Neudle.com: idiopathic cerebellar ataxia

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Differential
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abdominal x-ray

abducens nerve paralysis

abducens nerve paralysis, bilateral

abortion, spontaneous

abscess, intracerebral

achilles tendon, enlarged

acoustic neurinoma, bilateral

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome, heralded by neurologic invol

acute ataxia of childhood

acute cerebellar ataxia

Addison's disease

adrenomyeloneuropathy

advances in neurology

adverse drug reaction

agenesis of aqueduct of Sylvius

alcohol intolerance

alcohol, neurologic complications with

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

Alexanders disease

Alexanders disease, adult onset

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

amaurosis fugax

amnesia, concussion

AMPA receptor antibodies

amphiphysin antibodies

amyloid plaques

aneurysm, children

aneurysm, fusiform

aneurysm, vertebral basilar system

Angelman syndrome

angiitis, granulomatous of CNS

angiitis, isolated of CNS, benign focal

angiography, cerebral

angiography, vertebral artery

angiotensin-converting enzyme

ankle reflex, absent

anti GQ1b IgG antibody

anti GT1aIgG antibody

anti Hu antibody

anti mGluR1 encephalitis

anti Ri antibody

anti Ro antibody

anti Tr antibodies

anti Yo antibody

antiamphiphysin

antiarrhythmic drugs

antibiotics, neurologic complications with

anticardiolipin antibodies

anticholinesterase

antiganglioside antibodies

antineutrophil cytoplasmic autoantibodies

antithyroid antibodies

antiviral agents

apraxia of eye movements

aqueduct of Sylvius, stenosis

aqueductal stenosis

arterial dissection, vertebral

arteritis, temporal

ascending paralysis

ataxia telangiectasia

ataxia, acute onset

ataxia, cerebellar

ataxia, congenital

ataxia, hereditary

ataxia, paroxysmal

ataxia, progressive

ataxia, sensory

ataxia, truncal

ataxia, truncal, associated with ocular oscillations

ataxic-dystonia syndromes

atherosclerosis, premature

auditory evoked brainstem potentials

autoimmune basal ganglia encephalitis

autoimmune cerebellar ataxia

autoimmune disease

autoimmune encephalopathy

autonomic dysfunction

autonomic neuropathy

autosomal dominant leukodystrophy

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

axonal spheroid

B 12 deficiency

bacterial infection

bacterial infection, CNS

ballismus, bilateral

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basilar impression

Bassen-Kornzweig syndrome

behavior, combative

behavioral disorder

Behcet's syndrome

Bergmann's gliosis

Bickerstaff's brainstem encephalitis

bilirubin encephalopathy

biologic markers

bitemporal visual field defect

bladder dysfunction

blood dyscrasias, neurologic findings with

blue tongue virus

bone marrow biopsy

Borrelia burgdorferi infection

brain biopsy, stereotaxic

brainstem, atrophy

brainstem, dysfunction

brainstem, glioma

brainstem, glioma, adult

brainstem, infarction of

brainstem, lesion of

brainstem, neoplasms of

brucellosis, nervous system involvement with

bulbar dysfunction

bulbar palsy, acute

burning paresthesia

calcification, intracranial

carbon tetrachloride poisoning

carcinoembryonic antigen

carcinoma of bladder

carcinoma of breast

carcinoma of cervix

carcinoma of lung

carcinoma of ovary

carcinoma of testis

carcinoma of uterus

carpo-pedal spasm

CAT scan, abnormal

CAT scan, chest

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, pelvis

cataracts, congenital

cauda equina, enhancement

celiac disease, adult

celiac disease, childhood

central nervous system, infection of

central retinal artery occlusion

cerebellar ataxia, autosomal recessive

cerebellar ataxia, children

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 hemangioma

cerebellar hypoplasia

cerebellar infarction

cerebellar lesion

cerebellar peduncle

cerebellar vermis

cerebellitis, autoimmune

cerebellum, disease of

cerebellum, neoplasms of

cerebral arteries

cerebral cortex

cerebral cortical atrophy

cerebral embolism

cerebral embolism, cardiac origin

cerebral folate deficiency syndrome

cerebral infarction

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, cytology

cerebrospinal fluid, cytology, false negative

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, enzymes in

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, gold sol.curve of

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, pressure low

cerebrospinal fluid, protein of

cerebrospinal fluid, proteincytologic dissociation

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, clinical diagnosis

cerebrovascular accident, prognosis in

cerebrovascular accident, recurrent

cerebrovascular accident, young adult

cerebrovascular disease, risk factors in

Chamberlane's line

Charcot-Marie-Tooth

chelation therapy

chemotherapy, CNS treatment and complications with

chenodeoxycholic acid

cherry red spot

chest x-ray, abnormal

choreoathetosis

choroid plexus, tumor of

chromosomal abnormality

chronic progressive external ophthalmoplegia

cigarette smoking

ciguatera poisoning

cisterna magna, enlarged

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

cogwheel rigidty

collapsin response mediator protein 5 IgG

concentration, impaired

congenital infection, CNS

conjunctival biopsy

contactin associated protein like 2 antibodies

contractures, joint

controversies in neurology

copper metabolism, abnormal

cornea, abnormal

corpus callosum

corpus callosum, atrophy of

corpus callosum, thinning

counterimmunoelectrophoresis

cranial nerve palsies

cranial nerve palsies, bilateral

cranial neuropathy

cranial neuropathy, multiple

craniopharyngioma

C-reactive protein, elevated

creatine phosphokinase(CPK)elevated

Creutzfeldt-Jakob disease, genetic

Crigler-Najjar disease, type I

cryptococcal meningitis

cultured skin fibroblasts

Cushing's syndrome

cyst, epidermoid of CNS

cyst, neoplastic cerebellum

cyst, parenchymal

cyst, porencephalic

cyst, subcortical

cytosine arabinoside

deep gray nuclei

deep tendon reflexes

degenerative diseases of CNS

delay in diagnosis

delayed dentition

dementia, childhood

dementia, familial

dementia, frontotemporal

dementia, posttraumatic

dementia, rapidly progressive

dementia, transmissible

demyelinating disease

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

dermatitis herpetiformis

dermatoglyphics

dermatomyositis

developmental disability

developmental retardation

dexterity, impaired

diabetes insipidus

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diagnostic criteria

differential diagnosis

difficulty climbing stairs

diplegia, brachial

distal muscle atrophy

down-beat nystagmus

DPPX, antibodies, encephalitis

drug abuse, inhalation

drug abuse, neurologic complications of

drug induced neurologic disorders

dysdiadochokinesia

dyskinesia, buccal lingual facial

dyssynergia cerebellaris myoclonica

dystonia musculorum deformens

edema, periorbital

ejection fraction, abnormal

electrical injury of nervous system

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

electron microscopy

electrophoretic pattern, CSF

electrophoretic pattern, serum

embolism, vertebral-basilar artery

emotional lability

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, episodic

encephalitis, paraneoplastic

encephalitis, viral

encephalomyelitis

encephalomyelitis, postinfectious

encephalomyopathy

encephalopathy, parainfectious

epidemiology of neurology

Epstein-Barr virus

Erdheim-Chester disease

erythema migrans

evoked potentials

exercise intolerance

exome sequencing

eye movement, disorders of

facial appearance, abnormal

facial expression abnormality

facial nerve palsy

facial nerve palsy, bilateral

facial weakness

facial weakness, bilateral

familial hemiplegic migraine

familial periodic ataxia

feeding disorder

fine motor function, impaired

finger nose finger test

fingerprint bodies

Fisher's syndrome

Fisher's syndrome, atypical

flaccid paralysis

fluorescene in situ hybridization

folic acid deficiency

fourth ventricle, enlargement 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

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

gasoline sniffing

gastrointestinal disease, neurologic complications

gaze palsy, horizontal

gaze palsy, horizontal-bilateral

gaze palsy, supranuclear

gaze palsy, vertical

genetic counselling

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

Gerstmann-Straussler-Scheinker disease

giant cell arteritis

Gillespie syndrome

glioma, low-grade

gliomatosis cerebri

globus pallidus, lesion of

glucose tolerance test, abnormal

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

Hallervorden Spatz disease

Hallgren's syndrome

hallucination, auditory

hallucination, visual

Hand-Schuller-Christian disease

head turning, neurologic complications with

headache, elderly

headache, progressive

headache, severe

hearing loss, bilateral

heel-knee-shin test

hemangioblastoma

hematuria, microscopic

hemisensory loss

hemochromatosis

hemochromatosis, primary

hemophagocytic lymphohistiocytosis, cerebromeningeal

hemophagocytosis

hemorrhagic diathesis

hemosiderosis of CNS, superficial

hepatic encephalopathy

hepatic failure

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), screening for

hepatosplenomegaly

heralding manifestation

herpes simplex virus

herpes virus infection

herpes zoster, disseminated

heterophile antibody test

Hodgkin's disease

Hodgkin's disease, neurologic involvement with

Horner's syndrome

hot cross bun sign

human immunodeficiency virus type 1

human immunodeficiency virus type 1, false positive

human immunodeficiency virus type 2

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

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

Hurler's syndrome

hydranencephally

hydrocephalus, normal pressure

hydroxytryptophan L-5(L-5 HTP)

hyperadrenalism

hyperalimentation

hyperbilirubinemia

hyperbilirubinemia, CNS abnormality after

hyperinsulinism

hyperosmolality

hyperparathyroidism

hyperpigmentation of skin

hyperthyroidism

hypertriglyceridemia

hypertrophic intracranial pachymeningitis

hyperventilation

hypocalcemia, causes of

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

iatrogenic neurologic disorders

imbalance, postural

immune reconstitution inflammatory syndrome

immunization, neurologic complications with

immunocompetent

immunodeficiency

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

industrial neurologic disorders

infectious mononucleosis

infectious mononucleosis, neurologic findings with

influenza A virus

intellectual deficit

intellectual deterioration

internuclear ophthalmoplegia

internuclear ophthalmoplegia, bilateral

intestinal biopsy

intracerebral hemorrhage

intracerebral hemorrhage, recurrent

intracerebral hemorrhage, young adult

intracranial hypertension, benign

intracranial pressure, increased

intrathecal chemotherapy

intrathecal medication

intrinsic hand muscles, wasting of

islet cell tumor

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Jakob-Creutzfeldt disease, variant

Jakob-Creutzfeldt disease, young adult

jaw claudication

Kayser-Fleischer ring

Kearns-Sayre syndrome

kelch-like protein 11 antibodies

Korsakoff's psychosis

lactic acidemia

lactic dehydrogenase(LDH)

laryngismus stridulus

lateral medullary syndrome

lateral rectus palsy

laughing, pathologic

Laurence-Moon-Bardet-Biedl syndrome

learning disability

learning disability, in children

leg spasms, painful

leg weakness, bilateral

Legionella pneumophilia

Legionnaires'disease

Leigh's disease

leucine rich glioma inactivated 1 antibodies

leukemia, neurologic findings assoc.with

leukodystrophy, 4H

leukoencephalopathy

leukoencephalopathy, differential diagnosis

level of consciousness, decreased

life expectancy

limbic encephalitis

lipid storage disorder of CNS

listeria monocytogenes

listeriosis, CNS

liver function enzymes

liver transplantation

long bone lesion

lumbosacral radiculopathy

lymphadenopathy

lymphocytic meningoradiculitis

lymphoma involving CNS

lysosomal storage disease

macroglobulinemia

macular degeneration

malabsorption syndrome

malformation, CNS, congenital

malignancy screen

malignancy, occult

marche a petits pas

Marinesco-Sjogren syndrome

mediastinum, mass of

medulla oblongata, infarction of

memory, defect of recent

memory, impairment of

Meniere's disease

meningeal biopsy

meningeal enhancement

meningeal gliomatosis

meningitis, actinomycotic

meningitis, aseptic

meningitis, bacterial

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, helminthic

meningitis, histoplasma

meningitis, leptospira

meningitis, lymphomatous

meningitis, Mollaret's

meningitis, nocardia

meningitis, paracoccidioides

meningitis, post myelography

meningitis, recurrent

meningitis, syphilitic

meningitis, toxoplasma

meningoencephalitis

meningoencephalitis, toxoplasma

meningoencephalopathy

mental retardation

mental status, abnormal

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

methylhydrazine derivatives

microhemorrhage, intracerebral

midbrain, atrophy

midbrain, infarction of

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

migraine, children

migraine, hemiplegic

mitochondrial disease

mitochondrial encephalomyopathy

mitochondrial recessive ataxic syndrome

molecular genetics

monoamine oxidase inhibitors

monoclonal antibodies

monoclonal gammopathy

mononeuritis multiplex

motor neuron disease

movement disorder

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, hyperkinetic

movement disorder, treatment of

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, false negative

MRI, high signal foci on

MRI, high signal intensity of basal ganglia

MRI, optic nerve

MRI, punctate pattern

MRI, spinal cord

MRI, vessel wall

mucopolysaccharidoses

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple system atrophy

muscle stiffness

muscle weakness

muscle weakness, causes of

muscle weakness, proximal

myasthenia gravis

myasthenia gravis, paraneoplastic

myasthenic syndrome

mycoplasma pneumoniae

myelinolysis, extrapontine

myelitis, transverse

myelopathy, chronic progressive

myoclonic ataxia

myoclonic jerks

myoclonus, cortical

myoclonus, epilepsy

myoclonus, stimulus sensitive

myoclonus-ataxia syndrome

myopathy, mitochondrial

myxedema, neurologic manifestations of

Native Americans

nausea and vomiting

neonatal infection, viral

neoplasm, pituitary

neoplasm, primary intracerebral

neoplasm, primary of CNS

neoplasm, primary of CNS-classification

neoplasm, primary of CNS-metastasizing to subarachnoid space

nephrotic syndrome

nerve conduction studies

neuraminidase deficiency

neuroaxonal dystrophy

neuroaxonal dystrophy, infantile

neuroaxonal dystrophy, juvenile

neurocutaneous disease

neuroendocrinology

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic disease, multifocal

neurologic disease, tempo

neurologic signs

neurologic symptoms

neuromuscular junction

neuronal cell surface antigen

neuronal ceroid-lipofuscinosis

neuronal intranuclear inclusion disease

neuronopathy, sensory

neuroophthalmology

neuropathology, brain

neuropathy, acute

neuropathy, ataxic

neuropathy, demyelinating

neuropathy, painful

neuropathy, paraneoplastic

neuropathy, peripheral

neuropathy, recurrent

neuropathy, sensory

neuropathy, toxic

next-generation sequencing

Niemann-Pick disease

nitrogen mustard

NMDA antagonists

nodular infarction

nutritional deficiency

nystagmus, gaze-evoked

nystagmus, gaze-paretic

nystagmus, intermittent

nystagmus, monocular

nystagmus, primary position of gaze

nystagmus, rotary

nystagmus, upbeating on upgaze

nystagmus, vertical

ocular dysmetria

ocular motility, disorders of

ocular myopathy

oculocephalic reflex

oculomasticatory myorhythmia

old age, neurology of

onconeural antibodies

ophelia syndrome

ophthalmoplegia

ophthalmoplegia, acute

ophthalmoplegia, postinfectious

ophthalmoplegia, progressive external

ophthalmoplegia, recurrent

ophthalmoplegia, total

opportunistic infection

opportunistic infection, CNS

opsoclonus-myoclonus syndrome

optic disc edema

optic nerve, enhancement

optic neuropathy

optic neuropathy, ischemic

optical coherence tomography

oral ulcerations

orbit, tomograms of

orthostatic hypotension

osmotic demyelination syndrome

osteoblastic lesions, causes of

otitis, neurologic complications with

ovarian dysgenesis

Paget's disease

pain, abdominal

palatal myoclonus

paralysis, acute

paralysis, acute areflexic

paraneoplastic brainstem encephalitis

paraneoplastic cerebellar degeneration

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, spastic

parasitic infection, CNS

parathyroid adenoma

paresthesias, feet

parietal lobe, lesion of

Parkinson disease

Parkinson disease, drug induced

Parkinson disease, dystonia with

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

Parkinsonism, freezing phenomena in

paroxysmal hemiplegia

paroxysmal neurologic deficits

partial thromboplastin time, prolonged

PAS positive material in the brain

pathologic reflex

pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection

Pelizaeus Merzbacher

peripheral nerve, lesion of

peripheral pulse, absent

Perrault syndrome

personality change

pheochromocytoma

pigmentary retinopathy

pituitary, lesion of

pleocytosis of cerebrospinal fluid

pleural effusion

pneumoencephalogram(PEG)

poliomyelitis-like illness

polyclonal gammopathy

polymerase chain reaction

polyneuritis, acute sensory

polyneuropathy, acute sensory

polyneuropathy, chronic idiopathic

polyneuropathy, chronic idiopathic, ataxic

polyneuropathy, chronic relapsing

polyradiculoneuropathy

pons, lesion of

pontocerebellar atrophy

Poretti-Boltshauser syndrome

positional head-hanging test

post infectious cerebellar ataxia

posterior column disease

posterior inferior cerebellar artery occlusion

posterior inferior cerebellar artery syndrome

postural abnormality

potassium channel antibodies

practice guidelines

precipitating factors

prevention of neurologic disorders

primary aldosteronism

prion protein gene

progressive infantile poliodystrophy

progressive multifocal leucoencephalopathy

progressive neurologic disorder

proprioception, abnormal

protein 14-3-3, cerebrospinal fluid

pseudobulbar palsy

pseudointernuclear ophthalmoplegia

pseudoretinitis pigmentosa

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, neurologic problems

psychomotor retardation

ptosis, bilateral

puberty, delayed

pulmonary embolism

pulmonary infiltrates

punch-drunk syndrome

pupil, abnormality in neurologic disorders

pupil, dilated and fixed, bilateral

pupil, dilated, bilateral

purkinje cell cytoplastic autoantibody

pursuit eye movements, abnormal

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

radial pulse, unilateral decrease of

radiation hypersensitivity

ragged-red fibers

Ramsay Hunt syndrome

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

reading disorder, acquired

real-time quaking-induced conversion

reflex, brainstem

release phenomena

remote effect of cancer on the nervous system

renal cell carcinoma

respiratory failure

respiratory tract infection

reticulum cell sarcoma

retina, abnormal

retinal degeneration

retinal detachment

retinal hemangioma

retinitis pigmentosa

retroperitoneal mass

Rett's syndrome

rheumatoid arthritis factor(R.A.factor)

rhomboencephalopathy

Rosenthal fibers

rubella encephalitis

rubella encephalitis, progressive

rubella syndrome

Sabin-Feldman dye test

saccadic eye movements, abnormal

salivation, excessive

sarcoidosis, CNS

scalp tenderness

sclerosis, bone

sedimentation rate

sedimentation rate, elevated

seizure, intractable

seizure, laughing as manifestation

seizure, neonatal

seizure, psychomotor-temporal lobe

sensorineural hearing loss

sensory loss, crossed pattern

sensory loss, leg

sensory polyneuropathy

serologic testing

serologic testing of cerebrospinal fluid

serologic testing, false negative

serum glutamic oxaloacetic transaminase

shunt procedure, ventricular

shunt procedure, ventriculo-atrial

Shy-Drager syndrome

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skin, darkening of

skin, lesions in neurologic disorders

skull x-ray, abnormal

sleep pathology and physiology

slow virus infection of CNS

sodium channel dysfunction

spastic paraplegia, type 7

speech disorder

speech disorder, childhood

speech disorder, non aphasic

speech, delayed development of

Spielmeyer Vogt syndrome

spinal cord, lesion of

spinal muscular atrophy

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 10

spinocerebellar ataxia type 12

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

spirochete infection

splenium of corpus callosum

splinter hemorrhages

spongy degeneration of brain

sports medicine, neurology of

square wave jerks

standing difficulty

startle myoclonus

startle reaction

status epilepticus

status tetanicus

steroid therapy, CNS treatment and complications with

stiff man syndrome

stimulation, deep brain

storage disease of CNS

striatal encephalitis

striatonigral degeneration

striatum, lesion of

striatum, lesion of, bilateral

striopallidodentate calcifications, familial idiopathic

subconjunctival hemorrhage

subcortical U fibers

subdural hematoma

subdural hematoma, acute

superior cerebellar artery infarction

superior cerebellar artery syndrome

symmetric brain lesions

synucleinopathy

systemic illness

tandem gait, ataxic

teeth, abnormal

teeth, number of in infants

teeth, wide-spaced

temporal artery, biopsy

temporal lobe, lesion

temporal lobe, lesion, bilateral

tentorium cerebelli

teratogenesis, viral

tetany, normocalcemic

thalamus, lesion of

thalamus, lesion of-bilateral

third nerve palsy

thrombocytopenia

tongue, enlarged

tongue, protrusion of

toxic encephalopathy

toxins, nervous system

toxoplasma complement fixation test

toxoplasmosis, acquired

toxoplasmosis, CNS

transglutaminase antibodies

transient ischemic attack

transient neurologic deficit

treatment of neurologic disorder

tremor, cerebellar

tremor, intention

tremor, postural

tremor, treatment of

tremor, writing

trigeminal neuropathy

trigeminal neuropathy, sensory

trinucleotide repeats

Trousseau's sign

ultrasonography

upgaze, paralysis of

urinary gonadotropin

urinary incontinence

urinary retention

urinary urgency

Usher's syndrome

varicella zoster virus

varicella zoster virus, encephalitis

vertebral artery

vertebral artery disease

vertebral artery occlusion

vertebral artery stenosis

vertebral-basilar insufficiency

vestibular areflexia

vibratory sensation, abnormal

vincristine neurotoxicity

violent behavior

viral infection

viral infection, CNS

viral isolation

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 obscurations, transient

vitamin deficiency

vitamin E deficiency

vitamin supplementation

vocal cord paralysis

Vogt-Koyanagi-Harada syndrome

voice, abnormality of

von Bonsdorff's sign

Von Hippel Lindau

Waldenstrom's macroglobulinemia

walking, difficulty with

walking, difficulty with in dark

weakness, generalized

weakness, progressive

Wernekinck commissure syndrome

West Nile fever

Western immunoblot test

Whipple's disease

white matter disease

whole genome sequencing

wide based gait

Wolfram syndrome

xanthoma, eyelid

xanthoma, tendon

Showing articles 200 to 250 of 3658 << Previous Next >>

Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
Medicine 70:99-117, Gatti,R.A.,et al, 1991

Sarcoidosis of the Nervous System, A Clinical Approach
Arch Int Med 151:1317-1321, Sharma,Om.P.&Sharma,A.D., 1991

The Marinesco-Sjogren Syndrome Examined by CT, MR, and 18F-2-Fluoro-2-Deoxy-D-Glucose & PET
Arch Neurol 47:1239-1242, Bromberg,M.B.,et al, 1990

Progressive Myoclonic Ataxia (The Ramsay Hunt Syndrome)
Arch Neurol 47:1121-1125, Marsden,C.D.,et al, 1990

Idiopathic Cerebellar Ataxia of Late Onset:Natural History and MRI Morphology
JNNP 53:297-305, Klockgether,T.,et al, 1990

Migraine Assoc with Focal Cerebral Edema, CSF Pleocytosis, & Prog Cerebellar Ataxia:MRI Documentation
Neurol 40:1284-1287, Goldstein,J.M.,et al, 1990

Progressive Rubella Panencephalitis
In Handbk of Clin Neurol, Vinken & Bruyn, Ed, N Holland Publ Co, 56:405-416, Wolinsky,J.S., 1990

Cerebral Cortex and Brainstem Involvement in Marinesco-Sjogren Syndrome
Ann Neurol 27:448-449, Katafuchi,Y.,et al, 1990

Movement Disorders in Alcoholism:A Review
Neurol 40:741-746, Neiman,J.,et al, 1990

Neurologic Manifestations of Giant Cell Arteritis
Am J Med 89:67-72, Reich,K.A.,et al, 1990

Gerstmann-Straussler-Scheinker Disease, I, Extending the Clinical Spectrum
Neurol 39:1446-1452, Farlow,M.R.,et al, 1989

Late Onset of Distinct Neurologic Syndromes in Galactosemic Siblings
Neurol 39:741-742, Friedman,J.H.,et al, 1989

Syndrome of Cerebellar Ataxia and Hypogonadotrophic Hypogonadism:Evidence for Pituitary Gonadotrophin Deficiency
JNNP 52:407-409, Fox,A.C.K.,et al, 1989

Primary Progressive Cerebellar Ataxia
Neuroradiology 31:16-18, Bradac,G.B.,et al, 1989

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

Sensory Form of Acute Polyneuritis
Neurol 38:1728-1731, Dawson,D.M.,et al, 1988

Magnetic Resonance Imaging in Familial Paroxysmal Ataxia
Arch Neurol 45:547-549, Vighetto,A.,et al, 1988

Creutzfeldt-Jakob Disease Following Pituitary-Derived Human Growth Hormone Therapy:A New American Case
Neurol 38:1131-1133, Marzewski,D.J.,et al, 1988

The Minor Symptoms of Increased Intracranial Pressure:101 Pts with Benign Intracranial Hypertension
Neurol 38:1461-1464, Round,R.&Keane,J.R., 1988

Hereditary Dentatorubral-Pallidoluysian Atrophy:Clinical and Pathologic Variants in a Family
Neurol 38:1065-1070, Takahashi,H.,et al, 1988

Neurologic Manifestations of Heatstroke at the Mecca Pilgrimage
Neurol 37:1004-1006, Yaqub,B.A., 1987

Delayed Cerebellar Ataxia:A New Complication of Falciparum Malaria
BMJ 294:1253-1254, Senanayake,N., 1987

Acute Trimethyltin Limbic-Cerebellar Syndrome
Neurol 37:945-950, Besser,R.,et al, 1987

Clinicopath Conf
Kearns-Sayre Syndrome (Oculocraniosomatic Neuromuscular Disease with Mitochondrial Myopathy) , Case, 4-1,NEJM 317:493-501,1987., 1987

Neurologic Aspects of Boxing
Arch Neurol 44:453-459, Jordan,B.D., 1987

Tobacco Intolerance in Multiple System Atrophy
Neurol 36:986-988, Johnsen,J.A.,et al, 1986

Neurologic Sequelae of Chronic Solvent Vapor Abuse
Neurol 36:698-702, Hormes,J.T.,et al, 1986

Chronic Idiopathic Ataxic Neuropathy
Ann Neurol 19:545-554, Dalakas,M.C., 1986

Hyponatraemia as a Cause of Reversible Ataxia
et al BMJ 293:1346, Kelsey,S.M., 1986

Cerebellar Dysfunction & Nephrotic Syndrome in a 50-Year-Old Man, Clinicopath. Conference
Am J Med 79:621-628, Klahr,S., 1985

Paraneoplastic Cerebellar Disease, Remission with Excision of the Primary Tumor
Arch Neurol 42:1208-1210, Kearsley,J.H.,et al, 1985

Creutzfeldt-Jakob Disease after Administration of Human Growth Hormone
Lancet 2:244-246, Powell-Jackson,J.,et al, 1985

Central Nervous System Toxicity with High-Dose Ara-C
Neurol 35:1475-1479, Hwang,T.,et al, 1985

Relapsing Ophthalmoparesis-Sensory Neuropathy Syndrome
Neurol 35:595-596, Kaplan,J.G.,et al, 1985

Adrenoleukomyeloneuropathy with Onset in Early Childhood
Ann Neurol 17:311-312, Rosen,N.L.,et al, 1985

Ataxic Creutzfeldt-Jakob Disease:Diagnostic Techniques & Neuropathologic Observations in Early Disease
Neurol 35:254-257, Jones,H.R.,et al, 1985

Cerebellar Ataxia Due to Procainamide Toxicity
Arch Int Med 144:2260-2261, Schwartz,A.B.,et al, 1984

Long-Term Treatment of Cerebrotendinous Xanthomatosis with Chenodeoxycholic Acid
NEJM 311:1649-1652, Berginer,V.M.,et al, 1984

Long-Lasting Neurological Sequelae After Lithium Intoxication
Acta Psychiatr Scand 70:594-602, Schou,M., 1984

Herpes Zoster-Associated Encephalitis:Clinicopathologic Report of 12 Cases and Review of the Literature
Medicine 62:81-95, Jemsek,J.,et al, 1983

Gerstmann-Straussler-Scheinker Disease with Coincidental Familial Onset
Ann Neurol 14:670-678, Hudson,A.J.,et al, 1983

Persisting Neurologic Sequelae of Lithium Carbonate Therapy
Arch Neurol 40:747-751, MacDonaldson,I.,et al, 1983

Acute Cerebellar Ataxia & Hearing Loss as Initial Symptoms of Infectious Mononucleosis
Arch Neurol 40:760-762, Erzurum,S.,et al, 1983

Cerebellar Degeneration Caused by High-Dose Cytosine Arabinoside:A Clinicopathological Study
Ann Neurol 14:520-527, Winkelman,M.D.,et al, 1983

Cerebellar Dysfunction after Acute Carbon Tetrachloride Poisoning
Lancet 2:968, Forster,S.H.,et al, 1983

Permanent Neurological Deficits Due to Lithium Toxicity
Ann Neurol 13:453-455, Apte,S.N.,et al, 1983

Sensory Ataxia, A Residual Disability of Guillain-Barre Syndrome
Arch Neurol 40:86-89, Sobue,G.,et al, 1983

Neuroaxonal Dystrophy in Young Adults:A Clinicopathological Study of Two Unrelated Cases
Ann Neurol 11:335-343, Williamson,K.,et al, 1982

Primary Cerebellopontine Progressive Multifocal Leukoencephalopathy Diagnosed Premortem by Cerebellar Biopsy
Ann Neurol 11:199-202, Jones,H.R.,et al, 1982

Spinocerebellar Degeneration Secondary to Chronic Intestinal Malabsorption:A Vitamin E Deficiency Syndrome
Ann Neurol 12:419-424, Harding,A.E.,et al, 1982

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