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Differential
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abscess, brainstem

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome, congenital

acute ataxia of childhood

acute cerebellar ataxia

adverse drug reaction

alcohol, neurologic complications with

alexia without agraphia

alien hand syndrome

alternating rapid movement

ankle reflex, absent

anterior horn cell disease

anterior tibial muscle weakness

anti Yo antibody

antiviral agents

aqueduct of Sylvius, enlargement

arm swing, reduced

ataxia telangiectasia

ataxia, acute onset

ataxia, cerebellar

ataxia, hereditary

ataxia, progressive

ataxia, sensory

ataxia, truncal

attention deficit disorder with hyperactivity

autonomic dysfunction

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

axonal spheroid

B 12 deficiency

basal ganglia, calcification of

basal ganglia, lesion of

behavioral disorder

Benedikt's syndrome

benign essential tremor

benign essential tremor, refractory

beta adrenergic blocker

biologic markers

brainstem, infarction of

brainstem, lesion of

brainstem, syndrome

calcification, intracranial

carcinoma of breast

carcinoma of lung

CAT scan, abnormal

CAT scan, false negative

central nervous system, infection of

cerebellar ataxia, autosomal recessive

cerebellar ataxia, hereditary

cerebellar ataxia, neuropathy and vestibular areflexia syndrome

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar disease, eye movement disorder in

cerebellar hemorrhage

cerebellar hypoplasia

cerebellar lesion

cerebellum, disease of

cerebral cortical atrophy

cerebral embolism

cerebral embolism, cardiac origin

cerebral peduncle

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, cytology

cerebrospinal fluid, enzymes in

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, gold sol.curve of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, red cells in

cerebrovascular accident

chest x-ray, abnormal

chylomicron retention disease

Claude's syndrome

Clinical Pathologic Conference(C.P.C.)

cogwheel rigidty

congenital infection, viral

corpus callosum, lesion of

corpus callosum, thinning

cortical-basal ganglionic degeneration

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

cryptococcoma, cerebral

decerebrate posture

degenerative diseases of CNS

delay in diagnosis

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes mellitus

differential diagnosis

difficulty going down stairs

distal muscle weakness

drug induced neurologic disorders

dysdiadochokinesia

dystonia, focal

electroencephalogram, abnormalities of

electroencephalogram, focal delta activity

erythema nodosum

exome sequencing

eye movement, disorders of

facial weakness

facial weakness, bilateral

failed medical management

false positive VDRL

fine motor function, impaired

finger nose finger test

fingerprint bodies

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

Friedreich's ataxia

gastrointestinal perforation

gaze palsy, supranuclear

gaze palsy, vertical

genetic neurologic disorders

genetic screening

genetic testing

glucose tolerance test, abnormal

granular osmiphilic material

head injury, brain stem lesion after

head injury, delayed deterioration following

heavy metal intoxication

heel-knee-shin test

hemianopia, homonymous

hemochromatosis

hemochromatosis, primary

hepatic encephalopathy

hepatolenticular degeneration(Wilson's disease)

hepatosplenomegaly

high arched feet

human immunodeficiency virus type 1

hyperhomocysteinemia

hyperosmolality

hyperpigmentation of skin

hyperthyroidism

hypoparathyroidism

hypotonia, infants

ideomotor apraxia

immunocompetent

inappropriate antidiuretic(A.D.H.)hormone

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

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intranuclear

infant, evaluation of

infantile tremor syndrome

intellectual deficit

intellectual deterioration

internuclear ophthalmoplegia

internuclear ophthalmoplegia, bilateral

internuclear ophthalmoplegia, unilateral

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Krabbe's disease

lactic acidemia

lactic dehydrogenase(LDH)

laughing, pathologic

leg weakness, bilateral

Leigh's disease

leukoencephalopathy

leukoencephalopathy, hereditary diffuse

level of consciousness, decreased

liver function enzymes

lysosomal storage disease

memory, defect of recent

memory, impairment of

meningeal enhancement

meningitis, carcinomatous

meningoencephalitis

mental status, abnormal

mesencephalic artery syndrome

midbrain, atrophy

midbrain, infarction of

midbrain, lesion of

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

molecular genetics

movement disorder

movement disorder, delayed onset

movement disorder, drug induced

movement disorder, extrapyramidal

MRI, CAT scan compared to

MRI, diffusion weighted

MRI, face of giant panda sign on

MRI, functional

multiple sclerosis

multiple sclerosis, treatment of

multiple system atrophy

muscle stiffness

muscle weakness, proximal

myelinolysis, extrapontine

myoclonic jerks

myoclonus, epilepsy

nausea and vomiting

nerve conduction studies

neuroaxonal leukodystrophy

neurologic disease, diagnoses of

neuronal ceroid-lipofuscinosis

neuronal intranuclear inclusion disease

neuroophthalmology

neuropathy, demyelinating

neuropathy, peripheral

neuropathy, sensory

Nothnagel's syndrome

nutritional deficiency

nystagmus, rotary

nystagmus, upbeating on upgaze

nystagmus, vertical

ocular motility, disorders of

oculogyric crisis

ophthalmoplegia

opportunistic infection

opportunistic infection, CNS

opsoclonus, differential diagnosis of

optic neuropathy

optic neuropathy, bilateral

osmotic demyelination syndrome

palatal myoclonus

Parkinson disease

Parkinson disease, axial symptoms

Parkinson disease, benign tremulous

Parkinson disease, L-dopa nonresponsive

Parkinson disease, tremor, absence of

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

PAS positive material in the brain

penguin silhouette sign

pleocytosis of cerebrospinal fluid

pneumoencephalogram(PEG)

poison, neurologic problems with

polymerase chain reaction, false negative

pons, lesion of

positional head-hanging test

posterior cerebral artery

posterior cerebral artery embolism

posterior cerebral artery territory infarction

postural abnormality

prevention of neurologic disorders

progressive multifocal leucoencephalopathy

progressive neurologic disorder

progressive supranuclear palsy

prothrombin time, prolonged

pseudobulbar palsy

psychomotor retardation

pure sensory stroke

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

Raynaud's phenomenon

reading disorder, acquired

red nucleus, involvement of

remote effect of cancer on the nervous system

reversible neurologic disorder

rigidity, axial

Sabin-Feldman dye test

saccadic eye movements, abnormal

sedimentation rate, elevated

seizure, children

sequencing difficulty

serum glutamic oxaloacetic transaminase

skin, darkening of

skin, lesions in neurologic disorders

speech disorder

speech disorder, childhood

speech disorder, non aphasic

speech, delayed development of

speech, loss of

spinocerebellar ataxia

spinocerebellar ataxia type 12

spinocerebellar ataxia type 3/Machado Joseph disease

startle myoclonus

startle reaction

status epilepticus

stimulation, deep brain

storage disease of CNS

striatonigral degeneration

striatonigral degeneration, infantile

substantia nigra

systemic lupus erythematosus

systemic lupus erythematosus, neurologic complications with

systemic lupus erythematosus, skin changes in

tandem gait, ataxic

thalamus, focused ultrasound ablation

thalamus, infarction of

thalamus, lesion of

thalamus, lesion of-bilateral

third nerve palsy

third nerve palsy, bilateral

thrombocytopenia

thrombotic thrombocytopenia purpura

toxoplasma complement fixation test

toxoplasmosis, acquired

toxoplasmosis, CNS

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

tremor, thalamic stimulation for suppression of

tremor, treatment of

tremor, writing

trimethoprim-sulfamethoxazole

trinucleotide repeats

unconsciousness

unconsciousness, transient

upgaze, paralysis of

vagus nerve stimulation

Venereal Disease Research Laboratory test

vibratory sensation, abnormal

viral infection

viral infection, CNS

vision, blurred

visual field defect

visual symptoms

vitamin deficiency

vitamin E deficiency

voice, abnormality of

walking, delayed

walking, difficulty with

Wernekinck commissure syndrome

West Nile fever

white matter disease

wide based gait

Showing articles 1050 to 1073 of 1073 << Previous

Encephalomyelopathy of Leigh
Editorial BMJ 238, 1971, May., , 1971

Drug-Induced Movement Disorders
Postgrad Med 180, 1971, Sept., North,R., 1971

Supranuclear Abnorm. of the Vert. Ocular Motor Syst
Trans Ophth United King 90:433, Sanders,M.D.,et al, 1970

Diseases of the Extrapyramidal System
Disease-a-month-Jan 1970., Klawans,H.,et al, 1970

Infantile Nystagmus:A Prospec. Study of Spasmus Nutans, Congen. Nystag, & Unclass. Nystagmus of Infancy
J Pediatr 77:177, Jayalakshuni,R.,et al, 1970

Corticodentatonigral Degeneration with Neuronal Achromasia
Arch Neurol 18:20-33, Rebeiz,J.J.,et al, 1968

Spastic Pseudosclerosis (Creutzfeldt-Jakob Dis) Van Rossum A. , In:Vinken, P. J.
Handbk of Clin Neurol Vol 6 North-Holland Publ. Amster 1968 Ch 28, p 726., Bruyn,G.W., 1968

Neuropathological Findings in Three Cases of Persistent Dyskinesia following Phenothiazine Medication
J Neurol Sci 7:263, Hunter,R.,et al, 1968

Function of the Basal Ganglia
Handbook of Clinical Neurology 6:90-115, Ward,A., 1968

Parkinson's Disease
In Handbk of Clinical Neurology, Vinken, P. J. & Bruyn, G. W. , Ed, North-Holland Publ Co, Amsterdam, 6:173, 1968. Selby, G., 1968

The Neuro-Psychiatric Syndr. Assoc. with Chronic Liver Disease & an Extensive Portal-Systemic Collat. Circul
Quart J Med 36:135, 1967 Jan., Read,A.E.,et al, 1967

Sylvian Aqueduct Syndrome
Arch Neurol 15:215, Hatcher,M.,et al, 1966

The Neurologist's Experience with Pheochromocytoma
JAMA 197:100, Thomas,J.E.,et al, 1966

Treatment of Hepatolenticular Degeneration (Wilson's Disease)
Am J Gastro 52:121, After 1966., Spellberg,M., 1966

Metabolic Defects Associated with Mental Retardation
Am J Dis Child 104:401, Garell,D., 1962

Diseases of the Basal Ganglia-Their Relation to Disorders of Movement
Lancet 1099, 1960, Nov., Denny-Brown,D., 1960

Nystagmus Retractorius
Arch Opthalmol 62:156, Smith,J.S.,et al, 1959

Neurologic Manifestations of Chronic Carbon Monoxide Poisoning
NEJM 261:1217-1220, Gilbert,G.J.,et al, 1959

Neurologic Manifestations of Chronic Pulmonary Insufficiency
NEJM 257:579-590, Austen,F.K.,et al, 1957

Neoplasms within the Midbrain
Arch Neurol & Psych 68:116952., Netsky,M.G.,et al, 1952

Ocular Motor Manifestations of Brainstem & Cerebellar Dysfunction
Chap 9, p 104 Neuro-Ophthalmol ed J. L. Smith., Daroff,R.B., 1850

Cerebellar Ataxia in Children
Handout & References., Gilbert,J.J., 1850

MR Imaging of Central Nervous System Whipple Disease: A 15-Year Review
AJNR 31:1493-1497, Black,D.F.,et al,

An 81-Year-Old Man with Imbalance and Memory Impairment
, Golbe,L.I.,et al,

Showing articles 1050 to 1073 of 1073 << Previous