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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

caudate nucleus, 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

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

eye movement, disorders of

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

gene

gene mutation

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)

Hodgkin's disease

Huntington's chorea

Huntington's disease, children

hypoxic encephalopathy

iatrogenic neurologic disorders

inborn errors of metabolism

inclusion bodies, intranuclear

infantile hemiplegia

insomnia

intellectual deficit

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

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

psychosis

pull test

putamen, lesion of

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

seizure, unknown origin

sensorineural hearing loss

sensory tricks

serologic testing

serologic testing, false negative

seronegative

sinemet

sleep pathology and physiology

spasticity

speech disorder

status epilepticus

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

weakness, progressive

Showing articles 1050 to 1100 of 1826 << Previous Next >>

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Psychosis as the Initial Manifestation of Adult-Onset Niemann-Pick Disease Type C
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Post-Traumatic Movement Disorders:Central and Peripheral Mechanisms
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Urgent Therapy for Acute Stroke:Effects of a Stroke Trial on Untreated Patients
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Rapidly Evolving Myopathy with Myosin-Deficient Muscle Fibers
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Diagnosing the Severe Headache
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Antineuronal Antibodies in Acute Cerebellar Ataxia Following Epstein-Barr Virus Infection
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Clinicopath Conf
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Dopa-Responsive Dystonia:Pathological and Biochemical Observations in a Case
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Parkinson's Disease
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Discontinuing Antiepileptic Drugs in Children with Epilepsy
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Relapse Following Discontinuation of Antiepileptic Drugs:A Meta-Analysis
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Efficacy of Felbamate in Therapy for Partial Epilepsy in Children
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Early Presentation of Hemispheric Intracerebral Hemorrhage:Prediction of Outcome and Guidelines for Treatment Allocation
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Characteristics of the Dementia in Late-Onset Metachromatic Leukodystrophy
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Showing articles 1050 to 1100 of 1826 << Previous Next >>