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Differential
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abdominal reflex, absent

abducens nerve paralysis

abulia

achilles tendon, enlarged

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

acquired immunodeficiency syndrome, infants and children

acromicria

Addison's disease

adrenoleukodystrophy

adrenomyeloneuropathy

adult polyglucosan body disease

adult-onset leukodystrophy, with neuroaxonal spheroids

advances in neurology

adverse drug reaction

Africa

alcohol injection

alcohol intolerance

alcohol, neurologic complications with

alcoholism

Alexanders disease

Alexanders disease, adult onset

algorithm

alopecia

alternating rapid movement

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, atypical

amyotrophic lateral sclerosis, diagnosis of

amyotrophic lateral sclerosis, etiology of

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, treatment of

aqueduct of Sylvius, stenosis

aqueductal stenosis

areflexia

arm weakness

Arnold Chiari malformation

atherosclerosis, generalized

atypical

auditory evoked brainstem potentials

autoantibodies

autoimmune disease

autonomic dysfunction

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

basal ganglia, infarction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basilar impression

behavioral disorder

Behcet's syndrome

benign essential tremor

biotin

biotin deficiency

biotin deficiency, juvenile form

biotin-responsive basal ganglia disease

bladder dysfunction

brachial plexus neuropathy

brain atrophy

brain biopsy

brain biopsy, negative

brain biopsy, stereotaxic

brainstem

brainstem, atrophy

brainstem, dysfunction

brainstem, glioma

brainstem, glioma in children

brainstem, glioma, adult

brainstem, ischemia

brainstem, lesion of

brainstem, neoplasms of

calcification, intracranial

CAT scan, emission, abnormal

CAT scan, spine

cataracts

caudate nucleus, atrophy

caudate nucleus, lesion of

caudate nucleus, lesion of, bilateral

central nervous system, infection of

cerebellar ataxia, children

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar degeneration

cerebral palsy, associated problems with

cerebral venous thrombosis

cerebroretinal microangiopathy with calcifications and cysts

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, lactic acid concentration

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, recurrent

cerebrovascular disease

cervical myelopathy

cervical spondylosis

chenodeoxycholic acid

chromosomal abnormality

chronic progressive external ophthalmoplegia

cirrhosis

Clinical Pathologic Conference(C.P.C.)

clonus

clubfoot as related to neurologic disease

cobalamin C deficiency

concentration, impaired

confusion

congenital infection, CNS

consanguinity

constipation

controversies in neurology

conversion reaction

corpus callosum, atrophy of

corpus callosum, lesion of

corpus callosum, thinning

cortical blindness

cough

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

crossed adductor reflex

crying, pathologic

deafmute

deafness

deafness, bilateral progressive vs.unilateral acute

deafness, unilateral

deep gray nuclei

degenerative cervical myelopathy

degenerative diseases of CNS

dementia, rapidly progressive

dementia, subcortical

demyelinating disease

dentate nuclei, lesion of

depression

dermatitis

dermatomyositis

developmental milestones

developmental milestones, loss of

developmental retardation

differential diagnosis

diplegia, spastic cerebral

diplopia

disability, neurological

disorientation

distal muscle atrophy

distal muscle weakness

dysarthria

dysarthria-clumsy hand syndrome

dystonia musculorum deformens

dystrophic calcification

ears of the Lynx MR sign

eczema

efficacy

electrical sensation

electroencephalogram, abnormalities of

encephalitis lethargica

enzyme, muscle disease

epidemiology of neurology

epileptic encephalopathy

equinovarus

evoked potentials

executive dysfunction

exome sequencing

eye movement, disorders of

facial nerve palsy

facial nerve palsy, bilateral

facial nerve palsy, recurrent

facial weakness

facial weakness, bilateral

fatty acid, elevated plasma content

fever

fine motor function, impaired

finger nose finger test

finger tapping

fistula, arterio-venous

fistula, arterio-venous, dural

fistula, arterio-venous, dural, spinal

fluctuate

fluorescent treponema antibody absorption(FTA-ABS)

foot deformity

foot drop

Friedreich's ataxia

Friedreich's ataxia, late onset

frontal lobe, pathologic signs of

fundus, abnormality of

gammaglobulin therapy, intravenous

genetic neurologic disorders

Gerstmann-Straussler-Scheinker disease

GFAP gene

girdle sensation

glioblastoma multiforme(astrocytoma Gr.III)

glioma

glioma, low-grade

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

GLUT1 deficiency syndrome

glutamic acid decarboxylase, antibody

glycogen storage disease

granulomatosis with polyangiitis

granulomatous disease

grasp reflex

growth retardation

Guillain Barre syndrome

Hallervorden Spatz disease

headache, intermittent

hemangioma, vertebral

hepatolenticular degeneration, non-Wilsonian

hepatomegaly

hepatosplenomegaly

herniated disc

herniated disc, cervical

high arched feet

Hispanics

hoarseness

human immunodeficiency virus type 1

human T-lymphotropic virus type I(HTLV-I)

human T-lymphotropic virus type II(HTLV-II)

Huntington's chorea

Huntington's disease, children

hydrocephalus

hydrocephalus, non-communicating(obstructive)

hyperammonemic encephalopathy

hyperhomocysteinemia

hyperpigmentation of skin

hypotension, systemic

inborn errors of metabolism

intellectual deterioration

intrinsic hand muscles, wasting of

Jakob-Creutzfeldt disease

Jamaica ginger paralysis

laminectomy, cervical

leg weakness, bilateral

Leigh's disease

lenticular nucleus, lesion of, bilateral

level of consciousness, decreased

lymphoma involving CNS

lymphomatoid granulomatosis

Madonna facies

Maghreb

malformation, vascular

mania

marche a petits pas

marihuana

medulla oblongata, lesion of

Melkersson's syndrome

memory, defect of recent

memory, impairment of

meningeal gliomatosis

meningitis, CSF cell count-normal

meningomyelitis

mental retardation

mental status, abnormal

metabolic disorder, primary

methylmalonic acidemia

microangiopathy, brain

mitochondrial disease

mobility

mobility aids

molecular genetics

mononeuritis multiplex

mortality

motor neuron disease

movement disorder

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, brachial plexus

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, emergent

MRI, high signal foci on

MRI, high signal intensity of basal ganglia

MRI, negative

MRI, paramagnetic effect

MRI, spinal cord

MRI, spine

MRI, T1 weighted high signal foci

MRS

multinucleated giant cell

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple system atrophy

muscle weakness, proximal

mutism

myasthenia gravis

myelitis, longitudinal

myelomalacia

myeloneuropathy

myelopathy

myelopathy, chronic progressive

myelopathy, hepatic

myelopathy, tract-specific

myxedema, neurologic manifestations of

neoplasm, primary of CNS

neoplasm, primary of CNS-classification

neoplasm, primary of CNS-treatment of

nerve biopsy

nerve conduction studies

neuroendocrinology

neurogenic bladder

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic examination

neurologic examination, focal

neurologic signs

neurologic symptoms

neuropathology

neuropathology, brain

neuropathy

neuropathy, demyelinating

neuropathy, peripheral

neuropathy, sensory

neurosyphilis

neurotoxin

next-generation sequencing

night blindness

numb clumsy hands syndrome

numbness, extremity

nystagmus

nystagmus, dissociated

ophthalmoplegia, progressive external

optical coherence tomography

oral ulcerations

orthostatic hypotension

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, familial spastic, variants

paraparesis, spastic

paraparesis, spastic, tropical

Parkinson disease, arteriosclerotic

Parkinson disease, asymmetric onset

Parkinson disease, L-dopa nonresponsive

Parkinson disease, postencephalitic

Parkinson disease, tremor, absence of

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

pleocytosis of cerebrospinal fluid

poison, organophosphate

POLR3B

polyglucosan body

polyglucosan body disease

polymerase chain reaction

posterior column disease

postural abnormality

practice guidelines

precipitating factors

primary lateral sclerosis

prisoners of war, neurologic complications in

prognosis

progressive neurologic disorder

proprioception, abnormal

pseudobulbar palsy

psychiatric problems in neurologic disorders

psychological testing

psychological testing, neurologic problems

psychomotor retardation

psychosis

ptosis

pulmonary infiltrates

pupil, abnormality in neurologic disorders

pursuit eye movements, abnormal

pyramidal

pyramidal tract

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

quadriparesis

quadriparesis, progressive

quadriplegia

radiation therapy, CNS treatment and complications with

radiculopathy

Rankin score

rapidly progressing neurologic illness

respiratory dyskinesias

reticulum cell sarcoma

retinitis pigmentosa

Rett's syndrome

reversible neurologic disorder

review article

rigidity

risk factors

risk-benefit assessment

Romberg's sign

Rosenthal fibers

rubella encephalitis

rubella encephalitis, progressive

rubella syndrome

rubella virus

saccadic eye movements, abnormal

safety

Saudi Arabia

scissors gait

sclerae, hyperpigmented

scleritis

scleroderma

scleroderma, neurologic involvement with

scoliosis

scoliosis, neurologic association with

sedimentation rate, elevated

seizure

seizure, children

sensorineural hearing loss

sensory level

sensory loss

sensory loss, cutaneous

serologic testing

serologic testing of cerebrospinal fluid

short stature

shunt procedure, ventricular

sinusitis

skin, biopsy

skin, darkening of

skin, lesions in neurologic disorders

skull x-ray, abnormal

sleep apnea

slow virus infection of CNS

snout reflex

solitary scerlosis

somatosensory evoked potentials

spastic paraplegia, type 11

spastic paraplegia, type 7

spasticity

spasticity, treatment of

spastin

speech disorder

speech disorder, childhood

speech, loss of

spinal cord

spinal cord, cervical

spinal cord, compression of

spinal cord, lesion of

spinal cord, vascular disorders Affecting

spinal cord, vascular malformation of

spinal xanthomatosis

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar ataxia type 7

steroid therapy, CNS treatment and complications with

striatonigral degeneration

striatonigral degeneration, infantile

striatum, lesion of

striatum, lesion of, bilateral

subcortical U fibers

substantia nigra

superior cerebellar peduncle

symmetric brain lesions

syphilis, diagnosis and treatment

syphilis, meningomyelitis

syphilis, neurologic complications with

teeth, number of in infants

tone, muscle, increased

tongue, enlarged

tongue, impaired movements of

tongue, ulcer

tonic foot response

tonsillar herniation of cerebellum

toxins, nervous system

transient ischemic attack

treatment of neurologic disorder

trinucleotide repeats

urea-cycle enzymopathies

vibratory sensation, abnormal

visual acuity, decreased

visual evoked response

walking, difficulty with

war

weakness

weakness, progressive

weakness, proximal

weight loss

Western immunoblot test

wheelchair

white matter disease

wide based gait

word-finding difficulty

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Cerebellar Ataxia and Hearing Impairment
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