Neudle.com: extrapyramidal movement disorder progressive

Differential
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acanthocytosis

acquired immunodeficiency syndrome

adolescent medicine

adverse drug reaction

agitation

akathisia

akinesia of eyelid function

alcohol, neurologic complications with

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

aphasia, progressive, primary

apraxia

apraxia of eye movements

apraxia of eyelid opening

arbovirus

areflexia

ataxia

ataxia telangiectasia

autoimmune basal ganglia encephalitis

autoimmune cerebellar ataxia

autoimmune disease

autoimmune encephalopathy

autonomic dysfunction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavioral disorder

benign essential tremor

bent spine syndrome

bilirubin encephalopathy

biologic markers

biotin

biotin deficiency

biotin deficiency, juvenile form

biotin-responsive basal ganglia disease

bone marrow transplantation

botulinum toxin

botulinum toxin, complications of

brainstem, infarction of

carcinoembryonic antigen

carcinoma

carcinoma of breast

cardiomyopathy

carotid artery disease

carotid artery occlusion, neck

carotid artery stenosis

CAT scan

CAT scan, abnormal

CAT scan, chest

CAT scan, emission, abnormal

CAT scan, muscle

catalepsy

cataplexy

caudate nucleus, atrophy

celiac disease, adult

central nervous system, infection of

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar lesion

cerebellar vermis

cerebellitis, autoimmune

cerebellum, disease of

cerebral cortex

cerebral cortical atrophy

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

choreoathetosis, paroxysmal

chromosomal abnormality

chromosome 11

chromosome 20

chronic progressive external ophthalmoplegia

cirrhosis

Clinical Pathologic Conference(C.P.C.)

cognition

cogwheel rigidty

collagen vascular disease

concussion

confabulation

confusion

congenital infection, CNS

consanguinity

contractures, joint

controversies in neurology

conversion reaction

corpus callosum, thinning

cortical-basal ganglionic degeneration

cost

cost effectiveness

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

Cuba

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

dementia

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

dementia, reversible

dementia, subcortical

dementia, treatment of

Dengue fever

depression

developmental milestones, loss of

developmental retardation

differential diagnosis

difficulty climbing stairs

diplopia

disease modifying agents

disorientation

distal muscle atrophy

dopa responsive dystonia

DPPX

DPPX, antibodies, encephalitis

driving

drooling

drug abuse

drug abuse, neurologic complications of

dysarthria

dysdiadochokinesia

dyskinesia

dyskinesia, buccal lingual facial

dystonia, drug induced

dystonia, face

dystonia, focal

dystonia, painful

dystonia, treatment of

electroencephalogram, abnormalities of

electromyogram

encephalitis

encephalitis, autoimmune

encephalitis, episodic

encephalitis, paraneoplastic

encephalitis, viral

encephalomyelitis

encephalopathy

encephalopathy, neonatal

encephalopathy, progressive

endarterectomy, carotid

endemic area

enolase

enzyme, defect

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

fatal familial insomnia

fatigue

fever

fluctuate

fluorescent treponema antibody absorption/false positive

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

frontal behavioral spatial syndrome

frontal lobe, anatomy and physiology

gait disorder

gait speed

galactorrhea

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

gaze palsy

gaze palsy, supranuclear

genetic neurologic disorders

genetic testing

glabellar sign

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glutamic acid decarboxylase, antibody

gluten ataxia

gluten sensitivity

gluten-free diet

granulomatous disease

growth retardation

Guillain Barre syndrome

gyrus, abnormal

Hallervorden Spatz disease

Hallervorden Spatz disease, late onset

hallucination

hallucination, visual

hepatolenticular degeneration, non-Wilsonian

hepatomegaly

hepatosplenomegaly

heralding manifestation

hippocampus

hippocampus, hyperintense

Horner's syndrome

human immunodeficiency virus type 1

Huntington's chorea

Huntington's disease, children

hydrocephalus

hyperammonemic encephalopathy

hyperbilirubinemia

hyperbilirubinemia, CNS abnormality after

hypothalamus, disturbance of

hypothyroidism

hypotonia

hypoxia

hypoxic encephalopathy

inborn errors of metabolism

incidence

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intranuclear

intellectual deterioration

internal capsule

intracranial hypertension, benign

intravenous

iron, brain

Isaacs syndrome

Jakob-Creutzfeldt disease

lenticular nucleus, lesion of, bilateral

leukemia

leukoencephalopathy

Lewy body

Lewy body disease, diffuse

lid abnormalities

limbic encephalitis

lipid storage disorder of CNS

liver disease

lordosis

low back pain

lymphadenopathy, hilar

lymphoma

lysosomal storage disease

maculopathy

manganese intoxication

memory, defect of recent

memory, impairment of

meningitis

meningitis, aseptic

meningitis, carcinomatous

mental retardation

mental status, abnormal

metabolic acidosis

metabolic disorder, primary

methcathinone

methylmalonic acidemia

microcephaly

midbrain, atrophy

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

miglustat

migraine

mimics

Mini Mental Status Examination

misdiagnosis

mitochondrial disease

mitochondrial disease, pathogenesis

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, hyperkinetic

movement disorder, paroxysmal

MRI

MRI, abnormal

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, muscle

MRI, negative

MRI, paramagnetic effect

MRI, susceptibility weighted

MRI, T1 weighted high signal foci

MRS

multiple sclerosis

multiple system atrophy

muscle weakness, proximal

myoclonus, stimulus sensitive

myoclonus-ataxia syndrome

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

neuronopathy, sensory

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, peripheral

neurotoxic

neurotoxin

next-generation sequencing

Niemann-Pick disease

NOTCH2NLC

nutritional deficiency

nystagmus

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

optic atrophy

optic neuritis

orthostatic hypotension

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

PAS positive material in the brain

pathology

pericarditis

peripheral blood smear

peripheral nerve, lesion of

personality change

pigmentary retinopathy

pituitary, lesion of

pleocytosis of cerebrospinal fluid

POLG1 gene

polymerase chain reaction

polyneuropathy

portal caval shunt

posterior inferior cerebellar artery syndrome

postural abnormality

precipitating factors

preclinical

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

proteinopathy

pseudobulbar palsy

psychiatric disorder

psychiatric problems in neurologic disorders

psychomotor retardation

psychosis

ptosis

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

recurrent

remote effect of cancer on the nervous system

rubella encephalitis, progressive

rubella syndrome

rubella virus

Russia

saccadic eye movements

saccadic eye movements, abnormal

salivation, excessive

seizure, laughing as manifestation

sensorineural hearing loss

serologic testing

serologic testing of cerebrospinal fluid

shaking

sinemet

skin, biopsy

skin, lesions in neurologic disorders

skull x-ray

skull x-ray, abnormal

sleep pathology and physiology

slow virus infection of CNS

spastic dysphonia

spasticity

speech disorder

speech disorder, childhood

spinal cord, lesion of

spinal muscular atrophy

spinocerebellar ataxia

spinocerebellar ataxia type 2

splenomegaly

spongy degeneration of brain

status epilepticus, intractable

steroid therapy, CNS treatment and complications with

striatum, lesion of, bilateral

stridor

strokelike episodes

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

subarachnoid hemorrhage

subcortical U fibers

substantia nigra

subthalamic nucleus

symmetric brain lesions

synucleinopathy

systemic illness

systemic lupus erythematosus

systemic lupus erythematosus, neurologic complications with

temporal lobe, lesion

temporal lobe, lesion, bilateral

term infant

thalamus, lesion of

thalamus, lesion of-bilateral

transient ischemic attack

transient ischemic attack, limb shaking

transient neurologic deficit

travel history

treatment of neurologic disorder

trigeminal neuropathy

trinucleotide repeats

tyrosine hydroxylase deficiency

unconsciousness

unconsciousness, transient

visual evoked response

visual impairment

vitamin deficiency

walking frame

walking, difficulty with

weakness

weakness, generalized

weakness, progressive

Showing articles 700 to 750 of 18245 << Previous Next >>

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

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

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

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

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

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

Drug Therapy of Tardive Dyskinesia
NEJM 296:257, Kobayashi,R.M., 1977

Familial Nonprogressive Involuntary Movements of Childhood
Ann Neurol 1:602 1977., Damasio,H.,et al, 1977

Elevated Manganese Levels Associated with Dementia & Extrapyramidal Signs
Neurol 27:213, Banta,R.G.,et al, 1977

Meningoencephalopathy Secondary to Infectious Mononucleosis:Unusual Presentation with Stupor & Chorea
Arch Neurol 34:186, Friedland,R.,et al, 1977

Fisher's Syndrome:A Pharmacological Study of the Pupils
Ann Neurol 2:63, Okajima,T.,et al, 1977

Familial Idiopathic Cerebral Calcifications
et al. , JNNP 40:280977., Boller,F., 1977

Tonic Pupils with Acute Ophthalmoplegic Polyneuritis
Ann Neurol 2:393, Keane,J.R., 1977

The Impossible Meningioma
Arch Neurol 34:36, Susac,J.O.,et al, 1977

Familial Essential Myoclonus
Brain 93:131-138, Korten,J.J.,et al, 1977

Phenytoin-induced Ophthalmoplegia
Neurol 26:1031, Spector,R.H.,et al, 1976

Huntington's Chorea, Changes in Neurotransmitter Receptors in the Brain
NEJM 294:1305, Enna,S.J.,et al, 1976

Dystonia & Choreoathetosis in Multiple Sclerosis
Arch Neurol 33:590, Bachman,D.S.,et al, 1976

Treatment & Prognosis of Hemiballismus
NEJM 295:1348, Klawans,H.L.,et al, 1976

Normocalcemic Tetany
Neurol 26:825, Isgreen,W.P., 1976

Neurologic Disorders in Renal Failure (1st of Two Parts)
NEJM 294:143, Raskin,N.H.,et al, 1976

Blepharospasm-oromandibular Dystonia Dyndrome (Brueghel's syndrome) :A Variant of Adult-onset Torsion Dystonia
JNNP 39:1204, Marsden,C.D., 1976

Anticonvulsant-induced Dyskinesias:A Comparison with Dyskinesias Induced by Neuroleptics
JNNP 39:1210, Chadwick,D.,et al, 1976

Acute Dystonia, An Unusual Reaction to Diphenhydramine
JAMA 236:291, Lavenstein,B.L.&Cantor,F.K., 1976

Choline for Tardive Dyskinesia
NEJM 293:152, Davis,K.L.,et al, 1975

Huntington's Chorea-Deficiency of Y-Aminobutynic Acid in Brain
NEJM 288:337, 1973, 289:104, 1973, 292:10295., Perry,T.,et al, 1975

Catecholamines & Neurologic Diseases
NEJM 293:274, Moskowitz,M.A.,et al, 1975

Deanol in the Treatment of Tardive Dyskinesia
Am J Psych 132:864, Casey,D.E.,et al, 1975

Oral Facial Dyskinesia Assoc. with Prolonged use of Antihistamine Decongestants
NEJM 293:486, Thach,B.T.,et al, 1975

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

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

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

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

Showing articles 700 to 750 of 18245 << Previous Next >>