Neudle.com: optic ataxia

Differential
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abdominal distention

abdominal reflex, absent

abducens nerve paralysis

abducens nerve paralysis, bilateral

acoustic nerve

acquired immunodeficiency syndrome

Addison's disease

adrenoleukodystrophy

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

adverse drug reaction

ageusia

alcohol intolerance

alopecia

alternating hemiplegia

alternating hemiplegia of childhood

alternating rapid movement

amaurosis fugax

aminoglycoside

amphiphysin antibodies

amyloid angiopathy, cerebral

amyloid plaques

anemia

aneurysm

angiography, cerebral, false negative

angiography, cerebral, negative

angiotensin-converting enzyme

anorexia

anosmia

anti GQ1b IgG antibody

antibiotics

antibiotics, neurologic complications with

aphasia

apnea

apnea, primary central

apraxia of eye movements

ataxia telangiectasia

auditory evoked brainstem potentials

autoantibodies

autoimmune disease

autoimmune GFAP astrocytopathy

autonomic dysfunction

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basilar artery migraine

basilar impression

basophilic stippling of red blood cells

Bassen-Kornzweig syndrome

behavioral disorder

biotin deficiency

biotinidase deficiency

bitemporal visual field defect

brachial plexus neuropathy

brain biopsy

brain biopsy, stereotaxic

brain purpura

brain scan, abnormal

brainstem, atrophy

brainstem, infarction of

brainstem, lesion of

brainstem, neoplasms of

calcification, intracranial

carcinoma of pancreas

CAT scan, emission, abnormal

cataracts

central nervous system, infection of

central retinal artery occlusion

cerebellar ataxia, children

cerebellar atrophy, primary

cerebellar degeneration

cerebellar hemangioma

cerebellar lesion

cerebellar pontine angle

cerebellar pontine angle tumor

cerebellum

cerebellum, neoplasms of

cerebral cortical atrophy

cerebral edema

cerebral folate deficiency syndrome

cerebral infarction

cerebral venous thrombosis

cerebro hepato renal syndrome

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, cytology

cerebrospinal fluid, cytology, false negative

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, pressure increased

cerebrospinal fluid, xanthochromia of

cerebrovascular accident

cerebrovascular accident, bilateral

cerebrovascular accident, recurrent

cerebrovascular accident, women

cerebrovascular accident, young adult

cerebrovascular disease

Chamberlane's line

chemotherapy, CNS treatment and complications with

chest x-ray, abnormal

chronic progressive external ophthalmoplegia

Chvostek sign

cisterna magna

Clinical Pathologic Conference(C.P.C.)

clonus

clubfoot as related to neurologic disease

Cockayne's syndrome

coenzyme Q10 deficiency

cognition

cold intolerance

collagen vascular disease

collapsin response mediator protein 5 IgG

color vision, impaired

contactin associated protein like 2 antibodies

cornea, abnormal

corpus callosum

corpus callosum, lesion of

cough

cranial nerve palsies

cranial nerve palsies, unilateral

cranial nerves, toxins effecting

cranial neuropathy

cranial neuropathy, multiple

craniopharyngioma

cryopyrin-associated periodic syndrome

cultured skin fibroblasts

Cushing's syndrome

cyst

cyst, peritumoral

cyst, benign intracranial

cyst, neoplastic cerebellum

cyst, parenchymal

cytochrome c oxidase

cytochrome c oxidase, deficiency

Dandy Walker malformation

Dandy Walker malformation, adult

degenerative diseases of CNS

dementia, transmissible

dementia, treatment of

demyelinating disease

depression

dermatitis

dermatomyositis

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes insipidus

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diagnostic criteria

diarrhea

diarrhea, bloody

differential diagnosis

diplopia

disability, neurological

dizziness

DNA probes

downward gaze, paralysis of

drowsiness

drug abuse, inhalation

drug abuse, neurologic complications of

drug induced neurologic disorders

electroencephalogram, abnormalities of

electromyogram

electron microscopy

electronystagmography

electrophoretic pattern, CSF

electroretinograph

emotional lability

encephalitis

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, paraneoplastic

epidemiology of neurology

episodic disorders

episodic neurologic deficits

epistaxis

equinovarus

Erdheim-Chester disease

evoked potentials

exercise intolerance

exophthalmus

eye movement, disorders of

face, numbness of

facial nerve palsy

facial nerve palsy, recurrent

facial weakness

facial weakness, bilateral

finger nose finger test

fingerprint bodies

Fisher's syndrome

fluorescein angiography

fluorescent treponema antibody absorption(FTA-ABS)

folic acid

folic acid deficiency

fornix, lesion of

fourth ventricle, enlargement of

fourth ventricle, neoplasm of

Friedreich's ataxia

frontal bossing

fundus, abnormality of

gastrointestinal perforation

gaze palsy

gaze palsy, supranuclear

general paresis of the insane

genetic counselling

genetic linkage

genetic neurologic disorders

genetic testing

gentamicin

Gerstmann-Straussler-Scheinker disease

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glucagonoma

glycosuria

granulomatous disease

gray hair

gray matter

Guillain Barre syndrome

Guillain Barre syndrome, ophthalmoplegia in

Hallervorden Spatz disease

hallucination

hallucination, auditory

hallucination, visual

hand weakness

Hand-Schuller-Christian disease

hearing loss, bilateral

hearing loss, sudden, bilateral

hearing problems in children

heart block

heavy metal intoxication

heel-knee-shin test

hemangioblastoma

hematuria, gross

hemianopia, homonymous

hemifacial spasm

hemiparesis

hemiplegia

hemophagocytic lymphohistiocytosis, cerebromeningeal

hemophagocytosis

hepatomegaly

hepatosplenomegaly

herniated disc, thoracic

herpes zoster

herpes zoster, ophthalmicus

herpes zoster, oticus

Hispanics

histiocytosis

histochemistry

histochemistry of muscle

HLA

hoarseness

Hodgkin's disease, neurologic involvement with

human immunodeficiency virus type 1

hydrocephalus

hydrocephalus, non-communicating(obstructive)

hydrocephalus, normal pressure

hypertrophic intracranial pachymeningitis

hypofibrinogenemia

hypoglycorrhachia

hypokalemic periodic paralysis

hypothalamus, disturbance of

hypothalamus, neoplasm of

hypotonia

imbalance

immunoelectrophoresis, serum

immunologic disease

immunology and the nervous system

immunosuppressive agents

immunotherapy

impotence

impulsivity

inborn errors of metabolism

inclusion bodies

incontinence, fecal

incoordination

industrial neurologic disorders

infection

intellectual deficit

intellectual deterioration

intelligence quotient

internal capsule

internuclear ophthalmoplegia

internuclear ophthalmoplegia, bilateral

intestinal pseudoobstruction

intracerebral hemorrhage

intracranial hypertension, benign

intracranial pressure, increased

intrathecal chemotherapy

intrinsic hand muscles, wasting of

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, Heidenhain variant

jaw claudication

Kearns-Sayre syndrome

kyphoscoliosis, neurologic causes of

kyphosis

lactic acidemia

Laurence-Moon-Bardet-Biedl syndrome

lead and the nervous system

lead line, gingival

lead poisoning

Leber's hereditary optic neuropathy

leg weakness, bilateral

Leigh's disease

Leigh's disease, adult variety

lenticular nucleus, lesion of, bilateral

leucine rich glioma inactivated 1 antibodies

leukemia

leukemia, neurologic findings assoc.with

leukocyte enzyme abnormality

lymphoma involving CNS

lymphoma, primary of CNS

lymphomatoid granulomatosis

macular degeneration

malformation, CNS, congenital

Melkersson's syndrome

memory, defect of recent

memory, impairment of

meningeal biopsy

meningeal enhancement

meningismus

meningitis

meningitis, aseptic

meningitis, carcinomatous

meningitis, elderly

meningitis, lymphomatous

meningitis, syphilitic

meningoencephalitis

meningoencephalomyelitis

mental retardation

mental status, abnormal

MERRF syndrome

mesial temporal lobe

metabolic acidosis

metachromatic leukodystrophy

metachromatic leukodystrophy, juvenile

methyl benzene

microangiopathy, brain

microangiopathy, retina

microcephaly

microhemorrhage, intracerebral

microinfarcts

migraine

migraine, children

migraine, visual symptoms in

Mini Mental Status Examination

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

MNGIE syndrome

molecular genetics

mononeuritis multiplex

mononeuropathy

mononeuropathy multiplex

movement disorder, extrapyramidal

movement disorder, hyperkinetic

MRI

MRI, abnormal

MRI, brachial plexus

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, high signal foci on

mucopolysaccharidoses

multiple sclerosis

multiple sclerosis, children

multiple sclerosis, misdiagnosis

multiple sclerosis, presenting manifestations

multiple sclerosis, prognosis

muscle biopsy

muscle pain

muscle weakness

muscle weakness, causes of

muscle weakness, proximal

myasthenia gravis

myasthenia gravis, paraneoplastic

myelopathy, chronic progressive

myelopathy, tract-specific

myopathy, mitochondrial

myxedema, neurologic manifestations of

nasal septum, perforation of

nausea and vomiting

neck pain

neonatal screening, genetic neurologic disorders

neoplasm, metastatic to CNS

neoplasm, pituitary

neoplasm, posterior fossa

neoplasm, primary intracerebral

neoplasm, primary of CNS

neoplasm, primary of CNS-children

neoplasm, primary of CNS-surgical treatment of

nerve biopsy

nerve conduction studies

neuroaxonal dystrophy

neuroaxonal dystrophy, infantile

neuroendocrinology

neurogenic bladder

neurologic complications

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic disease, multifocal

neurologic examination

neurologic signs

neurologic symptoms

neuromuscular junction

neuronal cell surface antigen

neuronal ceroid-lipofuscinosis

neuronopathy, sensory

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, ataxia, retinitis pigmentosa

neuropathy, ataxic

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, medication induced

neuropathy, paraneoplastic

neuropathy, peripheral

neuropathy, vasculitic, systemic

nystagmus, dissociated

nystagmus, monocular

nystagmus, rotary

nystagmus, spontaneous

nystagmus, vertical

occipital cortex

occipital lobe, infarction

occipital lobe, infarction, bilateral

occipital lobe, lesion of

octreotide

ocular motility, disorders of

old age, neurology of

onconeural antibodies

one and a half syndrome

ophthalmoplegia

ophthalmoplegia, acute

ophthalmoplegia, bilateral, acute

ophthalmoplegia, progressive external

ophthalmoplegia, total

opisthotonus

opportunistic infection, CNS

opsoclonus-myoclonus syndrome

optic ataxia

optic atrophy

optic atrophy, bilateral

optic atrophy, hereditary

optic atrophy, unilateral

optic chiasm

optic disc edema

optic nerve

optic nerve, enhancement

optic neuritis

optic neuritis, children

optic neuropathy

optic neuropathy, bilateral

optic neuropathy, ischemic

optic neuropathy, toxic

optical coherence tomography

orthostatic hypotension

otitis, neurologic complications with

ototoxicity

overlap syndrome

Paget's disease

Paget's disease, psychosis in

Paget's disease, spinal cord problem in

paraneoplastic cerebellar degeneration

paranoia

paraparesis

paraparesis, familial spastic

parietal lobe, infarction

Parkinson disease, dystonia with

Parkinsonism syndrome

paroxysmal hemiplegia

paroxysmal neurologic deficits

peripheral nerve, lesion of

perivascular enhancement

pigmentary retinopathy

pituitary stalk

platelet inhibiting drugs

pleocytosis of cerebrospinal fluid

posterior cerebral artery occlusion

posterior column disease

posterior fossa

posterior fossa, lesion of

precipitating factors

pretectal syndrome

prevention of neurologic disorders

primary aldosteronism

prion disease

prognosis

progressive multifocal leucoencephalopathy

progressive neurologic disorder

prolactin, elevated

proprioception, abnormal

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing, neurologic problems

psychomotor retardation

psychosis

ptosis

ptosis, unilateral

pulmonary infiltrates

pupil, abnormality in neurologic disorders

pupil, tonic

Purkinje cell

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

quadriparesis

quadriplegia

radiation therapy, CNS treatment and complications with

radiation therapy, stereotactic

radiculopathy

ragged-red fibers

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

rash

real-time quaking-induced conversion

remote effect of cancer on the nervous system

renal cell carcinoma

respiratory failure

reticulum cell sarcoma

retina, abnormal

retinal artery occlusion

retinal branch artery occlusion

reversible neurologic disorder

review article

rheumatoid arthritis

rheumatoid arthritis factor(R.A.factor)

rubella encephalitis, progressive

scotomata, scintillating

screening

sea-blue histiocytes

sedimentation rate

sedimentation rate, elevated

seizure

seizure, children

seizure, neonatal

sensorineural hearing loss

sensory loss

sensory loss, cutaneous

serologic testing

serologic testing of cerebrospinal fluid

short stature

shunt procedure, ventricular

shunt procedure, ventriculo-atrial

simultanagnosia

sinusitis

skin, biopsy

skin, lesions in neurologic disorders

skull bone, thickening

skull x-ray

skull x-ray, abnormal

speech disorder, childhood

speech, loss of

spinal cord

spinal cord, compression of

spinal cord, lesion of

spinal cord, neoplasm

spinal cord, pathologic exam of

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 7

spinocerebellar degeneration

spinopontine atrophy, dominant

spirochete infection

splenomegaly

spongy degeneration of brain

startle myoclonus

status epilepticus

stereotaxic surgery

steroid responsive encephalopathy

steroid therapy, CNS treatment and complications with

strabismus

streptomycin

striatonigral degeneration

striatonigral degeneration, infantile

superior orbital fissure syndrome

suprasellar lesion

Susac's syndrome

syncope

syphilis, diagnosis and treatment

syphilis, meningomyelitis

syphilis, neurologic complications with

syphilis, ocular

systemic lupus erythematosus

tabes dorsalis

tachycardia

tandem gait, ataxic

tapetoretinal degeneration

taste

telangiectases

temporal lobe, lesion

tentorium cerebelli

term infant

testicular biopsy

testosterone, serum, low

tetany

thalamus, lesion of

thalamus, lesion of-bilateral

toxins, nervous system

transient ischemic attack

transient neurologic deficit

treatment of neurologic disorder

trigeminal neuropathy

trigeminal neuropathy, sensory

trinucleotide repeats

Trousseau's sign

tuberculosis

tuberculosis, miliary

Venereal Disease Research Laboratory test

vertebral-basilar insufficiency

vertigo

vestibulopathy

vibratory sensation, abnormal

viral infection, CNS

Virchow-Robin spaces, dilated

vision, blurred

vision, failure of in childhood

visual acuity, decreased

visual evoked response

visual field defect

visual impairment

visual loss

visual loss, progressive

visual loss, slow

visual loss, transient

visual obscurations, transient

vitamin deficiency

vitiligo

vitreous opacities

Vogt-Koyanagi-Harada syndrome

Von Hippel Lindau

walking frame

walking, difficulty with

weakness

weakness, generalized

weakness, progressive

Showing articles 1950 to 2000 of 2439 << Previous Next >>

Ataxia-Telangiectasia:A Multisystem Hereditary Disease with Immunodeficiency
Ann Int Med 99:367-379, Waldmann,T.A.,et al, 1983

Glutamate Dehydrogenase Deficiency in Patients with Olivopontocerebellar Atrophy
Neurol 33:1322-1326, Duvoisin,R.C.,et al, 1983

Ataxia Hemiparesis in Patients with Primary Pontine Hemorrhage
Stroke 14:762-764, Kobatake,K.,et al, 1983

Improvement of Ataxic Hemiparesis with Trihexyphenidyl
Neurol 33:1627-1628, Jabbari,B.,et al, 1983

Fatal Brain Oedema Due to Accidental Water Intoxication
BMJ 287:1181-1182, Anastassiades,E.,et al, 1983

Signs & Symptoms from a Cerebral Lesion that Suggest Cerebellar Dysfunction
Jr. , Arch Neurol 40:422-423983., Montgomery,E.B., 1983

Bilateral Optic Neuropathy with Remission in Young Men, Variation on a Theme by Leber
Arch Neurol 40:2-6, Lessell,S.,et al, 1983

Optic Neuritis & Multiple Sclerosis
NEJM 308:1294-1295, Link,H., 1983

Primary Position Vertical Nystagmus & Cerebellar Ataxia
Arch Neurol 40:310-314, Kattah,J.C.,et al, 1983

Acute Posterior Multifocal Placoid Pigment Epitheliopathy & Cerebral Vasculitis
Arch Neurol 40:48-50, Smith,C.G.,et al, 1983

Parainfectious Optic Neuritis
Arch Neurol 40:347-350, Selbst,R.G.,et al, 1983

Clin. Path. Conference
Multiple-System Atrophy with Parkinsonism, Case 28-13, NEJM 308:1406-1414983., , 1983

Myeloneuropathy & Macrocytosis Associated with Nitrous Oxide Abuse
Arch Neurol 40:416-418, Bianco,G.,et al, 1983

Sensory Neuropathy from Pyridoxine Abuse
NEJM 309:445-448, Schaumburg,H.,et al, 1983

Evoked Potentials in Olivopontocerebellar Atrophy
Arch Neurol 40:366-369, Hammond,E.J.,et al, 1983

Complications of Intravenous Phenytoin for Acute Treatment of Seizures
JAMA 249:762-765, Earnest,M.P.,et al, 1983

Delayed Neurologic Sequelae in Carbon Monoxide Intoxication
Arch Neurol 40:433-435, Choi,I.I.S., 1983

Phytanic Acid Storage Disease:Hearing Maintained After 15 Years of Dietary Treatment
Neurol 33:237-240, Djupesland,G.,et al, 1983

Osteosclerotic Myeloma & Peripheral Neuropathy
Neurol 33:202-210, Kelly,J.J.,et al, 1983

Ataxic Hemiparesis from Lesions of the Corona Radiata
Arch Neurol 40:449-450, Sage,J.L.,et al, 1983

Clin. Path. Conference
Pineocytoma, Case Record 35-1983, NEJM 309:542-549983., , 1983

Progressive Supranuclear Palsy:Clinical Features & Response to Treatment in 16 Patients
Ann Neurol 13:273-278, Jackson,J.A.,et al, 1983

Dominant Spinopontine Atrophy
Arch Neurol 40:259-260, Pogacar,S.,et al, 1983

Joseph Disease in a Non-Portuguese Family
Neurol 33:74-80, Sakai,T.,et al, 1983

Acetazolamide-Responsive Episodic Ataxia Syndrome
Neurol 33:1212-1214, Zasorin,N.L.,et al, 1983

Eye Movements in Friedreich's Ataxia
Arch Neurol 40:343-346, Furman,J.M.,et al, 1983

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

Sclerosteosis:Neurogenetic & Pathophysiologic Analysis of an American Kinship
Neurol 33:267-277, Stein,S.A.,et al, 1983

Nervous System Complications of Relapsing Polychondritis
Neurol 33:513-515, Sundaram,M.B.M.,et al, 1983

Supranuclear Gaze Palsy in Familial Creutzfeldt-Jakob Disease
Arch Neurol 40:618-622, Bertoni,J.M.,et al, 1983

Neuro-Ophthalmologic Signs in the Angiitic Form of Neurosarcoidosis
Neurol 33:1130-1135, Caplan,L.,et al, 1983

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

Sinusitis:Induced Subdural Empyema
Neurol 33:123-132, Kaufman,D.M.,et al, 1983

Case Report, Pseudotumor Cerebri:Computed Tomography of Resolving Papilledema
J Comput Assist Tomogr 7:364-366, O'Reilly,G.V.,et al, 1983

Visual Evoked Potentials in the Detection of Subclinical Optic Toxic Effects Secondary to Ethambutol
Arch Neurol 40:645-648, Yiannikas,C.,et al, 1983

Unilateral Papilledema in"Benign"Intracranial Hypertension (Pseudotumor Cerebri)
JAMA 250:2346-2347, Sher,N.A.,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

Clinicopathological Conference
Maroteaux-Lamy Syndrome, Case 44-1983, NEJM 309:1109-1117983., , 1983

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

Gait Disorders Among Elderly Patients
Arch Neurol 40:740-743, Sudarsky,L.,et al, 1983

Idiopathic Hemochromatosis (IHC) :Dementia & Ataxia as Presenting Signs
Neurol 33:1479-1483, Royden,H.,et al, 1983

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

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

Unrecognized Chronic Lithium Neurotoxic Reactions
JAMA 250:2029-2030, Lewis,D.A., 1983

A Progressive Syndrome of Autism, Dementia, Ataxia, & Loss of Purposeful Hand Use in Girls:Rett's Syndrome
Ann Neurol 14:471-491, Hagberg,B., 1983

Lymphomatous Leptomeningitis as a Presenting Syndrome of Hodgkin's Disease
Ann Int Med 99:342-343, Steinherz,P.G.,et al, 1983

Problems in the Diagnosis & Treatment of Pseudotumor Cerebri
Can J Neurol Sci 10:221-229, Corbett,J.J., 1983

Electro-oculographic Findings in Machado-Joseph Disease
Neurol 32:1272-1276, Dawson,D.M.,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

Subdural Tension Pneumocephalus Following Surgery
J Comput Assist Tomogr 6:903-906, Monajati,A.,et al, 1982

Showing articles 1950 to 2000 of 2439 << Previous Next >>