Neudle.com: muscle atrophy progressive

Differential
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abdominal distention

abdominal muscle paralysis

abdominal protrusion

abiotrophy

acanthocytosis

acetylcholine receptor antibody

acid maltase deficiency

acid maltase deficiency, adult

acne fulminans

acoustic neurinoma

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome, heralded by neurologic invol

ACTH, ectopic syndrome of

acute intermittant porphyria

Addison's disease

adult polyglucosan body disease

advance directives

advances in neurology

adverse drug reaction

agitation

alcohol intolerance

alcoholic polyneuropathy

alternating hemiplegia

alternating hemiplegia of childhood

alternating rapid movement

alveolar hypoventilation

Alzheimer's disease

Alzheimer's disease, early onset

Alzheimer's disease, familial

aminoacidopathies

aminoacidurias

amphiphysin antibodies

amyloid angiopathy, cerebral

amyloidosis

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

aneurysm, cavernous sinus

aneurysm, internal carotid artery

angiitis

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 edema

ankle reflex, absent

ankle reflex, preserved

ankylosing spondylitis

anoctaminopathy

anoxia

anterior horn cell disease

anterior interosseous neuropathy

anterior spinal artery infarction

anterior tibial muscle weakness

anti citrullinated antibody

anti Hu antibody

anti IgLON5

anti signal recognition particle antibody

antibiotics

antibiotics, neurologic complications with

antibodies to measles

antibodies to voltage-gated calcium channels

anticonvulsants

anticonvulsants, selection of

aphasia, progressive, primary

apraxia of eye movements

apraxia, constructional

arterial dissection, aorta

arterial dissection, vertebral

arteritides

arthralgia

arthrogryposis multiplex

asthma, poliomyelitis-like syndrome with

asymptomatic

ataxia

ataxia telangiectasia

atlanto axial dislocation, congenital

ATP1A3 gene

atrioventricular block

autonomic dysfunction

Barkhof MR criteria for MS

basal cistern

basal ganglia

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

benzodiazepine

biologic markers

BiPAP

bitemporal visual field defect

blood dyscrasias, neurologic findings with

Borrelia burgdorferi infection

botulinum toxin

botulinum toxin, complications of

botulism

brachial amyotrophic diplegia

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

brucellosis, nervous system involvement with

Brugada syndrome

bruit, supraclavicular

bulbar palsy

bulbar palsy, acute

bulbar palsy, childhood

bulbar palsy, progressive

calcification, intracranial

calcium channel dysfunction

carbon monoxide poisoning

carcinoembryonic antigen

cardiovascular disease

caregiver

carpal tunnel syndrome

CAT scan, disappearing lesion on

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, spine

cataracts

cauda equina

cauda equina, enhancement

caudate nucleus, atrophy

cavernous sinus, syndrome

CD4 counts

celiac disease, adult

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

cerebellar vermis

cerebellitis

cerebellum

cerebellum, disease of

cerebellum, neoplasms of

cerebral arteries

cerebral cortex

cerebral cortical atrophy

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

cerebrospinal fluid, proteincytologic dissociation

cerebrovascular accident

cerebrovascular accident, mimics

cerebrovascular accident, multiple

cerebrovascular accident, three territory involvement

cerebrovascular accident, women

cerebrovascular accident, young adult

cerebrovascular disease

cerebrovascular disease, cardiovascular disease with

cervical collar

cervical myelopathy

cervical osteoarthritis

cervical osteophyte

cervical rib

cervical spine

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

children

chills

Chinese paralytic syndrome

chromosomal abnormality

chronic polyneuritis, children

chronic progressive external ophthalmoplegia

Chvostek sign

ciguatera poisoning

Clarkson disease

claudication, extremity

climate change

Clinical Pathologic Conference(C.P.C.)

collapsin response mediator protein 5 IgG

color vision, impaired

compression neuropathy

concussion

conduction block

confusion

congenital heart disease

congenital infection, CNS

congenital myopathy

congestive heart failure

consanguinity

constipation

contactin associated protein like 2 antibodies

contractures, joint

controversies in neurology

conversion reaction

corpus callosum

corpus callosum, atrophy of

corpus callosum, lesion of

corpus callosum, thinning

cortical blindness

cortical hand knob

cortical muscular atrophy

cortical-basal ganglionic degeneration

coxsackievirus, myopathy with

CPAP

cranial nerve enhancement

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

craniopharyngioma

creatine phosphokinase(CPK)elevated

Creutzfeldt-Jakob disease, genetic

degenerative diseases of CNS

Dejerine-Sottas syndrome

delay in diagnosis

delusion

dementia

dementia, age at onset

dementia, cerebrovascular disease causing

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

depression

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

diarrhea

diet

differential diagnosis

difficulty climbing stairs

diffuse idiopathic skeletal hyperostosis

disability rating scale, neurological

disability, neurological

disorientation

distal muscle atrophy

distal muscle weakness

disulfiram

dizziness

DNA probes

dopa responsive dystonia

dopamine

downward gaze

drooling

dropped head syndrome

drowning

drug induced neurologic disorders

dyssynergia cerebellaris myoclonica

dysthyroid ocularmyopathy

dystonia

dystonia, children

dystrophic calcification

dystrophin

ears of the Lynx MR sign

edema, leg

edema, pedal

efficacy

electrical injury of nervous system

electrical sensation

electrocardiogram, abnormal

electrocorticogram

electroencephalogram, abnormalities of

electroencephalogram, periodic complexes

electromyogram

electromyogram, decremental response

electron microscopy

electrophoretic pattern, serum

Emery-Dreifuss muscular dystrophy

emotional lability

encephalitis

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, central European

encephalitis, episodic

encephalitis, paraneoplastic

encephalitis, Powassan

encephalitis, Rasmussen's

encephalitis, recurrent

encephalitis, viral

encephalocele

encephalomyelitis

encephalomyeloneuritis

encephalopathy

encephalopathy, acute

encephalopathy, anoxic

encephalopathy, neonatal

encephalopathy, post anoxic

encephalopathy, progressive

endemic area

endocarditis, subacute bacterial

enterovirus

enterovirus infection of CNS

entrapment neuropathy

enzyme, defect

enzyme, muscle disease

epidemiology of neurology

epilepsia partialis continua

episodic disorders

episodic neurologic deficits

episodic unconsciousness

erectile dysfunction

ethics in neurology

euthanasia

evidence-based research

exercise-induced vascular symptoms

exome sequencing

exophthalmus

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 pain

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

failed medical management

falling

familial

fasciculation

fasciculation, benign

fatigable chewing

fatigue

Fazio-Londe's disease

femoral neuropathy

fetal movements, reduced

fetus

fever

fibrillations

fine motor function, impaired

finger drop

finger flexor weakness

finger nose finger test

football neurologic injuries

fourth ventricle, compression

fragile-X syndrome

free radical

Friedreich's ataxia

Friedreich's ataxia, late onset

frontal behavioral spatial syndrome

frontal lobe, atrophy

frontal lobe, behavior with disease of

frontal lobe, lesion of

frontotemporal dementia, behavioral variant

fundus, abnormality of

funduscopic exam

F-wave response

gadolinium

gag reflex, depressed

gammaglobulin therapy, intravenous

ganglionitis

gangliosides

gangliosidosis GM2

gastrectomy, neurologic complications following

gastrocnemius muscle weakness

gastrointestinal disease, neurologic complications

gastrointestinal motility

gastroparesis

gastrostomy

gastrostomy, percutaneous endoscopic

gaze palsy

gaze palsy, horizontal

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

globus pallidus, hemorrhage

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glutamic acid

glutamic acid decarboxylase, antibody

gluten ataxia

gluten sensitivity

gluten-free diet

glycogen storage disease

GM1 ganglioside

GM1 ganglioside antibodies

Gowers maneuver

granular atrophy, cerebral cortex

granular osmiphilic material

granulomatous disease

Graves ophthalmopathy

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, variant forms of

Hallervorden Spatz disease

Hallervorden Spatz disease, late onset

hallucination

hallucination, auditory

hammertoes

hand weakness

handlebar palsy

Hand-Schuller-Christian disease

headache, progressive

health insurance

hearing loss

hearing loss, bilateral

hearing loss, sudden, bilateral

heart block

heart block, complete

heart murmur

heavy metal intoxication

hemianopia, transient

hemiatrophy, cerebral

hemidiaphragm, paralysis of

hemifacial atrophy

hemiparesis

hemiplegia

hemiplegia, progressive

hemispherectomy

hemophilia

hepatosplenomegaly

heralding manifestation

hereditary myopathy with early respiratory failure

herniated disc

herpes simplex encephalitis

herpes simplex encephalitis, diagnosis of

highly active antiretroviral therapy

hip pain

histochemistry

histochemistry of muscle

Hodgkin's disease, neurologic involvement with

Horner's syndrome

Horner's syndrome, etiologies of

hospice

human immunodeficiency virus type 1

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

hunger

huntingtin

Huntington's chorea

Huntington's disease, children

hydrocephalus

hydrocephalus, exvacuo

hyperpigmentation of skin

hypogammaglobulinemia

hypokalemic alkalosis

hypokalemic paralysis

hypokalemic periodic paralysis

hypopigmentation of skin

hypopnea

hyporeflexia

hypotelorism

hypotension, systemic

hypothalamus

hypothalamus, disturbance of

hypoxic encephalopathy

iatrogenic neurologic disorders

immunoelectrophoresis, serum

immunohistochemistry

immunologic disease

immunology and the nervous system

immunosuppression

immunosuppressive agents

immunotherapy

impotence

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

incontinentia pigmenti

incoordination

India

industrial neurologic disorders

infant, evaluation of

infantile neuronal degeneration

infantile tremor syndrome

infection

inflexibility, mental

insect sting

insomnia

intellectual deficit

intellectual deterioration

intermittent positive pressure breathing

internal capsule

internet

intestinal pseudoobstruction

intracranial hypertension, benign

intracranial pressure, increased

intrinsic hand muscles, wasting of

ischemic exercise test

islet cell tumor

Jackson's syndrome

Jakob-Creutzfeldt disease

juvenile distal and segmental muscular atrophy

Kearns-Sayre syndrome

Kernig's sign

ketogenic diet

klippel feil syndrome

Klumpke palsy

Kugelberg-Welander syndrome

kyphoscoliosis, neurologic causes of

laboratory values, normal

lactic acidemia

Lafora's disease

laminectomy, cervical

lead and the nervous system

lead poisoning

Leber's hereditary optic neuropathy

leg atrophy

leg numbness

leg weakness, bilateral

leg weakness, unilateral

Leigh's disease

Leigh's disease, adult variety

lenticular nucleus, lesion of, bilateral

lethargy

leucine rich glioma inactivated 1 antibodies

leukemia

leukemia, neurologic findings assoc.with

leukodystrophy

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

lumbosacral plexopathy

Lyme disease

lymph node biopsy

lymphadenopathy

lymphadenopathy, hilar

lymphocytic meningoradiculitis

lymphoma

lymphoma involving CNS

lysosomal storage disease

Madonna facies

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

malignancy screen

malignancy, occult

manganese intoxication

Man-In-The-Barrel syndrome

marche a petits pas

masked facies

masseter muscle wasting

masseter muscle weakness

McArdle's disease

median neuropathy

medical-legal aspects of neurology

MELAS syndrome

memory, defect of recent

memory, impairment of

meningeal enhancement

meningitis, carcinomatous

meningitis, chronic

meningitis, fungal

meningitis, fungal-negative CSF culture

meningitis, neutrophilic

meningitis, TB

meningoencephalitis

mental retardation

mental status, abnormal

merosin

MERRF syndrome

metabolic acidosis

metabolic disorder, primary

microangiopathy, brain

microangiopathy, retina

mild cognitive impairment

Millard Gubler syndrome

Mills syndrome

mimics

Mini Mental Status Examination

minimally conscious state

miosis

misdiagnosis

misdirection

mitochondrial disease

mitochondrial encephalomyopathy

mitochondrial recessive ataxic syndrome

monoclonal antibodies

monoclonal gammopathy

monomelic amyotrophy

mononeuritis multiplex

mononeuropathy

mononeuropathy chronic inflammatory demyelinating

mononeuropathy, motor

motor neuron disease, juvenile form

motor neuron disease, misdiagnosis

motor neuron disease, spontaneous recovery

motor system

movement disorder

movement disorder, extrapyramidal

movement disorder, hyperkinetic

MRI

MRI, abnormal

MRI, angiography

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, eye of tiger sign

MRI, FLAIR

MRI, functional

MRI, gradient-echo

MRI, high signal foci on

MRI, lumbosacral plexus

MRI, muscle

MRI, paramagnetic effect

MRI, peripheral nerve

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRI, spine

MRI, susceptibility weighted

MRS

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 biopsy

muscle cramp

muscle diseases, characteristics of

muscle hypertrophy

muscle pain

muscle phosphorylase deficiency

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

muscular dystrophy, neurogenic hypothesis of

mutism

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

myelitis

myelitis, longitudinal

myelitis, transverse

myelogram

myelogram, cervical

myeloma, osteosclerotic

myelopathy, carcinomatous

myelopathy, chronic progressive

myelopathy, necrotizing

myelopathy, radiation induced

myeloradiculitis

myeloradiculopathy

myocardial biopsy

myocardial infarction

myoclonus, stimulus sensitive

myoclonus-ataxia syndrome

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, inflammatory

myopathy, mitochondrial

myopathy, necrotizing

myopathy, neurogenic hypothesis of

myopathy, proximal

myopathy, quadriceps

myopathy, steroid induced

myopathy, thyroid disease causing

myxedema, neurologic manifestations of

N-acetyl-L-aspartic acid

nemaline rod myopathy

nemaline rod myopathy, adult onset

neoplasm, hormone producing

neoplasm, hormone producing, ectopic

neoplasm, intracranial

neoplasm, pituitary

neoplasm, primary intracerebral

neoplasm, primary intracranial

neoplasm, primary of CNS

nerve biopsy

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

neurofibromatosis 1

neurofibromatosis 2

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

neurologic testing

neuromuscular blockade

neuromuscular disease, electrodiagnosis of

neuromuscular junction

neuromuscular junction, abnormality of

neuromyotonia

neuronal cell surface antigen

neuronal ceroid-lipofuscinosis

neuronal degeneration

neuronal intranuclear inclusion disease

neuronal migration disorder

neuronopathy

neuronopathy, sensory

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy, diphtheritic

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, iatrogenic

neuropathy, medication induced

neuropathy, motor

neuropathy, motor, multifocal

neuropathy, multifocal

neuropathy, onion bulb

neuropathy, painful

neuropathy, paraneoplastic

neuropathy, peripheral

neuropathy, peripheral, treatment

neuropathy, sensory

neuropathy, short-fiber

neuropathy, toxic

neuropathy, vasculitic, systemic

neuroprotective agents

newborn, evaluation of

next-generation sequencing

nystagmus, primary position of gaze

nystagmus, rotary

occupational neurologic disorders

occupational neuropathies

ocular motility, disorders of

ocular myopathy

oculopharyngeal muscular dystrophy

old age, neurology of

olivary degeneration, hypertrophic

onconeural antibodies

Onufrowicz nucleus

ophthalmoplegia

ophthalmoplegia, painful

ophthalmoplegia, progressive external

ophthalmoplegia, total

opiate

Oppenheim muscular dystrophy

opportunistic infection, CNS

opsoclonus-myoclonus syndrome

optic atrophy

optic atrophy, hereditary

orthostatic hypotension

osmotic demyelination syndrome

osteomalacia

osteoporosis

otitis, neurologic complications with

overlap syndrome

owl's eye sign of spinal cord

oxygen therapy

pacemaker, cardiac-transvenous

pain, increased response

pain, leg

pain, management of chronic

paralysis, acute areflexic

paralysis, asymmetric

paralysis, use-related

paraneoplastic cerebellar degeneration

paraneoplastic ganglionopathy

paranoia

paraoxonase

paraparesis

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraspinal muscle weakness

parathyroid adenoma

paratonia

paratrigeminal syndrome

paresthesias

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

PAS positive

pathology

patient information and support

penguin silhouette sign

penicillamine

percussion induced muscle contraction

periodic paralysis

periodic paralysis, thyrotoxic

peripheral blood smear

peripheral nerve, lesion of

peripheral vascular disease

peroneal muscle atrophy, causes of

peroxisomal disease

persistent vegetative state

personality change

pes cavus

pheochromocytoma

phosphorylase b kinase deficiency

phrenic nerve

phrenic nerve pacemaker

physical activity

physical therapy

physician assisted suicide

phytanic acid

Pick's disease

pigmentary retinopathy

pituitary, lesion of

placebo

plasma cell dyscrasia

plasmacytoma

plasmapheresis

pleocytosis of cerebrospinal fluid

pleural effusion

pneumoencephalogram(PEG)

pneumonia

POEMS syndrome

poison, mercury

poison, neurologic problems with

poliomyelitis

poliomyelitis, provocation

poliomyelitis-like illness

POLR3B

polyclonal gammopathy

polyglucosan body

polyglucosan body disease

polymerase chain reaction

polymyositis

polyneuropathy

polyneuropathy, chronic inflammatory demyelinating

pontocerebellar atrophy

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

preclinical

pregnancy, neurologic complications in

pressure sores

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

proprioception, abnormal

proximal muscle atrophy

psychiatric problems in neurologic disorders

psychomotor retardation

pulmonary function tests

pulmonary infiltrates

pupil

pupil, abnormality in neurologic disorders

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

rabies, nervous system involvement with

radiation hypersensitivity

radiation therapy, CNS treatment and complications with

radiation therapy, salivary gland

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

rash

Raynaud's phenomenon

real-time quaking-induced conversion

recombinant DNA

recurrent

Red flags

reflex sympathetic dystrophy

reflex sympathetic dystrophy, children

Refsum's disease

release phenomena

REM sleep behavior disorder

remote effect of cancer on the nervous system

renal cell carcinoma

renal failure

renal stones

renal transplantation

renal tubular acidosis

repetitive nerve stimulation

respirator

respiratory arrest

respiratory depression

respiratory failure

respiratory tract infection

retina, abnormal

retinal artery occlusion

retinal branch artery occlusion

retrograde axonal flow

retrovirus

reverse split hand sign

reversible neurologic disorder

rheumatoid arthritis, neurologic complications of

rippling muscle disease

risdiplam

risk factors

risk-benefit assessment

rubella encephalitis, progressive

rubella syndrome

rubella virus

rubeola virus

saccadic eye movements, abnormal

safety

salivation, excessive

scleroderma, neurologic involvement with

sclerosis, bone

scoliosis

scoliosis, neurologic association with

second wind phenomena

sedation

segmental demyelination

seizure, surgical treatment of

seizure, treatment of

self-mutilation

semialdehyde dehydrogenase deficiency

sensorineural hearing loss

sensory ganglia

sensory ganglia, abnormal

sequencing difficulty

serologic testing

serologic testing of cerebrospinal fluid

serologic testing, false negative

serum alanine aminotransferase

shell fish poisoning

short stature

shoulder, subluxation

shoulder-girdle wasting

sicca syndrome

sinemet

single photon emission computed tomography

single-fiber electromyography

sinuses, diseases of

sinusitis

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skin, biopsy

skin, lesions in neurologic disorders

skin, temperature difference

skull x-ray

skull x-ray, abnormal

sleep

sleep apnea

sleep pathology and physiology

slit lamp examination

slow virus infection of CNS

slurred speech

smell

Smell Identification Test

SMN1 gene

solvent

somatosensory evoked potentials

somatosensory evoked potentials, dermatomal

somnolence

spastic ataxia

spastic paraplegia, type 11

spastic paraplegia, type 7

spasticity

speech disorder

speech disorder, childhood

spinal cord degeneration

spinal cord, biopsy

spinal cord, cervical

spinal cord, compression of

spinal cord, enlargement

spinal cord, infarction of

spinal cord, injury of

spinal cord, injury, management of

spinal cord, ischemic lesion of

spinal cord, lesion of

spinal cord, neoplasm

spinal cord, neoplasm, extramedullary

spinal cord, neoplasm, 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

spongy degeneration of brain

spontaneous remission

sports medicine, neurology of

stem cell transplantation

steppage gait

stereotaxic surgery

stereotyped behavior

sternocleidomastoid muscle

steroid

steroid therapy, CNS treatment and complications with

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

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

subarachnoid hemorrhage

subclavian artery stenosis

superior cerebellar peduncle

superoxide dismutase

suprasellar lesion

survival motor neuron gene

Susac's syndrome

symmetric brain lesions

sympathetic block

symptomatic

synucleinopathy

syphilis, neurologic complications with

teeth, number of in infants

temporal lobe, atrophy

temporalis muscle wasting

temporalis muscle weakness

temporomandibular joint, dislocation

tensilon test

tensilon test, false positive

thalamus, lesion of-bilateral

thermography

Thies's sign

thoracic outlet syndromes

thyrotropin-releasing hormone

tick bite

tick paralysis

tick-borne encephalitis

tongue, fasciculations of

tongue, impaired movements of

transient ischemic attack

transient neurologic deficit

transverse smile

trauma

treatment of neurologic disorder

tremor

tremor, postural

tremulousness

triangle of Guillain and Mollaret

tricresylphosphate

trigger finger

trinucleotide repeats

tyrosine hydroxylase deficiency

ubiquitin

ulcers, fingertip

ulnar nerve

ulnar nerve, deep palmar branch of

ulnar neuropathy

unconsciousness

unconsciousness, episodic

unconsciousness, transient

Unverricht-Lundborg disease

upgaze, paralysis of

urea-cycle enzymopathies

urinary incontinence

urinary urgency

urine test for metabolic disorders

urine, dark

uveitis

valium

vascular endothelial growth factor

vasculitides

vasculopathy

venous thrombosis, non-cerebral

ventricular enlargement

vertigo

vestibular function, tests of

vibratory sensation, abnormal

visual acuity, decreased

visual evoked response

visual field defect

visual fields, constricted

visual loss

visual symptoms

visuospatial disturbance

Waldenstrom's macroglobulinemia

walking frame

walking, difficulty with

weakness, generalized

weakness, infant

weakness, progressive

weakness, proximal

weakness, rapidly progressive

weaning from respirator, failure to

Werdnig-Hoffman disease

West disease

West Nile fever

wheelchair

whistle, inability to

white matter disease

white matter disease, subcortical

wide based gait

winging of scapula

word-finding difficulty

X-linked bulbospinal neuronopathy

X-linked myopathy

x-linked myopathy with excessive autophagy

zinc

Showing articles 300 to 350 of 5301 << Previous Next >>

Competent Pts with Adv States of Perm Paralysis Have the Right to Forgo Life-Sustaining Therapy
Neurol 43:224-225, Bernat,J.L.,et al, 1993

Intramedullary Spinal Sarcoidosis:Clinical and Magnetic Resonance Imaging Characteristics
Neurol 43:333-337, Junger,s.S.,et al, 1993

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

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

Decreased Glutamate Transport by the Brain and Spinal Cord in Amyotrophic Lateral Sclerosis
NEJM 326:1464-1468, 14931992., Rothstein,J.D.,et al, 1992

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

Werdnig-Hoffman Disease & Chronic Distal Spinal Muscular Atrophy with Apparent Autosomal Dom Inherit
Ann Neurol 32:404-407, Boylan,K.B.&Cornblath,D.R., 1992

Anti-Hu-Associated Pareneoplastic Encephalomyelitis/Sensory Neuronopathy
Medicine 71:59-72, Dalmau,J.,et al, 1992

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

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

Diagnosis and Treatment of Ossification of the Posterior Longitudinal Ligament of the Spine:8 Cases and Lit Review
Am J Med 92:296-306, Trojan,D.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

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

Acute Paralytic Poliomyelitis Presenting as Guillain-Barre Syndrome
J Infection 22:129-133, Yohannan,M.D.,et al, 1991

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

Olfactory Impairment in Motor Neuron Disease:A Pilot Study
JNNP 54:927-928, Elian,M., 1991

Subacute, Reversible Motor Neuron Disease
Neurol 41:1541-1544, Tucker,T.,et al, 1991

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

Pancuronium-Induced Prolonged Neuromuscular Blockade
Crit Care Med 19:1583-1587, Rossiter,A.,et al, 1991

Pick's Disease:A Case Clinically Resembling Amyotrophic Lateral Sclerosis
Neurol 41:1831-1833, Sam,M.,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

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

Progressive Motor Neuron Disease Associated with Electrical Injury
Muscle & Nerve 14:977-980991., Sirdofsky,M.D.,et al, 1991

Lymphoma, Motor Neuron Diseases, and Amyotrophic Lateral Sclerosis
Ann Neurol 29:78-86, Younger,D.S.,et al, 1991

Angiofollicular Lymph Node Hyperplasia & Peripheral Neuropathy, Case Report & Literature Review
Arch Int Med 151:789-790, Scherokman,B.,et al, 1991

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

Poliomyelitis-Like paralysis During Recovery from Acute Bronchial Asthma:Possible Etiology and Risk Fators
Pediatrics 88:276-279, Shahar,E.M.,et al, 1991

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

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

Autosomal Recessive Distal Dystrophy
Neurol 41:1365-1370, Barohn,R.J.,et al, 1991

Progressive Myoclonic Ataxia (The Ramsay Hunt Syndrome)
Arch Neurol 47:1121-1125, Marsden,C.D.,et al, 1990

Graves Orbitopathy:Correlation of CT and Clinical Findings
Radiology 177:675-682, Nugent,R.A.,et al, 1990

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

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

X-Linked Spinal Muscular Atrophy (Kennedy's Syndrome) A Kindred with Hypobetalipoproteinemia
Arch Neurol 47:1117-1120, Warner,C.L.,et al, 1990

Quadriceps Myopathy:Forme Fruste of Becker Muscular Dystrophy
Ann Neurol 28:634-639, Sunohara,N.,et al, 1990

Phenotypic Heterogeneity of Spinal Muscular Atrophy Mapping to Chromosome 5q11. 2-12. 3 (SMA5q)
Neurol 40:1831-1836, Munsat,T.L.,et al, 1990

What Causes Motoneuron Disease?
Editorial, Lancet 336:1033-10351990., , 1990

Misdiagnosis in Patients with Amyotrophic Lateral Sclerosis
Arch Int Med 150:2301-2305, Belsh,J.M.&Schiffman,P.L., 1990

Non Alzheimer's Disease Forms of Cerebral Atrophy
Editorial, JNNP 53:929-9311990., Neary,D., 1990

Anti-GM1 IgM Antibodies in Motor Neuron Disease and Neuropathy
Neurol 40:1747-1750, Nobile-Orazio,E.,et al, 1990

Showing articles 300 to 350 of 5301 << Previous Next >>