Neudle.com: biopsy muscle

Differential
(Click to cross reference)

abdominal distention

abdominal muscle paralysis

abdominal protrusion

abducens nerve paralysis

abortion, spontaneous

abscess, brainstem

abscess, intracerebral

abscess, lung

acetylcholine receptor antibody

acid maltase deficiency

acid maltase deficiency, adult

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

acquired immunodeficiency syndrome, infants and children

acquired immunodeficiency syndrome-related complex

acrocyanosis

acute disseminated encephalomyelitis

acyl CoA dehydrogenase deficiency

Addison's disease

adrenomyeloneuropathy

adult polyglucosan body disease

advances in neurology

adverse drug reaction

alcohol, heart involvement with

alcohol, neurologic complications with

alternating hemiplegia

alternating rapid movement, impaired

alveolar hypoventilation

amaurosis fugax

amaurosis fugax, alternating

aminoacidopathies

aminoacidurias

amphiphysin antibodies

amyloid

amyloid angiopathy, cerebral

amyloidosis

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, atypical

amyotrophic lateral sclerosis, diagnosis of

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, misdiagnosis

amyotrophic lateral sclerosis, sensory symptoms in

amyotrophic lateral sclerosis, work up

amyotrophic lateral sclerosis-like syndrome

ANA

ANA-negative systemic lupus erythematosus

aneurysm, abdominal aortic

aneurysm, aortic arch

aneurysm, intracranial

angiitis

angiitis, granulomatous of CNS

angiitis, isolated of CNS

angina pectoris

angiography, cerebral, beaded vessels

angiography, cerebral

angiography, cerebral, false negative

angiography, cerebral, negative

angiography, neurologic complications with

angiotensin-converting enzyme

anterior horn cell disease

anterior tibial muscle weakness

antibiotics, neurologic complications with

antibodies to measles

anticoagulant, complications of

anticonvulsants

antifibrinolytic drugs

antimetabolite

anti-myeloperoxidase

antiphospholipid antibodies

antistriational muscle antibody

aortic arch ulcerated plaques

aqueduct of Sylvius, stenosis

arterial dissection, aorta

arthrogryposis multiplex

arylsulfatase A

ascending paralysis

ascites

aspartate aminotransferase

atherosclerosis, generalized

atrioventricular block

atrophy, muscle

atypical

audiogram

auditory evoked brainstem potentials

autoantibodies

autoimmune disease

autonomic dysfunction

basal ganglia, calcification of

basal ganglia, infarction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basement membrane

basement membrane thickening

bat bite

BCG treatment

behavior, combative

behavioral disorder, acute

blood dyscrasias, neurologic findings with

blue toe syndrome

bone biopsy

bone density

bone density, increased

bone marrow biopsy

bone marrow transplantation

bone pain

bone scanning

bovine spongiform encephalopathy

brain biopsy, false negative

brain biopsy, indication

brain biopsy, negative

brain biopsy, stereotaxic

brain natriuretic peptide

brain purpura

brain scan, abnormal

brainstem, infarction of

brainstem, lesion of

Brown Sequard syndrome

bruit

bulbar palsy

bulbar palsy, acute

bulbar palsy, progressive

BUN, elevated

burning feet

burning feet, differential diagnosis of

calcification, intracranial

cancer associated myopathy

carbamazepine

carbon monoxide poisoning

cardiac surgery, neurologic complications with

cardiomegaly

cardiomyopathy

cardiotoxicity

cardiovascular disease

caribbean

carnitine deficiency

carnitine deficiency myopathy

carpal tunnel syndrome

CAT scan, angiography

CAT scan, chest

CAT scan, contrast enhanced

CAT scan, emission, abnormal

CAT scan, false negative

cataracts, congenital

cauda equina

cauda equina, enhancement

cauda equina, lesion of

cavernous sinus

cavernous sinus, expansion

cavernous sinus, lesion of

CD4 counts

cecum perforation

celiac disease, adult

celiac disease, childhood

central core disease

central nervous system, infection of

central pontine myelinolysis

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar lesion

cerebellar peduncle

cerebellum, disease of

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortex

cerebral cortical atrophy

cerebral embolism

cerebral infarction

cerebral venous thrombosis

cerebroretinal microangiopathy with calcifications and cysts

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, cytology

cerebrospinal fluid, cytology, false negative

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, pressure increased

cerebrospinal fluid, protein of

cerebrospinal fluid, red cells in

cerebrospinal fluid, xanthochromia of

cerebrovascular accident

cerebrovascular accident, bilateral

cerebrovascular accident, infancy and childhood

cerebrovascular accident, mimics

cerebrovascular accident, misdiagnosis

cerebrovascular accident, multiple

cerebrovascular accident, nonvascular territory

cerebrovascular accident, recurrent

cerebrovascular accident, women

cerebrovascular accident, young adult

cerebrovascular disease

cerebrovascular disease, cardiovascular disease with

cerebrovascular disease, surgical treatment of

chemotherapy, CNS treatment and complications with

cherry red spot

cherry red spot-myoclonus syndrome

chest pain

chest x-ray, abnormal

chondroitin sulfate C

chorea

choreoathetosis

choroid plexus

chromosomal abnormality

chromosome 19

chronic fatigue syndrome

chronic graft versus host disease

chronic idiopathic anhidrosis

chronic progressive external ophthalmoplegia

Churg-Strauss syndrome

Chvostek sign

cirrhosis

cirrhosis, infancy

Clinical Pathologic Conference(C.P.C.)

clubbing of fingers

coenzyme Q10

coenzyme Q10 deficiency

collagen vascular disease

congenital heart disease

congenital infection, CNS

congenital myopathy

congenital myopathy, inflammatory

congenital paresis

congestive heart failure

controversies in neurology

conversion reaction

cornea, abnormal

cornea, opacity of

corneal reflex, abnormal

corneal reflex, absent

corona radiata

coronary artery bypass

coronavirus

corpus callosum

corpus callosum, hypoplastic

corpus callosum, infarction of

corpus callosum, lesion of

cortical blindness

cortical blindness, transient

cranial nerve enhancement

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

C-reactive protein, elevated

creatine phosphokinase MB isoenzyme elevation

creatine phosphokinase(CPK)elevated

cryptococcal meningitis

cultured skin fibroblasts

cyclic vomiting

cyclophosphamide

cylindrical spiral

cysticercosis, cerebral

cysticercosis, disseminated

cysticercosis, intraventricular

cysticercosis, miliary

cystinosis

cytochrome c oxidase

cytochrome c oxidase, deficiency

cytomegalic inclusion disease

cytomegalovirus infection

degenerative diseases of CNS

dementia, cerebrovascular disease causing

dementia, childhood

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

dementia, transmissible

demyelinating disease

denervation of muscle

denervation potentials

depression

dermatitis

dermatitis herpetiformis

dermatomyositis

desmin

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes insipidus

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diabetic amyotrophy

diabetic muscle infarction

diagnosis

diagnostic criteria

dialysis

diaphragmatic paralysis

diarrhea

differential diagnosis

difficulty climbing stairs

dilantin

diplopia

disability rating scale, neurological

disability, neurological

disorientation

dissociated sensory loss

distal muscle atrophy

distal muscle weakness

dizziness

DNA probes

DNA sequencing

downward gaze, paralysis of

dropped head syndrome

drug abuse

drug abuse, inhalation

drug abuse, neurologic complications of

drug induced neurologic disorders

drug interactions

dura, thickened

dural sinus thrombosis

duvalumab

dysarthria

dysdiadochokinesia

dysequilibrium syndrome

DYSF gene

dysferlin

dysferlinopathy

dyskinesia, buccal lingual facial

dysthyroid ocularmyopathy

dystonia

dystonia, focal

dystroglycanopathies

dystrophic calcification

dystrophin

dystrophin associated proteins

ear, abnormal

ecchymoses

echocardiogram

echocardiogram, transesophageal

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, periodic complexes

electromyogram

electromyogram, decremental response

electron microscopy

electronystagmography

electrophoretic pattern, serum

ELISA

embolism

embolism, atheromatous

embolism, cholesterol

embolism, platelet

embolism, retinal

emergencies, neurologic

Emery-Dreifuss muscular dystrophy

encephalitis

encephalitis, autoimmune

encephalitis, focal

encephalitis, human immunodeficiency virus type 1

encephalitis, viral

encephalomyelitis, paraneoplastic

encephalomyopathy

encephalopathy

encephalopathy, metabolic

encephalopathy, progressive

endarterectomy, carotid

endocarditis, neurologic manifestations with

entrapment neuropathy

enzyme treatment

enzyme, defect

enzyme, muscle disease

enzyme, serum

eosinophilia

eosinophilia-myalgia syndrome

eosinophilic fasciitis

eosinophilic granulomatosis with polyangiitis

epidemiology of neurology

epilepsia partialis continua

episcleritis

episodic disorders

episodic neurologic deficits

epistaxis

epsilon-aminocaproic acid(E.A.C.A.)

exercise-induced neurologic dysfunction

exophthalmus

extraocular muscle enlargement

extraocular muscle lesion

extraocular muscle, metastasis to

eye closure

eye movement, disorders of

eye, pain in

face, elongated

face, numbness of

facial appearance, abnormal

facial movement disorder

facial pain

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

femoral artery catheterization

femoral neuropathy

fetal movements, reduced

fluorescein angiography

foam cells

folic acid deficiency

frontal lobe, pathologic signs of

fundus, abnormality of

funduscopic exam

fungal infection, CNS

F-wave response

gadolinium

gag reflex, depressed

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

ganglionitis

gangrene

gastric dilatation, acute

gastrocnemius muscle weakness

gastrointestinal bleeding

gastrointestinal disease, neurologic complications

gastrointestinal motility

gastrointestinal perforation

gastroparesis

gaze palsy

gaze palsy, horizontal

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

globus pallidus, lesion of

gluten-free diet

glycogen storage disease

GM1 ganglioside antibodies

granular atrophy, cerebral cortex

granuloma, eosinophilic

granulomatosis with polyangiitis

granulomatosis, allergic

granulomatous disease

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, infantile and childhood form

Guillain Barre syndrome, variant forms of

hallucination, visual

headache, chronic daily

headache, elderly

headache, new onset

headache, positional

headache, progressive

headache, recurrent

headache, sudden onset of

headache, vascular

hearing loss

hearing loss, bilateral

hearing loss, sudden, bilateral

hearing loss, unilateral

heart block

heart block, complete

heart murmur

heliotrope rash

hematuria, gross

hematuria, microscopic

hemianopia, homonymous

hemiballismus

hemiparesis

hemiparesis, transient

hemiplegia

hemiplegia, progressive

hemophilia

hemorrhagic diathesis

hepatolenticular degeneration(Wilson's disease)

hepatomegaly

hepatosplenomegaly

heralding manifestation

highly active antiretroviral therapy

histochemistry of muscle

HMGcoA reductase inhibitors

hoarseness

Hodgkin's disease

H-reflex testing

human diploid cell rabies vaccine

human immunodeficiency virus type 1

human immunodeficiency virus type 1, pathogenesis

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

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

hypereosinophilic syndrome(HES)

hyperesthesia

hypergammaglobulinemia

hyperpigmentation of skin

hyperreflexia

hypertension

hypertensive encephalopathy

hyperthermia

hypertonia

hypertrichosis

hypertrophic intracranial pachymeningitis

hypertrophic spinal pachymeningitis

hypoparathyroidism, idiopathic

hypophonia

hypopigmentation of skin

hypoproteinemia

hypoprothrombinemia

hyporeflexia

hypothalamus, disturbance of

hypothalamus, lesion of

iatrogenic neurologic disorders

idiopathic CD4+lymphopenia

idiopathic inflammatory myopathy

idiopathic polyneuropathy

immune checkpoint inhibitors

immune reconstitution inflammatory syndrome

immune-related adverse events

immunocompetent

immunoelectrophoresis, serum

immunofluorescence

immunofluorescent"band"test

immunosuppressive agents

immunotherapy

impotence

impulsivity

inability to stand on tiptoes

inborn errors of metabolism

incidence

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

inclusion body myositis

India

infant, evaluation of

intellectual deterioration

interferonopathy

interstitial pulmonary fibrosis

intestinal biopsy

intestinal pseudoobstruction

intraaortic balloon pump

intracerebral hemorrhage

intracranial pressure, increased

intranasal medication

intrauterine

intrauterine infection

intrauterine infection, viral of CNS

intrinsic hand muscles, wasting of

ischemic exercise test

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Jakob-Creutzfeldt disease, variant

Kearns-Sayre syndrome

Kugelberg-Welander syndrome

kuru plaques

kyphosis

lacrimal gland enlargement

lactate

lactic acidemia

lactic dehydrogenase(LDH)

Lafora body

Lafora's disease

laminar necrosis, cortical

lateral rectus palsy

lead and the nervous system

leg weakness, bilateral

leg weakness, unilateral

Legionella pneumophilia

Legionnaires'disease

Leigh's disease

leishmaniasis

lenticular nucleus, lesion of, bilateral

leukemia, neurologic findings assoc.with

leukocytosis

leukodystrophy

leukoencephalopathy

leukoencephalopathy, differential diagnosis

leukopenia

level of consciousness, decreased

Lewy body disease, diffuse

lid abnormalities

lid closure, weakness of

lid lag

lid twitch

life expectancy

life support, withdrawal of

limb hypertrophy

limb-girdle weakness

limbic encephalitis

lipid storage myopathy

lipomatosis

lipomatosis, multiple symmetrical

liver function enzymes

liver transplantation

lumbosacral plexopathy

lumbosacral radiculopathy

lymphadenopathy, hilar

lymphadenopathy, paraaortic

lymphocytic meningoradiculitis

lymphoma

lymphoma involving CNS

lymphoma, primary of CNS

lysosomal storage disease

lysosomes, abnoral

macrocephaly

malabsorption

malabsorption syndrome

malaise

malignant hyperpyrexia

malignant papulosis

masked facies

masseter muscle wasting

mastoiditis

McArdle's disease

McArdle's disease, adult onset

memory, defect of recent

memory, impairment of

meningeal biopsy

meningeal biopsy, false negative

meningeal enhancement

meningitis, leptospira

meningitis, leukemic

meningitis, lupus

meningitis, lymphomatous

meningitis, melanomatous

meningitis, recurrent

meningoencephalitis

mental retardation

mental status, abnormal

mental status, abnormal, acute

merosin

mestinon

metabolic acidosis

metabolic disorder, primary

metachromatic leukodystrophy

metachromatic leukodystrophy, juvenile

methotrexate

mexiletine

microaneurysm, retinal

microangiopathy, brain

microangiopathy, retina

microcephaly

microinfarcts

middle cerebellar peduncle, lesion

migraine

mimics

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

mitral valve lesion

MNGIE syndrome

molecular genetics

monoclonal antibodies

monoclonal gammopathy

monocytosis

monomelic amyotrophy

mononeuritis multiplex

mononeuritis multiplex, causes of

mononeuropathy

mononeuropathy chronic inflammatory demyelinating

mononeuropathy multiplex

movement disorder, drug induced

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, angiography

MRI, angiography, false negative

MRI, contrast enhanced

MRI, cortical enhancement

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, extraocular muscle enhancement

MRI, false negative

MRI, fetal

MRI, gray matter enhancement

MRI, high signal foci on

MRI, high signal intensity of basal ganglia

MRI, lumbosacral plexus

MRI, muscle

MRI, negative

MRI, orbit

MRI, peripheral nerve

MRI, serial

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRI, spine

MRS

multicore myopathy

multifocal acquired demyelinating sensory motor neuropathy

multinucleated giant cell

multiple myeloma

multiple organ failure

multiple sclerosis

multiple sclerosis, misdiagnosis

muscle atrophy, focal

muscle atrophy, progressive

muscle atrophy, static

muscle biopsy

muscle biopsy, extraocular

muscle biopsy, needle

muscle cramp

muscle culture

muscle diseases, characteristics of

muscle hypertrophy

muscle hypertrophy, congenital

muscle pain

muscle phosphorylase deficiency

muscle spasm

muscle stiffness

muscle strength, testing

muscle swelling

muscle tenderness

muscle wasting, diffuse

muscle weakness

muscle weakness, insidious onset of

muscle weakness, proximal

muscle weakness, sudden onset of

muscle-eye-brain disease

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, dystrophin normal

muscular dystrophy, facioscapulohumeral

muscular dystrophy, female occurrence of

muscular dystrophy, limb-girdle

muscular dystrophy, neurogenic hypothesis of

myasthenia gravis

myasthenia gravis, diagnosis

myasthenia gravis, differential diagnosis

myasthenia gravis, distal weakness

myasthenia gravis, drug induced

myasthenia gravis, familial incidence of

myasthenia gravis, limb-girdle

myasthenia gravis, misdiagnosis of

myasthenia gravis, non motor symptoms

myasthenia gravis, ocular

myasthenia gravis, presenting manifestations

myasthenia gravis, prognosis of

myasthenia gravis, remission of

myasthenia gravis, seronegative

myasthenia gravis, thymectomy in

myasthenia gravis, treatment of

myasthenic syndrome

mycobacterial infection

myelopathy, chronic progressive

myelopathy, radiation induced

myelopathy, vacuolar

myeloradiculopathy

myocardial biopsy

myocardial infarction

myopathy, carcinomatous

myopathy, centronuclear

myopathy, critically ill

myopathy, desmin

myopathy, distal

myopathy, distal Laing

myopathy, distal, vacuolar

myopathy, distal, Welander's

myopathy, drug-induced

myopathy, focal

myopathy, genetic

myopathy, hereditary

myopathy, hypokalemic

myopathy, inclusion body

myopathy, inclusion body with Paget's disease

myopathy, inclusion body, hereditary

myopathy, inflammatory

myopathy, inflammatory, classification

myopathy, metabolic

myopathy, mitochondrial

myopathy, monomelic

myopathy, myofibrillar

myopathy, necrotizing

myopathy, necrotizing, autoimmune

myopathy, necrotizing, immune-mediated

myopathy, neurogenic hypothesis of

myopathy, painful

myopathy, proximal

myopathy, quadriceps

myopathy, radiation-induced

myopathy, steroid induced

myopathy, steroid responsive

myopathy, thyroid disease causing

myositis, acute of childhood

myositis, bacterial

myositis, focal

myositis, granulomatous

myositis, ocular

myositis, post infectious

nasal septum, perforation of

necrotizing granuloma

necrotizing vasculitis

negative

nemaline rod myopathy

nemaline rod myopathy, adult onset

neoplasm, metastatic to CNS

neoplasm, metastatic to muscle

neoplasm, metastatic to orbit

neoplasm, primary of CNS

neoplastic angioendotheliosis

nephritis

nephrotic syndrome

nerve biopsy

nerve biopsy, indication

nerve conduction studies

nerve conduction studies, motor

nerve conduction studies, sensory

nerve culture

nerve enlargement

nerve root biopsy

nerve root enhancement

nerve root hypertrophy

neuroaxonal dystrophy

neuroaxonal dystrophy, infantile

neurocutaneous disease

neuroendocrinology

neurogenic bladder

neurogenic vs.myopathic atrophy

neuroleptic malignant syndrome

neurolipidosis IV

neurologic complications of, chronic pulmonary disease

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic disease, tempo

neurologic evaluation

neurologic examination, focal

neurologic history

neurologic signs

neurological intensive care

neurolymphomatosis

neuromuscular blockade

neuromuscular disease, electrodiagnosis of

neuromuscular junction

neuromuscular junction, abnormality of

neuromyotonia

neuronal ceroid-lipofuscinosis

neuronopathy

neuronopathy, sensory

neuronopathy, sensory and motor

neuroophthalmology

neuropathology

neuropathology, brain

neuropathology, peripheral nerves

neuropathy

neuropathy, acute

neuropathy, amyloid

neuropathy, asymmetric

neuropathy, asymptomatic

neuropathy, chronic

neuropathy, classification of

neuropathy, cryoglobulinemic

neuropathy, diabetic

neuropathy, hypertrophic

neuropathy, iatrogenic

neuropathy, idiopathic

neuropathy, ischemic

neuropathy, medication induced

neuropathy, motor

neuropathy, motor, multifocal

neuropathy, onion bulb

neuropathy, painful

neuropathy, peripheral

neuropathy, peripheral, treatment

neuropathy, recurrent

neuropathy, sensory

neuropathy, short-fiber

neuropathy, small-fiber

neuropathy, small-fiber, painful sensory

neuropathy, toxic

neuropathy, vasculitic, nonsystemic

neuropathy, vasculitic, systemic

neuropathy, work up for

neurosyphilis

neurotoxic

neurotoxin

newborn, evaluation of

next-generation sequencing

nonsteroidal anti-inflammatory drug

normal

nortriptyline

nucleotidase-5 activity

numbness, extremity

numbness, generalized

nystagmus

nystagmus, vertical

occipital lobe, infarction

occipital lobe, infarction, bilateral

occipital lobe, lesion of

occupational neurologic disorders

ocular motility, disorders of

ocular myopathy

oculomasticatory myorhythmia

oculopharyngeal muscular dystrophy

oculovestibular reflex

old age, neurology of

ophthalmoplegia

ophthalmoplegia, neonatal

ophthalmoplegia, plus syndrome

ophthalmoplegia, progressive external

ophthalmoplegia, total

opsoclonus

optic atrophy

optic atrophy, infants

optic neuropathy

optic neuropathy, ischemic

optic neuropathy, ischemic, anterior

orange peel appearance of skin

orbit

orbit, biopsy

orbit, inflammation in

orbit, lesions of

orbit, mass

orbital apex

organ transplantation

otitis, neurologic complications with

overuse syndrome

pacemaker, cardiac-transvenous

pachymeningitis, cranial

pain, management of chronic

paralysis, asymmetric

parasitic infection, CNS

paraspinal muscle

paraspinal muscle weakness

Parkinson disease, surgical treatment of

Parkinson disease, treatment of

Parkinsonism syndrome

parotid gland swelling

parvovirus

PAS positive

PAS positive material in the brain

percussion induced muscle contraction

periarteritis nodosa

pericardial friction rub

peripheral nerve, lesion of

peripheral vascular disease

persistent vegetative state

personality change

petechiae

phenylketonuria

phosphorylase b kinase deficiency

pituitary stalk, lesion of

pituitary, hormones of

pituitary, lesion of

plasma cell dyscrasia

plasmacytoma

plasmapheresis

PLEDs

PLEDs, bilateral independent

PLEDs, etiology of

pleocytosis of cerebrospinal fluid

poison, neurologic problems with

POLG1 gene

poliomyelitis

poliomyelitis-like illness

polyglucosan body

polyglucosan body disease

polymerase chain reaction

polymicrogyria

polymyalgia rheumatica

polymyositis

polymyositis, eosinophilic

polymyositis, infantile

polyneuritis

polyneuropathy

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, chronic inflammatory demyelinating, childhood

polyneuropathy, critically ill

polyneuropathy, subacute idiopathic demyelinating

polyneuropathy, uremic

polyradiculoneuropathy

Pompe's disease of glycogen storage

positive sharp waves

post polio syndrome

posterior column disease

posterior interosseous neuropathy

posterior leukoencephalopathy syndrome

precipitating factors

pregnancy, neurologic complications in

prenatal

prenatal diagnosis by amniocentesis

pressure sores

prion disease

prognosis

progressive multifocal leucoencephalopathy

progressive myoclonic epilepsy

progressive neurologic disorder

progressive spinal muscular atrophy

proprioception, abnormal

proptosis

proptosis, unilateral

prostigmine

protein 14-3-3, cerebrospinal fluid

proteinuria

prothrombin time, prolonged

protozoan infection

proximal muscle atrophy

proximal myotonic myopathy

pruritus

pseudohypertrophy

pseudointernuclear ophthalmoplegia

pseudomyasthenia

pseudomyotonia

psychiatric disorder

psychiatric problems in neurologic disorders

psychomotor retardation

pulmonary hypertension

pulmonary infiltrates

quadriparesis, progressive

quadriplegia

quadriplegia, transient

quality of life

quinine

rabies, nervous system involvement with

radial nerve, palsy of

radiation therapy, CNS treatment and complications with

radiculitis

radiculopathy

radionuclide imaging, heart

ragged-red fibers

Rankin score

rapidly progressing neurologic illness

rash

rash, hand

Raynaud's phenomenon

reading disorder, acquired

recombinant DNA

recurrent

recurrent laryngeal nerve paralysis

refractory sprue

regional enteritis

rehabilitation for neurologic disorders

release phenomena

remote effect of cancer on the nervous system

renal transplantation

repetitive nerve stimulation

research

respirator

respiratory distress syndrome, neurologic status with

respiratory failure

respiratory paralysis, pharmacologic

respiratory tract infection

restless leg syndrome

reticulum cell sarcoma

retina, abnormal

retinal artery occlusion

retinal branch artery occlusion

retinal microvascular disease

retinopathy

retropulsion

reversible neurologic disorder

rheumatoid arthritis factor(R.A.factor)

rippling muscle disease

risk factors

risus sardonicus

rituximab

Rocky Mountain spotted fever

rubella encephalitis, progressive

rubella syndrome

rubella virus

rubeola virus

Sabin-Feldman dye test

saccadic eye movements

saccadic eye movements, abnormal

safety

salivary gland enlargement

salivation, excessive

Schwartz-Jampel syndrome

sciatic neuropathy

sclerodactyly

scleroderma

scleroderma, neurologic involvement with

second wind phenomena

sedimentation rate

sedimentation rate, elevated

sensorineural hearing loss

sensory ganglia

sensory ganglia, abnormal

sensory loss

sensory loss, asymmetric

sensory loss, patchy

sensory polyneuropathy

sensory polyneuropathy, cryptogenic

sensory symptoms

sensory testing

sensory testing, quantitative

septicemia

serologic testing

serologic testing of cerebrospinal fluid

seronegative

serum alanine aminotransferase

serum glutamic oxaloacetic transaminase

serum lipase, elevated

severe acute respiratory syndrome

sex reassignment surgery

single-fiber electromyography

Sjogren's syndrome, neurologic manifestations of

skin, biopsy

skin, darkening of

skin, lesions in neurologic disorders

skin, thickened

skull x-ray, abnormal

sleep

sleep apnea, obstructive

sleep pathology and physiology

slit lamp examination

slow virus infection of CNS

slurred speech

small vessel disease

small vessel vasculitis

snout reflex

somatosensory evoked potentials

speech disorder, childhood

speech, unintelligible

spinal cord

spinal cord, biopsy

spinal cord, compression of

spinal cord, enlargement

spinal cord, infarction of

spinal cord, lesion of

spinal muscular atrophy

spinal pachymeningitis

spinal stenosis

spinal stenosis, cervical canal

spinocerebellar degeneration

spirochete infection

splenic infarcts

splenium of corpus callosum

splenomegaly

splinter hemorrhages

spongy degeneration of brain

statin therapy, discontinuation

status asthmaticus

status epilepticus

steatorrhea

stem cell transplantation

steroid therapy, CNS treatment and complications with

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

subacute sclerosing panencephalitis, adult onset

subarachnoid hemorrhage

superior sagittal sinus thrombosis

sural nerve

Susac's syndrome

sweating

sweating, abnormality of

Sweet's syndrome

symmetric brain lesions

syphilis, neurologic complications with

systemic illness

systemic lupus erythematosus

systemic lupus erythematosus, neurologic complications with

tachycardia

tandem gait, ataxic

telangiectases

telangiectases, periungual

temporal artery, biopsy

temporal artery, tender

temporal lobe, lesion

temporalis muscle wasting

temporalis muscle weakness

temporomandibular joint, dislocation

tender points

tenderness

tensilon

tensilon test, false negative

tensilon test, false positive

tensilon test, paradoxical

thalamus, lesion of-bilateral

third nerve palsy

thrombocytopenia

thrombocytosis

thrombotic thrombocytopenia purpura

tongue, fasciculations of

tongue, weakness

torticollis

toxic encephalopathy

toxins, nervous system

toxoplasma complement fixation test

toxoplasma gondii

toxoplasmosis, acquired

toxoplasmosis, CNS

toxoplasmosis, muscle

transgender

transient ischemic attack

transient neurologic deficit

transluminal angioplasty, coronary artery

transplacental virus infections

transverse smile

travel, foreign

treatment of neurologic disorder

trigeminal nerve, abnormality of

trigeminal neuralgia

trigeminal neuropathy

trigeminal neuropathy, sensory

trinucleotide repeats

uremic encephalopathy

Venereal Disease Research Laboratory test

ventricular enlargement

vertigo

vibratory sensation, abnormal

vincristine neurotoxicity

vision, failure of in childhood

visual acuity, decreased

visual evoked response

visual field defect

visual fields, constricted

visual impairment

visual loss

visual loss, alternating

visual loss, sudden-unilateral

visual loss, transient

visual symptoms

visuospatial disturbance

vital capacity

vitreous opacities

vocal cord paralysis

Waldenstrom's macroglobulinemia

walking frame

walking, difficulty with

weakness, fluctuating

weakness, generalized

weakness, progressive

weakness, proximal

weakness, rapidly progressive

weakness, severe

weaning from respirator, failure to

weight loss

Wernicke's encephalopathy

West Nile fever

Western immunoblot test

wheelchair

Whipple's disease

whistle, inability to

white matter disease

white matter disease, subcortical

whites

wide based gait

winging of scapula

word-finding difficulty

workup

wrist drop

xerostomia

x-linked mental retardation

X-linked myopathy

x-linked myopathy with excessive autophagy

Showing articles 250 to 300 of 3683 << Previous Next >>

Pravastatin-Associated Inflammatory Myopathy
NEJM 327:649-650, Schalke,B.B.,et al, 1992

The Dropped Head Syndrome
Neurol 42:1625-1627, Suarez,G.A.&Kelly,J.J., 1992

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

Subacute Idiopathic Demyelinating Polyradiculoneuropathy
Arch Neurol 49:612-616, Hughes,R.,et al, 1992

Drug Induced Creutzfeldt-Jakob Like Syndrome
J Psychiatr Neurosci 17:103-105, Finelli,P.F., 1992

Polymyalgia Rheumatica and Mitochondrial Myopathy:Clinicopathologic and Biochemical Studies in Five Cases
Am J Med 92:167-172, Harle,J.,et al, 1992

ELISA Quantitation of Dystrophin for the Diagnosis of Duchenne and Becker Muscular Dystrophies
Neurol 42:570-576, Byers,T.J.,et al, 1992

Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes (MELAS) :Clin Features & DNA Mutation
Neurol 42:545-550, Goto,Y.,et al, 1992

Cholesterol Emboli Neuropathy
Neurol 42:428-430, Bendixen,B.H.,et al, 1992

Clinicopath Conf
Churg-Strauss Syndrome, Case 18-1992, NEJM 326:1204-1212992., , 1992

Transeophageal Echocardiographic Detection of Aortic Arch Disease in Patients with Cerebral Infarction
Stroke 23:1005-1009, Amarenco,P.,et al, 1992

Fibromyalgia:The Copenhagen Declaration
Lancet 340:663-664, Csillag,C., 1992

Myopathy in Severe Asthma
Am Rev Respir Dis 146:517-519, Douglass,J.A.,et al, 1992

McArdle's Disease with Late-Onset Symptoms:Case Report & Review of the Literature
JNNP 55:407-408, Felice,K.J.,et al, 1992

Clinicopath Conf
Case 40-1991, Inclusion-Body Myositis, NEJM 325:1026-1035991., , 1991

Polymyositis, Dermatomyositis, and Inclusion-Body Myositis
NEJM 325:1487-1498, Dalakas,M.C., 1991

Myopathy and Prolonged Neuromuscular Blockade after Lung Transplant
Crit Care Med 19:1580-1582, 14571991., Subramony,S.H.,et al, 1991

Prolonged Paralysis after Treatment with Neuromuscular Junction Blocking Agents
Crit Care Med 19:1125-1131, Gooch,J.L.,et al, 1991

Legionella Myositis
Neurol 41:750-752, Warner,C.L.,et al, 1991

Autosomal Recessive Distal Dystrophy
Neurol 41:1365-1370, Barohn,R.J.,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

Mononuclear Cell Analysis of Muscle Biopsies in Prednisone-Treated & Untreated Duchenne Muscular Dystrophy
Neurol 41:667-672, Kissel,J.T.,et al, 1991

Mitochondrial Dysfunction in Multiple Symmetrical Lipomatosis
Ann Neurol 29:566-569, Berkovic,S.F.,et al, 1991

Continuous Muscle Fiber Activity, Peripheral Neuropathy, and Thymoma
Ann Neurol 29:215-218, Garcia-Merino,A.,et al, 1991

Eosinophilia-Myalgia Syndrome, A Clinical Case Series of 21 Patients
Arch Int Med 151:533-537, Philen,R.M.,et al, 1991

Congenital Monomelic Hypertrophy with Progressive Myopathy
Arch Neurol 48:107-110, Shukla,A.,et al, 1991

Eosinophilia-Myalgia Syndrome Associated with Ingestion of L-Tryptophan:Muscle Biopsy Findings in 4 Patients
Neurol 41:319-321, Hollander,D.&Adelman,L.S., 1991

Polymyositis Mediated by T Lymphocytes that Express the y/8 Receptor
NEJM 324:877-881, Hohlfeld,R.,et al, 1991

Clinicopath Conf
Cerebral Amyloid Angiopathy, Case 27-1991, NEJM 325:42-54991., , 1991

Prognosis in AZT Myopathy
Neurol 41:1181-1184, Chalmers,A.C.,et al, 1991

Myopathy in Human Immunodeficiency Virus-Infected Children Receiving Long-Term Zidovudine Therapy
J Pediatr 119:152-155, Walter,E.B.,et al, 1991

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

Infantile CNS Spongy Degeneration-14 Cases:Clinical Update
Neurol 40:1876-1882, Gascon,G.G.,et al, 1990

Eosinophilia-Myalgia Syndrome (L-Tryptophan-Associated Neuromyopathy)
Neurol 40:1793-1796, Turi,G.K.,et al, 1990

Myopathy with Human Immunodeficiency Virus Type I (HIV-1) Infection:HIV-1 or Zidovudine?
Ann Int Med 113:492-493, Till,M.&MacDonell,K., 1990

Human Immunodeficiency Virus Assoc Myopathy:Immunocytochemical Ident of an HIV Antigen (gp41) in Muscle Macrophages
Ann Neurol 28:579-582, Chad,D.A.,et al, 1990

Neurologic Crises in Hereditary Tyrosinemia
NEJM 322:432-437, Mitchell,G.,et al, 1990

Clinicopath Conf
Primary CNS Lymphoma with AIDS, Am J Med 88:169-1761990., , 1990

Clinicopath Conf
Acute Febrile Neutrophilic Dermatosis (Sweet's Syndrome) , Case 30-1990, NEJM 323:254-2630., , 1990

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

Molecular Genetics of Duchenne and Becker Muscular Dystrophy
J Pediatr 117:1-15, Darras,B.T., 1990

Congenital Inflammatory Myopathy
Neurol 40:1111-1114, Shevell,M.,et al, 1990

The Clinical Spectrum of the Eosinophilia-Myalgia Syndrome Associated with L-Tryptophan Ingestion
Ann Int Med 113:124-134, Martin,R.W.,et al, 1990

L-Tryptophan-Associated Eosinophilic Perimyositis, Neuritis, and Fasciitis
Medicine 69:187-199, Kaufman,L.D.,et al, 1990

Clinicopath Conf
Eosinophilic Fasciitis, Case Study 4-1990, NEJM 322:252-261, 93190., , 1990

Development of Diffuse Fasciitis with Eosinophilia During L-Tryptophan Treatment:Elevated Type I Collagen Gene
Ann Int Med 112:344-351, Varga,J.,et al, 1990

Skeletal Muscle Pathology in AIDS:An Autopsy Study
Muscle & Nerve, 13:508-51590., Wrzolek,M.A.,et al, 1990

Adult Phosphorylase b Kinase Deficiency
Ann Neurol 28:529-538, Clemens,P.R.,et al, 1990

Human Leptospirosis-A Review of 50 Cases
Infection 17:10-14, Lecour,H.,et al, 1989

HTLV-1 Associated Myelopathy and Polymyositis in a US Native
Neurol 39:1572-1575, Evans,B.K.,et al, 1989

Showing articles 250 to 300 of 3683 << Previous Next >>