Neudle.com: muscle atrophy distal

Differential
(Click to cross reference)

abdominal muscle paralysis

abductor pollicis brevis

abiotrophy

abscess, vertebral

acanthocytosis

acetylcholine receptor antibody

acid maltase deficiency

acid maltase deficiency, adult

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

aggression

alcohol intoxication

alcohol, neurologic complications with

alcoholic polyneuropathy

alcoholism

algorithm

alpha-fetoprotein

alveolar hypoventilation

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

analgesic

anatomy of

anemia

anemia, megaloblastic

anesthesia, general

aneurysm

aneurysm, cavernous sinus

aneurysm, internal carotid artery

aneurysm, intracranial

angiitis

angiography, neurologic complications with

ankle reflex, preserved

ankylosing spondylitis

anorexia

anterior horn cell disease

anterior interosseous neuropathy

anterior spinal artery infarction

anterior tibial muscle weakness

anti citrullinated antibody

anti Hu antibody

anti IgLON5

antibodies to voltage-gated calcium channels

anticoagulant, complications of

anticoagulant, treatment

anticonvulsants

antineurofascin antibodies

antiviral agents

anxiety

aphasia

aphasia, progressive, primary

aphonia

apnea

apraxia

apraxia of eye movements

arterial dissection, aorta

arterial dissection, carotid

arterial dissection, vertebral

arthralgia

arthrogryposis multiplex

ascending paralysis

aspiration

asthma

asthma, poliomyelitis-like syndrome with

asymptomatic

ataxia

ataxia telangiectasia

atlanto axial dislocation, congenital

atrioventricular block

atrophy, muscle

attention deficit disorder with hyperactivity

autoantibodies

autoimmune disease

autonomic dysfunction

basal ganglia, degeneration

basal ganglia, lesion of

basement membrane

basement membrane thickening

basophilic stippling of red blood cells

behavioral disorder

Bence Jones protein

benign congenital hypotonia

benign essential tremor

benzodiazepine

biologic markers

BiPAP

bitemporal visual field defect

bladder dysfunction

blink reflex

bone marrow biopsy

bone marrow suppression

border zone infarct

botulinum toxin

botulinum toxin, complications of

botulism

brachial amyotrophic diplegia

brachial neuritis

brachial plexus

brachial plexus injury

brachial plexus neuropathy

brachial plexus neuropathy, familial

brachial plexus neuropathy, recurrent

brachial plexus, lesion of

brainstem, infarction of

brainstem, lesion of

bright tongue sign

Brown Sequard syndrome

Brugada syndrome

bruit

bruit, supraclavicular

bulbar palsy

bulbar palsy, acute

bulbar palsy, childhood

bulbar palsy, progressive

calcification, intracranial

calcium channel dysfunction

campylobacter infection

cane

carbon monoxide poisoning

carcinoembryonic antigen

carcinoma

carcinoma of breast

carcinoma of lung

cardiac catheterization, neurologic complications

cardiomegaly

cardiomyopathy

cardiovascular disease

caregiver

carotid artery atherosclerosis

carotid artery disease

carotid artery occlusion, neck

carotid artery stenosis

carpal tunnel syndrome

CAT scan, emission, abnormal

cataracts

cauda equina

cavernous sinus, syndrome

CD4 counts

central core disease

central nervous system, infection of

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar lesion

cerebellar vermis

cerebellum

cerebellum, neoplasms of

cerebral cortex

cerebral cortical atrophy

cerebral death

cerebral embolism

cerebral embolism, artery to artery

cerebral embolism, cardiac origin

cerebral infarction

cerebral infarction, small, deep

cerebral ischemia

cerebral peduncle

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, cell count

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, protein of

cerebrospinal fluid, proteincytologic dissociation

cerebrovascular accident

cerebrovascular accident, incidence of

cerebrovascular accident, location of

cerebrovascular accident, mimics

cerebrovascular accident, non atherosclerotic cause of

cerebrovascular accident, young adult

cerebrovascular disease, cardiovascular disease with

cervical band

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

cheiralgia paresthetica

chelation therapy

chest x-ray, abnormal

chewing, impaired

children

chills

Chinese paralytic syndrome

chromosomal abnormality

chronic polyneuritis, children

Chvostek sign

ciguatera poisoning

cimetidine

claudication, extremity

climate change

Clinical Pathologic Conference(C.P.C.)

collagen vascular disease

coma

coma, episodic

compartment syndrome

compartment syndrome, medial brachial fascial

complications

compression neuropathy

concussion

conduction block

confusion

confusional state, acute

congenital heart disease

congenital myopathy

congestive heart failure

constipation

contactin associated protein like 1 antibodies

contactin associated protein like 1 auto antibodies.(CNTN1)

contractures, joint

controversies in neurology

conversion reaction

corneal reflex, abnormal

corneal reflex, absent

corona radiata

corpus callosum, infarction of

corpus callosum, lesion of

cortical hand knob

cortical hand knob infarct

cortical infarction

cortical infarction, small

cortical muscular atrophy

coxsackievirus, myopathy with

CPAP

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

craniopharyngioma

creatine phosphokinase(CPK)elevated

degenerative diseases of CNS

Dejerine-Sottas syndrome

dementia, age at onset

dementia, cerebrovascular disease causing

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

denervation of muscle

denervation potentials

dentatorubral-pallidoluysian atrophy

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diabetic mononeuropathy

diagnostic criteria

diaphragmatic paralysis

diaphragmatic paralysis, causes of

diarrhea

diet

differential diagnosis

difficulty climbing stairs

difficulty going down stairs

disability rating scale, neurological

disability, neurological

disc space infection

disc space narrowing

discitis

dissociated sensory loss

distal muscle atrophy

distal muscle weakness

DNA probes

dopamine

drooling

dropped head syndrome

dystrophic calcification

dystrophin

edema, pedal

efficacy

electrical injury of nervous system

electrical sensation

electrical stimulation, spinal nerves

electrocardiogram, abnormal

electromyogram

electromyogram, decremental response

electron microscopy

electrophoretic pattern, serum

embolism

emotional lability

empyema, epidural-spinal

encephalitis

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, central European

encephalitis, episodic

encephalitis, paraneoplastic

encephalitis, Powassan

encephalitis, viral

encephalocele

encephalomyelitis

encephalomyeloneuritis

encephalopathy

encephalopathy, anoxic

encephalopathy, neonatal

encephalopathy, post anoxic

endocarditis, subacute bacterial

enterovirus

enterovirus infection of CNS

entrapment neuropathy

enzyme, defect

enzyme, muscle disease

eosinophilia

epidemiology of neurology

episodic disorders

episodic neurologic deficits

episodic unconsciousness

evidence-based research

exercise-induced vascular symptoms

exome sequencing

exophthalmus

extremity, cold

eye movement, disorders of

face, numbness of

facial appearance, abnormal

facial pain

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

failed medical management

falling

familial

fasciculation

fasciculation, benign

fatigable chewing

fatigue

Fazio-Londe's disease

fever

fibrillations

fine motor function, impaired

finger drop

finger flexor weakness

finger weakness

fingernails, abnormal

football neurologic injuries

fracture, long bones, nerve injury with

fragile-X syndrome

free radical

Friedreich's ataxia

frontal lobe, atrophy

frontal lobe, behavior with disease of

frontal lobe, lesion of

frontotemporal dementia, behavioral variant

F-wave response

gag reflex, depressed

gait disorder

gait, spastic

gait, waddling

gammaglobulin therapy, intravenous

gammaglobulin therapy, intravenous, refractory

gastrectomy, neurologic complications following

gastrocnemius muscle weakness

gastroenteritis

gastrostomy

gastrostomy, percutaneous endoscopic

gaze palsy

gaze palsy, horizontal

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

glycogen debranching enzyme deficiency

glycogen storage disease

GM1 ganglioside

GM1 ganglioside antibodies

granular atrophy, cerebral cortex

granulomatous disease

growth retardation

guanidine

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, prognosis of

Guillain Barre syndrome, variant forms of

hallucination, auditory

Hand-Schuller-Christian disease

heart block, complete

heavy metal intoxication

hemangioma

hemidiaphragm, paralysis of

hemiplegia, progressive

hemoglobinuria

hepatitis

hepatomegaly

heralding manifestation

hereditary myopathy with early respiratory failure

herniated disc

herniated disc, thoracic

herpes simplex encephalitis

herpes simplex encephalitis, diagnosis of

highly active antiretroviral therapy

histamine-2 receptor blockers

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)

hyperhidrosis, palmar

hyperpigmentation of skin

hypogammaglobulinemia

hypoglycemia

hypoglycemic coma

hypokalemia

hypokalemic alkalosis

hypokalemic periodic paralysis

hypotension, systemic

hypothalamus

hypothalamus, disturbance of

hypoxic encephalopathy

iatrogenic neurologic disorders

immunoelectrophoresis, serum

immunohistochemistry

immunologic disease

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, intracytopasmic

inclusion bodies, intranuclear

inclusion bodies, ubiquitin

inclusion body myositis

incontinentia pigmenti

incoordination

India

infant, evaluation of

infantile neuronal degeneration

infantile tremor syndrome

infection

inflexibility, mental

insomnia

insulinoma

intellectual deficit

intellectual deterioration

intermittent positive pressure breathing

internal capsule

internet

interosseous muscles

intestinal pseudoobstruction

intracerebral hemorrhage

intrinsic hand muscles

intrinsic hand muscles, wasting of

Jakob-Creutzfeldt disease

juvenile distal and segmental muscular atrophy

klippel feil syndrome

Klumpke palsy

Krabbe's disease

Kugelberg-Welander syndrome

kyphoscoliosis, neurologic causes of

laboratory values, normal

lactic acidemia

lactic dehydrogenase(LDH)

laminectomy, cervical

lathyrism

laughing

laughing, pathologic

lead and the nervous system

lead poisoning

leg atrophy

leg numbness

leg weakness, bilateral

leg weakness, unilateral

leprosy

leukemia

leukemia, neurologic findings assoc.with

leukodystrophy

leukoencephalopathy

leukoencephalopathy, differential diagnosis

leukopenia

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

liver disease

liver function enzymes

lymphadenopathy, hilar

lymphoma

lymphoma involving CNS

lysosomal storage disease

Madonna facies

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

Man-In-The-Barrel syndrome

Martin-Gruber anastamosis

masseter muscle wasting

masseter muscle weakness

median nerve

median nerve, lesion of

median neuropathy

medical-legal aspects of neurology

Mees lines

memory, defect of recent

memory, impairment of

meningismus

meningitis

mental retardation

mental status, abnormal

metabolic disorder, primary

methotrexate

methylmalonic acid, serum

methylmalonic acidemia

microangiopathy, brain

microinfarcts

middle cerebral artery territory infarction

middle cerebral artery, emboli to

middle cerebral artery, occlusion of

middle cerebral artery, stenosis of

migraine

Millard Gubler syndrome

Mills syndrome

mimics

minimally conscious state

monoclonal antibodies

monoclonal gammopathy

monoclonal gammopathy of uncertain significance

monomelic amyotrophy

mononeuritis multiplex

mononeuropathy

mononeuropathy, motor

motor neuron disease, juvenile form

motor neuron disease, misdiagnosis

motor neuron disease, spontaneous recovery

motor system

movement disorder

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, brachial plexus

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, FLAIR

MRI, functional

MRI, gradient-echo

MRI, lumbosacral plexus

MRI, muscle

MRI, negative

MRI, paramagnetic effect

MRI, peripheral nerve

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRI, spine

MRI, susceptibility weighted

MRI, T1 weighted fat suppression

MRS

multifocal acquired demyelinating sensory motor neuropathy

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 spasm, paraspinal

muscle stiffness

muscle strength, testing

muscle swelling

muscle tenderness

muscle twitching

muscle wasting, diffuse

muscle weakness

muscle weakness, causes of

muscle weakness, insidious onset of

muscle weakness, proximal

muscle, metabolic disorders of

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, Becker, carrier

muscular dystrophy, cardiovascular changes with

muscular dystrophy, classification

muscular dystrophy, differential diagnosis of

muscular dystrophy, distal, Miyoshi

muscular dystrophy, Duchenne

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

muscular dystrophy, neurogenic hypothesis of

mutism

myasthenia gravis

myasthenia gravis, distal weakness

myasthenia gravis, drug induced

myasthenia gravis, limb-girdle

myasthenia gravis, treatment of

myasthenic crisis

myasthenic syndrome

myelitis

myelitis, longitudinal

myelopathy, carcinomatous

myelopathy, chronic progressive

myelopathy, necrotizing

myelopathy, radiation induced

myelopathy, tract-specific

myeloradiculitis

myeloradiculopathy

myocardial infarction

myopathy, carcinomatous

myopathy, centronuclear

myopathy, desmin

myopathy, distal

myopathy, distal, vacuolar

myopathy, distal, Welander's

myopathy, hereditary

myopathy, inclusion body

myopathy, inclusion body, hereditary

myopathy, inflammatory

myopathy, mitochondrial

myopathy, myofibrillar

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, intracranial, differential diagnosis of

neoplasm, pituitary

neoplasm, primary intracerebral

neoplasm, primary intracranial

neoplasm, primary of CNS

nephrotic syndrome

nerve biopsy

nerve conduction studies

nerve conduction studies, motor

nerve conduction studies, sensory

nerve repair, end to end

nerve root enhancement

nerve root hypertrophy

neuritis

neuritis, causes of

neuritis, heavy metals causing

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 evaluation

neurologic examination

neurologic examination, focal

neuromuscular blockade

neuromuscular disease, electrodiagnosis of

neuromuscular junction

neuromuscular junction, abnormality of

neuromyotonia

neuronal ceroid-lipofuscinosis

neuronal degeneration

neuronal intranuclear inclusion disease

neuronal migration disorder

neuronopathy

neuronopathy, sensory

neuronopathy, sensory and motor

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, acute

neuropathy, amyloid

neuropathy, autoimmune

neuropathy, bicycle

neuropathy, demyelinating

neuropathy, diabetic

neuropathy, diphtheritic

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, iatrogenic

neuropathy, medication induced

neuropathy, motor

neuropathy, motor, multifocal

neuropathy, multifocal

neuropathy, painful

neuropathy, paraneoplastic

neuropathy, peripheral

neuropathy, peripheral, treatment

neuropathy, sensory

neuropathy, short-fiber

neuropathy, toxic

neuroprotective agents

newborn, evaluation of

next-generation sequencing

nodopathy, autoimmune

nonresponsive

numbness, ascending

numbness, extremity

numbness, generalized

nusinersen

nystagmus

nystagmus, primary position of gaze

nystagmus, rotary

occupational neurologic disorders

occupational neuropathies

ocular motility, disorders of

old age, neurology of

olivary degeneration, hypertrophic

Onufrowicz nucleus

ophthalmoplegia

ophthalmoplegia, painful

ophthalmoplegia, progressive external

ophthalmoplegia, total

opiate

Oppenheim muscular dystrophy

opportunistic infection, CNS

osteomyelitis, spinal

otitis, neurologic complications with

overlap syndrome

owl's eye sign of spinal cord

pain, increased response

pain, interscapular

pain, management of chronic

paralysis, acute areflexic

paralysis, asymmetric

paralysis, use-related

paraneoplastic ganglionopathy

paranoia

paraoxonase

paraparesis

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraspinal muscle weakness

parathyroid adenoma

paratrigeminal syndrome

paresthesias

paresthesias, feet

paresthesias, hands

parietal lobe, lesion of

parietal lobe, syndromes of

Parkinson disease

Parkinson disease, L-dopa nonresponsive

Parkinson disease, motor neuron disease with

Parkinson disease, treatment of

Parkinsonism syndrome

Parkinsonism-dementia complex

paroxysmal neurologic deficits

pathology

patient information and support

penicillamine

percussion induced muscle contraction

pericardial effusion

periodic paralysis

periodic paralysis, thyrotoxic

peripheral blood smear

peripheral blood smear, abnormal

peripheral vascular disease

pernicious anemia

peroneal muscle atrophy, causes of

peroxisomal disease

persistent vegetative state

phrenic nerve pacemaker

physical activity

physical therapy

physician assisted suicide

Pick's disease

placebo

plasma cell dyscrasia

plasmacytoma

plasmapheresis

pleocytosis of cerebrospinal fluid

pleural effusion

pneumoencephalogram(PEG)

POEMS syndrome

poison, mercury

poison, neurologic problems with

poliomyelitis

poliomyelitis, provocation

poliomyelitis-like illness

polyclonal gammopathy

polyglucosan body

polyglucosan body disease

polymerase chain reaction

polymyositis

polyneuropathy

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, chronic inflammatory demyelinating, variant form

polyneuropathy, chronic inflammatory demyelinating-pure motor syn

polyneuropathy, chronic inflammatory demyelinating-sens atax var

polyneuropathy, chronic inflammatory demyelinating-variant forms

polyneuropathy, familial

porphyria

position sensation, abnormal

positive sharp waves

post polio syndrome

posterior column disease

posterior fossa

posterior fossa, differential diagnosis of lesions of

posterior fossa, lesion of

posterior inferior cerebellar artery syndrome

posterior interosseous neuropathy

practice guidelines

precentral gyrus

preclinical

pregnancy, neurologic complications in

pressure sores

prevention of neurologic disorders

primary aldosteronism

primary lateral sclerosis

prisoners of war, neurologic complications in

progeria

prognosis

progranulin

progressive multifocal leucoencephalopathy

progressive muscular dystrophy

progressive neurologic disorder

progressive spinal muscular atrophy

pronator syndrome

proprioception

proprioception, abnormal

proximal muscle atrophy

pseudoathetosis

pseudobulbar palsy

pseudohypertrophy

pseudomedian nerve palsy

pseudomyotonia

pseudoperipheral palsy

pseudoradial nerve palsy

pseudoulnar palsy

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

pulmonary function tests

pupil

pupil, abnormality in neurologic disorders

pure motor stroke

pyramidal tract

pyramidal tract dysfunction

rabies, nervous system involvement with

radial nerve

radial nerve, palsy of

radial pulse, unilateral decrease of

radiation hypersensitivity

radiation therapy, CNS treatment and complications with

radiation therapy, salivary gland

radiculitis

radiculopathy

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

REM sleep behavior disorder

remote effect of cancer on the nervous system

renal cell carcinoma

renal stones

repetitive nerve stimulation

respirator

respiratory arrest

respiratory depression

respiratory failure

respiratory tract infection

retinitis pigmentosa

retrograde axonal flow

retrovirus

reverse split hand sign

review article

RFLPs

rheumatoid arthritis

rheumatoid arthritis, neurologic complications of

risk-benefit assessment

saccadic eye movements, abnormal

safety

salivation, excessive

sarcoidosis

sarcoidosis, CNS

scalenus anticus syndrome

schizophrenia

scissors gait

scleroderma

scleroderma, neurologic involvement with

scoliosis

scoliosis, neurologic association with

sedimentation rate, elevated

segmental demyelination

seizure

seizure, children

seizure, treatment of

sensorimotor stroke

sensorineural hearing loss

sensory ganglia

sensory ganglia, abnormal

sensory level

sensory loss

sensory loss, cortical

sensory loss, glove-stocking

sensory loss, patchy

sensory loss, pseudoradicular

sensory loss, truncal

sensory symptoms

sensory testing

sensory testing, quantitative

serologic testing

serologic testing of cerebrospinal fluid

serologic testing, false negative

serum alanine aminotransferase

shoulder, subluxation

shoveling

single photon emission computed tomography

skin, biopsy

skin, lesions in neurologic disorders

sleep

sleep apnea

sleep pathology and physiology

slit lamp examination

small vessel disease

smell

Smell Identification Test

SMN1 gene

solvent

somatosensory evoked potentials

somatosensory evoked potentials, dermatomal

spinal cord degeneration

spinal cord, cervical

spinal cord, compression of

spinal cord, compression, epidural abscess causing

spinal cord, enlargement

spinal cord, infarction of

spinal cord, injury of

spinal cord, injury, management of

spinal cord, 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

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar degeneration

spirometry

spitting

splenium of corpus callosum

splenomegaly

spondylosis

spontaneous muscle activity

sports medicine, neurology of

standing difficulty

stem cell tourism

stem cell transplantation

steppage gait

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

survival motor neuron gene

swallow evaluation

sweating, abnormality of

swimming

symptomatic

syphilis, neurologic complications with

temporal lobe, atrophy

temporalis muscle wasting

temporalis muscle weakness

temporomandibular joint, dislocation

tensilon test

tensilon test, false positive

thoracic outlet syndromes

thromboangiitis obliterans cerebri

thyrotropin-releasing hormone

tick bite

tick paralysis

tick-borne encephalitis

tongue, fasciculations of

tongue, impaired movements of

transient neurologic deficit

trauma

treatment of neurologic disorder

tremor

tremor, intention

tremor, postural

triangle of Guillain and Mollaret

tricresylphosphate

trigeminal nerve, abnormality of

trigger finger

trinucleotide repeats

ulnar nerve, compression of

ulnar nerve, deep palmar branch of

ulnar neuropathy

ultrasonography

unconsciousness

unconsciousness, episodic

unconsciousness, transient

upgaze, paralysis of

urea-cycle enzymopathies

uremia

urinary incontinence

urine test in toxic screen

urine, dark

valium

vascular endothelial growth factor

vasculopathy

venous thrombosis, non-cerebral

vertebral erosion

vestibular function, tests of

vibratory sensation, abnormal

visual evoked response

Waldenstrom's macroglobulinemia

walking frame

walking, delayed

walking, difficulty with

weakness, generalized

weakness, infant

weakness, progressive

weakness, proximal

weaning from respirator, failure to

web sites

Weber's syndrome

weight loss

Werdnig-Hoffman disease

West disease

West Nile fever

wheelchair

whistle, inability to

white matter disease

wide based gait

winging of scapula

word-finding difficulty

workup

wrist drop

xerostomia

X-linked bulbospinal neuronopathy

yelling

zinc

Showing articles 650 to 700 of 5189 << Previous Next >>

Dysthyroid Orbitopathy
Semin Neurol 20:43-54, Jacobson,D.M., 2000

Distal Myopathies:Clinical and Molecular Diagnosis and Classification
JNNP 67:703-709, Mastaglia,F.J.&Laing,N.G., 1999

Hypertrophy of Multiple Cranial Nerves and Spinal Roots in Chronic Inflammatory Demyelinating Neuropathy
JNNP 67:685-687, Duarte,J.,et al, 1999

The Roussy-Levy Family:From the Original Description to the Gene
Ann Neurol 46:770-773, Plante-Bordeneuve,V.,et al, 1999

Pathologic Heterogeneity in Clinically Diagnosed Corticobasal Degeneration
Neurol 53:795-800, Boeve,B.F.,et al, 1999

Neurologic Complications Associated with Hepatitis C Virus Infection
Neurol 53:861-864, Tembl,J.I.,et al, 1999

Infantile Neuroaxonal Dystrophy,Clinical Spectrum and Diagnostic Criteria
Neurol 52:1472-1478, Nardocci,N.,et al, 1999

Compression of Spinal Cord and Cauda Equina in Charcot-Marie-Tooth Disease Type 1A
Neurol 52:890-891, Butefisch,C.,et al, 1999

Rapidly Progressive Dementia
Lancet 353:1150, Bornke,C.,et al, 1999

Suprascapular Neuropathy
J Am Acad Orthop Surg 7:358-367, Romeo, A.A.,et al, 1999

Clinicopath Conf,Syndrome of Mitochondrial Encephalopathy,Lactic Acidosis,and Stroke-Like Episodes (MELAS),Case 39-1998
NEJM 339:1914-1923, , 1998

Dipsticks and Convulsions
Lancet 352:1824, Koch,H., 1998

Prader-Willi and Angelman Syndromes
Medicine 77:140-151, Cassidy,S.B.&Schwartz,S., 1998

PCR-Based Strategy for Dx of Hered Neuropathy with Liability to Pressure Palsies & Charcot-Marie-Tooth Dis Type 1A
Neurol 50:760-763, Young,P.,et al, 1998

Mucolipidosis Type IV; Characteristic MRI Findings
Neurol 51:565-569, Frei,K.P.,et al, 1998

Clinical Presentation and Pharmacological Therapy in Corticobasal Degeneration
Arch Neurol 55:957-961, Kompoliti,K.,et al, 1998

Fluid Attenuation Inversion Recovery (FLAIR) Images of Dentatorubropalliodoluysian Atrophy:Case Report
JNNP 65:396-399, Yoshii,F.,et al, 1998

MR of Extraocular Muscles in Chronic Progressive External Ophthalmoplegia
AJNR 19:95-99, Carlow,T.J.,et al, 1998

Congenital Muscular Dystrophy:Use of Brain MR Imaging to Predict Merosin Deficiency
Radiology 206:811-816, Lamer,S.,et al, 1998

Retinocochleocerebral Vasculopathy
Medicine 77:12-40, Petty,G.W.,et al, 1998

Clinicopath Conf
Acute Critical-Illness Myopathy, with Loss of Myosin Filaments, ? Induced by Steroid, Case 11-1997,, EJM 379-1088,1997., 1997

Clinical Characteristics of Patients with Motor Disability Due to Conversion Disorder:A Prospective Study
JNNP 63:83-88, Binzer,M.,et al, 1997

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

Paramedian Pontine Infarction
Stroke 28:809-815, Kataoka,S.,et al, 1997

Mononeuropathy of a Distal Branch of the Femoral Nerve in a Body Building Champion
JNNP 63:669-671, Padua,L.,et al, 1997

Atrophy of Bilateral Extraocular Muscles
J Neuro-Ophthalmol 16:286-288, Okamoto,K.,et al, 1996

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

Twelfth-Nerve Palsy:Analysis of 100 Cases
Arch Neurol 53:561-566, Keane,J.R., 1996

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

Congenital Muscular Dystrophy:Clinical & Pathologic Study of 50 Pts with Classical (Occidental) Merosin-Positive Form
Neurol 46:815-818, Kobayashi,O.,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

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

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

Effect of GPi Pallidotomy on Motor Function in Parkinson's Disease
Lancet 346:1383-1387, Lozano,A.M.,et al, 1995

Critical Illness Neuromuscular Disease in Children Manifested as Ventilatory Dependence
J Pediatr 126:259-261, Sheth,R.D.,et al, 1995

Lyme Neuroborreliosis
Ann Neurol 37:691-702, Garcia-Monco,J.C.&Benach,J.L., 1995

Mitochondrial DNA and Disease
NEJM 333:638-644, Johns,D.R., 1995

Clinical and Genetic Studies of Fatal Familial Insomnia
Neurol 45:1068-1075, Reder,A.T.,et al, 1995

Dentatorubral-Pallidoluysian Atrophy:Clin Features Closely Related to Unstable Expansion of Trinucleotide (CAG) Repeat
Ann Neurol 37:769-775, Ikeuchi,T.,et al, 1995

Reflex Sympathetic Dystrophy
BMJ 310:1645-1648, Paice,E., 1995

Reflex Sympathetic Dystrophy in Children
BMJ 310:1648-1649, Lloyd-Thomas,A.R.&Lauder,G., 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

Adverse Outcomes of Bacterial meningitis in School-Age Survivors
Pediatrics 95:646-655, Grimwood,K.,et al, 1995

Clinical Genetics in Neurological Disease
JNNP 57:7-15, MacMillan,J.C.&Harper,P.S., 1994

Cerebral Involvement in McLeod Syndrome
Neurol 44:117-120, Danek,A.,et al, 1994

Phenotype of Chromosome 14-Linked Familial Alzheimer's Disease in a Large Kindred
Ann Neurol 36:368-378, Lampe,T.H.,et al, 1994

Mitochondrial Neurogastrointestinal Encephalomyopathy (MMGIE) :Clin Biochem & Genetic Features of Auto Recess Mitochond Disorder
Neurol 44:721-727, Hirano,M.,et al, 1994

Becker Muscular Dystrophy with Onset after 60 Years
Neurol 44:2388-2390, Heald,A.,et al, 1994

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