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Differential
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acquired immunodeficiency syndrome

acute ataxia of childhood

acute cerebellar ataxia

adverse drug reaction

alcohol, neurologic complications with

alien hand syndrome

alternating rapid movement

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, misdiagnosis

amyotrophic lateral sclerosis-like syndrome

ankle reflex, absent

anterior horn cell disease

anterior tibial muscle weakness

anti citrullinated antibody

anti Yo antibody

anticholinergic drugs

anticonvulsants

anticonvulsants, blood level determination of

anticonvulsants, mechanism of action of

anticonvulsants, teratogenicity of

anticonvulsants, untoward effects of

antiviral agents

arylsulfatase A

ataxia telangiectasia

ataxia, acute onset

ataxia, cerebellar

ataxia, hereditary

ataxia, progressive

ataxia, truncal

attention deficit disorder with hyperactivity

autonomic dysfunction

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

axonal spheroid

basal ganglia, calcification of

basal ganglia, lesion of

behavioral disorder

benign essential tremor

benign essential tremor, refractory

beta adrenergic blocker

biologic markers

calcification, intracranial

carcinoma of lung

CAT scan, abnormal

central nervous system, infection of

cerebellar ataxia, autosomal recessive

cerebellar ataxia, hereditary

cerebellar atrophy, primary

cerebellar degeneration

cerebellar disease, eye movement disorder in

cerebellar hemorrhage

cerebellar hypoplasia

cerebellar lesion

cerebellum, disease of

cerebral cortical atrophy

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

Clinical Pathologic Conference(C.P.C.)

cogwheel rigidty

conduction block

conversion reaction

corpus callosum, lesion of

corpus callosum, thinning

cortical-basal ganglionic degeneration

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

cyclophosphamide

decerebrate posture

degenerative diseases of CNS

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes mellitus

differential diagnosis

difficulty going down stairs

dilantin, factors influencing metabolism of

distal muscle weakness

drug induced neurologic disorders

dysdiadochokinesia

dystonia, focal

dystonia, post traumatic

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, focal delta activity

entrapment neuropathy

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

gamma amino butyric acid

gammaglobulin therapy, intravenous

gastrointestinal perforation

genetic counselling

genetic neurologic disorders

genetic screening

genetic testing

glucose tolerance test, abnormal

granular osmiphilic material

head injury, delayed deterioration following

heavy metal intoxication

hemochromatosis

hemochromatosis, primary

hepatic encephalopathy

hepatolenticular degeneration(Wilson's disease)

hepatosplenomegaly

high arched feet

Huntington's chorea

hyperosmolality

hyperthyroidism

hypoparathyroidism

hypotonia, infants

immunosuppressive agents

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intranuclear

infantile spasm

intellectual deficit

intellectual deterioration

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Krabbe's disease

lactic acidemia

lactic dehydrogenase(LDH)

laminectomy, lumbar

laughing, pathologic

leg weakness, bilateral

Leigh's disease

leukoencephalopathy

leukoencephalopathy, hereditary diffuse

liver function enzymes

lysosomal storage disease

memory, impairment of

meningeal enhancement

meningitis, carcinomatous

meningoencephalitis

mental retardation

metachromatic leukodystrophy

metachromatic leukodystrophy, juvenile

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

molecular genetics

motor neuron disease

movement disorder

movement disorder, delayed onset

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, psychogenic

MRI, diffusion weighted

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

nerve conduction studies, motor

neuroaxonal leukodystrophy

neuroendocrinology

neurologic disease, diagnoses of

neuromuscular disease, electrodiagnosis of

neuronal ceroid-lipofuscinosis

neuronal intranuclear inclusion disease

neuropathology, brain

neuropathy, demyelinating

neuropathy, motor

neuropathy, motor, multifocal

neuropathy, peripheral

nutritional deficiency

nystagmus, rotary

nystagmus, vertical

occupational neuropathies

oculogyric crisis

ophthalmoplegia

optic neuropathy

optic neuropathy, bilateral

orthostatic hypotension

osmotic demyelination syndrome

Parkinson disease

Parkinson disease, benign tremulous

Parkinson disease, L-dopa nonresponsive

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

PAS positive material in the brain

pleocytosis of cerebrospinal fluid

pneumoencephalogram(PEG)

poison, neurologic problems with

polymerase chain reaction, false negative

pons, lesion of

postoperative neurologic complications

prevention of neurologic disorders

progressive neurologic disorder

prothrombin time, prolonged

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

Raynaud's phenomenon

reflex sympathetic dystrophy

remote effect of cancer on the nervous system

respiratory myoclonus

respiratory tract infection

rheumatoid arthritis

rheumatoid arthritis, neurologic complications of

Sabin-Feldman dye test

saccadic eye movements, abnormal

sedimentation rate, elevated

seizure, children

seizure, minor motor

seizure, petit mal

seizure, tonic-clonic

seizure, treatment of

serum glutamic oxaloacetic transaminase

skin, darkening of

sodium valproate

sodium valproate, toxicity

speech disorder

speech disorder, childhood

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

systemic lupus erythematosus

systemic lupus erythematosus, neurologic complications with

systemic lupus erythematosus, skin changes in

tandem gait, ataxic

thalamus, focused ultrasound ablation

thrombocytopenia

thrombotic thrombocytopenia purpura

tongue, fasciculations of

tonic foot response

torticollis, post traumatic

toxoplasma complement fixation test

toxoplasmosis, acquired

toxoplasmosis, CNS

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, writing

trimethoprim-sulfamethoxazole

trinucleotide repeats

ulnar nerve, compression of

ulnar neuropathy

vagus nerve stimulation

Venereal Disease Research Laboratory test

viral infection

viral infection, CNS

vitamin E deficiency

walking, delayed

walking, difficulty with

West Nile fever

white matter disease

wide based gait

X-linked bulbospinal neuronopathy

Showing articles 1250 to 1277 of 1277 << Previous

Electrodiagnosis Studies in Neuromuscular Disease
NEJM 285:1244, Samaha,F., 1971

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

Early Recognition of Heterozygotes for the Gene for Dystrophia Myotonica
JNNP 33:279, Bundey,S.,et al, 1970

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

The Neuromyopathy of Vincristine in Man, Clinical, Electrophysiol & Pathological Studies
J Neurol Sci 10:107-131, Bradley,W.G.,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

Anterior Interosseous Nerve Palsy
BMJ 2:555, Mills,R.H.B.,et al, 1969

Foot Drop
G P 40:89, Goldner,J.,et al, 1969

Diabetes Mellitus Presenting with Bilateral Foot Drop
Lancet 2:930, Shahani,B.,et al, 1969

Myopathy of the Quadriceps Muscles
J Neurol Sci 7:201, VanWijngaarden,G.K.,et al, 1968

The Oculopharyngeal Syndrome
JAMA 203:1003, Murphy,S.F.,et al, 1968

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

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

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

A Spectrum of Myopathy Associated with Alcoholism (I. Clinical & Laboratory Features)
Ann Int Med 67:481, Perkoff,G.T.,et al, 1967

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

A Critical Survey of Stiff-Man Syndrome
Am J Med 42:582-599, Gordon,E.E.,et al, 1967

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

Mononeuritis Multiplex in Polyarteritis Nodosa
Neurol 14:434, Lovelace,R.E., 1964

Syndrome of Intention of Action Myoclonus as a Sequel to Hypoxic Encephalopathy
Brain 86:111, Lance,J.,et al, 1963

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

Clinical Picture in Creutzfeldt-Jakob Disease
Trans of Amer Neuro Assn 5:l47, Fisher,C.M., 1960

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

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

Showing articles 1250 to 1277 of 1277 << Previous