Neudle.com: "optic ataxia"

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Differential
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abdominal distention

abdominal reflex, absent

abducens nerve paralysis

abducens nerve paralysis, bilateral

acquired immunodeficiency syndrome

Addison's disease

adrenoleukodystrophy

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

adverse drug reaction

alcohol intolerance

alternating rapid movement

amaurosis fugax

amphiphysin antibodies

amyloid angiopathy, cerebral

amyloid plaques

angiography, cerebral, false negative

angiography, cerebral, negative

angiotensin-converting enzyme

anti GQ1b IgG antibody

antibiotics, neurologic complications with

apnea, primary central

arteritis, temporal

arylsulfatase A

ataxia telangiectasia

ataxia, cerebellar

ataxia, hereditary

ataxia, progressive

ataxia, sensory

ataxia, truncal

auditory evoked brainstem potentials

autoimmune disease

autoimmune GFAP astrocytopathy

autonomic dysfunction

autonomic neuropathy

B 12 deficiency

ballismus, bilateral

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

bladder dysfunction

blindness, transient

brachial plexus neuropathy

brain biopsy, stereotaxic

brain scan, abnormal

brainstem, atrophy

brainstem, infarction of

brainstem, lesion of

brainstem, neoplasms of

burning paresthesia

calcification, intracranial

carcinoma of breast

carcinoma of lung

carcinoma of pancreas

carcinoma of stomach

carpo-pedal spasm

CAT scan, abnormal

CAT scan, emission, abnormal

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, neoplasms of

cerebral cortical atrophy

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, recurrent

cerebrovascular accident, women

cerebrovascular accident, young adult

cerebrovascular disease

Chamberlane's line

chemotherapy, CNS treatment and complications with

chest x-ray, abnormal

choreoathetosis

chorioretinitis

chronic progressive external ophthalmoplegia

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

Cockayne's syndrome

coenzyme Q10 deficiency

cold intolerance

collagen vascular disease

collapsin response mediator protein 5 IgG

color vision, impaired

compression fracture

cone-rod dystrophy

conjunctival biopsy

contactin associated protein like 2 antibodies

cornea, abnormal

corpus callosum

corpus callosum, lesion of

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, peritumoral

cyst, benign intracranial

cyst, neoplastic cerebellum

cyst, parenchymal

cytochrome c oxidase

cytochrome c oxidase, deficiency

Dandy Walker malformation

Dandy Walker malformation, adult

deafness, bilateral

deafness, sudden

deafness, unilateral

deep gray nuclei

degenerative diseases of CNS

dementia, childhood

dementia, reversible

dementia, transmissible

dementia, treatment of

demyelinating disease

dermatomyositis

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes insipidus

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diagnostic criteria

diarrhea, bloody

differential diagnosis

disability, neurological

downward gaze, paralysis of

drug abuse, inhalation

drug abuse, neurologic complications of

drug induced neurologic disorders

electrical sensation

electroencephalogram, abnormalities of

electron microscopy

electronystagmography

electrophoretic pattern, CSF

electroretinograph

emotional lability

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, paraneoplastic

encephalomyelitis

epidemiology of neurology

episodic disorders

episodic neurologic deficits

Erdheim-Chester disease

evoked potentials

exercise intolerance

eye movement, disorders of

face, numbness of

facial nerve palsy

facial nerve palsy, recurrent

facial weakness

facial weakness, bilateral

fever, recurrent

finger nose finger test

fingerprint bodies

Fisher's syndrome

fluorescein angiography

fluorescent treponema antibody absorption(FTA-ABS)

folic acid deficiency

fornix, lesion of

fourth ventricle, enlargement of

fourth ventricle, neoplasm of

Friedreich's ataxia

frontal bossing

fundus, abnormality of

funduscopic exam

gastrointestinal perforation

gaze palsy, supranuclear

gaze palsy, vertical

general paresis of the insane

genetic counselling

genetic linkage

genetic neurologic disorders

genetic testing

Gerstmann-Straussler-Scheinker disease

girdle sensation

gliomatosis cerebri

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

granulomatous disease

Guillain Barre syndrome

Guillain Barre syndrome, ophthalmoplegia in

Hallervorden Spatz disease

hallucination, auditory

hallucination, visual

Hand-Schuller-Christian disease

head circumference

headache, elderly

headache, occipital

headache, severe

hearing loss, bilateral

hearing loss, sudden, bilateral

hearing problems in children

heavy metal intoxication

heel-knee-shin test

hemangioblastoma

hematuria, gross

hemianopia, homonymous

hemifacial spasm

hemophagocytic lymphohistiocytosis, cerebromeningeal

hemophagocytosis

hepatosplenomegaly

herniated disc, thoracic

herpes zoster, ophthalmicus

herpes zoster, oticus

histochemistry of muscle

Hodgkin's disease, neurologic involvement with

human immunodeficiency virus type 1

hydrocephalus, non-communicating(obstructive)

hydrocephalus, normal pressure

hyperadrenalism

hyperinsulinism

hyperparathyroidism

hypersegmented polys

hyperthyroidism

hypertriglyceridemia

hypertrophic intracranial pachymeningitis

hypofibrinogenemia

hypoglycorrhachia

hypokalemic periodic paralysis

hypomyelination

hypoparathyroidism

hypopituitarism

hypothalamus, disturbance of

hypothalamus, neoplasm of

immunoelectrophoresis, serum

immunologic disease

immunology and the nervous system

immunosuppressive agents

inborn errors of metabolism

inclusion bodies

incontinence, fecal

industrial neurologic disorders

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

islet cell tumor

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, Heidenhain variant

jaw claudication

Kearns-Sayre syndrome

kyphoscoliosis, neurologic causes of

lactic acidemia

Laurence-Moon-Bardet-Biedl syndrome

lead and the nervous system

lead line, gingival

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, neurologic findings assoc.with

leukocyte enzyme abnormality

Lhermitte's sign

libido, decreased

limbic encephalitis

long bone lesion

lymphadenopathy

lymphoma involving CNS

lymphoma, primary of CNS

lymphomatoid granulomatosis

macular degeneration

malformation, CNS, congenital

malignancy screen

malignancy, occult

malignant papulosis

marche a petits pas

melanoma, malignant

Melkersson's syndrome

memory, defect of recent

memory, impairment of

meningeal biopsy

meningeal enhancement

meningitis, aseptic

meningitis, carcinomatous

meningitis, elderly

meningitis, lymphomatous

meningitis, syphilitic

meningoencephalitis

meningoencephalomyelitis

mental retardation

mental status, abnormal

mesial temporal lobe

metabolic acidosis

metachromatic leukodystrophy

metachromatic leukodystrophy, juvenile

microangiopathy, brain

microangiopathy, retina

microhemorrhage, intracerebral

migraine, children

migraine, visual symptoms in

Mini Mental Status Examination

mitochondrial disease

mitochondrial encephalomyopathy

molecular genetics

mononeuritis multiplex

mononeuropathy multiplex

monoparesis, focal

motor neuron disease

movement disorder

movement disorder, extrapyramidal

MRI, brachial plexus

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, high signal foci on

MRI, optic nerve

MRI, spinal cord

mucopolysaccharidoses

multiple sclerosis

multiple sclerosis, children

multiple sclerosis, misdiagnosis

multiple sclerosis, presenting manifestations

multiple sclerosis, prognosis

muscle weakness

muscle weakness, causes of

muscle weakness, proximal

myasthenia gravis

myasthenia gravis, paraneoplastic

myasthenic syndrome

myelopathy, chronic progressive

myoclonic jerks

myoclonus, epilepsy

myopathy, mitochondrial

myopathy, vacuolar

myositis, ocular

myxedema, neurologic manifestations of

nasal septum, perforation of

nausea and vomiting

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 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, brain

neuropathy, ataxia, retinitis pigmentosa

neuropathy, ataxic

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, medication induced

neuropathy, paraneoplastic

neuropathy, peripheral

neuropathy, vasculitic, systemic

night blindness

NMDA antagonists

nystagmus, dissociated

nystagmus, rotary

nystagmus, spontaneous

nystagmus, vertical

occipital cortex

occipital lobe, lesion of

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

opportunistic infection, CNS

opsoclonus-myoclonus syndrome

optic atrophy, bilateral

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

orthostatic hypotension

otitis, neurologic complications with

overlap syndrome

Paget's disease

Paget's disease, psychosis in

Paget's disease, spinal cord problem in

pain, abdominal

pain, testicular

palatal myoclonus

paraneoplastic cerebellar degeneration

paraparesis, familial spastic

paraparesis, spastic

parathyroid adenoma

Parkinsonism syndrome

Pelizaeus Merzbacher

periarteritis nodosa

peripheral nerve, lesion of

perivascular enhancement

pernicious anemia

peroxisomal disease

personality change

pheochromocytoma

pigmentary retinopathy

pituitary stalk

platelet inhibiting drugs

pleocytosis of cerebrospinal fluid

pons, lesion of

posterior column disease

posterior fossa

posterior fossa, lesion of

pretectal syndrome

prevention of neurologic disorders

primary aldosteronism

progressive multifocal leucoencephalopathy

progressive neurologic disorder

prolactin, elevated

proprioception, abnormal

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing, neurologic problems

psychomotor retardation

ptosis, unilateral

pulmonary infiltrates

pupil, abnormality in neurologic disorders

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

radiation therapy, CNS treatment and complications with

radiation therapy, stereotactic

ragged-red fibers

rapidly progressing neurologic illness

real-time quaking-induced conversion

refractive errors

Refsum's disease

regional enteritis

release phenomena

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

retinal degeneration

retinal detachment

retinal hemangioma

retinal hemorrhages

retinal infarction

retinitis pigmentosa

retroperitoneal mass

reversible neurologic disorder

rheumatoid arthritis

rheumatoid arthritis factor(R.A.factor)

root lesion, nerve

rubella encephalitis

rubella encephalitis, progressive

sarcoidosis, CNS

sclerosis, bone

scotomata, scintillating

sea-blue histiocytes

sedimentation rate

sedimentation rate, elevated

seizure, children

seizure, neonatal

sensorineural hearing loss

sensory loss, cutaneous

serologic testing

serologic testing of cerebrospinal fluid

shunt procedure, ventricular

shunt procedure, ventriculo-atrial

skin, lesions in neurologic disorders

skull bone, thickening

skull x-ray, abnormal

spastic diplegia

speech disorder

speech disorder, childhood

speech, loss of

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

spongy degeneration of brain

startle myoclonus

status epilepticus

stereotaxic surgery

steroid responsive encephalopathy

steroid therapy, CNS treatment and complications with

striatonigral degeneration

striatonigral degeneration, infantile

subcortical U fibers

subdural effusion

subdural hygroma

substantia nigra

superior orbital fissure syndrome

suprasellar lesion

Susac's syndrome

syphilis, diagnosis and treatment

syphilis, meningomyelitis

syphilis, neurologic complications with

syphilis, ocular

systemic lupus erythematosus

tandem gait, ataxic

tapetoretinal degeneration

temporal lobe, lesion

tentorium cerebelli

testicular biopsy

testosterone, serum, low

thalamus, lesion of

thalamus, lesion of-bilateral

third nerve palsy

thrombocytopenia

toxic encephalopathy

toxins, nervous system

transient ischemic attack

transient neurologic deficit

treatment of neurologic disorder

tremor, intention

tremor, postural

trigeminal neuralgia

trigeminal neuropathy

trigeminal neuropathy, sensory

trinucleotide repeats

Trousseau's sign

tuberculosis, miliary

ulcerative colitis

upgaze, paralysis of

urinary frequency

urinary incontinence

urinary urgency

Usher's syndrome

Venereal Disease Research Laboratory test

vertebral-basilar insufficiency

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, progressive

visual loss, slow

visual loss, transient

visual obscurations, transient

vitamin deficiency

vitreous opacities

Vogt-Koyanagi-Harada syndrome

Von Hippel Lindau

walking, difficulty with

weakness, generalized

weakness, progressive

weakness, proximal

Whipple's disease

white matter disease

Wolfram syndrome

Showing articles 0 to 50 of 2382 Next >>

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

Expanding Clinical Spectrum an Anti-GQ1b Antibody Syndrome, A Review
JAMA Neurol 81:762-770, Lee,S-U.,et al, 2024

A 35-Year-Old Woman with Personality Change and Gait Impairment
Neurol 104:e210252, Bernardes,C.,et al, 2024

Neuroimaging Features of Biotinidase Deficiency
AJNR 44:328-333, Biswas,A.,et al, 2023

A 55-Year-Old Woman with Recurrent Episodes of Aphasia and Vision Changes
Neurol 98:330-335, Jeanneret, V.,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

Homonymous Hemianopia with Normal Magnetic Resonance Imaging
JAMA Ophthalmol doi:10.1001/JAMAOphthalmol.2020.0447, Cai, S.,et al, 2020

Progressive Neurological Impairment and an Enhancing Brainstem Lesion in a Middle-Aged Man
JAMA Neurol 76:1397-1398, Gupta, S.,et al, 2019

Autoimmune Glial Fibrillary Acidic Protein Astrocytopathy
JAMA Neurol 73:1297-1307, Fang, B.,et al, 2016

Neurological Management of Von Hippel-Lindau Disease
Neurologist 21:73-78, Hodgson, T.S.,et al, 2016

A 40-year old Woman with Difficulty Going Down Stairs in High-Heeled Shoes
Ann Neurol 77:1-7, Scripko, P.,et al, 2015

Diseases of the Nervous System Caused by Nutritional Deficiency, Vitamin B12 (Cobalamin) Deficiency (Subacute Combined Degeneration)
Adams & Victors Principles of Neurology Chp 41, pg 1172, Ropper, A.H.,et al, 2014

Infections of the Nervous System, (Bacterial, Fungal, Spirochetal, Parasitic) and Sarcoidosis, Neurosyphilis
Adams & Victors Principles of Neurology, Chp 32, pg 723, Ropper, A.H.,et al, 2014

Intracranial Neoplasms and Paraneoplastic Disorders, Hemangioblastoma of the Cerebellum
Adams & Victors Principles of Neurology, Chp 31, pg 668, Ropper, A.H.,et al, 2014

Disorders of the Nervous System Caused by Drugs, Toxins, and Chemical Agents, Lead
Adams & Victors Principles of Neurology Chp 43, pg 1220, Ropper, A.H.,et al, 2014

Paraneoplastic Neurological Syndromes
Clin Exp Immunol 175:336-348, Leypoldt, F. & Wandinger, K.-P., 2014

Diagnosis and Therapy in Neuromuscular Disorders: Diagnosis and New Treatments in Mitochondrial Diseases
JNNP 80:943-953, Rahman,S. &Hanna,M.G., 2009

A 23-Year-Old Man With Seizures and Visual Deficit
Neurol 70:73-78, Boustany,R.-M.,et al, 2008

Clinicopath Conf., Degoss Disease
NEJM 355:2575-2584, Case 38-2006, 2006

Autoantibodies to Folate Receptors in the Cerebral Folate Deficiency Syndrome
NEJM 352:1985-1991, Ramaekers,V.T.,et al, 2005

Mitochondrial Respiratory-Chain Diseases
NEJM 348:2656-2668, DiMauro,S. &Schon,E.A., 2003

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
Neurol 53:478-484, Ruggieri,M.,et al, 1999

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

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

Chronic Lymphocytic Leukemia and the Central Nervous System:A clinical and Pathological Study
Neurol 46:19-25, Cramer,S.C.,et al, 1996

Wolfram Syndrome:Hereditary Diabetes Mellitus with Brainstem and Optic Atrophy
Ann Neurol 39:352-360, Scolding,N.J.,et al, 1996

Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities
Ann Neurol 39:343-351, Rahman,S.,et al, 1996

Neurotox of Antimicrob & Antimalarial Agents
In Intox of Nervous System, Part II, Handbk Clin Neurol, Elsevier Science 21 (65) :471., Moorhouse,D.F.,et al, 1995

Mitochondrial DNA and Disease
NEJM 333:638-644, Johns,D.R., 1995

Ependymomas of the Posterior Cranial Fossa:CT and MRI Findings
Neuroradiology 37:238-243, Tortori-Donati,P.,et al, 1995

Neurodegeneration and Diabetes:UK Nationwide Study of Wolfram (DIDMOAD) Syndrome
Lancet 1458-1463, Barrett,T.G.,et al, 1995

Neurologic Aspects of Inflammatory Bowel Disease
Neurol 45:416-421, Lossos,A.,et al, 1995

Clinicopath Conf
Primary Malignant Lymphoma of CNS, Diffuse, Large-Cell]B-Cell Type, Case 36-1994, NEJM 331:861-8684., , 1994

Cranial Pachymeningitis of Unknown Origin:A Study of Seven Cases
Neurol 43:1329-1334, Masson,C.,et al, 1993

Clinicopath Conf
Infantile Striatonigral Regeneration, with Cerebellar Degeneration, Familial, Case 30-1992, NEJM 327, 261-1992., 1992

Wolfram Syndrome:Evidence of a Diffuse Neurodegenerative Disease by Magnetic Resonance Imaging
Neurol 42:1220-1224, 1992,, Rando,T.A.,et al, 1992

MR Imaging of the Spinal Cord in 23 Subjects with ALD-AMN Complex
AJR 158:413-416, Snyder,R.D.,et al, 1992

Cerebromeningeal Haemophagocytic Lymphohistiocytosis
Lancet 239:104-107, Henter,J.&Elinder,G., 1992

Hallervorden-Spatz Syndrome and Brain Iron Metabolism
Arch Neurol 48:1285-1293, Swaiman,K.F., 1991

Reversal of a Neurologic Paraneoplastic Syndrome with Octreotide (Sandostatin) in a Pt with Glucagonoma
Am J Med 91:434-436, Holmes,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

Neurologic Aspects of Cobalamin Deficiency
Medicine 70:229-245, Healton,E.B.,et al, 1991

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

Demyelinating Diseases
In Rowlands Merritt's Textbk of Neurology, Lea & Febiger, Phila, 8th Ed, p. 749, Sibley,W.A.,et al, 1989

Friedreich Ataxia
In Rowland, L. P. Merritt's Textbook of Neurology, 8th Ed, Lea & Febiger, Phila, Ch 13, p627, Rosenberg,R.N., 1989

Retinitis Pigmentosa
Surv Ophthalmol 33:137-177, Pagon,R.A., 1988

Clinicopath Conf
Adenocarcinoma of Lung, with Metastasis to Meninges of Brain, Spinal Cord & Optic Nerves, Case Recor, 14-1EJM 318:903-915,1988., 1988

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

Showing articles 0 to 50 of 2382 Next >>