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Differential
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abdominal distention

abdominal reflex, absent

abducens nerve paralysis

abscess, intracerebral

abscess, spinal cord

aceruloplasminemia

achilles tendon, enlarged

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

acquired immunodeficiency syndrome myelopathy

acquired immunodeficiency syndrome, congenital

acquired immunodeficiency syndrome, infants and children

acquired immunodeficiency syndrome-related complex

activities of daily living

acute disseminated encephalomyelitis

acute disseminated encephalomyelitis, multiphasic

acute respiratory distress syndrome

addiction, heroin

addiction, heroin-neurologic complications with

Addison's disease

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 injection

alcohol intolerance

alcohol, neurologic complications with

Alexanders disease

Alexanders disease, adult onset

altered states of consciousness

alternating rapid movement

Alzheimer's disease

aminoacidopathies

amyloid plaques

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, bulbar

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, juvenile

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, treatment of

anemia, megaloblastic

anesthesia, general

aneurysm, vertebral basilar system

angiitis, granulomatous of CNS

angiitis, isolated of CNS

angiography, neurologic complications with

ankle reflex, absent

antecedent illness

anterior horn cell disease

anterior spinal artery

anterior tibial muscle weakness

anti GQ1b IgG antibody

anticholinergic drugs

anticoagulant, complications of

anticoagulant, treatment

antispasticity drugs

antiviral agents

Argyll Robertson pupil

arm swing, reduced

Arnold Chiari malformation

arteritis, temporal

asterixis, causes of

asterixis, unilateral

ataxia, cerebellar

ataxia, hereditary

ataxia, progressive

ataxia, sensory

ataxia, truncal

atherosclerosis, generalized

atherosclerosis, premature

atlanto-axial subluxation

atrioventricular block

attention deficit disorder with hyperactivity

auditory evoked brainstem potentials

autoimmune disease

autonomic dysfunction

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

axonal degeneration

axonal spheroid

azidodeoxythymidine

B 12 deficiency

Babinski sign in new born

bacterial infection

bacterial infection, CNS

ballismus, bilateral

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, infarction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavioral disorder

Behcet's syndrome

Bickerstaff's brainstem encephalitis

bladder dysfunction

blood dyscrasias, neurologic findings with

blood transfusion

bone marrow biopsy

bone marrow transplantation

brain biopsy, false negative

brain biopsy, stereotaxic

brainstem, dysfunction

brainstem, glioma

brainstem, glioma in children

brainstem, glioma, adult

brainstem, hypoplasia

brainstem, infarction of

brainstem, ischemia

brainstem, lesion of

brainstem, malformation

brainstem, neoplasms of

Brown Sequard syndrome

brucellosis, nervous system involvement with

Brudzinski's sign

bulbar palsy, progressive

burning paresthesia

calcification, intracranial

calcifications, intracranial, punctate

carcinoma of lung

carotid angiogram

CAT scan, abnormal

CAT scan, demyelinating disease

CAT scan, emission, abnormal

CAT scan, metrizamide

CAT scan, myelogram with

CAT scan, serial

CAT scan, spinal cord

CAT scan, spine

cavernous hemangioma

central nervous system, infection of

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar degeneration

cerebellar hemangioma

cerebellar infarction

cerebellar lesion

cerebellar peduncle

cerebellar plaques, amyloid

cerebellar vermis

cerebral cortex

cerebral cortical atrophy

cerebral embolism

cerebral embolism, cardiac origin

cerebral folate deficiency syndrome

cerebral infarction

cerebral peduncle

cerebral venous thrombosis

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, amonia

cerebrospinal fluid, culture of, viral

cerebrospinal fluid, cytology

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, glutamine

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, pressure increased

cerebrospinal fluid, proteincytologic dissociation

cerebrospinal fluid, red cells in

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, prognosis in

cerebrovascular accident, vascular territory involved

cerebrovascular disease

ceruloplasmin, serum

cervical spine injury, compression

cervical spondylosis

Chaddock's sign

Charcot-Marie-Tooth

cherry red spot

cherry red spot-myoclonus syndrome

chilbran skin lesions

chorea, causes of

chorea, familial

choreoathetosis

choroid plexus, tumor of

chromosomal abnormality

chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids

chronic progressive external ophthalmoplegia

claudication, intermittent of cauda equina

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

cobalamin C deficiency

coccidioidomycosis

color vision, impaired

compression fracture

concentration, impaired

congenital bilateral perisylvian syndrome

congenital malformation

congenital malformation, non CNS

controversies in neurology

copper deficiency

cornea, opacity of

corpus callosum

corpus callosum, atrophy of

corpus callosum, lesion of

corpus callosum, thinning

cortical blindness

cortical-basal ganglionic degeneration

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

C-reactive protein, elevated

critical care unit

crossed adductor reflex

crying, pathologic

cryptococcal meningitis

cultured skin fibroblasts

cyst, epidermoid of CNS

deafness, bilateral progressive vs.unilateral acute

deafness, unilateral

decerebrate posture

decompressive spinal cord surgery

deep gray nuclei

deep tendon reflexes

degenerative diseases of CNS

Dejerine's sign

Dejerine-Sottas syndrome

delay in diagnosis

dementia, childhood

dementia, familial

dementia, presenile

dementia, subcortical

dementia, thalamic

demyelinating disease

dental procedure, neurologic complications with

dentate nuclei, lesion of

developmental abnormality of brain

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes mellitus

diagnostic criteria

diaphragmatic paralysis

diaphragmatic paralysis, causes of

differential diagnosis

difficulty climbing stairs

difficulty going down stairs

digiti quinti sign

digits, abnormal

disability, neurological

distal muscle atrophy

distal muscle weakness

dopa responsive dystonia

Dravet syndrome

dropped head syndrome

drug abuse, inhalation

drug abuse, neurologic complications of

dyskinesia, buccal lingual facial

dystonia musculorum deformens

dystonia, children

dystonia, focal

dystonia, treatment of

ears of the Lynx MR sign

electrical sensation

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, triphasic delta waves

emergencies, neurologic

emergencies, neurosurgical

emotional lability

Emperor's clothes syndrome

empyema, epidural-spinal

encephalitis lethargica

encephalitis, brainstem

encephalitis, paraneoplastic

encephalitis, viral

encephalomyelitis

encephalomyelitis, paraneoplastic

encephalopathy, acute

encephalopathy, Hashimoto's

encephalopathy, metabolic

encephalopathy, progressive

enzyme, muscle disease

epicanthal folds

epidemiology of neurology

epileptic encephalopathy

episodic neurologic deficits

erythema migrans

evoked potentials

exome sequencing

eye movement, disorders of

face, numbness of

facial anomalies

facial appearance, abnormal

facial nerve palsy

facial nerve palsy, bilateral

facial weakness

facial weakness, bilateral

failure to thrive

FARS2 deficiency

fatal familial insomnia

fatty acid, elevated plasma content

feeding disorder

ferritin, elevated

fetal alcohol syndrome

fine motor function, impaired

finger nose finger test

fingers, abnormal

Fisher's syndrome

fistula, arterio-venous, dural

flaccid paralysis

folic acid deficiency

fourth ventricle, enlargement of

fragile-X syndrome

Friedreich's ataxia

Friedreich's ataxia, late onset

frontal lobe, pathologic signs of

gag reflex, depressed

galactocerebrosidase

gamma amino butyric acid-mimetic drug

gammaglobulin therapy, intravenous

gangliosidosis GM2

gastric partitioning

gaze palsy, congenital horizontal

gaze palsy, horizontal

gaze palsy, horizontal-bilateral

gaze palsy, supranuclear

gaze palsy, vertical

genetic counselling

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

geographic location

Gerstmann-Straussler-Scheinker disease

girdle sensation

glioblastoma multiforme(astrocytoma Gr.III)

glioma, low-grade

gliomatosis cerebri

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glutamate dehydrogenase deficiency

glutamic acid decarboxylase, antibody

gram negative rod

granular osmiphilic material

granulomatosis with polyangiitis

granulomatous disease

Guillain Barre syndrome

Guillain Barre syndrome, axonal form

Guillain Barre syndrome, variant forms of

Hallervorden Spatz disease

headache, positional

headache, recurrent

headache, severe

hearing problems in children

heart block, complete

heel-knee-shin test

hemangioma, vertebral

hematoma, epidural-spinal

hematoma, intracerebral

hematopoietic tissue, extramedullary

hematuria, microscopic

hemiplegia, progressive

hemoglobin abnormality, neurologic complications of

hemorrhage, putamenal

hemorrhage, thalamic

hemosiderosis of CNS, superficial

hepatic encephalopathy

hepatic failure

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration, non-Wilsonian

hepatosplenomegaly

herniated disc, cervical

herpes virus infection

hexosaminidase-A

high arched feet

hip flexor weakness

history of neurology

Hodgkin's disease

Hoffmann's sign

homocysteine, serum

Horner's syndrome

human herpesvirus 6

human immunodeficiency virus type 1

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

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

hydrocephalus, congenital

hydrocephalus, fetal

hydrocephalus, intrauterine

hyperammonemic encephalopathy

hypereosinophilic syndrome(HES)

hyperhomocysteinemia

hyperparathyroidism

hyperpigmentation of skin

hyperpyrexia, CNS disorder causing

hypersegmented polys

hyperthyroidism

hypoglycorrhachia

hypoglycorrhachia, causes of

hypomyelination

hypopigmentation of skin

hypothalamus, disturbance of

hypothermia, causes of

iatrogenic neurologic disorders

immunosuppression

immunosuppressive agents

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic intranuclear

incontinence, fecal

intellectual deficit

intellectual deficit, treatable causes of

intellectual deterioration

intelligence quotient

interferon alpha

internal capsule

internuclear ophthalmoplegia

interobserver agreement

intracerebral hemorrhage

intrathecal antispasticity drugs

intrinsic hand muscles, wasting of

ipsilateral hemiplegia

iron, serum, low

Jakob-Creutzfeldt disease

Jamaica ginger paralysis

jaw jerk, abnormal

Krabbe's disease

kyphoscoliosis, neurologic causes of

lactic acidemia

lacunar infarction

laminectomy, cervical

laminectomy, lumbar

laughing, pathologic

left-right orientation

leg spasms, painful

leg weakness, bilateral

Leigh's disease

Leigh's disease, adult variety

lenticular nucleus, lesion of, bilateral

leukemia, neurologic findings assoc.with

leukocyte enzyme abnormality

leukoencephalopathy

leukoencephalopathy, adult onset, sporadic

leukoencephalopathy, differential diagnosis

level of consciousness, decreased

Lhermitte's sign

life expectancy

lipid storage disorder of CNS

locked-in syndrome

lymphadenopathy

lymphadenopathy, hilar

lymphocytic pneumonitis

lymphoma involving CNS

lymphoma, primary of CNS

lymphomatoid granulomatosis

lysosomal storage disease

magnetic stimulation

magnetic stimulation, brain

malformation, CNS, congenital

malformation, vascular

malformation, vascular, treatment of

meconium staining

medial lemniscus

mediastinum, lymph-node biopsy

mediastinum, mass of

medulla oblongata

medulla oblongata, lesion of

medulla oblongata, malformation

memory, defect of recent

memory, impairment of

meningeal biopsy

meningeal enhancement

meningeal gliomatosis

meningitis, actinomycotic

meningitis, aseptic

meningitis, bacterial

meningitis, blastomyces

meningitis, brucellosis

meningitis, candida

meningitis, carcinomatous

meningitis, chronic

meningitis, chronic benign lymphocytic

meningitis, cladosporium

meningitis, coenurosis

meningitis, CSF cell count-normal

meningitis, cysticercosis

meningitis, echinococcal

meningitis, eosinophilic

meningitis, fungal

meningitis, helminthic

meningitis, histoplasma

meningitis, leptospira

meningitis, lymphomatous

meningitis, Mollaret's

meningitis, neutrophilic

meningitis, nocardia

meningitis, paracoccidioides

meningitis, pneumococcal

meningitis, post myelography

meningitis, recurrent

meningitis, syphilitic

meningitis, toxoplasma

meningoencephalitis

meningoencephalitis, toxoplasma

meningomyelitis

meningovascular syphilis

mental retardation

mental retardation, familial

mental status, abnormal

metabolic acidosis

metabolic disorder, primary

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

metachromatic leukodystrophy, late-infantile

methylmalonic acid, serum

methylmalonic acidemia

methylmalonic aciduria

midbrain, lesion of

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

mitochondrial disease

molecular genetics

mononeuropathy multiplex

Morquio syndrome

motor neuron disease

movement disorder

movement disorder, extrapyramidal

movement disorder, treatment of

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, contrast enhanced, high dose

MRI, demyelinating disease

MRI, diffusion tensor

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, false negative

MRI, functional

MRI, gradient-echo

MRI, high signal foci on

MRI, high signal intensity of basal ganglia

MRI, hypointense signal foci on

MRI, linear enhancement

MRI, nodular enhancement

MRI, paramagnetic effect

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRI, susceptibility weighted

MRI, T1 weighted high signal foci

MRI, target sign

mucopolysaccharidoses

multinucleated giant cell

multiple sclerosis

multiple sclerosis, chronic progressive

multiple sclerosis, diagnosis of

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple sclerosis, prognosis

multiple sclerosis, spinal form

multiple sclerosis, treatment of

multiple system atrophy

muscle atrophy, progressive

muscle twitching

muscle wasting, diffuse

muscle weakness

mycoplasma pneumoniae

myelitis, longitudinal

myelitis, post infectious

myelitis, transverse

myelogram, cervical

myelogram, thoracic

myeloneuropathy

myelopathy hand

myelopathy, ascending

myelopathy, chronic progressive

myelopathy, hepatic

myelopathy, vacuolar

myeloradiculopathy

myoclonic jerks

myoclonus, epilepsy

Native Americans

nausea and vomiting

neoplasm, primary intracerebral

neoplasm, primary of CNS

neoplasm, primary of CNS-classification

neoplasm, primary of CNS-metastasizing to subarachnoid space

neoplasm, primary of CNS-treatment of

nerve conduction studies

nerve root enhancement

nerve root hypertrophy

neuroaxonal leukodystrophy

neurocutaneous disease

neuroendocrinology

neurogenic bladder

neuroichthyosis

neurologic complications

neurologic complications of, surgery

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic examination

neurologic examination, focal

neurologic signs

neurologic symptoms

neuromuscular disease, electrodiagnosis of

neuronal ceroid-lipofuscinosis

neuronal intranuclear inclusion disease

neuroophthalmology

neuropathology, brain

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, peripheral

neuropathy, sensory

neuropathy, vasculitic, systemic

neuropsychiatry

next-generation sequencing

numbness, ascending

nutritional deficiency

nystagmus, dissociated

nystagmus, gaze-evoked

nystagmus, rotary

nystagmus, upbeating on upgaze

nystagmus, vertical

occupational neurologic disorders

ocular dysmetria

ocular motility, disorders of

oculodentodigital dysplasia

oculogyric crisis

odontoid process

operculum syndrome, bilateral

ophthalmoplegia

ophthalmoplegia, progressive external

ophthalmoplegia, total

opportunistic infection

optic atrophy, hereditary

optic chiasm, enlarged

optic nerve, enlarged

optic nerve, lesion of

optic neuropathy

oral contraceptives

oral ulcerations

orthostatic hypotension

osteomyelitis, spinal

pain, abdominal

pain, interscapular

palatal myoclonus

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, familial spastic, variants

paraparesis, flaccid

paraparesis, painful

paraparesis, spastic

paraparesis, spastic, tropical

paraplegia, progressive

parathyroid adenoma

paresthesias, feet

paresthesias, hands

Parkinson disease

Parkinson disease, arteriosclerotic

Parkinson disease, asymmetric onset

Parkinson disease, hemiparesis in

Parkinson disease, L-dopa nonresponsive

Parkinson disease, postencephalitic

Parkinson disease, tremor, absence of

Parkinson disease, unilateral

Parkinson disease, young onset

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

paroxysmal neurologic disorder

PAS positive material in the brain

pathologic reflex

pediatric neurology

Pelizaeus Merzbacher

perivascular enhancement

pernicious anemia

peroneal nerve palsy

peroneal nerve, lesion of

peroxisomal disease

personality change

phenylketonuria

phenylketonuria, adult onset

pituitary stalk

pituitary stalk, lesion of

pleocytosis of cerebrospinal fluid

poison, organophosphate

polycythemia, primary

polyglucosan body

polyglucosan body disease

polymerase chain reaction

polyneuropathy, familial

pons, hypoplasia

pons, lesion of

portal caval shunt

position sensation, abnormal

posterior column disease

posterior inferior cerebellar artery syndrome

posterior leukoencephalopathy syndrome

posterior longitudinal ligament, ossification of

postictal neurologic deficits

postural abnormality

precentral gyrus

precipitating factors

precocious puberty

prenatal diagnosis by amniocentesis

primary lateral sclerosis

prisoners of war, neurologic complications in

progressive encephalomyelitis with rigidity syndrome

progressive myoclonic epilepsy

progressive neurologic disorder

proprioception, abnormal

pseudobulbar palsy

pseudomonas aeruginosa

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, neurologic problems

psychomotor retardation

pulmonary infiltrates

pupil, abnormality in neurologic disorders

pure dysarthria

pursuit eye movements, abnormal

pyramidal tract

pyramidal tract dysfunction

pyramidal tract dysfunction, unilateral

pyramidal tract, uncrossed

pyruvate metabolism, abnormality of

quadriparesis, progressive

radiation encephalopathy, delayed

radiation therapy, CNS treatment and complications with

Raynaud's phenomenon

release phenomena

respiratory dyskinesias

respiratory failure

respiratory tract infection

reticulum cell sarcoma

retinal degeneration

retinal detachment

retinal exudates

retinitis pigmentosa

reversible neurologic disorder

rheumatoid arthritis

rheumatoid arthritis, neurologic complications of

Rosenthal fibers

rubella encephalitis, progressive

saccadic eye movements, abnormal

saddle anesthesia

sarcoidosis, CNS

scalp tenderness

Schilder's disease

sclerae, hyperpigmented

scleroderma, neurologic involvement with

scoliosis, neurologic association with

sea-blue histiocytes

sedimentation rate, elevated

seizure, children

seizure, familial

seizure, febrile

seizure, hysterical

seizure, intractable

seizure, neonatal

seizure, tonic-clonic

sensorineural hearing loss

sensory loss, cutaneous

serologic testing

serologic testing of cerebrospinal fluid

severe acute respiratory syndrome

sickle cell disease

single photon emission computed tomography

Sjogren-Larsson syndrome

Sjogren's syndrome

skin, darkening of

skin, lesions in neurologic disorders

skin, temperature difference

skull x-ray, abnormal

sleep pathology and physiology

slow virus infection of CNS

sodium channel dysfunction

somatosensory evoked potentials

spastic diplegia

spastic paraplegia, type 11

spastic paraplegia, type 15

spastic paraplegia, type 7

spasticity, treatment of

speech disorder

speech disorder, childhood

speech, loss of

spinal cord, biopsy

spinal cord, cervical

spinal cord, compression of

spinal cord, enlargement

spinal cord, herniation

spinal cord, infarction of

spinal cord, injury of

spinal cord, injury, management of

spinal cord, ischemic lesion of

spinal cord, lesion of

spinal cord, neoplasm

spinal cord, neoplasm, extramedullary

spinal cord, neoplasm, meningioma

spinal cord, pathologic exam of

spinal cord, vascular disorders Affecting

spinal cord, vascular malformation of

spinal stenosis

spinal stenosis, familial

spinal xanthomatosis

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar ataxia type 7

spinocerebellar degeneration

spirochete infection

spongy degeneration of brain

spontaneous remission

startle myoclonus

startle reaction

status epilepticus

steroid therapy, CNS treatment and complications with

striatonigral degeneration

striatonigral degeneration, infantile

striopallidodentate calcifications, familial idiopathic

subarachnoid hemorrhage

subcortical U fibers

substantia nigra

superior cerebellar artery infarction

superior sagittal sinus thrombosis

symmetric brain lesions

syphilis, meningomyelitis

syphilis, neurologic complications with

systemic illness

systemic lupus erythematosus

systemic lupus erythematosus, neurologic complications with

tandem gait, ataxic

Tay-Sachs disease

teeth, abnormal

temporal lobe, lesion

temporal lobe, lesion, bilateral

tendon, enlarged

testicular atrophy

testicular enlargement

thalamus, lesion of

thalamus, lesion of-bilateral

thrombocytopenia

tone, muscle, increased

tongue, atrophy

tongue, fasciculations of

tongue, impaired movements of

tongue, weakness

tonic foot response

toxins, nervous system

toxoplasmosis, acquired

toxoplasmosis, CNS

transient neurologic deficit

transposition of the great vessels

transsynaptic degeneration

treatment of neurologic disorder

tremor, cerebellar

tremor, intention

trigeminal nerve

trigeminal nerve, abnormality of

trinucleotide repeats

tuberculoma of CNS

tuberculosis, spinal

unconsciousness

upgaze, paralysis of

urinary frequency

urinary incontinence

urinary retention

urinary urgency

vaccination, neurologic complications with

valsalva maneuver

ventricular enlargement

vertebral artery

vertebral artery occlusion

vertebral-basilar insufficiency

vertigo, episodic

vibratory sensation, abnormal

viral infection

viral infection, CNS

viral isolation

visual acuity, decreased

visual evoked response

visual fields, constricted

vitamin deficiency

vitamin E deficiency

Vogt-Koyanagi-Harada syndrome

walking, delayed

walking, difficulty with

Wallerian degeneration

watershed infarcts

weakness, generalized

weakness, progressive

weaning from respirator, failure to

Werner's syndrome

Western immunoblot test

white matter disease

white matter disease, periventricular

wide based gait

xanthoma, tendon

x-linked hydrocephalus

x-linked mental retardation

x-ray, thoracic spine

Showing articles 150 to 200 of 535 << Previous Next >>

Isolated Granulomatous Angiitis of the Spinal Cord
Ann Neurol 32:580-582, Caccamo,D.V.&Garcia,J.H., 1992

Human T Lymphotropic Virus Type I-Assoc Myelopathy, A Rpt of 10 Pts Born in US
Arch Neurol 49:1113-1118, Sheremata,W.A.,et al, 1992

Chronic Myelopathy Associated with Human T-Lymphotropic Virus Type I (HTLV-I)
Ann Int Med 117:933-946, Gessain,A.&Gout,O., 1992

Brain MRI and Electrophysiologic Abnormalities in Preclinical and Clinical Adrenomyeloneuropathy
Neurol 42:85-91, Aubourg,P.,et al, 1992

MR Imaging of the Spinal Cord in 23 Subjects with ALD-AMN Complex
AJR 158:413-416, Snyder,R.D.,et al, 1992

Fatal Familial Insomnia:Clinical and Pathologic Study of Five New Cases
Neurol 42:312-319, Manetto,V.,et al, 1992

Recurrent Encephalopathy and Seizures in a US Native with HTLV-I-Associated Myelopathy/Tropical Spastic Paraparesis
Neurol 42:658-661, Smith,C.R.,et al, 1992

Presence of HTLV-I Proviral DNA in Central Nervous System of Patients with HTLV-I-Associated Myelopathy
Ann Neurol 31:39-45, Kira,J.,et al, 1992

Chronic Neurodegenerative Disease Associated with HTLV-II Infection
Lancet 339:645-646, Hjelle,B.,et al, 1992

Idiopathic Hemiparetic Parkinsonism, A Syndrome Distinct from Idiopathic Parkinsonism
Lancet 339:149-150, DeKeyser,J.,et al, 1992

Clinicopath Conf
Infantile Striatonigral Regeneration, with Cerebellar Degeneration, Familial, Case 30-1992, NEJM 327, 261-1992., 1992

Myelopathy Associated with Human T Cell Lymphotropic Virus Type 1 in a White European Native to England
BMJ 305:453, Ali,A.&Rudge,P., 1992

Primary Lateral Sclerosis, Clin Features, Neuropath & Dx Criteria
Brain 115:495-520, Pringle,C.E.,et al, 1992

Hallervorden-Spatz Syndrome and Brain Iron Metabolism
Arch Neurol 48:1285-1293, Swaiman,K.F., 1991

The Sensitivity of Transcranial Cortical Magnetic Stimulation in Detecting Pyramidal Tract Lesions in Clin Definite MS
Neurol 41:566-569, Mayr,N.,et al, 1991

Neurologic Aspects of Cobalamin Deficiency
Medicine 70:229-245, Healton,E.B.,et al, 1991

HTLV-I-Associated Myelopathy/Tropical Spastic Paraparesis in the United States
Neurol 41:1355-1357, Janssen,R.S.,et al, 1991

HTLV-I-Associated Myelopathy Endemic in Texas-Born Residents and Isolation of Virus from CSF Cells
Neurol 41:831-836, McKendall,R.R.,et al, 1991

HTLV-I-Associated Myelopathy Associated with Blood Transfusion in the US:Epidemiologic & Molecular Evidence
Neurol 41:192-197, Kaplan,J.E.,et al, 1991

Syphilitic Meningomyelitis
Neurol 41:325-326, Strom,T.&Schneck,S.A., 1991

Myelopathic Neurosarcoidosis:Diagnostic Value of Enhanced MRI
Neurol 41:150-151, Sauter,M.K.,et al, 1991

Dopa-Responsive Dystonia:Long-Term Treatment Response and Prognosis
Neurol 41:174-181, Nygaard,T.G.,et al, 1991

Magnetic Stimulation of the Motor Cortex in Cervical Spondylosis
Neurol 41:75-80, deNoordhout,A.M.,et al, 1991

Idiopathic Myelopathies with White Matter Vacuolation in Non-AIDS Patients
Human Pathol 22:816-824, Kamin,S.S.&Petito,C.K., 1991

Clinical Features and Associations of 560 Cases of Motor Neuron Disease
JNNP 53:1043-1045, Li,T.,et al, 1990

Selective Involvement of the Pyramidal Tract on Magnetic Resonance Imaging in Primary Lateral Sclerosis
Neurol 40:1799-1800, Marti-Fabregas,J.&Pujol,J., 1990

Excessive Muscular Fatigue in Patients with Spastic Paraparesis
Neurol 40:1271-1274, Miller,R.G.,et al, 1990

Transvrse Myelitis and Spastic Paraparesis in a Patient with HIV Infection
NEJM 322:1322, Dodson,D., 1990

Familial Spastic Paraparesis Syndrome Associated with HTLV-I Infection
NEJM 323:732-737, Salazar-Grueso,E.F.,et al, 1990

Neuronal Intranuclear Inclusion Disease in a Child:Diagnosis by Rectal Biopsy
Ann Neurol 27:103-106, Goutieres,F.,et al, 1990

Wallerian Degeneration of the Pyramidal Tract in Capsular Infarction Studied by Magnetic Resonance Imaging
Stroke 21:404-409, Pujol,J.,et al, 1990

Demyelinating Diseases
In Rowlands Merritt's Textbk of Neurology, Lea & Febiger, Phila, 8th Ed, p. 749, Sibley,W.A.,et al, 1989

Subacute Combined Degeneration of the Spinal Cord
In Rowland's, Merritt's Textbk of Neurology, Lea & Febiger, Phila, 8th Ed, p. 691, Mancall,E.L., 1989

Familial Idiopathic Striopallidodentate Calcifications
Neurol 39:381-385, Ellie,E.,et al, 1989

Endemic Fluorosis with Spinal Cord Compression, A Case Report and Review
Arch Int Med 149:697-700, Fisher,R.L.,et al, 1989

Gerstmann-Straussler-Scheinker Disease, I, Extending the Clinical Spectrum
Neurol 39:1446-1452, Farlow,M.R.,et al, 1989

Primary Lateral Sclerosis in a Child
Neurol 39:1530-1532, Grunnet,M.L.,et al, 1989

Spinal Cord Pathology in Pediatric Acquired Immunodeficiency Syndrome
Neurol 39:227-235, Dickson,D.W.,et al, 1989

Chronic Myelopathies Associated with HTLV-I, A Clinical, Serologic, and Immunovirologic Study of 10 Patients in France
Arch Neurol 46:255-260, Gout,O.,et al, 1989

Adrenoleukodystrophy
JAMA 262:1504-1506, Ladenson,P.W., 1989

The Acquired Immunodeficiency Syndrome (AIDS) Dementia Complex
Ann Int Med 111:400-410, Ho,D.D.,et al, 1989

Clinicopath Conf
HTLV-I Infection, with Adult T-Cell Lymphoma and Tropical Spastic Paraparesis, Case 36-2989, NEJM 32, :6675,1989., 1989

HTLV-I-Associated Myelopathy with Adult T-Cell Leukemia
Neurol 39:1129-1131, Kawai,H.,et al, 1989

HTLV-I Myeloneuropathy in the Solomon Islands
NEJM 321:615-616, Ajdukiewicz,A.,et al, 1989

Detection of Human T-Cell Leukemia/Lymphoma Virus Type I in a Transfusion Recipient with Chronic Myelopathy
Neurol 39:841-844, Saxton,E.H.,et al, 1989

Clinicopath Conf
Chronic Osteomyelitis of Spine, with Intervertebral Diskitis (T3-T4) & Epidural Abscess (Staph Aureu, ) , Cas9,NEJM 320:1610-1618,1989., 1989

Lyme Disease
NEJM 321:586-596, Steere,A.C., 1989

Compression Syndromes Due to Hypertrophic Nerve Roots in Hereditary Motor Sensory Neuropathy Type I
Neurol 39:1173-1177, Rosen,S.A.,et al, 1989

Intrathecal Baclofen for Severe Spinal Spasticity
NEJM 320:1517-1521, 1553-15551989., Penn,R.D.,et al, 1989

Treatment of Spastic Paresis
NEJM 320:1553-1555, Young,R.R., 1989

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