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acetylcholine receptor antibody

Addison's disease

adrenergic blocker

advances in neurology

adverse drug reaction

airway obstruction

alcohol, neurologic complications with

Alexanders disease

Alexanders disease, adult onset

alpha adrenergic blocker

alternating rapid movement

Alzheimer's disease

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, misdiagnosis

anemia, hemolytic

aneurysm, intracranial

ankle reflex, absent

ankle, swelling of

anticholinergic drugs

anticonvulsants

anticonvulsants, untoward effects of

aorta, atherosclerosis

Arnold Chiari malformation

arylsulfatase A

aspartate aminotransferase

ataxia telangiectasia

ataxia, cerebellar

ataxia, hereditary

ataxia, progressive

ataxia, sensory

ataxia, truncal

ataxic-dystonia syndromes

athetosis, causes of

attention deficit disorder with hyperactivity

auditory evoked brainstem potentials

auditory evoked potentials

autonomic dysfunction

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

axonal spheroid

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basilar artery occlusion

behavioral disorder

Behcet's syndrome

benign essential tremor

benign essential tremor, refractory

beta adrenergic blocker

biologic markers

blinking, reduced

blood dyscrasias, neurologic findings with

bone marrow suppression

botulinum toxin

botulinum toxin, complications of

brain transplantation

brainstem, lesion of

Brueghel's syndrome

calcification, intracranial

calcium antagonist

carbon monoxide poisoning

carbonic anhydrase inhibitor

carcinoma of pancreas

CAT scan, abnormal

CAT scan, emission

CAT scan, emission, abnormal

caudate nucleus, lesion of

caudate nucleus, lesion of, bilateral

central nervous system, infection of

central pontine myelinolysis

cerebellar ataxia, autosomal recessive

cerebellar ataxia, children

cerebellar ataxia, children, differential diagnosis of

cerebellar ataxia, hereditary

cerebellar ataxia, neuropathy and vestibular areflexia syndrome

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar lesion

cerebellum, disease of

cerebral blood flow

cerebral cortex

cerebral cortical atrophy

cerebral infarction

cerebral infarction, hemorrhagic

cerebral venous thrombosis

cerebral venous thrombosis, deep

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, lactic acid concentration

cerebrovascular accident

ceruloplasmin, serum

Charcot-Marie-Tooth

chelation therapy

cherry red spot

cherry red spot-myoclonus syndrome

chorea, causes of

choreoathetosis

chromosomal abnormality

cingulate island sign

cirrhosis, causes of childhood

Clinical Pathologic Conference(C.P.C.)

clubbing of fingers

clubfoot as related to neurologic disease

coat-hanger pain

cogwheel rigidty

complicated migraine

copper metabolism, abnormal

cornea, abnormal

coronary artery bypass

corpus callosum, lesion of

corpus callosum, thinning

Cushing's syndrome

cyst, parenchymal

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

delayed dentition

dementia, childhood

dementia, familial

developmental milestones

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetic coma, diagnosis and treatment

differential diagnosis

disability, neurological

distal muscle atrophy

distal muscle weakness

dopa responsive dystonia

dopamine agonist

dopamine receptor, D2

drug induced neurologic disorders

dysdiadochokinesia

dyskinesia, buccal lingual facial

dyskinesia, causes of

dyskinesia, drug induced

dystonia musculorum deformens

dystonia, cervical

dystonia, classification

dystonia, etiology of

dystonia, evaluation of

dystonia, focal

dystonia, laryngeal

dystonia, post traumatic

dystonia, prevalence of

dystonia, symptomatic

dystonia, treatment of

electroencephalogram, abnormalities of

electrolyte imbalance

electron microscopy

electronystagmography

emotional lability

encephalitis, Japanese

encephalitis, viral

epidemiology of neurology

erectile dysfunction

esophageal varices

evoked potentials

exome sequencing

eye movement, disorders of

Fabry's disease

facial appearance, abnormal

facial expression abnormality

failed medical management

failure to thrive

familial hemiplegic migraine

fatal familial insomnia

fine motor function, impaired

finger nose finger test

fingerprint bodies

fracture, long bone

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

Friedreich's ataxia

frontal lobe, lesion of

frontal lobe, pathologic signs of

gait, festinating

gamma knife therapy

gaze fixation, distractable

gaze palsy, supranuclear

genetic counselling

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

gests antagoniste

Gilles de la Tourette syndrome

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glucose tolerance test, abnormal

granular osmiphilic material

Hallervorden Spatz disease

heavy metal intoxication

heel-knee-shin test

hemochromatosis

hemochromatosis, primary

hemorrhagic diathesis

hepatic encephalopathy

hepatic failure

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), late onset

hepatolenticular degeneration(Wilson's disease), presymptomatic

hepatolenticular degeneration(Wilson's disease), screening for

hepatolenticular degeneration, non-Wilsonian

hepatosplenomegaly

heralding manifestation

Huntington's chorea

hyperadrenalism

hyperbilirubinemia

hyperparathyroidism

hyperthyroidism

hypoalbuminemia

hypometric saccades

hypomyelination

hypoparathyroidism

hypotension, neurologic causes of

hypotension, systemic

hypoxic encephalopathy

iatrogenic neurologic disorders

imbalance, postural

inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, intranuclear

inclusion bodies, ubiquitin

intellectual deficit

intellectual deterioration

intelligence quotient

intracerebral hemorrhage

intrinsic hand muscles, wasting of

Jakob-Creutzfeldt disease

jaw contractures

joint hypermobility

Kayser-Fleischer ring

kinesia paradoxica

kyphoscoliosis, neurologic causes of

lactic acidemia

laminectomy, lumbar

L-dopa, drug interactions with and side effects of

leg weakness, bilateral

Leigh's disease

lenticular nucleus, lesion of

lenticular nucleus, lesion of, bilateral

leukoencephalopathy

leukoencephalopathy, differential diagnosis

leukoencephalopathy, hereditary diffuse

level of consciousness, decreased

Lewy body disease, diffuse

lipid storage disorder of CNS

liver function enzymes

liver transplantation

locus ceruleus, lesion of

lymphoma involving CNS

lysosomal storage disease

marche a petits pas

Marinesco-Sjogren syndrome

memory, impairment of

mental retardation

metabolic disorder, primary

metachromatic leukodystrophy

metachromatic leukodystrophy, juvenile

midbrain, atrophy

midbrain, lesion of

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

migraine, hemiplegic

mitochondrial disease

molecular genetics

movement disorder

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, treatment of

MRI, CAT scan compared to

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, face of giant panda sign on

MRI, false negative

MRI, high signal foci on

MRI, high signal intensity of basal ganglia

MRI, paramagnetic effect

MRI, T1 weighted high signal foci

multiple sclerosis

multiple sclerosis, cognitive presenttion

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple system atrophy

muscle stiffness

myasthenia gravis

myoclonic jerks

myoclonus, epilepsy

myoclonus, essential

nausea and vomiting

neoplasm, intracranial

neoplasm, primary of CNS

nerve conduction studies

neuroaxonal leukodystrophy

neuroendocrinology

neurofibromatosis 1

neurologic complications of, burns

neurologic complications of, surgery

neurologic disease

neurologic disease, diagnoses of

neurologic signs

neurologic symptoms

neuronal ceroid-lipofuscinosis

neuroophthalmology

neuropathology, brain

neuropathy, peripheral

neuropathy, sensory

neuropsychiatry

nigrostriatal pathway

nutritional deficiency

nystagmus, pendular

nystagmus, primary position of gaze

nystagmus, rotary

nystagmus, upbeating-in primary position of gaze

nystagmus, vertical

obsessive-compulsive disorder

ocular motility, disorders of

oculogyric crisis

old age, neurology of

organ transplantation

orthostatic hypotension

osmotic demyelination syndrome

ovarian insufficiency

pain, abdominal

palatal myoclonus

paraparesis, spastic

parenteral alimentation

Parkinson disease

Parkinson disease, arteriosclerotic

Parkinson disease, atypical

Parkinson disease, benign tremulous

Parkinson disease, diagnosis

Parkinson disease, differential diagnosis of

Parkinson disease, drug induced

Parkinson disease, familial

Parkinson disease, fluctuations in

Parkinson disease, freezing phenomena in

Parkinson disease, L-dopa nonresponsive

Parkinson disease, misdiagnosis

Parkinson disease, pathogenesis of

Parkinson disease, surgical treatment of

Parkinson disease, treatment of

Parkinson disease, young onset

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

paroxysmal neurologic deficits

PAS positive material in the brain

patient information and support

Pelizaeus Merzbacher

pernicious anemia

personality change

phenylketonuria

phenylketonuria, adult onset

pheochromocytoma

poison, neurologic problems with

pons, lesion of

positional head-hanging test

postoperative neurologic complications

postural abnormality

practice guidelines

pregnancy, neurologic complications in

progressive neurologic disorder

progressive supranuclear palsy

prothrombin time, prolonged

pseudobulbar palsy

psychiatric disorder

psychiatric manifestations of brain tumors

psychiatric problems in neurologic disorders

psychomotor retardation

psychosis, cause of

psychosocial aspects

pulmonary function tests

pursuit eye movements, abnormal

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

quality of life

radiation therapy, stereotactic

reading disorder, acquired

reflex sympathetic dystrophy

rehabilitation for neurologic disorders

remote effect of cancer on the nervous system

respirations in CNS disease

respiratory failure

retinal degeneration

retinitis pigmentosa

reversible neurologic disorder

rheumatoid arthritis

risus sardonicus

Rosenthal fibers

saccadic eye movements, abnormal

salivation, excessive

sea-blue histiocytes

seizure, children

seizure, differential diagnosis of

seizure, psychomotor-temporal lobe

serum alanine aminotransferase

shoulder, pain in

single photon emission computed tomography

skin, darkening of

sleep pathology and physiology

slit lamp examination

Smell Identification Test

SNCA duplication

somatosensory evoked potentials

spastic dysphonia

speech disorder

speech disorder, childhood

speech disorder, non aphasic

speech, delayed development of

speech, loss of

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 12

spinocerebellar ataxia type 28

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar degeneration

spinopontine atrophy, dominant

splenium of corpus callosum

spongy degeneration of brain

status epilepticus

stereotaxic surgery

stimulation, deep brain

stimulation, thalamic

storage disease of CNS

striatonigral degeneration

striatonigral degeneration, infantile

striatum, lesion of

striatum, lesion of, bilateral

striopallidodentate calcifications, familial idiopathic

substantia nigra

subthalamic nucleus

subthalamic nucleus deep brain stimulation

symmetric brain lesions

syphilis, neurologic complications with

systemic illness

systemic lupus erythematosus

tandem gait, ataxic

tardive dyskinesia

tardive dystonia

teeth, abnormal

teeth, number of in infants

testicular enlargement

tetrathiomolybdate

thalamic tumors

thalamic tumors, bilateral

thalamotuberal artery

thalamus, focused ultrasound ablation

thalamus, infarction of

thalamus, infarction, bilateral

thalamus, lesion of

thalamus, lesion of-bilateral

thiazide diuretic

thrombocytopenia

thrombus, mural

thymus and neuromuscular function

tongue, fasciculations of

tongue, protrusion of

tonic foot response

torticollis, post traumatic

transient neurologic deficit

treatment of neurologic disorder

tremor, cerebellar

tremor, classification

tremor, differential diagnosis of

tremor, intention

tremor, orthostatic

tremor, physiologic

tremor, post traumatic

tremor, postural

tremor, psychogenic

tremor, resting

tremor, surgical treatment of

tremor, thalamic stimulation for suppression of

tremor, treatment of

tremor, wing beating

tremor, writing

trientine dihydrochloride

trinucleotide repeats

ultrasonography

ultrasonography, head

ultrasonography, high-intensity focused

urine test for metabolic disorders

ventricular enlargement

vertigo, migraine causing

vibratory sensation, abnormal

viral infection

visual acuity, decreased

visual evoked response

visual fields, constricted

vitamin deficiency

vitamin E deficiency

voice, abnormality of

Von Hippel Lindau

walking, difficulty with

Wernicke's encephalopathy

white matter disease

wide based gait

X-linked bulbospinal neuronopathy

x-linked intellectual deficit

x-linked mental retardation

Showing articles 2000 to 2050 of 2512 << Previous Next >>

Arteriovenous Malformation Presenting as Hemidystonia
Neurol 36:1590-1593, Friedman,D.I.,et al, 1986

Familial Myoclonic Dementia Masquerading as Creutzfeldt-Jakob Disease
Ann Neurol 20:231-239, Little,B.W.,et al, 1986

Gerstmann-Straussler-Scheinker Disease:Autopsy Study of a Familial Case
Ann Neurol 20:540-543, Vinters,H.V.,et al, 1986

Identical Twins with Hereditary Hemorrhagic Telangiectasia Concordant for Cerebrovascular Arteriovenous Malformations
Am J Med 81:931-934, Lesser,B.A.,et al, 1986

Familial Hyperlipidemia in Stroke in the Young
Stroke 17:1142-1145, Bansal,B.C.,et al, 1986

Metoclopramide-Induced Parkinsonism in Hemodialysis Patients
Arch Int Med 146:2070-2071, Sirota,R.A.,et al, 1986

Tardive Dyskinesia Associated with High-Dose Intravenous Metoclopramide
NEJM 315:518-519, Breitbart,W., 1986

Locus Ceruleus Lesions & Eosinophilic Inclusions in MPTP-Treated Monkeys
Ann Neurol 20:449-455, Forno,L.S.,et al, 1986

Computed Tomography of Familial Pineoblastoma
J Comput Assist Tomogr 10:32-33, Peyster,R.G.,et al, 1986

Inherited Multiple Meningiomas:A Clinical, Pathological & Cytogenetic Study of an Affected Family
JNNP 49:362-368, Battersby,R.D.E.,et al, 1986

Pharmacologic Treatment of Parkinsonian Tremor
Arch Neurol 43:126-127, Koller,W.C., 1986

On Heredity, Twins, & Parkinson's Disease
Ann Neurol 19:409-411, Duvoisin,R.C., 1986

Parkinson's Disease in Monozygotic Twins
Ann Neurol 19:405-408, Jankovic,J.&Reches,A., 1986

Monozygotic Twins with Parkinson's Disease
Ann Neurol 19:402-405, Koller,W.,et al, 1986

Infantile Bilateral Striatal Necrosis, Clinicopathological Classification
Arch Neurol 43:677-680, Mito,T.,et al, 1986

Familial Amyloidosis with Cranial Neuropathy & Corneal Lattice Dystrophy
Neurol 36:432-435, Darras,B.T.,et al, 1986

Familial Association of Intracranial Aneurysms & Multiple Congenital Anomalies
Arch Neurol 43:30-33, Berg,H.W.M.,et al, 1986

Chronic Demyelinating Peripheral Neuropathy in Cerebrotendinous Xanthomatosis
Ann Neurol 20:89-91, Argov,Z.,et al, 1986

Recurrent Cerebral Infarctions in Two Brothers with Antiphospholipid Antibodies that Block Coagulation Reactions
Stroke 17:98-102, Jacobson,D.M.,et al, 1986

Cerebrospinal Fluid Findings in Healthy Siblings of Multiple Sclerosis Patients
Neurol 36:727-729, Duquette,P.&Charest,L., 1986

Parkinsonism, Tardive Dyskinesia, Akathisia, & Depression Induced by Flunarizine
Lancet 1:1303-1304, Chouza,C.,et al, 1986

Alzheimer's Disease
NEJM 314:964-973, Katzman,R., 1986

Narcolepsy & Immunity
BMJ 292:359-360, Parkes,J.D.,et al, 1986

Autosomal Dominant Osteosclerosis Associated with Familial Spinal Canal Stenosis
Neurol 36:687-692, Yasuda,Y.,et al, 1986

Adynamia Episodica & Paralysis Periodica Paramyotonica
Neurol 36:682-686, Ricker,K.,et al, 1986

Neurological Manifestations in Xeroderma Pigmentosum
Ann Neurol 20:70-75, Mimaki,T.,et al, 1986

Successful Treatment with Tocainide of Recessive Generalized Congenital Myotonia
Ann Neurol 19:501-504, Streib,E.W., 1986

Familial Adult Motor Neuron Disease:Amyotrophic Lateral Sclerosis
Neurol 36:511-517, Mulder,D.W.,et al, 1986

Myasthenia Gravis in Identical Twins
Neurol 36:78-80, Murphy,J.&Murphy,S.F., 1986

Clinicopathological Conference
Paget's Disease of Bone, Giant-Cell Reparative Granuloma, Case 1-1986, NEJM 314:105-11386., , 1986

Progressive Myoclonus Epilepsies:Specific Causes & Diagnosis
NEJM 315:296-305, Berkovic,S.F.,et al, 1986

The Neuroleptic Malignant Syndrome:Agent and Host Interaction
Acta Psychiatr Scand 73:337-347, Shaley,A.&Munitz,H., 1986

Segmental Myoclonus Clinical and Pharmacologic Study
Arch Neurol 43:1025-1031, Jankovic,J.&Pardo,R., 1986

Facioscapulohumeral Dystrophy, in Myology, Basic & Clinical
McGraw-Hill Book Co, NY, p1251986., Munsat,T.L., 1986

Phosphorylase Deficiency
In Englel & Banker, Myology, McGraw-Hill Book Co, Ch 52, 1585-1601, DiMauro,S.&Bresolin,N., 1986

Acid Maltase Deficiency
Engel, A. G. in Engel and Banker, Myology, McGraw-Hill Co, New York, Ch 55, p. 1629-1651, , 1986

GM1 Gangliosidosis:Clinical and Laboratory Findings in Eight Families
Hum Genet 70:347-354, Giugliani,R.,et al, 1985

Conjugal Multiple Sclerosis
In Handbook of Clinical Neurol, Elsivier Publ, Amsterdam 47:291985., Myrianthopoulos,N.C., 1985

Deep Brain Stimulation for Pain Relief
in Neurosurgery, Wilkins, R. H. & Rengachary, S. S. (Eds) , McGraw-Hill Book Co, NY, Vol 3, p 2421, Richardson,D.E., 1985

Biotinidase Deficiency:Initial Clinical Features & Rapid Diagnosis
Ann Neurol 18:614-617, Wolf,B.,et al, 1985

Association of High Cyanide & Low Sulphur Intake in Cassava-Induced Spastic Paraparesis
Lancet 2:1211-1213, Cliff,J.,et al, 1985

Acute Exacerbation of Parkinson's Disease with Sulindac
Ann Neurol 17:104-105, Sandyk,R.,et al, 1985

Extrapyramidal Reactions with Metoclopramide
BMJ 291:930-932, Bateman,D.N.,et al, 1985

Colpocephaly:Clinical, Radiologic, & Pathogenetic Aspects
Neurol 35:1594-1598, Herskowitz,J.,et al, 1985

Intracranial Calcification in Nephrogenic Diabetes Insipidus
JAMA 254:3349-3350, Kanzaki,S.,et al, 1985

Carbonic Anhydrase II Deficiency in 12 Families with Osteopetrosis with Renal Tubular Acidosis & Cerebral Calcification
NEJM 313:139-181, Sly,W.S.,et al, 1985

Portal-Systemic Myelopathy after Portacaval Shunt Surgery
Arch Int Med 145:1921-1922, Lebovics,E.,et al, 1985

Familial Syringomyelia
JNNP 48:936-938, Busis,N.A.&Hochberg,F.H., 1985

Metachromatic Leukodystrophy Manifesting as a Schizophrenic Disorder:Computed Tomographic Correlation
Ann Neurol 18:94-95, Finelli,P.F., 1985

Limb Shaking-A Carotid TIA
Stroke 16:444-448, Baquis,G.D.,et al, 1985

Showing articles 2000 to 2050 of 2512 << Previous Next >>