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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

dementia, presenile

developmental retardation

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

executive dysfunction

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

hepatosplenomegaly

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

life expectancy

lipid storage disorder of CNS

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

Niemann-Pick disease

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

psychological testing

psychomotor retardation

psychotic behavior

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

seizure, laughing as manifestation

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

visuospatial disturbance

vocal cord paralysis

walking, difficulty with

weakness, progressive

Whipple's disease

white matter disease

whole genome sequencing

wide based gait

Showing articles 900 to 950 of 1219 << Previous Next >>

Clinicopath Conf
HTLV-I Infection, with Adult T-Cell Lymphoma and Tropical Spastic Paraparesis, Case 36-2989, NEJM 32, :6675,1989., 1989

Human T-Lymphotropic Virus Type I-Associated Myelopathy Presenting as Spinocerebellar Syndrome
Ann Neurol 25:419-420, Iwasaki,Y.,et al, 1989

Falling and Postural Deficits Due to Acute Unilateral Basal Ganglia Lesions
Arch Neurol 46:492-496, Labadie,E.L.,et al, 1989

Guillain-Barre Syndrome Presenting as High-Altitude Cerebral Edema
NEJM 321:545, Shlim,D.R.&Cohen,M.T., 1989

Usefulness of a Writing Aid in Writer's Cramp
Neurol 39:149-150, Koller,W.C.&Vetere-Overfield,B., 1989

The"Yips":A Focal Dystonia of Golfers
Neurol 39:192-195, McDaniels,K.D.,et al, 1989

Treatment of Focal Dystonias of the Hand with Botulism Toxin Injections
JNNP 52:355-363, Cohen,L.G.,et al, 1989

Clinicopath Conf
Primary (Granulomatous) Angiitis of Central Nervous System, Case Record 8-1989, NEJM 320:514-5249., , 1989

Diabetic Truncal Neuropathy Presenting as Abdominal Hernia
Neurol 39:1488-1490, Parry,G.J.&Floberg,J., 1989

Post-Traumatic Torticollis
Neurol 39:1642-1643, Isaac,K.&Cohen,J.A., 1989

Cerebral Palsy Diplegia:Improvements for Walking
BMJ 299:1115-1116, Patrick,J., 1989

Demyelinating Diseases
In Rowlands Merritt's Textbk of Neurology, Lea & Febiger, Phila, 8th Ed, p. 749, Sibley,W.A.,et al, 1989

Refsum Disease
In Rowland's Merritt's Textbk of Neurology, Lea & Febiger, Phila, 8thEd, p. 509, Menkes,J.H., 1989

Magnetic Resonance Imaging in Pathologically Proven Hallervorden-Spatz Disease
Neurol 39:440-442, Schaffert,D.A.,et al, 1989

Brain White-Matter Changes in the Elderly Prone to Falling
Arch Neurol 46:1292-1296, Masdeu,J.C.,et al, 1989

Hypothyroidism
In Neurologic Clinics, W. B. Saunders Co, Phila, 7:492-493., Kaminski,H.J.&Ruff,R.L., 1989

Diphenhydramine-Induced Dystonia
Clin Pharmacy 8:471, Santora,J.,et al, 1989

Friedreich Ataxia
In Rowland, L. P. Merritt's Textbook of Neurology, 8th Ed, Lea & Febiger, Phila, Ch 13, p627, Rosenberg,R.N., 1989

Life-Threatening Cranial Dystonia Following Trihexyphenidyl Withdrawal
Movement Disorders 4:349-353, Gimenez-Roldan,S.,et al, 1989

Antecollis in Parkinsonism
Lancet 1:1320-1321, Jorens,P.G.,et al, 1989

Cervical Myelopathy Secondary to Movement Disorders:Case Report
Neurosurgery 24:902-905, El-Mallakh,R.S.,et al, 1989

Paroxysmal Cerebellar Ataxia
Aust NZ J Med 19:113-117, Feeney,G.F.&Boyle,R.S., 1989

Hemifacial Spasm, In Movement Disorders, A Comprehensive Survey
Futura Publ., NY. Ch. 9 p.510, Weiner,W.J. &LangA.E., 1989

Transient Paroxysmal Dystonia in Infancy
Neuropediatr 19:171-174, Angelini,L.,et al, 1988

Chronic Progressive Spinobulbar Spasticity, A Rare Form of Primary Lateral Sclerosis
Arch Neurol 45:509-513, Gastaut,J.L.,et al, 1988

Rapidly Progressive Dementia Caused by Spongiform Encephalopathy
West J Med 148:313-319, Enos,B.E.&Vinters,H.V., 1988

Brain Metabolism in Mitochondrial Encephalomyopathy:A PET Study
J Comput Assist Tomogr 12:854-857, DeVolder,A.,et al, 1988

Primary Lateral Sclerosis, A Clinical Diagnosis Reemerges
Arch Neurol 45:1304-1307, Younger,D.S.,et al, 1988

Idiopathic Hypoparathyroidism and Paroxysmal Dystonic Choreoathetosis
Ann Neurol 24:585, Barabas,G.&Tucker,S.M., 1988

Dystonic-Parkinsonian Syndrome after Cyanide Poisoning:Clinical and MRI Findings
JNNP 51:1345-1348, Carella,F.,et al, 1988

Acute Extrapyramidal Syndrome in Methylmalonic Acidemia:"Metabolic Stroke"Involving the Globus Pallidus
J Pediatr 113:1022-1027, Heidenreich,R.,et al, 1988

Blepharospasm
Editorial, Lancet 2:10591988., , 1988

Hyperthyroidism Presenting as Pyramidal Tract Disease
BMJ 297:1395-1396, Shaw,P.J.,et al, 1988

Clinicopath Conf
Paraneoplastic Encephalitis (Limbic and Brain-Stem Encephalitis) , Case Record 39-1988, NEJM 319:849, 860,, 1988

Dystonia and Tremor Induced by Peripheral Trauma:Predisposing Factors
JNNP 51:1512-1519, Jankovic,J.&VanDer Linden,C., 1988

Diagnostic Criteria for Rett Syndrome
The Rett Syndrome Diagnostic Criteria Work Group, Ann Neurol 23:425-4281988., , 1988

Rett Syndrome:Natural History and Management
Pediatrics 82:1-10, Moeschler,J.B.,et al, 1988

Clinicopath Conf
Progressive Multifocal Leukoencephalopathy, Chronic Lymphocytic Leukemia, Case Record 45-1988, NEJM, 19:8-1280,1988., 1988

Acute Upper Airway Obstruction Due to Supraglottic Dystonia Induced by a Neuroleptic
BMJ 297:964-965, Newton-John,H., 1988

Brain-Stem Auditory-Evoked Potentials in Spasmodic Torticollis
Arch Neurol 45:174-175, Drake,M.E., 1988

Tetrabenazine Therapy of Dystonia, Chorea, Tics, & Other Dyskinesias
Neurol 38:391-394, Jankovic,J.&Orman,J., 1988

Hemidystonia Due to Subdural Hematoma
Neurol 38:507, Eaton,J.M., 1988

Clinicopath Conf
Infiltrating Carcinoma of Breast (Paraneoplastic Opsoclonus Syndrome & SIADH) Case 9-1988, NEJM 318:, 63-578., 1988

Dystonia in Parkinson's Disease:Clinical & Pharmacological Features
Ann Neurol 23:73-78, Poewe,W.H.,et al, 1988

Clinicopath Conf
Adenocarcinoma of Lung, with Metastasis to Meninges of Brain, Spinal Cord & Optic Nerves, Case Recor, 14-1EJM 318:903-915,1988., 1988

CT and Hemifacial Spasm
Neurol 38:1111-1113, Digre,K.B.,et al, 1988

The Clinical Course of Spasmodic Torticollis
Neurol 38:530-532, Lowenstein,D.H.,et al, 1988

Hemifacial Spasm Caused by a Tortuous Vertebral Artery:MR Demonstration
J Comput Assist Tomogr 12:492-494, Tash,R.R.,et al, 1988

Neuropsychiatric Disorders Caused by Cobalamin Deficiency in the Absence of Anemia or Macrocytosis
NEJM 318:1720-1728, 1752-17541988., Lindenbaum,J.,et al, 1988

Hereditary Defect of Cobalamin Metabolism (cblG Mutation) Presenting as a Neurologic Disorder in Adulthood
NEJM 318:1738-1741, 1752-17541988., Carmel,R.,et al, 1988

Showing articles 900 to 950 of 1219 << Previous Next >>