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abstract reasoning

accomodation, abnormal

acquired immunodeficiency syndrome

acute cerebellar ataxia

addiction, heroin

addiction, heroin-neurologic complications with

Addison's disease

adrenoleukodystrophy

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

adult polyglucosan body disease

adult-onset leukodystrophy, with neuroaxonal spheroids

advances in neurology

affect, inappropriate

agnosia, visual

Aicardi-Goutieres syndrome

alcohol intolerance

alcohol, neurologic complications with

Alexanders disease

alpha-fetoprotein

alternating hemiplegia

alternating rapid movement

alternating rapid movement, impaired

Alzheimer's disease

Alzheimer's disease, diagnosis of

Alzheimer's disease, preclinical

Alzheimer's disease, visual variant

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, treatment of

anemia, hemolytic

Angelman syndrome

angiography, cerebral

ankle, swelling of

anti La antibody

anti Ro antibody

antibiotics, neurologic complications with

anticholinergic drugs

aphasia, children

aphasia, progressive

aphasia, progressive, primary

aphasia, transcortical

aphasia, transcortical-sensory

apraxia of eye movements

apraxia, speech

arm swing, reduced

arthrogryposis multiplex

arylsulfatase A

ataxia telangiectasia

ataxia, cerebellar

ataxia, hereditary

ataxia, progressive

ataxia, truncal

attention deficit disorder with hyperactivity

auditory processing, impaired

automobile accidents

autonomic dysfunction

autonomic nervous system

axonal degeneration

axonal spheroid

B 12 deficiency

B cell lymphoma

Balint's syndrome

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, infarction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavior, combative

behavioral disorder

Behcet's syndrome

Benedict's solution test

biologic markers

bladder dysfunction

blinking, reduced

blood brain barrier

bone marrow biopsy

bone marrow transplantation

brainstem, atrophy

brainstem, infarction of

brainstem, lesion of

bulbar palsy, progressive

burning feet, differential diagnosis of

cafe au lait spots

calcification, intracranial

calf hypertrophy

carbon monoxide poisoning

carcinoembryonic antigen

carcinoid syndrome

carcinoid tumor

carcinoma of thymus

carotid artery occlusion, bilateral

carotid artery occlusion, intracranial

carotid artery occlusion, neck

carotid-siphon occlusion

carpo-pedal spasm

CAT scan, abnormal

CAT scan, angiography

CAT scan, angiography, false negative

CAT scan, chest

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, venography

caudate nucleus

caudate nucleus, infarction

caudate nucleus, lesion of, bilateral

central hypoventilation

central nervous system, infection of

central pontine myelinolysis

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar atrophy, primary

cerebellar cognitive affective syndrome

cerebellar degeneration

cerebellar disease, eye movement disorder in

cerebellar hypoplasia

cerebellar lesion

cerebellar vermis

cerebellum, disease of

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortex

cerebral cortical atrophy

cerebral dominance

cerebral infarction

cerebral infarction, small, deep

cerebral infarction, subcortical

cerebral palsy, associated problems with

cerebral palsy, pure ataxic

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, enzymes in

cerebrospinal fluid, gammaglobulin of

cerebrovascular accident

cerebrovascular accident, bilateral

cerebrovascular accident, complications with

cerebrovascular accident, familial occurrence

cerebrovascular accident, multiple

cerebrovascular accident, recurrent

cerebrovascular accident, silent

cerebrovascular disease

ceruloplasmin, serum

chasing the dragon

chelation therapy

chemotherapy, CNS treatment and complications with

chest x-ray, abnormal

chilbran skin lesions

choreoathetosis

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

cognition, slowed

cognitive delay

cogwheel rigidty

comprehension, impaired

congenital bilateral perisylvian syndrome

congenital infection, CNS

congenital malformation

congenital myasthenic syndromes

conjunctival biopsy

contractures, joint

controversies in neurology

convergence, impaired

copper metabolism, abnormal

corpus callosum, hypoplastic

corpus callosum, lesion of

corpus callosum, thinning

cortical blindness

cortical-basal ganglionic degeneration

cranial nerve palsies

cranial nerve palsies, bilateral

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

Creutzfeldt-Jakob disease, genetic

crying, pathologic

cryptococcal antigen

cryptococcal meningitis

cultured skin fibroblasts

cytomegalic inclusion disease

cytomegalovirus infection

decerebrate posture

deep gray nuclei

deep tendon reflexes

degenerative diseases of CNS

delay in diagnosis

dementia, age at onset

dementia, childhood

dementia, differential diagnosis of

dementia, familial

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

dementia, subcortical

dementia, thalamic

dementia, transmissible

demyelinating disease

denervation of muscle

denervation potentials

dentate nuclei, lesion of

developmental abnormality of brain

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetes insipidus

diabetes mellitus

diagnostic criteria

dialysis dementia

dichotic hearing

differential diagnosis

difficulty climbing stairs

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

diplegia, atonic

diplegia, spastic cerebral

disability rating scale, neurological

disability, neurological

distal muscle weakness

dopamine agonist

drug abuse, inhalation

drug abuse, neurologic complications of

drug induced neurologic disorders

dural arteriovenous malformation

dysdiadochokinesia

dysequilibrium syndrome

dyskinesia, buccal lingual facial

dysplasia of C.N.S.

dystonia, children

ears of the Lynx MR sign

electroencephalogram

electroencephalogram, abnormalities of

electron microscopy

electrophoretic pattern, CSF

emotional lability

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, viral

encephalomalacia

encephalomyelitis, postinfectious

encephalopathy, delayed

encephalopathy, metabolic

epilepsia partialis continua

Epstein-Barr virus

esophageal varices

executive dysfunction

exome sequencing

eye movement, disorders of

face, inexpressive

face, numbness of

facial appearance, abnormal

facial expression abnormality

facial weakness

facial weakness, bilateral

failure to thrive

feeding disorder

ferric chloride test

fetal alcohol syndrome

fine motor function, impaired

finger nose finger test

fingerprint bodies

fistula, arterio-venous, dural

fluorescene in situ hybridization

food-borne infection

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

Friedreich's ataxia

frontal lobe, atrophy

frontal lobe, behavior with disease of

frontal lobe, pathologic signs of

frontotemporal dementia, behavioral variant

fungal infection

fungal infection, CNS

gag reflex, depressed

gait, festinating

gammaglobulin therapy, intravenous

gastroenteritis

gaze palsy, horizontal

gaze palsy, supranuclear

gaze palsy, vertical

genetic counselling

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

genital ulcerations

Gerstmann syndrome

Gerstmann-Straussler-Scheinker disease

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glycogen storage disease

GM1 ganglioside antibodies

Gowers maneuver

granular osmiphilic material

growth retardation

gyrus, abnormal

Hallervorden Spatz disease

Hallervorden Spatz disease, late onset

hallucination, visual

head circumference

headache, intermittent

headache, intractable

headache, severe

headache, sudden onset of

headache, vascular

hearing problems in children

heel-knee-shin test

hemianopia, homonymous

hemifacial spasm

hemiparesis, transient

hemorrhage, thalamic

hepatic encephalopathy

hepatic failure

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), presymptomatic

hepatolenticular degeneration(Wilson's disease), screening for

hepatosplenomegaly

heralding manifestation

high arched palate

human immunodeficiency virus type 1

Huntington's chorea

hydroxyglutaric aciduria

hyperlipoproteinemia

hyperpigmentation of skin

hyperpyrexia, CNS disorder causing

hypersegmented polys

hypoalbuminemia

hypoglycorrhachia

hypometric saccades

hypopigmentation of skin

hypotension, systemic

hypothyroidism, congenital

hypotonia, infants

imbalance, postural

immunocompetent

immunodeficiency

immunohistochemistry

immunosuppression

inborn errors of metabolism

inclusion bodies

inclusion bodies, intracytopasmic

incontinence, fecal

infection, recurrent

infectious mononucleosis

infectious mononucleosis, neurologic findings with

inflexibility, mental

initiative, lack of

intellectual deficit

intellectual deficit, treatable causes of

intellectual deterioration

intelligence quotient

interferon alpha

internal capsule

internuclear ophthalmoplegia

intracranial pressure, increased

intrinsic hand muscles, wasting of

iodine deficiency

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Jakob-Creutzfeldt disease, variant

jaw jerk, abnormal

joint hypermobility

Kayser-Fleischer ring

kinesia paradoxica

klippel feil syndrome

Kluver-Bucy syndrome

lactic acidemia

language development, neurologic basis of

language disorder in adults

language disorders in children

laughing, pathologic

learning disability

learning disability, in children

left-right orientation

leg weakness, bilateral

leg weakness, unilateral

Leigh's disease

lenticular nucleus, lesion of, bilateral

leukocyte alkaline phosphotase

leukoencephalopathy

leukoencephalopathy, toxic

lid abnormalities

life expectancy

limbic encephalitis

lipid storage disorder of CNS

listeria monocytogenes

listeriosis, CNS

liver function enzymes

liver transplantation

locked-in syndrome

long bone lesion

loss of sympathy

lumbar puncture, complications of

lymphoma involving CNS

lymphoma, primary of CNS

lysosomal storage disease

magnetic source image

magnetoencephalography

malformation, CNS, congenital

maple syrup urine disease

marche a petits pas

masseter muscle wasting

mediastinum, mass of

megalencephaly, idiopathic

memory, defect of recent

memory, impairment of

meningeal enhancement

meningeal enhancement, nodular

meningitis, fungal

meningitis, neutrophilic

meningitis, neutrophilic, persistent

mental retardation

mental status, abnormal

mesial temporal lobe

metabolic disorder, primary

metachromatic leukodystrophy

metachromatic leukodystrophy, juvenile

microangiopathy, brain

microangiopathy, retina

microhemorrhage, intracerebral

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

midline defect in children

mitochondrial disease

molecular genetics

monoclonal gammopathy

Montreal cognitive assessment

motor neuron disease

movement disorder

movement disorder, extrapyramidal

MRI, angiography

MRI, angiography, false negative

MRI, contrast enhanced

MRI, diffusion weighted

MRI, eye of tiger sign

MRI, false negative

MRI, functional

MRI, nodular enhancement

MRI, paramagnetic effect

MRI, punctate pattern

MRI, spinal cord

MRI, venography

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, familial

multiple sclerosis, misdiagnosis

multiple system atrophy

muscle atrophy, progressive

muscle spasm, face

muscle stiffness

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, central nervous system abnormality

muscular dystrophy, Duchenne

myasthenia gravis

myasthenia gravis, congenital

myasthenia gravis, familial incidence of

myeloneuropathy

myoclonic jerks

myoclonus, epilepsy

myoclonus, stimulus sensitive

myxedema, neurologic manifestations of

nausea and vomiting

neoplasm, primary of CNS

neoplasm, primary of CNS-treatment of

neoplastic angioendotheliosis

nerve conduction studies

neurocutaneous disease

neuroendocrinology

neurofibrillary degeneration

neurofibromatosis 1

neurogenic bladder

neurologic complications

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic examination, focal

neurologic examination, non-focal

neurologic signs

neurologic symptoms

neurologic testing

neuromuscular junction

neuronal ceroid-lipofuscinosis

neuroophthalmology

neuropathology, brain

neuroprotective agents

next-generation sequencing

Niemann-Pick disease

ocular motility, disorders of

old age, neurology of

operculum syndrome

operculum syndrome, bilateral

ophthalmoplegia

optokinetic nystagmus, abnormal

oral ulcerations

otitis, neurologic complications with

ovarian insufficiency

pain, increased response

palatal myoclonus

palatopharyngeal incompetence

palmomental response

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, spastic

paraplegia, in flexion

Parkinson disease

Parkinson disease, diagnosis

Parkinson disease, freezing phenomena in

Parkinson disease, pathogenesis of

Parkinson disease, surgical treatment of

Parkinson disease, treatment of

Parkinsonism syndrome

PAS positive material in the brain

patent foramen ovale

pathologic reflex

peripheral blood smear

peripheral blood smear, abnormal

peroxisomal disease

personality change

phenylketonuria

pheochromocytoma

philtrum, tented

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

pleocytosis of cerebrospinal fluid, neutrophilic

pneumoencephalogram(PEG)

polycythemia, primary

polyglucosan body

polyglucosan body disease

polyneuropathy, uremic

pons, infarction of

post infectious cerebellar ataxia

posterior cortical atrophy

postural abnormality

pregnancy, neurologic complications in

prevention of neurologic disorders

primary lateral sclerosis

prion protein gene

progressive multifocal leucoencephalopathy

progressive myoclonic epilepsy

progressive neurologic disorder

progressive supranuclear palsy

protein 14-3-3, cerebrospinal fluid

pseudobulbar palsy

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychological testing, neurologic problems

psychomotor retardation

psychosis, childhood

psychosocial aspects

ptosis, bilateral

ptosis, unilateral

pursuit eye movements, abnormal

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

radiation hypersensitivity

rapidly progressing neurologic illness

real-time quaking-induced conversion

rehabilitation for neurologic disorders

release phenomena

remote effect of cancer on the nervous system

renal transplantation

repetition, impaired

respirations in CNS disease

respiratory failure

restless leg syndrome

reticulum cell sarcoma

retina, abnormal

retinal branch artery occlusion

retinal infarction

retinitis pigmentosa

Rett's syndrome

rigidity, axial

roaming behavior

Rosenthal fibers

rubella encephalitis

rubella encephalitis, progressive

rubella syndrome

saccadic eye movements, abnormal

salivation, excessive

sea-blue histiocytes

seizure, advice to parents and teachers regarding

seizure, psychosocial aspects of

seizure, recurrent

seizure, surgical treatment of

seizure, treatment of

seizure, workup of

semantic dementia

sensorineural hearing loss

serologic testing

serologic testing of cerebrospinal fluid

single photon emission computed tomography

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skin, lesions in neurologic disorders

sleep apnea, obstructive

sleep pathology and physiology

slit lamp examination

slow virus infection of CNS

spastic diplegia

spastic paraplegia, type 11

speech disorder

speech disorder, childhood

speech disorder, non aphasic

speech lateralization

speech, absence of

speech, delayed development of

speech, loss of

speech, pressured

spinal muscular atrophy

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 7

spinopontine atrophy, dominant

splenium of corpus callosum

spongy degeneration of brain

square wave jerks

startle myoclonus

startle reaction

stem cell rescue

stem cell transplantation

stereotyped behavior

stooped posture

striopallidodentate calcifications, familial idiopathic

stuttering following CVA

subdural hematoma

substantia nigra

Susac's syndrome

symmetric brain lesions

syphilis, diagnosis and treatment

syphilis, neurologic complications with

systemic illness

tandem gait, ataxic

teeth, wide-spaced

temporal lobe, atrophy

temporal lobe, lesion

temporal lobe, lesion, bilateral

testicular enlargement

thalamus, lesion of

thalamus, lesion of-bilateral

third nerve palsy

third nerve palsy, bilateral

thrombocytopenia

thrombosis, cerebral

tongue, atrophy

tongue, enlarged

tongue, fasciculations of

tongue, impaired movements of

tongue, protrusion of

toxoplasmosis, acquired

toxoplasmosis, CNS

treatment of neurologic disorder

tremor, intention

tremor, resting

tremor, wing beating

tremor, writing

trientine dihydrochloride

trinucleotide repeats

Trousseau's sign

upgaze, paralysis of

uremic encephalopathy

uremic twitching

urinary incontinence

urine test for metabolic disorders

Venereal Disease Research Laboratory test

venous hypertension

venous ischemia

very long chain fatty acids

viral infection

viral infection, CNS

viral isolation

vision, blurred

vision, failure of in childhood

visual acuity, decreased

visual evoked response

visual impairment

visual loss, progressive

visual loss, slow

vitamin deficiency

vitamin supplementation

vocal cord paralysis

voice, abnormality of

Waldenstrom's macroglobulinemia

walking, difficulty with

weakness, fatiguable

weakness, generalized

weakness, progressive

weakness, proximal

Wernicke's aphasia

Wernicke's encephalopathy

Whipple's disease

white matter disease

whole genome sequencing

wide based gait

Wolfram syndrome

word-finding difficulty

x-linked intellectual deficit

x-linked mental retardation

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Pyruvate Dehydrogenase Deficiency (PDCD)
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