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acanthocytosis

acetazolamide

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome-related complex

Adies pupil

advances in neurology

adverse drug reaction

alcohol, neurologic complications with

algorithm

alien hand syndrome

alternating hemiplegia

alternating hemiplegia of childhood

alveolar hypoventilation

amimia

aminoacidopathies

aminoacidurias

AMPA receptor antibodies

amphiphysin antibodies

amyotrophic chorea-acanthocytosis

anemia

anti basal ganglia antibodies

anti GQ1b IgG antibody

anti IgLON5

anticonvulsants

anticonvulsants, blood level determination of

anticonvulsants, untoward effects of

antihistamines

anxiety

apraxia

apraxia of eye movements

apraxia, constructional

attention deficit disorder with hyperactivity

autoantibodies

autoimmune basal ganglia encephalitis

autoimmune disease

autoimmune encephalopathy

autoimmune epilepsy

autonomic dysfunction

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, infarction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basilar artery migraine

behavioral disorder

behavioral disorder, acute

benign essential tremor

beta adrenergic blocker

biotin

biotin deficiency

biotin deficiency, juvenile form

biotin-responsive basal ganglia disease

calcification, intracranial

calcium antagonist

carbamazepine

carbamazepine, toxicity

carbon monoxide poisoning

CAT scan, emission, abnormal

CAT scan, isodense lesion with acute hemorrhage

cataracts

catatonia

catecholamine

caudate nucleus, atrophy

central nervous system, infection of

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar lesion

cerebral cortex

cerebral cortical atrophy

cerebral edema

cerebral ischemia

cerebral palsy

cerebral palsy, adults

cerebral palsy, associated problems with

cerebral vasculature, calcification

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, cell count, normal

cerebrovascular accident

cerebrovascular accident, complications with

cerebrovascular accident, young adult

choreoathetosis, paroxysmal

chromosomal abnormality

chromosome 1

chromosome 7

chronic progressive external ophthalmoplegia

Clinical Pathologic Conference(C.P.C.)

clonazepam

cognition

cold intolerance

collapsin response mediator protein 5 IgG

coma

coma, causes of

coma, episodic

coma, unknown etiology

complications

compression fracture

computers, neurologic diagnosis and

confusion

conjugate gaze, forced

consanguinity

contactin associated protein like 2 antibodies

conversion reaction

copper metabolism, abnormal

cortical-basal ganglionic degeneration

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

cultured skin fibroblasts

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

dementia

dementia, childhood

dementia, rapidly progressive

dementia, reversible

dementia, treatment of

depression

developmental milestones, loss of

developmental retardation

differential diagnosis

disability, neurological

DPPX, antibodies, encephalitis

drooling

dysarthria

dyskinesia

dyskinesia, buccal lingual facial

dyskinesia, drug induced

dystonia musculorum deformens

dystonia, children

dystonia, delayed onset

dystonia, drug induced

dystonia, psychogenic

dystonia, treatment of

dystonic reaction, acute

DYT1 mutation

efficacy

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

electromyogram

ELISA

emergencies, neurologic

emotional lability

encephalitis

encephalitis lethargica

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, clinical picture and treatment of

encephalitis, etiology

encephalitis, focal

encephalitis, paraneoplastic

encephalitis, viral

encephalopathy

encephalopathy, neonatal

encephalopathy, post anoxic

enuresis

enzyme, defect

epileptic encephalopathy

episodic disorders

episodic neurologic deficits

epsilon sarcoglycan gene

exercise

exercise intolerance

exome sequencing

extralimbic encephalitis

eye color

eye movement, disorders of

face, contractions

facial nerve palsy

faciobrachial dystonic seizure

gamma amino butyric acid

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

gaze deviation

gaze palsy

gaze palsy, supranuclear

genetic neurologic disorders

genetic testing

Gilles de la Tourette syndrome

globus pallidus

globus pallidus, lesion of

GLUT1

GLUT1 deficiency syndrome

glutamic acid decarboxylase, antibody

glycine receptor antibodies

grimacing

Hallervorden Spatz disease

hemiparesis, transient

hemiplegia

hepatic encephalopathy

hepatic encephalopathy, treatment of

hepatic failure

hepatitis

hepatolenticular degeneration(Wilson's disease)

hepatosplenomegaly

heralding manifestation

herpes simplex encephalitis

hippocampus

Hodgkin's disease

homovanillic acid

human immunodeficiency virus type 1

Huntington's chorea

Huntington's disease, children

hypotension, systemic

hypotonia

hypotonia, infants

hypoxia, newborn

hypoxic encephalopathy

imbalance

immunologic disease

immunosuppression

immunosuppressive agents

immunotherapy

inappropriate antidiuretic(A.D.H.)hormone

inborn errors of metabolism

intellectual deterioration

intestinal pseudoobstruction

intracerebral hemorrhage

iron, brain

islet cell tumor

Jakob-Creutzfeldt disease

karyotyping

Kayser-Fleischer ring

Kearns-Sayre syndrome

Leber's hereditary optic neuropathy

left handedness

Leigh's disease

lenticular nucleus, lesion of

lenticular nucleus, lesion of, bilateral

leucine rich glioma inactivated 1 antibodies

leukodystrophy

level of consciousness, decreased

levitation

Lewy body disease, diffuse

limbic encephalitis

lipid storage disorder of CNS

liver disease

lobar atrophy

lumbar puncture

lysosomal storage disease

masked facies

mediastinum, mass of

medical-legal aspects of neurology

MELAS syndrome

memory

memory, defect of recent

memory, impairment of

meningitis, carcinomatous

mental retardation

mental status, abnormal

MERRF syndrome

mesial temporal lobe

metabolic disorder, primary

metabolic disorder, primary-screening tests

mitochondrial disease

mitochondrial encephalomyopathy

molecular genetics

monoamines

monoclonal antibodies

mortality

motor neuron disease

movement disorder

movement disorder, delayed onset

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, hyperkinetic

movement disorder, paroxysmal

movement disorder, psychogenic

movement disorder, treatment of

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, false negative

MRI, FLAIR

MRI, negative

MRI, paramagnetic effect

MRI, pelvis

MRS

multiple sclerosis

multiple sclerosis, paroxysmal symptoms in

myelitis, transverse, recurrent

myopathy, mitochondrial

myorhythmia

mysoline

neoplasm, intracranial

neoplasm, primary intracerebral

neoplasm, primary of CNS

neurexin-3 alpha antibodies

neuroendocrinology

neuroleptic

neuroleptic malignant syndrome

neurologic complications

neurologic complications of, systemic cancer

neurologic disease

neurologic disease, diagnoses of

neurologic disease, diagnoses of, clinical bedside

neurologic disease, multifocal

neuronal cell surface antigen

neuropathology

neuropathology, brain

occupational neurologic disorders

ocular motility, disorders of

optokinetic nystagmus, abnormal

Parkinson disease, differential diagnosis of

Parkinson disease, drug induced

Parkinson disease, dystonia with

Parkinson disease, L-dopa nonresponsive

Parkinson disease, postencephalitic

Parkinson disease, psychogenic

Parkinson disease, tremor, absence of

Parkinsonism syndrome

paroxysmal dystonic choreoathetosis

paroxysmal exertion-induced dyskinesia

paroxysmal hemiplegia

paroxysmal hypnogenic dyskinesia

paroxysmal kinesigenic dyskinesia

paroxysmal neurologic deficits

paroxysmal neurologic disorder

paroxysmal nonkinesigenic dyskinesia

pathognomonic

pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection

penicillamine

peroxisomal disease

personality change

phencyclidine poisoning

phenylketonuria

pigmentary retinopathy

pitfalls

PLEDs

pleocytosis of cerebrospinal fluid

poison, neurologic problems with

polymyositis

pons, lesion of

potassium channel antibodies

practice guidelines

precipitating factors

primary episodic ataxia

primary familial brain calcification

prognosis

progressive neurologic disorder

propranolol

pseudohypoparathyroidism

psychiatric disorder

psychiatric problems in neurologic disorders

psychomotor retardation

pupil, abnormality in neurologic disorders

pupil, tonic

pyramidal tract

pyramidal tract dysfunction

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

quadriplegia

ragged-red fibers

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

rectal biopsy

recurrent

release phenomena

remote effect of cancer on the nervous system

respirator

respiratory failure

respiratory tract infection

retinitis pigmentosa

retinopathy

Rett's syndrome

reversible neurologic disorder

salivation, excessive

sedimentation rate, elevated

seizure

seizure, adult onset

seizure, children

seizure, differential diagnosis of

seizure, dystonic

seizure, focal

seizure, neonatal

seizure, psychomotor-temporal lobe

seizure, stimulus sensitive

seizure, unknown origin

self harm

self-mutilation

semialdehyde dehydrogenase deficiency

sensorineural hearing loss

sensory loss

sensory loss, cortical

serologic testing

serologic testing, false negative

seronegative

sexual behavior, disorder of

short stature

sicca syndrome

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skin, lesions in neurologic disorders

sleep apnea, obstructive

sleep pathology and physiology

speech disorder, childhood

spinal cord, lesion of

spinocerebellar ataxia type 16

status epilepticus, intractable

stereotaxic surgery

stereotypy

steroid

steroid therapy, CNS treatment and complications with

stimulation, deep brain

stimulation, deep brain, bilateral

strabismus

striatal encephalitis

striatum, lesion of

striatum, lesion of, bilateral

striopallidodentate calcifications, familial idiopathic

subarachnoid hemorrhage

substantia nigra

sugarcane, mildewed

symmetric brain lesions

tardive dyskinesia

tardive dystonia

tauopathy

temporal lobe, lesion

temporal lobe, lesion, bilateral

thalamus, lesion of-bilateral

toxins, nervous system

toxoplasmosis, CNS

transient neurologic deficit

transient paroxysmal dystonia in infancy

trauma

treatment of neurologic disorder

trinucleotide repeats

twitching, face

undiagnosed

urea-cycle enzymopathies

urine test for metabolic disorders

urine test in toxic screen

visual evoked response

visual impairment

visuospatial disturbance

walking, difficulty with

white matter disease, subcortical

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Localization of a Gene for Myoclonus-Dystonia to Chromosome 7q21-q31
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Delayed Movement Disorders After Carbon Monoxide Poisoning
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