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Differential
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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 600 to 650 of 822 << Previous Next >>

Abnormalities of Eyelid Closure
In Walsh & Hoyt's Clinical Neuro-ophthalmology, Williams & Wilkins, Baltimore, 2:967, Miller,M.R., 1985

Early Neurological Complications of Coronary Artery Bypass Surgery
BMJ 291:1384-1387, Shaw,P.J.,et al, 1985

Cardiac Involvement in Myotonic Muscular Dystrophy
Medicine 64:371-387, Moorman,J.R.,et al, 1985

Cardiac Side Effects of Phenytoin & Carbamazepine, A Dose-Related Phenomenon
Arch Neurol 42:1067-1068, Durelli,L.,et al, 1985

A Microangiopathic Syndrome of Encephalopathy, Hearing Loss & Retinal Arteriolar Occlusions
Neurol 35:1113-1121, Monteiro,M.L.R.,et al, 1985

Prenatal Diagnosis & Carrier Detection of Duchenne Muscular Dystrophy with Closely Linked RFLPs
Lancet 1:655-658, Bakker,E.,et al, 1985

Increased Head Circumference in Patients with Duchenne Muscular Dystrophy
Ann Neurol 17:620-621, Schmidt,B.,et al, 1985

Facioscapulohumeral Dystrophy Presenting in Infancy with Facial Diplegia & Sensorineural Deafness
Ann Neurol 17:513-516, Korf,B.R.,et al, 1985

Tubular Aggregates, Their Association with Neuromuscular Diseases, Including the Syndrome of Myalgias/Cramps
Arch Neurol 42:973-976, Rosenberg,N.L.,et al, 1985

Steroid-Responsive Ophthalmoplegia in a Child, Diagnostic Considerations
Arch Neurol 42:589-591, Kandt,R.S.,et al, 1985

Chronic Ocular Ischemia & Carotid Vascular Disease
Stroke 16:721-728, Carter,J.E., 1985

Clin. Path. Conference
External Ophthalmoplegia with Mitochondrial Myopathy, Case Record 3-1985, NEJM 312:171-177985., , 1985

Migrainous Ischemic Optic Neuropathy
Neurol 35:112-114, Katz,B.,et al, 1985

Blind Loop Syndrome, Vitamin E Malabsorption, & Spinocerebellar Degeneration
Neurol 35:338-342, Brin,M.F.,et al, 1985

Autosomal Recessive Distal Muscular Dystrophy:A Comparative Study with Distal Myopathy with Rimmed Vacuole Formation
Ann Neurol 17:51-59, Nonaka,I.,et al, 1985

Computed Tomographic Changes of Hypertensive Encephalopathy
AJNR 6:395-398, Weingarten,K.L.,et al, 1985

Oculomotor Nerve
Savino, P. J. , Trobe, J. D. , In Clinical Decisions in Neuro-Ophthalmology, The C. V. Mosby Co, St., Louis, 1985, ChBurde, R. M., 1985

Acquired Immune Defieiency Syndrome, Pathogenic Mechanisms of Ocular Disease
Ophthalmology 92:472-484, Pepose,J.S.,et al, 1985

A Prospective Study of the Ophthalmologic Findings in the Acquired Immune Deficiency Syndrome
Am J Ophthalmol 97:133-142, Freeman,W.R.,et al, 1984

Ophthalmologic Findings in Acquired Immune Deficiency Syndrome (AIDS)
Arch Ophthmol 102:201-206, Khadem,M.,et al, 1984

Sudden Visual Loss in Pseudotumor Cerebri Due to Central Retinal Artery Occlusion
Arch Neurol 41:1274-1276, Baker,R.S.,et al, 1984

Iatrogenic Causalgia
Arch Neurol 41:821-824, Horowitz,S.H., 1984

Neurologic Complications of Hemoglobin SC Disease
Arch Neurol 41:289-292, Fablan,R.H.,et al, 1984

The Cerebrohepatorenal (Zellweger) Syndrome
NEJM 310:1141-1146, Moser,A.E.,et al, 1984

Computed Tomographic Patterns of Muscles in Neuromuscular Diseases
Arch Neurol 41:383-387, Hawley,R.J.,et al, 1984

The Terminology of Transient Visual Loss Due to Vascular Insufficiency
Stroke 15:907-908, Hedges,T.R., 1984

Graves'Disease Presenting with Bilateral Acute Painful Proptosis, Ptosis, Ophthalmoplegia, & Visual Loss
Lancet 2:431-433, Leonard,T.J.K.,et al, 1984

Neurological Complications of Acquired Immune Deficiency Syndrome:Analysis of 50 Patients
Ann Neurol 14:403-418, Snider,W.D.,et al, 1983

Chronic Progressive External Ophthalmoplegia (CPEO) :Clinical, Morphologic, & Biochemical Studies
Neurol 33:452-461, Mitsumoto,H.,et al, 1983

Duchenne Muscular Dystrophy:Carrier Detection by Ultrasound & Computerised Tomography
Lancet 2:1199-1200, Rott,H., 1983

Implications of Diagnostic Delay in Duchenne Muscular Dystrophy
BMJ 287:1106-1107, Zellweger,H., 1983

Recognising & Preventing Duchenne Muscular Dystrophy
BMJ 287:1083-1084, Firth,M.A.,et al, 1983

Abnormal Visual Evoked Potentials in Myotonic Dystrophy
Neurol 33:1622-1625, Cott,P.S.,et al, 1983

Families with Myotonic Dystrophy with & without Cardiac Involvement
Arch Int Med 143:2134-2136, Hawley,R.J.,et al, 1983

Clinicopathological Conference
Maroteaux-Lamy Syndrome, Case 44-1983, NEJM 309:1109-1117983., , 1983

Monocular Polyopia
Arch Neurol 40:756-757, Hirst,L.W.,et al, 1983

Isolated Ocular Myopathy & Celiac Disease in Childhood
Neurol 33:792, Sandyk,R.,et al, 1983

Reflex Sympathetic Dystrophy (Causalgia) Treatment with Guanethidine
Arch Neurol 40:430-432, Tabira,T.,et al, 1983

Neuro-Ophthalmologic Signs in the Angiitic Form of Neurosarcoidosis
Neurol 33:1130-1135, Caplan,L.,et al, 1983

Herpes Zoster & Central Retinal Artery Occlusion
Ann Neurol 13:217-218, Hall,S.,et al, 1983

Quadriceps Myopathy:A Varient of the Limb-Girdle Dystrophy Syndrome
JNNP 46:355-357, Swash,M.,et al, 1983

Radionuclide Angiocardiographic Analysis of Myocardial Function in Myotonic Muscular Dystrophy
Neurol 33:657-660, Hartwign,G.B.,et al, 1983

The Treatment of Myotonia:Evaluation of Chronic Oral Taurine Therapy
Neurol 33:599-603, Durelli,L.,et al, 1983

Mucopolysaccaridosis IV (Morquio Syndrome) , in The Metabolic Basis of Inherited Disease
(Ed) 5th Ed. , McGraw-Hill, New York, p. 766, Stanbury,J.B., 1983

Respiratory Muscle Function and Ventilatory Control in Patients with Myotonic Dystrophy
Q J Med 202:205-226, Serisier,D.E.,et al, 1982

Inflammatory Facioscapulohumeral Muscular Dystrophy & Coats Syndrome
Ann Neurol 12:398-401, Wulff,J.D.,et al, 1982

Ophthalmoscopy of the Retinal Nerve Fiber Layer
Arch Neurol 39:226-233, Newman,N.M.,et al, 1982

External Carotid-Cavernous Sinus Fistula Simulating Unilateral Graves Ophthalmopathy
J Comput Assist Tomogr 6:1006-1009, Merlis,A.L.,et al, 1982

Leber's Idiopathic Stellate Retinopathy
Am J Ophthalmol 93:96-101, Carroll,D.M.,et al, 1982

Co-occurring Ophthalmoplegia & Hemiparesis in a Case of Migraine
Arch Neurol 39:445-446, Whitehouse,P.J.,et al, 1982

Showing articles 600 to 650 of 822 << Previous Next >>