Neudle.com: myoclonus dystonia

Differential
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acquired immunodeficiency syndrome

acquired immunodeficiency syndrome-related complex

acrocyanosis

Aicardi-Goutieres syndrome

akathisia

alcohol

alcohol, neurologic complications with

alien hand syndrome

altered states of consciousness

anemia

anorexia

anti basal ganglia antibodies

anti IgLON5

anticholinergic drugs

anxiety

apraxia

apraxia of eye movements

apraxia, constructional

basal ganglia, calcification of

basal ganglia, infarction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

benign essential tremor

beta adrenergic blocker

calcification, intracranial

carbon monoxide poisoning

CAT scan, emission, abnormal

cataracts

central nervous system, infection of

cerebral cortical atrophy

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gold sol.curve of

cerebrospinal fluid, xanthochromia of

cerebrovascular accident

cerebrovascular accident, complications with

cerebrovascular accident, young adult

ceruloplasmin, serum

chilbran skin lesions

choreoathetosis, paroxysmal

chromosomal abnormality

chromosome 7

chronic progressive external ophthalmoplegia

cisternogram, radionuclide

Clinical Pathologic Conference(C.P.C.)

clonazepam

coccidioidomycosis

cold intolerance

conjugate gaze, forced

consanguinity

conversion reaction

copper metabolism, abnormal

cortical-basal ganglionic degeneration

crying

delay in diagnosis

dementia

dentate nuclei, lesion of

depression

developmental retardation

dexterity, impaired

diabetes mellitus

diagnostic criteria

differential diagnosis

disability, neurological

drooling

dysarthria

dyskinesia

dyskinesia, buccal lingual facial

dyskinesia, drug induced

dystonia, delayed onset

dystonia, face

dystonia, focal

dystonia, psychogenic

dystonia, treatment of

dystonic reaction, acute

electroencephalogram

electromyogram

emergencies, neurologic

encephalitis

encephalitis lethargica

encephalitis, paraneoplastic

encephalitis, viral

encephalopathy

encephalopathy, post anoxic

epileptic encephalopathy

epsilon sarcoglycan gene

extralimbic encephalitis

face, contractions

faciobrachial dystonic seizure

familial

feeding disorder

fever

frontal lobe, pathologic signs of

gait disorder

gamma amino butyric acid receptor antibody

gaze palsy

gaze palsy, supranuclear

gene

gene mutation

genetic diagnosis, prenatal

genetic neurologic disorders

hepatolenticular degeneration(Wilson's disease)

heralding manifestation

human immunodeficiency virus type 1

hydrocephalus

hydrocephalus, normal pressure

hyperekplexia

hyperpyrexia, CNS disorder causing

hypoxic encephalopathy

intestinal pseudoobstruction

intracerebral hemorrhage

intrauterine

irritability

Kayser-Fleischer ring

Kearns-Sayre syndrome

L-dopa

Leber's hereditary optic neuropathy

left handedness

Leigh's disease

leucine rich glioma inactivated 1 antibodies

leukodystrophy

leukoencephalopathy

levitation

Lewy body disease, diffuse

medical-legal aspects of neurology

MELAS syndrome

memory, defect of recent

memory, impairment of

meningismus

meningitis

meningitis, fungal

meningitis, syphilitic

mitochondrial disease

mitochondrial encephalomyopathy

molecular genetics

mortality

movement disorder

movement disorder, delayed onset

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, paroxysmal

movement disorder, psychogenic

movement disorder, treatment of

myopathy, mitochondrial

myorhythmia

mysoline

neoplasm, intracranial

neoplasm, primary intracerebral

neoplasm, primary of CNS

neurologic complications of, systemic cancer

neurologic disease, diagnoses of

neurologic disease, diagnoses of, clinical bedside

neurologic disease, multifocal

Parkinson disease, differential diagnosis of

Parkinson disease, drug induced

Parkinson disease, L-dopa nonresponsive

Parkinson disease, postencephalitic

Parkinson disease, psychogenic

Parkinson disease, tremor, absence of

Parkinsonism syndrome

paroxysmal dystonic choreoathetosis

paroxysmal kinesigenic dyskinesia

paroxysmal neurologic deficits

paroxysmal nonkinesigenic dyskinesia

pathognomonic

penicillamine

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

pneumoencephalogram(PEG)

prenatal

prognosis

progressive neurologic disorder

propranolol

psychiatric problems in neurologic disorders

psychomotor retardation

ptosis

pyramidal tract dysfunction

ragged-red fibers

remote effect of cancer on the nervous system

salivation, excessive

seizure

seizure, dystonic

seizure, stimulus sensitive

sensorineural hearing loss

sensory loss

sensory loss, cortical

short stature

skin, lesions in neurologic disorders

sleep apnea, obstructive

sleep pathology and physiology

somnolence

spastic dysphonia

speech disorder

speech disorder, childhood

spinocerebellar ataxia type 16

spongy degeneration of brain

startle reaction

status dystonicus

status epilepticus, intractable

stereotypy

steroid therapy, CNS treatment and complications with

subarachnoid hemorrhage

treatment of neurologic disorder

visuospatial disturbance

Showing articles 750 to 800 of 858 << Previous Next >>

Myoclonus with Electrocerebral Silence in a Patient Receiving Pencillin
Arch Neurol 36:857-858, Sackellares,J.C.,et al, 1979

Dialysis Encephalopathy Treated with Clonazepan
Ann Neurol 6:555-556, Trauner,D.,et al, 1979

Microangiopathy of the Brain & Retina
Neurol 29:313-316, Susac,J.O.,et al, 1979

Familial Subacute Necrotizing Encephalomyelopathy of the Adult Form (Adult Leigh Syndrome)
Ann Neurol 6:200-206, Kalimo,H.,et al, 1979

Drug Therapy, Bromocriptine
NEJM 301:873-878, Parkes,D., 1979

Adult Type Neuronal Storage Disease with Neuraminidase Deficiency
Ann Neurol 6:232-244, Miyatake,T.,et al, 1979

Hereditary Myoclonus & Progressive Distal Muscular Atrophy
Ann Neurol 6:227-231, Jankovic,J.,et al, 1979

Paroxysmal Choreoathetosis Associated with Thyrotoxicosis
Ann Neurol 6:453-454, Fischblek,K.H.,et al, 1979

Familial Psychosis & Diverse Neurologic Abnormalities in Adult-Onset Gaucher's Disease
Arch Neurol 36:95-99, Neil,J.F.,et al, 1979

Neurologic Disturbances in Pagets Disease of Bone:Response to Calcitonin
Neurol 29:448-457, Chen,J.R.,et al, 1979

Uraemic Myoclonus:An Example of Reticular Reflex Myoclonus
JNNP 42:52-55, Chadwick,D.,et al, 1979

Blepharospasm:Successful Treatment with Clonazepam
Ann Neurol 5:401-402, Merikangas,J.R.,et al, 1979

Early-Morning Dystonia-A Late Side Effect of Long-Term Levodopa Therapy
Arch Neurol 36:308-310, Melamed,E., 1979

Postanoxic Action Myoclonus (Lance-Adams Syndrome) Responding to Valproate
Arch Neurol 36:44-45, Rollinson,R.D.,et al, 1979

Myoclonus Following Spinal Anesthesia
Neurol 29:379-380, Fox,E.J.,et al, 1979

Clinical Similarity of Alzheimer & Creutzfeldt-Jakob Disease
Ann Neurol 6:368-369, Watson,C.P., 1979

Meige's Disease, A Clinical Form of Facial Convulsion, Bilateral & Medial
Arch Neurol 36:635-637, Tolosa,E.S.,et al, 1979

Meige Disease:Striatal Dopaminergic Preponderance
Neurol 29:1126-1130, Tolosa,E.S.,et al, 1979

Subacute Spongiform Encephalopathy (Creutzfeldt-Jakob Disease)
Brain 101:333-344, Masters,C.L.,et al, 1978

Progressive Dialysis Encephalopathy
Ann Neurol 4:199-204, Lederman,R.J.,et al, 1978

Treatment of Myoclonus with Pheneturide
JNNP 41:598-602, Ward,C.D., 1978

Imipramine in Absence & Myoclonic-astatic Seizures
Neurol 28:953-957, Fromm,G.H.,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

Diagnosis of Treatable Wilson's Disease
NEJM 298:1347, Cartwright,G.E., 1978

Dominant Spinopontine Atrophy
Arch Neurol 35:156, Pogacar,S.,et al, 1978

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

Autosomal Dominant System Degeneration in Portugese Families of the Azores Islands
Neurol 28:703, Coutinho,P.,et al, 1978

Clinical Aspects of Spasmodic Dysphonia
JNNP 41:361, Aminoff,M.J.,et al, 1978

Hemifacial Spasm
Arch Neurol 35:481, Maroon,J.C., 1978

Hemifacial Spasm Due to Aneurysmal Compression of the Facial Nerve
Arch Neurol 35:545, Maroon,J.C.,et al, 1978

Glycine Encephalopathy
NEJM 298:687, Ch'ien,L.T., 1978

Gaze-evoked Blepharoclonus
Ann Neurol 3:243, Keane,J.R., 1978

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

A Case of Schwartz-Jampel Syndrome with Unusual Muscle Biopsy Findings
Ann Neurol 3:93, Fariello,R.,et al, 1978

Juvenile Neuroaxonal Dystrophy:Clinical, Electrophysiological, & Neuropathological Features
Ann Neurol 3:419, Dorfman,L.J.,et al, 1978

Post-anoxic Action Myoclonus:Improvement with Valproic Acid
NEJM 299:313, Fah,S., 1978

The Cherry-red Spot-Myoclonus Syndrome
Ann Neurol 3:234, Rapin,I.,et al, 1978

Drug Therapy, Clonazepam
NEJM 299:812-816, Brown,T.R., 1978

Sodium Valproate & Clonazepam in the Treatment of Intractable Epilepsy
Arch Neurol 34:14, Lance,W.,et al, 1977

Familial Spasmodic Torticollis
Neurol 27:11, Gilbert,G.J., 1977

Clonazepam & Branchial Myoclonus
Ann Neurol 1:306, Gledhill,R.F., 1977

Subacute Measles Encephalitis Complicating Hodgkin's Disease in an Adult
Ann Neurol 1:452, Wolinsky,J.S.,et al, 1977

Paroxysmal Choreoathetosis Following Head Injury
Ann Neurol 2:447, Robin,J.J., 1977

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

A Syndrome of Early Recognition of Occult Hydrocephalus & Cerebral Atrophy
Quart J Med 183:365, Botez,M.I.,et al, 1977

Clinical Pathologic Conference, Creutzfeldt-Jakob Disease, (Case record 43-1977)
NEJM 297:930, Scully,R.E.,et al, 1977

Effects of Learning on Visceral Functions-Biofeedback
NEJM 296:1274, Miller,N.E.,et al, 1977

Serotonin & Myoclonic Seizures
NEJM 296:101, Munsat,T.L., 1977

Long-term Therapy of Myoclonus & Other Neurologic Disorders with L-5-Hydroxytryptophan & Carbidopa
NEJM 296:70, VanWoert,M.H.,et al, 1977

Showing articles 750 to 800 of 858 << Previous Next >>