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Differential
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achilles tendon, enlarged

acromicria

Addison's disease

adrenoleukodystrophy

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

adult polyglucosan body disease

advances in neurology

affect, inappropriate

amniocentesis

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, atypical

amyotrophic lateral sclerosis, diagnosis of

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, epidemiology of

amyotrophic lateral sclerosis, etiology of

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, treatment of

asymmetric crying facies

ataxia

autonomic dysfunction

axonal degeneration

Babinski sign

basal ganglia, calcification of

basal ganglia, lesion of

bone marrow transplantation

botulinum toxin

botulism

botulism antitoxin

botulism immune globulin

botulism, infant

brainstem, infarction of

brainstem, lesion of

bulbar palsy

bulbar palsy, childhood

bulbar palsy, progressive

cachexia

calcification, intracranial

caries

CAT scan, abnormal

CAT scan, emission, abnormal

cataracts

cerebral dominance

cerebrovascular accident

cerebrovascular accident, bilateral

children

chromosomal abnormality

chromosome 15

Clinical Pathologic Conference(C.P.C.)

Cockayne's syndrome

congenital birth defects

congenital heart disease

congenital malformation

creatine phosphokinase(CPK)elevated

cultured skin fibroblasts

cystatin C mutation

deafness

decerebrate posture

degenerative diseases of CNS

dementia

dementia, frontotemporal

depression

developmental disability

developmental retardation

differential diagnosis

disability rating scale, neurological

disability, neurological

distal muscle weakness

electroencephalogram, abnormalities of

electromyogram

emotional lability

epidemiology of neurology

Erdheim-Chester disease

eye movement, disorders of

eyes, sunken

facial appearance, abnormal

facial asymmetry

facial weakness

facial weakness, bilateral

gammaglobulin therapy, intravenous

gaze palsy

gaze palsy, horizontal

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic neurologic disorders

genetic testing

glycogen storage disease

growth hormone deficiency

heralding manifestation

hyperpigmentation of skin

hypopigmentation of skin

hyporeflexia

hypotension, systemic

hypotonia

hypotonia, infants

imbalance

inappropriate antidiuretic(A.D.H.)hormone

inclusion bodies

infant, evaluation of

intellectual deficit

intellectual deterioration

internal capsule

internuclear ophthalmoplegia

intrinsic hand muscles, wasting of

leg weakness, unilateral

memory, defect of recent

memory, impairment of

mental retardation

merosin

middle cerebellar peduncle, lesion

multiple sclerosis, differential diagnosis of

muscle biopsy

muscle cramp

muscle wasting, diffuse

muscular dystrophy

muscular dystrophy, congenital

neurologic disease, diagnoses of

neurologic signs

neurologic symptoms

neuromuscular blockade

neuromuscular disease, electrodiagnosis of

neuromuscular junction, abnormality of

neuroophthalmology

neuropathology

neuropathy

neuroprotective agents

neurotoxin

next-generation sequencing

Parkinsonism syndrome

pathologic reflex

peroxisomal disease

personality change

photosensitivity, skin

pigmentary retinopathy

polyglucosan body

polyglucosan body disease

polymerase chain reaction

polymicrogyria

pons, infarction of

Prader-Labhart-Willi syndrome

prenatal diagnosis by amniocentesis

primary lateral sclerosis

prognosis

progressive neurologic disorder

progressive supranuclear palsy

pseudobulbar palsy

psychomotor retardation

ptosis

ptosis, bilateral

pyramidal tract

pyramidal tract dysfunction

saccadic eye movements, abnormal

seizure

sensorineural hearing loss

sertraline

short stature

skew deviation

skin, lesions in neurologic disorders

sleep

sleep pathology and physiology

symmetric brain lesions

tongue, fasciculations of

tongue, impaired movements of

tongue, protrusion of

toxins, nervous system

tracheostomy

trauma

treatment of neurologic disorder

very long chain fatty acids

walking, difficulty with

weakness

weakness, generalized

weakness, infant

weakness, progressive

wheelchair

white matter disease

wide based gait

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Cognitive and Brain Magnetic Resonance Imaging Findings in Adrenomyeloneuropathy
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Autonomic Ganglionitis with Severe Hypertension, Migraine, and Episodic but Fatal Hypotension
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The Stroke Syndrome of Cortical Vein Thrombosis
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Internal Carotid Artery Dissection:MR Imaging Features and Clinical-Radiologic Correlation
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Mechanical Ventilation in Stroke Patients-Is It Worthwhile
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Campylobacter Jejuni Infection and Anti-GM1 Antibodies in Guillain-Barre Syndrome
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Progressive Deterioration of Intellect and Motor Function Occurring Several Decades after Cranial Irradiation
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Human T-Cell Lymphotropic Virus Type 1-Associated Myelopathy, Sjogren Syndrome, and Lymphocytic Pneumonitis
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Intravenous Immunoglobulin Treatment of Neurological Disease
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Delayed Radiation-Induced Bulbar Palsy
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Cost-Effectiveness Analysis:What Is It and How Will It Influence Neurology
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Pure Motor Hand Weakness
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Intravenous IgG in Guillain-Barre Syndrome
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