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adolescent medicine

adverse drug reaction

akinesia of eyelid function

alexia without agraphia

alien hand syndrome

alpha-fetoprotein

Alzheimer's disease

anticholinergic drugs

anticholinesterase

aphasia, progressive, primary

apraxia of eye movements

apraxia of eyelid opening

arm swing, reduced

arylsulfatase A

ataxia telangiectasia

ataxia, cerebellar

ataxia, hereditary

ataxia, paroxysmal

ataxia, progressive

ataxia, truncal

ataxic-dystonia syndromes

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavioral disorder

bent spine syndrome

biologic markers

biopterin deficiency

biotin deficiency

biotin deficiency, juvenile form

biotin-responsive basal ganglia disease

botulinum toxin

brainstem, dysfunction

brainstem, lesion of

bulbar dysfunction

calcification, intracranial

carcinoembryonic antigen

CAT scan, abnormal

CAT scan, false negative

CAT scan, muscle

caudate nucleus, atrophy

central hypoventilation

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar degeneration

cerebellar pontine angle

cerebellar pontine angle tumor

cerebral cortex

cerebral cortical atrophy

cerebral embolism

cerebral embolism, cardiac origin

cerebral palsy, associated problems with

cerebral peduncle

cerebrovascular accident

ceruloplasmin, serum

choreoathetosis

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

cogwheel rigidty

cold intolerance

conjugate gaze, forced

conversion reaction

cortical-basal ganglionic degeneration

cranial nerve palsies

creatine phosphokinase(CPK)elevated

crying, pathologic

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

dexterity, impaired

diabetes mellitus

diagnostic criteria

differential diagnosis

diurnal variation

dopa responsive dystonia

down-beat nystagmus

drug induced neurologic disorders

dysarthria-clumsy hand syndrome

dysdiadochokinesia

dyskinesia, buccal lingual facial

dyskinesia, facial

dystonia musculorum deformens

dystonia, cervical

dystonia, classification

dystonia, drug induced

dystonia, etiology of

dystonia, evaluation of

dystonia, focal

dystonia, painful

dystonia, post traumatic

dystonia, treatment of

dystonia, truncal

dystonic reaction, acute

emotional lability

encephalitis, autoimmune

episodic disorders

episodic neurologic deficits

esophageal varices

ethics in neurology

exercise-induced neurologic dysfunction

exome sequencing

extrapyramidal movement disorder, progressive

eye movement, disorders of

facial expression abnormality

fine motor function, impaired

fourth ventricle, enlargement of

fourth ventricle, neoplasm of

frontal behavioral spatial syndrome

gangliosidosis GM1

gaze palsy, supranuclear

gaze palsy, vertical

genetic counselling

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic testing

gests antagoniste

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

globus pallidus, stimulation

growth retardation

Hallervorden Spatz disease

Hallervorden Spatz disease, late onset

health insurance

hemianopia, homonymous

hemifacial spasm

hepatic encephalopathy

hepatic failure

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), presymptomatic

heralding manifestation

Huntington's chorea

Huntington's chorea, genetic counselling

Huntington's disease, children

hypoalbuminemia

hypometric saccades

iatrogenic neurologic disorders

ideomotor apraxia

imbalance, postural

immunodeficiency

immunosuppression

inclusion bodies, intranuclear

incontinence, fecal

intellectual deficit

intellectual deterioration

intracranial pressure, increased

Jakob-Creutzfeldt disease

jaw jerk, abnormal

Kayser-Fleischer ring

laughing, pathologic

leg spasms, painful

leg weakness, bilateral

lenticular nucleus, lesion of, bilateral

liver function enzymes

lysosomal storage disease

manganese intoxication

memory, defect of recent

memory, impairment of

mental retardation

metabolic disorder, primary

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

midbrain, atrophy

midbrain, infarction of

molecular genetics

movement disorder

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, extrapyramidal-treatment of

movement disorder, psychogenic

movement disorder, treatment of

MRI, CAT scan compared to

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, eye of tiger sign

MRI, high signal foci on

MRI, high signal intensity of basal ganglia

MRI, mouse ears

MRI, paramagnetic effect

MRI, T1 weighted high signal foci

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple system atrophy

muscle hypertrophy

muscle spasm, face

muscle weakness

muscular dystrophy

myasthenia gravis

myelopathy, chronic progressive

myoclonic jerks

myopathy, metabolic

neoplasm, posterior fossa

neoplasm, primary of CNS

neoplasm, primary of CNS-children

neurocutaneous disease

neuroendocrinology

neuroleptic, atypical

neurologic disease, diagnoses of

neurologic disease, diagnoses of, clinical bedside

neurologic disease, tempo

neurologic evaluation

neurologic examination

neurologic signs

neurologic symptoms

neuronal intranuclear inclusion disease

neuroophthalmology

numb clumsy hands syndrome

nystagmus, vertical

obsessive-compulsive disorder

ocular motility, disorders of

ocular myopathy

ocular myopathy, differential diagnosis

old age, neurology of

ophthalmoplegia

paraspinal muscle

paraspinal muscle weakness

Parkinson disease

Parkinson disease, axial symptoms

Parkinson disease, differential diagnosis of

Parkinson disease, dystonia with

Parkinson disease, juvenile

Parkinson disease, L-dopa nonresponsive

Parkinson disease, treatment of

Parkinson disease, tremor, absence of

Parkinsonism syndrome

penguin silhouette sign

personality change

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

polycythemia, secondary

posterior cerebral artery

posterior cerebral artery embolism

posterior cerebral artery territory infarction

postural abnormality

precipitating factors

pregnancy, neurologic complications in

primary episodic ataxia

progressive neurologic disorder

progressive supranuclear palsy

pseudobulbar palsy

psychiatric disorder

psychiatric problems in neurologic disorders

psychomotor retardation

pure sensory stroke

pyramidal tract

pyramidal tract dysfunction

radiation hypersensitivity

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

release phenomena

respirations in CNS disease

retinal degeneration

retinitis pigmentosa

Rett's syndrome

reversible neurologic disorder

rigidity, axial

saccadic eye movements, abnormal

salivation, excessive

sea-blue histiocytes

sensorineural hearing loss

sensory loss, cortical

sequencing difficulty

shoulder, elevation

single photon emission computed tomography

skin, lesions in neurologic disorders

sleep apnea, obstructive

sleep pathology and physiology

slit lamp examination

speech disorder

speech disorder, childhood

spinal cord, lesion of

spinal muscular atrophy

spinocerebellar ataxia

spinocerebellar ataxia type 28

spinocerebellar degeneration

stem cell transplantation

stimulation, deep brain

stimulation, deep brain, bilateral

stooped posture

striatum, lesion of

striatum, lesion of, bilateral

substantia nigra

swallow evaluation

symmetric brain lesions

tardive dystonia

tetrahydrobiopterin

thalamus, infarction of

thrombocytopenia

tonic foot response

treatment of neurologic disorder

treatment, empirical

tremor, intention

tremor, postural

tricyclic antidepressant

trientine dihydrochloride

trinucleotide repeats

upgaze, paralysis of

urinary incontinence

urinary sulfatidase excretion

vision, blurred

visual evoked response

visual field defect

visual symptoms

vocal cord paralysis

walking, difficulty with

weakness, progressive

Whipple's disease

white matter disease

wide based gait

Showing articles 1050 to 1100 of 1200 << Previous Next >>

Familial Paroxysmal Dystonic Choreoathetosis & Response to Alternate-Day Oxazepam Therapy
Ann Neurol 13:456-457, Kurlan,R.,et al, 1983

Progressive Supranuclear Palsy:Clinical Features & Response to Treatment in 16 Patients
Ann Neurol 13:273-278, Jackson,J.A.,et al, 1983

Blepharospasm & Orofacial-Cervical Dystonia:Clinical & Pharmacological Findings in 100 Patients
Ann Neurol 13:402-411, Jankovic,J.,et al, 1983

Treatment of Dystonia with Tetrahydrobiopterin
NEJM 308:157-158, LeWitt,P.A.,et al, 1983

Delayed Neurologic Sequelae in Carbon Monoxide Intoxication
Arch Neurol 40:433-435, Choi,I.I.S., 1983

High Dosage Anticholinergic Therapy in Dystonia
Neurol, 33:1255-12611983., Fahn,S., 1983

Herpes Zoster-Associated Encephalitis:Clinicopathologic Report of 12 Cases and Review of the Literature
Medicine 62:81-95, Jemsek,J.,et al, 1983

Blinking & Blepharospasm, Mechanism, Diagnosis, & Management
JAMA 248:3160-3164, Jankovic,J.,et al, 1982

Decongestant-Induced Blepharospasm & Orofacial Dystonia
JAMA 247:3244-3245, Powers,J.M., 1982

Abnormal Brainstem Auditory Evoked Potentials in Chronic Paint Sniffers
Ann Neurol 12:553-556, Metrick,S.A.,et al, 1982

Delayed-onset Posthemiplegic Dystonia:CT Demonstration of Basal Ganglia Pathology
Neurol 32:1033-1035, Grimes,J.D.,et al, 1982

Tardive Dystonia:Late-onset & Persistent Dystonia Caused by Antipsychotic Drugs
Neurol 32:1335-1346, Burke,R.E.,et al, 1982

Severe Dystonia & Myoglobinuria
Neurol 32:1195-1197, Jankovic,J.,et al, 1982

Dystonia Musculorum Deformans, Implications of Therapeutic Response to Levodopa & Carbamazepine
Arch Neurol 39:376-377, Garg,B.P., 1982

Writers'Cramp-A Focal Dystonia
Brain 105:461-480, Sheehy,M.P.,et al, 1982

Hydrocephalus as a Cause of Disturbances of Gait in the Elderly
Neurol 32:1358-1363, Fisher,C.M., 1982

Adult Dystonic Lipidosis, Clin Histo & Biochem Findings of a Neurovisceral Storage Dis
Neurol 32:1295-1299, Longstreth,W.T.Jr.,et al, 1982

Truncal Ataxia in Terminal Bronchial Carcinoma
Arch Neurol 39:787-788, Puvanendran,K., 1982

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

Lithium Therapy in Torsion Dystonia
Ann Neurol 11:106-107, Marti-Masso,J.F.,et al, 1982

Carbamazepine for Hemifacial Spasm
Neurol 32:286-287, Alexander,G.E.,et al, 1982

Thoracic Root Pain in Diabetes:The Spectrum of Clinical & Electromyographic Findings
Ann Neurol 11:80-85, Kikta,D.G.,et al, 1982

Progressive Dyskinesia Due to Internal Cerebral Vein Thrombosis
Neurol 32:769-772, Solomon,G.E.,et al, 1982

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

Clusters of Tonic Spasms as an Initial Manifestation of Multiple Sclerosis
Ann Neurol 12:494-495, Heath,P.D.,et al, 1982

Hemifacial Spasm; A Long Term Follow-up of Patients Treated by Posterior Fossa Surgery & Facial Nerve Wrapping
JNNP 44:1100-1103, Kaye,A.H.,et al, 1981

Choline For Blepharospasm
NEJM 305:957-958, Skarf,B.,et al, 1981

Neurologic Complications of Hyperthyroidism
Arch Neurol 38:669-670, Bulens,C., 1981

Meningeal Carcinomatosis
Arch Neurol 38:696-699, Theodore,W.H.,et al, 1981

Neurologic Signs In Uncomplicated Aging (Senscence)
Seminars In Neurology, Thieme-Stratton Inc. , New York, N. Y. pp. 21-30, Jenkyn,L.R.&Reeves,A.G., 1981

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

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

Prolonged Relief of Dystonic Movements with Diazepam
Neurol 31:1457-1458, Ziegler,D.K., 1981

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

Toxic Substances & the Nervous System:The Role of Clinical Observation
JNNP 44:1-8, LeQuesne,P.M., 1981

A Progressive Neurologic Syndrome In Children With Chronic Liver Disease
NEJM 304:503-508, Rosenblum,J.L.,et al, 1981

Chronic GM1 Gangliosidosis Presenting as Dystonia:I. Clinical & Pathological Features
Ann Neurol 9:465-475, Goldman,J.E.,et al, 1981

Clin. Path. Conference
Fibrillary Astrocytoma of Medulla, with Invasion of Subarachnoid Space, Case Record 6-1981, NEJM 304, 3430,1981., 1981

Diabetic Thoracoabdominal Neuropathy:Clinical & Electrodiagnostic Features
Ann Neurol 9:75-79, Sun,S.F.,et al, 1981

Diabetic Truncal Polyneuropathy
Arch Neurol 38:46-47, Waxman,S.G.,et al, 1981

Benign Paroxysmal Torticollis in Infancy
Arch Dis Child 56:956-959, Deonna,T.,et al, 1981

Temporal Arteritis Presenting as Ataxia and Dementia
Post Grad Med 69:246-249, Shenberger,K.N.,et al, 1981

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

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

Clinical Criteria for Diagnosis of Machado-Joseph Disease:Report of a Non-Azorean Portuguese Family
Neurol 30:319-322, Lima,L.,et al, 1980

Focal Neurologic symptoms in hypercalcemia
Neurol 30:200-201, Longo,D.L.,et al, 1980

Dystonic Foot Response of Parkinsonism
Arch Neurol 37:132-136, Nausieda,P.A.,et al, 1980

L-Dopa in Children with Progressive Neurological Disorders
Ann Neurol 7:93, Bugiani,O.,et al, 1980

Clin. Path. Conference
Olivopontocerebellar atrophy, sporadic form. Case Record 39-1980, NEJM 303:803-80980., , 1980

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

Showing articles 1050 to 1100 of 1200 << Previous Next >>