Neudle.com: atrophy muscle

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abdominal contractions

abdominal distention

abdominal muscle paralysis

abdominal protrusion

abducens nerve paralysis

abductor pollicis brevis

abscess, intracerebral

abscess, intracerebral, multiple

abscess, intracerebral, treatment of

abscess, vertebral

acid maltase deficiency

acid maltase deficiency, adult

acoustic neurinoma

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

acquired immunodeficiency syndrome, congenital

acquired immunodeficiency syndrome, heralded by neurologic invol

acquired immunodeficiency syndrome, infants and children

acral sensory symptoms

acridine orange-RNA fluorescence

ACTH, ectopic syndrome of

addiction, heroin

addiction, heroin-neurologic complications with

Addison's disease

adrenoleukodystrophy

adult polyglucosan body disease

advance directives

advances in neurology

adverse drug reaction

agenesis of corpus callosum

Aicardi-Goutieres syndrome

airway obstruction

alcohol intolerance

alcohol intoxication

alcohol, blood level of

alcohol, heart involvement with

alcohol, neurologic complications with

alcoholic blackout

alcoholic dementia

alcoholic polyneuropathy

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

Alexanders disease

alien hand syndrome

alkylating agents

alpha glucosidase

alpha-fetoprotein

altered states of consciousness

alternating hemiplegia

alternating hemiplegia of childhood

alternating rapid movement

alveolar hypoventilation

Alzheimer's disease

Alzheimer's disease, early onset

Alzheimer's disease, familial

amaurosis fugax

amobarbitol interview

amphiphysin antibodies

amyloid angiopathy, cerebral

amyloid plaques

amyotrophic chorea-acanthocytosis

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, bulbar

amyotrophic lateral sclerosis, atypical

amyotrophic lateral sclerosis, childhood

amyotrophic lateral sclerosis, cluster

amyotrophic lateral sclerosis, complications with

amyotrophic lateral sclerosis, conjugal

amyotrophic lateral sclerosis, diagnosis of

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, epidemiology of

amyotrophic lateral sclerosis, etiology of

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, guamian type of

amyotrophic lateral sclerosis, hospitalization

amyotrophic lateral sclerosis, juvenile

amyotrophic lateral sclerosis, misdiagnosis

amyotrophic lateral sclerosis, myasthenic syndrome with

amyotrophic lateral sclerosis, Parkinson-dementia-complex

amyotrophic lateral sclerosis, post-encephalitic

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, sensory symptoms in

amyotrophic lateral sclerosis, treatment of

amyotrophic lateral sclerosis, work up

amyotrophic lateral sclerosis-like syndrome

anemia, megaloblastic

anesthesia, general

aneurysm, anterior communicating

aneurysm, cavernous sinus

aneurysm, internal carotid artery

aneurysm, intracranial

aneurysm, intracranial, treatment of

Angelman syndrome

angiitis, granulomatous of CNS

angiitis, isolated of CNS

angiography, cerebral, beaded vessels

angiography, cerebral

angiography, cerebral, false negative

angiography, cerebral, negative

angiography, neurologic complications with

angiography, posterior fossa

angiotensin-converting enzyme

animal exposure

ankle reflex, absent

ankylosing spondylitis

anoctaminopathy

anterior horn cell disease

anterior interosseous neuropathy

anterior spinal artery infarction

anterior tibial muscle weakness

anti citrullinated antibody

anti Hu antibody

anti signal recognition particle antibody

antibiotics, neurologic complications with

antibodies to measles

antibodies to voltage-gated calcium channels

anticholinergic drugs

anticoagulant, complications of

anticoagulant, treatment

anticonvulsants

anticonvulsants, selection of

antiviral agents

aortic valve, stenosis

aphasia, progressive

aphasia, progressive, primary

apnea, primary central

apraxia of eye movements

apraxia, constructional

apraxia, speech

aqueduct of Sylvius, obstruction

aqueduct of Sylvius, stenosis

aqueductal stenosis

arm swing, reduced

arrhythmia, cardiac

arterial dissection

arterial dissection, carotid

arterial dissection, vertebral

arteriovenous malformation

arteriovenous malformation, brainstem

arteriovenous malformation, cerebral

arteritis, temporal

arthrogryposis multiplex

arylsulfatase A

arylsulfatase B

ascending paralysis

aspartate aminotransferase

asthma, poliomyelitis-like syndrome with

ataxia telangiectasia

ataxia, cerebellar

ataxia, hereditary

ataxia, progressive

ataxia, sensory

ataxia, truncal

atlanto axial dislocation, congenital

atrioventricular block

atrophy, muscle

attention deficit disorder with hyperactivity

auditory and vestibular pathways

auditory evoked brainstem potentials

autoimmune disease

autoimmune GFAP astrocytopathy

autonomic cardiovascular reflexes

autonomic dysfunction

autonomic neuropathy

axonal degeneration

axonal spheroid

azidodeoxythymidine

B 12 deficiency

Babinski sign in new born

bacterial infection

Barkhof MR criteria for MS

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, infarction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basement membrane

basement membrane thickening

basilar impression

basophilic stippling of red blood cells

behavior, combative

behavioral disorder

Bence Jones protein

benign congenital hypotonia

benign essential tremor

bicaudate index

biologic markers

biotin deficiency

biotinidase deficiency

bitemporal visual field defect

bladder dysfunction

blinking, reduced

blood dyscrasias, neurologic findings with

bone density, increased

bone marrow biopsy

bone marrow suppression

bone marrow transplantation

border zone infarct

Borrelia burgdorferi infection

botulinum toxin

botulinum toxin, complications of

brachial neuritis

brachial neuritis, acute

brachial neuritis, bilateral

brachial neuritis, prognosis of

brachial plexus

brachial plexus injury

brachial plexus injury, treatment of

brachial plexus neuropathy

brachial plexus neuropathy, bilateral

brachial plexus neuropathy, children

brachial plexus neuropathy, familial

brachial plexus neuropathy, recurrent

brachial plexus, lesion of

brachial plexus, postoperative palsy of

brain biopsy, false negative

brain biopsy, negative

brain natriuretic peptide

brainstem, atrophy

brainstem, infarction of

brainstem, lesion of

brainstem, vascular malformation of

breech delivery

bright tongue sign

Brown Sequard syndrome

brucellosis, nervous system involvement with

Brueghel's syndrome

Brugada syndrome

bruit, supraclavicular

bulbar palsy, acute

bulbar palsy, childhood

bulbar palsy, progressive

bulging of biceps

burning paresthesia

calcification, intracranial

calcium channel dysfunction

calf amyotrophy

calf hypertrophy

caloric testing

campylobacter infection

Canavan's disease

carbon monoxide poisoning

carcinoembryonic antigen

carcinoma of breast

carcinoma of lung

carcinoma of ovary

carcinoma of pancreas

carcinoma of thyroid

cardiac arrest and resuscitation

cardiac catheterization, neurologic complications

cardiovascular disease

carotid artery atherosclerosis

carotid artery disease

carotid artery occlusion, neck

carotid artery stenosis

carotid sinus syndrome

carpal tunnel syndrome

carpo-pedal spasm

cashew nut sign

Castleman's disease

CAT scan, abdomen

CAT scan, abnormal

CAT scan, abscess, cerebral

CAT scan, contrast enhanced

CAT scan, disappearing lesion on

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, metrizamide

CAT scan, myelogram with

CAT scan, orbits

CAT scan, pelvis

CAT scan, serial

CAT scan, spine

cataracts, congenital

cauda equina, enhancement

cauda equina, lesion of

caudate nucleus

caudate nucleus, atrophy

cavernous sinus

cavernous sinus, lesion of

cavernous sinus, syndrome

Central America

central core disease

central hypoventilation, congenital

central nervous system, infection of

central pontine myelinolysis

cerebellar ataxia, autosomal recessive

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar disease, eye movement disorder in

cerebellar edema

cerebellar hemorrhage

cerebellar hypoplasia

cerebellar lesion

cerebellar plaques, amyloid

cerebellar pontine angle tumor

cerebellar vermis

cerebellum, disease of

cerebellum, neoplasms of

cerebral arteries

cerebral cortex

cerebral cortical atrophy

cerebral embolism

cerebral embolism, artery to artery

cerebral embolism, cardiac origin

cerebral infarction

cerebral infarction, small, deep

cerebral infarction, subcortical

cerebral ischemia

cerebral peduncle

cerebral vasculature

cerebral venous thrombosis

cerebro hepato renal syndrome

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, cell count

cerebrospinal fluid, culture of

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, eosinophilia of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, gold sol.curve of

cerebrospinal fluid, IgG index, elevated

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, pressure low

cerebrospinal fluid, protein of

cerebrospinal fluid, red cells in

cerebrospinal fluid, xanthochromia of

cerebrovascular accident

cerebrovascular accident, clinical diagnosis

cerebrovascular accident, etiology

cerebrovascular accident, incidence of

cerebrovascular accident, infancy and childhood

cerebrovascular accident, location of

cerebrovascular accident, mimics

cerebrovascular accident, misdiagnosis

cerebrovascular accident, multiple

cerebrovascular accident, non atherosclerotic cause of

cerebrovascular accident, prevention of

cerebrovascular accident, recurrent

cerebrovascular accident, three territory involvement

cerebrovascular accident, topographic pattern

cerebrovascular accident, vascular territory involved

cerebrovascular accident, women

cerebrovascular accident, young adult

cerebrovascular disease

cerebrovascular disease, cardiovascular disease with

cerebrovascular disease, risk factors in

cervical collar

cervical myelopathy

cervical osteoarthritis

cervical osteophyte

cervical spine injury

cervical spine injury, treatment of

cervical spondylosis

cervical spondylosis, differential diagnosis of

cervical spondylosis, misdiagnosis

Charcot-Marie-Tooth

cheiralgia paresthetica

chelation therapy

chemotherapy, CNS treatment and complications with

cherry red spot

cherry red spot-myoclonus syndrome

chest x-ray, abnormal

chewing, impaired

chilbran skin lesions

cholesterol, HDL

chorea, familial

chorea, Sydenham's

choreoathetosis

chorioretinitis

chromosomal abnormality

chronic polyneuritis, children

chronic progressive external ophthalmoplegia

cigarette smoking

cisternogram, radionuclide

Clarkson disease

claudication, extremity

claudication, intermittent of cauda equina

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

cluster, geographic

cobalamin C deficiency

coccidioidomycosis

cogwheel rigidty

cold hands sign

cold temperature

collagen vascular disease

collapsin response mediator protein 5 IgG

color vision, impaired

compartment syndrome

compartment syndrome, medial brachial fascial

compression fracture

compression neuropathy

conduction block

confusional state, acute

congenital heart disease

congenital infection, CNS

congenital infection, viral

congenital myopathy

congestive heart failure

conjugate gaze, forced

conjunctival injection

contactin associated protein like 2 antibodies

contractures, joint

controversies in neurology

conversion reaction

copper deficiency

cornea, opacity of

corneal reflex, abnormal

corneal reflex, absent

coronary thrombolysis

corpus callosum

corpus callosum, atrophy of

corpus callosum, hypoplastic

corpus callosum, infarction of

corpus callosum, lesion of

corpus callosum, neoplasm of

corpus callosum, thinning

cortical blindness

cortical blindness, transient

cortical hand knob

cortical hand knob infarct

cortical hemorrhage

cortical infarction

cortical infarction, small

cortical muscular atrophy

cortical topography

cortical wrist drop

cortical-basal ganglionic degeneration

cost effectiveness

coxsackievirus, myopathy with

cranial nerve enhancement

cranial nerve enlargement

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

craniopharyngioma

creatine phosphokinase(CPK)elevated

Creutzfeldt-Jakob disease, genetic

critical care unit

crying, pathologic

cultured skin fibroblasts

Cushing's syndrome

cycad seed flour

cyclophosphamide

cyst, benign intracranial

cyst, cortical parenchyma

cyst, parenchymal

cyst, perineural

cyst, ventricular

cysticercosis, cerebral

cysticercosis, intraventricular

cysticercosis, subarachnoid

cytochrome c oxidase

cytochrome c oxidase, deficiency

cytomegalic inclusion disease

cytomegalovirus infection

cytomegalovirus infection, congenital

dantrolene sodium

deafness, bilateral

deafness, sudden

deep gray nuclei

degenerative diseases of CNS

Dejerine-Sottas syndrome

delay in diagnosis

delayed dentition

delivery, complicated

dementia, cerebrovascular disease causing

dementia, childhood

dementia, familial

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

dementia, reversible

dementia, treatment of

demyelinating disease

denervation of muscle

denervation potentials

dental procedure, neurologic complications with

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

dermatomyositis

descending paralysis

developmental disability

developmental evaluation

developmental milestones

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetes insipidus

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diabetic amyotrophy

diabetic mononeuropathy

diagnostic criteria

diaphragmatic paralysis

diaphragmatic paralysis, causes of

diethylene glycol

differential diagnosis

difficulty climbing stairs

difficulty going down stairs

diffuse idiopathic skeletal hyperostosis

diplegia, atonic

diplegia, brachial

diplopia, transient

diplopia, vertical

disability rating scale, neurological

disability, neurological

disc space infection

disc space narrowing

dislocated hip, congenital

dissociated sensory loss

distal muscle atrophy

distal muscle weakness

dopa responsive dystonia

down-beat nystagmus

down-beat nystagmus, primary position of gaze

downward gaze, paralysis of

dropped head syndrome

drug abuse, neurologic complications of

drug induced neurologic disorders

drug interactions

dural sinus thrombosis

dysdiadochokinesia

dysferlinopathy

dyskinesia, buccal lingual facial

dyssynergia cerebellaris myoclonica

dysthyroid ocularmyopathy

dystonia, children

dystonia, focal

dystonia, post traumatic

dystrophic calcification

ears of the Lynx MR sign

eating disorder

ectatic basilar artery

edema, periorbital

educational status

electrical injury of nervous system

electrical sensation

electrical stimulation, spinal nerves

electrocardiogram, abnormal

electrocorticogram

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, inflammatory disease

electroencephalogram, periodic complexes

electromyogram, decremental response

electron microscopy

electrophoretic pattern, serum

electroretinograph

Emery-Dreifuss muscular dystrophy

emotional lability

empyema, epidural-spinal

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, episodic

encephalitis, focal

encephalitis, paraneoplastic

encephalitis, Powassan

encephalitis, Rasmussen's

encephalitis, recurrent

encephalitis, viral

encephalomyelitis

encephalomyelitis, parainfectious

encephalopathy, acute

encephalopathy, anoxic

encephalopathy, metabolic

encephalopathy, neonatal

encephalopathy, post anoxic

encephalopathy, progressive

endocarditis, subacute bacterial

enterovirus infection of CNS

entrapment neuropathy

enzyme treatment

enzyme, muscle disease

epidemiology of neurology

epilepsia partialis continua

episodic neurologic deficits

erectile dysfunction

erythema migrans

ethics in neurology

evidence-based research

evoked potentials

exercise intolerance

exercise-induced vascular symptoms

exome sequencing

extraocular muscle atrophy

extraocular muscle enlargement

extraocular muscle lesion

extrapyramidal movement disorder, progressive

extremity, cold

eye movement, disorders of

face, numbness of

facial appearance, abnormal

facial nerve palsy

facial nerve palsy, bilateral

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

failed medical management

failure to thrive

fatal familial insomnia

fatigable chewing

Fazio-Londe's disease

feeding disorder

femoral neuropathy

fetal alcohol syndrome

fetal movements, reduced

fibrinolytic agents

fibrinolytic agents, complications

fine motor function, impaired

finger flexor weakness

finger nose finger test

finger swelling

finger weakness

fingernails, abnormal

fingerprint bodies

flaccid paralysis

flail arm syndrome

flu-like illness

foot drop, bilateral

football neurologic injuries

foramen magnum, lesion of

fourth ventricle, compression

fourth ventricle, cyst

fracture, long bone

fracture, long bones, nerve injury with

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

Friedreich's ataxia

Friedreich's ataxia, late onset

frontal behavioral spatial syndrome

frontal lobe, atrophy

frontal lobe, behavior with disease of

frontal lobe, pathologic signs of

frontal lobe, space occupying lesion of

frontotemporal dementia, behavioral variant

fundus, abnormality of

funduscopic exam

F-wave response

gag reflex, depressed

gammaglobulin therapy, intravenous

gangliosidosis GM2

Gantzer's muscle

gastric partitioning

gastrocnemius muscle weakness

gastroenteritis

gastrointestinal bleeding

gastrointestinal disease, neurologic complications

gastrointestinal motility

gastrostomy, percutaneous endoscopic

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

genital hypoplasia

genu of corpus callosum

girdle sensation

glaucoma, low tension

glioblastoma multiforme(astrocytoma Gr.III)

globus pallidus

globus pallidus, hemorrhage

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glutamic acid decarboxylase, antibody

glycogen debranching enzyme deficiency

glycogen storage disease

GM1 ganglioside antibodies

Gowers maneuver

granular atrophy, cerebral cortex

granular osmiphilic material

granuloma, pulmonary

granulomatosis with polyangiitis

granulomatous disease

Graves ophthalmopathy

growth hormone deficiency

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, prognosis of

Gulf War syndrome

gyrate atrophy of choroid and retina

gyrus, abnormal

Hallervorden Spatz disease

Hallervorden Spatz disease, late onset

hallucination, auditory

handcuff neuropathy

handlebar palsy

Hand-Schuller-Christian disease

hanging leg syndrome

head circumference

headache, positional

headache, progressive

headache, severe

headache, sudden onset of

headache, worst of life

health insurance

hearing loss, bilateral

hearing loss, sudden, bilateral

heart block, complete

heavy metal intoxication

heel-knee-shin test

helminthic infection of CNS

hematoma, intracerebral

hemianopia, homonymous

hemianopia, transient

hemiatrophy, cerebral

hemidiaphragm, paralysis of

hemifacial atrophy

hemifacial spasm

hemiparesis, transient

hemiplegia, progressive

hemispherectomy

hepatic encephalopathy

hepatosplenomegaly

heralding manifestation

hereditary myopathy with early respiratory failure

herniated disc, thoracic

herpes simplex encephalitis

herpes simplex encephalitis, diagnosis of

hexosaminidase-A

high arched feet

high arched palate

highly active antiretroviral therapy

hip flexor weakness

hippocampal atrophy

Hirschprung's disease

histamine-2 receptor blockers

histochemistry of muscle

history of neurology

Hodgkin's disease

Hodgkin's disease, neurologic involvement with

Holter monitoring

Horner's syndrome

Horner's syndrome, bilateral

Horner's syndrome, congenital

human immunodeficiency virus type 1

Huntington's chorea

Huntington's disease, children

hydrocephalus, communicating

hydrocephalus, congenital

hydrocephalus, exvacuo

hydrocephalus, non-communicating(obstructive)

hydrocephalus, normal pressure

hydrocephalus, transient

hydroxychloroquine

hyperadrenalism

hyperamylasemia

hyperbilirubinemia

hyperhidrosis, palmar

hyperhomocysteinemia

hyperinsulinism

hyperornithinemia

hyperparathyroidism

hyperpyrexia, CNS disorder causing

hypersegmented polys

hypertension, cerebrovascular disease with

hyperthyroidism

hypertrophic cardiomyopathy

hypertrophic intracranial pachymeningitis

hypoglycemic coma

hypoglycorrhachia

hypokalemic alkalosis

hypokalemic paralysis

hypokalemic periodic paralysis

hypomyelination

hypoparathyroidism

hypopigmentation of skin

hypotension, systemic

hypothalamus, disturbance of

hypotonia, infants

hypoxic encephalopathy

iatrogenic neurologic disorders

ideomotor apraxia

idiopathic hypertrophic subaortic stenosis

IgG4-related disease

imbalance, postural

immediate recall

immune complexes

immunodeficiency

immunoelectrophoresis, serum

immunologic disease

immunology and the nervous system

immunosuppression

immunosuppressive agents

inability to sit up

inability to stand on tiptoes

inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

inclusion bodies, ubiquitin

inclusion body myositis

incontinence, fecal

industrial neurologic disorders

infant, evaluation of

infantile tremor syndrome

infraspinatus muscle

intellectual deficit

intellectual deterioration

intelligence quotient

interferon alpha

intermittent positive pressure breathing

internal capsule

internuclear ophthalmoplegia

interosseous muscles

intestinal pseudoobstruction

intracardiac electrophysiologic testing

intracerebral hemorrhage

intracerebral hemorrhage, causes of

intracerebral hemorrhage, differential diagnosis of

intracerebral hemorrhage, lobar

intracerebral hemorrhage, multiple

intracerebral hemorrhage, volume

intracranial hemorrhage

intracranial hypertension, benign

intracranial pressure, increased

intranasal medication

intrauterine infection

intrauterine infection, viral

intrauterine infection, viral of CNS

intrinsic hand muscles

intrinsic hand muscles, wasting of

iodine deficiency

Isaacs syndrome

ischemic exercise test

islet cell tumor

Jackson's syndrome

Jakob-Creutzfeldt disease

jaw closure weakness

jaw jerk, abnormal

juvenile distal and segmental muscular atrophy

juxtacortical hemorrhage

Kearns-Sayre syndrome

klippel feil syndrome

Korsakoff's psychosis

Krabbe's disease

Kugelberg-Welander syndrome

kyphoscoliosis, neurologic causes of

lacrimal gland enlargement

lactic acidemia

lactic dehydrogenase(LDH)

lacunar infarction

lacunar infarction, differential diagnosis of

lacunar infarction, hemorrhagic

Lafora's disease

laminar necrosis, cortical

laminectomy, cervical

laminectomy, lumbar

language disorder in adults

laughing, pathologic

lead and the nervous system

learning disability

learning disability, in children

Leber's hereditary optic neuropathy

leg weakness, bilateral

leg weakness, unilateral

Leigh's disease

Leigh's disease, adult variety

lens, dislocation of

lenticular nucleus, lesion of, bilateral

leucine rich glioma inactivated 1 antibodies

leukemia, neurologic findings assoc.with

leukoencephalitis, acute necrotizing hemorrhagic

leukoencephalopathy

leukoencephalopathy, differential diagnosis

level of consciousness, decreased

Lewy body disease, diffuse

Lhermitte's sign

lid closure, weakness of

life expectancy

life support, withdrawal of

life support, withholding of

life sustaining treatment

limbic encephalitis

livedo reticularis

liver function enzymes

locked-in syndrome

long bone lesion

lumbar puncture

lumbar puncture, complications of

lumbosacral plexopathy

lumbosacral plexus

lumbosacral plexus, neuritis

lumbrical muscles

lymph node biopsy

lymphadenopathy

lymphadenopathy, cervical

lymphadenopathy, hilar

lymphocytic meningoradiculitis

lymphoma involving CNS

lysosomal storage disease

lysosomes, abnoral

macular degeneration

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

malignancy screen

malignancy, occult

malignant hyperpyrexia

manganese intoxication

Man-In-The-Barrel syndrome

marche a petits pas

Marchiafava-Bignami disease

Marinesco-Sjogren syndrome

Martin-Gruber anastamosis

masseter muscle spasm

masseter muscle wasting

masseter muscle weakness

maxillary nerves

McArdle's disease

McLeod syndrome

median nerve, lesion of

median neuropathy

medical-legal aspects of neurology

medulla oblongata, lesion of

memory, defect of recent

memory, impairment of

meningeal biopsy

meningeal enhancement

meningitis, aseptic

meningitis, bacterial

meningitis, basilar

meningitis, carcinomatous

meningitis, children

meningitis, chronic

meningitis, cysticercosis

meningitis, eosinophilic

meningitis, factors influencing mortality in

meningitis, fungal

meningitis, fungal-negative CSF culture

meningitis, late neurologic sequelae in

meningitis, leptospira

meningitis, melanomatous

meningitis, neurologic aspects and complications of

meningitis, neutrophilic

meningitis, recurrent

meningitis, syphilitic

meningocele, traumatic

meningoencephalitis

meningoencephalomyelitis

meningoencephalopathy

meningomyelitis

mental retardation

mental status, abnormal

mercaptopropionyl glycine

metabolic acidosis

metabolic disorder, primary

metachromatic leukodystrophy

metachromatic leukodystrophy, juvenile

methylene tetrahydrofolate reductase

methylenetetrahydrofolate reductase deficiency

methylhydrazine derivatives

methylmalonic acid, serum

methylmalonic acidemia

microangiopathy, brain

microangiopathy, retina

midbrain, atrophy

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

middle cerebral artery territory infarction

middle cerebral artery, emboli to

middle cerebral artery, occlusion of

middle cerebral artery, stenosis of

migraine, seizures in

mild cognitive impairment

Millard Gubler syndrome

Mini Mental Status Examination

minimally conscious state

mitochondrial disease

mitochondrial encephalomyopathy

mitochondrial recessive ataxic syndrome

mitral valve lesion

mitral valve prolapse

molecular genetics

monoamine oxidase inhibitors

monoclonal antibodies

monoclonal gammopathy

monoclonal gammopathy of uncertain significance

monomelic amyotrophy

mononeuritis multiplex

mononeuropathy chronic inflammatory demyelinating

mononeuropathy multiplex

mononeuropathy, motor

monoparesis, focal

Motor Band Sign

motor dysfunction

motor neuron disease

motor neuron disease, juvenile form

motor neuron disease, spontaneous recovery

movement disorder

movement disorder, extrapyramidal

movement disorder, hyperkinetic

MRI, angiography

MRI, brachial plexus

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, cranial nerves

MRI, diffusion tensor

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, eye of tiger sign

MRI, functional

MRI, gradient-echo

MRI, high signal foci on

MRI, lumbosacral plexus

MRI, optic nerve

MRI, paramagnetic effect

MRI, peripheral nerve

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRI, susceptibility weighted

MRI, T1 weighted fat suppression

mucopolysaccharidoses

multifocal acquired demyelinating sensory motor neuropathy

multinucleated giant cell

multiple endocrine neoplasia

multiple myeloma

multiple organ failure

multiple sclerosis

multiple sclerosis, diagnosis of

multiple sclerosis, diet in

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple sclerosis, treatment of

multiple system atrophy

muscle atrophy, focal

muscle atrophy, progressive

muscle atrophy, static

muscle biopsy, extraocular

muscle diseases, characteristics of

muscle hypertrophy

muscle phosphorylase deficiency

muscle relaxant

muscle spasm, paraspinal

muscle stiffness

muscle strength, testing

muscle swelling

muscle tenderness

muscle twitching

muscle wasting, diffuse

muscle weakness

muscle weakness, causes of

muscle weakness, insidious onset of

muscle weakness, proximal

muscle weakness, sudden onset of

muscle, metabolic disorders 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, distal, Miyoshi

muscular dystrophy, Duchenne

muscular dystrophy, Duchenne, carrier

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

myasthenia gravis

myasthenia gravis, differential diagnosis

myasthenia gravis, distal weakness

myasthenia gravis, drug induced

myasthenia gravis, limb-girdle

myasthenia gravis, misdiagnosis of

myasthenia gravis, paraneoplastic

myasthenia gravis, treatment of

myasthenic crisis

myasthenic syndrome

myasthenic syndrome, treatment of

mycoplasma pneumoniae

myelin protein zero gene

myelinolysis, extrapontine

myelitis, longitudinal

myelogram, cervical

myeloma, osteosclerotic

myeloneuropathy

myelopathy, ischemic

myelopathy, carcinomatous

myelopathy, chronic progressive

myeloradiculopathy

myocardial biopsy

myocardial infarction

myocardial infarction, acute

myocardial injury

myoclonic jerks

myoclonus, abdominal

myoclonus, cortical

myoclonus, epilepsy

myoclonus, segmental

myoclonus, stimulus sensitive

myopathy, acute

myopathy, alcoholic

myopathy, amyloid

myopathy, autoimmune

myopathy, carcinomatous

myopathy, centronuclear

myopathy, critically ill

myopathy, desmin

myopathy, distal

myopathy, distal, vacuolar

myopathy, distal, Welander's

myopathy, drug-induced

myopathy, hereditary

myopathy, inclusion body

myopathy, inclusion body with Paget's disease

myopathy, inclusion body, hereditary

myopathy, mitochondrial

myopathy, myofibrillar

myopathy, necrotizing

myopathy, proximal

myopathy, quadriceps

myopathy, radiation-induced

myopathy, steroid induced

myopathy, steroid responsive

myopathy, thyroid disease causing

myopathy, toxic

myopathy, vacuolar

myositis, focal

myositis, ocular

myotonia congenita

myotonia dystrophica

myotonic discharges

myxedema, neurologic manifestations of

N-acetyl-L-aspartic acid

narcotic analgesics

nausea and vomiting

necrotizing vasculitis

nemaline rod myopathy

nemaline rod myopathy, adult onset

neonatal infection, viral

neoplasm, hormone producing

neoplasm, hormone producing, ectopic

neoplasm, intracranial

neoplasm, intracranial, differential diagnosis of

neoplasm, metastatic to CNS

neoplasm, pituitary

neoplasm, primary intracerebral

neoplasm, primary intracranial

neoplasm, primary of CNS

nerve conduction studies

nerve conduction studies, motor

nerve conduction studies, sensory

nerve enlargement

nerve growth factor

nerve hypertrophy

nerve repair, end to end

nerve root enhancement

nerve root hypertrophy

neuritis, causes of

neuritis, heavy metals causing

neuroaxonal dystrophy

neuroaxonal dystrophy, infantile

neuroaxonal dystrophy, juvenile

neurocutaneous disease

neuroendocrinology

neurofibrillary degeneration

neurogenic atrophy

neurogenic bladder

neurogenic stunned myocardium

neurogenic vs.myopathic atrophy

neurolipidosis IV

neurologic complications

neurologic complications of, burns

neurologic complications of, surgery

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic consultation

neurologic disease

neurologic disease, diagnoses of

neurologic disease, diagnoses of, clinical bedside

neurologic disease, incurable

neurologic disease, multifocal

neurologic disease, tempo

neurologic evaluation

neurologic examination

neurologic examination, focal

neurologic signs

neurologic symptoms

neurolymphomatosis

neuromuscular blockade

neuromuscular disease, electrodiagnosis of

neuromuscular junction

neuromuscular junction, abnormality of

neuronal cell surface antigen

neuronal ceroid-lipofuscinosis

neuronal degeneration

neuronal intranuclear inclusion disease

neuronal migration disorder

neuronopathy, sensory

neuronopathy, sensory and motor

neuroophthalmology

neuropathology, brain

neuropathy, ataxic

neuropathy, bicycle

neuropathy, classification of

neuropathy, demyelinating

neuropathy, diabetic

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, iatrogenic

neuropathy, medication induced

neuropathy, motor

neuropathy, motor, multifocal

neuropathy, multifocal

neuropathy, onion bulb

neuropathy, painful

neuropathy, paraneoplastic

neuropathy, peripheral

neuropathy, peripheral, treatment

neuropathy, sensory

neuropathy, toxic

neuropathy, vasculitic, systemic

neuropathy, work up for

neuroprotective agents

neurotoxicity, acute

neurotransmitter

newborn, evaluation of

next-generation sequencing

night blindness

nitrogen mustard

NMDA antagonists

numbness, ascending

numbness, extremity

numbness, generalized

nutritional deficiency

nystagmus, dissociated

nystagmus, monocular

nystagmus, primary position of gaze

nystagmus, rotary

nystagmus, vertical

obstetric neurologic injuries

occipital lobe, lesion of

occupational neurologic disorders

occupational neuropathies

ocular motility, disorders of

ocular myopathy

oculopharyngeal muscular dystrophy

old age, neurology of

olivary degeneration, hypertrophic

onconeural antibodies

Onufrowicz nucleus

ophthalmoplegia

ophthalmoplegia, painful

ophthalmoplegia, progressive external

ophthalmoplegia, total

Oppenheim muscular dystrophy

opportunistic infection

opportunistic infection, CNS

opsoclonus-myoclonus syndrome

optic atrophy, hereditary

optic atrophy, infants

optic atrophy, unilateral

optic disc edema

optic nerve sheath enhancement

optic nerve, compression of

optic nerve, enlarged

optic nerve, hypoplasia of

optic nerve, lesion of

optic neuropathy

optic neuropathy, bilateral

optic neuropathy, ischemic

optic neuropathy, ischemic, anterior

optic neuropathy, nutritional

orbit, inflammation in

orbit, lesions of

orthostatic hypotension

osmotic demyelination syndrome

osteomyelitis, spinal

otitis, neurologic complications with

owl's eye sign of spinal cord

pacemaker, cardiac-transvenous

Paget's disease

Paget's disease, psychosis in

Paget's disease, spinal cord problem in

pain, abdominal

pain, interscapular

pain, management of chronic

palatal myoclonus

palliative care

paracentral lobule

paralysis, acute

paralysis, acute areflexic

paralysis, asymmetric

paralysis, recurrent

paraneoplastic cerebellar degeneration

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, spastic

paraproteinemia

parasitic infection, CNS

paraspinal muscle

paraspinal muscle weakness

parathyroid adenoma

paresthesias, feet

paresthesias, hands

paresthesias, lower extremity

parietal lobe, lesion of

parietal lobe, syndromes of

Parkinson disease

Parkinson disease, axial symptoms

Parkinson disease, dystonia with

Parkinson disease, L-dopa nonresponsive

Parkinson disease, motor neuron disease with

Parkinson disease, surgical treatment of

Parkinson disease, treatment of

Parkinson disease, tremor, absence of

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

Parkinsonism-dementia complex

paroxysmal hemiplegia

paroxysmal neurologic deficits

PAS positive material in the brain

patient information and support

pediatric neurology

penguin silhouette sign

percussion induced muscle contraction

pericardial effusion

perineuritis, optic

periodic paralysis

periodic paralysis, thyrotoxic

peripheral blood smear

peripheral blood smear, abnormal

peripheral nerve, lesion of

peripheral vascular disease

periventricular leukomalacia

pernicious anemia

peroneal muscle atrophy, causes of

peroxisomal disease

persistent vegetative state

personality change

personality disorder

pheochromocytoma

phosphorylase b kinase deficiency

phrenic nerve pacemaker

physical activity

physical therapy

physician assisted suicide

pigmentary retinopathy

pituitary, lesion of

plasma cell dyscrasia

pleocytosis of cerebrospinal fluid

pleural effusion

pneumoencephalogram(PEG)

poison, mercury

poison, neurologic problems with

poliomyelitis, neonatal

poliomyelitis-like illness

polyclonal gammopathy

polyglucosan body

polyglucosan body disease

polymerase chain reaction

polymyalgia rheumatica

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, chronic inflammatory demyelinating, variant form

polyneuropathy, chronic inflammatory demyelinating-pure motor syn

polyneuropathy, chronic inflammatory demyelinating-sens atax var

polyneuropathy, chronic inflammatory demyelinating-variant forms

polyneuropathy, critically ill

polyneuropathy, critically ill, children

polyneuropathy, familial

polyradiculoneuropathy

Pompe's disease of glycogen storage

pons, infarction of

pons, lesion of

pontocerebellar atrophy

position sensation, abnormal

positive sharp waves

post polio syndrome

posterior column disease

posterior fossa

posterior fossa, arteriovenous malformation

posterior fossa, differential diagnosis of lesions of

posterior fossa, lesion of

posterior fossa, signs of

posterior inferior cerebellar artery syndrome

posterior interosseous neuropathy

posterior longitudinal ligament, ossification of

postoperative neurologic complications

postural abnormality

practice guidelines

Prader-Labhart-Willi syndrome

precentral gyrus

precipitating factors

pregnancy, neurologic complications in

premature infant

prenatal diagnosis by amniocentesis

pretectal syndrome

prevention of neurologic disorders

primary aldosteronism

primary lateral sclerosis

primary thrombocythemia

prisoners of war, neurologic complications in

progressive multifocal leucoencephalopathy

progressive muscular dystrophy

progressive myoclonic epilepsy

progressive neurologic disorder

progressive pallidum atrophy

progressive spinal muscular atrophy

progressive supranuclear palsy

prolactin, elevated

pronator syndrome

proprioception, abnormal

proptosis, unilateral

proximal muscle atrophy

pseudobulbar palsy

pseudohypertrophy

pseudomedian nerve palsy

pseudoperipheral palsy

pseudoradial nerve palsy

pseudoulnar palsy

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychomotor retardation

ptosis, bilateral

ptosis, familial

ptosis, unilateral

pulmonary embolism

pulmonary function tests

pulmonary infiltrates

pupil, abnormality in neurologic disorders

pupil, dilated and fixed, bilateral

pure motor hemiplegia

pure motor stroke

pure sensory stroke

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

quadriceps atrophy

quadriceps weakness

quadriplegia, transient

quality of life

rabies, nervous system involvement with

radial nerve, palsy of

radial pulse, unilateral decrease of

radiation hypersensitivity

radiation therapy, CNS treatment and complications with

radiation therapy, salivary gland

radionuclide imaging, heart

ragged-red fibers

Ramsay Hunt syndrome

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

Raynaud's phenomenon

reading disorder, acquired

real-time quaking-induced conversion

recombinant DNA

recruitment, reduced

reflex sympathetic dystrophy

reflex sympathetic dystrophy, children

Refsum's disease

rehabilitation for neurologic disorders

release phenomena

remote effect of cancer on the nervous system

renal transplantation

renal tubular acidosis

repetitive nerve stimulation

respirations in CNS disease

respiratory depression

respiratory failure

respiratory tract infection

restrictive ophthalmopathy

retina, abnormal

retinal artery occlusion

retinal branch artery occlusion

retinal degeneration

retinal dysplasia

retinal hemorrhages

retinal infarction

retinitis pigmentosa

Rett's syndrome

reverse split hand sign

reversible neurologic disorder

rheumatoid arthritis

rheumatoid arthritis, neurologic complications of

rigid spine syndrome

rigidity, axial

rippling muscle disease

risk-benefit assessment

Rolandic artery

root lesion, nerve

Rosenthal fibers

Roussy Levy syndrome

rubella encephalitis

rubella encephalitis, progressive

rubella syndrome

saccadic eye movements, abnormal

salivary gland enlargement

salivation, excessive

sarcoidosis, CNS

scalenus anticus syndrome

Schilder's disease

sciatic neuropathy

scleroderma, neurologic involvement with

sclerosis, bone

scoliosis, neurologic association with

scotomata, scintillating

sea-blue histiocytes

second wind phenomena

sedimentation rate

sedimentation rate, elevated

seizure, children

seizure, intractable

seizure, neonatal

seizure, paradoxical

seizure, repetitive

seizure, surgical treatment of

seizure, treatment of

seizure, withdrawal

self-mutilation

semialdehyde dehydrogenase deficiency

sensorimotor stroke

sensorineural hearing loss

sensory ganglia

sensory ganglia, abnormal

sensory loss, cortical

sensory loss, cutaneous

sensory loss, glove-stocking

sensory loss, patchy

sensory loss, pseudoradicular

sensory loss, truncal

sensory nerve action potentials

sensory symptoms

sensory testing

sensory testing, quantitative

sequencing difficulty

serologic testing

serologic testing of cerebrospinal fluid

serum alanine aminotransferase

shock, hypovolemic

shoulder, numbness

shoulder, pain in

shoulder, subluxation

shoulder, weakness

shoulder-girdle wasting

shunt procedure, ventricular

single photon emission computed tomography

single-fiber electromyography

sinuses, diseases of

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skin, discoloration

skin, lesions in neurologic disorders

skin, temperature difference

skull x-ray, abnormal

sleep pathology and physiology

slit lamp examination

slow virus infection of CNS

small for dates infant, problems in

small vessel disease

Smell Identification Test

somatosensory evoked potentials

somatosensory evoked potentials, dermatomal

spastic paraplegia, type 11

spastic paraplegia, type 7

speech disorder

speech disorder, childhood

speech, delayed development of

speech, loss of

spinal cord degeneration

spinal cord, biopsy

spinal cord, cervical

spinal cord, compression of

spinal cord, compression, epidural abscess causing

spinal cord, enlargement

spinal cord, infarction of

spinal cord, injury of

spinal cord, injury, management of

spinal cord, injury, New Born

spinal cord, intramedullary cyst of

spinal cord, ischemic lesion of

spinal cord, lesion of

spinal cord, neoplasm

spinal cord, neoplasm, extramedullary

spinal cord, neoplasm, intramedullary

spinal cord, pathologic exam of

spinal cord, transection

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinal muscular atrophy, classification

spinal muscular atrophy, intermediate form

spinal stenosis

spinal stenosis, cervical canal

spinal stenosis, familial

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar ataxia type 7

spinocerebellar degeneration

spirochete infection

splenium of corpus callosum

splinter hemorrhages

spongy degeneration of brain

spontaneous muscle activity

spontaneous remission

sports medicine, neurology of

standing difficulty

startle myoclonus

startle reaction

status epilepticus

stellate-ganglion block

stem cell tourism

stem cell transplantation

stereotaxic surgery

stereotyped behavior

sternocleidomastoid muscle

steroid therapy, CNS treatment and complications with

stiff man syndrome

Stokes-Adams syndrome

storage disease of CNS

striatonigral degeneration

striatonigral degeneration, infantile

striatum, lesion of

striatum, lesion of, bilateral

strokelike episodes

subacute myelo-opticoneuropathy(S.M.O.N.)complex

subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease

subarachnoid hemorrhage

subclavian artery stenosis

subdural effusion

subdural hematoma

subdural hematoma, interhemispheric

substantia nigra

subtraction of x-rays

sulfite oxidase deficiency

superior cerebellar peduncle

superior orbital fissure syndrome

superior sagittal sinus

superior sagittal sinus thrombosis

superoxide dismutase

suprascapular nerve

suprascapular neuropathy

suprasellar lesion

supraspinatus muscle

survival motor neuron gene

Susac's syndrome

swallow evaluation

sweating, abnormality of

symmetric brain lesions

sympathetic block

syncope, differential diagnosis of

synucleinopathy

syphilis, neurologic complications with

systemic illness

systemic lupus erythematosus

systemic lupus erythematosus, neurologic complications with

tandem gait, ataxic

Tangier's disease

Tay-Sachs disease

teeth, abnormal

teeth, number of in infants

temper tantrums

temporal artery, biopsy

temporal artery, tender

temporal lobe, atrophy

temporalis muscle wasting

temporalis muscle weakness

temporomandibular joint, dislocation

tensilon test, false positive

testicular atrophy

thalamus, atrophy of

thalamus, lesion of

thalamus, lesion of-bilateral

thallium poisoning

thoracic outlet syndromes

Three territory sign

thromboangiitis obliterans cerebri

thrombocytopenia

thrombophlebitis

thrombosis, cerebral

thyrotropin-releasing hormone

tick-borne encephalitis

tissue plasminogen activator, intravenous

Tolosa Hunt syndrome

tomaculous neuropathy

tongue, atrophy

tongue, enlarged

tongue, fasciculations of

tongue, protrusion of

tongue, swelling

tongue, weakness

tonic foot response

torticollis, post traumatic

toxic encephalopathy

toxins, nervous system

toxoplasmosis, CNS

tram-track sign

transdermal medication

transient ischemic attack

transient neurologic deficit

transilumination of skull

transplacental virus infections

transverse smile

travel, foreign

treatment of neurologic disorder

tremor, cerebellar

tremor, intention

tremor, post traumatic

tremor, postural

tremor, resting

triangle of Guillain and Mollaret

trichopoliodystrophy

tricresylphosphate

trigeminal nerve

trigeminal nerve, abnormality of

trigeminal nerve, hypertrophy

trigeminal nerve, lesion of

trigeminal neuralgia

trinucleotide repeats

Trousseau's sign

tuberous sclerosis

tubular aggregates, muscle

tumor necrosis factor inhibitor

type 2 muscle fiber

tyrosine hydroxylase deficiency

ulcers, fingertip

ulnar nerve, compression of

ulnar nerve, deep palmar branch of

ulnar neuropathy

ultrasonography

ultrasonography, head

ultrasonography, head, fetus-neonate

ultrasonography, nerve

unconsciousness

Unverricht-Lundborg disease

upgaze, paralysis of

upright-tilt test

upward deviation of eyes

urinalysis, abnormal

urinary incontinence

urinary urgency

urine test for metabolic disorders

urine test in toxic screen

vascular endothelial growth factor

vascular syndromes

vasospasm, cerebral

venous thrombosis, non-cerebral

ventricular enlargement

vertebral erosion

vertebral-basilar insufficiency

vertigo, cervical

vertigo, positional

vertigo, treatment of

vestibular function, tests of

vibratory sensation, abnormal

vincristine neurotoxicity

violent behavior

viral infection

viral infection, CNS

viral isolation

vision, blurred

vision, failure of in childhood

visual acuity, decreased

visual evoked response

visual field defect

visual field defect, altitudinal

visual fields, constricted

visual impairment

visual loss, transient

visual symptoms

visual tracking

visuospatial disturbance

vitamin deficiency

vitamin E deficiency

vitreous opacities

vocal cord paralysis

Volkmann's ischemia

Waldenstrom's macroglobulinemia

Walker-Warburg syndrome

walking, delayed

walking, difficulty with

watershed infarcts

weakness, acute

weakness, congenital

weakness, fatiguable

weakness, focal

weakness, generalized

weakness, infant

weakness, progressive

weakness, proximal

weakness, rapidly progressive

weaning from respirator, failure to

Weber's syndrome

Werdnig-Hoffman disease

Wernicke's encephalopathy

West Nile fever

Whipple's disease

whistle, inability to

white matter disease

white matter disease, periventricular

white matter disease, subcortical

wide based gait

winging of scapula

Wolfram syndrome

word-finding difficulty

X-linked bulbospinal neuronopathy

X-linked myopathy

x-linked myopathy with excessive autophagy

X-linked neuropathy

Zika virus infection

Showing articles 500 to 550 of 4226 << Previous Next >>

Neuromuscular Blockade
Lancet 335:382-384, , 1990

Clinical Study of 227 Patients with Lacunar Infarcts
Stroke 21:842-847, Arboix,A.,et al, 1990

Benign Plexus Neuropathy in Children
J Pediatr 116:276-278, Zeharia,A.,et al, 1990

Cortical-Basal Ganglionic Degeneration
Neurol 40:1203-1212, Riley,D.E.,et al, 1990

The Spectrum of Neurologic Disease Associated with Anti-GM1 Antibodies
Neurol 40:1067-1072, Sadiq,S.A.,et al, 1990

Progressive Rubella Panencephalitis
In Handbk of Clin Neurol, Vinken & Bruyn, Ed, N Holland Publ Co, 56:405-416, Wolinsky,J.S., 1990

Polyclonal IgM Anti-GM1 Ganglioside Antibody in Patients with Motor Neuron Disease and Variants
Ann Neurol 27:558-563, Salazar-Grueso,E.F.,et al, 1990

Immunologic Reactivity Against Borrelia Burgdorfi in Patients with Motor Neuron Disease
Arch Neurol 47:586-594, Halperin,J.J.,et al, 1990

2-Amino-3- (methylamino) -Propanoic Acid (BMAA) in Cycad Flour:An Unlikely Cause of ALS & Parkinsonism-Dementia of Guam
Neurol 40:767-772, Duncan,M.W.,et al, 1990

Mapping of Acute (Type 1) Spinal Muscular Atrophy to Chromosome 5q12-q14
Lancet 336:271-273, Melki,J.,et al, 1990

Spinal Muscular Atrophies
Editorial, Lancet 336:280-2811990., , 1990

Genetic Linkage of Hereditary Motor & SensoryNeuro Type I (Charcot-Marie-Tooth Disease) to Chrom 1 & 17
Neurol 40:1450-1453, Defesche,J.C.,et al, 1990

Cerebral Cortex and Brainstem Involvement in Marinesco-Sjogren Syndrome
Ann Neurol 27:448-449, Katafuchi,Y.,et al, 1990

Syncope:Current Diagnostic Evaluation and Management
Ann Int Med 112:850-863, Manolis,A.S.,et al, 1990

A Disorder of Azonal Development, Necrotizing Myopathy, Cardiomyopathy, and Cataracts:A New Familial Disease
Ann Neurol 27:193-199, Lyon,G.,et al, 1990

MRI Demonstration of Cortical Laminar Necrosis and Delyaed White Matter Injury in Anoxic Encephalopathy
Neuroradiology 32:319-321, Sawada,H.,et al, 1990

Hypoxic-Ischemic Damage of the Basal Ganglia
Mov Disord 5:219-224, Hawker, K. & Lang, A.E., 1990

DNA Restriction Fragment Length Polymorphisms in Diff Dx of Genetic Disease:Appl in Neuromusc Dis
Hum Genet 82:55-58, Defesche,J.C.,et al, 1989

Trochanteric Sciatic Neuropathy
Neurol 39:1539-1541, Crisci,C.,et al, 1989

Neuromuscular Involvement in Mild, Asymptomatic Primary Hyperparathyroidism
Am J Med 87:553-557, Turken,S.A., 1989

Respiratory Muscle Weakness in Charcot-Marie-Tooth Disease, A Field Study
Arch Int med 149:1389-1391, Nathanson,B.N.,et al, 1989

Hereditary Motor & Sensory Neuropathy with Optic Atrophy, Ultrastructural and Morphometic Observations
Arch Neurol 46:973-977, Sommer,C.&Schroder,J.M., 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

Rising Mortality From Motoneuron Disease in the USA, 1962-84
Lancet 1:710-712, Lilienfeld,D.E.,et al, 1989

Amyotrophic Lateral Sclerosis:Abnormalities of the Tongue on Magnetic Resonance Imaging
Ann Neurol 25:468-472, Cha,C.H.&Patten,B.M., 1989

Ethanol and the Nervous System
NEJM 321:442-454, Charness,M.E.,et al, 1989

Inclusion Body Myositis, Observations in 40 Patients
Brain 112:727-747, Lotz,B.P.,et al, 1989

Congenital AIDS:Review of Neurological Problems
Child's Nerv Syst 5:9-11, Curles,R.G., 1989

Respiratory Complications and Their Management in Motor Neuron Disease
Brain 112:1155-1170, Howard,R.S.,et al, 1989

Refsum Disease
In Rowland's Merritt's Textbk of Neurology, Lea & Febiger, Phila, 8thEd, p. 509, Menkes,J.H., 1989

The Effects of Alcoholism on Skeletal and Cardiac Muscle
NEJM 320:409-415, 458-4601989., Urbano-Marquez,A.,et al, 1989

Sulfite Oxidase Deficiency:Clinical, Neuroradiologic, and Biochemical Features in Two New Patients
Neurol 39:252-257, Brown,G.K.,et al, 1989

Clinicopath Conf
Subacute Cerebellar Degeneration, Cystadenocarcinoma of Ovary, (with Paraneoplastic Syndrome) , Case, 34-1EJM 321:524-535,1989., 1989

Compressive Mononeuropathy of the Deep Palmar Branch of the Ulnar Nerve in Cyclists
JNNP 51:1588-1590, Hankey,G.J.&Gubbay,S.S., 1988

The Peroxisome:Nervous System Role of a Previously Underrated Organelle, The 1987 Robert Wartenberg Lecture
Neurol 38:1617-1627, Moser,H.W., 1988

Nontraumatic Frontal Lobe Hemorrhages:Clinical-computed Tomographic Correlations
Neuroradiology 30:500-505, Weisberg,L.A.&Stazio,A., 1988

Dystonia and Tremor Induced by Peripheral Trauma:Predisposing Factors
JNNP 51:1512-1519, Jankovic,J.&VanDer Linden,C., 1988

Magnetic Resonance Imaging in Amyotrophic Lateral Sclerosis
Ann Neurol 23:418-420, Goodin,D.S.,et al, 1988

A Double-Blind Study of the Effectiveness of Cyclosporine in Amyotrophic Lateral Sclerosis
Arch Neurol 45:381-386, Appel,S.H.,et al, 1988

Respiratory Muscle Dysfunction in Hereditary Motor Sensory Neuropathy, Type I
Arch Int Med 148:1739-1740, Eichacker,P.Q.,et al, 1988

Motoneuron Disease and Past Poliomyelitis in England and Wales
Lancet 1:1319-1322, Martyn,C.N.,et al, 1988

Distal Vacuolar Myopathy with Complete Heart Block
Arch Neurol 45:698-699, Krendel,D.A.,et al, 1988

Neurologic and Cognitive Deficits in Children with Cystinosis
J Pediatr 112:912-914, Trauner,D.A.,et al, 1988

Severe Polymyositis-Like Syndrome Associated with Zidovudine Therapy of AIDS & ARC
NEJM 318:708, Bessen,L.J.,et al, 1988

Amyotrophic Lateral Sclerosis, Recent Advances in Pathogenesis & Therapeutic Trials
Arch Neurol 45:189-202, Mitsumoto,H.,et al, 1988

The Natural History of Motoneuron Loss in Amyotrophic Lateral Sclerosis
Neurol 38:409-413, Munsat,T.L.,et al, 1988

Use of Composite Scores (Megascores) to Measure Deficit in Amyotrophic Lateral Sclerosis
Neurol 38:405-408, Andres,P.L.,et al, 1988

Deep Branch Ulnar Neuropathy Due to Giant Cell Tumor:Report of a Case
Neurol 38:327-329, Rafecas,J.C.,et al, 1988

Early-Onset Benign Autosomal Dominant Limb-Girdle with Contractures (Bethlem Myopathy)
Neurol 38:573-580, Mohire,M.D.,et al, 1988

Amyotrophic Lateral Sclerosis Presenting with Sleep Hypopnea Syndrome
Chest 93:1309-1312, Carre,P.C.,et al, 1988

Showing articles 500 to 550 of 4226 << Previous Next >>