileptic Seizures:Features in 19 Patients
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The Risk of Seizure Recurrence After a First Unprovoked Afebrile Seizure in Childhood:An Extended Follow-up
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Efficacy of Gabapentin Therapy in Children with Refractory Partial Seizures
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The Use of Parenteral Antiepileptic Drugs & The Role of Fosphenytoin
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Accidental Injury is a Serious Risk in Children with Typical Absence Epilepsy
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Amyloid Angiopathy-Related Cerebellar Hemorrhage
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Cerebral Achromatopsia as a Presentation of Trousseaus Syndrome
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The Landau-Kleffner Syndrome
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Withdrawal of Antiepileptic Drug Treatment in Childhood Epilepsy:Factors Related to Age
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Multiple Subpial Transection:A Review of 21 Cases
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Comparison of Therapeutic Effects & Mortality Data of Levodopa & Levodopa with Selegiline in Pts with Early, Mild Parkinson's
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MRI In Patients with Suspected Vascular Parkinsonism
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Early Differential Diagnosis of Parkinson's Disease with F-flurodeoxyglucose and Positron Emission Tomography
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Clinical and[18F]dopa PET Findings in Early Parkinson's Disease
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Hereditary Adult-Onset Alexander's Disease with Palatal Myoclonus, Spastic Paraparesis and Cerebellar Ataxia
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Psychogenic Movement Disorders:Frequency, Clinical Profile and Characteristics
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Progressive Muscular Atrophy, Case 36-1995, NEJM 333:1406-1412995., , 1995

Statement of Use of Apolipoprotein E Testing for Alzheimer Disease
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Lamotrigine for the Treatment of Epilepsy in Childhood
J Pediatr 127:991-997, Besag,F.M.C.,et al, 1995

Delayed Onset of Fatal Basilar Thrombotic Embolus After Whiplash Injury
Stroke 26:2194-2196, Viktrup,L.,et al, 1995

Is Blood Pressure Really a Trigger for the Circadian Rhythm of Subarachnoid Hemorrhage?
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Paroxysmal Dyskinesias:Clinical Features and Classification
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Phenobarbitone, Phenytoin, Carbamazepine, or Sodium Valproate for Newly Diagnosed Adult Epilepsy:A Randomized Monotherapy Trial
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Do Anticonvulsants Alter the Natural Course of Epilepsy
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Showing articles 1000 to 1050 of 1853 << Previous Next >>