Neudle.com: anterior horn cell disease

Differential
(Click to cross reference)

abiotrophy

acid maltase deficiency

acid maltase deficiency, adult

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome, heralded by neurologic invol

ACTH, ectopic syndrome of

acute intermittant porphyria

Addison's disease

adult polyglucosan body disease

advances in neurology

adverse drug reaction

algorithm

alpha glucosidase

alpha-fetoprotein

alveolar hypoventilation

Alzheimer's disease

aminoacidopathies

amyloidosis

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, bulbar

amyotrophic lateral sclerosis, atypical

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, juvenile

amyotrophic lateral sclerosis, misdiagnosis

amyotrophic lateral sclerosis, myasthenic syndrome with

amyotrophic lateral sclerosis, Parkinson-dementia-complex

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

aneurysm

aneurysm, cavernous sinus

aneurysm, internal carotid artery

animal exposure

ankle edema

ankle reflex, preserved

anorexia

anterior horn cell disease

anterior interosseous neuropathy

anterior spinal artery infarction

anterior tibial muscle weakness

anti citrullinated antibody

aphasia, progressive, primary

aphonia

apnea

apraxia

apraxia of eye movements

arterial dissection, aorta

arterial dissection, vertebral

arthrogryposis multiplex

ascending paralysis

aspartate aminotransferase

aspiration

asthma

asthma, poliomyelitis-like syndrome with

asymptomatic

ataxia

ataxia telangiectasia

atlanto axial dislocation, congenital

autoantibodies

autoimmune disease

autonomic dysfunction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

bitemporal visual field defect

bladder dysfunction

bone marrow biopsy

botulinum toxin

botulinum toxin, complications of

botulism

brachial amyotrophic diplegia

bulbar palsy, childhood

bulbar palsy, progressive

C0ORF72

cachexia

calcification, intracranial

calf hypertrophy

camptocormia

cane

carcinoembryonic antigen

CAT scan, emission, abnormal

cataracts

cauda equina

cauda equina, enhancement

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

cerebral cortex

cerebral cortical atrophy

cerebral embolism

cerebral peduncle

cerebral venous thrombosis

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, proteincytologic dissociation

cerebrovascular accident

cerebrovascular accident, young adult

cerebrovascular disease, cardiovascular disease with

cervical collar

cervical rib

cervical spine injury

cervical spondylosis

Charcot-Marie-Tooth

chest x-ray, abnormal

chewing, impaired

children

chills

Chinese paralytic syndrome

chorea

choreoathetosis

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

compression neuropathy

conduction block

confusion

congenital heart disease

congenital myopathy

congestive heart failure

coxsackievirus, myopathy with

CPAP

cranial nerve enhancement

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

craniopharyngioma

creatine phosphokinase(CPK)elevated

critical care unit

critical illness

crying, pathologic

cultured skin fibroblasts

degenerative diseases of CNS

Dejerine-Sottas syndrome

delay in diagnosis

delusion

dementia

dementia, age at onset

dementia, cerebrovascular disease causing

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

denervation of muscle

denervation potentials

dentate nuclei

dentate nuclei, lesion of

depression

dermatomyositis

developmental milestones

developmental retardation

dexterity, impaired

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diabetic mononeuropathy

diagnostic criteria

diaphragmatic paralysis

diaphragmatic paralysis, causes of

diarrhea

differential diagnosis

diphtheria

diplegia, atonic

diplegia, brachial

disability, neurological

distal muscle atrophy

distal muscle weakness

DNA probes

dog bite

drooling

drug induced neurologic disorders

electrical injury of nervous system

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electromyogram

electromyogram, decremental response

electrophoretic pattern, serum

embolism

embolism, nucleus pulposus

emotional lability

encephalitis

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, central European

encephalitis, Japanese

encephalitis, paraneoplastic

encephalitis, Powassan

encephalitis, viral

encephalocele

encephalomyelitis

encephalomyeloneuritis

encephalopathy

encephalopathy, anoxic

encephalopathy, neonatal

enterovirus

enterovirus infection of CNS

entrapment neuropathy

enzyme treatment

enzyme, defect

enzyme, muscle disease

epidemiology of neurology

episodic disorders

episodic neurologic deficits

episodic unconsciousness

eye movement, disorders of

facial pain

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

falling

familial

fasciculation

fasciculation, benign

fatigable chewing

fatigue

Fazio-Londe's disease

fever

fibrillations

fine motor function, impaired

football neurologic injuries

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

ganglionitis

gangliosides

gangliosidosis GM2

gastrectomy, neurologic complications following

gastroenteritis

gaze palsy

gaze palsy, horizontal

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

glycogen storage disease

GM1 ganglioside

GM1 ganglioside antibodies

granular atrophy, cerebral cortex

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, variant forms of

Guyon's canal

gynecomastia

hallucination

hallucination, auditory

hand weakness

handlebar palsy

Hand-Schuller-Christian disease

head injury

headache

hearing loss

heavy metal intoxication

heralding manifestation

herpes zoster

heterochromia iridis

highly active antiretroviral therapy

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)

hyperpigmentation of skin

hypogammaglobulinemia

hypoglycemia

hypoglycemic coma

hypokalemia

hypokalemic alkalosis

hypokalemic periodic paralysis

hypotension, systemic

hypothalamus

hypothalamus, disturbance of

hypotonia

hypotonia, infants

hypoxia

hypoxic encephalopathy

imbalance

immunodeficiency

immunoelectrophoresis, serum

immunohistochemistry

immunosuppression

immunosuppressive agents

immunotherapy

impotence

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, ubiquitin

inclusion body myositis

incontinentia pigmenti

India

infant, evaluation of

infantile neuronal degeneration

infantile tremor syndrome

infection

inflexibility, mental

insomnia

intellectual deficit

intellectual deterioration

intermittent positive pressure breathing

internal capsule

internet

intestinal pseudoobstruction

intrinsic hand muscles, wasting of

iron, brain

Isaacs syndrome

islet cell tumor

Jakob-Creutzfeldt disease

jaw jerk, abnormal

Jewish

juvenile distal and segmental muscular atrophy

klippel feil syndrome

Klumpke palsy

Kugelberg-Welander syndrome

kyphoscoliosis, neurologic causes of

laboratory values, normal

lead and the nervous system

lead poisoning

leg atrophy

leg weakness, bilateral

leg weakness, unilateral

leukemia

leukemia, neurologic findings assoc.with

leukodystrophy

leukoencephalopathy

Lewy body disease, diffuse

lid closure, weakness of

life expectancy

life support, withdrawal of

life sustaining treatment

lumbosacral radiculopathy

Lyme disease

lymphadenopathy

lymphadenopathy, hilar

lymphoma

lymphoma involving CNS

lysosomal storage disease

lysosomes, abnoral

malaise

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

Man-In-The-Barrel syndrome

masseter muscle wasting

median neuropathy

medical-legal aspects of neurology

memory, defect of recent

memory, impairment of

meningeal enhancement

meningismus

meningitis

meningitis, aseptic

meningitis, neutrophilic

mental retardation

mental status, abnormal

metabolic disorder, primary

monoclonal antibodies

monoclonal gammopathy

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, contrast enhanced

MRI, disappearing lesion on

MRI, FLAIR

MRI, gradient-echo

MRI, paramagnetic effect

MRI, ring sign

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRI, susceptibility weighted

MRS

multiple myeloma

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, treatment of

multiple system atrophy

muscle atrophy, progressive

muscle atrophy, static

muscle biopsy

muscle cramp

muscle diseases, characteristics of

muscle hypertrophy

muscle pain

muscle twitching

muscle wasting, diffuse

muscle weakness

muscle weakness, causes of

muscle weakness, proximal

muscle, metabolic disorders of

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, Becker, carrier

muscular dystrophy, differential diagnosis of

muscular dystrophy, Duchenne

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

muscular dystrophy, neurogenic hypothesis of

mutism

myasthenia gravis

myasthenia gravis, distal weakness

myasthenia gravis, limb-girdle

myasthenic crisis

myasthenic syndrome

myelitis

myelitis, longitudinal

myelopathy, carcinomatous

myelopathy, chronic progressive

myelopathy, necrotizing

myelopathy, radiation induced

myeloradiculitis

myeloradiculopathy

myocardial infarction

myopathy, carcinomatous

myopathy, centronuclear

myopathy, critically ill

myopathy, distal

myopathy, mitochondrial

myopathy, neurogenic hypothesis of

myopathy, thyroid disease causing

myxedema, neurologic manifestations of

N-acetyl-L-aspartic acid

nemaline rod myopathy

neoplasm, hormone producing

neoplasm, hormone producing, ectopic

neoplasm, pituitary

nerve biopsy

nerve conduction studies

nerve conduction studies, motor

nerve growth factor

nerve root enhancement

neuralgia

neuralgia, intercostal

neuritis, causes of

neurocutaneous disease

neuroendocrinology

neurofibrillary degeneration

neurofibromatosis 1

neurofibromatosis 2

neurogenic bladder

neurogenic vs.myopathic atrophy

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic evaluation

neurologic signs

neurologic symptoms

neurologic testing

neuromuscular disease, electrodiagnosis of

neuromuscular junction

neuromuscular junction, abnormality of

neuromyotonia

neuronal degeneration

neuronal intranuclear inclusion disease

neuronopathy

neuronopathy, sensory

neurons

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy, diphtheritic

neuropathy, hereditary peripheral

neuropathy, motor

neuropathy, motor, multifocal

neuropathy, multifocal

neuropathy, painful

neuropathy, paraneoplastic

neuropathy, peripheral

neuropathy, short-fiber

neuroprotective agents

newborn, evaluation of

next-generation sequencing

nystagmus, primary position of gaze

nystagmus, rotary

occupational neurologic disorders

occupational neuropathies

ocular motility, disorders of

oculogyric crisis

old age, neurology of

olivary degeneration, hypertrophic

Onufrowicz nucleus

ophthalmoplegia

ophthalmoplegia, painful

ophthalmoplegia, progressive external

ophthalmoplegia, total

otitis, neurologic complications with

owl's eye sign of spinal cord

pain, increased response

paralysis, acute areflexic

paralysis, asymmetric

paralysis, use-related

paraneoplastic ganglionopathy

paranoia

paraparesis, familial spastic

paraparesis, familial spastic, classification

paratrigeminal syndrome

paresthesias

Parkinson disease

Parkinson disease, motor neuron disease with

Parkinson disease, treatment of

Parkinsonism syndrome

Parkinsonism-dementia complex

paroxysmal neurologic deficits

pathology

patient information and support

penicillamine

periodic paralysis

periodic paralysis, thyrotoxic

peripheral vascular disease

peroneal muscle atrophy, causes of

phrenic nerve pacemaker

physical activity

physician assisted suicide

Pick's disease

placebo

plasma cell dyscrasia

pleocytosis of cerebrospinal fluid

poison, mercury

poison, neurologic problems with

poliomyelitis

poliomyelitis, provocation

poliomyelitis-like illness

polyclonal gammopathy

polyglucosan body

polyglucosan body disease

polymerase chain reaction

polymerase chain reaction, false negative

polymyositis

polyneuropathy

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, critically ill

Pompe's disease of glycogen storage

posterior inferior cerebellar artery syndrome

posterior interosseous neuropathy

preclinical

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

primary aldosteronism

primary lateral sclerosis

progeria

prognosis

progressive neurologic disorder

progressive spinal muscular atrophy

proprioception

proprioception, abnormal

proximal muscle atrophy

pseudoathetosis

pseudobulbar palsy

pseudohypertrophy

psychiatric problems in neurologic disorders

psychomotor retardation

psychosis

public health

pupil

pupil, abnormality in neurologic disorders

pyramidal tract

pyramidal tract dysfunction

quadriparesis

quadriplegia

quality of life

rabies, nervous system involvement with

radiation hypersensitivity

radiation therapy, CNS treatment and complications with

radiculitis

radiculopathy

rapidly progressing neurologic illness

rehabilitation for neurologic disorders

release phenomena

REM sleep behavior disorder

remote effect of cancer on the nervous system

renal cell carcinoma

renal stones

repetitive nerve stimulation

respirator

respiratory arrest

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

right to die

riluzole

risk factors

risk-benefit assessment

rodents

root lesion, nerve

Roussy Levy syndrome

saccadic eye movements, abnormal

safety

salivation, excessive

sarcoidosis

scleroderma

scoliosis

scoliosis, neurologic association with

screening

sedation

segmental demyelination

seizure

sensorineural hearing loss

sensory loss

sensory symptoms

serologic testing

serologic testing of cerebrospinal fluid

serologic testing, false negative

serum alanine aminotransferase

shell fish poisoning

shoulder, subluxation

single photon emission computed tomography

skin, biopsy

skin, lesions in neurologic disorders

sleep

sleep apnea

sleep pathology and physiology

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, infarction of

spinal cord, injury of

spinal cord, ischemic lesion of

spinal cord, lesion of

spinal cord, neoplasm

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 degeneration

sports medicine, neurology of

standing difficulty

stem cell transplantation

stereotyped behavior

sternocleidomastoid muscle

stiff man syndrome

stuttering

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

subarachnoid hemorrhage

survival motor neuron gene

syphilis, neurologic complications with

temporal lobe, atrophy

temporalis muscle wasting

tensilon test

tensilon test, false positive

thalamus, lesion of-bilateral

Thies's sign

thoracic outlet syndromes

thyrotoxicosis

tick bite

tick paralysis

tick-borne encephalitis

Tolosa Hunt syndrome

tongue, atrophy

tongue, enlarged

tongue, fasciculations of

tongue, impaired movements of

treatment of neurologic disorder

tremor

tremor, intention

triangle of Guillain and Mollaret

tricresylphosphate

trigger finger

trinucleotide repeats

ulnar nerve, deep palmar branch of

ulnar neuropathy

unconsciousness

unconsciousness, episodic

unconsciousness, transient

upgaze, paralysis of

urea-cycle enzymopathies

vestibular function, tests of

Waldenstrom's macroglobulinemia

walking, difficulty with

weakness, generalized

weakness, infant

weakness, progressive

weakness, proximal

weaning from respirator, failure to

web sites

weight loss

Werdnig-Hoffman disease

West Nile fever

wheelchair

whistle, inability to

white matter disease

winging of scapula

word-finding difficulty

workup

xerostomia

X-linked bulbospinal neuronopathy

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