Neudle.com: retinal dystrophy

Differential
(Click to cross reference)

abdominal distention

acanthocytosis

adrenoleukodystrophy

adverse drug reaction

antiretinal antibodies

aphasia

apraxia of eye movements

aqueduct of Sylvius, stenosis

aqueductal stenosis

areflexia

Argyll Robertson pupil

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

Bassen-Kornzweig syndrome

battered child syndrome

brainstem, hypoplasia

bulbar palsy

cachexia

calcification, intracranial

carotid artery occlusion, neck

CAT scan

CAT scan, abnormal

CAT scan, false negative

cataracts

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

cerebral palsy

cerebro hepato renal syndrome

cerebrospinal fluid, elevated protein of

cerebrovascular accident

cerebrovascular accident, young adult

cherry red spot

cherry red spot-myoclonus syndrome

chromosomal abnormality

chromosome 17

chromosome 20

chronic progressive external ophthalmoplegia

cisterna magna, enlarged

Clinical Pathologic Conference(C.P.C.)

Coats syndrome

Cockayne's syndrome

color vision

color vision, impaired

cone-rod dystrophy

congenital heart disease

congenital infection, CNS

corpus callosum, hypoplastic

cranial nerve palsies

craniopharyngioma

creatine phosphokinase(CPK)elevated

cytochrome c oxidase, deficiency

deafmute

deafness

deep gray nuclei

degenerative diseases of CNS

dementia

developmental abnormality of brain

developmental milestones, loss of

developmental retardation

diabetes insipidus

diabetes mellitus

diarrhea

differential diagnosis

diplegia, spastic cerebral

DNA probes

drug induced neurologic disorders

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electron microscopy

electronystagmography

electroretinograph

encephalocele

enzyme, defect

epidermal nevus syndrome

extraocular muscle lesion

eye injury

eye movement, disorders of

eyes, sunken

facial appearance, abnormal

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

fatty acid dehydrogenase deficiency

feeding disorder

fingerprint bodies

fluorescein angiography

fluorescent treponema antibody absorption(FTA-ABS)

foot deformity

fourth ventricle, enlargement of

Friedreich's ataxia

fundus, abnormality of

funduscopic exam

gait disorder

gargoylism

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

growth retardation

Hallervorden Spatz disease

Hallervorden Spatz disease, late onset

hearing loss, bilateral

hearing loss, congenital

hearing problems in children

heart block

hepatomegaly

heralding manifestation

Hurler's syndrome

hydrocephalus

hydrocephalus, congenital

hyperpigmentation of skin

immunosuppressive agents

inborn errors of metabolism

inclusion bodies

inclusion bodies, intracytopasmic

incoordination

intellectual deficit

intellectual deterioration

internuclear ophthalmoplegia

intestinal pseudoobstruction

intrauterine infection, viral of CNS

Kearns-Sayre syndrome

keratoconus

kyphoscoliosis, neurologic causes of

kyphosis

lactic acidemia

Laurence-Moon-Bardet-Biedl syndrome

Leber's hereditary optic neuropathy

Leigh's disease

lens, dislocation of

lenticular nucleus, lesion of, bilateral

leukodystrophy

leukoencephalopathy

life expectancy

light-near dissociation, causes of

lissencephaly

lymphocyte fingerprint profiles

lysosomal storage disease

macular degeneration

malabsorption

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

marche a petits pas

Marcus Gunn pupil

medial longitudinal fasciculus(MLF)

MELAS syndrome

memory, impairment of

mitochondrial disease

mitochondrial encephalomyopathy

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, CAT scan compared to

MRI, eye of tiger sign

MRI, paramagnetic effect

MRI, serial

MRS

mucopolysaccharidoses

muscle atrophy, progressive

muscle biopsy

muscle weakness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, differential diagnosis of

muscular dystrophy, facioscapulohumeral

myopathy, mitochondrial

myopia

myotonia dystrophica

nausea and vomiting

neuraminidase deficiency

neuritis

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

neuropathology, brain

neuropathy

neuropathy, ataxic

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, onion bulb

neuropathy, peripheral

ophthalmoplegia, progressive external

optic atrophy

optic atrophy, hereditary

optic glioma

optic nerve

optic nerve, lesion of

optic nerve, neoplasm of

optic neuropathy

optic neuropathy, hereditary

optical coherence tomography

Parkinsonism syndrome

PAS positive material in the brain

patent ductus arteriosus

photosensitivity, eye

photosensitivity, skin

phytanic acid

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

polydactyly

polymyositis

polyneuropathy

Poretti-Boltshauser syndrome

postural abnormality

progeria

prognosis

progressive neurologic disorder

pseudohypertrophy

pseudoretinitis pigmentosa

psychiatric disorder

psychiatric problems in neurologic disorders

psychomotor retardation

ptosis

pupil

pupil, abnormality in neurologic disorders

pupil, light reflex, abnormal

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

remote effect of cancer on the nervous system

retina, abnormal

retinal arteriole attenuation

scotoma, paracentral-homonymous

sea-blue histiocytes

sedimentation rate, elevated

seizure

seizure, children

seizure, neonatal

sensorineural hearing loss

sensory loss

serologic test for syphilis

sheathing of retinal veins

short stature

Sjogren-Larsson syndrome

skin, biopsy

skin, lesions in neurologic disorders

skull x-ray, abnormal

spastic diplegia

spasticity

speech disorder

speech disorder, childhood

Spielmeyer Vogt syndrome

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 7

spinocerebellar degeneration

spongy degeneration of brain

steatorrhea

steroid

steroid therapy, CNS treatment and complications with

stooped posture

substantia nigra

sudden death

syphilis, diagnosis and treatment

syphilis, neurologic complications with

tapetoretinal degeneration

telangiectases

telangiectases, retinal

treatment of neurologic disorder

tremor

trinucleotide repeats

Usher's syndrome

uveitis

ventricular enlargement

viral infection, CNS

vision loss, sequential

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

Walker-Warburg syndrome

walking, difficulty with

weakness

weakness, generalized

weakness, progressive

weaning from respirator, failure to

Showing articles 700 to 750 of 822 << Previous Next >>

Behcet's Syndrome
NEJM 301:431-432, James,D.G., 1979

Clinical Pathological Conference
Candida Endocarditis with Cerebral Embolism, Case 27-1979, NEJM 301:34-42979., , 1979

Allopurinol Not Effective In Muscular Dystrophy
NEJM 301:785, Bakouche,P.,et al, 1979

5'-Nucleotidase Activity in Duchenne Muscular Dystrophy
NEJM 301:726, Scholte,H.R.,et al, 1979

Carrier Detection in Duchenne Muscular Dystrophy
Neurol 29:1423-1425, Tagliavini,J.,et al, 1979

Cholestasis & Myotonic Dystrophy
(letter) NEJM 301:329-330979., Theodore,Ch.,et al, 1979

Lymphocyte Capping in Muscular Dystrophy
Neurol 29:1419-1421, Hauser,S.L.,et al, 1979

Insulin-Induced Weakness in Hypokalemic Myopathy
Ann Neurol 6:139-140, Ruff,R.L., 1979

Muscular Dystrophy in Six Young Girls
Neurol 29:1486-1491, Hazama,R.,et al, 1979

Quadriceps Myopathy in Two Brothers
Rhode Island Med J 62:125, Finelli,P.F., 1979

Microangiopathy of the Brain & Retina
Neurol 29:313-316, Susac,J.O.,et al, 1979

Effects of Acetazolamide on Myotonia
Ann Neurol 3:531, Griggs,R.C.,et al, 1978

Papillophlebitis:Benign Retinopathy Resembling Papilledema or Paillitis
Ann Neurol 3:438, Ellenberger,C.,et al, 1978

A Case of Schwartz-Jampel Syndrome with Unusual Muscle Biopsy Findings
Ann Neurol 3:93, Fariello,R.,et al, 1978

Normal Pressure Hydrocephalus, Recog & Relation to Neuro Abnormalities in Cockayne's Sydrome
Arch Neurol 35:337, Brumback,R.A.,et al, 1978

Juvenile Neuroaxonal Dystrophy:Clinical, Electrophysiological, & Neuropathological Features
Ann Neurol 3:419, Dorfman,L.J.,et al, 1978

Peripheral Neuropathy in Myotonic Dystrophy
Arch Neurol 35:741-745, Olson,N.D.,et al, 1978

Deformed Erythrocytes in Muscular Dystrophies
Neurol 28:842-844, Grassi,E.,et al, 1978

Erythrocyte Metabolism in Muscular Dystrophy
Arch Neurol 35:592-595, Danon,M.J.,et al, 1978

Alteration in Erythrocyte Membrane Structure in Duchenne Muscular Dystrophy
Ann Neurol 4:253-256, Wakayama,Y.,et al, 1978

Systemic Membrane Defect in the Proximal Muscular Dystrophies
NEJM 299:841-846, Pickard,N.A.,et al, 1978

Weakness in Malignancy:Evidence for a Remote Effect of Tumor on Distal Axons
Ann Neurol 4:268-274, Barron,S.A.,et al, 1978

Human Pneumatic Tourniquet Paralysis
Neurol 28:787-793, Bolton,C.F.,et al, 1978

Clinical Symposia, Scoliosis
CIBA, 30:21978., Keim,H.A., 1978

Pseudoxanthoma Elasticum:A Review of Neurological Complications
Ann Neurol 4:18, Iqbal,A.,et al, 1978

Migraine Presenting as Acute Confusion & Delirium:A Case Report
Neurol 28:1201, Finelli,P.F., 1978

The Clinical Significance of Spontaneous Pulsations of the Retinal Vein
Arch Neurol 35:37, Levin,B., 1978

Neurological Manifestations of Fabry Disease in Female Carriers
Ann Neurol 4:537-540, Bird,T.D.,et al, 1978

Clinical pathological conference
Von Hippel-Lindau disease, Case Record 1-1978, NEJM 298:95978., , 1978

Sarcoidosis & Its Ophthalmic Manifestations
Am J Ophthmol 86:648-655, Obenauf,C.D.,et al, 1978

Amaurosis Fugax From Disease of the External Carotid Artery
Arch Neurol 34:532, Burnbaum,M.D.,et al, 1977

Amaurosis Fugax Due to Isolated Atherosclerotic Carotid Artery Disease in a Young Woman
Ann Neurol 2:541, Feldon,S.E.,et al, 1977

Clinical Pathological Conference
Giant-cell Arteritis of Temporal Artery (temporal arteritis) , Case Record 35-1977, NEJM 297:4927., , 1977

Subacute meningitis heralding a diffuse granulomatous angiitis: (Wegener's granulomatosis? )
Neurol, 27:2621977., Atcheson,S.G.,et al, 1977

Clofibrate-Induced Muscle Damage with Myoglobinuria & Cardiomyopathy
NEJM 296:942, Smals,A.G.H., 1977

The Spectrum of Mild X-Linked Recessive Muscular Dystrophy
Arch Neurol 34:408, Ringer,S.P.,et al, 1977

Myasthenia Gravis & Myotonic Dystrophy in a 13-year-old Girl
Neurol 27:546, Schoen,R.T., 1977

Solitary Oculomotor Nerve Palsy In Childhood
Am J Ophthal 83:106-111, Miller,N.R., 1977

Globoid cells, Glial nodules, & Peculiar Fibrillary Changes in the cerebro-hepato-renal Syndrome of Zellweger
Ann Neurol 2:473, deLeon,G.A.,et al, 1977

Retinal Hemorrhage as a Complication of Gas Encephalography & Gas Myelography
JNNP 40:1049, Slagsvold,J.E.,et al, 1977

Bone Scanning & Diagnosis of Reflex Sympathetic Dystrophy Secondary to Herniated Lumbar Disks
Neurol 27:791, Carlson,D.H.,et al, 1977

Prenatal Diagnosis of Duchenne's Muscular Dystrophy
NEJM 297:968, Mahoney,M.J.,et al, 1977

X-linked Muscular Dystrophy
Ann Neurol 2:414, Furukawa,T.,et al, 1977

Neurological Complications of Infections of the Head & Neck
Otolaryng Clin North Am 9:729, Kaplan,R.J., 1976

Neuropsychiatric Manifest. of SLE:Diagnosis, Clinical Spectrum, & Relationship to Other Features of the Disease
Medicine 55:323, Feinglass,E.J.,et al, 1976

Carrier Detection in Duchenne Muscular Dystrophy
NEJM 294:193, Roses,A.D.,et al, 1976

Bilateral Altitudinal Anopia Caused by Infarction of the Calcarine Cortex
Neurol 26:1176, Bettinger,I.H.,et al, 1976

Episodic Disorders of Vision
MCV Quart 12:99-109, Harbison,J.W., 1976

Brachial Plexus Injuries
NEJM 291:1059, 1974 & 292, 4285., Leffert,R., 1975

Polymyositis & Dermatomyositis
NEJM 292:344, 1975, 292:403975., Bohan,A.,et al, 1975

Showing articles 700 to 750 of 822 << Previous Next >>