Neudle.com: rapid alternating 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

autosomal dominant leukodystrophy

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

celiac disease, adult

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

cortical ribbon sign

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

gluten ataxia

gluten sensitivity

gluten-free diet

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

middle cerebellar peduncle, lesion, bilateral

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

myoclonus, stimulus sensitive

myoclonus-ataxia syndrome

myopathy

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

ocular dysmetria

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 1450 to 1500 of 1870 << Previous Next >>

Hypertensive Putaminal Hemorrhage Presenting with Hemichorea
Stroke 16:130-131, Jones,H.R.,et al, 1985

Reversible Parkinsonism Related to Meperidine
NEJM 312:509, Lieberman,A.N.,et al, 1985

Tetrabenazine Induces Acute Dystonic Reactions
Ann Neurol 17:200-202, Burke,R.E.,et al, 1985

Diaphragmatic Paralysis Following Chiropractic Manipulation of the Cervical Spine
Arch Int Med 145:562-564, Heffner,J.E., 1985

Acute Exacerbation of Parkinson's Disease with Sulindac
Ann Neurol 17:104-105, Sandyk,R.,et al, 1985

Spinal Cord Degeneration in AIDS
Neurol 35:103-106, Goldstick,L.,et al, 1985

Delayed Choreoathetosis Following Acute Carbon Monoxide Poisoning
Neurol 35:98-99, Schwartz,A.,et al, 1985

Clin. Path. Conference
External Ophthalmoplegia with Mitochondrial Myopathy, Case Record 3-1985, NEJM 312:171-177985., , 1985

"Apraxia"of Eyelid Opening:An Involuntary Levator Inhibition
Neurol 35:423-427, Lepore,F.E.,et al, 1985

Persistent Rheumatic Chorea
Neurol 35:101-102, Gibb,W.R.G.,et al, 1985

Wernicke's Encephalopathy
NEJM 312:1035-1039, Reuler,J.B.,et al, 1985

Cerebral Lateralization, Biological Mechanisms, Associations, & Pathology:II
Arch Neurol 42:521-552, Geschwind,N.&Galaburda,A.M., 1985

Limb Shaking-A Carotid TIA
Stroke 16:444-448, Baquis,G.D.,et al, 1985

Repetitive Involuntary Movement Associated with Episodic Cerebral Ischemia
Ann Neurol 18:244-250, Yanagihara,T.,et al, 1985

The Syndrome of Posterior Thalamic Hemorrhage
Neurol 35:998-1002, Hirose,G.,et al, 1985

Generalized Chorea Due to Bilateral Small, Deep Cerebral Infarcts
Neurol 35:588-589, Tabaton,M.,et al, 1985

Acute Traumatic Midbrain Hemorrhage
Ann Neurol 18:80-86, Ropper,A.H.,et al, 1985

Non-Penetrating Arterial Trauma & Cerebral Infarction in the Young
Lancet 1:1435-1438, Hilton-Jones,D.,et al, 1985

The Gait Abnormality of Huntington's Disease
Neurol 35:1450-1454, Koller,W.C.&Trimble,J., 1985

Presymptomatic Testing for Huntington's Disease
JAMA 253:3286-3291, Bird,S.J., 1985

Genetic Prediction & Family Structure in Huntington's Chorea
BMJ 290:1929-1931, Harper,P.S.,et al, 1985

Atypical Presentation of Progressive Supranuclear Palsy
Ann Neurol 17:334-343, Davis,P.H.,et al, 1985

Olivopontocerebellar Atrophy with Dementia, Blindness, & Chorea, Response to Baclofen
Arch Neurol 42:757-758, Trauner,D.A., 1985

The Clinical Spectrum of Internuclear Ophthalmoplegia in Multiple Sclerosis
Arch Neurol 42:851-855, Muri,R.M.&Meienberg,O., 1985

The Clinical Syndrome of Striatal Dopamine Deficiency, Parkinsonism Induced by MPTP
NEJM 312:1418-1421, Burns,R.S.,et al, 1985

Permanent Human Parkinsonism Due to 1-Methyl-4-Phenyl-1, 2, 3, 6-Tetrahydropyridine (MPTP) :Seven Cases
Neurol 35:949-956, Ballard,P.A.,et al, 1985

Heterogeneity in Dementia of the Alzheimer Type:Evidence of Subgroups
Neurol 35:453-461, Mayeux,R.,et al, 1985

Vacuolar Myelopathy Pathologically Resembling Subacute Combined Degeneration in Patients with AIDS
NEJM 312:874-879, Petito,C.K.,et al, 1985

Clinicopathological Conference
Schistosoma Mansoni Infection (with Involvement of Spinal Cord) , Case 21-1985, NEJM 312:1376-13835., , 1985

Inflammatory Myopathies
Ann Neurol 17:215-227, 317-3231985., Mastaglia,F.L.,et al, 1985

Mirror Movement Asymmetries in Congenital Hemiparesis:The Inhibition Hypothesis Revisited
Neurol 35:1059-1062, Nass,R., 1985

Haemorrhagic Shock & Encephalopathy
Editorial, Lancet 2:534-5361985., , 1985

Does Head-Turning During a Seizure Have Lateralizing or Localizing Significance
Neurol 34:884-890, Ochs,R.,et al, 1984

Cervical Spondylotic Radiculo-Myelopathy in Patients with Athetoid-Dystonic Cerebral Palsy:Evaluation & Treatment
JNNP 47:775-780, Hirose,G.,et al, 1984

Conjugate Eye Deviation after Acute Hemispheric Stroke:Delayed Recovery after Previous Contralateral Damage
Ann Neurol 16:509-511, Steiner,I.,et al, 1984

Creutzfeldt-Jakob Disease of Long Duration:Clinicopathological Characteristics
Ann Neurol 16:295-304, Brown,P.,et al, 1984

Nystagmus in Motor Neuron Disease:Clinicopathological Study of Two Cases
Ann Neurol 16:71-77, Kushner,M.J.,et al, 1984

Extrapyramidal Signs in Alzheimer's Disease
Neurol 34:1114-1116, Molsa,P.K.,et al, 1984

Unusual Spontaneous Movements in Brain-Dead Patients
Neurol 34:1089-1092, Ropper,A.H., 1984

Neurologic Disorder of Vitamin E Deficiency in Acquired Intestinal Malabsorption
Neurol 34:1561-1565, Weder,B.,et al, 1984

Metoclopramide & Tardive Dyskinesia in the Elderly
BMJ 289:397-398, Orme,M.L., 1984

Increased Rate of Suicide Among Patients with Huntington's Disease
JNNP 47:1283-1287, Schoenfeld,M.,et al, 1984

Genetic Testing in Huntington's Disease
Ann Neurol 16:511-513, Koller,W.C.,et al, 1984

Phenobarbital-Induced Dyskinesia in a Neurologically Impaired Child
Neurol 34:1600-1601, Wiznitzer,M.,et al, 1984

Tardive Dyskinesia:Current Clinical Issues
Neurol 34:1348-1353, Burke,R.E., 1984

Involvement of Upper-Airway Muscles in Extrapyramidal Disorders
NEJM 311:438-442, Vincken,W.G.,et al, 1984

Drug-Induced Parkinsonism in the Elderly
Lancet 2:1082-1083, Stephen,P.J.,et al, 1984

Midbrain Paresis of Horizontal Gaze
Ann Neurol 16:495-504, Zackon,D.H.,et al, 1984

Ocular Dipping
Neurol 34:391-393, Stark,S.R.,et al, 1984

Bilateral Adie's Tonic Pupil with Anhidrosis & Hyperthermia
Arch Neurol 41:342-343, Spector,R.H.,et al, 1984

Showing articles 1450 to 1500 of 1870 << Previous Next >>