Neudle.com: ataxia cerebellar

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Differential
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abdominal distention

abdominal reflex, absent

abdominal x-ray

abducens nerve paralysis

abducens nerve paralysis, bilateral

abortion, spontaneous

abscess, intracerebral

achilles tendon, enlarged

acoustic nerve, vestibular division of

acoustic neurinoma

acoustic neurinoma, bilateral

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

acquired immunodeficiency syndrome myelopathy

acquired immunodeficiency syndrome, heralded by neurologic invol

acral sensory symptoms

acute ataxia of childhood

acute cerebellar ataxia

acute disseminated encephalomyelitis

addiction, heroin

addiction, heroin-neurologic complications with

Addison's disease

adrenoleukodystrophy

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

adult-onset leukodystrophy, with neuroaxonal spheroids

advances in neurology

adverse drug reaction

agenesis of aqueduct of Sylvius

agranulocytosis

alcohol intolerance

alcohol, neurologic complications with

alcoholic amblyopia

alcoholic polyneuropathy

alcoholic withdrawal states, DT's, convulsions, etc.

Alexanders disease

Alexanders disease, adult onset

alien hand syndrome

alkalosis, respiratory

alkylating agents

alpha-fetoprotein

alpha-synuclein

altered states of consciousness

alternating hemiplegia

alternating hemiplegia of childhood

alternating rapid movement

alternating rapid movement, impaired

Alzheimer's disease

amaurosis fugax

aminoacidopathies

amnesia, concussion

amnestic syndrome

AMPA receptor antibodies

amphiphysin antibodies

amyloid angiopathy, cerebral

amyloid angiopathy, cerebral, inflammatory type

amyloid plaques

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, differential diagnosis

anemia, hemolytic

anemia, megaloblastic

anesthesia, general

aneurysm, asymptomatic

aneurysm, children

aneurysm, fusiform

aneurysm, intracranial

aneurysm, vertebral basilar system

Angelman syndrome

angiitis, granulomatous of CNS

angiitis, isolated of CNS, benign focal

angiography, cerebral, beaded vessels

angiography, cerebral

angiography, cerebral, false negative

angiography, cerebral, negative

angiography, posterior fossa

angiography, vertebral artery

angiotensin-converting enzyme

animal exposure

ankle reflex, absent

antecedent illness

anterior choroidal artery

anterior horn cell disease

anterior tibial muscle weakness

anti GQ1b IgG antibody

anti GT1aIgG antibody

anti Hu antibody

anti La antibody

anti MAG antibodies

anti mGluR1 encephalitis

anti Ri antibody

anti Ro antibody

anti Tr antibodies

anti Yo antibody

antiamphiphysin

antiarrhythmic drugs

antibiotics, neurologic complications with

antibodies to measles

antibodies to voltage-gated calcium channels

anticardiolipin antibodies

anticholinesterase

anticonvulsants

anticonvulsants, effectiveness

anticonvulsants, untoward effects of

antiendomysial antibodies

antiganglioside antibodies

antineurofascin antibodies

antineutrophil cytoplasmic autoantibodies

antithyroid antibodies

antiviral agents

aortic valve, insufficiency

apnea, primary central

apraxia of eye movements

aqueduct of Sylvius, enlargement

aqueduct of Sylvius, obstruction

aqueduct of Sylvius, stenosis

aqueductal obstruction

aqueductal stenosis

arm swing, reduced

Arnold Chiari malformation

arrhythmia, cardiac

arterial dissection

arterial dissection, intracranial

arterial dissection, precipitating events

arterial dissection, ruptured

arterial dissection, vertebral

arteritis, temporal

artificial intelligence

arylsulfatase A

ascending paralysis

aspartate aminotransferase

ataxia telangiectasia

ataxia, acute onset

ataxia, cerebellar

ataxia, congenital

ataxia, frontal

ataxia, hereditary

ataxia, paroxysmal

ataxia, progressive

ataxia, sensory

ataxia, truncal

ataxia, truncal, associated with ocular oscillations

ataxic hemiparesis

ataxic-dystonia syndromes

atherosclerosis, premature

atrial fibrillation

attention deficit disorder with hyperactivity

atypical lymphocytes

auditory evoked brainstem potentials

autoimmune basal ganglia encephalitis

autoimmune cerebellar ataxia

autoimmune disease

autoimmune encephalopathy

autoimmune GFAP astrocytopathy

automatism, postictal

automobile accidents

autonomic dysfunction

autonomic neuropathy

autosomal dominant leukodystrophy

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

axonal degeneration

axonal spheroid

axonopathy, distal

Ayurvedic medicine

B 12 deficiency

bacterial endocarditis, neurologic manifestations of

bacterial infection

bacterial infection, CNS

ballismus, bilateral

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, infarction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basilar artery aneurysm, twitching of face with

basilar artery migraine

basilar artery occlusion

basilar artery stenosis

basilar impression

basophilic stippling of red blood cells

Bassen-Kornzweig syndrome

behavior, combative

behavioral disorder

behavioral disorder, acute

Behcet's syndrome

Benedikt's syndrome

benign positional vertigo

Bergmann's gliosis

Bickerstaff's brainstem encephalitis

bilirubin encephalopathy

Binswanger disease

biologic markers

biological warfare

biotin deficiency

biotin deficiency, juvenile form

biotinidase deficiency

bitemporal visual field defect

bladder dysfunction

blindness, monocular

blindness, transient

blood dyscrasias, neurologic findings with

blood transfusion

blue tongue virus

bone marrow biopsy

bone marrow transplantation

border zone infarct

Borrelia burgdorferi infection

bovine spongiform encephalopathy

brachial neuritis

BRAF protooncogene

brain biopsy, negative

brain biopsy, stereotaxic

brainstem, atrophy

brainstem, dysfunction

brainstem, dysfunction, eye movement disorders with

brainstem, glioma

brainstem, glioma in children

brainstem, glioma, adult

brainstem, hematoma

brainstem, hemorrhage, primary

brainstem, infarction of

brainstem, lesion of

brainstem, neoplasms of

brainstem, syndrome

brucellosis, nervous system involvement with

Brudzinski's sign

bulbar dysfunction

bulbar palsy, acute

burning paresthesia

cafe au lait spots

calcification, intracranial

calcification, periventricular

calcium antagonist

calcium channel dysfunction

cancer of colon

carbamazepine, toxicity

carbon monoxide poisoning

carbon monoxide poisoning, chronic

carbon tetrachloride poisoning

carcinoembryonic antigen

carcinoid syndrome

carcinoma of bladder

carcinoma of breast

carcinoma of cervix

carcinoma of lung

carcinoma of ovary

carcinoma of pancreas

carcinoma of testis

carcinoma of uterus

carpo-pedal spasm

CAT scan, abdomen

CAT scan, abnormal

CAT scan, angiography

CAT scan, chest

CAT scan, contrast enhanced

CAT scan, contrast enhanced, subepend.

CAT scan, dense artery sign

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, metrizamide

CAT scan, negative

CAT scan, pelvis

CAT scan, ring sign

cataracts, congenital

cat-scratch disease

cauda equina, enhancement

caudate nucleus, lesion of, bilateral

celiac disease, adult

celiac disease, childhood

central core disease

central hypoventilation

central nervous system, infection of

central pontine myelinolysis

central retinal artery occlusion

cerebellar ataxia, autosomal recessive

cerebellar ataxia, children

cerebellar ataxia, children, differential diagnosis of

cerebellar ataxia, hereditary

cerebellar ataxia, neuropathy and vestibular areflexia syndrome

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar calcification

cerebellar cognitive affective syndrome

cerebellar degeneration

cerebellar disease, eye movement disorder in

cerebellar edema

cerebellar hemangioma

cerebellar hemorrhage

cerebellar hypoplasia

cerebellar infarction

cerebellar lesion

cerebellar peduncle

cerebellar plaques, amyloid

cerebellar pontine angle

cerebellar pontine angle tumor

cerebellar vermis

cerebellitis, autoimmune

cerebellum, clinico-path correlations

cerebellum, disease of

cerebellum, neoplasms of

cerebral arteries

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortex

cerebral cortical atrophy

cerebral embolism

cerebral embolism, cardiac origin

cerebral embolism, mechanical extraction

cerebral folate deficiency syndrome

cerebral glucose metabolism

cerebral infarction

cerebral infarction, hemorrhagic

cerebral ischemia

cerebroretinal microangiopathy with calcifications and cysts

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, culture of, viral

cerebrospinal fluid, cytology

cerebrospinal fluid, cytology, false negative

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, enzymes in

cerebrospinal fluid, eosinophilia of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, gold sol.curve of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, pressure low

cerebrospinal fluid, protein of

cerebrospinal fluid, proteincytologic dissociation

cerebrospinal fluid, red cells in

cerebrospinal fluid, xanthochromia of

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, acute management of

cerebrovascular accident, bilateral

cerebrovascular accident, clinical diagnosis

cerebrovascular accident, etiology

cerebrovascular accident, mimics

cerebrovascular accident, prognosis in

cerebrovascular accident, recurrent

cerebrovascular accident, surgical treatment of

cerebrovascular accident, vascular territory involved

cerebrovascular accident, women

cerebrovascular accident, young adult

cerebrovascular disease

cerebrovascular disease, risk factors in

cerebrovascular disease, surgical treatment of

Chamberlane's line

Charcot-Marie-Tooth

chasing the dragon

Cheiro-oral syndrome

chelation therapy

chemical weapons

chemotherapy, CNS treatment and complications with

chenodeoxycholic acid

cherry red spot

chest x-ray, abnormal

chewing movements

chloride channel dysfunction

choline chloride

chorea, familial

choreoathetosis

chorioretinitis

choroid plexus, tumor of

chromosomal abnormality

chronic fatigue syndrome

chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids

chronic progressive external ophthalmoplegia

cigarette smoking

ciguatera poisoning

cisterna magna, enlarged

Claude's syndrome

Clinical Pathologic Conference(C.P.C.)

clubbing of fingers

clubfoot as related to neurologic disease

coccidioidomycosis

Cockayne's syndrome

coenzyme Q10 deficiency

Cogan's syndrome

cognition, slowed

cognitive delay

cogwheel rigidty

collagen vascular disease

collapsin response mediator protein 5 IgG

color vision, impaired

compression fracture

concentration, impaired

cone-rod dystrophy

confusional state, acute

congenital infection, CNS

congenital infection, viral

congenital malformation

congenital paresis

congestive heart failure

conjunctival biopsy

contactin associated protein like 1 antibodies

contactin associated protein like 2 antibodies

contractures, joint

controversies in neurology

conus medullaris, lesion of

conversion reaction

copper deficiency

copper metabolism, abnormal

corkscrew hairs

cornea, abnormal

corneal reflex, abnormal

corneal reflex, depressed

corpus callosum

corpus callosum, atrophy of

corpus callosum, lesion of

corpus callosum, thinning

cortical blindness

cortical infarction

cortical infarction, small

cortical ribbon sign

cortical-basal ganglionic degeneration

counterimmunoelectrophoresis

Coxiella burnetti

cranial nerve enhancement

cranial nerve enlargement

cranial nerve palsies

cranial nerve palsies, bilateral

cranial nerve palsies, unilateral

cranial neuropathy

cranial neuropathy, multiple

cranio-cervical junction

craniopharyngioma

C-reactive protein, elevated

creatine phosphokinase(CPK)elevated

creatinine, elevated

Creutzfeldt-Jakob disease, genetic

Crigler-Najjar disease, type I

crying, pathologic

cryptococcal antigen

cryptococcal meningitis

cultured skin fibroblasts

Cushing's syndrome

cyst, peritumoral

cyst, arachnoid

cyst, arachnoid, posterior fossa

cyst, benign intracranial

cyst, epidermoid of CNS

cyst, neoplastic cerebellum

cyst, parenchymal

cyst, porencephalic

cyst, subcortical

cystatin C mutation

cystic fibrosis, neurologic complications with

cytochrome c oxidase

cytochrome c oxidase, deficiency

cytomegalovirus infection

cytosine arabinoside

Dandy Walker malformation

Dandy Walker malformation, adult

deafness, bilateral

deafness, sudden

deafness, unilateral

decerebrate posture

decontamination

deep gray nuclei

deep tendon reflexes

degenerative diseases of CNS

delay in diagnosis

delayed dentition

dementia, childhood

dementia, differential diagnosis of

dementia, familial

dementia, frontotemporal

dementia, posttraumatic

dementia, presenile

dementia, rapidly progressive

dementia, reversible

dementia, subcortical

dementia, transmissible

dementia, treatment of

demyelinating disease

dense basilar artery sign

dense middle cerebral artery sign

dental procedure, neurologic complications with

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

depersonalization

dermatitis herpetiformis

dermatoglyphics

dermatomyositis

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetes insipidus

diabetes mellitus

diabetes mellitus, chemical

diabetes mellitus, neurologic manifestations of

diagnostic criteria

dialysis dementia

dietary supplement

differential diagnosis

difficulty climbing stairs

difficulty going down stairs

digital health, wearable technology

digital subtraction angiography

dilantin, toxicity

diplegia, brachial

disability, neurological

disease modifying agents

dissociated sensory loss

distal muscle atrophy

distal muscle weakness

diurnal variation

doll's head maneuver

down-beat nystagmus

down-beat nystagmus, primary position of gaze

downward gaze, paralysis of

DPPX, antibodies

DPPX, antibodies, encephalitis

Dravet syndrome

drug abuse, inhalation

drug abuse, neurologic complications of

drug abuse, symptoms of

drug induced neurologic disorders

drug induced neurologic disorders in children

drug withdrawal

dysdiadochokinesia

dyskinesia, buccal lingual facial

dyssynergia cerebellaris myoclonica

dystonia musculorum deformens

dystonia, focal

dystonia, psychogenic

eating disorder

edema, periorbital

ejection fraction, abnormal

Ekbom's Syndrome

electrical injury of nervous system

electrical sensation

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, periodic complexes

electroencephalogram, triphasic delta waves

electron microscopy

electrophoretic pattern, CSF

electrophoretic pattern, serum

electroretinograph

embolism, paradoxical

embolism, septic

embolism, systemic

embolism, vertebral-basilar artery

emotional lability

empyema, epidural-spinal

encephalitis, amebic

encephalitis, autoimmune

encephalitis, bacterial

encephalitis, balamuthia

encephalitis, brainstem

encephalitis, diagnosis of

encephalitis, episodic

encephalitis, etiology

encephalitis, human immunodeficiency virus type 1

encephalitis, paraneoplastic

encephalitis, Powassan

encephalitis, viral

encephalitis, viral-causes of

encephalomyelitis

encephalomyelitis, parainfectious

encephalomyelitis, postinfectious

encephalomyopathy

encephalopathy, acute

encephalopathy, delayed

encephalopathy, Hashimoto's

encephalopathy, parainfectious

encephalopathy, progressive

encephalopathy, salmonella

endocarditis, neurologic manifestations with

endocarditis, subacute bacterial

endolymphatic sac tumors

endovascular therapy

enterovirus infection of CNS

eosinophilia-myalgia syndrome

epicanthal folds

epidemiology of neurology

episodic disorders

episodic neurologic deficits

Epstein-Barr virus

Erdheim-Chester disease

erectile dysfunction

erythema migrans

ethics in neurology

evoked potentials

executive dysfunction

exercise intolerance

exome sequencing

exophthalmus, bilateral

extraocular muscle lesion

eye movement, disorders of

Fabry's disease

face, numbness of

facial appearance, abnormal

facial expression abnormality

facial movement disorder

facial nerve palsy

facial nerve palsy, bilateral

facial pain, atypical

facial weakness

facial weakness, bilateral

failure to thrive

familial hemiplegic migraine

familial periodic ataxia

family planning

fatal familial insomnia

feeding disorder

fine motor function, impaired

finger nose finger test

finger numbness

fingerprint bodies

Fisher's syndrome

Fisher's syndrome, atypical

fistula, perilymphatic

flaccid paralysis

flu-like illness

fluorescein angiography

fluorescene in situ hybridization

fluorescent treponema antibody absorption(FTA-ABS)

fluorescent treponema antibody absorption/false positive

folic acid deficiency

food-borne infection

foot ulcer, neuropathic

fornix, lesion of

fourth ventricle, compression

fourth ventricle, enlargement of

fourth ventricle, neoplasm of

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

Friedreich's ataxia

Friedreich's ataxia, late onset

frontotemporal dementia, behavioral variant

fundus, abnormality of

funduscopic exam

fungal infection

fungal infection, CNS

gait analysis technology

GALOP syndromes

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

gammaglobulin therapy, intravenous, refractory

gasoline sniffing

gasserian ganglia

gastrectomy, neurologic complications following

gastric partitioning

gastroenteritis

gastrointestinal disease, neurologic complications

gastrointestinal motility

gastrointestinal perforation

gaze palsy, horizontal

gaze palsy, horizontal-bilateral

gaze palsy, supranuclear

gaze palsy, vertical

general paresis of the insane

genetic counselling

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

genital ulcerations

genu of corpus callosum

Gerstmann-Straussler-Scheinker disease

giant cell arteritis

Gillespie syndrome

gingival hyperplasia

girdle sensation

gliadin antibodies

glioblastoma multiforme(astrocytoma Gr.III)

glioma, low-grade

gliomatosis cerebri

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glucose tolerance test, abnormal

GLUT1 deficiency syndrome

glutamate dehydrogenase deficiency

glutamic acid decarboxylase, antibody

gluten sensitivity

gluten-free diet

gram negative rod

gram positive rod

granular osmiphilic material

granulomatous disease

growth hormone deficiency

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, ataxic form

Guillain Barre syndrome, axonal form

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, etiology of

Guillain Barre syndrome, infantile and childhood form

Guillain Barre syndrome, ophthalmoplegia in

Guillain Barre syndrome, prognosis of

Guillain Barre syndrome, sensory

Guillain Barre syndrome, variant forms of

Gulf War syndrome

gyrus, abnormal

Hallervorden Spatz disease

Hallgren's syndrome

hallucination, auditory

hallucination, visual

hand-foot-mouth disease

Hand-Schuller-Christian disease

Hartnup's disease

head circumference

head injury, brain stem lesion after

head injury, delayed deterioration following

head injury, severe

head turning, neurologic complications with

headache, awakened by

headache, awakening with

headache, bifrontal

headache, elderly

headache, episodic

headache, intractable

headache, occipital

headache, progressive

headache, recurrent

headache, severe

headache, sudden onset of

headache, worst of life

hearing loss, bilateral

hearing loss, sudden, bilateral

hearing problems in children

heavy metal intoxication

heel-knee-shin test

hemangioblastoma

hematoma, intracerebral

hematuria, gross

hematuria, microscopic

hemifacial spasm

hemisensory loss

hemisensory syndrome

hemochromatosis

hemochromatosis, primary

hemophagocytic lymphohistiocytosis, cerebromeningeal

hemophagocytosis

hemorrhage, thalamic

hemorrhagic diathesis

hemosiderosis of CNS, superficial

hepatic encephalopathy

hepatic failure

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), screening for

hepatolenticular degeneration, non-Wilsonian

hepatosplenomegaly

heralding manifestation

herniated disc, thoracic

herniation syndromes, intracranial

herpes simplex virus

herpes virus infection

herpes zoster, disseminated

herpes zoster, ophthalmicus

herpes zoster, oticus

heterophile antibody test

high altitude sickness

high arched feet

highly active antiretroviral therapy

histochemistry of muscle

HIV CSF viral escape syndrome

Hodgkin's disease

Hodgkin's disease, neurologic involvement with

homocysteine, serum

Horner's syndrome

hot cross bun sign

human immunodeficiency virus type 1

human immunodeficiency virus type 1, false positive

human immunodeficiency virus type 1, pathogenesis

human immunodeficiency virus type 2

human T-lymphotropic virus type I(HTLV-I)

human T-lymphotropic virus type II(HTLV-II)

Huntington's chorea

Hurler's syndrome

hydranencephally

hydrocephalus, non-communicating(obstructive)

hydrocephalus, normal pressure

hydroxyglutaric aciduria

hydroxytryptophan L-5(L-5 HTP)

hyperadrenalism

hyperalimentation

hyperammonemic encephalopathy

hyperbilirubinemia

hyperbilirubinemia, CNS abnormality after

hyperhomocysteinemia

hyperinsulinism

hyperintense vessel sign

hyperosmolality

hyperparathyroidism

hyperphosphatasia

hyperpigmentation of skin

hypersegmented polys

hypertension, cerebrovascular disease with

hyperthyroidism

hypertriglyceridemia

hypertrophic intracranial pachymeningitis

hyperventilation

hypocalcemia, causes of

hypocholesterolemia

hypofibrinogenemia

hypoglycorrhachia

hypoglycorrhachia, causes of

hypogonadism, hypogonadotropic

hypokalemic periodic paralysis

hypometric saccades

hypomyelination

hypoparathyroidism

hypoparathyroidism, idiopathic

hypophosphatemia

hypopigmentation of skin

hypoproteinemia

hypoprothrombinemia

hypotension, systemic

hypothalamus, damage to

hypothalamus, disturbance of

hypotonia, infants

hypoxic encephalopathy

iatrogenic neurologic disorders

IgG4-related disease

imbalance, postural

immediate recall

immune reconstitution inflammatory syndrome

immune-mediated pathogenesis

immunization, neurologic complications with

immunocompetent

immunodeficiency

immunoelectrophoresis, serum

immunofluorescent exam of CSF cells

immunohistochemistry

immunologic disease

immunology and the nervous system

immunomodulation

immunosuppression

immunosuppressive agents

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

inclusion bodies, ubiquitin

incontinence, fecal

industrial neurologic disorders

infectious mononucleosis

infectious mononucleosis, neurologic findings with

inferior olivary nucleus

inferior vermian artery

influenza A virus

insect repellent

intellectual deficit

intellectual deterioration

intelligence quotient

interferon alpha

internal capsule

internuclear ophthalmoplegia

internuclear ophthalmoplegia, bilateral

internuclear ophthalmoplegia, bilateral wall-eyed

internuclear ophthalmoplegia, unilateral

intestinal biopsy

intestinal pseudoobstruction

intracerebral hemorrhage

intracerebral hemorrhage, clot evacuation

intracerebral hemorrhage, recurrent

intracerebral hemorrhage, small

intracerebral hemorrhage, young adult

intracranial hypertension, benign

intracranial hypotension

intracranial pressure, increased

intrathecal chemotherapy

intrathecal medication

intrauterine infection

intrauterine infection, viral

intrauterine infection, viral of CNS

intrinsic hand muscles, wasting of

inverted V sign

islet cell tumor

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Jakob-Creutzfeldt disease, variant

Jakob-Creutzfeldt disease, young adult

jaw claudication

JC virus cerebellar granule cell neuronopathy

JC virus encephalopathy

joint hypermobility

judgement, impaired

juvenile paresis

Kayser-Fleischer ring

Kearns-Sayre syndrome

kelch-like protein 11 antibodies

keratitis, interstitial

keratoconjunctivitis

Korsakoff's psychosis

Krabbe's disease

kyphoscoliosis, neurologic causes of

labyrinth, disorder of

lactic acidemia

lactic dehydrogenase(LDH)

lacunar infarction

lacunar infarction, differential diagnosis of

language disorders in children

laryngismus stridulus

lateral medullary syndrome

lateral rectus palsy

laughing, pathologic

Laurence-Moon-Bardet-Biedl syndrome

lead and the nervous system

lead line, gingival

learning disability

learning disability, in children

Leber's hereditary optic neuropathy

leg spasms, painful

leg weakness, bilateral

Legionella pneumophilia

Legionnaires'disease

Leigh's disease

Leigh's disease, adult variety

lenticular nucleus, lesion of, bilateral

leucine rich glioma inactivated 1 antibodies

leukemia, neurologic findings assoc.with

leukocyte enzyme abnormality

leukodystrophy, 4H

leukoencephalopathy

leukoencephalopathy, adult onset, sporadic

leukoencephalopathy, differential diagnosis

leukoencephalopathy, hereditary diffuse

leukoencephalopathy, toxic

level of consciousness, decreased

Lhermitte's sign

libido, decreased

life expectancy

light-near dissociation, causes of

limbic encephalitis

lipid storage disorder of CNS

lipomatosis, multiple symmetrical

listeria monocytogenes

listeriosis, CNS

liver function enzymes

liver transplantation

locked-in syndrome

long bone lesion

lumbosacral radiculopathy

lymph node biopsy

lymphadenopathy

lymphadenopathy, cervical

lymphadenopathy, hilar

lymphocytic choriomeningitis

lymphocytic meningoradiculitis

lymphoma involving CNS

lymphoma, primary of CNS

lymphomatoid granulomatosis

lysosomal storage disease

macroglobulinemia

macular degeneration

malabsorption syndrome

malaria, cerebral

malformation, CNS, congenital

malignancy screen

malignancy, occult

malignant hyperpyrexia

mammillary bodies

maple syrup urine disease

marche a petits pas

Marchiafava-Bignami disease

Marcus Gunn pupil

Marinesco-Sjogren syndrome

mediastinum, mass of

medulla oblongata

medulla oblongata, infarction of

medulla oblongata, lesion of

medulla oblongata, neoplasm of

memory, defect of recent

memory, impairment of

Meniere's disease

meningeal biopsy

meningeal enhancement

meningeal enhancement, nodular

meningeal gliomatosis

meningitis, actinomycotic

meningitis, aseptic

meningitis, bacterial

meningitis, basilar

meningitis, blastomyces

meningitis, brucellosis

meningitis, candida

meningitis, carcinomatous

meningitis, chronic

meningitis, chronic benign lymphocytic

meningitis, cladosporium

meningitis, coenurosis

meningitis, cysticercosis

meningitis, echinococcal

meningitis, elderly

meningitis, eosinophilic

meningitis, fungal

meningitis, fungal-negative CSF culture

meningitis, helminthic

meningitis, histoplasma

meningitis, leptospira

meningitis, lymphomatous

meningitis, Mollaret's

meningitis, neutrophilic

meningitis, neutrophilic, persistent

meningitis, nocardia

meningitis, paracoccidioides

meningitis, post myelography

meningitis, recurrent

meningitis, syphilitic

meningitis, toxoplasma

meningoencephalitis

meningoencephalitis, mumps

meningoencephalitis, toxoplasma

meningoencephalomyelitis

meningoencephalopathy

meningovascular syphilis

mental retardation

mental status, abnormal

meralgia paresthetica

mesial temporal lobe

metabolic acidosis

metabolic disorder, primary

metabolic disorder, primary-screening tests

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

metachromatic leukodystrophy, juvenile

methylglutaconic aciduria

methylhydrazine derivatives

methylmalonic acid, serum

methylmalonic acidemia

microangiopathy, brain

microangiopathy, retina

microglial nodules

microhemorrhage, intracerebral

midbrain, atrophy

midbrain, hemorrhage

midbrain, infarction of

midbrain, lesion of

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

migraine, children

migraine, hemiplegic

migraine, visual symptoms in

Minamata disease

Mini Mental Status Examination

mitochondrial disease

mitochondrial disease, pathogenesis

mitochondrial encephalomyopathy

mitochondrial recessive ataxic syndrome

mitral valve lesion

mitral valve prolapse

mitral valve regurgitation

molecular genetics

monoamine oxidase inhibitors

monoclonal antibodies

monoclonal gammopathy

mononeuritis multiplex

mononeuropathy multiplex

monoparesis, focal

motor dysfunction

motor neuron disease

movement disorder

movement disorder, delayed onset

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, hyperkinetic

movement disorder, psychogenic

movement disorder, treatment of

MRI, angiography

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, contrast enhanced, high dose

MRI, contrast enhanced, subependymal

MRI, cranial nerves

MRI, curvilinear peppering enhancement

MRI, demyelinating disease

MRI, diffusion tensor

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, false negative

MRI, FLAIR, hyperintense vessels

MRI, high signal foci on

MRI, high signal intensity of basal ganglia

MRI, lumbosacral plexus

MRI, nodular enhancement

MRI, optic nerve

MRI, paramagnetic effect

MRI, punctate pattern

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRI, T1 weighted high signal foci

MRI, vessel wall

mucopolysaccharidoses

multimodal neuroimaging

multinucleated giant cell

multiple sclerosis

multiple sclerosis, children

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple sclerosis, pain in

multiple sclerosis, paroxysmal symptoms in

multiple sclerosis, presenting manifestations

multiple sclerosis, prognosis

multiple system atrophy

muscle atrophy, progressive

muscle spasm, face

muscle stiffness

muscle weakness

muscle weakness, causes of

muscle weakness, proximal

muscular dystrophy

myasthenia gravis

myasthenia gravis, paraneoplastic

myasthenic syndrome

mycoplasma pneumoniae

mycotic aneurysm

myelinolysis, extrapontine

myelitis, autoimmune

myelitis, longitudinal

myelitis, transverse

myeloneuropathy

myelopathy, chronic progressive

myelopathy, hepatic

myelopathy, tract-specific

myelopathy, vacuolar

myeloradiculitis

myoclonic ataxia

myoclonic jerks

myoclonus, cortical

myoclonus, epilepsy

myoclonus, segmental

myoclonus, stimulus sensitive

myoclonus-ataxia syndrome

myopathy, mitochondrial

myopathy, proximal

myotonia congenita

myotonia dystrophica

myxedema, neurologic manifestations of

N-acetylcysteine

Native Americans

nausea and vomiting

neonatal infection, viral

neonatal screening, genetic neurologic disorders

neoplasm, metastatic to CNS

neoplasm, metastatic to CNS-treatment of

neoplasm, pituitary

neoplasm, posterior fossa

neoplasm, primary intracerebral

neoplasm, primary of CNS

neoplasm, primary of CNS-children

neoplasm, primary of CNS-classification

neoplasm, primary of CNS-metastasizing to subarachnoid space

neoplasm, primary of CNS-surgical treatment of

neoplasm, primary of CNS-survival

neoplasm, primary of CNS-treatment of

neoplastic angioendotheliosis

nephrotic syndrome

nerve conduction studies

nerve conduction studies, sensory

nerve growth factor

nerve hypertrophy

nerve root enhancement

nerve root hypertrophy

neuraminidase deficiency

neuroaxonal dystrophy

neuroaxonal dystrophy, infantile

neuroaxonal dystrophy, juvenile

neuroaxonal leukodystrophy

neurocutaneous disease

neuroendocrinology

neurofibrillary degeneration

neurofibromatosis 1

neurogenic bladder

neurologic complications

neurologic complications of, surgery

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic disease, multifocal

neurologic disease, tempo

neurologic evaluation

neurologic examination

neurologic examination, focal

neurologic signs

neurologic symptoms

neurologic symptoms, unexplained

neurologic testing

neuromuscular disease, electrodiagnosis of

neuromuscular junction

neuromuscular junction, abnormality of

neuronal cell surface antigen

neuronal ceroid-lipofuscinosis

neuronal intranuclear inclusion disease

neuronopathy, sensory

neuroophthalmology

neuropathology, brain

neuropathy, acute

neuropathy, ataxic

neuropathy, autoimmune

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, iatrogenic

neuropathy, medication induced

neuropathy, motor

neuropathy, onion bulb

neuropathy, painful

neuropathy, paraneoplastic

neuropathy, peripheral

neuropathy, peripheral, treatment

neuropathy, recurrent

neuropathy, sensory

neuropathy, small-fiber

neuropathy, small-fiber, painful sensory

neuropathy, toxic

neurotoxicity, acute

neurotransmitter

next-generation sequencing

Niemann-Pick disease

night blindness

nitrogen mustard

NMDA antagonists

node of Ranvier

nodopathy, autoimmune

nodular infarction

non-dominant hemisphere

Nothnagel's syndrome

numbness, ascending

numbness, extremity

numbness, generalized

nutritional deficiency

nystagmus, dissociated

nystagmus, gaze-evoked

nystagmus, gaze-paretic

nystagmus, hereditary

nystagmus, intermittent

nystagmus, monocular

nystagmus, pendular

nystagmus, periodic

nystagmus, periodic alternating

nystagmus, positional

nystagmus, primary position of gaze

nystagmus, rotary

nystagmus, upbeating on upgaze

nystagmus, upbeating-in primary position of gaze

nystagmus, vertical

occupational neurologic disorders

ocular dysmetria

ocular motility, disorders of

ocular myopathy

oculocephalic reflex

oculodentodigital dysplasia

oculogyric crisis

oculomasticatory myorhythmia

old age, neurology of

olivary degeneration, hypertrophic

onconeural antibodies

one and a half syndrome

ophelia syndrome

ophthalmoplegia

ophthalmoplegia, acute

ophthalmoplegia, bilateral, acute

ophthalmoplegia, plus syndrome

ophthalmoplegia, postinfectious

ophthalmoplegia, progressive external

ophthalmoplegia, recurrent

ophthalmoplegia, total

opportunistic infection

opportunistic infection, CNS

opsoclonus, differential diagnosis of

opsoclonus-myoclonus syndrome

optic atrophy, hereditary

optic atrophy, unilateral

optic disc edema

optic nerve, enhancement

optic neuritis, children

optic neuropathy

optic neuropathy, bilateral

optic neuropathy, ischemic

optic neuropathy, toxic

optical coherence tomography

optokinetic nystagmus(O.K.N.)

optokinetic nystagmus, abnormal

oral ulcerations

orbit, lesions of

orbit, tomograms of

organ transplantation

orthostatic hypotension

osmotic demyelination syndrome

osteoblastic lesions, causes of

osteolytic lesion, causes of

otitis, neurologic complications with

ovarian dysgenesis

ovarian insufficiency

ovary, enlarged

overlap syndrome

Paget's disease

Paget's disease, psychosis in

Paget's disease, spinal cord problem in

pain, abdominal

palatal myoclonus

paralysis, acute

paralysis, acute areflexic

paramyotonia congenita

paraneoplastic brainstem encephalitis

paraneoplastic cerebellar degeneration

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, spastic

parasitic infection

parasitic infection, CNS

parathyroid adenoma

parenteral alimentation

paresthesias, feet

paresthesias, generalized

paresthesias, hands

parietal lobe, lesion of

parietal lobe, tests of

Parkinson disease

Parkinson disease, arteriosclerotic

Parkinson disease, drug induced

Parkinson disease, dystonia with

Parkinson disease, familial

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

Parkinsonism, freezing phenomena in

parotid gland neoplasm

paroxysmal hemiplegia

paroxysmal neurologic deficits

paroxysmal tonic upgaze

partial thromboplastin time, prolonged

PAS positive material in the brain

patent foramen ovale

pathologic reflex

patient information and support

pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection

Pelizaeus Merzbacher

Penumbra System

periaqueductal lesion

periarteritis nodosa

perifollicular hemorrhage

periodic paralysis

perioral numbness

peripheral blood smear

peripheral blood smear, abnormal

peripheral nerve, lesion of

peripheral pulse, absent

perivascular enhancement

perivascular inflammation

pernicious anemia

peroxisomal disease

Perrault syndrome

personality change

personality disorder

phencyclidine poisoning

phenylketonuria

pheochromocytoma

photosensitivity, skin

pigmentary retinopathy

pituitary stalk

pituitary stalk, lesion of

pituitary, enlargement

pituitary, lesion of

platelet inhibiting drugs

platelet transfusion

pleocytosis of cerebrospinal fluid

pleocytosis of cerebrospinal fluid, neutrophilic

pleural effusion

pneumoencephalogram(PEG)

poison, mercury

poison, neurologic problems with

poison, organophosphate

poliomyelitis-like illness

polyarthropathy

polyclonal gammopathy

polymerase chain reaction

polymerase chain reaction, false negative

polyneuritis, acute sensory

polyneuropathy, acute sensory

polyneuropathy, chronic idiopathic

polyneuropathy, chronic idiopathic, ataxic

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, chronic relapsing

polyradiculoneuropathy

pons, infarction of

pons, lesion of

pontine hemorrhage

pontocerebellar atrophy

Poretti-Boltshauser syndrome

portal caval shunt

position sensation

position sensation, abnormal

positional head-hanging test

post infectious cerebellar ataxia

post transplant lymphoproliferative disease

posterior cerebral artery

posterior column disease

posterior fossa

posterior fossa, lesion of

posterior fossa, mass of

posterior inferior cerebellar artery occlusion

posterior inferior cerebellar artery syndrome

posterior leukoencephalopathy syndrome

postoperative neurologic complications

postural abnormality

potassium channel antibodies

potassium channel dysfunction

practice guidelines

Prader-Labhart-Willi syndrome

precipitating factors

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

pretectal syndrome

prevention of neurologic disorders

primary aldosteronism

primary episodic ataxia

primary intracranial hypotension

prion protein gene

prisoners of war, neurologic complications in

progressive ataxia and palatal tremor

progressive infantile poliodystrophy

progressive multifocal leucoencephalopathy

progressive myoclonic epilepsy

progressive neurologic disorder

progressive pallidum atrophy

proprioception, abnormal

protein 14-3-3, cerebrospinal fluid

protein 14-3-3, cerebrospinal fluid, false negative

protozoan infection

pseudoathetosis

pseudobulbar palsy

pseudocerebellar signs

pseudointernuclear ophthalmoplegia

pseudoretinitis pigmentosa

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, neurologic problems

psychomotor retardation

psychotic behavior

ptosis, bilateral

ptosis, unilateral

puberty, delayed

pulmonary edema

pulmonary embolism

pulmonary infection

pulmonary infiltrates

pulmonary nodules

punch-drunk syndrome

pupil, abnormality in neurologic disorders

pupil, dilated and fixed, bilateral

pupil, dilated, bilateral

pupil, light reflex, abnormal

pure motor hemiplegia

pure sensory stroke

purkinje cell cytoplastic autoantibody

Purkinje cell surface antibody

pursuit eye movements, abnormal

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

radial pulse, unilateral decrease of

radiation hypersensitivity

radiation induced neoplasm

radiation necrosis

radiation therapy, CNS treatment and complications with

radiation therapy, stereotactic

ragged-red fibers

Ramsay Hunt syndrome

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

reading disorder, acquired

real-time quaking-induced conversion

red nucleus, involvement of

reflex, brainstem

Refsum's disease

rehabilitation for neurologic disorders

relapsing polychondritis

release phenomena

remote effect of cancer on the nervous system

renal cell carcinoma

renal transplantation

respirations in CNS disease

respiratory depression

respiratory failure

respiratory tract infection

reticular activating system

reticulum cell sarcoma

retina, abnormal

retinal artery occlusion

retinal branch artery occlusion

retinal degeneration

retinal detachment

retinal hemangioma

retinal hemorrhages

retinal infarction

retinal vasculitis

retinitis pigmentosa

retroperitoneal fibrosis

retroperitoneal mass

Rett's syndrome

reversible cerebral vasoconstrictive syndromes

reversible neurologic disorder

rheumatoid arthritis factor(R.A.factor)

rhomboencephalopathy

rickettsial organism

Riley-Day syndrome

root lesion, nerve

Rosenthal fibers

rubella encephalitis

rubella encephalitis, progressive

rubella syndrome

Sabin-Feldman dye test

saccadic eye movements, abnormal

sagging of the brain

salivation, excessive

sarcoidosis, CNS

scalp tenderness

sclerosis, bone

scotomata, scintillating

sedimentation rate

sedimentation rate, elevated

seizure, children

seizure, differential diagnosis of

seizure, drug-induced

seizure, familial

seizure, febrile

seizure, intractable

seizure, laughing as manifestation

seizure, neonatal

seizure, paradoxical

seizure, photosensitive

seizure, psychomotor-temporal lobe

seizure, tonic-clonic

seizure, treatment of

seizure, withdrawal

self-mutilation

semialdehyde dehydrogenase deficiency

sensorimotor stroke

sensorineural hearing loss

sensory ganglia

sensory ganglia, abnormal

sensory loss, asymmetric

sensory loss, crossed pattern

sensory loss, cutaneous

sensory loss, leg

sensory loss, patchy

sensory nerve action potentials

sensory polyneuropathy

sensory symptoms

serologic testing

serologic testing of cerebrospinal fluid

serologic testing, false negative

serum alanine aminotransferase

serum glutamic oxaloacetic transaminase

shell fish poisoning

shunt procedure, ventricular

shunt procedure, ventriculo-atrial

Shy-Drager syndrome

single photon emission computed tomography

sinuses, diseases of

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skew deviation, alternating

skin, darkening of

skin, lesions in neurologic disorders

skull x-ray, abnormal

sleep apnea, obstructive

sleep pathology and physiology

slow virus infection of CNS

small vessel disease

sodium channel dysfunction

somatosensory evoked potentials

spastic paraplegia, type 7

spatial orientation

speech disorder

speech disorder, childhood

speech disorder, non aphasic

speech, delayed development of

speech, loss of

Spielmeyer Vogt syndrome

spinal cord, cervical

spinal cord, compression of

spinal cord, dorsal subpial enhancement

spinal cord, lesion of

spinal cord, neoplasm

spinal cord, pathologic exam of

spinal muscular atrophy

spine, metastasis to

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 10

spinocerebellar ataxia type 12

spinocerebellar ataxia type 14

spinocerebellar ataxia type 17

spinocerebellar ataxia type 2

spinocerebellar ataxia type 28

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar ataxia type 5

spinocerebellar ataxia type 6

spinocerebellar ataxia type 7

spinocerebellar ataxia type 8

spinocerebellar degeneration

spinopontine atrophy, dominant

spirochete infection

splenium of corpus callosum

splinter hemorrhages

spongy degeneration of brain

spontaneous remission

sports medicine, neurology of

square wave jerks

standing difficulty

staphylococcal protein A column therapy

startle myoclonus

startle reaction

starvation, therapeutic

status epilepticus

status tetanicus

stem cell rescue

stem cell transplantation

stereotaxic surgery

stereotyped behavior

steroid responsive encephalopathy

steroid therapy, CNS treatment and complications with

stiff man syndrome

stimulation, deep brain

storage disease of CNS

stress, emotional

striatal encephalitis

striatonigral degeneration

striatonigral degeneration, infantile

striatum, lesion of

striatum, lesion of, bilateral

striopallidodentate calcifications, familial idiopathic

strokelike episodes

subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease

subarachnoid hemorrhage

subarachnoid hemorrhage, cerebral convexity

subarachnoid hemorrhage, recurrent

subconjunctival hemorrhage

subcortical U fibers

subcutaneous nodules

subdural hematoma

subdural hematoma, acute

superior cerebellar artery infarction

superior cerebellar artery syndrome

superior cerebellar peduncle

superior colliculus

superior orbital fissure syndrome

suprasellar lesion

supratentorial lymphocytic inflam parenchy perivasc enhanc responsive to steroids

Susac's syndrome

sweating, abnormality of

symmetric brain lesions

synucleinopathy

syphilis, asymptomatic

syphilis, diagnosis and treatment

syphilis, meningomyelitis

syphilis, neurologic complications with

syphilis, ocular

systemic illness

systemic lupus erythematosus

systemic lupus erythematosus, neurologic complications with

tandem gait, ataxic

teeth, abnormal

teeth, number of in infants

teeth, wide-spaced

temper tantrums

temporal artery, biopsy

temporal lobe, lesion

temporal lobe, lesion, bilateral

tentorium cerebelli

teratogenesis, viral

teratoma, ovarian

testicular enlargement

tetany, normocalcemic

thalamic ataxia syndrome

thalamic syndrome

thalamus, infarction of

thalamus, lesion of

thalamus, lesion of-bilateral

thiamine deficiency

third nerve palsy

third nerve palsy, bilateral

third nerve palsy, partial

third ventricle, wall

thrombocytopenia

thyrotropin-releasing hormone

tick-borne encephalitis

tongue, enlarged

tongue, numbness of

tongue, protrusion of

tonsillar herniation of cerebellum

toxic encephalopathy

toxins, nervous system

toxoplasma complement fixation test

toxoplasmosis, acquired

toxoplasmosis, CNS

transglutaminase antibodies

transient ischemic attack

transient neurologic deficit

transplacental virus infections

treatment of neurologic disorder

tremor, cerebellar

tremor, intention

tremor, postural

tremor, psychogenic

tremor, resting

tremor, thalamic

tremor, treatment of

tremor, writing

triangle of Guillain and Mollaret

trigeminal neuralgia

trigeminal neuropathy

trigeminal neuropathy, sensory

trinucleotide repeats

triphenyltin intoxication

trochlear nerve

trochlear nerve palsy

Trousseau's sign

twitching, face

ultrasonography

unconsciousness

Unverricht-Lundborg disease

upgaze, paralysis of

upgaze, sustained

upside-down vision

upward deviation of eyes

urea-cycle enzymopathies

urinary frequency

urinary gonadotropin

urinary incontinence

urinary retention

urinary urgency

urine test for metabolic disorders

urine test in toxic screen

Usher's syndrome

vaccination, neurologic complications with

valsalva maneuver

varicella zoster virus

varicella zoster virus, encephalitis

vasogenic edema

vasospasm, cerebral

Venereal Disease Research Laboratory test

vertebral artery

vertebral artery disease

vertebral artery occlusion

vertebral artery stenosis

vertebral-basilar insufficiency

vertigo, episodic

vertigo, positional

vertigo, treatment of

vestibular areflexia

vibratory sensation

vibratory sensation, abnormal

vincristine neurotoxicity

violent behavior

viral infection

viral infection, CNS

viral isolation

Virchow-Robin spaces, dilated

vision, blurred

vision, failure of in childhood

visual acuity, decreased

visual evoked response

visual field defect

visual fields, constricted

visual impairment

visual loss, progressive

visual loss, slow

visual loss, sudden-unilateral

visual loss, transient

visual obscurations, transient

visuospatial disturbance

vitamin deficiency

vitamin E deficiency

vitamin supplementation

vitamin, multiple

vitreous opacities

vocal cord paralysis

Vogt-Koyanagi-Harada syndrome

voice, abnormality of

voluntary nystagmus

von Bonsdorff's sign

Von Hippel Lindau

Waldenstrom's macroglobulinemia

walking, delayed

walking, difficulty with

walking, difficulty with in dark

weakness, generalized

weakness, progressive

weakness, proximal

weaning from respirator, failure to

Wernekinck commissure syndrome

Wernicke's encephalopathy

West Nile fever

Western immunoblot test

Whipple's disease

white matter disease

white matter disease, periventricular

white matter disease, subcortical

whole genome sequencing

wide based gait

Wolfram syndrome

word-finding difficulty

xanthoma, eyelid

xanthoma, tendon

xeroderma pigmentosa

X-linked bulbospinal neuronopathy

x-linked intellectual deficit

x-linked mental retardation

zoster sine herpete

Showing articles 350 to 400 of 1829 << Previous Next >>

Infantile Neuroaxonal Dystrophy,Clinical Spectrum and Diagnostic Criteria
Neurol 52:1472-1478, Nardocci,N.,et al, 1999

Multiple Sclerosis in Children Under 6 Years of Age
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Clinicopath Conf,Multifocal Inflammatory Leukoencephalopathy Related to Combination Chemo with Fluorouracil/levamisole
NEJM 341:512-519, Case 24-1999, 1999

Dancing Eyes-Dancing Feet
Lancet 354:390, Imtiaz,K.E.&Vora,J.P., 1999

Clinicopath Conf, Creutzfeldt-Jakob Disease,Case 28-1999
NEJM 341:901-908, , 1999

Neurologic Complications in Children with Enterovirus 71 Infection
NEJM 341:936-942, Huang,C-C.,et al, 1999

Opsoclonus as a Dominant Sign in Primary Sjogrens Syndrome
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Leukoencephalopathy and Raised Brain Lactate from Heroin Vapor Inhalation ("Chasing the Dragon")
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Subcotical Arteriosclerotic Encephalopathy (Binswangers Disease)
, Ghika,J. &Bogousslavsky, J., 1998

Usefulness of CT and MR Imaging in the Diagnosis of Acute Wernickes Encephalopathy
AJR 171:1131-1137, Antunez, E.,et al, 1998

Adult Brainstem Gliomas
Neurol 51:1136-1139, Landolfi,J.C.,et al, 1998

Ion Channels and Neurological Disease:DNA Based Diagnosis is Now Possible,and Ion Channels May be Important in Common Paroxysmal Disorders
JNNP 65:427-431, Hanna,M.G.,et al, 1998

Neuroradiologic Findings in Marinesco-Sjogren Syndrome
AJNR 19:281-283, Georgy,B.A.,et al, 1998

Slater Revisited:6 Year Follow Up Study of Pts with Medically Unexplained Motor Symptoms
BMJ 316:582-586, 5641998., Crimlisk,H.L.,et al, 1998

Consequences of the Delayed Diagnosis of Ataxia-Telangiectasia
Pediatrics 102:98-100, Cabana,M.D.,et al, 1998

Fluid Attenuation Inversion Recovery (FLAIR) Images of Dentatorubropalliodoluysian Atrophy:Case Report
JNNP 65:396-399, Yoshii,F.,et al, 1998

Neurological Channelopathies, Dysfunctional Ion Channels May Cause Many Neurological Diseases
BMJ 316:1104-1105, Rose,M.R., 1998

Myelopathy Caused by Nitrous Oxide Toxicity
AJNR 19:894-896, 9941998., Pema,P.J.,et al, 1998

Prader-Willi and Angelman Syndromes
Medicine 77:140-151, Cassidy,S.B.&Schwartz,S., 1998

Clinical Usefulness of Magnetic Resonance Imaging in Multiple System Atrophy
JNNP 65:65-71, Schrag,A.,et al, 1998

CAG Repeat Number Correlates with the Rate of Brainstem and Cerebellar Atrophy in Machado-Joseph Disease
Neurol 51:882-884, Abe,Y.,et al, 1998

Incidence of Dominant Spinocerebellar and Friedreich Triplet Repeats Among 361 Ataxic Families
Neurol 51:1666-1671, Moseley,M.L.,et al, 1998

Ataxic Hemiparesis,Critical Appraisal of a Lacunar Syndrome
Stroke 29:2549-2555, Gorman,M. J.,et al, 1998

Acute Inflammatory Demyelinating Polyradiculopathy in Children:Clinical and Electrodiagnostic Studies
Ann Neurol 44:350-356, Delanoe,C.,et al, 1998

Retinocochleocerebral Vasculopathy
Medicine 77:12-40, Petty,G.W.,et al, 1998

Susac Syndrome
Medicine 77:3-11, Papo,T.,et al, 1998

Progressive Atrophy of Cerebellum & Brainstem, Age & Size of Expanded CAG Repeats in the MJDI Gene in Machado-Joseph Dis
Ann Neurol 43:288-296, Onokera,O.,et al, 1998

Chronic Progressive Leukoencephalopathy in Adult Celiac Disease
Neurol 50:820-822, Beyenburg,S.,et al, 1998

Cerebellar Degeneration Associated With Human Immunodeficiency Virus Infection
Neurol 50:244-251, Tagliati,M.,et al, 1998

Lateral Medullary Infarction
Stroke, Pathophysiology, Diagnosis and management, Churchhill Livingstone, NY 3rd Ed, Ch 22, p. 534, Amarenco,P.,et al, 1998

Clinical,Radiological,Neurophysiological,and Neuropathological Characteristics of Gluten Ataxia
Lancet 352:1582-1585, Hadjivassiliou,M.,et al, 1998

Hypophosphatemia-Induced Neuropathy: Clinical and Electrophysiologic Findings
Muscle Nerve 21:650-652, Siddiqui,M.F. &Bertorini,T.E., 1998

Cerebral & Cerebellar Atrophy on Serial MRI in an Initially Symptom Free Subject at Risk of Familial Prion Disease
BMJ 315:856-857, Fox,N.C.,et al, 1997

Cerebral Manifestation of Erdheim-Chester Disease:Clinical and Radiologic Findings
Neurol 49:1702-1705, Bohlega,S.,et al, 1997

Ocular Findings in Ramsay Hunt Syndrome
J Neuro-Ophthalmol 17:199-201, Mansour,A.M.&Bailey,B.J., 1997

Adult-Onset Neimann-Pick Type C Disease, Clinical, Biochemical and Genetic Study
Arch Neurol 54:1536-1541, Lossos,A.,et al, 1997

Friedreich's Ataxia GAA Repeat Expansion in Pts with Recessive or sporadic Ataxia
Neurol 49:1004-1009, Geschwind,D.H.,et al, 1997

Broadened Friedreich's Ataxia Phenotype after Gene Cloning, Minimal GAA Expan Causes Late Spastic Ataxia
Neurol 49:1617-1620, Ragno,M.,et al, 1997

Atrophy of Cerebellum & Brainstem in Dentatorubral Pallidoluysian Atrophy, CAG Repeat Size on MRI Findings
Neurol 49:1605-1612, Koide,R.,et al, 1997

Pain After Thalamic Stroke:Right Diencephalic Predominance and Clinical Features in 180 Patients
Neurol 48:1196-1199, Nasreddine,Z.S.&Saver,J.L., 1997

Calcium Channels in Neurological Disease
Ann Neurol 42:275-282, Greenberg,D.A., 1997

Rapid Spongiform Degeneration of the Cerebrum and Cerebellum in Creutzfeldt-Jakob Encephalitis:Serial MR Findings
AJNR 18:583-586, Tzeng,B-C.,et al, 1997

Ataxia and Slurred Speech after Artesunate Treatment for Falciparum Malaria
NEJM 336:1328, Miller,L.G.&Panosian,C.B., 1997

Clinicopath Conf
Hodgkin's Disease, Paraneoplastic Cerebellar Degeneration, Case 21-1997, NEJM 337:115-12297., , 1997

Paraneoplastic Cerebellar Degeneration
Arch Int Med 157:1258-1262, Bolla,L.&Palmer,R.M., 1997

New Variant Creutzfeldt-Jakob Disease:Neurological Features and Diagnostic Tests
Lancet 350:903-907, Zeidler,M.,et al, 1997

The Expansion of the CAG Repeat in Ataxin-2 is a Frequent Cause of Autosomal Dominant Spinocerebellar Ataxia
Neurol 49:1009-1013, Lorenzetti,D.,et al, 1997

Spinocerebellar Ataxia Type 6, Molecular & Clin Features of 35 Japanese Pts (1 Homozygous for CAG Repeat Expan)
Neurol 49:1238-1243, 11961997., Matsumura,R.,et al, 1997

Clinical and Molecular Features of Spinocerebellar Ataxia Type 6
Neurol 49:1243-1246, 11961997., Stevanin,G.,et al, 1997

Spinocerebellar Ataxia Type 6, Frequency of the Mutation & Genotype-Phenotype Correl
NEurol 49:1247-1251, Geschwind,D.H.,et al, 1997

Showing articles 350 to 400 of 1829 << Previous Next >>