Neudle.com: retinal atrophy

Differential
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abdominal distention

abducens nerve paralysis

abducens nerve paralysis, bilateral

acoustic nerve

acquired immunodeficiency syndrome

adrenoleukodystrophy

adverse drug reaction

amphiphysin antibodies

angiitis

angiitis, granulomatous of CNS

angiography, cerebral, false negative

angiography, cerebral, negative

anisocoria

anosmia

antibodies to measles

anticardiolipin antibodies

antiphospholipid antibodies

antiretinal antibodies

apraxia

apraxia of eye movements

aqueduct of Sylvius, stenosis

aqueductal stenosis

areflexia

Argyll Robertson pupil

Arnold Chiari malformation

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basilar impression

Bassen-Kornzweig syndrome

battered child syndrome

brainstem, hypoplasia

calcification, intracranial

carotid artery occlusion, neck

CAT scan

CAT scan, abnormal

CAT scan, false negative

cataracts

cataracts, congenital

central nervous system, infection of

central retinal artery occlusion

cerebellar ataxia, children

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar hemorrhage

cerebellar hypoplasia

cerebellar lesion

cerebellar vermis

cerebral cortical atrophy

cerebral edema, vasogenic

cerebral infarction

cerebral ischemia

cerebro hepato renal syndrome

cerebro retinal arterio venous aneurysm

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, oligoclonal IgG in

cerebrovascular accident

cerebrovascular accident, multiple

cerebrovascular accident, women

cerebrovascular accident, young adult

cerebrovascular disease, risk factors in

chemotherapy, CNS treatment and complications with

chemotherapy, intra-arterial

cherry red spot

cherry red spot-myoclonus syndrome

chromosomal abnormality

chromosome 17

chromosome 20

chronic progressive external ophthalmoplegia

cis-platinum

cisterna magna, enlarged

cisternogram, radionuclide

Clinical Pathologic Conference(C.P.C.)

Cockayne's syndrome

collapsin response mediator protein 5 IgG

color vision

color vision, impaired

congenital infection, CNS

congenital infection, viral

conjunctival biopsy

consanguinity

contactin associated protein like 2 antibodies

contractures, joint

cornea, opacity of

corpus callosum

corpus callosum, hypoplastic

corpus callosum, lesion of

cortical blindness

cotton-wool spots

cranial nerve palsies

cranial neuropathy, multiple

craniopharyngioma

creatine phosphokinase(CPK)elevated

cry, weak

cryptococcal meningitis

cytochrome c oxidase, deficiency

cytoid bodies

cytomegalovirus infection

cytomegalovirus infection, congenital

degenerative diseases of CNS

dementia

demyelinating disease

dermatomyositis

developmental abnormality of brain

developmental milestones, loss of

developmental retardation

drug abuse, neurologic complications of

drug induced neurologic disorders

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electron microscopy

electronystagmography

electroretinograph

embolism, fat

emergencies, ocular

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, paraneoplastic

encephalocele

encephalomyelitis

encephalopathy

endocarditis, marantic

enophthalmous

enzyme, defect

epidermal nevus syndrome

exophthalmus

extraocular muscle lesion

eye injury

eye movement, disorders of

eye, pain in

eyes, sunken

facial appearance, abnormal

facial nerve palsy

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

fatty acid dehydrogenase deficiency

feeding disorder

fever

fingerprint bodies

fluorescein angiography

fluorescent treponema antibody absorption(FTA-ABS)

foot deformity

Foster Kennedy syndrome

fourth ventricle, enlargement of

fundus, abnormality of

funduscopic exam

fungal infection, CNS

gait disorder

gastrointestinal disease, neurologic complications

gastrointestinal motility

gastroparesis

gaze palsy

gaze palsy, supranuclear

gene

gene mutation

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

gray matter

growth retardation

Hallervorden Spatz disease

Hallervorden Spatz disease, late onset

Hallgren's syndrome

hallucination

hallucination, visual

hearing loss, bilateral

hearing loss, sudden, bilateral

heart block

hemifacial spasm

hemiparesis

hemoglobin abnormality, neurologic complications of

hepatomegaly

heralding manifestation

herpes simplex virus

herpes simplex virus infection, newborn

herpes zoster

homosexual

Horner's syndrome

human immunodeficiency virus type 1

hydrocephalus

hydrocephalus, congenital

hydrocephalus, non-communicating(obstructive)

hydrocephalus, normal pressure

hydrocephalus, normal pressure in children

hyperpigmentation of skin

hypothalamus, lesion of

hypotonia

iatrogenic neurologic disorders

immunology and the nervous system

immunosuppression

immunosuppressive agents

immunotherapy

inborn errors of metabolism

inclusion bodies

inclusion bodies, intracytopasmic

intellectual deterioration

internuclear ophthalmoplegia

intestinal pseudoobstruction

intracerebral hemorrhage

intracranial hypertension, benign

intrauterine

intrauterine infection

intrauterine infection, viral

intrauterine infection, viral of CNS

Kearns-Sayre syndrome

keratoconjunctivitis

kyphoscoliosis, neurologic causes of

lactic acidemia

Laurence-Moon-Bardet-Biedl syndrome

Leber's hereditary optic neuropathy

Leigh's disease

lens, dislocation of

lenticular nucleus, lesion of, bilateral

leucine rich glioma inactivated 1 antibodies

leukemia

leukemia, neurologic findings assoc.with

light-near dissociation, causes of

lymphocyte fingerprint profiles

lymphoma

lymphoma involving CNS

lymphoma, primary of CNS

lysosomal storage disease

macular degeneration

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

medial longitudinal fasciculus(MLF)

MELAS syndrome

memory, impairment of

meningitis

meningitis, aseptic

meningitis, bacterial

meningitis, lymphomatous

meningitis, pneumococcal

meningoencephalitis

mental retardation

mental retardation, familial

MERRF syndrome

microaneurysm, retinal

microangiopathy, brain

microangiopathy, retina

microcephaly

micropthalmia

migraine

migraine, visual symptoms in

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

mitral valve vegetation

MNGIE syndrome

molecular genetics

monoclonal antibodies

mortality

motor neuron disease

movement disorder

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, disappearing lesion on

MRI, eye of tiger sign

MRI, high signal foci on

MRI, paramagnetic effect

MRI, serial

MRS

mucopolysaccharidoses

multiple sclerosis

multiple sclerosis, misdiagnosis

muscle atrophy, progressive

muscle biopsy

muscle weakness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, differential diagnosis of

muscular dystrophy, facioscapulohumeral

myasthenia gravis

myasthenia gravis, paraneoplastic

myopathy, mitochondrial

myopia

myotonia dystrophica

nausea and vomiting

neoplasm, primary of CNS

neoplasm, second primary

neuraminidase deficiency

neurocutaneous disease

neuroendocrinology

neurogenic vs.myopathic atrophy

neuroichthyosis

neurolipidosis IV

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic disease, multifocal

neurologic signs

neuromuscular junction

neuronal cell surface antigen

neuronal ceroid-lipofuscinosis

neuronopathy, sensory

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, ataxic

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, onion bulb

neuropathy, paraneoplastic

neuropathy, peripheral

occipital lobe, infarction

occipital lobe, infarction, bilateral

occipital lobe, lesion of

onconeural antibodies

ophthalmic migraine

ophthalmoplegia

ophthalmoplegia, progressive external

opportunistic infection

opportunistic infection, CNS

opsoclonus-myoclonus syndrome

optic atrophy

optic atrophy, bilateral

optic atrophy, hereditary

optic atrophy, unilateral

optic nerve, compression of

optic nerve, lesion of

optic nerve, neoplasm of

optic neuritis

optic neuropathy

optic neuropathy, hereditary

optic neuropathy, ischemic

optic neuropathy, ischemic, anterior

optic neuropathy, toxic

optic tract, lesion of

optical coherence tomography

osmotic demyelination syndrome

Paget's disease

Paget's disease, psychosis in

Paget's disease, spinal cord problem in

paraneoplastic cerebellar degeneration

paranoia

paraparesis

parasitic infection, CNS

Parkinson disease

Parkinsonism syndrome

PAS positive material in the brain

peripheral nerve, lesion of

photosensitivity, eye

photosensitivity, skin

phytanic acid

pigmentary retinopathy

pituitary

pituitary, metastasis to

platelet inhibiting drugs

pleocytosis of cerebrospinal fluid

pneumonia

polymyositis

polyneuropathy

Poretti-Boltshauser syndrome

progressive multifocal leucoencephalopathy

progressive neurologic disorder

proptosis

proptosis, bilateral

prothrombin time, prolonged

psychiatric disorder

psychiatric problems in neurologic disorders

psychomotor retardation

psychosis

ptosis

pupil

pupil, abnormality in neurologic disorders

pupil, light reflex, abnormal

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

quadrantanopsia, homonymous

quadriparesis

quadriplegia

rabies, nervous system involvement with

red free light, fundus exam with

refractive errors

Refsum's disease

remote effect of cancer on the nervous system

renal failure

retina, abnormal

retinal arteriole attenuation

retinal artery occlusion

retinal atrophy

retinal branch artery occlusion

retinal nerve fiber layer

retinal tumor

retinal vasculitis

retinal vasculopathy

retinal vasculopathy with cerebral leukodystrophy

rheumatoid arthritis factor(R.A.factor)

scotoma, paracentral-homonymous

scotomata, scintillating

screening

sea-blue histiocytes

sedimentation rate, elevated

sensorineural hearing loss

sensory loss

serologic test for syphilis

sheathing of retinal veins

Sjogren-Larsson syndrome

skin, biopsy

skin, lesions in neurologic disorders

skull x-ray, abnormal

spastic diplegia

spasticity

speech disorder

speech disorder, childhood

spinal cord, compression of

spinal cord, pathologic exam of

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 7

spinocerebellar degeneration

spongy degeneration of brain

Spot sign

spot sign, retrobulbar

steroid

steroid therapy, CNS treatment and complications with

stooped posture

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

subarachnoid hemorrhage

subdural hematoma

substantia nigra

sudden death

superior orbital fissure syndrome

Susac's syndrome

syphilis, congenital

syphilis, diagnosis and treatment

syphilis, neurologic complications with

syphilis, ocular

systemic illness

systemic lupus erythematosus

systemic lupus erythematosus, neurologic complications with

systemic lupus erythematosus, neuro-opthal.complications with

tabes dorsalis

tapetoretinal degeneration

testicular atrophy

thalamus, lesion of

thalamus, lesion of-bilateral

toxoplasmosis, acquired

toxoplasmosis, CNS

toxoplasmosis, congenital

transient ischemic attack

transplacental virus infections

trauma

treatment of neurologic disorder

tremor

trigeminal neuralgia

trinucleotide repeats

tuberous sclerosis

ultrasonography

ultrasonography, orbit

Usher's syndrome

uveitis

vasculopathy

ventricular enlargement

vertebral artery occlusion

vertebral-basilar insufficiency

vertigo

viral infection, CNS

vision, blurred

vision, failure of in childhood

visual acuity

visual acuity, decreased

visual acuity, decreased, monocular

visual evoked response

visual field defect

visual field defect, altitudinal

visual fields, constricted

visual impairment

visual loss

visual loss, progressive

visual loss, slow

visual loss, slow-unilateral

visual loss, sudden

visual loss, sudden-unilateral

vitreous hemorrhage

vitreous opacities

Walker-Warburg syndrome

walking, difficulty with

weakness

weakness, generalized

weakness, progressive

weaning from respirator, failure to

Showing articles 1400 to 1450 of 2631 << Previous Next >>

Leber's Hereditary Optic Neuropathy Mitochondrial DNA Mutations in Multiple Sclerosis
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Mitochondrial DNA mutations in an Outbreak of Optic Neuropathy in Cuba
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Eye Movements in Parkinsonian Syndromes:Vidailhet
M. , et al, Neurol 35:420-42694., , 1994

Diff Diag of parkinson's Disease, Multiple Sys Atrophy, & Steele-Richardson-Olszewski Syndrome:Striatal F-Dopa PET Data
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Rapidly Progressing Atrophy of Medial Temporal Lobe in Alzheimer's Disease
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Moderate Alcohol Consumption and Loss of Cerebellar Purkinje Cells
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Friedreich's Ataxia:MR Findings Involving the Cervical Portion of the Spinal Cord
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Bilateral Distal Upper Limb Amyotrophy and Watershed Infarcts from Vertebral Dissection
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Central Retinal Artery Occlusion from Carotid Dissection Diagnosed by Cervical Computed Tomography
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Susac's Syndrome:Triad of Microangiopathy of the Brain and Retina with Hearing Loss in Young Women
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Ataxia-Telangiectasia:MR and CT Findings
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Initial and Follow-up Brain MRI Findings and Correlation with the Clinical Course in Wilson's Disease
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Phenotype of Chromosome 14-Linked Familial Alzheimer's Disease in a Large Kindred
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Psychiatric Manifest of Systemic Lupus Erythematosus:Clin Features, Symptoms, & Signs of CNS Activity in 43 Pts
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Clinicopath Conf
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Distal Vacuolar Myopathy in Nephropathic Cystinosis
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Posterior Cortical Atrophy:Neuropathologic Correlations
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Neuro-Ophthalmological Presentation of Non-Invasive Aspergillus Sinus Disease in the Non-Immunocompromised Host
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Neurocysticercosis in Houston, Texas:A Report of 112 Cases
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Cerebral Involvement in McLeod Syndrome
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The Clinical Correlates of High-Titer IgG Anti-GM1 Antibodies
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Clinical Genetics in Neurological Disease
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Conjugal Amyotrophic Lateral Sclerosis:A Report on Two Couples from Southern France
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Amyotrophic Lateral Sclerosis Patient Antibodies Label CA2+Channel a1 Subunit
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Intravenous Immunoglobulin Trtm in Pts with Motor Neuron Syndromes Assoc with Anti-GM Antibodies:A Contrld Study
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The Brain in Infantile Autism:Posterior Fossa Structures are Abnormal
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MRI in Chronic Progressive Radiation Myelopathy
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Superoxide Dismutase and ALS
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Monomelic Amyotrophy
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Regional Brain Abnormalities in Schizophrenia Measured with Magnetic Resonance Imaging
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Showing articles 1400 to 1450 of 2631 << Previous Next >>