Neudle.com: retinal dystrophy

Neurology Specific Literature Search

Differential
(Click to cross reference)

abdominal distention

adrenoleukodystrophy

adverse drug reaction

Alzheimer's disease

antiretinal antibodies

apraxia of eye movements

aqueduct of Sylvius, stenosis

aqueductal stenosis

Argyll Robertson pupil

arrhythmia, cardiac

ataxia, cerebellar

ataxia, hereditary

ataxia, progressive

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

Bassen-Kornzweig syndrome

battered child syndrome

behavioral disorder

bladder dysfunction

brainstem, atrophy

brainstem, hypoplasia

calcification, intracranial

calf hypertrophy

carcinoma of lung

carotid artery occlusion, neck

CAT scan, abnormal

CAT scan, false negative

cataracts, congenital

central nervous system, infection of

cerebellar ataxia, children

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar hypoplasia

cerebellar lesion

cerebellar vermis

cerebral cortical atrophy

cerebro hepato renal syndrome

cerebrospinal fluid, elevated protein of

cerebrovascular accident

cerebrovascular accident, young adult

cherry red spot

cherry red spot-myoclonus syndrome

choreoathetosis

chorioretinitis

chromosomal abnormality

chronic progressive external ophthalmoplegia

cisterna magna, enlarged

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

Cockayne's syndrome

color vision, impaired

cone-rod dystrophy

congenital heart disease

congenital infection, CNS

conjunctival biopsy

contractures, joint

cornea, abnormal

cornea, opacity of

corpus callosum

corpus callosum, hypoplastic

cranial nerve palsies

craniopharyngioma

creatine phosphokinase(CPK)elevated

cyst, parenchymal

cyst, subcortical

cytochrome c oxidase

cytochrome c oxidase, deficiency

deep gray nuclei

degenerative diseases of CNS

developmental abnormality of brain

developmental milestones, loss of

developmental retardation

diabetes insipidus

diabetes mellitus

differential diagnosis

diplegia, spastic cerebral

drug induced neurologic disorders

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electron microscopy

electronystagmography

electroretinograph

epidermal nevus syndrome

extraocular muscle lesion

eye movement, disorders of

facial appearance, abnormal

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

false negative VDRL

fatty acid dehydrogenase deficiency

feeding disorder

fingerprint bodies

fluorescein angiography

fluorescent treponema antibody absorption(FTA-ABS)

fourth ventricle, enlargement of

Friedreich's ataxia

fundus, abnormality of

funduscopic exam

gastrointestinal disease, neurologic complications

gastrointestinal motility

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic testing

glare, light-induced

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

growth retardation

Hallervorden Spatz disease

Hallervorden Spatz disease, late onset

Hallgren's syndrome

hearing loss, bilateral

hearing loss, congenital

hearing problems in children

heralding manifestation

Hurler's syndrome

hydrocephalus, congenital

hyperpigmentation of skin

hypocholesterolemia

hypoparathyroidism

immunofluorescence

immunosuppressive agents

inborn errors of metabolism

inclusion bodies

inclusion bodies, intracytopasmic

intellectual deficit

intellectual deterioration

internuclear ophthalmoplegia

intestinal pseudoobstruction

intrauterine infection, viral of CNS

iris, atrophy of

Joubert syndrome

Kearns-Sayre syndrome

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

leukoencephalopathy

life expectancy

light-near dissociation, causes of

lymphocyte fingerprint profiles

lysosomal storage disease

macular degeneration

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

marche a petits pas

Marcus Gunn pupil

medial longitudinal fasciculus(MLF)

memory, impairment of

mental retardation

mitochondrial disease

mitochondrial encephalomyopathy

molecular genetics

motor neuron disease

movement disorder

movement disorder, extrapyramidal

MRI, CAT scan compared to

MRI, eye of tiger sign

MRI, paramagnetic effect

mucopolysaccharidoses

muscle atrophy, progressive

muscle weakness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, differential diagnosis of

muscular dystrophy, facioscapulohumeral

myoclonic jerks

myopathy, mitochondrial

myotonia dystrophica

nausea and vomiting

neuraminidase deficiency

neurocutaneous disease

neuroendocrinology

neurogenic vs.myopathic atrophy

neuroichthyosis

neurolipidosis IV

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic signs

neuronal ceroid-lipofuscinosis

neuroophthalmology

neuropathology, brain

neuropathy, ataxic

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, onion bulb

neuropathy, peripheral

night blindness

nystagmus, pendular

ocular myopathy

ophthalmoplegia

ophthalmoplegia, progressive external

optic atrophy, hereditary

optic nerve, lesion of

optic nerve, neoplasm of

optic neuropathy

optic neuropathy, hereditary

optical coherence tomography

pain, abdominal

paraparesis, spastic

Parkinson disease

Parkinsonism syndrome

PAS positive material in the brain

patent ductus arteriosus

peroxisomal disease

photosensitivity, eye

photosensitivity, skin

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

Poretti-Boltshauser syndrome

postural abnormality

progressive neurologic disorder

pseudohypertrophy

pseudoretinitis pigmentosa

psychiatric disorder

psychiatric problems in neurologic disorders

psychomotor retardation

pupil, abnormality in neurologic disorders

pupil, light reflex, abnormal

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

ragged-red fibers

refractive errors

Refsum's disease

remote effect of cancer on the nervous system

retina, abnormal

retinal arteriole attenuation

retinal degeneration

retinal detachment

retinal dysplasia

retinitis pigmentosa

roving eye movements

rubella syndrome

scotoma, central

scotoma, paracentral-homonymous

sea-blue histiocytes

sedimentation rate, elevated

seizure, children

seizure, neonatal

sensorineural hearing loss

serologic test for syphilis

sheathing of retinal veins

Sjogren-Larsson syndrome

skin, lesions in neurologic disorders

skull x-ray, abnormal

spastic diplegia

speech disorder

speech disorder, childhood

Spielmeyer Vogt syndrome

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 7

spinocerebellar degeneration

spongy degeneration of brain

steroid therapy, CNS treatment and complications with

stooped posture

substantia nigra

syphilis, diagnosis and treatment

syphilis, neurologic complications with

syphilis, ocular

systemic illness

Tangier's disease

tapetoretinal degeneration

telangiectases, retinal

testicular atrophy

third nerve palsy

treatment of neurologic disorder

trinucleotide repeats

Usher's syndrome

ventricular enlargement

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 field defect, altitudinal

visual fields, constricted

visual impairment

visual loss, progressive

visual loss, slow

visual loss, sudden

vitamin deficiency

vitamin E deficiency

Walker-Warburg syndrome

walking, difficulty with

weakness, generalized

weakness, progressive

weaning from respirator, failure to

white matter disease

wide based gait

Wolfram syndrome

Showing articles 650 to 700 of 822 << Previous Next >>

The Female Carrier of Duchenne Muscular Dystrophy
BMJ 284:1423-1424, Dubowitz,V., 1982

Progressive Muscle Disease in a Young Woman With Family History of Duchenne's Muscular Dystrophy
Arch Neurol 39:378-380, Olson,B.J.,et al, 1982

Serial Two-dimensional Echocardiography in Duchenne Muscular Dystrophy
Neurol 32:1101-1105, Goldberg,S.J.,et al, 1982

An Autosomal-dominant Dystrophy with Humeropelvic Distribution & Cardiomyopathy
Neurol 32:1399-1401, Fenichel,G.M.,et al, 1982

Distal Myopathy, Histochemical & Ultrastructural Studies
Arch Neurol 39:367-371, Kumamoto,T.,et al, 1982

Prolonged Migraine Aura Status
Ann Neurol 11:197-199, Haas,D.C., 1982

Diagnostic Delay in Duchenne's Muscular Dystrophy
JAMA 247:478-480, Crisp,D.E.,et al, 1982

Temporal Arteritis Associated With Normal Sedimentation Rate
JAMA 247:486-487, Biller,J.,et al, 1982

Neuroaxonal Dystrophy in Young Adults:A Clinicopathological Study of Two Unrelated Cases
Ann Neurol 11:335-343, Williamson,K.,et al, 1982

Examination of Dental Pulp to Diagnose Infantile Neuroaxonal Dystrophy
Arch Neurol 39:422-423, Carlo,J.,et al, 1982

Ocular Disorders Associated with a New Severe Acquired Cellular Immunodeficiency Syndrome
Am J Ophthalmol 93:393-402, Holland,G.N.,et al, 1982

Retinal Cotton-Wool Spots in a Patient with Pneumocystis Carinii Infection
NEJM 314:184-185, Kwok,S.,et al, 1982

Myotonic Dystrophy, Mitral Valve Prolapse, and Cerebral Embolism
Stroke 13:93-94, Morris,L.K.,et al, 1982

Carotid-retinal Embolism with Coexistent Mitral Valve Prolapse
Neurol 31:1192-1193, Baker,R.S.,et al, 1981

Cholesterol Embolism as a Cause of Transient Ischemic Attacks & Cerebral Infarction
Neurol 31:860-865, Beal,M.F.,et al, 1981

Hypersomnia Associated with Alveolar Hypoventilation in Myotonic Dystrophy
Neurol 31:1336-1337, Hansotia,P.,et al, 1981

Acute Thallium Poisoning, Toxicological & Morphological Studies of the Nervous System
Ann Neurol 10:38-44, Davis,L.E.,et al, 1981

A Progressive Neurologic Syndrome In Children With Chronic Liver Disease
NEJM 304:503-508, Rosenblum,J.L.,et al, 1981

Ischemic Oculopathy, a Manifestation of Carotid Artery Disease
Arch Neurol 38:358-361, Young,L.H.Y.,et al, 1981

High-Altitude Retinopathy
JAMA 245:581-586, McFadden,D.M.,et al, 1981

Sudden Blindness in Acute Pancreatitis
Arch Int Med 141:134-136, Jacob,H.S.,et al, 1981

An Ultramicroscopic Study of Skin & Conjunctival Biopsies in Chronic Neuro. Disorders of Childhood
Ann Neurol 9:163-173, Arsenio-Nunes,M.L.,et al, 1981

The Reflex Sympathetic Dystrophy Syndrome (RSDS)
Am J Med 70:23-30, Kozin,F.,et al, 1981

Anterior Ischemic Optic Neuropathy
Arch Neurol 38:675-678, Hayreh,S.S., 1981

Peripheral Source of MB Band of Creatine Kinase in Alcoholic Rhabdomyolysis
JAMA 244:580-582, Siegel,A.J., 1980

Neurologic Manifestations in Macroglobulinemia
In Vinken PJ, Bruyn GW, Eds, Handbook of Clin Neurol, Vol 39, North-Holland Publ Co, p. 189, Abramsky,O., 1980

Electrocardiogram Abnormalities in Carriers of Duchenne Muscular Dystrophy
Neurol 30:497-501, Lane,R.J.M.,et al, 1980

Echocardiographic Evaluation of Cardiac Abnormalities in Duchenne's Dystrophy & Myotonic Muscular Dystrophy
Arch Neurol 37:273-277, Reeves,W.C.,et al, 1980

Congenital Myotonic Dystrophy
Arch Neurol 37:693-696, Argov,Z.,et al, 1980

Hypoparathyroidism & Elevated Muscle Enzymes
Neurol 30:192-195, Shane,E.,et al, 1980

Horner Syndrome with Causalgia
Neurol 30:534-535, Bernad,P.G.,et al, 1980

Diagnosis of Infatile Neuroaxonal Dystrophy by Skin Biopsy
Ann Neurol 7:377-379, Wisniewski,K.,et al, 1980

Myotonic Dystrophy
In Harrison's Principles of Internal Medicine, 9th Ed, McGraw-Hill Book Co, NY 206180., Adams,R.D.,et al, 1980

Cockayne Syndrome:Unusual Neuropathological Findings & Review of the Literature
Ann Neurol 6:340-348, 1979, Soffer,D.,et al, 1979

Creatine Phosphokinase MB Band In Oculopharyngeal Muscular Dystrophy
(Letter) NEJM 301:270979., Diskin,C.J., 1979

Extraocular Muscle Biopsy in Chronic Progressive External Ophthalmoplegia
Ann Neurol 6:326-339, Ringel,S.P.,et al, 1979

Senile Disciform Macular Degeneration
Editioral, BMJ 1:1444-14451979., , 1979

Retinal Hemorrhages, Its Significance in 100 Patients With Acute Encephalopathy of Unknown Cause
Arch Neurol 36:691-694, Keane,J.R., 1979

Unilateral Visual Loss in Bright Light, An Unusual Symptom of Carotid Artery Occusive Disease
Arch Neurol 36:675-676, Furlan,A.J.,et al, 1979

Serum LDH-5 in Carriers of Duchenne Muscular Dystrophy
Neurol 29:239-241, Burt,D.,et al, 1979

Cerebral & Retinal Vascular Complications of Inflammatory Bowel Disease
Ann Neurol 5:331-337, Schneiderman,J.H.,et al, 1979

Visual Evoked Responses in Pernicious Anemia
Arch Neurol 36:168-169, Troncoso,J.,et al, 1979

Marfan Syndrome
NEJM 300:772-777, Pyeritz,R.E.,et al, 1979

Elevated Skeletal-Muscle Enzymes During Quinidine Therapy
NEJM 300:1218, Weiss,M.,et al, 1979

Emery-Dreifuss Muscular Dystrophy
Ann Neurol 5:111-117, Rowland,L.P.,et al, 1979

Neurologic Disturbances in Pagets Disease of Bone:Response to Calcitonin
Neurol 29:448-457, Chen,J.R.,et al, 1979

Retraction of the Lower Eyelid
Neurol 29:386-389, Cohen,M.M.,et al, 1979

Prenatal Genetic Diagnosis in 3000 Amniocenteses
NEJM 300:157-163, Golbus,M.S.,et al, 1979

Ocular Complications of Temporal Arteritis
Editorial, BMJ 1:14431979., , 1979

Haemophilic Neuromyopathy
JNNP 42:600-605, Defaria,C.R.,et al, 1979

Showing articles 650 to 700 of 822 << Previous Next >>