Neudle.com: alternating rapid movement impaired

Differential
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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

Showing articles 1500 to 1550 of 1850 << Previous Next >>

A Genetic Marker for Huntington's Chorea
BMJ 287:1567-1568, Harper,P.S., 1983

Developmental Learning Disabilities of the Right Hemisphere
Arch Neurol 40:463-468, Weintraub,S.,et al, 1983

Clin. Path. Conference
Pineocytoma, Case Record 35-1983, NEJM 309:542-549983., , 1983

Downbeat Nystagmus
Arch Neurol 40:754-755, Coppeto,J.R.,et al, 1983

Clinicopathological Conference
Case 49-1983, Creutzfeldt-Jakob, NEJM 309:1440-1449983., , 1983

Cauda Equina Syndrome Secondary to Long-Standing Ankylosing Spondylitis
Ann Neurol 14:662-669, Bartleson,J.D.,et al, 1983

Syndromes of Amytrophic Lateral Sclerosis & Dementia:Relation to Transmissible Creutzfeldt-Jakob Disease
Ann Neurol 14:17-26, Salazar,A.M.,et al, 1983

Chorea Caused by Caudate Infarction
Arch Neurol 40:590-591, Saris,S., 1983

Chorea in Long-Term Use of Pemoline
Ann Neurol 13:218, Singh,B.K.,et al, 1983

Huntington's Chorea:Neglected Opportunities for Preventive Medicine
Lancet 1:634-636, Martindale,B.,et al, 1983

Maternal Transmission in Huntington's Disease
Lancet 1:208-210, Myers,R.H.,et al, 1983

Progressive Supranuclear Palsy:Clinical Features & Response to Treatment in 16 Patients
Ann Neurol 13:273-278, Jackson,J.A.,et al, 1983

Nuclear Magnetic Resonance Imaging in Movement Disorders
Ann Neurol 13:690-691, Lukes,S.A.,et al, 1983

Edentulous Orodyskinesia
Ann Neurol 13:97-99, Koller,W.C., 1983

Parkinson's Disease in a Chemist Working with l-Methyl-4-Phenyl-1, 2, 5, 6-Tetrahydropyridine
NEJM 309:310, Langston,J.W.,et al, 1983

Blepharospasm & Orofacial-Cervical Dystonia:Clinical & Pharmacological Findings in 100 Patients
Ann Neurol 13:402-411, Jankovic,J.,et al, 1983

Eye Movements in Friedreich's Ataxia
Arch Neurol 40:343-346, Furman,J.M.,et al, 1983

Permanent Neurological Deficits Due to Lithium Toxicity
Ann Neurol 13:453-455, Apte,S.N.,et al, 1983

Three Cases of Lumbar Disc Rupture & One of Cauda Equina Associated with Spinal Manipulation (Chiropraxis)
Lancet 1:411, Gallinaro,P., 1983

Supranuclear Gaze Palsy in Familial Creutzfeldt-Jakob Disease
Arch Neurol 40:618-622, Bertoni,J.M.,et al, 1983

Carpal Tunnel Syndrome, Complication of Toxic Shock Syndrome
Arch Neurol 40:414-415, Sahs,A.L.,et al, 1983

The One- & -A-Half Syndrome-A Unilateral Disorder of the Pontine Tegmentum:A Study of 20 Cases & Review of the Liter
Neurol 33:971-980, Wall,M.,et al, 1983

Clin. Path. Conference
Multiple-System Atrophy with Parkinsonism, Case 28-13, NEJM 308:1406-1414983., , 1983

Positron Computed Tomography for Studies of Myocardial & Cerebral Function
Ann Int Med 98:339-359, Phelps,M.E.,et al, 1983

Toxic Neurological Reaction to Lithium/Thioridazine
Lancet 1:771, Standish-Barry,H.M.A.S.,et al, 1983

Two Spinal Cord Lesions in a Patient With Ankylosing Spondylitis & Cervical Spine Injury
Neurol 33:245-249, Foo,D.,et al, 1983

The Lateralizing & Localizing Value of Adversion in Epileptic Seizures
Neurol 33:1241-1242, Robillard,A.,et al, 1983

Choreoathetosis and Seizures Associated with Systemic Lupus Erythematosus - A Case Report
Singapore Med J 24:56-58, Chew, S.K.,et al, 1983

Delayed-onset Posthemiplegic Dystonia:CT Demonstration of Basal Ganglia Pathology
Neurol 32:1033-1035, Grimes,J.D.,et al, 1982

Tardive Dystonia:Late-onset & Persistent Dystonia Caused by Antipsychotic Drugs
Neurol 32:1335-1346, Burke,R.E.,et al, 1982

Neuroleptics & Abnormal Movements
BMJ 285:463-464, Lader,M.H., 1982

Electro-oculographic Findings in Machado-Joseph Disease
Neurol 32:1272-1276, Dawson,D.M.,et al, 1982

Estrogen Treatment of Dyskinetic Disorders
Neurol 32:547-549, Koller,W.C.,et al, 1982

Cauda Equina Syndrome Caused By Chiropraxis On A Patient Previously Free Of Lumbar Spine Symptoms
Lancet 2:986-987, Malmivaara,A.,et al, 1982

Choreoathetosis in an Infant With Tuberculous Meningitis
Arch Neurol 39:596, Riela,A.,et al, 1982

Chorea after Legionnaire's Disease
BMJ 284:1232-1233, Fraser,D.W.,et al, 1982

Inclusion Body Myositis
Arch Neurol 39:760-764, Danon,M.J.,et al, 1982

Peripheral Neuropathy & Starvation After Gastric Partitioning for Morbid Obesity
Ann Int Med 96:453-455, Feit,H.,et al, 1982

Clinical Features of Ciguatera Fish Poisoning, A Study of the Disease in the US Virgin Islands
Jr. , et al, Arch Int Med 142:1090-109282., Morris,J.G., 1982

Methanol Optic Neuropathy:A Histopathological Study
Neurol 32:1093-1100, Sharpe,J.A.,et al, 1982

Amitriptyline:Another Cause of Internuclear Ophthalmoplegia with Coma, Letter
Ann Neurol 12:62, Hotson,J.R.,et al, 1982

Vertical Supranuclear Gaze Palsy with Secondary Syphilis
JNNP 45:86-88, Page,N.G.R.,et al, 1982

Chronic Orbital Myositis
Arch Ophthalmol 100:1749-1751, Bullen,C.L.,et al, 1982

Neuro-ophthalmic Signs & Symptoms of Hysteria
Neurol 32:757-762, Keane,J.R., 1982

Drug-induced Asterixis in Parkinson Disease
Neurol 32:553-555, Glantz,R.,et al, 1982

Neuroaxonal Dystrophy in Young Adults:A Clinicopathological Study of Two Unrelated Cases
Ann Neurol 11:335-343, Williamson,K.,et al, 1982

Lithium Therapy in Torsion Dystonia
Ann Neurol 11:106-107, Marti-Masso,J.F.,et al, 1982

Occipitoatlantal Instability & Vertebrobasilar Ischemia:Case Report
Neurol 32:303-305, Coria,F.,et al, 1982

Progressive Dyskinesia Due to Internal Cerebral Vein Thrombosis
Neurol 32:769-772, Solomon,G.E.,et al, 1982

Episodic Dyskinesias & Transient Cerebral Ischemia
Neurol 32:1379-1380, Margolin,D.I.,et al, 1982

Showing articles 1500 to 1550 of 1850 << Previous Next >>