Neudle.com: rapid alternating movement

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

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

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 1800 to 1850 of 1887 << Previous Next >>

Computerized Axial Tomography-Use in the Dx. of Dementia
JAMA 234:754, Menzer,L.,et al, 1975

Oculogyric Crisis
In Ocular Differential Diagnosis, Lea & Febiger, Phila. 1975 p. 133, Roy,F.H., 1975

Internal Ophthalmoplegia, In Ocular Differential Diagnosis
Lea & Febiger, Phila. p 3375., Roy,F.H., 1975

Chronic Progressive Panencephalitis due to Rubella Virus Simulating Subacute Sclerosing Panencephalitis
NEJM 292:994-998,1023, Weil, M.L.,et al, 1975

Neuro Complica of Coeliac Disease & Trop Sprue, Neurology of GI Disease
1974, Major Problems in Neurology V-3, W. B. Saunders Co, Ltd., Pallis,C.A.&Lewis,P.D., 1974

Acquired Pendular Nystagmus with Oscillopsia in Multiple Sclerosis:A Sign of Cerebellar Nuclei Disease
JNNP 37:570, Aschoff,J.C.,et al, 1974

Case Records of MGH
NEJM 290:1130, 1974. Tuberculous Meningencephalitis with Vasculitis & Cerebral Infarcts., , 1974

Case Records of MGH
NEJM 290:1426, 1974. Neurofibromatosis, , 1974

Neuromuscular Disease in Primary Hyperparathyroidism
Ann Int Med 80:182, Patten,B.M.,et al, 1974

Dyskinesia After Fenfluramine
NEJM 291:422, Sananman,M., 1974

Pseudointernuclear Ophthalmoplegia in Acute Idiopathic Polyneuritis (Fisher's Syndrome)
Am J Ophthalmol 77:725, Swick,H.M., 1974

Facial Hyperkinesis
BMJ 626, Jun1974., , 1974

Neurologic Syndrome Associated with Antipsychotic Drug Use
NEJM 289:20, 1973, 290:110974., , 1974

Case Records of MGH
NEJM 288:674, Cerebral Abscess-Bacterial1973., , 1973

Neurologic Manifest. of Infective Endocarditis:A Review
Stroke 4:958, Greenlee,J.E.,et al, 1973

Clinical Neuropathological Conference
(Ed) , Dis Ner Sys 34:124, 1973, Pick's Disease., Aronson,S.&Aronson,B., 1973

Huntington's Disease in Children
Neurol 23:561, Byers,R.,et al, 1973

Tardive Dyskinesia Associated with Antipsychotic Drugs
FDA Drug Bulletin, May 1973., , 1973

Kinesiogenic Choreoathetosis & Idiopathic H Hypoparathyroidism
NEJM 286:762, 1972, 287 569973., Tabace-Zadeh,J.J.,et al, 1973

Case Records of MGH-NEJM 289:366
1973 Tuberculoma of Cerebral hemisphere & Brain Stem., , 1973

Neurologic Complications of Heroin Addiction
Bull NY Acad Sci 49:4, Ritcher,R.W.,et al, 1973

Anticholinergics
NEJM 288:1215, Greenblatt,D.J.,et al, 1973

Reserpine for Athetosis-Correspondence
NEJM 289:1375, Gordon,E., 1973

Impaired Peripheral Chemosensitivity & Acute Respiratiory Failure in Arnold-Chiari Malfor & Syringomyelia
NEJM 288:947, Bokinsky,G.E.,et al, 1973

Neurologic Manifestations of Rheumatic Fever
Postgrad Med 54:82, Aita,J.A., 1973

The Facioscapulohumeral Synd, in Clinical Studies in Myology, Amsterdam, Excerpta Medica
p498-501, VanWijngaarden,G.K.&Bethlem,J., 1973

Recent Advances in the Therapy of Thyroid Eye Disease
In Neuroophthalmology, C V Mosby Co, St. Louis, 6:1-102., Smith,J.L., 1972

Implications of Amphetamine-Induced Stereotyped Behavior as a Model for Tardive Dyskinesias
Arch Gen Psychiat 27:502-507, Rubovits,R.,et al, 1972

The EEG in Huntington's Chorea:A Clinical & Neuropathological Study
JNNP 35:97-102, Scott,D.F.,et al, 1972

Enlargement of the Sylvian Aqueduct:A Sequel of Head Injuries
JNNP 35:463-467, Boller,F.C.,et al, 1972

Thromboangiitis Obliterans Cerebri
Edited by, Vinken, E. , Handbook Clinical Neurol 12:3842., Bernsmeier,A.&Held,K., 1972

Use of L-Dopa in the Detection of Presymptomatic Huntington's Chorea
NEJM 286:1332, Klawans,H.,et al, 1972

Neurologic Manifestations of SLE 1972
Nebraska State Journ Med, Oct 1972, pp 395., Aita,J., 1972

Ocular Dyskinesia in Cerebellar Disease
Brain 95:685, Ellenberger,C.,et al, 1972

Neuropsychiatric Problems in SLE
BMJ 4:342, Bennett,R.,et al, 1972

Treatment of Sydenham's Chorea with Haloperidol
Neurol 22:418, Lansky,L., 1972

Benign Essential Tremor
Lancet 471, 1972 Sept., , 1972

Clinical Diagnosis of the Dyskinesias
Med Clin of North Am 56:1321, Duvoisin,R., 1972

Huntington's Disease-Newspaper Article-Boston Globe
May 7, 1972, , 1972

Huntington's Chorea, Effect of Serotonin Depletion
Arch Neurol 26:282, Chase,T.,et al, 1972

Presymptomatic Detection of Huntington's Chorea
BMJ 540, 1972 Sept., , 1972

Tapetoretinal Degeneration in Childhood Presenting as a Disturbance of Behavior
BMJ 202, 1972 Jan., Harcourt,B.,et al, 1972

Cholinergic & Dopaminergic Mechanisms in Huntington's Chorea
Life Sciences 10:405 1971., Aquilonius,S.,et al, 1971

Hemifacial Spasm
Arch Neurol 25:81, Eckman,P.,et al, 1971

Neurological Involvement in SLE
Singapore Med J 12:18, Tay,C.H.,et al, 1971

Drug-Induced Movement Disorders
Postgrad Med 180, 1971, Sept., North,R., 1971

Bilateral Traumatic Abducens Palsy
J Neurosurg 34:33, 1971, Schneider,R.,et al, 1971

Encephalomyelopathy of Leigh
Editorial BMJ 238, 1971, May., , 1971

Reversed Pupillary Reflexes, In System of Ophthalmology
the C. V. Mosby Co. , 1971, pp 690-691., Duke-Elder,S.&Scott,G.I.:Vol XII St.Louis, 1971

Diseases of the Extrapyramidal System
Disease-a-month-Jan 1970., Klawans,H.,et al, 1970

Showing articles 1800 to 1850 of 1887 << Previous Next >>