Neudle.com: retinal dystrophy

Differential
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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 750 to 800 of 822 << Previous Next >>

Cardiac Features of Unusual X-linked Humeroperoneal Neuromuscular Disease
et al NEJM 293:1017, Waters,D.D., 1975

Progressive Supranuclear Palsy-Case Study
NEJM 293:346, Richardson,E.P., 1975

Limitations & Complications of Myelography, in Myelography
3rd Year Book Med Publ Inc, Chicago, 1975, p. 455-462., Shapiro,R., 1975

Quadriceps Myopathy-Entity or Syndrome
Arch Neurol 31:60, Boddie,H.,et al, 1974

Transient Benign Unilateral Pupillary Dilation in Young Adults
Arch Neurol 31:12-14, Edelson,R.N.,et al, 1974

Wyburn-Mason Syndrome, Report of Two Cases Without Retinal Involvement
Arch Neurol 28:67-68, Brown,D.G.,et al, 1973

Placoid Pigment Epitheliopathy With Swelling of the Optic Disks
Arch Neurol 29:204-205, Jenkins,R.B.,et al, 1973

Case Records of MGH-NEJM 289:366
1973 Tuberculoma of Cerebral hemisphere & Brain Stem., , 1973

Epidemiology of Motor-Neuron Diseases
NEJM 288:1047, Bobwick,A.R.,et al, 1973

Visual Symptoms in the Migraine Syndrome
Neurol 23:570, Hachinski,V.,et al, 1973

Pathology of Malignant Hyperpyrexia
BMJ Editorial 249, 1973, Feb., , 1973

Possible Neurogenic Factor in Muscular Dystrophy:Its Similarity to Denervation Atrophy
JNNP 36:399-410, Dastur,D.K.,et al, 1973

Neurologic Manifestations of Rheumatic Fever
Postgrad Med 54:82, Aita,J.A., 1973

Air Embolism Complicating Percutaneous Needle Biopsy of the Lung
Chest 63:108-110, Westcott,J.L., 1973

The Facioscapulohumeral Synd, in Clinical Studies in Myology, Amsterdam, Excerpta Medica
p498-501, VanWijngaarden,G.K.&Bethlem,J., 1973

Neurologic Manifestations of Periarteritis Nodosa (1972)
Nebraska Med J 57:326, Aita,J.A., 1972

Congenital Dystrophia Myotonica
Neurol 22:443, Dyken,P.D., 1972

Preclinical Detection of Dystrophia Myotonica
BMJ 124, 1972 April., , 1972

Corneal Opacification in Infancy
MCV Quart 8:230, Ching,F., 1972

Mollaret's Meningitis & Differential Diagnosis of Recurrent Meningitis
Am J Med 52:128, Hermans,P.,et al, 1972

Isolated Ophthalmic Migraine:Its Frequency, Mechanism & Diff. Diagnosis
Neuro-Ophthalmol 1972-Bascom Palmer Instit Symp, Ed, J. S. Smith., Hedges,T., 1972

Diphenylhydantoin for Myotonia Congenita-Correspondence
NEJM 286:893, , 1972

Retinal Ischemic Symptoms in Cardiovascular Diagnosis
Postgrad Med 85, Oct 1972., Hoyt,W., 1972

Optic Disc Vasculitis
Br J Ophthalmol 56:652, Hayreh,S., 1972

Thalmic Neuronal Inclusion Disease
Neurol 22, 3961972., Segarra,J., 1972

Peripheral NR. Injuries & their Repairs
Surg Clin North Am Oct 1972., , 1972

Mucopolysaccaridosis IV (Morquio Syndrome) , in Heritable Disorders of Connective Tissue
(Ed) 4th Ed, The C. V. Mosby Co, St. Louis, p. 583, McKusick,V.A., 1972

Ophthalmoplegia In Myotonic Dystrophy
Am J Ophthalmol 71:1231-1235, Lessell,S.,et al, 1971

Electrodiagnosis of Neuromuscular Disease
Bull Univ Maryland School Med 56:33, Kemble,F., 1971

"Sick"Motoneurones A Unifying Concept of Muscle Disease
Lancet 321, 1971 Feb., McComas,A.J.,et al, 1971

Neurological Involvement in SLE
Singapore Med J 12:18, Tay,C.H.,et al, 1971

Comprehensive Mangagement of Duchenne Muscular Distrophy
Arch Phys Med & Rehab Mar 1971, pp110., Johnson,E.,et al, 1971

Acute Chorioretinal Infarction in Sickle Cell Trait
Arch Ophthalmol 84:485, Stein,M.,et al, 1970

The Nervous System in Sickle Cell Disease
Afr J Med Sci 1:33, Adelove,A.,et al, 1970

Retinal Lesions in Subacute Sclerosing Panencephalitis
Arch Ophthalmol 84:6l3, Nelson,D.,et al, 1970

Complains of Muscle Weakness
Patient Care Clinical Concepts, 21, 1970 Jan., , 1970

Early Recognition of Heterozygotes for the Gene for Dystrophia Myotonica
JNNP 33:279, Bundey,S.,et al, 1970

Chronic Progressive External Ophthalmoplegia
Arch Ophthalmol 82:845, Daroff,R., 1969

Chronic Spinal Muscular Atrophy in Adults
J Neurol Sci 9:527, Meadows,J.C.,et al, 1969

Ocular Myopathy
Arch Neurol 20:1, Magora,A.,et al, 1969

Whipple's Disease & Papilledema
Arch Int Med 123:74, Switz,D.M.,et al, 1969

Ophthalmic Complications in General MedicalDisorders
Trans Opthal Soc of United Kingdom 89:167, Russell,R., 1969

Biochemical Abnormalities of the Sarcoplasmic Reticulum in Muscular Dystrophy
NEJM 290:184, Samaha,F.,et al, 1969

The Use of Serum Lactate Dehydrogenase Isoenzymens in the Diagnosis of Muscle Disease
Neurol 19:26, Hooshmard,H.,et al, 1969

Neurogenic Muscular Atrophy Simulating Facioscapulohumeral Muscular Dystrophy
J Neurol Sci 9:389, Furukawa,T.,et al, 1969

Nine Neuropathies
Med Ann of the Dist of Columbia 37:89, Stevens,H., 1968

Whipple's Disease Presenting with Ocular Inflammation & Minimal Intestinal Symptoms
John's Hopkin's Med Jour 123:175, Knox,D.L.,et al, 1968

Progressive Ophthalmoplegia
Arch Neurol 19:362, Rosenberg,R.,et al, 1968

The Oculopharyngeal Syndrome
JAMA 203:1003, Murphy,S.F.,et al, 1968

Diseases of Muscles-Clinical Manifestations & Differential Diagnosis
The New Physic 263, 1967, Oct., Boshes,L., 1967

Showing articles 750 to 800 of 822 << Previous Next >>