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abdominal distention

abdominal muscle paralysis

abdominal protrusion

acid maltase deficiency

acid maltase deficiency, adult

acoustic neurinoma

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome, heralded by neurologic invol

Addison's disease

adult polyglucosan body disease

advance directives

advances in neurology

adverse drug reaction

alcohol intolerance

alcoholic polyneuropathy

alien hand syndrome

alpha-fetoprotein

alternating hemiplegia

alternating hemiplegia of childhood

alternating rapid movement

alveolar hypoventilation

Alzheimer's disease

Alzheimer's disease, early onset

Alzheimer's disease, familial

amphiphysin antibodies

amyloid angiopathy, cerebral

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

anesthesia, general

aneurysm, cavernous sinus

aneurysm, internal carotid artery

angiitis, granulomatous of CNS

angiitis, isolated of CNS

angiography, cerebral, beaded vessels

angiography, cerebral, false negative

angiography, cerebral, negative

angiotensin-converting enzyme

animal exposure

ankle reflex, absent

ankylosing spondylitis

anoctaminopathy

anterior horn cell disease

anterior interosseous neuropathy

anterior tibial muscle weakness

anti Hu antibody

anti signal recognition particle antibody

antibiotics, neurologic complications with

antibodies to measles

antibodies to voltage-gated calcium channels

anticonvulsants

anticonvulsants, selection of

antiviral agents

aphasia, progressive

aphasia, progressive, primary

apraxia of eye movements

apraxia, constructional

arm swing, reduced

arrhythmia, cardiac

arthrogryposis multiplex

ataxia telangiectasia

ataxia, cerebellar

ataxia, hereditary

ataxia, progressive

ataxia, truncal

atlanto axial dislocation, congenital

atrioventricular block

autoimmune disease

autonomic dysfunction

autonomic neuropathy

axonal degeneration

azidodeoxythymidine

B 12 deficiency

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

basophilic stippling of red blood cells

behavioral disorder

Bence Jones protein

benign congenital hypotonia

biologic markers

bitemporal visual field defect

bladder dysfunction

blinking, reduced

blood dyscrasias, neurologic findings with

bone marrow biopsy

Borrelia burgdorferi infection

botulinum toxin

botulinum toxin, complications of

brachial neuritis

brachial neuritis, acute

brachial neuritis, bilateral

brachial plexus neuropathy

brachial plexus neuropathy, bilateral

brachial plexus neuropathy, familial

brachial plexus neuropathy, recurrent

brain biopsy, false negative

brain natriuretic peptide

brainstem, atrophy

brainstem, infarction of

brainstem, lesion of

bright tongue sign

Brown Sequard syndrome

brucellosis, nervous system involvement with

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

carbon monoxide poisoning

carcinoembryonic antigen

carcinoma of breast

carcinoma of lung

cardiovascular disease

carpal tunnel syndrome

carpo-pedal spasm

Castleman's disease

CAT scan, abdomen

CAT scan, abnormal

CAT scan, disappearing lesion on

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, spine

cauda equina, enhancement

caudate nucleus, atrophy

cavernous sinus, syndrome

central core disease

central nervous system, infection of

central pontine myelinolysis

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar edema

cerebellar lesion

cerebellar plaques, amyloid

cerebellum, disease of

cerebellum, neoplasms of

cerebral arteries

cerebral cortex

cerebral cortical atrophy

cerebral embolism

cerebral peduncle

cerebral vasculature

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, cell count

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, IgG index, elevated

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, protein of

cerebrovascular accident

cerebrovascular accident, mimics

cerebrovascular accident, multiple

cerebrovascular accident, three territory involvement

cerebrovascular accident, women

cerebrovascular accident, young adult

cerebrovascular disease

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

chelation therapy

cherry red spot-myoclonus syndrome

chest x-ray, abnormal

chewing, impaired

chorea, familial

chorea, Sydenham's

choreoathetosis

chromosomal abnormality

chronic polyneuritis, children

chronic progressive external ophthalmoplegia

Clarkson disease

claudication, extremity

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

cluster, geographic

cogwheel rigidty

cold temperature

collapsin response mediator protein 5 IgG

color vision, impaired

compression neuropathy

conduction block

congenital heart disease

congenital infection, CNS

congenital myopathy

congestive heart failure

contactin associated protein like 2 antibodies

contractures, joint

controversies in neurology

corpus callosum

corpus callosum, atrophy of

corpus callosum, lesion of

corpus callosum, thinning

cortical blindness

cortical muscular atrophy

cortical-basal ganglionic degeneration

cost effectiveness

coxsackievirus, myopathy with

cranial nerve enhancement

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

craniopharyngioma

creatine phosphokinase(CPK)elevated

Creutzfeldt-Jakob disease, genetic

crying, pathologic

Cushing's syndrome

cycad seed flour

cyclophosphamide

cyst, perineural

deafness, bilateral

deafness, sudden

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

dementia, familial

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

denervation of muscle

denervation potentials

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

dermatomyositis

descending paralysis

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetes insipidus

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diabetic mononeuropathy

diagnostic criteria

diaphragmatic paralysis

diaphragmatic paralysis, causes of

differential diagnosis

difficulty climbing stairs

diffuse idiopathic skeletal hyperostosis

diplegia, atonic

diplegia, brachial

disability rating scale, neurological

disability, neurological

distal muscle atrophy

distal muscle weakness

dopa responsive dystonia

dropped head syndrome

drug induced neurologic disorders

drug interactions

dysferlinopathy

dyssynergia cerebellaris myoclonica

dysthyroid ocularmyopathy

dystonia, children

dystrophic calcification

ears of the Lynx MR sign

electrical injury of nervous system

electrical sensation

electrocardiogram, abnormal

electrocorticogram

electroencephalogram, abnormalities of

electroencephalogram, periodic complexes

electromyogram, decremental response

electron microscopy

electrophoretic pattern, serum

Emery-Dreifuss muscular dystrophy

emotional lability

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, episodic

encephalitis, paraneoplastic

encephalitis, Powassan

encephalitis, Rasmussen's

encephalitis, recurrent

encephalitis, viral

encephalomyelitis

encephalopathy, acute

encephalopathy, anoxic

encephalopathy, neonatal

encephalopathy, post anoxic

encephalopathy, progressive

endocarditis, subacute bacterial

enterovirus infection of CNS

entrapment neuropathy

enzyme, muscle disease

epidemiology of neurology

epilepsia partialis continua

episodic neurologic deficits

erectile dysfunction

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

facial appearance, abnormal

facial nerve palsy

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

failed medical management

fatigable chewing

Fazio-Londe's disease

femoral neuropathy

fetal movements, reduced

fine motor function, impaired

finger flexor weakness

finger nose finger test

finger weakness

flaccid paralysis

flail arm syndrome

flu-like illness

foot drop, bilateral

football neurologic injuries

fourth ventricle, compression

fragile-X syndrome

Friedreich's ataxia

Friedreich's ataxia, late onset

frontal behavioral spatial syndrome

frontal lobe, atrophy

frontotemporal dementia, behavioral variant

fundus, abnormality of

funduscopic exam

F-wave response

gag reflex, depressed

gammaglobulin therapy, intravenous

gastrocnemius muscle weakness

gastrointestinal disease, neurologic complications

gastrointestinal motility

gastrostomy, percutaneous endoscopic

gaze palsy, horizontal

gaze palsy, supranuclear

gaze palsy, vertical

genetic counselling

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

girdle sensation

globus pallidus

globus pallidus, hemorrhage

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glutamic acid decarboxylase, antibody

glycogen storage disease

GM1 ganglioside antibodies

Gowers maneuver

granular osmiphilic material

granulomatous disease

Graves ophthalmopathy

growth retardation

Guillain Barre syndrome

Gulf War syndrome

gyrus, abnormal

Hallervorden Spatz disease

Hallervorden Spatz disease, late onset

hallucination, auditory

handlebar palsy

Hand-Schuller-Christian disease

headache, positional

headache, progressive

health insurance

hearing loss, bilateral

hearing loss, sudden, bilateral

heart block, complete

heavy metal intoxication

heel-knee-shin test

hemianopia, transient

hemiatrophy, cerebral

hemidiaphragm, paralysis of

hemiplegia, progressive

hemispherectomy

hepatosplenomegaly

heralding manifestation

hereditary myopathy with early respiratory failure

herpes simplex encephalitis

herpes simplex encephalitis, diagnosis of

high arched feet

high arched palate

highly active antiretroviral therapy

histochemistry of muscle

history of neurology

Hodgkin's disease

Hodgkin's disease, neurologic involvement with

human immunodeficiency virus type 1

Huntington's chorea

Huntington's disease, children

hydrocephalus, exvacuo

hydroxychloroquine

hyperadrenalism

hyperinsulinism

hyperparathyroidism

hyperthyroidism

hypoglycemic coma

hypoglycorrhachia

hypokalemic paralysis

hypokalemic periodic paralysis

hypoparathyroidism

hypopigmentation of skin

hypotension, systemic

hypothalamus, disturbance of

hypotonia, infants

hypoxic encephalopathy

iatrogenic neurologic disorders

ideomotor apraxia

imbalance, postural

immune complexes

immunodeficiency

immunoelectrophoresis, serum

immunologic disease

immunology and the nervous system

immunosuppression

immunosuppressive agents

inability to sit up

inability to stand on tiptoes

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intranuclear

inclusion bodies, ubiquitin

inclusion body myositis

industrial neurologic disorders

infant, evaluation of

infantile tremor syndrome

intellectual deficit

intellectual deterioration

intermittent positive pressure breathing

internal capsule

intestinal pseudoobstruction

intracranial hypertension, benign

intracranial pressure, increased

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

Kearns-Sayre syndrome

klippel feil syndrome

Kugelberg-Welander syndrome

kyphoscoliosis, neurologic causes of

lactic acidemia

Lafora's disease

laminectomy, cervical

laughing, pathologic

lead and the nervous system

Leber's hereditary optic neuropathy

leg weakness, bilateral

leg weakness, unilateral

Leigh's disease

Leigh's disease, adult variety

lenticular nucleus, lesion of, bilateral

leucine rich glioma inactivated 1 antibodies

leukemia, neurologic findings assoc.with

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

locked-in syndrome

long bone lesion

lumbar puncture

lumbosacral plexopathy

lymph node biopsy

lymphadenopathy

lymphadenopathy, hilar

lymphocytic meningoradiculitis

lymphoma involving CNS

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

malignancy screen

malignancy, occult

manganese intoxication

Man-In-The-Barrel syndrome

marche a petits pas

masseter muscle wasting

masseter muscle weakness

McArdle's disease

median neuropathy

medical-legal aspects of neurology

memory, defect of recent

memory, impairment of

meningeal enhancement

meningitis, aseptic

meningitis, basilar

meningitis, carcinomatous

meningitis, chronic

meningitis, fungal

meningitis, fungal-negative CSF culture

meningitis, neutrophilic

meningoencephalitis

mental retardation

mental status, abnormal

metabolic acidosis

microangiopathy, brain

microangiopathy, retina

midbrain, atrophy

mild cognitive impairment

Millard Gubler syndrome

Mini Mental Status Examination

minimally conscious state

mitochondrial disease

mitochondrial encephalomyopathy

mitochondrial recessive ataxic syndrome

molecular genetics

monoclonal antibodies

monoclonal gammopathy

monomelic amyotrophy

mononeuropathy chronic inflammatory demyelinating

mononeuropathy, motor

monoparesis, focal

Motor Band Sign

motor neuron disease

motor neuron disease, juvenile form

motor neuron disease, spontaneous recovery

movement disorder

movement disorder, extrapyramidal

movement disorder, hyperkinetic

MRI, angiography

MRI, CAT scan compared to

MRI, contrast enhanced

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, paramagnetic effect

MRI, peripheral nerve

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRI, susceptibility weighted

multinucleated giant cell

multiple myeloma

multiple sclerosis

multiple sclerosis, diagnosis of

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 diseases, characteristics of

muscle hypertrophy

muscle phosphorylase deficiency

muscle relaxant

muscle stiffness

muscle swelling

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

myelinolysis, extrapontine

myelogram, cervical

myeloma, osteosclerotic

myeloneuropathy

myelopathy, ischemic

myelopathy, chronic progressive

myocardial biopsy

myocardial infarction

myocardial injury

myoclonic jerks

myoclonus, cortical

myoclonus, epilepsy

myoclonus, stimulus sensitive

myopathy, acute

myopathy, autoimmune

myopathy, carcinomatous

myopathy, centronuclear

myopathy, critically ill

myopathy, distal

myopathy, distal, vacuolar

myopathy, drug-induced

myopathy, hereditary

myopathy, inclusion body

myopathy, inclusion body with Paget's disease

myopathy, inclusion body, hereditary

myopathy, mitochondrial

myopathy, necrotizing

myopathy, proximal

myopathy, quadriceps

myopathy, steroid induced

myopathy, thyroid disease causing

myopathy, toxic

myopathy, vacuolar

myotonia congenita

myotonia dystrophica

myotonic discharges

myxedema, neurologic manifestations of

N-acetyl-L-aspartic acid

narcotic analgesics

nausea and vomiting

nemaline rod myopathy

nemaline rod myopathy, adult onset

neoplasm, intracranial

neoplasm, pituitary

neoplasm, primary intracerebral

neoplasm, primary intracranial

neoplasm, primary of CNS

nerve conduction studies

nerve conduction studies, motor

nerve enlargement

nerve growth factor

nerve root enhancement

nerve root hypertrophy

neuritis, causes of

neurocutaneous disease

neuroendocrinology

neurofibrillary degeneration

neurogenic bladder

neurogenic vs.myopathic atrophy

neurologic complications

neurologic complications of, surgery

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic consultation

neurologic disease

neurologic disease, diagnoses of

neurologic disease, incurable

neurologic disease, multifocal

neurologic disease, tempo

neurologic evaluation

neurologic examination

neurologic signs

neurologic symptoms

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

neuroophthalmology

neuropathology, brain

neuropathy, ataxic

neuropathy, bicycle

neuropathy, diabetic

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, iatrogenic

neuropathy, medication induced

neuropathy, motor

neuropathy, motor, multifocal

neuropathy, multifocal

neuropathy, onion bulb

neuropathy, paraneoplastic

neuropathy, peripheral

neuropathy, peripheral, treatment

neuropathy, sensory

neuropathy, toxic

neuropathy, vasculitic, systemic

neuroprotective agents

neurotoxicity, acute

neurotransmitter

newborn, evaluation of

next-generation sequencing

night blindness

NMDA antagonists

nystagmus, monocular

nystagmus, primary position of gaze

nystagmus, rotary

occupational neurologic disorders

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, CNS

opsoclonus-myoclonus syndrome

optic atrophy, hereditary

optic disc edema

optic neuropathy

orbit, lesions of

orthostatic hypotension

osmotic demyelination syndrome

owl's eye sign of spinal cord

pacemaker, cardiac-transvenous

Paget's disease

pain, abdominal

pain, management of chronic

palatal myoclonus

palliative care

paralysis, acute

paralysis, acute areflexic

paralysis, asymmetric

paraneoplastic cerebellar degeneration

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, spastic

paraproteinemia

paraspinal muscle

paraspinal muscle weakness

parathyroid adenoma

paresthesias, hands

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

patient information and support

penguin silhouette sign

percussion induced muscle contraction

periodic paralysis

periodic paralysis, thyrotoxic

peripheral blood smear

peripheral nerve, lesion of

peroxisomal disease

persistent vegetative state

personality change

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-like illness

polyclonal gammopathy

polyglucosan body

polyglucosan body disease

polymerase chain reaction

polyneuropathy, chronic inflammatory demyelinating

pontocerebellar atrophy

positive sharp waves

post polio syndrome

posterior fossa

posterior fossa, differential diagnosis of lesions of

posterior fossa, lesion of

posterior inferior cerebellar artery syndrome

posterior interosseous neuropathy

posterior longitudinal ligament, ossification of

postural abnormality

practice guidelines

precipitating factors

pregnancy, neurologic complications in

prevention of neurologic disorders

primary aldosteronism

primary lateral sclerosis

progressive multifocal leucoencephalopathy

progressive muscular dystrophy

progressive myoclonic epilepsy

progressive neurologic disorder

progressive pallidum atrophy

progressive spinal muscular atrophy

progressive supranuclear palsy

prolactin, elevated

proprioception, abnormal

proximal muscle atrophy

pseudobulbar palsy

pseudohypertrophy

psychiatric disorder

psychiatric problems in neurologic disorders

psychomotor retardation

ptosis, bilateral

ptosis, familial

pulmonary embolism

pulmonary function tests

pulmonary infiltrates

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

quadriceps atrophy

quadriceps weakness

quality of life

radiation hypersensitivity

radiation therapy, salivary gland

ragged-red fibers

Ramsay Hunt syndrome

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

Raynaud's phenomenon

real-time quaking-induced conversion

reflex sympathetic dystrophy

reflex sympathetic dystrophy, children

Refsum's disease

release phenomena

remote effect of cancer on the nervous system

renal transplantation

renal tubular acidosis

repetitive nerve stimulation

respiratory depression

respiratory failure

respiratory tract infection

retina, abnormal

retinal artery occlusion

retinal branch artery occlusion

retinal infarction

retinitis pigmentosa

reverse split hand sign

reversible neurologic disorder

rigid spine syndrome

rigidity, axial

rippling muscle disease

risk-benefit assessment

rubella encephalitis

rubella encephalitis, progressive

rubella syndrome

saccadic eye movements, abnormal

salivation, excessive

sarcoidosis, CNS

sciatic neuropathy

scleroderma, neurologic involvement with

sclerosis, bone

scoliosis, neurologic association with

sea-blue histiocytes

second wind phenomena

seizure, children

seizure, intractable

seizure, paradoxical

seizure, repetitive

seizure, surgical treatment of

seizure, treatment of

self-mutilation

semialdehyde dehydrogenase deficiency

sensorineural hearing loss

sensory ganglia

sensory ganglia, abnormal

sensory loss, patchy

sensory symptoms

sensory testing

sequencing difficulty

serologic testing

serologic testing of cerebrospinal fluid

serum alanine aminotransferase

shoulder, subluxation

shoulder-girdle wasting

single photon emission computed tomography

single-fiber electromyography

sinuses, diseases of

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skin, lesions in neurologic disorders

skin, temperature difference

skull x-ray, abnormal

sleep pathology and physiology

slit lamp examination

slow virus infection of CNS

Smell Identification Test

somatosensory evoked potentials

somatosensory evoked potentials, dermatomal

spastic paraplegia, type 11

spastic paraplegia, type 7

speech disorder

speech disorder, childhood

spinal cord degeneration

spinal cord, biopsy

spinal cord, cervical

spinal cord, compression of

spinal cord, enlargement

spinal cord, injury of

spinal cord, injury, management of

spinal cord, lesion of

spinal cord, neoplasm

spinal cord, neoplasm, extramedullary

spinal cord, neoplasm, intramedullary

spinal cord, pathologic exam of

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinal muscular atrophy, classification

spinal muscular atrophy, intermediate form

spinal stenosis

spinal stenosis, cervical canal

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar ataxia type 7

spinocerebellar degeneration

spirochete infection

splinter hemorrhages

spongy degeneration of brain

spontaneous remission

sports medicine, neurology of

standing difficulty

status epilepticus

stem cell tourism

stem cell transplantation

stereotaxic surgery

sternocleidomastoid muscle

steroid therapy, CNS treatment and complications with

stiff man syndrome

striatum, lesion of

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 hematoma

substantia nigra

superior cerebellar peduncle

superoxide dismutase

suprasellar lesion

survival motor neuron gene

Susac's syndrome

symmetric brain lesions

sympathetic block

synucleinopathy

systemic illness

tandem gait, ataxic

teeth, abnormal

teeth, number of in infants

temporal lobe, atrophy

temporalis muscle wasting

temporalis muscle weakness

temporomandibular joint, dislocation

tensilon test, false positive

testicular atrophy

thalamus, lesion of

thalamus, lesion of-bilateral

thoracic outlet syndromes

Three territory sign

thrombophlebitis

thyrotropin-releasing hormone

tick-borne encephalitis

Tolosa Hunt syndrome

tongue, atrophy

tongue, enlarged

tongue, fasciculations of

tongue, weakness

toxic encephalopathy

transient ischemic attack

transient neurologic deficit

transverse smile

treatment of neurologic disorder

tremor, postural

triangle of Guillain and Mollaret

tricresylphosphate

trinucleotide repeats

Trousseau's sign

tuberous sclerosis

type 2 muscle fiber

tyrosine hydroxylase deficiency

ulcers, fingertip

ulnar nerve, deep palmar branch of

ulnar neuropathy

unconsciousness

Unverricht-Lundborg disease

upgaze, paralysis of

urinary incontinence

urinary urgency

urine test for metabolic disorders

vascular endothelial growth factor

venous thrombosis, non-cerebral

ventricular enlargement

vestibular function, tests of

vibratory sensation, abnormal

viral infection

viral infection, CNS

viral isolation

vision, blurred

visual acuity, decreased

visual evoked response

visual fields, constricted

visual symptoms

visuospatial disturbance

vitamin E deficiency

Waldenstrom's macroglobulinemia

walking, difficulty with

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

West Nile fever

whistle, inability to

white matter disease

white matter disease, subcortical

wide based gait

winging of scapula

X-linked bulbospinal neuronopathy

X-linked myopathy

x-linked myopathy with excessive autophagy

Showing articles 950 to 1000 of 5218 << Previous Next >>

Accuracy of the Clinical Diagnosis of Corticobasal Degeneration:A clinicopathologic Study
Neurol 48:119-125, Litvan,I.,et al, 1997

Adult Botulism
Muscle & Nerve, 20:100-10297., Shapiro,B.E.,et al, 1997

CIDP:Clinical Features & Responses to Trtm in 67 Consecutive Pts with/without a Monoclonal Gammopathy
Neurol 48:321-328, Gorson,K.G.,et al, 1997

Bilirubin Metabolism and Kernicterus
Adv Pediatr 44:173-229, Gourley,G.R., 1997

Symmetrical Necrosis of Globus Pallidus with Severe Gait Disturbance in a Patient with Myelodysplastic Syndrome Given Allogeneic Marrow Transplantation
Ann Hematol 75:235-237, Rabitsch,W.,et al, 1997

Charcot-Marie-Tooth Disease and Related Inherited Neuropathies
Medicine 75:233-250, Murakami,T.,et al, 1996

Erroneous Diagnosis Corrected After 28 Years
Arch Neurol 53:1194-1196, Gordon,P.H.,et al, 1996

Unusual Clinical Presentations of Cortical-Basal Ganglionic Degeneration
Ann Neurol 40:893-900, Bergeron,C.,et al, 1996

Total Alopecia, Diabetes Mellitus, and Falls
Lancet 348:1420, Mueller-Schoop,J.W., 1996

Congenital Muscular Dystrophy with Primary Laminin a2 (Merosin) Deficiency Presenting as Inflammatory Myopathy
Ann Neurol 40:782-791, Pegoraro,E.,et al, 1996

Investigation of Muscle Disease
JNNP 60:256-274, Mastaglia,F.L.&Laing,N.G., 1996

Inclusion Body Myositis:Clinical and Pathological Boundaries
Ann Neurol 40:581-586, Amato,A.A.,et al, 1996

Human T-Cell Lymphotrophic Virus Type II-Associated Myelopathy:Clinical and Immunologic Profiles
Ann Neurol 40:714-723, Lenky,T.J.,et al, 1996

Inclusion Body Myositis
JNNP 60:251-255, Garlepp,M.J.&Mastaglia,F.L., 1996

Creutzfeldt-Jakob Disease in a Young Woman
Lancet 347:945-948, Tabrizi,S.J.,et al, 1996

Wolfram Syndrome:Hereditary Diabetes Mellitus with Brainstem and Optic Atrophy
Ann Neurol 39:352-360, Scolding,N.J.,et al, 1996

AAEM Case Report#13:Diabetic Amyotrophy
Muscle & Nerve 19:939-945996., Chokroverty,S.&Sander,H.W., 1996

Ethylene Oxide Neurotoxicity:A Cluster of 12 Nurses with Peripheral and Central Nervous System Toxicity
Neurol 46:992-998, Brashear,A.,et al, 1996

Progressive Encephalomyelitis with Rigidity Responsive to Plasmapheresis and Immunosuppression
Ann Neurol 40:451-453, Fogan,L., 1996

Treatment of Advanced Parkinson's Disease by Posterior GPi Pallidotomy:1-Year Results of a Pilot Study
Ann Neurol 40:355-366, 3411996., Baron,M.S.,et al, 1996

Hereditary Spastic Paraplegia:Advances in Genetic Research
Neurol 46:1507-1514, Fink,J.K.,et al, 1996

Clinicopath Conf
Tangier Disease, Case 16-1996, NEJM 334:1389-1394996., , 1996

Yelling Attacks and Wasted Hands
Lancet 348:238, Bosboom,W.M.J.,et al, 1996

Acute Focal Neuropathy in Male Weight Lifters
Muscle & Nerve 19:897-899996., Bird,S.J.&Brown,M.J., 1996

Congenital Muscular Dystrophy Syndromes Distinguished by Alkaline and Acid Phosphatase, Merosin, & Dystrophin Staining
Neurol 46:810-814, Connolly,A.M.,et al, 1996

Wilson Disease:Findings at MR Imaging and CT of the Brain with Clinical Correlation
Radiology 198:531-536, van Wassenaer-van Hall,H.N.,et al, 1996

Bent Spine Syndrome
JNNP 60:51-54, Serratrice,G.,et al, 1996

Brief Report:Deficiency of a Dystrophin-Assoc Glycoprotein (Adhalin) in Pt with Muscular Dystrophy & Cardiomyopathy
NEJM 334:362-366, Fadic,R.,et al, 1996

Campylobacter Jejuni Infection and Anti-GM1 Antibodies in Guillain-Barre Syndrome
Ann Neurol 40:181-187, Jacobs,B.C.,et al, 1996

Antiamphiphysin Antibodies with Small-Cell Lung Carcinoma and Paraneoplastic Encephalomyel; itis
Ann Neurol 39:659-667, Dropcho,E.J., 1996

Neuroimaging Findings in Patients with AIDS
Clin Inf Dis 22:906-919, Walot,I.,et al, 1996

Manganese Toxicity in Children Receiving Long-Term Parental Nutrition
Lancet 347:1218-1221, Fell,J.M.E.,et al, 1996

Evolution of High-Intensity Basal Ganglia Lesions on T1-Weighted MR in Neurofibramotisis Type 1
AJNR 17:755-760, Terada,H.A.,et al, 1996

Cognitive Dysfunction as the Major Presenting Feature of Becker's Muscular Dystrophy
Neurol 46:461-465, North,K.N.,et al, 1996

Clinical Heterogeneity of Adhalin Deficiency
Ann Neurol 39:196-202, Morandi,L.,et al, 1996

Diagnosis of Merosin (Laminin-2) Deficient Congenital Muscular Dystrophy by Skin Biopsy
Lancet 347:582-584, Sewry,C.A.,et al, 1996

Autonomic Ganglionitis with Severe Hypertension, Migraine, and Episodic but Fatal Hypotension
Neurol 47:817-821, Lee,H.C.,et al, 1996

Clinical, Neuroimaging, and Pathologic Features of Progressive Nonfluent Aphasia
Ann Neurol 39:166-173, Turner,R.S.,et al, 1996

A Case of Creutzfeldt-Jakob Disease (CJD) Started with Monoparesis of the Left Arm
Rinshi Shinkeigaku 36:1245-1248, Obi, T.,et al, 1996

Neurodegeneration and Diabetes:UK Nationwide Study of Wolfram (DIDMOAD) Syndrome
Lancet 1458-1463, Barrett,T.G.,et al, 1995

Neurological Sequelae of Cyanide Intoxication-The Patterns of Clinical MRI & Pet Findings
Ann Neurol 38:825-828, Rosenow,F.,et al, 1995

Myasthenic Symptoms in Patients with Mitochondrial Myopathies
Muscle & Nerve 18:1338-1340995., Forestier,N.L.,et al, 1995

Canavan Disease:From Spongy Degeneration to Molecular Analysis
J Pediatr 127:511-517, Matalon,R.,et al, 1995

Stereotactic Ventral Pallidotomy for Parkinson's Disease
Neurol 45:753-761, Dogali,M.,et al, 1995

Clinicopath Conf
Multiple Myeloma with Bilateral Carpal Tunnel Syndrome Probably Due to Secondary Amyloid Deposit, Ca, e38-1995,NEJM 333:1625-1630,1995., 1995

Bilateral Ulnar Handcuff Neuropathies with Segmental Conduction Block
Muscle & Nerve 18:1021-1023995., Satkunam,L.&Zochodne,D., 1995

X-Linked Pure Familial Spastic Paraparesis
Arch Neurol 52:665-669, Cambi,F.,et al, 1995

Persistence of MRI Hyperintensity of the Globus Pallidus in Cirrhotic Patients:A 2-year Follow-up Study
Neurol 45:995-997, Kulisevsky,J.,et al, 1995

Amyloidosis Causing A Progressive Myopathy
Muscle & Nerve 18:1016-1018995., Nadkarni,N.,et al, 1995

Encephalopathy with Parkinsonian Features in Children Following Bone Marrow Transplantations and High-Dose Amphotericin B
Ann Neurol 37:810-814, Mott,S.H.,et al, 1995

Showing articles 950 to 1000 of 5218 << Previous Next >>