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acanthocytosis

acetazolamide

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome-related complex

Adies pupil

advances in neurology

adverse drug reaction

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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

anti La antibody

anticonvulsants

anticonvulsants, blood level determination of

anticonvulsants, untoward effects of

antihistamines

anxiety

apraxia

apraxia of eye movements

apraxia, constructional

attention deficit disorder with hyperactivity

atypical

autoantibodies

autoimmune basal ganglia encephalitis

autoimmune disease

autoimmune encephalopathy

autoimmune epilepsy

autonomic dysfunction

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, infarction

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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

caudate nucleus, atrophy

central nervous system, infection of

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

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cerebral ischemia

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cerebrospinal fluid

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cerebrospinal fluid, cell count, normal

cerebrovascular accident

cerebrovascular accident, complications with

cerebrovascular accident, nonarterial territory

cerebrovascular accident, young adult

choreoathetosis, paroxysmal

chromosomal abnormality

chromosome 1

chromosome 7

chronic progressive external ophthalmoplegia

Clinical Pathologic Conference(C.P.C.)

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cognition

cold intolerance

collapsin response mediator protein 5 IgG

coma

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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 ribbon sign

cortical-basal ganglionic degeneration

cranial neuropathy

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creatine phosphokinase(CPK)elevated

cultured skin fibroblasts

deep gray nuclei

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developmental retardation

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disease modifying agents

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enuresis

enzyme, defect

epileptic encephalopathy

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epsilon sarcoglycan gene

executive dysfunction

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

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genetic neurologic disorders

genetic testing

Gilles de la Tourette syndrome

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glycine receptor antibodies

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hypoxic encephalopathy

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inattention

inborn errors of metabolism

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intellectual deficit

intellectual deterioration

intestinal pseudoobstruction

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karyotyping

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Kearns-Sayre syndrome

Leber's hereditary optic neuropathy

left handedness

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lenticular nucleus, lesion of, bilateral

leucine rich glioma inactivated 1 antibodies

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level of consciousness, decreased

levitation

Lewy body disease, diffuse

life expectancy

limbic encephalitis

lipid storage disorder of CNS

lysosomal storage disease

masked facies

mediastinum, mass of

medical-legal aspects of neurology

MELAS syndrome

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memory, defect of recent

memory, impairment of

meningitis, carcinomatous

mental retardation

mental retardation, etiology of

mental status, abnormal

MERRF syndrome

mesial temporal lobe

metabolic disorder, primary

metabolic disorder, primary-screening tests

Mini Mental Status Examination

misdiagnosis

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

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myopathy, mitochondrial

myorhythmia

mysoline

neoplasm, intracranial

neoplasm, primary intracerebral

neoplasm, primary of CNS

neurexin-3 alpha antibodies

neuroendocrinology

neuroimmunology

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neuroleptic malignant syndrome

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neurologic disease, multifocal

neurologic examination, focal

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

psychological testing

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, laughing as manifestation

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

strokelike episodes

subarachnoid hemorrhage

substantia nigra

sugarcane, mildewed

symmetric brain lesions

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

whole genome sequencing

x-linked mental retardation

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