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Differential
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abdominal contractions

abdominal protrusion

abductor pollicis brevis

abscess, intracerebral

abscess, intracerebral, multiple

abscess, intracerebral, treatment of

abscess, lung

abscess, vertebral

acanthocytosis

acetylcholine receptor antibody

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

acute necrotizing encephalitis

addiction, heroin

addiction, heroin-neurologic complications with

Addison's disease

Adies pupil

adult polyglucosan body disease

advances in neurology

agenesis of corpus callosum

aggression

agitation

Aicardi-Goutieres syndrome

alcohol intoxication

alcohol, neurologic complications with

alcoholic polyneuropathy

alcoholism

algorithm

alien hand syndrome

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

amphiphysin antibodies

amyloid

amyloid angiopathy, cerebral

amyloid plaques

amyloidosis

amyotrophic chorea-acanthocytosis

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, bulbar

amyotrophic lateral sclerosis, atypical

amyotrophic lateral sclerosis, complications with

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, misdiagnosis

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, treatment of

amyotrophic lateral sclerosis-like syndrome

anatomy of

anemia

anemia, megaloblastic

aneurysm

aneurysm, anterior communicating

aneurysm, intracranial

angiitis

angiitis, granulomatous of CNS

angiitis, isolated of CNS

angiography, neurologic complications with

anisocoria

ankle reflex, absent

ankylosing spondylitis

anoctaminopathy

anorexia

anterior horn cell disease

anterior interosseous neuropathy

anterior spinal artery infarction

anterior tibial muscle weakness

anti citrullinated antibody

anti Hu antibody

antibiotics

antibodies to measles

anticoagulant, complications of

anticoagulant, treatment

antiviral agents

aphasia

aphasia, progressive

aphasia, progressive, primary

aphonia

applause sign

apraxia

apraxia of eye movements

apraxia, constructional

apraxia, speech

aqueduct of Sylvius, obstruction

arterial dissection, carotid

arterial dissection, vertebral

arthralgia

arthrogryposis multiplex

asthma, poliomyelitis-like syndrome with

autonomic dysfunction

Babinski sign in new born

bacterial infection

BAL

basal ganglia

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, infarction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basement membrane

basement membrane thickening

basophilic stippling of red blood cells

behavioral disorder

Bence Jones protein

benign essential tremor

biologic markers

BiPAP

bitemporal visual field defect

bone marrow suppression

botulinum toxin, complications of

brachial amyotrophic diplegia

brachial neuritis

brachial neuritis, acute

brachial neuritis, bilateral

brachial neuritis, prognosis of

brachial plexus

brachial plexus injury

brachial plexus neuropathy

brachial plexus neuropathy, bilateral

brachial plexus neuropathy, familial

brachial plexus neuropathy, recurrent

brachial plexus, lesion of

bradykinesia

brain atrophy

brain biopsy

brain biopsy, false negative

brain biopsy, negative

brain scan

brainstem, atrophy

brainstem, infarction of

brainstem, lesion of

Brueghel's syndrome

bruit

bruit, supraclavicular

bulbar palsy

bulbar palsy, progressive

calcification, intracranial

cardiac catheterization, neurologic complications

cardiomegaly

cardiomyopathy

cardiovascular disease

caribbean

carotid artery atherosclerosis

carotid artery disease

carotid artery occlusion, neck

carotid artery stenosis

carpal tunnel syndrome

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, serial

CAT scan, spine

cataracts

cataracts, congenital

CD4 counts

central hypoventilation, congenital

central nervous system, infection of

cerebellar ataxia, children

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar lesion

cerebellar plaques, amyloid

cerebellum

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

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, culture of

cerebrospinal fluid, cytology

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, gold sol.curve of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

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, recurrent

cerebrovascular accident, topographic pattern

cerebrovascular accident, vascular territory involved

cerebrovascular accident, young adult

cerebrovascular disease, risk factors in

cheiralgia paresthetica

chelation therapy

chemotherapy, CNS treatment and complications with

chromosomal abnormality

chromosome 17

chromosome 3

chronic progressive external ophthalmoplegia

Chvostek sign

cisterna magna

cisternogram, radionuclide

claudication, extremity

Clinical Pathologic Conference(C.P.C.)

collapsin response mediator protein 5 IgG

coma

comorbidities

compartment syndrome

compartment syndrome, medial brachial fascial

complications

compression neuropathy

conduction block

confusion

confusional state, acute

congenital infection, CNS

congenital infection, viral

congestive heart failure

conjugate gaze, forced

conjunctivitis

contactin associated protein like 2 antibodies

contractures, joint

conversion reaction

corneal reflex, abnormal

corneal reflex, absent

corona radiata

corpus callosum, atrophy of

corpus callosum, infarction of

corpus callosum, lesion of

corpus callosum, neoplasm of

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

cough

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

craniopharyngioma

creatine phosphokinase(CPK)elevated

Creutzfeldt-Jakob disease, genetic

crying, pathologic

cultured skin fibroblasts

Cushing's syndrome

cyclophosphamide

cyst

cyst, cortical parenchyma

cysticercosis, cerebral

cysticercosis, intraventricular

cysticercosis, subarachnoid

cystinosis

cytomegalic inclusion disease

cytosine arabinoside

deep gray nuclei

degenerative diseases of CNS

dementia, age at onset

dementia, childhood

dementia, familial

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

demyelinating disease

denervation of muscle

denervation potentials

dental abscess

depression

depression, psychotic

dermatitis

dermatomyositis

developmental disability

developmental evaluation

developmental milestones

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diabetic amyotrophy

diabetic mononeuropathy

diagnostic criteria

diarrhea

differential diagnosis

difficulty climbing stairs

diffuse idiopathic skeletal hyperostosis

disability rating scale, neurological

disability, neurological

dissociated sensory loss

distal muscle atrophy

distal muscle weakness

downward gaze

drooling

dropped head syndrome

drug abuse

drug abuse, neurologic complications of

dural sinus thrombosis

dying

dysarthria

dysferlinopathy

dyskinesia, buccal lingual facial

dystonia, post traumatic

dystrophic calcification

electrical stimulation, spinal nerves

electrocardiogram, abnormal

electrocorticogram

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, periodic complexes

electromyogram

electromyogram, decremental response

electron microscopy

embolism

emotional lability

empyema, epidural-spinal

encephalitis

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, episodic

encephalitis, focal

encephalitis, paraneoplastic

encephalitis, Rasmussen's

encephalitis, viral

encephalomyelitis

encephalopathy

encephalopathy, acute

encephalopathy, metabolic

encephalopathy, progressive

endemic area

enterovirus

enterovirus infection of CNS

entrapment neuropathy

enzyme, defect

enzyme, muscle disease

eosinophilia

epidemiology of neurology

epilepsia partialis continua

episodic neurologic deficits

exercise-induced vascular symptoms

exome sequencing

exophthalmus

extremity, cold

eye movement, disorders of

face, numbness of

facial nerve palsy

facial weakness

facial weakness, bilateral

failed medical management

fetal movements, reduced

fetus

fever

fibrillations

fine motor function, impaired

finger flexor weakness

finger weakness

fingernails, abnormal

fourth ventricle, cyst

fracture, long bones, nerve injury with

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

frontal behavioral spatial syndrome

frontal lobe, atrophy

frontal lobe, behavior with disease of

frontal lobe, lesion of

frontal lobe, pathologic signs of

frontal lobe, space occupying lesion of

frontotemporal dementia, behavioral variant

gammaglobulin therapy, intravenous

gaze palsy, horizontal

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic neurologic disorders

genetic testing

genu of corpus callosum

girdle sensation

glabellar sign

glioblastoma multiforme(astrocytoma Gr.III)

glioma

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glycogen debranching enzyme deficiency

glycogen storage disease

granular osmiphilic material

granuloma, pulmonary

granulomatous disease

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, variant forms of

Guyon's canal

gynecomastia

hallucination

hallucination, auditory

Hand-Schuller-Christian disease

hearing loss, bilateral

heavy metal intoxication

helminthic infection of CNS

hematoma, intracerebral

hemianopia, homonymous

hemiatrophy, cerebral

hemidystonia

hemiparesis

hemiparesis, transient

hemiplegia

hemiplegia, progressive

heralding manifestation

herniated disc

herniated disc, thoracic

herpes labialis

herpes simplex encephalitis

herpes simplex encephalitis, diagnosis of

herpes simplex encephalitis, differential diagnosis of

herpes simplex encephalitis, recurrent

herpes simplex encephalitis, treatment of

herpes simplex myelitis

herpes simplex virus

herpes simplex virus infection, immunosuppressed patient

herpes simplex virus, human nervous system and

herpes simplex virus, localization of

herpes simplex virus, malignancy with

herpes simplex virus, pathogenesis of

herpes simplex virus, pathology of

herpes simplex, neurocutaneous lesions in

highly active antiretroviral therapy

hip flexor weakness

Hirschprung's disease

Hispanics

histochemistry

histochemistry of muscle

Hodgkin's disease, neurologic involvement with

Horner's syndrome

hospice

human immunodeficiency virus type 1

Huntington's chorea

hydrocephalus

hydrocephalus, communicating

hydrocephalus, congenital

hydrocephalus, exvacuo

hydrocephalus, non-communicating(obstructive)

hydrocephalus, normal pressure

hydrocephalus, transient

hyperhidrosis, palmar

hypertension, cerebrovascular disease with

hyperthyroidism

hypoglycemia

hypoglycorrhachia

hypokalemic periodic paralysis

hypotension, systemic

hypothalamus

hypothalamus, disturbance of

hypotonia

hypotonia, infants

hypoxia

iatrogenic neurologic disorders

ideomotor apraxia

imbalance

imbalance, postural

immunofluorescent exam of CSF cells

immunologic disease

immunology and the nervous system

immunosuppression

immunosuppressive agents

immunotherapy

impotence

inability to stand on tiptoes

inborn errors of metabolism

incidence

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intranuclear

inclusion bodies, ubiquitin

inclusion body myositis

incoordination

India

infection

infectious mononucleosis

inflexibility, mental

infraspinatus muscle

insulinoma

intellectual deficit

intellectual deterioration

interferon

interferon alpha

interferon inducer

internuclear ophthalmoplegia

interosseous muscles

intracerebral hemorrhage

intracerebral hemorrhage, causes of

intracerebral hemorrhage, differential diagnosis of

intracerebral hemorrhage, lobar

intracerebral hemorrhage, multiple

intracranial hypertension, benign

intracranial pressure, increased

intranasal medication

intrauterine

intrauterine infection

intrauterine infection, viral

intrauterine infection, viral of CNS

intrinsic hand muscles

intrinsic hand muscles, wasting of

iododeoxyuridine

islet cell tumor

Jakob-Creutzfeldt disease

juvenile distal and segmental muscular atrophy

juxtacortical hemorrhage

ketogenic diet

klippel feil syndrome

Kugelberg-Welander syndrome

kyphoscoliosis, neurologic causes of

lactic acidemia

lactic dehydrogenase(LDH)

lacunar infarction

lacunar infarction, differential diagnosis of

lacunar infarction, hemorrhagic

laminectomy

laminectomy, lumbar

language disorder in adults

leg weakness, bilateral

leg weakness, unilateral

leucine rich glioma inactivated 1 antibodies

leukemia

leukodystrophy

leukoencephalitis, acute necrotizing hemorrhagic

leukoencephalopathy

leukopenia

level of consciousness, decreased

levitation

Lewy body disease, diffuse

Lhermitte's sign

lid closure, weakness of

life expectancy

life support, withdrawal of

liver function enzymes

lobar atrophy

locked-in syndrome

low back pain

lumbar puncture, complications of

lumbosacral plexopathy

lumbosacral plexus, neuritis

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

malignancy screen

malignancy, occult

Man-In-The-Barrel syndrome

Marinesco-Sjogren syndrome

Martin-Gruber anastamosis

masked facies

mastoiditis

median nerve

median nerve, lesion of

median neuropathy

Mees lines

MELAS syndrome

memory, defect of recent

memory, impairment of

meningitis, carcinomatous

meningitis, chronic

meningitis, cysticercosis

meningitis, eosinophilic

meningitis, fungal

meningitis, leptospira

meningitis, syphilitic

meningitis, TB

meningoencephalitis

mental retardation

mental status, abnormal

merosin

metabolic disorder, primary

methotrexate

methylmalonic acid, serum

Mexican

Mexico

microangiopathy, brain

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

mitochondrial disease

mitochondrial encephalomyopathy

molecular genetics

monoamines

monoamines, brain

monoclonal gammopathy

monomelic amyotrophy

mononeuritis multiplex

mononeuropathy

mononeuropathy chronic inflammatory demyelinating

mononeuropathy, motor

motor neuron disease, spontaneous recovery

movement disorder

movement disorder, extrapyramidal

movement disorder, hyperkinetic

MRI

MRI, abnormal

MRI, brachial plexus

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, FLAIR

MRI, functional

MRI, gradient-echo

MRI, lumbosacral plexus

MRI, muscle

MRI, negative

MRI, peripheral nerve

MRI, serial

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRI, spine

MRI, susceptibility weighted

MRI, T1 weighted fat suppression

MRS

multinucleated giant cell

multiple myeloma

multiple sclerosis

multiple sclerosis, diagnosis of

multiple sclerosis, differential diagnosis of

multiple system atrophy

muscle atrophy, focal

muscle atrophy, progressive

muscle atrophy, static

muscle biopsy

muscle cramp

muscle diseases, characteristics of

muscle hypertrophy

muscle pain

muscle spasm

muscle spasm, paraspinal

muscle stiffness

muscle swelling

muscle wasting, diffuse

muscle weakness

muscle weakness, causes of

muscle weakness, proximal

muscle, metabolic disorders of

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, cardiovascular changes with

muscular dystrophy, central nervous system abnormality

muscular dystrophy, classification

muscular dystrophy, congenital

muscular dystrophy, congenital, Fukuyama type

muscular dystrophy, distal, Miyoshi

muscular dystrophy, Duchenne

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

myasthenia gravis

myasthenia gravis, differential diagnosis

myasthenia gravis, distal weakness

myasthenia gravis, limb-girdle

myasthenia gravis, misdiagnosis of

myasthenia gravis, paraneoplastic

myelopathy, chronic progressive

myelopathy, necrotizing

myoclonus, stimulus sensitive

myopathy, carcinomatous

myopathy, distal

myopathy, distal, vacuolar

myopathy, distal, Welander's

myopathy, inclusion body

myopathy, inclusion body with Paget's disease

myopathy, inclusion body, hereditary

myopathy, inflammatory

myopathy, necrotizing

myopathy, quadriceps

myopathy, radiation-induced

myopathy, thyroid disease causing

myxedema, neurologic manifestations of

neoplasm, intracranial

neoplasm, intracranial, differential diagnosis of

neoplasm, metastatic to CNS

neoplasm, pituitary

neoplasm, primary intracerebral

neoplasm, primary intracranial

neoplasm, primary of CNS

nephritis

nerve biopsy

nerve conduction studies

nerve conduction studies, motor

nerve conduction studies, sensory

nerve repair, end to end

nerve root enhancement

nerve root hypertrophy

neuritis

neuritis, causes of

neuritis, heavy metals causing

neuroendocrinology

neurogenic bladder

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic disease, diagnoses of, clinical bedside

neurologic disease, multifocal

neurologic disease, tempo

neurologic examination

neurologic examination, focal

neurologic signs

neurologic symptoms

neurolymphomatosis

neuromuscular disease, electrodiagnosis of

neuromuscular junction

neuronal cell surface antigen

neuronal ceroid-lipofuscinosis

neuronal intranuclear inclusion disease

neuronopathy

neuronopathy, sensory

neuronopathy, sensory and motor

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, bicycle

neuropathy, diabetic

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, iatrogenic

neuropathy, medication induced

neuropathy, motor

neuropathy, motor, multifocal

neuropathy, multifocal

neuropathy, paraneoplastic

neuropathy, peripheral

neuropathy, peripheral, treatment

neuropathy, sensory

neuropathy, toxic

neuroprotective agents

nutritional deficiency

nystagmus

nystagmus, monocular

nystagmus, rotary

occipital lobe, lesion of

occupational neurologic disorders

occupational neuropathies

ocular bobbing

ocular motility, disorders of

old age, neurology of

onconeural antibodies

ophthalmoplegia

ophthalmoplegia, progressive external

ophthalmoplegia, total

opportunistic infection

opportunistic infection, CNS

opsoclonus-myoclonus syndrome

optic atrophy

optic neuropathy

osteomyelitis

osteomyelitis, spinal

otitis, neurologic complications with

overlap syndrome

owl's eye sign of spinal cord

pain, increased response

paralysis, acute areflexic

paralysis, asymmetric

paralysis, recurrent

paraneoplastic cerebellar degeneration

paraneoplastic ganglionopathy

parasitic infection, CNS

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, tremor, absence of

Parkinsonism syndrome

parotitis

paroxysmal hemiplegia

paroxysmal neurologic deficits

PAS positive

PAS positive material in the brain

penguin silhouette sign

pericardial effusion

peripheral blood smear

peripheral blood smear, abnormal

peripheral nerve, lesion of

pernicious anemia

persistent vegetative state

pleocytosis of cerebrospinal fluid

pleural effusion

pneumoencephalogram(PEG)

poliomyelitis

poliomyelitis, neonatal

poliomyelitis-like illness

polyclonal gammopathy

polyglucosan body

polyglucosan body disease

polyinosinic cytidic acid(poly IC)

polymerase chain reaction

polymyositis

polyneuropathy

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, familial

polyradiculoneuropathy

pons, infarction of

pons, lesion of

porphyria

position sensation, abnormal

positive sharp waves

posterior fossa

posterior fossa, lesion of

posterior inferior cerebellar artery syndrome

posterior interosseous neuropathy

posterior longitudinal ligament, ossification of

postoperative neurologic complications

postpartum

precentral gyrus

precipitating factors

pregnancy, neurologic complications in

premature infant

prenatal diagnosis by amniocentesis

primary aldosteronism

primary lateral sclerosis

primary thrombocythemia

prion disease

prisoners of war, neurologic complications in

prognosis

progranulin

progressive multifocal leucoencephalopathy

progressive neurologic disorder

progressive spinal muscular atrophy

progressive supranuclear palsy

pronator syndrome

proprioception, abnormal

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

psychomotor retardation

pupil, abnormality in neurologic disorders

pupil, tonic

pure motor hemiplegia

pure motor stroke

pure sensory stroke

pyramidal tract

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

quadriplegia, transient

quality of life

radial nerve

radial nerve, palsy of

radial pulse, unilateral decrease of

radiation therapy, CNS treatment and complications with

radiculopathy

ragged-red fibers

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

rash

Raynaud's phenomenon

reading disorder, acquired

real-time quaking-induced conversion

reflex sympathetic dystrophy

release phenomena

remote effect of cancer on the nervous system

repetitive nerve stimulation

respirations in CNS disease

respirator

respiratory failure

respiratory tract infection

retinopathy

retrocollis

retrovirus

reverse split hand sign

reversible neurologic disorder

review article

rheumatoid arthritis

rheumatoid arthritis, neurologic complications of

saccadic eye movements, abnormal

salivation, excessive

sarcoidosis

scalenus anticus syndrome

scleroderma, neurologic involvement with

sclerosis, bone

scotoma

scotomata, scintillating

screening

sedimentation rate

sedimentation rate, elevated

seizure, psychomotor-temporal lobe

seizure, repetitive

seizure, surgical treatment of

seizure, treatment of

sensorimotor stroke

sensorineural hearing loss

sensory loss

sensory loss, cortical

sensory loss, pseudoradicular

sensory loss, truncal

sensory symptoms

sensory testing, quantitative

sequencing difficulty

shunt procedure, ventricular

sicca syndrome

sinemet

single photon emission computed tomography

sinusitis

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skew deviation

skin, lesions in neurologic disorders

sleep

sleep pathology and physiology

slow virus infection of CNS

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, ischemic lesion of

spinal cord, lesion of

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinal stenosis

spinal stenosis, cervical canal

spinocerebellar ataxia type 3/Machado Joseph disease

spirochete infection

spitting

splenium of corpus callosum

splenomegaly

spondylosis

spongy degeneration of brain

spontaneous muscle activity

sports medicine, neurology of

steroid therapy, CNS treatment and complications with

stiff man syndrome

storage disease of CNS

striatonigral degeneration

striatonigral degeneration, infantile

striatum, lesion of

strokelike episodes

stuttering

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

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

subclavian artery stenosis

subdural effusion

subdural hematoma

subdural hematoma, interhemispheric

subtemporal decompression

suck reflex

suck, poor

sulfite oxidase deficiency

sulfone

superior sagittal sinus

superior sagittal sinus thrombosis

suprascapular nerve

suprascapular neuropathy

supraspinatus muscle

swallow evaluation

sweating, abnormality of

swimming

symmetric brain lesions

systemic illness

systemic lupus erythematosus

systemic lupus erythematosus, neurologic complications with

temporal lobe, atrophy

temporalis muscle wasting

tetany

thoracic outlet syndromes

thromboangiitis obliterans cerebri

tomaculous neuropathy

tongue, atrophy

tongue, fasciculations of

torticollis, post traumatic

toxoplasmosis, CNS

transient ischemic attack

transient neurologic deficit

transilumination of skull

transplacental virus infections

trauma

travel, foreign

treatment of neurologic disorder

tremor

tremor, intention

tremor, post traumatic

trichopoliodystrophy

trigeminal nerve, abnormality of

trigeminal neuralgia

trinucleotide repeats

ulnar nerve, compression of

ulnar nerve, deep palmar branch of

urine test for metabolic disorders

urine test in toxic screen

visual acuity, decreased

visual evoked response

visual impairment

visual loss

visual loss, transient

visual symptoms

visuospatial disturbance

Volkmann's ischemia

walking, difficulty with

weakness, generalized

weakness, progressive

weakness, proximal

weight loss

weightlifting

Werdnig-Hoffman disease

white matter disease, periventricular

white matter disease, subcortical

wide based gait

winging of scapula

word-finding difficulty

Showing articles 850 to 900 of 5834 << Previous Next >>

Intrafamilial Heterogeneity in Hereditary Motor Neuron Disease
Neurol 42:1488-1492, Applebaum,J.S.,et al, 1992

Duplication of Part of Chromosome 17 is Commonly Associated with HMSN Type I (Charcot-Marie-Tooth Disease Type 1)
Ann Neurol 31:570-572, Hallam,P.J.,et al, 1992

De-Novo Mutation in Hereditary Motor and Sensory Neuropathy Type I
Lancet 339:1081-1082, Hoogendijk,J.E.,et al, 1992

Amyotrophic Lateral Sclerosis and Lymphoma:Bone Marroe Examination and Other Diagnostic Tests
Neurol 42:1101-1102, Rowland,L.P.,et al, 1992

Characteristics of Intractable Seizures Following Meningitis and Encephalitis
Neurol 42:1513-1518, Marks,D.A.,et al, 1992

Morphometry, Histopathology, and Tomography of Cerebral Atrophy in the Acquired Immunodeficiency Syndrome
F. C. , Ann Neurol 32:31-40-1992., Gelman,B.B.&Guinto,Jr, 1992

Clinicopath Conf
Emery-Dreifus Muscular Dystrophy, NEJM 327:548-5571992., , 1992

Motor Neurone Disease
BMJ 304:459-460, Norris,F.H., 1992

Motor Neurone Disease:A Hospice Perspective
BMJ 304:471-473, O'Brien,T.,et al, 1992

Lethal Cytomegalovirus Infection in Preterm Infants:Clinical, Radiological, and Neuropathological Findings
Ann Neurol 31:64-68, Perlman,J.M.&Argyle,C., 1992

GM-1 Ganglioside for Spinal-Cord Injury
NEJM 326:493, Schonhofer,P.S., 1992

Crossed Cerebellar Diaschisis and Crossed Cerebellar Atrophy:MR Findings & Clin Symptoms in 26 Pts
AJR 158:1155-1159, Tien,R.D.&Ashdown,B.C., 1992

CNS Complications of Cocaine Abuse:Prevalence, Pathophysiology, and Neuroradiology
AJR 159:137-147, Brown,E.,et al, 1992

Dementia Associated with lacunar Infarction
Stroke 23:1225-1229, Loeb,C.,et al, 1992

Transsection of the Spinal Cord Associated with Breech Delivery
Am J Dis Child 146:351-352, DiMario,F.J.&Wood,B.P., 1992

Diagnosis of Sturge-Weber Syndrome:Comparison of the Efficacy of CT & MR Imaging in 14 Cases
AJR 158:867-871, Marti-Bonmati,L.,et al, 1992

Clinicopath Conf
Pick's Diseae, Case 6-1992, NEJM 326:397-405992., , 1992

Multifocal Demyelinating Motor Neuropathy:Cranial Nerve Involvement and Immunoglobulin Therapy
Neurol 42:506-509, Kaji,R.,et al, 1992

Multifocal Motor Neuropathy with Conduction Block:Is It a Distinct Clinical Entity?
Neurol 42:497-505, Lange,D.J.,et al, 1992

Surgical Treatment of Cervical Spondylotic Myelopathy:Time for a Controlled Trial
Neurol 42:5-13, Rowland,L.P., 1992

Quantitative Cerbral Anatomy of the Aging Human Brain:A Cross-Sectional Study Using Magnetic Resonance Imaging
Neurol 42:527-536, Coffey,C.E.,et al, 1992

Progressive Language Disorder Due to Lobar Atrophy
Ann Neurol 31:174-183, Snowden,J.S.,et al, 1992

Detection in Life of Confirmed Alzheimer's Disease, Medial Temporal Lobe Atrophy by Computed Tomography
Lancet 340:1179-1183, Jobst,K.A.,et al, 1992

Serum Antibodies to L-Type Calcium Channels in Patients with Amyotrophic Lateral Sclerosis
NEJM 327:1721-1728, 17521992., Smith,R.G.,et al, 1992

Clinicopath Conf
Motor Neuron Disease, Progressive-Muscular-Atrophy Type, Case 43-1992, NEJM 327:1298-130592., , 1992

Familial Adult-Onset Muscular Dystrophy with Leukoencephalopathy
Ann Neurol 32:577-580, vanEngelen,B.G.M.,et al, 1992

MRI and SPECT in Amyotrophic Lateral Sclerosis, Demonstr of Upper Motor Neurone Invol by Neuroimaging
Neuroradiology 34:389-393, Udaka,F.,et al, 1992

Facioscapulohumeral Dystrophy, In Skeletal Muscle Pathology
Churchhill Livingstone, NY, p285, 30392., Mastaglia,F.L.&Walton,J., 1992

CT of 338 Active Professional Boxers
Radiology 185:509-512, Jordan,B.D.,et al, 1992

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

Angelman Syndrome: Clinical Profile
J Child Neurol 7:270-280, Zori,R.T.,et al, 1992

Alzheimer's Disease in a Patient with Posterior Cortical Atrophy
JNNP 54:1110-1111, Berthier,M.L.,et al, 1991

Magnetic Resonance Imaging-based Volume Studies in Temporal Lobe Epilepsy:Pathological Correlations
Ann Neurol 30:31-36, Cascino,G.D.,et al, 1991

Welander's Distal Myopathy:Clinical Neurophysiol & Muscle Biopsy Obser in Young & Middle Aged Adults with Early Symptoms
JNNP 54:494-498, Borg,K., 1991

Serial MR Imaging in Creutzfeldt-Jakob Disease
Neuroradiology 33:364-367, Uchino,A.,et al, 1991

Sarcoidosis of the Nervous System, A Clinical Approach
Arch Int Med 151:1317-1321, Sharma,Om.P.&Sharma,A.D., 1991

Staphylococcal Pyomyositis in Patients Infected by the Human Immunodeficiency Virus
Am J Med 90:595-600, Schwartzman,W.A.,et al, 1991

Pyomyositis in Patients with the Human Immunodeficiency Virus:An Unusual Form of Disseminated Bacterial Infection
Am J Med 91:129-136, Widrow,C.A.,et al, 1991

Clinical and Electrodignostic Features of X-Linked Recessive Bulbospinal Neuronopathy
Neurol 41:823-828, Olney,R.K.,et al, 1991

Parental Sex Effect in Familial Amyotrophic Lateral Sclerosis
Neurol 41:1292-1294, Leone,M., 1991

Linkage of a Gene Causing Familial ALS to Chromosome 21 & Evidence of Genetic-Locus Heterogeneity
NEJM 324:1381-1384, 1430-14321991., Siddique,T.,et al, 1991

Computed Tomography of Intracranial Tuberculosis
Neuroradiology 33:126-135, Jinkins,J.R., 1991

Diagnostic Tests for Choreoacanthocytosis
Neurol 41:1000-1006, Feinberg,T.E.,et al, 1991

Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
Medicine 70:99-117, Gatti,R.A.,et al, 1991

Therapeutic Uses Of Botulinum Toxin
NEJM 324:1186-1194, Jankovic,J.&Brin,M.F., 1991

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

Zidovudine Myopathy:A Distinctive Disorder Associated with Mitochondrial Dysfunction
Ann Neurol 29:606-614, Mhiri,C.,et al, 1991

Posterior Cortical Dementia with Alexia:Neurobehavioural, MRI, and PET Findings
JNNP 54:443-448, Freedman,L.,et al, 1991

Membranous Lipodystrophy:MR Imaging Appearance of the Brain
Radiology 180:793-797, Araki,T.,et al, 1991

Frontal Lobe Degeneration:Clinical, Neuropsychologicaland SPECT Characteristics
Neurol 41:1374-1382, Miller,B.L.,et al, 1991

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