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.)

clubfoot as related to neurologic disease

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 800 to 822 of 822 << Previous

Some Neuro-ophthalmological Observations
JNNP 30:383, Fisher,C.M., 1967

Contributions of Serum Enzymes & Isozymes to the Diagnosis of Myocardial Injury
Med Concept of CVD 36:43, Cohen,L., 1967

The Cerebral Defect & Myopathy in Myotonic Dystrophy
Neurol 17:1106, Rosman,N.,et al, 1967

Contributions of Serum Enzymes to the Diagnosis of Myocardial Injury
Med Concepts of CVD 36:49, , 1967

Sickle Cell Trait & Central Retinal Artery Occlusion
Am J Ophthalmol 63:465, Conrad,W.C.,et al, 1967

Mental Deficiency Associated with Muscular Dystrophy
Brain 89:769, Rosman,N.P.,et al, 1966

The Uveomeningoencephalitic Syndrome
Neurol 16, 6031966., Riehl,J.L.,et al, 1966

Incidence of Uveitis in Multiple Sclerosis
Am J Ophthalmol 52:540, Riehl,J.L.,et al, 1966

Alternating Exophathalmos with Plainful Ophthalmoplegia
Arch Ophthalmol 74:625, Hedges,T., 1965

SLE Case Report-Pathology of the Cardiac Conduction System in SLE
Am J Med 264:255, 1972 Ann Int Med 63:4021965., James,T.,et al, 1965

The Muscular Dystrophies
NEJM 273:537, 5961965., Zundel,W.,et al, 1965

Central Nervous System Manifestations of Periarteritis Nodosa
Neurol 15:114, Ford,R.G.,et al, 1965

Muscular Dystrophy
Am J Med 35:632, Pearson,C.M., 1963

Ophthalmoplegic Migraine
Arch Neurol 7:320, Friednam,A.P., 1962

Angiokeratoma Corporis Diffusum
Quart J Med 31:177, 1962 April., Wise,D.,et al, 1962

Abnormal Hemoglobin as a Cause of Neurolic Disease
Neurol 12:114, Greer,M.,et al, 1962

Painful Ophthalmoplegia
Neurol 11:56, Hunt,W.,et al, 1961

Aetiology & Neurological Complications of Retinal Vasculitis
Brain 84:262, White,R., 1961

Sarcoid of the Fundus
Arch Ophthalmol 65:161, Gould,H.,et al, 1961

Basilar Artery Migraine
Lancet 1:15-17, Bickerstaff,E.R., 1961

Neuro CPC of MGH
Myopathy, Severe, Generalized, Chronic, NEJM 258:388-3938., , 1958

Causalgia of the Face, Two Cases Successfully Treated by Sympathectomy
BMJ 1:804-805, Bingham,J.A.W., 1947

Five Types of Dystrophy
Together with Other Conditions Producing Insidious Muscle Weakness-Table 1-Hospital Med p. 60., , 1850

Showing articles 800 to 822 of 822 << Previous