Neudle.com: idiopathic cerebellar ataxia

Neurology Specific Literature Search

Differential
(Click to cross reference)

abdominal x-ray

abducens nerve paralysis

abortion, spontaneous

abscess, intracerebral

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

alkylating agents

alpha-fetoprotein

alpha-synuclein

altered states of consciousness

alternating hemiplegia

alternating hemiplegia of childhood

alternating rapid movement

alternating rapid movement, impaired

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

angiotensin-converting enzyme

ankle reflex, absent

anti GQ1b IgG 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

anticholinesterase

antithyroid antibodies

antiviral agents

apraxia of eye movements

aqueduct of Sylvius, stenosis

aqueductal stenosis

arterial dissection, vertebral

arteritis, temporal

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 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

bilirubin encephalopathy

biologic markers

bitemporal visual field defect

bladder dysfunction

blood dyscrasias, neurologic findings with

blue tongue virus

bone marrow biopsy

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

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

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

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

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, clinical diagnosis

cerebrovascular accident, prognosis in

cerebrovascular disease, risk factors in

Chamberlane's line

Charcot-Marie-Tooth

chelation therapy

chemotherapy, CNS treatment and complications with

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

cornea, abnormal

corpus callosum

corpus callosum, atrophy of

corpus callosum, thinning

counterimmunoelectrophoresis

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

craniopharyngioma

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

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

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

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, etiology of

Guillain Barre syndrome, variant forms of

Hallervorden Spatz disease

Hallgren's syndrome

hallucination, auditory

hallucination, visual

Hand-Schuller-Christian disease

headache, progressive

headache, severe

hearing loss, bilateral

heel-knee-shin test

hemangioblastoma

hematuria, microscopic

hemisensory loss

hemochromatosis

hemochromatosis, primary

hemorrhagic diathesis

hemosiderosis of CNS, superficial

hepatic encephalopathy

hepatic failure

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

hyperbilirubinemia

hyperbilirubinemia, CNS abnormality after

hyperinsulinism

hyperosmolality

hyperparathyroidism

hyperpigmentation of skin

hyperthyroidism

hypoglycorrhachia

hypoglycorrhachia, causes of

hypogonadism, hypogonadotropic

hypokalemic periodic paralysis

hypomyelination

hypoparathyroidism

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

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

Kearns-Sayre syndrome

kelch-like protein 11 antibodies

Korsakoff's psychosis

lactic acidemia

lactic dehydrogenase(LDH)

lateral medullary syndrome

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

long bone lesion

lymphadenopathy

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

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 jerks

myoclonus, epilepsy

myoclonus, stimulus sensitive

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, demyelinating

neuropathy, painful

neuropathy, paraneoplastic

neuropathy, peripheral

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, monocular

nystagmus, primary position of gaze

nystagmus, rotary

nystagmus, upbeating on upgaze

nystagmus, vertical

ocular motility, disorders of

ocular myopathy

oculocephalic reflex

oculomasticatory myorhythmia

old age, neurology of

onconeural antibodies

ophelia syndrome

ophthalmoplegia

ophthalmoplegia, progressive external

ophthalmoplegia, total

opportunistic infection

opportunistic infection, CNS

opsoclonus-myoclonus syndrome

optic disc edema

optic nerve, enhancement

optic neuropathy

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

paraneoplastic brainstem encephalitis

paraneoplastic cerebellar degeneration

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, spastic

parathyroid adenoma

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

PAS positive material in the brain

pathologic reflex

pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection

Pelizaeus Merzbacher

peripheral nerve, lesion of

Perrault syndrome

personality change

pheochromocytoma

pigmentary retinopathy

pituitary, lesion of

pleocytosis of cerebrospinal fluid

pleural effusion

pneumoencephalogram(PEG)

poliomyelitis-like illness

polymerase chain reaction

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

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

purkinje cell cytoplastic autoantibody

pursuit eye movements, abnormal

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

radiation hypersensitivity

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

sarcoidosis, CNS

scalp tenderness

sclerosis, bone

sedimentation rate, elevated

seizure, intractable

seizure, laughing as manifestation

seizure, psychomotor-temporal lobe

sensorineural hearing loss

sensory loss, crossed pattern

sensory loss, leg

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

spongy degeneration of brain

sports medicine, neurology of

square wave jerks

standing difficulty

startle myoclonus

startle reaction

status epilepticus

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

teratogenesis, viral

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 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

vestibular areflexia

vibratory sensation, abnormal

vincristine neurotoxicity

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

vitamin deficiency

vitamin E deficiency

vitamin supplementation

vocal cord paralysis

Vogt-Koyanagi-Harada syndrome

voice, abnormality of

Von Hippel Lindau

Waldenstrom's macroglobulinemia

walking, difficulty with

walking, difficulty with in dark

weakness, progressive

Wernekinck commissure syndrome

West Nile fever

Western immunoblot test

Whipple's disease

white matter disease

wide based gait

Wolfram syndrome

xanthoma, eyelid

Showing articles 250 to 300 of 3612 << Previous Next >>

Neurologic Abnormalities of Lyme Disease
Medicine 58:281-294, Reik,L.,et al, 1979

Kearns-Sayre Syndrome with Hypoparathyroidism
Ann Neurol 3:513, Horwitz,S.J.,et al, 1978

Juvenile Neuroaxonal Dystrophy:Clinical, Electrophysiological, & Neuropathological Features
Ann Neurol 3:419, Dorfman,L.J.,et al, 1978

Varicella & Acute Cerebellar Ataxia
Arch Neurol 35:769-771, Peters,A.C.B.,et al, 1978

Acute & Chronic Progressive Encephalopathy Due to Gasoline Sniffing
Neurol 28:507-510, Valpey,R.,et al, 1978

Cerebrovascular diseases
In Harrison's Principles of Internal Medicine, 1977. McGraw-Hill Book Co. , p1., , 1977

Physostigmine in Familial Ataxias
Neurol 27:70, Kark,R.A.,et al, 1977

Reversible Cerebellocerebral Disorder in Primary Hemochromatosis
Arch Neurol 34:123, Singh,N.,et al, 1977

Persistent Cerebellar Ataxia after Exposure to Toluene
Ann Neurol 2:440, Boor,J.W.,et al, 1977

Chronic Meningitis
Medicine 55:341, Ellner,J.J.,et al, 1976

Ocular Motor Abnormalities in Hereditary Cerebellar Ataxia
Brain 99:207-234, Zee,D.S.,et al, 1976

The Thyroid Gland:Its Relationship to Neurology
In Handbook of Clin Neurol, Vinken & Bruyn (Ed) , North Holland Publ Co, Amsterdam 27:255, Greene,R., 1976

Adult Toxoplasmosis Presenting as Polymyositis & Cerebellar Ataxia
Ann Int Med 82:367, Greenlee,J.,et al, 1975

Neurotoxicity of Commonly Used Antineoplastic Agents
NEJM 291:75, 1271974., Weiss,H.,et al, 1974

Neuro Complica of Coeliac Disease & Trop Sprue, Neurology of GI Disease
1974, Major Problems in Neurology V-3, W. B. Saunders Co, Ltd., Pallis,C.A.&Lewis,P.D., 1974

Effects of Viral Infection on the Developing Nervous System
Seminars in Medicine of the Beth Israel Hosp, Boston NEJM 287:5991972., Johnson,R., 1972

Genetic Counseling in Retinitis Pigmentosa
MCV Quart 8:283, Noah,V., 1972

Neurological Problems in Endocrine Diseases
Med Clin North Am 56:1029, Dale,A., 1972

Mollaret's Meningitis & Differential Diagnosis of Recurrent Meningitis
Am J Med 52:128, Hermans,P.,et al, 1972

Neurological Disorders Associated with Adult Celiac Disease
Brain 89:683, Cooke,W.T.,et al, 1966

Acute Cerebellar Syndrome Secondary to Infectious Mononucleosis in a Fifty-Two Yealr Old Man
Ann Int Med 55:147-149, Bennett,D.R.&Peters,H.A., 1961

A Case of Cerebellar Ataxia, with a Discussion of Classification
Arch Neurol 3:71, Locke,S.,et al, 1960

An Acute Syndrome of Ocular Oscillations & Truncal Ataxis
p. 96-99., Winkler,G.,et al, 1850

A 59-Year-Old Man with Progressive Dysarthria and Gait Instability
Neurol 104:e213729, Shen,D.,et al, 2025

A Toddler with Acute-Onset Hypotonia, Areflexia, and Ataxia
Neurol 104:e213593, Pence, K.L. &Clark, R.A., 2025

Juvenile-Onset Dopa-Responsive Dystonia-Until It Isnt
Neurol 104:e213436, Paredes,N.C.,et al, 2025

Recurrent Rhombencephalitis Associatedwith Anti-GAD65 Antibody
Neurol 102:e208040, Alferes,A.R.,et al, 2024

A 24-Year-Old Man with Spastic Ataxia and Hypodontia
JAMA Neurol 81:658-659, Marien,L.,et al, 2024

Anti-NMDA Receptor Encephalitis Presenting with Cerebellitis in a Pediatric Patient
Neurol 102:e209259, Moehlman,M. & Kornbluh,A.B., 2024

A 24-Year-Old Man with Gait Impairment, Hearing Loss, and Recurrent Fever
Neurol 102:e209358, Barbosa,A.R.,et al, 2024

Clinicopathological Conference, Glutamic Acid Decarborylase 65 Autoantibody-Associated Stiff-Person Syndrome
NEJM 390:1712-1719, Case 14-2024, 2024

Unpacking the CNS Manifestations of Epstein-Barr Virus:An Imaging Perspective
AJNR 44:1002-1008, Soni,N.,et al, 2023

Pachymeningitis and Aortitis as the Initial Presentation of Granulomatosis with Polyangiitis
Neurol 101:979-980, Li,X.,et al, 2023

Extracranial Etiology of Acute Onset Ataxia and Weakness
Neurol 99:898-899, Nordli,D.,et al, 2022

Fragile X-Associated Tremor or Ataxia Syndrome in a Patient with Difficulty Walking, Falls, a Tremor, and Erectile Dysfunction
Lancet 400:1144, Sabino de Oliveira, D.,et al, 2022

A 67-Year-Old Woman with Progressive Diplopia, Vertigo, and Ataxia
Neurol 98:e669-e674, Sakoda, M.,et al, 2022

Progressive Vertebrobasilar Vasculopathy and Stroke Secondary to Giant Cell Arteritis
Stroke 53:e435-e438, Mahjoub, Y.,et al, 2022

A 6-Year-Old Girl with Progressive Toe Walking
Neurol 98:e769-e773, Libdeh, A.A. & Ibrahim, A., 2022

Bilateral Middle Cerebellar Peduncle Stroke in Giant Cell Arteritis
Neurol 98:e105-e106, Aghajan, Y.,et al, 2022

A 28-Year-Old Woman with Vision Loss and an Unusual Gait
Neurol 97:e1860-e1865, Dohlman, J.C.,et al, 2021

A 65-Year-Old Woman with Tremor
Neurol 97:e1257-e1261, Ye, J.,et al, 2021

Clinicopathologic Conference, Normal Pressure Hydrocephalus
NEJM 384:1350-1358, Case 10-2021, 2021

A 71-Year-Old Man with Horizontal Gaze Palsy, Anarthria, and Quadriparesis
Neurol 96:1146-1150, Cheema, I.,et al, 2021

Spontaneous Intracranial Hypotension: Atypical Radiologic Appearances, Imaging Mimickers, and Clinical Look-Alikes
AJNR 41:1339-1347, Bond, K.M.,et al, 2020

Sensory Ganglionopathy
NEJM 383:1657-1662, Amato, A.A. & Ropper, A.H., 2020

A 16-year-old Girl with Ataxia, Oscillopsia, and Behavioral Changes
Neurol 94:713-717, Silverman, A.,et al, 2020

Toxic Diffuse Isolated Cerebellar Edema from Over-the-Counter Health Supplements
Neurol 92:965-966, Kim, D.D.,et al, 2019

Clinicopathologic Conference, Powassan Virus Encephalitis
NEJM 380:380-387, Case 3-2019, 2019

Kelch-Like Protein 11 Antibodies in Seminoma-Associated Paraneoplastic Encephalitis
NEJM 381:47-54, Mandel-Brehm, C.,et al, 2019

Oculodentodigital Dysplasia: A Hypomyelinating Leukodystrophy with a Characteristic MRI Pattern of Brain Stem Involvement
AJNR 40:903-907, Hartin, I.,et al, 2019

Showing articles 250 to 300 of 3612 << Previous Next >>