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abducens nerve paralysis

adolescent medicine

adrenoleukodystrophy

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

advances in neurology

adverse drug reaction

alcohol intolerance

alternating hemiplegia

alternating hemiplegia of childhood

alternating rapid movement

amyloid angiopathy, cerebral

amyloidosis, oculoleptomeningeal, familial

anti MAG antibodies

apnea, primary central

arrhythmia, cardiac

arteritis, temporal

arylsulfatase A

arylsulfatase B

ataxia, cerebellar

ataxia, hereditary

ataxia, progressive

ataxia, truncal

auditory evoked brainstem potentials

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

Bassen-Kornzweig syndrome

battered child syndrome

behavioral disorder

Behr's optic atrophy

biotin deficiency

biotinidase deficiency

bitemporal visual field defect

blindness, sudden

bone density, increased

bone marrow transplantation

brainstem, atrophy

brainstem, lesion of

bulbar palsy, childhood

bulbar palsy, progressive

calcification, intracranial

Canavan's disease

CAT scan, abnormal

CAT scan, false negative

cerebellar ataxia, children

cerebellar atrophy, primary

cerebral cortical atrophy

cerebral edema, vasogenic

cerebro hepato renal syndrome

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, protein of

cerebrovascular accident

cerebrovascular accident, multiple

cerebrovascular accident, young adult

Charcot-Marie-Tooth

cherry red spot

choreoathetosis

chromosomal abnormality

chronic progressive external ophthalmoplegia

cisternogram, radionuclide

Clinical Pathologic Conference(C.P.C.)

clubbing of fingers

clubfoot as related to neurologic disease

Cockayne's syndrome

coenzyme Q10 deficiency

color vision, impaired

compression neuropathy

cone-rod dystrophy

contractures, joint

cornea, abnormal

cornea, opacity of

corpus callosum

corpus callosum, hypoplastic

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

craniopharyngioma

cryopyrin-associated periodic syndrome

cultured skin fibroblasts

degenerative diseases of CNS

dementia, childhood

dementia, thalamic

demyelinating disease

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes insipidus

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diabetes mellitus, ocular complications in

diabetic cranialneuropathies

diagnostic criteria

diplegia, brachial

dissociated sensory loss

drug induced neurologic disorders

dyschromatopsia

electroencephalogram, abnormalities of

electron microscopy

electronystagmography

electroretinograph

emergencies, ocular

encephalopathy, neonatal

encephalopathy, progressive

entrapment neuropathy

episodic disorders

evoked potentials

exome sequencing

eye movement, disorders of

facial appearance, abnormal

facial nerve palsy

facial nerve palsy, bilateral

failure to thrive

feeding disorder

fever, recurrent

finger nose finger test

flaccid paralysis

flow study, carotid artery

fluorescein angiography

Friedreich's ataxia

frontal bossing

frontal lobe, pathologic signs of

fundus, abnormality of

funduscopic exam

galactocerebrosidase

gangliosidosis GM2

genetic counselling

genetic diagnosis, prenatal

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genetic neurologic disorders

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globus pallidus

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globus pallidus, lesion of, bilateral

granulomatosis with polyangiitis

growth retardation

Hallervorden Spatz disease

head circumference

hearing problems in children

heel-knee-shin test

hemophagocytic lymphohistiocytosis, cerebromeningeal

hemophagocytosis

hepatosplenomegaly

hexosaminidase-A

Horner's syndrome

hydrocephalus, normal pressure

hydrocephalus, normal pressure in children

hydrocephalus, viral induced

hyperostosis corticalis generalisata familiaris

hypertriglyceridemia

hypertrophic intracranial pachymeningitis

hypofibrinogenemia

hypomyelination

hypotonia, infants

immunofluorescence

immunologic disease

inborn errors of metabolism

inclusion bodies

infantile bilateral striatal necrosis

intellectual deficit

intellectual deterioration

intestinal pseudoobstruction

intracerebral hemorrhage

intracerebral hemorrhage, familial

intracranial hypertension, benign

intracranial pressure, increased

Kearns-Sayre syndrome

Krabbe's disease

kyphoscoliosis, neurologic causes of

lactic acidemia

Laurence-Moon-Bardet-Biedl syndrome

Leber's hereditary optic neuropathy

Leigh's disease

Leigh's disease, adult variety

lenticular nucleus, lesion of, bilateral

leukocyte enzyme abnormality

light-near dissociation, causes of

lymphadenopathy

lysosomal storage disease

lysosomes, abnoral

macular degeneration

Marcus Gunn pupil

memory, impairment of

meningitis, aseptic

meningitis, carcinomatous

meningitis, chronic

mental retardation

metabolic acidosis

metabolic disorder, primary

metachromatic leukodystrophy

metachromatic leukodystrophy, juvenile

methylmalonic aciduria

mitochondrial disease

mitochondrial encephalomyopathy

molecular genetics

mononeuropathy multiplex

motor neuron disease

movement disorder

movement disorder, extrapyramidal

movement disorder, hyperkinetic

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, optic nerve

MRI, spinal cord

mucopolysaccharidoses

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, familial

muscle atrophy, progressive

muscle weakness

muscle weakness, proximal

myasthenia gravis, differential diagnosis

myasthenia gravis, misdiagnosis of

myelitis, longitudinal

myelitis, transverse

myoclonic jerks

myoclonus, epilepsy

myopathy, mitochondrial

nausea and vomiting

nerve conduction studies

neuroaxonal dystrophy

neuroendocrinology

neurolipidosis IV

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic examination

neurologic signs

neuromyelitis optica (Devic's disease)

neuromyelitis optica spectrum disorder

neuromyelitis optica, IgG

neuronal ceroid-lipofuscinosis

neuroophthalmology

neuropathology, brain

neuropathy, ataxia, retinitis pigmentosa

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, peripheral

neuropathy, vasculitic, systemic

night blindness

nutritional deficiency

nystagmus, monocular

nystagmus, rotary

nystagmus, upbeating-in primary position of gaze

nystagmus, vertical

ophthalmoplegia

ophthalmoplegia, progressive external

optic atrophy, bilateral

optic atrophy, hereditary

optic chiasm, enlarged

optic chiasm, lesion of

optic disc edema

optic foramina, abnormal

optic nerve, compression of

optic nerve, enhancement

optic nerve, enlarged

optic nerve, lesion of

optic nerve, neoplasm of

optic neuritis, bilateral

optic neuritis, treatment of

optic neuropathy

optic neuropathy, bilateral

optic neuropathy, hereditary

optic neuropathy, ischemic

optic neuropathy, nutritional

optic neuropathy, toxic

optic tract, lesion of

optical coherence tomography

owl's eye sign of spinal cord

palatal myoclonus

paraparesis, familial spastic

paraparesis, spastic

Parkinson disease

Parkinson disease, dystonia with

Parkinsonism syndrome

paroxysmal hemiplegia

paroxysmal neurologic deficits

PAS positive material in the brain

Pelizaeus Merzbacher

peroxisomal disease

personality change

photosensitivity, skin

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

polyneuropathy, familial

posterior leukoencephalopathy syndrome

precipitating factors

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

pretectal syndrome

prisoners of war, neurologic complications in

progressive neurologic disorder

propionic aciduria

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychological testing, neurologic problems

psychomotor retardation

pupil, abnormality in neurologic disorders

pupil, light reflex, abnormal

pyramidal tract

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

ragged-red fibers

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

red free light, fundus exam with

refractive errors

Refsum's disease

release phenomena

respiratory failure

retina, abnormal

retinal degeneration

retinal detachment

retinal ischemia

retinal nerve fiber layer

retinal vasculitis

retinal vasculopathy

retinal vasculopathy with cerebral leukodystrophy

retinitis pigmentosa

scotoma, central

sea-blue histiocytes

sedimentation rate, elevated

seizure, children

seizure, neonatal

sensorineural hearing loss

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, pathologic exam of

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 7

spinocerebellar degeneration

spinopontine atrophy, dominant

spongy degeneration of brain

startle myoclonus

startle reaction

status epilepticus

stem cell transplantation

steroid therapy, CNS treatment and complications with

stooped posture

striatonigral degeneration

striatonigral degeneration, infantile

striatum, lesion of

striatum, lesion of, bilateral

strokelike episodes

subarachnoid hemorrhage

subcortical U fibers

substantia nigra

symmetric brain lesions

systemic illness

Tangier's disease

tapetoretinal degeneration

Tay-Sachs disease

thalamus, lesion of

thrombocytopenia

tongue, enlarged

treatment of neurologic disorder

tremor, intention

trigeminal nerve, lesion of

trigeminal neuropathy

trinucleotide repeats

umbilical-cord blood transplantation

upgaze, paralysis of

urea-cycle enzymopathies

urinary incontinence

urine test for metabolic disorders

Usher's syndrome

vestibular function, tests of

viral infection, CNS

vision loss, sequential

vision, blurred

vision, failure of in childhood

visual acuity, decreased

visual acuity, decreased, monocular

visual evoked response

visual field defect

visual impairment

visual loss, progressive

visual loss, slow

visual loss, sudden

vitamin deficiency

vitreous opacities

walking, difficulty with

water channel antibodies

white matter disease

white matter disease, subcortical

Wolfram syndrome

Showing articles 600 to 650 of 5752 << Previous Next >>

Clinicopath Conf
Mastoiditis with Right Transverse-Sinus and Sigmoid-Sinus Thrombosis, Case Record 20-1988, NEJM 318:, 321328,1988., 1988

Guillain-Barre Syndrome and Optic Neuropathy in Acute Leukemia
Neurol 38:1324-1326, Phanthumchinda,K.,et al, 1988

Clinicopath Conf
Leukemia, Mycotic Aneurysm, Asperigillosis, Subarachnoid Hemorrhage, Fungal Intracran Aneurysm, Case, 7-198M 319:427-440,1988., 1988

Neurologic Disease in Biopsy-Proven Giant Cell (Temporal) Arteritis
Neurol 38:352-359, Caselli,R.J.,et al, 1988

Paraneoplastic Optic Neuritis & Encephalomyelitis, Report of A Case
Arch Neurol 45:353-356, Boghen,D.,et al, 1988

Risk of Developing Multiple Sclerosis after Uncomplicated Optic Neuritis:A Long-Term Prospective Study
Neurol 38:185-190, Rizzo,J.F.&Lessell,S., 1988

Magnetic Resonance Imaging of the Optic Nerve in Optic Neuritis
Neurol 38:175-179, Miller,D.H.,et al, 1988

Varicella Optic Neuritis
Neurol 38:501-503, Purvin,V.,et al, 1988

Visual System Toxicity Following Intra-arterial Chemotherapy
Neurol 38:284-289, Kupersmith,M.J.,et al, 1988

Computed Tomography and Magnetic Resonance Imaging in Adult-Onset Leukodystrophy
Arch Neurol 45:1004-1008, Schwankhaus,J.D.,et al, 1988

Postmarketing Surveillance for Neurologic Adverse Events after Hepatitis B Vaccination, Exp of the First 3 Yrs
Am J Epidemiol 127:337-352, Shaw,F.E.,et al, 1988

Paraneoplastic Syndromes Involving the Eyes
In Walsh & Hoyt's Clin Neuro-ophthal, 4th ed, Williams & Wilkins, Vol 3, p 1735-1746, Miller,N.R., 1988

Bilateral Optic Neuropathy and Osteolytic Sinusitis
JAMA 259:72-74, Newman,N.M.,et al, 1988

Sarcoidosis of the Anteroir Visual Pathway: Successes and Failures
JNNP 51:1473-1480, Gelwan,M.J., 1988

Hereditary Motor & Sensory Neuropathy, X-Linked:A Half Century Follow-Up
Neurol 37:1460-1465, Rozear,M.P.,et al, 1987

Disseminated Cholesterol Embolism Presenting as Neuromyelitis Optica
BMJ 295:697, Goldman,M.,et al, 1987

Cytochrome c Oxidase Deficiency in Leigh Syndrome
Ann Neurol 22:498-506, DiMauro,S.,et al, 1987

Clinicopath Conf
Castleman's Disease, Synd of Polyneuropathy, Organomegally, Endocrinopathy, Monoclonal Gammopathy, &, Skin CPOEM Synd),NEJM 316:606-618,1987., 1987

A Reassessment of the Risk of Multiple Sclerosis Developing in Patients with Optic Neuritis After Extended Follow-up
JNNP 50:758-765, Francis,D.A.,et al, 1987

Does Neuroretinitis Rule Out Multiple Sclerosis
CPT, et al, Arch Neurol 44:1045-1048987., Parmley,V.C., 1987

Anterior Ischaemic Optic Neuropathy in the Acquired Immune Deficiency Syndrome
BMJ 295:696-697, Brack,M.J.,et al, 1987

Unilateral Optic Neuropathy in Non-Hodgkin's Lymphoma
Neurol 37:1563-1564, Lanska,D.J.,et al, 1987

Familial Recurrent Bell's Palsy with Ocular Motor Palsies
Neurol 37:1369-1371, Aldrich,M.S.,et al, 1987

Lyme Disease, A Neuro-Ophthalmologic View
J Clin Neuro-ophthalmol 7:185-190, MacDonald,A.B., 1987

Genetic Linkage in Neurologic Diseases
Editorial, NEJM 316:1018-10201987., Martin,J.B., 1987

Optico-Cerebral Syndrome:Simultaneous Hemodynamic Infarction of Optic Nerve & Brain
Neurol 37:263-268, Bogousslavsky,J.,et al, 1987

Computed Tomography and Magnetic Resonance Imaging in the Diagnosis of Inflammatory Disease of the Optic Nerve
Surv Ophthalmol 31:352-355, McCrary,J.A.,et al, 1987

Bilateral Retrobulbar Optic Nerve Infarctions After Blood Loss & Hypotension, A Clinicopath Case Study
Ophthalmol 94:1577-1584, Johnson,M.W.,et al, 1987

Subacute Polyradiculopathy With Optic and Auditory Nerve Involvement
Arch Neurol 44:885-887, Pall,H.S. &Williams,A.C., 1987

Hereditary Neuropathy with Liability to Pressure Palsies
In Handbk of Clin Neurol, Elsevier Sci Publ Co, NY 51:551-562987., Cherry,S.&Mayer,R.F., 1987

Familial Long Thoracic Nerve Palsy:A Manifestation of Brachial Plexus Neuropathy
Neurol 36:1251-1253, Phillips,L.H., 1986

Fatal Familial Insomnia & Dysautonomia with Selective Degeneration of Thalamic Nuclei
NEJM 315:997-1003, Lugaresi,E.,et al, 1986

Optic-Nerve Degeneration in Alzheimer's Disease
NEJM 315:485-487, Hinton,D.R.,et al, 1986

The Role of Glutamate in Neurotransmission & in Neurologic Disease
Arch Neurol 43:1058-1063, Greenamyre,J.T., 1986

Lyme Disease Associated with Optic Neuropathy
Am J Med 81:143-145, Schechter,S.L., 1986

Visual & Auditory Neurotoxicity in Patients Receiving Subcutaneous Deferoxamine Infusions
NEJM 314:869-873, Olivieri,N.F.,et al, 1986

Silent Brain Lesions in Patients with Isolated Idiopathic Optic Neuritis
Arch Neurol 43:452-455, Jacobs,L.,et al, 1986

Isolated Idiopathic Optic Neuritis, Analysis of Free K-Light Chains in CSF & NMR
Arch Neurol 43:456-458, Rudick,R.A.,et al, 1986

Familial Amyloidosis with Cranial Neuropathy & Corneal Lattice Dystrophy
Neurol 36:432-435, Darras,B.T.,et al, 1986

Chronic Demyelinating Peripheral Neuropathy in Cerebrotendinous Xanthomatosis
Ann Neurol 20:89-91, Argov,Z.,et al, 1986

Neurological Manifestations in Xeroderma Pigmentosum
Ann Neurol 20:70-75, Mimaki,T.,et al, 1986

Neurosyphilis
Arch Neurol 42:606-613, Simon,R.P., 1985

Sarcoidosis & Its Neurological Manifestations
Arch Neurol 42:909-917, Stern,B.J.,et al, 1985

Carbonic Anhydrase II Deficiency in 12 Families with Osteopetrosis with Renal Tubular Acidosis & Cerebral Calcification
NEJM 313:139-181, Sly,W.S.,et al, 1985

Peripheral Neuropathy in Cerebrotendinous Xanthomatosis
Arch Neurol 42:1008-1010, Katz,D.A.,et al, 1985

The Risk of Cerebrovascular & Cardiovascular Disease in Patients with Anterior Ischemia Optic Neuropathy
Arch Ophthalmol 103:1136-1142, Guyer,D.R.,et al, 1985

Optic Neuritis & Multiple Sclerosis
Arch Neurol 42:702-704, Ebers,G.C., 1985

Optic Neuritis or Multiple Sclerosis
Arch Neurol 42:704-710, Kurtzke,J.F., 1985

Permanent Visual Loss after Shunt Malfunction
Neurol 35:25-29, Arroyo,H.A.,et al, 1985

Presentation & Management of Parasellar & Suprasellar Metastatic Mass Lesions
JNNP 48:44-49, Kattah,J.C.,et al, 1985

Showing articles 600 to 650 of 5752 << Previous Next >>