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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

genetic linkage

genetic neurologic disorders

genetic testing

globus pallidus

globus pallidus, lesion of

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 550 to 600 of 5752 << Previous Next >>

Hereditary Motor and Sensory Neuropathies and Hereditary Spastic Paraplegia:A Magnetic Stimulation Study
Ann Neurol 28:43-49, Claus,D.,et al, 1990

Familial Multiple Symmetric Lipomatosis with Peripheral Neuropathy
Neurol 40:1246-1250, Chalk,C.H.,et al, 1990

A Long-Term Prospective Study of Optic Neuritis:Evaluation of Risk Factors
Ann Neurol 27:386-393, Sandberg-Wollheim,M.,et al, 1990

Optic Neuritis:A Prospective Study
Neurol 40:919-923, Celesia,G.G.,et al, 1990

Clioquinol (lodochlorhydrozyquin
Vioform) and Iodoquinol (Diiodohydrozyquin) :Blindness and Neuropathy, Pediatrics 86:797-7980., , 1990

Magnetic Resonance Imaging of Radiation Optic Neuropathy
Am J Ophthalmol 110:389-394, Zimmerman,C.F.,et al, 1990

Neurosarcoidosis:Signs, Course and Treatment in 35 Confirmed Cases
Medicine 69:261-276, Chapelon,C.,et al, 1990

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

Neurofibromatosis 2 (Bilateral Acoustic Neurofibromatosis) An Update
Ann Int Med 113:39-52, Mulvihill,J.J.,et al, 1990

Acute Disseminated Encephalomyelitis, MRI Findings & the Distinction from Multiple Sclerosis
Brain 113:291-302, Kesselring,J.,et al, 1990

Polyneuropathy, Ophthalmoplegia, Leukoencephalopathy, and Intestinal Pseudo-Obstruction:POLIP Syndrome
Ann Neurol 28:349-360, Simon,L.T.,et al, 1990

Migraine-Related Stroke in the Context of the International Headache Society Classification of Head Pain
Arch Neurol 47:458-462, Welch,K.M.A.&Levine,S.R., 1990

Genetic Linkage of Hereditary Motor & SensoryNeuro Type I (Charcot-Marie-Tooth Disease) to Chrom 1 & 17
Neurol 40:1450-1453, Defesche,J.C.,et al, 1990

Hyperostosis Cranialis Interna
NEJM 322:450-463, Manni,J.J.,et al, 1990

Clinicopath Conf
Familial Visceral Myopathy (Oculogastrointestinal Muscular Dystrophy) , Case 12-1990, NEJM 322:829-8, 1, 19, 1990

Neurologic Crises in Hereditary Tyrosinemia
NEJM 322:432-437, Mitchell,G.,et al, 1990

Spontaneous Visual Phenomena with Visual Loss:104 Patients with Lesions of Retinal and Neural Afferent Pathways
Neurol 40:444-447, Lepore,F.E., 1990

Graves Orbitopathy:Correlation of CT and Clinical Findings
Radiology 177:675-682, Nugent,R.A.,et al, 1990

Refsum Disease
In Rowland's Merritt's Textbk of Neurology, Lea & Febiger, Phila, 8thEd, p. 509, Menkes,J.H., 1989

Surgical Treatment of Progressive Visual Loss in Traumatic Optic Neuropathy, Report of Two Cases
J Neurosurg 70:799-801, Guy,J.,et al, 1989

Respiratory Muscle Weakness in Charcot-Marie-Tooth Disease, A Field Study
Arch Int med 149:1389-1391, Nathanson,B.N.,et al, 1989

Cancer-Associated Retinopathy (Car Syndrome) with Antibodies Reacting with Retinal, Optic-Nerve, and Cancer Cells
NEJM 321:1589-1594, 1607-16081989., Thirkill,C.E.,et al, 1989

Multifocal Fibrosclerosis with Hypertrophic Intracranial Pachymeningitis
Neurol 39:1345-1349, Berger,J.R.,et al, 1989

Peripheral Neuropathy in Amyotrophic Chorea-Acanthocytosis
Ann Neurol 26:583-587, Vista,G.,et al, 1989

Compression Syndromes Due to Hypertrophic Nerve Roots in Hereditary Motor Sensory Neuropathy Type I
Neurol 39:1173-1177, Rosen,S.A.,et al, 1989

Neurologic Eye Signs Following Motorcycle Accidents
Arch Neurol 46:761-762, Keane,J.R., 1989

The Diagnosis of Neurofibromatosis-1 in the Child Under the Age of 6 Years
Am J Dis Child 143:717-719, Obringer,A.C.,et al, 1989

Aseptic Meningitis Complicating Adult Kawasaki Disease:Case Report and Review of the Literature
Am J Med 87:106-110, McIlroy,M.A.,et al, 1989

Ethanol and the Nervous System
NEJM 321:442-454, Charness,M.E.,et al, 1989

Neurofibromatosis and Other Disorders Among Children with CNS Tumors and Their Families
Neurol 39:487-492, Baptiste,M.,et al, 1989

Lyme Disease
NEJM 321:586-596, Steere,A.C., 1989

Neurobrucellosis:Clinical Characteristics, Diagnosis, and Outcome
Neurol 39:498-501, AlDeeb,S.M.,et al, 1989

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

Molecular Genetics of Amyloid Neuropathy in Europe
Lancet 1:524-526, Holt,I.J.,et al, 1989

Hereditary Sensory Neuropathy with Deafness:A Familial Multisystem Atrophy
Neurol 39:244-248, Horoupian,D.S., 1989

Transient Ocular Motor Paresis Associated with Acute Internal Carotid Artery Occlusion
Ann Neurol 25:286-290, Wilson,W.B.,et al, 1989

Neurological Disease Associated with Antiphospholipid Antibodies
Ann Neurol 25:221-227, Briley,D.P.,et al, 1989

Multiple Sclerosis-Like Illness Occurring with Human Immunodeficiency Virus Infection
Neurol 39:324-329, Berger,J.R.,et al, 1989

Follow-up and Diagnostic Reappraisal of 75 Patients with Leber's Congenital Amaurosis
Am J Ophthalmol 107:624-631, Lambert,S.R.,et al, 1989

REcurrent Familial Brachial Plexus Palsies as the ONly Clinical Expression of'Tomaculous'Neuropathy
Eur Neurol 29:61-66, Martinelli,P.,et al, 1989

The Peroxisome:Nervous System Role of a Previously Underrated Organelle, The 1987 Robert Wartenberg Lecture
Neurol 38:1617-1627, Moser,H.W., 1988

The Clinical Neuro-Ophthalmologic Spectrum of Temporal Arteritis
Am J Med 85:839-844, Mehler,M.F.&Rabinowich,L., 1988

Pituitary Apoplexy
BMJ 297:1526-1527, Lewin,I.G.,et al, 1988

The Early Risk of Multiple Sclerosis after Optic Neuritis
JNNP 51:1569-1571, Miller,D.H.,et al, 1988

Optic Neuritis in the Elderly:Prognosis for Visual Recovery and Long-Term Follow-Up
Neurol 38:1834-1837, Jacobson,D.M.,et al, 1988

Chronic Unilateral Optic Neuropathy:A Magnetic Resonance Study
Ann Neurol 24:3-11, Eidelberg,D.,et al, 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

Detection of HTLV-I DNA & Antigen in Spinal Fluid & Blood of Pts with Chronic Progressive Myelopathy
NEJM 318:1141-1147, 11951988., Bhagavati,S.,et al, 1988

Respiratory Muscle Dysfunction in Hereditary Motor Sensory Neuropathy, Type I
Arch Int Med 148:1739-1740, Eichacker,P.Q.,et al, 1988

Chiasmal Neuritis as a Complication of Epstein-Barr Virus Infection
Arch Neurol 45:458-460, Purvin,V.,et al, 1988

Showing articles 550 to 600 of 5752 << Previous Next >>