Neudle.com: alternating rapid movement

Differential
(Click to cross reference)

abscess, intracerebral

abscess, intracerebral, multiple

achilles tendon, enlarged

acute ataxia of childhood

acute cerebellar ataxia

adolescent medicine

adult-onset leukodystrophy, with neuroaxonal spheroids

advances in neurology

adverse drug reaction

alternating hemiplegia

alternating hemiplegia of childhood

alternating rapid movement

alternating rapid movement, impaired

Alzheimer's disease, misdiagnosis

amphetamines

amyotrophic lateral sclerosis

anemia

angiography, cerebral

ataxia telangiectasia

autoimmune cerebellar ataxia

autoimmune disease

autoimmune encephalopathy

automatic behavior

automobile accidents

autonomic dysfunction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavioral disorder

Benedikt's syndrome

biologic markers

bovine spongiform encephalopathy

carbon monoxide poisoning

carcinoma

carcinoma of breast

CAT scan, abnormal

CAT scan, angiography

CAT scan, angiography, false negative

CAT scan, emission, abnormal

cauda equina, enhancement

caudate nucleus, lesion of, bilateral

central nervous system, infection of

cerebellar ataxia, autosomal recessive

cerebellar ataxia, hereditary

cerebellar ataxia, neuropathy and vestibular areflexia syndrome

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar cognitive affective syndrome

cerebellar degeneration

cerebellar lesion

cerebellitis

cerebellitis, autoimmune

cerebellum, disease of

cerebral cortex

cerebral cortical atrophy

cerebral edema

cerebrospinal fluid, abnormal

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, protein of

cerebrovascular accident, mimics

chromosomal abnormality

cingulate island sign

Claude's syndrome

Clinical Pathologic Conference(C.P.C.)

controversies in neurology

conversion reaction

corpus callosum, lesion of

cough

cranial nerve enhancement

cranial neuropathy

cranial neuropathy, multiple

Creutzfeldt-Jakob disease, genetic

crying, pathologic

cystatin C mutation

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

delusion

dementia

dementia, age at onset

dementia, familial

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

dementia, reversible

dementia, thalamic

dementia, transmissible

dementia, treatment of

depression

developmental retardation

differential diagnosis

difficulty climbing stairs

diplopia

disability, neurological

dizziness

dopa responsive dystonia

down-beat nystagmus

DPPX

DPPX, antibodies, encephalitis

driving

drooling

drowsiness

dural arteriovenous malformation

electroencephalogram, periodic complexes

electromyogram

encephalitis

encephalitis, acanthamoeba

encephalitis, amebic

encephalitis, autoimmune

encephalomyelitis, postinfectious

encephalopathy

encephalopathy, delayed

encephalopathy, progressive

enolase

epidemiology of neurology

episodic disorders

episodic neurologic deficits

episodic unconsciousness

Epstein-Barr virus

Erdheim-Chester disease

escherichia coli

esophageal varices

executive dysfunction

exercise intolerance

eye movement, disorders of

facial expression abnormality

faciobrachial dystonic seizure

fatal familial insomnia

fatigue

fever

fine motor function, impaired

finger nose finger test

finger numbness

fingerprint bodies

Fisher C.M.

fistula, arterio-venous, dural

frontal lobe, anatomy and physiology

frontal lobe, atrophy

frontotemporal dementia, behavioral variant

gait disorder

gait, festinating

gamma amino butyric acid

gammaglobulin therapy, intravenous

gaze palsy, horizontal

gene

gene mutation

genetic counselling

genetic neurologic disorders

genetic testing

genu of corpus callosum

granular osmiphilic material

growth hormone

gyrus, abnormal

hallucination

hallucination, hypnagogic

hallucination, visual

hepatic encephalopathy

hepatic failure

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), presymptomatic

heralding manifestation

herniation syndromes, intracranial

hypersomnia, idiopathic

iatrogenic neurologic disorders

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, intranuclear

incontinence, fecal

incoordination

infectious mononucleosis

infectious mononucleosis, neurologic findings with

inferior olivary nucleus

insight, loss

insomnia

intellectual deficit

intellectual deterioration

intracranial hypertension, benign

intracranial pressure, increased

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Jakob-Creutzfeldt disease, variant

Jakob-Creutzfeldt disease, young adult

Kayser-Fleischer ring

leg weakness, bilateral

lesions too numerous to count

leucine rich glioma inactivated 1 antibodies

leukocytosis

leukodystrophy

leukoencephalopathy

leukoencephalopathy, adult onset, sporadic

leukopenia

Lewy body

Lewy body disease, diffuse

limbic encephalitis

liver disease

liver function enzymes

lobar atrophy

logopenia

lumbar puncture, complications of

lymphoma

lymphoma involving CNS

lymphoma, primary of CNS

masked facies

MELAS syndrome

memory, defect of recent

memory, impairment of

meningeal enhancement

meningitis

meningitis, acinetobacter calcoaceticus var.antitratus

meningitis, carcinomatous

meningoencephalitis

meningoencephalitis, amoebic

mental status, abnormal

microcephaly

microhemorrhage, intracerebral

midbrain

midbrain, atrophy

midbrain, infarction of

midbrain, lesion of

middle cerebellar peduncle, lesion

migraine

mild cognitive impairment

mimics

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

modafinil

molecular genetics

monoclonal antibodies

mood change

mortality

motor neuron disease

motor neuron disease, misdiagnosis

movement disorder

movement disorder, extrapyramidal

movement disorder, hyperkinetic

MRI

MRI, abnormal

MRI, angiography

MRI, angiography, false negative

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, punctate pattern

MRI, venography

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple sleep latency test

multiple system atrophy

muscle biopsy

muscle weakness, proximal

mutism

myasthenia gravis

myelinolysis, extrapontine

myopathy, mitochondrial

myxedema, neurologic manifestations of

narcolepsy

nausea and vomiting

negative

nerve conduction studies

nerve root biopsy

neuroaxonal dystrophy

neuroaxonal leukodystrophy

neuroleptic

neuroleptic sensitivity

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic examination, focal

neurologic signs

neuron specific enolase

neuronal ceroid-lipofuscinosis

neuronal intranuclear inclusion disease

neuronal loss

neuronopathy, sensory

neuropathology

neuropathology, brain

neuropathy

neuropathy, sensory

next-generation sequencing

night sweats

Nothnagel's syndrome

numbness, generalized

nutritional deficiency

nystagmus

nystagmus, monocular

nystagmus, primary position of gaze

old age, neurology of

olivary degeneration, hypertrophic

ophthalmoplegia

ophthalmoplegia, progressive external

opportunistic infection

opportunistic infection, CNS

optic atrophy

orthostatic hypotension

osmotic demyelination syndrome

otitis, neurologic complications with

palatal myoclonus

paraneoplastic cerebellar degeneration

parasitic infection

parasitic infection, CNS

paresthesias

paresthesias, hands

parietal lobe, atrophy

Parkinson disease

Parkinson disease, dementia with

Parkinson disease, dystonia with

Parkinson disease, juvenile

Parkinson disease, L-dopa nonresponsive

Parkinson disease, nonmotor problems of

Parkinson disease, presymptomatic detection

Parkinsonism syndrome

paroxysmal hemiplegia

paroxysmal neurologic deficits

PAS positive

PAS positive material in the brain

pituitary, hormones of

pleocytosis of cerebrospinal fluid

pleocytosis of cerebrospinal fluid, neutrophilic

POLG1 gene

polymerase chain reaction

polyneuropathy, chronic inflammatory demyelinating

polysomnogram

pons, lesion of

positional head-hanging test

post infectious cerebellar ataxia

posterior cortical atrophy

postinfectious

postural abnormality

potassium channel antibodies

practice guidelines

precipitating factors

pregnancy, neurologic complications in

prion disease

PRKN gene

prognosis

progressive ataxia and palatal tremor

progressive neurologic disorder

protein 14-3-3, cerebrospinal fluid

protein 14-3-3, cerebrospinal fluid, false negative

psychiatric problems in neurologic disorders

psychomotor retardation

pupil, dilated and fixed, bilateral

pursuit eye movements, abnormal

rapid onset dystonia parkinsonism

rapidly fatal neurologic illness

rapidly progressing neurologic illness

reading disorder, acquired

real-time quaking-induced conversion

recurrent

regional cerebral blood flow

rehabilitation for neurologic disorders

release phenomena

REM sleep

REM sleep behavior disorder

remote effect of cancer on the nervous system

saccadic eye movements, abnormal

safety

salivation, excessive

sarcoidosis

schizophrenia

seizure

seizure, psychomotor-temporal lobe

selective serotonin reuptake inhibitors

sensorineural hearing loss

single photon emission computed tomography

sleep

sleep apnea

sleep offset paralysis

sleep onset paralysis

sleep paralysis

sleep pathology and physiology

slit lamp examination

speech disorder, non aphasic

spinocerebellar ataxia

spinocerebellar ataxia type 7

splenomegaly

spongy degeneration of brain

spontaneous remission

storage disease of CNS

symmetric brain lesions

temporal lobe, atrophy

temporal lobe, lesion

temporal lobe, lesion, bilateral

thalamus, lesion of

thalamus, lesion of-bilateral

third nerve palsy

third nerve palsy, bilateral

thrombocytopenia

titubation

tongue, fasciculations of

tonic foot response

treatment of neurologic disorder

trientine dihydrochloride

trinucleotide repeats

uncal herniation

unconsciousness

unconsciousness, episodic

unconsciousness, transient

vibratory sensation, abnormal

viral infection

viral infection, CNS

vision, blurred

visual acuity, decreased

visuospatial disturbance

voice, abnormality of

walking frame

walking, difficulty with

walking, difficulty with in dark

weakness

weakness, generalized

weakness, progressive

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