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abdominal distention

abdominal muscle paralysis

abscess, intracerebral

abscess, intracranial

abscess, perivalvular

aceruloplasminemia

achilles tendon, enlarged

acid maltase deficiency

acid maltase deficiency, adult

acoustic nerve, vestibular division of

acoustic neurinoma, bilateral

acquired immunodeficiency syndrome

acral sensory symptoms

activities of daily living

activities of daily living scale

Addison's disease

adenosine deaminase deficiency

adrenoleukodystrophy

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

adult polyglucosan body disease

adult-onset leukodystrophy, with neuroaxonal spheroids

advances in neurology

adverse drug reaction

agenesis of corpus callosum

Aicardi-Goutieres syndrome

alcohol intolerance

alcohol intoxication

alcohol, blood level of

alcohol, neurologic complications with

alcoholic blackout

alcoholic dementia

alcoholic polyneuropathy

alcoholic withdrawal states, DT's, convulsions, etc.

alpha galactosidase A deficiency

alpha glucosidase

alpha-fetoprotein

alternating hemiplegia

alternating hemiplegia of childhood

alternating rapid movement

alternating rapid movement, impaired

alternative medicine

alveolar hypoventilation

Alzheimer's disease

Alzheimer's disease, age of onset

Alzheimer's disease, behavioral symptoms

Alzheimer's disease, conjugal

Alzheimer's disease, diagnosis of

Alzheimer's disease, driving with

Alzheimer's disease, early onset

Alzheimer's disease, early symptoms

Alzheimer's disease, familial

Alzheimer's disease, familial, late onset

Alzheimer's disease, incidence

Alzheimer's disease, pathogenesis

Alzheimer's disease, preclinical

Alzheimer's disease, risk factors in

Alzheimer's disease, telling patient diagnosis of

Alzheimer's disease, treatment of

aminoacidopathies

amyloid angiopathy, cerebral

amyloid angiopathy, cerebral, Dutch type

amyloid angiopathy, hereditary cystatin C

amyloid beta protein

amyloid imaging

amyloid plaques

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, diagnosis of

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, guamian type of

amyotrophic lateral sclerosis, Parkinson-dementia-complex

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, treatment of

anesthesia, general

aneurysm, asymptomatic

aneurysm, intracranial

aneurysm, intracranial, detection

aneurysm, intracranial, familial

aneurysm, intracranial, natural history

aneurysm, intracranial, screening for

aneurysm, intracranial, treatment of

aneurysm, multiple intracranial

aneurysm, ruptured

aneurysm, unruptured

Angelman syndrome

angiofibroma, facial

angiography, cerebral

angiography, posterior fossa

angioid streaks

angiomyolipomas

animal exposure

ankle reflex, absent

anterior horn cell disease

anterior tibial muscle weakness

antibiotic prophylaxis

anticholinergic drugs

anticholinesterase

anticonvulsants

anticonvulsants, discontinuation in seizure-free epileptics

anticonvulsants, effectiveness

anticonvulsants, hypersensitivity syndrome

anticonvulsants, rectal administration

anticonvulsants, selection of

anticonvulsants, untoward effects of

antiphospholipid antibodies

aortic valve, bicuspid

aortic valve, lesion of

aphasia, progressive

aphasia, progressive, primary

apolipoprotein E

apraxia of eye movements

apraxia, constructional

arrhythmia, cardiac

arterial dissection

arterial dissection, multiple

arterial dissection, recurrent

arterial dissection, renal artery

arterial dissection, ruptured

arterial dissection, vertebral

arteriovenous malformation

arteriovenous malformation, cerebral

arteriovenous malformation, pulmonary

arthropathy, neuropathic

artificial nutrition and hydration

arylsulfatase A

aspartate aminotransferase

Asperger's syndrome

ataxia telangiectasia

ataxia, cerebellar

ataxia, congenital

ataxia, hereditary

ataxia, progressive

ataxia, sensory

ataxia, truncal

atrial enlargement

atrial fibrillation

attention deficit disorder with hyperactivity

auditory and vestibular pathways

auditory evoked brainstem potentials

autism, screening for

autistic behavior

automatic implantable cardioverter-defibrillator

autonomic dysfunction

autonomic neuropathy

autonomic neuropathy, idiopathic

autosomal dominant leukodystrophy

axonal degeneration

axonal spheroid

bacterial endocarditis, neurologic manifestations of

bacterial infection

basal cell carcinoma

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, infarction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

Bassen-Kornzweig syndrome

battered child syndrome

behavior modification

behavior, combative

behavioral disorder

benign essential tremor

benign essential tremor, refractory

bent spine syndrome

beta adrenergic blocker

bicaudate index

bilateral periventricular nodular heterotopia

biologic markers

biotin deficiency

biotin deficiency, juvenile form

biotinidase deficiency

biotin-responsive basal ganglia disease

bladder dysfunction

blinking, reduced

blood transfusion

bone density, increased

bone marrow transplantation

bovine spongiform encephalopathy

brachial neuritis

brachial plexus neuropathy

brachial plexus neuropathy, familial

brachial plexus neuropathy, recurrent

brain transplantation

brainstem, atrophy

brainstem, hypoplasia

brainstem, lesion of

brainstem, neoplasms of

brainstem, vascular malformation of

Brugada syndrome

bulbar palsy, childhood

bulbar palsy, progressive

burning feet, differential diagnosis of

burning paresthesia

cafe au lait spots

calcification, gyral

calcification, intracranial

calf hypertrophy

Canavan's disease

carbonic anhydrase II deficiency

carcinoembryonic antigen

carcinoma of pancreas

cardiac surgery

carnitine deficiency

carnitine deficiency myopathy

carotid artery disease

carotid artery occlusion, bilateral

carotid artery occlusion, neck

CAT scan, abdomen

CAT scan, abnormal

CAT scan, angiography

CAT scan, chest

CAT scan, contrast enhanced

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, isodense lesion with acute hemorrhage

CAT scan, muscle

cataracts, congenital

caudate nucleus

caudate nucleus, atrophy

cavernous hemangioma

central nervous system, infection of

central pontine myelinolysis

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar hemorrhage

cerebellar hypoplasia

cerebellar infarction

cerebellar lesion

cerebellar plaques, amyloid

cerebellar vermis

cerebellum, disease of

cerebellum, neoplasms of

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortex

cerebral cortical atrophy

cerebral edema, vasogenic

cerebral embolism

cerebral embolism, cardiac origin

cerebral glucose metabolism

cerebral infarction

cerebral infarction, small, deep

cerebral infarction, subcortical

cerebral ischemia

cerebral vasculature

cerebral vasculature, calcification

cerebro hepato renal syndrome

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, culture of, viral

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, protein of

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, acute management of

cerebrovascular accident, cardiac disease causing

cerebrovascular accident, cost of

cerebrovascular accident, familial occurrence

cerebrovascular accident, infancy and childhood

cerebrovascular accident, mimics

cerebrovascular accident, multiple

cerebrovascular accident, neonatal

cerebrovascular accident, non atherosclerotic cause of

cerebrovascular accident, nonarterial territory

cerebrovascular accident, nonvascular territory

cerebrovascular accident, prognosis in

cerebrovascular accident, recurrent

cerebrovascular accident, rehabilitation of

cerebrovascular accident, time of presentation

cerebrovascular accident, young adult

cerebrovascular disease

cerebrovascular disease, surgical treatment of

ceruloplasmin, serum

Charcot-Marie-Tooth

Chediak-Higashi syndrome

chenodeoxycholic acid

cherry red spot

cherry red spot-myoclonus syndrome

chest x-ray, abnormal

chewing movements

chilbran skin lesions

choline acetyltransferase

chorea, causes of

chorea, familial

choreoathetosis

choroid plexus, abnormality of

chromosomal abnormality

chronic progressive external ophthalmoplegia

cingulate island sign

cirrhosis, infancy

cisterna magna, enlarged

Clinical Pathologic Conference(C.P.C.)

clubbing of fingers

clubfoot as related to neurologic disease

coat-hanger pain

cobalamin C deficiency

Cockayne's syndrome

codfish vertebrae

cognition, slowed

cogwheel rigidty

cold hands sign

collagen vascular disease

coma, causes of

coma, prognosis of

compression fracture

compression neuropathy

conduction block

congenital deformities

congenital heart disease

congenital heart disease, CNS complications with

congenital malformation

congenital myasthenic syndromes

congenital myopathy

congenital ocular motor apraxia

congestive heart failure

contractures, joint

contraindications

controversies in neurology

contusion, cerebral

conversion reaction

copper deficiency

copper metabolism, abnormal

cornea, abnormal

cornea, opacification in infancy-causes of

cornea, opacity of

corneal dystrophy

corneal transplant

corpus callosum

corpus callosum, atrophy of

corpus callosum, hypoplastic

corpus callosum, lesion of

corpus callosum, thinning

cortical blindness

cortical blindness, transient

cortical infarction

cost effectiveness

cranial nerve palsies

cranial nerve tumor

creatine phosphokinase(CPK)elevated

Creutzfeldt-Jakob disease, genetic

crying, pathologic

cryopyrin-associated periodic syndrome

cultured skin fibroblasts

cyst, peritumoral

cyst, benign intracranial

cyst, cortical parenchyma

cyst, neoplastic cerebellum

cyst, odontogenic

cyst, parenchymal

cyst, porencephalic

cytomegalovirus infection

deep gray nuclei

deep tendon reflexes

degenerative diseases of CNS

delay in diagnosis

delayed dentition

dementia, age at onset

dementia, cerebrovascular disease causing

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

dementia, treatment of

demyelinating disease

dental procedure, neurologic complications with

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

developmental abnormality of brain

developmental disability

developmental evaluation

developmental milestones

developmental milestones, loss of

developmental retardation

developmental venous anomalies

dexterity, impaired

diabetes insipidus

diabetes mellitus

diagnostic criteria

diaphragmatic paralysis

diazepam rectal gel

differential diagnosis

difficulty climbing stairs

digits, abnormal

dilantin, hypersensitivity to

diplegia, brachial

disability rating scale, neurological

disability, neurological

disconnection syndrome

disease modifying agents

disinhibition-dementia-parkinsonism-amyotrophic complex

distal muscle atrophy

distal muscle weakness

diurnal variation

dopa responsive dystonia

dopamine agonist

dopaminergic dysfunction

Dravet syndrome

drug induced neurologic disorders

Durett hemorrhages

dysdiadochokinesia

dysostosis multiplex

dyssynergia cerebellaris myoclonica

dystonia musculorum deformens

dystonia, cervical

dystonia, children

dystonia, etiology of

dystonia, focal

dystonia, painful

dystonia, treatment of

dystroglycanopathies

ears of the Lynx MR sign

eating disorder

echocardiogram, transesophageal

echocardiogram, transesophageal, false negative

echocardiogram, transthoracic

echocardiogram, transthoracic, false negative

ectatic basilar artery

edema, periorbital

Ehlers-Danlos syndrome

ejection fraction

ejection fraction, abnormal

electrocardiogram, abnormal

electroconvulsive therapy

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, monitoring, continuous

electroencephalogram, pediatric patients

electroencephalogram, periodic complexes

electroencephalogram, video monitoring with

electron microscopy

electronystagmography

electroretinograph

embolism, paradoxical

embolism, septic

embolization, therapeutic

emergencies, neurologic

emergencies, ocular

emergency medical technicians

Emery-Dreifuss muscular dystrophy

emotional lability

encephalitis, viral

encephalomalacia

encephalopathy, acute necrotizing

encephalopathy, acute necrotizing of childhood

encephalopathy, anoxic

encephalopathy, metabolic

encephalopathy, neonatal

encephalopathy, post traumatic

encephalopathy, progressive

endocarditis, acute bacterial

endocarditis, prophylaxis

endolymphatic sac tumors

endovascular therapy

entrapment neuropathy

enzyme treatment

enzyme, muscle disease

epicanthal folds

epidemiology of neurology

epileptic encephalopathy

episodic disorders

episodic neurologic deficits

erectile dysfunction

esophageal varices

ethics in neurology

evoked potentials

executive dysfunction

exercise intolerance

exome sequencing

extraocular muscle lesion

eye movement, disorders of

Fabry's disease

face, elongated

facial anomalies

facial appearance, abnormal

facial expression abnormality

facial hypoplasia

facial nerve palsy

facial nerve palsy, bilateral

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

failed medical management

failure to thrive

familial hemiplegic migraine

familial rectal pain

family conference

family function

Farber's disease

FARS2 deficiency

fatal familial insomnia

fatty acid dehydrogenase deficiency

fatty acid, elevated plasma content

feeding disorder

ferric chloride test

ferritin, elevated

fetal alcohol syndrome

fever, recurrent

fibrinolytic agents, contraindications

fibroma, ungual

fine motor function, impaired

finger nose finger test

fingerprint bodies

fistula, arterio-venous

fistula, arterio-venous, dural

fistula, arterio-venous, pulmonary

flow study, carotid artery

fluorescein angiography

fluorescene in situ hybridization

fourth ventricle, enlargement of

fracture, pathologic

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

Friedreich's ataxia

frontal bossing

frontal lobe, atrophy

frontal lobe, behavior with disease of

frontal lobe, pathologic signs of

frontotemporal dementia, behavioral variant

fundus, abnormality of

funduscopic exam

gait, festinating

galactocerebrosidase

gangliosidosis GM1

gangliosidosis GM2

gastrointestinal bleeding

gastrointestinal disease, neurologic complications

gastrointestinal motility

gastrointestinal perforation

Gaucher's disease

Gaucher's disease, adult onset

gaze palsy, horizontal

gaze palsy, supranuclear

gaze palsy, vertical

genetic counselling

genetic diagnosis

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

Gerstmann-Straussler-Scheinker disease

giant axonal neuropathy

Gilles de la Tourette syndrome

Gillespie syndrome

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

GLUT1 deficiency syndrome

glutaric acidemia

glycogen storage disease

Gorlin-Goltz syndrome

Gowers maneuver

granular osmiphilic material

growth hormone deficiency

growth retardation

guanidinoacetate methyltransferase deficiency

gyrus, abnormal

Hallervorden Spatz disease

Hallervorden Spatz disease, late onset

Hallgren's syndrome

hallucination, visual

head circumference

head injury, pediatric

headache, children

headache, positional

headache, recurrent

headache, throbbing

headache, thunderclap

headache, unilateral

health insurance

hearing loss, bilateral

hearing loss, sudden, unilateral

hearing problems in children

heart valve surgery

heel-knee-shin test

hemangioblastoma

hemangioma, facial

hemangioma, leptomeningeal

hemangioma, skin

hematuria, gross

hemianopia, homonymous

hemianopia, transient

hemihypertrophy, congenital

hemiparesis, transient

hemochromatosis

hemochromatosis, primary

hemophagocytic lymphohistiocytosis

hemophagocytic lymphohistiocytosis, cerebromeningeal

hemophagocytosis

hemorrhagic diathesis

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

hereditary hemorrhagic telangiectasia(HHT)

herpes simplex encephalitis

herpes simplex encephalitis, differential diagnosis of

hexosaminidase-A

hexosaminidase-A and B

high arched feet

high arched palate

hippocampal atrophy

hockey stick sign

holoprosencephaly

Hunter's syndrome

Huntington's chorea

Huntington's chorea, genetic counselling

Huntington's chorea, late onset

Huntington's chorea, misdiagnosis of

Huntington's chorea, presymptomatic detection of

Huntington's disease, children

Hurler's syndrome

hydrocephalus, communicating

hydrocephalus, complications with

hydrocephalus, congenital

hydrocephalus, etiology

hydrocephalus, exvacuo

hydrocephalus, fetal

hydrocephalus, intrauterine

hydrocephalus, treatment of

hyperglycinemia

hyperglycinemia, nonketotic

hyperhomocysteinemia

hyperostosis corticalis generalisata familiaris

hyperpigmentation of skin

hyperpyrexia, CNS disorder causing

hypersensitivity reaction

hyperthyroidism

hypertriglyceridemia

hypertrophic cardiomyopathy

hypertrophic intracranial pachymeningitis

hypoalbuminemia

hypofibrinogenemia

hypoglycemic coma

hypoglycorrhachia

hypokalemic periodic paralysis

hypomelanosis of Ito

hypometric saccades

hypomyelination

hypoparathyroidism

hypopigmentation of skin

hypotension, neurologic causes of

hypotension, systemic

hypotonia, infants

hypoxic encephalopathy

hypoxic-ischemic leukoencephalopathy

iatrogenic neurologic disorders

ileus, paralytic

imbalance, postural

immunodeficiency

immunofluorescence

immunohistochemistry

immunologic disease

immunosuppression

inappropriate behavior

inborn errors of metabolism

inborn errors of metabolism, screening

incidental finding

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

incontinentia pigmenti

infant, evaluation of

infantile bilateral striatal necrosis

infantile spasm

infection, recurrent

inflexibility, mental

influenza, avian

insulin resistance

intellectual deficit

intellectual deficit, treatable causes of

intellectual deterioration

intelligence quotient

interferon alpha

interstitial pulmonary fibrosis

intestinal pseudoobstruction

intracerebral hemorrhage

intracerebral hemorrhage, familial

intracerebral hemorrhage, lobar

intracerebral hemorrhage, recurrent

intracerebral hemorrhage, young adult

intracranial hemorrhage

intracranial pressure, increased

intrauterine infection

intraventricular hemorrhage

intrinsic hand muscles, wasting of

iron, serum, low

ischemic exercise test

islet cell tumor

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Jakob-Creutzfeldt disease, medical precaution with

Jakob-Creutzfeldt disease, variant

Jervell Lange-Neilson syndrome

joint hypermobility

Joubert syndrome

juvenile myoclonus epilepsy

Kayser-Fleischer ring

Kearns-Sayre syndrome

kinesia paradoxica

Kluver-Bucy syndrome

Krabbe's disease

Kugelberg-Welander syndrome

kyphoscoliosis, neurologic causes of

lactic acidemia

lactic dehydrogenase(LDH)

lacunar infarction

Lafora's disease

language disorder in adults

laughing, pathologic

Laurence-Moon-Bardet-Biedl syndrome

L-dopa, drug interactions with and side effects of

learning disability

learning disability, in children

Leber's congenital amaurosis

leg spasms, painful

leg weakness, bilateral

Leigh's disease

Leigh's disease, adult variety

lens, dislocation of

lenticular nucleus, lesion of, bilateral

Lesch-Nyhan syndrome

leukodystrophy, pigmented orthochromatic

leukoencephalopathy

leukoencephalopathy with calcification and cysts

leukoencephalopathy, differential diagnosis

leukoencephalopathy, hereditary diffuse

level of consciousness, decreased

Lewy body disease, diffuse

Lhermitte-Duclos disease

libido, decreased

lid abnormalities

lid closure, weakness of

life expectancy

life support, withdrawal of

life support, withholding of

life sustaining treatment

lifestyle modification

lipid storage disorder of CNS

lipomembranous polycystic osteodysplasia

livedo reticularis

liver function enzymes

liver transplantation

locus ceruleus, lesion of

long bone lesion

long QT syndrome

low birth weight

Lowe's syndrome

lumbar puncture

lymphadenopathy

lymphangiomyomatosis

lymphoma involving CNS

lysosomal storage disease

lysosomes, abnoral

macular degeneration

magnetic susceptibility

magnetoencephalography

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

malformation, vascular, familial

malformation, vascular, screening for

malignant hyperpyrexia

manic-depressive

maple syrup urine disease

marche a petits pas

Marinesco-Sjogren syndrome

McArdle's disease

McLeod syndrome

medical-legal aspects of neurology

medulla oblongata, neoplasm of

medulloblastoma

megalencephaly, idiopathic

melanomatosis, primary malignant

memory, defect of recent

memory, evaluation of

memory, impairment of

meningeal enhancement

meningitis, aseptic

meningitis, carcinomatous

meningitis, CSF cell count-normal

mental retardation

mental retardation, etiology of

mental retardation, familial

mental retardation, family psychological problems in

mental status, abnormal

mesial temporal lobe

mesial temporal lobe epilepsy

mesial temporal sclerosis

metabolic acidosis

metabolic disorder, primary

metabolic disorder, primary-screening tests

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

metachromatic leukodystrophy, juvenile

methylmalonic acidemia

microangiopathy, brain

microhemorrhage, intracerebral

microspherophakia

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

migraine with aura

migraine, children

migraine, hemiplegic

migratory lesion pattern

mild cognitive impairment

Miller-Dieker syndrome

Minamata disease

Mini Mental Status Examination

mitochondrial disease

mitochondrial encephalomyopathy

molecular genetics

molybdenum cofactor deficiency

monomelic amyotrophy

motor neuron disease

movement disorder

movement disorder, extrapyramidal

movement disorder, hyperkinetic

movement disorder, treatment of

moyamoya, adult

MRI, angiography

MRI, blooming effect

MRI, brachial plexus

MRI, CAT scan compared to

MRI, complications with

MRI, contrast enhanced

MRI, diffusion tensor

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, eye of tiger sign

MRI, functional

MRI, gradient-echo

MRI, incidental finding

MRI, paramagnetic effect

MRI, punctate pattern

MRI, spinal cord

MRI, susceptibility weighted

MRI, T1 weighted high signal foci

mucopolysaccharidoses

multiple endocrine neoplasia

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, familial

multiple sclerosis, misdiagnosis

multiple system atrophy

muscle atrophy, focal

muscle atrophy, progressive

muscle diseases, characteristics of

muscle hypertrophy

muscle phosphorylase deficiency

muscle stiffness

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

muscle weakness, sudden onset of

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, Becker, carrier

muscular dystrophy, cardiovascular changes with

muscular dystrophy, central nervous system abnormality

muscular dystrophy, classification

muscular dystrophy, congenital

muscular dystrophy, congenital, Fukuyama type

muscular dystrophy, differential diagnosis of

muscular dystrophy, Duchenne

muscular dystrophy, Duchenne, carrier

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

myasthenia gravis

myasthenia gravis, congenital

myasthenia gravis, differential diagnosis

myasthenia gravis, familial incidence of

myasthenia gravis, misdiagnosis of

myelination of nervous system

myeloneuropathy

myocardial abscess

myocardial biopsy

myoclonic jerks

myoclonus, epilepsy

myopathy, alcoholic

myopathy, metabolic

myopathy, mitochondrial

myopathy, quadriceps

myopathy, vacuolar

myotonia congenita

myotonia dystrophica

nasal bridge, wide

nausea and vomiting

neonatal epilepsy syndromes

neonatal epileptic encephalopathy

neoplasm, intracranial

neoplasm, metastatic to CNS

neoplasm, peripheral nerve

neoplasm, posterior fossa

neoplasm, primary intracerebral

neoplasm, primary of CNS

neoplasm, primary of CNS-recurrent

nerve conduction studies

nerve hypertrophy

neuroaxonal dystrophy

neuroaxonal dystrophy, infantile

neuroaxonal dystrophy, juvenile

neuroaxonal leukodystrophy

neurocardiology

neurocutaneous disease

neurodegeneration with brain iron accumulation

neuroendocrinology

neurofibrillary degeneration

neurofibromatosis 1

neurofibromatosis 2

neurofibromatosis 2, presymptomatic

neurogenic bladder

neurogenic vs.myopathic atrophy

neuroichthyosis

neuroleptic, atypical

neurolipidosis IV

neurologic complications of, surgery

neurologic complications of, systemic disease

neurologic consultation

neurologic disease

neurologic disease, diagnoses of

neurologic evaluation

neurologic examination

neurologic examination, focal

neurologic signs

neurologic symptoms

neurologic testing

neuromuscular junction

neuronal ceroid-lipofuscinosis

neuronal degeneration

neuronal intranuclear inclusion disease

neuronal migration disorder

neuroophthalmology

neuropathology, brain

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, painful

neuropathy, peripheral

neuropathy, sensory

neuropathy, sensory, hereditary

neuropsychiatry

neurotransmitter

nevoid basal cell carcinoma syndrome

newborn, evaluation of

next-generation sequencing

Niemann-Pick disease

night blindness

nigrostriatal pathway

Noonan Syndrome

numbness, extremity

nystagmus, monocular

obsessive-compulsive disorder

occipital lobe, infarction

occipital lobe, lesion of

ocular dysmetria

ocular motility, disorders of

ocular myopathy

oculodentodigital dysplasia

old age, neurology of

ophthalmoplegia

ophthalmoplegia, progressive external

optic atrophy, bilateral

optic foramina, abnormal

optic nerve, hypoplasia of

optic neuropathy

optokinetic nystagmus, abnormal

orthostatic hypotension

ovarian insufficiency

pacemaker, cardiac-transvenous

pain, abdominal

pain, increased response

palatal myoclonus

palliative care

pallido-ponto-nigral degeneration

palmoplantar keratoderma

pancreatic cyst

paralysis, acute areflexic

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, spastic

paraspinal muscle

paraspinal muscle weakness

Parkinson disease

Parkinson disease, arteriosclerotic

Parkinson disease, atypical

Parkinson disease, benign tremulous

Parkinson disease, classification

Parkinson disease, dementia with

Parkinson disease, diagnosis

Parkinson disease, differential diagnosis of

Parkinson disease, dystonia with

Parkinson disease, etiology of

Parkinson disease, familial

Parkinson disease, freezing phenomena in

Parkinson disease, heterogeneity of

Parkinson disease, L-dopa nonresponsive

Parkinson disease, nonmotor problems of

Parkinson disease, pathogenesis of

Parkinson disease, presymptomatic detection

Parkinson disease, rapid progression

Parkinson disease, subtypes

Parkinson disease, surgical treatment of

Parkinson disease, treatment of

Parkinson disease, young onset

Parkinsonism syndrome

Parkinsonism-dementia complex

paroxysmal extreme pain disorder

paroxysmal hemiplegia

paroxysmal neurologic deficits

PAS positive material in the brain

patient information and support

pectus carinatum

pectus excavatum

Pelizaeus Merzbacher

percussion induced muscle contraction

periodic paralysis

periodic paralysis, thyrotoxic

peripheral blood smear

periventricular leukomalacia

peroxisomal disease

persistent vegetative state

personality change

phenylketonuria

phenylketonuria, adult onset

pheochromocytoma

philtrum, tented

phosphorylase b kinase deficiency

photosensitivity, skin

physical therapy

physician assisted suicide

pigmentary retinopathy

Pittsburgh Compound B

pituitary, hormones of

platelet inhibiting drugs

pleocytosis of cerebrospinal fluid

poison, mercury

poison, neurologic problems with

polycystic kidneys

polycystic lipomembranous osteodysplasia

polyglucosan body

polyglucosan body disease

polymerase chain reaction

polyneuropathy, familial

polyps, gastrointestinal tract

Pompe's disease of glycogen storage

pontocerebellar atrophy

port wine nevus

portal caval shunt

positive sharp waves

posterior cerebral artery territory infarction

postural abnormality

practice guidelines

Prader-Labhart-Willi syndrome

precipitating factors

precocious puberty

pregnancy, neurologic complications in

premature infant

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

primary familial brain calcification

prion protein gene

progressive myoclonic epilepsy

progressive neurologic disorder

progressive pallidum atrophy

progressive subcortical gliosis

protein 14-3-3, cerebrospinal fluid

pseudobulbar palsy

pseudohypoparathyroidism

pseudoretinitis pigmentosa

pseudoxanthoma elasticum

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychological testing, neurologic problems

psychomotor retardation

psychosis, acute

psychosocial aspects

psychotic behavior

PTEN hamartoma tumor syndrome

ptosis, bilateral

puberty, delayed

pulmonary embolism

pulmonary infiltrates

pulmonary stenosis

pursuit eye movements, abnormal

pyramidal tract

pyramidal tract dysfunction

quality of life

radiation hypersensitivity

radiation therapy, CNS treatment and complications with

radiation therapy, stereotactic

ragged-red fibers

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

reading problem, causes of

real-time quaking-induced conversion

recombinant DNA

recruitment, reduced

refractive errors

Refsum's disease

rehabilitation for neurologic disorders

release phenomena

renal cell carcinoma

renal dysplasia

renal tubular acidosis

repetitive questioning

respiratory depression

respiratory failure

respiratory tract infection

retina, abnormal

retinal degeneration

retinal hamartoma

retinal hemangioma

retinal hemorrhages

retinal ischemia

retinal vasculitis

retinal vasculopathy

retinal vasculopathy with cerebral leukodystrophy

retinitis pigmentosa

Rett's syndrome

reversible neurologic disorder

rhabdomyosarcoma of heart

rigid spine syndrome

rippling muscle disease

risk factors, modification

Romano-Ward syndrome

root lesion, nerve

saccadic eye movements, abnormal

salivation, excessive

Sandhoff's disease

Sanfilippo syndrome

Schilder's disease

scoliosis, neurologic association with

sea-blue histiocytes

second wind phenomena

sedimentation rate, elevated

seizure, cardiac arrhythmia causing

seizure, children

seizure, classification of

seizure, complications following

seizure, diagnosis of

seizure, differential diagnosis of

seizure, drug resistance

seizure, etiology of

seizure, familial

seizure, febrile

seizure, home treatment

seizure, incidence of

seizure, injury following

seizure, intractable

seizure, laughing as manifestation

seizure, neonatal

seizure, nonepileptic

seizure, paradoxical

seizure, photosensitive

seizure, prevalence of

seizure, prognosis in adults

seizure, prognosis in childhood

seizure, psychomotor-temporal lobe

seizure, repetitive

seizure, surgical treatment of

seizure, teenager

seizure, tonic-clonic

seizure, treatment of

seizure, workup of

selective serotonin reuptake inhibitors

self-mutilation

semialdehyde dehydrogenase deficiency

sensorineural hearing loss

sensory polyneuropathy

shaken infant syndrome

shoulder, pain in

shunt procedure, ventricular

shunt procedure, ventricular-complications of

single photon emission computed tomography

Sjogren-Larsson syndrome

skin, lesions in neurologic disorders

skull bone, thickening

skull x-ray, abnormal

skull x-ray, bony defect on

sleep pathology and physiology

slit lamp examination

sloped shoulders

slow virus infection of CNS

small vessel disease

small vessel disease, cerebral

Smell Identification Test

SNCA duplication

Sneddon's syndrome

sodium channel dysfunction

sodium valproate

somatosensory evoked potentials

Southern immunoblot test

spastic diplegia

spastic paraplegia, type 11

spastic paraplegia, type 15

speech disorder

speech disorder, childhood

speech, absence of

speech, delayed development of

sphingolipodoses

Spielmeyer Vogt syndrome

spinal cord degeneration

spinal cord, infarction of

spinal cord, lesion of

spinal cord, neoplasm

spinal cord, neoplasm, intramedullary

spinal cord, pathologic exam of

spinal cord, vascular malformation of

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinal muscular atrophy, classification

spinal muscular atrophy, intermediate form

spine, metastasis to

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 17

spinocerebellar ataxia type 2

spinocerebellar ataxia type 7

spinocerebellar ataxia type 8

spinocerebellar degeneration

spinopontine atrophy, dominant

splenium of corpus callosum

spongy degeneration of brain

spontaneous remission

staphylococcus aureus

startle myoclonus

startle reaction

status epilepticus

stem cell transplantation

stereotaxic surgery

stereotyped behavior

stereotyped behavior, drug induced

steroid therapy, CNS treatment and complications with

stimulant drugs

stimulation, deep brain

stooped posture

storage disease of CNS

streptococcal infection

streptococcus viridans

stress, emotional

striatum, lesion of

striatum, lesion of, bilateral

striopallidodentate calcifications, familial idiopathic

strokelike episodes

Sturge-Weber syndrome

subarachnoid hemorrhage

subarachnoid hemorrhage, familial

subarachnoid hemorrhage, prognosis

subcortical U fibers

subdural hematoma

subdural hematoma, neonates and infants

subependymal nodules

substantia nigra

subthalamic nucleus

subthalamic nucleus deep brain stimulation

superoxide dismutase

suprascapular neuropathy

survival motor neuron gene

sweating, abnormality of

symmetric brain lesions

syncope, recurrent

syncope, triggers of

systemic illness

tandem gait, ataxic

tapetoretinal degeneration

Tay-Sachs disease

teeth, abnormal

teeth, number of in infants

teeth, wide-spaced

telangiectases, retinal

temper tantrums

temporal lobe, atrophy

temporal lobe, lesion

temporal lobe, lesion, bilateral

temporalis muscle wasting

temporalis muscle weakness

temporomandibular joint, dislocation

tentorium cerebelli

testicular enlargement

thalamus, focused ultrasound ablation

thalamus, atrophy of

thalamus, lesion of

thalamus, lesion of-bilateral

thromboangiitis obliterans cerebri

thrombocytopenia

thrombophlebitis

thyroid function tests

tomaculous neuropathy

tongue, enlarged

tongue, fasciculations of

tongue, protrusion of

tongue, weakness

tonic foot response

torsades de points

toxins, nervous system

transient ischemic attack

transient ischemic attack, recurrent

transient neurologic deficit

transverse smile

treatment of neurologic disorder

treatment, non-pharmacologic

tremor, intention

tremor, postural

tremor, resting

tremor, surgical treatment of

tremor, thalamic stimulation for suppression of

tremor, treatment of

tremor, wing beating

trichopoliodystrophy

trientine dihydrochloride

trinucleotide repeats

tuberous sclerosis

tuberous sclerosis, screening for

tumefactive lesion

tumor suppressor gene

ultrasonography

umbilical-cord blood transplantation

unconsciousness

Unverricht-Lundborg disease

upgaze, paralysis of

urea-cycle enzymopathies

urinary catecholamines

urinary frequency

urinary incontinence

urine test for metabolic disorders

Usher's syndrome

vanishing white matter

venous thrombosis, non-cerebral

ventricular tachycardia

ventriculostomy, endoscopic

vertebral-basilar insufficiency

vertigo, episodic

very long chain fatty acids

vestibular function, tests of

vibratory sensation, abnormal

violent behavior

viral infection

viral infection, CNS

viral isolation

vision, failure of in childhood

visual acuity, decreased

visual evoked response

visual field defect

visual fields, constricted

visual impairment

visual loss, congenital

visual loss, slow

visuospatial disturbance

vitamin deficiency

vomiting, recurrent

Von Hippel Lindau

Von Hippel Lindau, carrier

Von Hippel Lindau, screening protocol for

von Hippel-Lindau, screening

walking, difficulty with

weakness, chronic

weakness, congenital

weakness, episodic

weakness, fatiguable

weakness, generalized

weakness, progressive

weakness, proximal

weaning from respirator, failure to

Wernicke's aphasia

Wernicke's encephalopathy

white matter disease

white matter disease, subcortical

white matter disease, unilateral

whole genome sequencing

wide based gait

winging of scapula

Wolff-Parkinson-White syndrome

Wolfram syndrome

word-finding difficulty

wound healing, poor

xanthoma, tendon

xeroderma pigmentosa

x-linked hydrocephalus

x-linked intellectual deficit

X-linked lissencephaly

x-linked mental retardation

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