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acquired immunodeficiency syndrome

adolescent medicine

adverse drug reaction

akinesia of eyelid function

alcohol, neurologic complications with

alien hand syndrome

alpha-fetoprotein

alternating hemiplegia

alternating hemiplegia of childhood

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, Parkinson-dementia-complex

anticardiolipin antibodies

anticonvulsants, untoward effects of

antiphospholipid antibody syndrome

aphasia, progressive, primary

apraxia of eye movements

apraxia of eyelid opening

ataxia telangiectasia

ataxia, cerebellar

ataxia, hereditary

ataxia, progressive

ataxia, truncal

autoimmune basal ganglia encephalitis

autoimmune cerebellar ataxia

autoimmune disease

autoimmune encephalopathy

autonomic dysfunction

B 12 deficiency

bacterial infection

basal ganglia, lesion of

basal ganglia, lesion, bilateral

benign essential tremor

bent spine syndrome

bilirubin encephalopathy

biologic markers

biotin deficiency

biotin deficiency, juvenile form

biotin-responsive basal ganglia disease

blinking, reduced

bone marrow transplantation

botulinum toxin

botulinum toxin, complications of

bradykinesia, facial

brainstem, infarction of

brainstem, lesion of

Brueghel's syndrome

carcinoembryonic antigen

carcinoma of breast

carotid artery disease

carotid artery occlusion, neck

carotid artery stenosis

CAT scan, abnormal

CAT scan, chest

CAT scan, muscle

caudate nucleus, atrophy

central nervous system, infection of

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar lesion

cerebellitis, autoimmune

cerebellum, disease of

cerebral cortex

cerebral hypoperfusion

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, enzymes in

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, oligoclonal IgG in

cerebrovascular accident

cerebrovascular accident, multiple

cerebrovascular accident, three territory involvement

chewing movements

choreoathetosis

choreoathetosis, paroxysmal

chromosomal abnormality

chronic progressive external ophthalmoplegia

Clinical Pathologic Conference(C.P.C.)

cogwheel rigidty

collagen vascular disease

congenital infection, CNS

contractures, joint

controversies in neurology

conversion reaction

corpus callosum, thinning

cortical-basal ganglionic degeneration

cost effectiveness

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

dementia, reversible

dementia, subcortical

dementia, treatment of

developmental milestones, loss of

developmental retardation

diabetes insipidus

diabetes mellitus

diagnostic criteria

differential diagnosis

distal muscle atrophy

dopa responsive dystonia

DPPX, antibodies, encephalitis

drug abuse, neurologic complications of

dysdiadochokinesia

dyskinesia, buccal lingual facial

dystonia, cervical

dystonia, children

dystonia, drug induced

dystonia, focal

dystonia, painful

dystonia, treatment of

electroencephalogram, abnormalities of

encephalitis, autoimmune

encephalitis, episodic

encephalitis, paraneoplastic

encephalitis, viral

encephalomyelitis

encephalopathy, neonatal

encephalopathy, progressive

endarterectomy, carotid

epidemiology of neurology

episodic neurologic deficits

evidence-based research

exercise intolerance

exome sequencing

extralimbic encephalitis

extrapyramidal movement disorder, progressive

eye movement, disorders of

facial appearance, abnormal

facial expression abnormality

facial movement disorder

facial nerve palsy

fatal familial insomnia

fluorescent treponema antibody absorption/false positive

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

frontal behavioral spatial syndrome

frontal lobe, anatomy and physiology

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

gaze palsy, supranuclear

gaze palsy, vertical

genetic counselling

genetic linkage

genetic neurologic disorders

genetic testing

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glutamic acid decarboxylase, antibody

granulomatous disease

growth retardation

Guillain Barre syndrome

gyrus, abnormal

Hallervorden Spatz disease

Hallervorden Spatz disease, late onset

hallucination, visual

hemifacial spasm

hepatic failure

hepatolenticular degeneration, non-Wilsonian

hepatosplenomegaly

heralding manifestation

hippocampus, hyperintense

Horner's syndrome

human immunodeficiency virus type 1

Huntington's chorea

Huntington's disease, children

hyperammonemic encephalopathy

hyperbilirubinemia

hyperbilirubinemia, CNS abnormality after

hypocomplementemia

hypothalamus, disturbance of

hypoxic encephalopathy

imbalance, postural

immunocompetent

immunodeficiency

immunomodulation

immunosuppression

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intranuclear

intellectual deficit

intellectual deterioration

internal capsule

intracranial hypertension, benign

Isaacs syndrome

Jakob-Creutzfeldt disease

jaw jerk, abnormal

leg spasms, painful

lenticular nucleus, lesion of, bilateral

leukoencephalopathy

Lewy body disease, diffuse

lid abnormalities

limbic encephalitis

lymphadenopathy, hilar

manganese intoxication

marche a petits pas

mediastinum, mass of

memory, defect of recent

memory, impairment of

meningitis, aseptic

meningitis, carcinomatous

mental retardation

mental status, abnormal

metabolic acidosis

metabolic disorder, primary

methylmalonic acidemia

midbrain, atrophy

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

Mini Mental Status Examination

mitochondrial disease

mitochondrial disease, pathogenesis

molecular genetics

movement disorder

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, hyperkinetic

movement disorder, paroxysmal

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, eye of tiger sign

MRI, false negative

MRI, gradient-echo

MRI, high signal intensity of basal ganglia

MRI, paramagnetic effect

MRI, susceptibility weighted

MRI, T1 weighted high signal foci

multiple sclerosis

multiple system atrophy

muscle stiffness

muscle weakness

muscular dystrophy

myasthenia gravis

myelopathy, hepatic

myoclonic jerks

myoclonus, cortical

myoclonus, epilepsy

myoclonus, segmental

myopathy, metabolic

nausea and vomiting

neurocutaneous disease

neurodegeneration with brain iron accumulation

neuroendocrinology

neurologic complications of, systemic disease

neurologic consultation

neurologic disease

neurologic disease, diagnoses of

neurologic disease, multifocal

neurologic disease, tempo

neurologic signs

neuron specific enolase

neuronal intranuclear inclusion disease

neuronopathy, sensory

neuroophthalmology

neuropathology, brain

neuropathy, peripheral

next-generation sequencing

nutritional deficiency

nystagmus, gaze-evoked

nystagmus, monocular

ocular motility, disorders of

ocular myopathy

ocular myopathy, differential diagnosis

oculomasticatory myorhythmia

old age, neurology of

ophthalmoplegia

ophthalmoplegia, progressive external

orthostatic hypotension

paraparesis, spastic

paraspinal muscle

paraspinal muscle weakness

parenteral alimentation

Parkinson disease

Parkinson disease, arteriosclerotic

Parkinson disease, atypical

Parkinson disease, dementia with

Parkinson disease, diagnosis

Parkinson disease, differential diagnosis of

Parkinson disease, drug induced

Parkinson disease, dystonia with

Parkinson disease, juvenile

Parkinson disease, L-dopa nonresponsive

Parkinson disease, misdiagnosis

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

Parkinsonism, freezing phenomena in

paroxysmal hemiplegia

paroxysmal neurologic deficits

PAS positive material in the brain

peripheral nerve, lesion of

personality change

pigmentary retinopathy

pituitary, lesion of

pleocytosis of cerebrospinal fluid

polymerase chain reaction

portal caval shunt

posterior inferior cerebellar artery syndrome

postural abnormality

precipitating factors

premature infant

prevention of neurologic disorders

progressive multifocal leucoencephalopathy

progressive neurologic disorder

progressive supranuclear palsy

prolactin, elevated

protein 14-3-3, cerebrospinal fluid

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

pseudobulbar palsy

psychiatric disorder

psychiatric problems in neurologic disorders

psychomotor retardation

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

radiation hypersensitivity

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

reading disorder, acquired

reading problem, causes of

remote effect of cancer on the nervous system

retinitis pigmentosa

rigidity, axial

rubella encephalitis, progressive

rubella syndrome

saccadic eye movements

saccadic eye movements, abnormal

sarcoidosis, CNS

sea-blue histiocytes

sensorineural hearing loss

serologic testing

serologic testing of cerebrospinal fluid

skin, lesions in neurologic disorders

skull x-ray, abnormal

sleep pathology and physiology

slow virus infection of CNS

spastic dysphonia

speech disorder

speech disorder, childhood

spinal cord, lesion of

spinal muscular atrophy

spinocerebellar ataxia

spinocerebellar ataxia type 2

spongy degeneration of brain

standing difficulty

startle reaction

status epilepticus

status epilepticus, intractable

steroid therapy, CNS treatment and complications with

stiff limb syndrome

stiff man syndrome

stimulant drugs

stooped posture

striatum, lesion of

striatum, lesion of, bilateral

strokelike episodes

subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease

subarachnoid hemorrhage

substantia nigra

subthalamic nucleus

symmetric brain lesions

synucleinopathy

systemic illness

systemic lupus erythematosus

systemic lupus erythematosus, neurologic complications with

tandem gait, ataxic

temporal lobe, lesion

temporal lobe, lesion, bilateral

thalamus, lesion of

thalamus, lesion of-bilateral

Three territory sign

thrombophlebitis

tonic foot response

transient ischemic attack

transient ischemic attack, limb shaking

transient neurologic deficit

treatment of neurologic disorder

tremor, intention

tremor, postural

tremor, writing

trigeminal neuropathy

trinucleotide repeats

tyrosine hydroxylase deficiency

unconsciousness

unconsciousness, transient

viral infection

viral infection, CNS

visual evoked response

visual impairment

vitamin deficiency

walking, difficulty with

weakness, generalized

weakness, progressive

Whipple's disease

white matter disease

wide based gait

Showing articles 650 to 700 of 17967 << Previous Next >>

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

Treatment of Hyperkinetic Movement Disorders with Tetrabenazine:A Double-blind Crossover Study
Ann Neurol 11:41-47, Jankovic,J., 1982

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

Movement Disorders of Familial Neuroacanthocytosis Syndrome
Arch Neurol 39:298-301, Yamamoto,T.,et al, 1982

Neurotransmitters & CNS Disease, Basal Ganglia Disease
Lancet 2:1141-1147, Marsden,C.D., 1982

Acute Akathisia After Oral Droperidol & Metoclopramide Preoperative Medication
Lancet 2:48-49, Barnes,T.R.E.,et al, 1982

Metoclopramide-Induced Parkinsonism
Arch Neurol 39:494-496, Indo,T.,et al, 1982

A Danger In Making The Diagnosis Of Parkinson's Disease
Lancet 1:1212-1213, Murdoch,P.S.,et al, 1982

Reversible Drug-Induced Parkinsonism
Arch Neurol 39:644-646, Rajput,A.H.,et al, 1982

Extrapyramidal Side-Effects Of Metoclopramide
Lancet 2:1254-1255, Kataria,M.,et al, 1981

Parkinsonism & Tardive Dyskinesia Associated With Long-Term Metoclopramide Therapy
NEJM 305:1417, Grimes,J.D., 1981

Meige Syndrome (blepharospasm-oromandibular Dystonia) after Long-term Neuroleptic Therapy
Neurol 31:1555-1556, Weiner,W.J.,et al, 1981

Biochemical Evidence Of Dysfunction Of Brain Neurotransmitters In The Lesch-Nyhan Syndrome
NEJM 305:1106-1111, Lloyd,K.G.,et al, 1981

Tetrabenazine & Movement Disorders
Neurol 31:1051-1054, Asher,S.W., 1981

Tardive Dyskinesia
Editorial, BMJ 282:1257-12581981., , 1981

Depression-Dependent Dyskinesias In Two Cases Of Manic-Depressive Illness
NEJM 304:1088-1089, Cutler,N.R.,et al, 1981

Dystonia With Droperidol Therapy
NEJM 305:227, Arrowsmith,J.,et al, 1981

Tardive Dyskinesia and Abnormal Tongue Movements
Br J Psych 139:526-528, Pi,E.H.&Simpson,G.M., 1981

Delayed-onset Dystonia in Patients with"Static"Encephalopathy
JNNP 43:789-797, Burke,R.E.,et al, 1980

A Family with Hereditary Ataxia:HLA Typing
Neurol 30:12-20, Nino,H.E.,et al, 1980

Amyloid Neuropathy & Tremor in Waldenstrom's Macroglobulinemia
Arch Neurol 37:240-242, Bajada,S.,et al, 1980

Haloperidol-Induced Tardive Dyskinesia in a Child With Gilles de la Tourette's Disease
Arch Neurol 37:780, Mizrahi,E.M.,et al, 1980

Facial Dyskinesia From Overdose Of An Anti-histamine
NEJM 303:107, Barone,D.A.,et al, 1980

Methanol Poisoning:A Clinical & Pathological Study
Ann Neurol 8:161-167, McLean,D.R.,et al, 1980

Carbamazepine-induced Orofacial Dyskinesia
Neurol 30:1333-1334, Joyce,R.P.,et al, 1980

Nervous System Toxicity of Chemo Agents
Young, DF, in Vinken PJ, Bruyn GW, Handbook of Clin Neurol, North-Holland Publ Co, Amster, Vol 39, 1, 80, p 104, 1980

Exacerbation of Parkinsonism by Methyldopa
JAMA 244:2727-2728, Rosenblum,A.M.&Montgomery,E.B., 1980

Myotonic Dystrophy
In Harrison's Principles of Internal Medicine, 9th Ed, McGraw-Hill Book Co, NY 206180., Adams,R.D.,et al, 1980

Tardive Dyskinesia
Editorial, BMJ 2:13131979., , 1979

Neurology:An Annotated Bibliography of Recent Literature
Ann Int Med 91:658-663, , 1979

Poliomyelitis & Parkinsonism
NEJM 298:688, Vincent,F.M.,et al, 1978

Onset & End-of-dose Levodopa-induced Dyskinesias
Arch Neurol 35:261, Lhermitte,F.,et al, 1978

Normal Pressure Hydrocephalus, Recog & Relation to Neuro Abnormalities in Cockayne's Sydrome
Arch Neurol 35:337, Brumback,R.A.,et al, 1978

Celiac Sprue & Refractory Sprue
Gastroenter. 75:3071978., Trier,J.S.,et al, 1978

Tics & Tourette's:A Continuum of Symptoms
Ann Neurol 4:145-148, Golden,G.S., 1978

Familial Chorea & Myoclonus Epilepsy
Neurol 28:913-919, Takahata,N.,et al, 1978

Juvenile Amaurotic Idiocy (Neuronal Ceroid Lipofuscinosis) & Lymphocyte Fingerprint Profiles
Ann Neurol 4:531-536, Baumann,R.J.,et al, 1978

Corticosteroids in the Treatment of Sydenham's Chorea
Arch Neurol 35:53, Green,L.N., 1978

Respiratory Dyskinesias:Extrapyramidal Dysfunction & Dyspnea
Ann Int Med 88:327, Weiner,W.J.,et al, 1978

Aggravation of Tardive Dyskinesia by Phenytoin
NEJM 298:457, DeVeaugh-Geiss,J., 1978

Lecithin Can Suppress Tardive Dyskinesia
NEJM 298:1029, Growdon,J.H.,et al, 1978

Phenyton & Choreic Movements
NEJM 298:1093, Nausieda,P.A.,et al, 1978

Bilateral Ballismus in Phenytoin Intoxication
Ann Neurol 3:186, Opida,C.L.,et al, 1978

Apomorphine Hydrochloride-Induced Improvement in Huntington's Chorea
Arch Neurol 35:27, Corsini,G.U.,et al, 1978

Familial Paroxysmal Dystonic Choreoathetosis & its Differentiation From Related Syndromes
Ann Neurol 2:285, Lance,J.W., 1977

Oral Choline Administration to Patients with Tardive Dyskinesia
NEJM 297:524, Growdon,J.H.,et al, 1977

Hereditary Chorea Without Dementia
JNNP 40:687, Behan,P.O.,et al, 1977

Paroxysmal Choreoathetosis as a Presenting Symptom in Idiopathic Hypoparathyroidism
JNNP 40:692, Soffer,D.,et al, 1977

Showing articles 650 to 700 of 17967 << Previous Next >>