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abducens nerve paralysis

adolescent medicine

adrenoleukodystrophy

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

advances in neurology

adverse drug reaction

alcohol intolerance

alternating hemiplegia

alternating hemiplegia of childhood

alternating rapid movement

amyloid angiopathy, cerebral

amyloidosis, oculoleptomeningeal, familial

anti MAG antibodies

apnea, primary central

arrhythmia, cardiac

arteritis, temporal

arylsulfatase A

arylsulfatase B

ataxia, cerebellar

ataxia, hereditary

ataxia, progressive

ataxia, truncal

auditory evoked brainstem potentials

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

Bassen-Kornzweig syndrome

battered child syndrome

behavioral disorder

Behr's optic atrophy

biotin deficiency

biotinidase deficiency

bitemporal visual field defect

blindness, sudden

bone density, increased

bone marrow transplantation

brainstem, atrophy

brainstem, lesion of

bulbar palsy, childhood

bulbar palsy, progressive

calcification, intracranial

Canavan's disease

CAT scan, abnormal

CAT scan, false negative

cerebellar ataxia, children

cerebellar atrophy, primary

cerebral cortical atrophy

cerebral edema, vasogenic

cerebro hepato renal syndrome

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, protein of

cerebrovascular accident

cerebrovascular accident, multiple

cerebrovascular accident, young adult

Charcot-Marie-Tooth

cherry red spot

choreoathetosis

chromosomal abnormality

chronic progressive external ophthalmoplegia

cisternogram, radionuclide

Clinical Pathologic Conference(C.P.C.)

clubbing of fingers

clubfoot as related to neurologic disease

Cockayne's syndrome

coenzyme Q10 deficiency

color vision, impaired

compression neuropathy

cone-rod dystrophy

contractures, joint

cornea, abnormal

cornea, opacity of

corpus callosum

corpus callosum, hypoplastic

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

craniopharyngioma

cryopyrin-associated periodic syndrome

cultured skin fibroblasts

degenerative diseases of CNS

dementia, childhood

dementia, thalamic

demyelinating disease

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes insipidus

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diabetes mellitus, ocular complications in

diabetic cranialneuropathies

diagnostic criteria

diplegia, brachial

dissociated sensory loss

drug induced neurologic disorders

dyschromatopsia

electroencephalogram, abnormalities of

electron microscopy

electronystagmography

electroretinograph

emergencies, ocular

encephalopathy, neonatal

encephalopathy, progressive

entrapment neuropathy

episodic disorders

evoked potentials

exome sequencing

eye movement, disorders of

facial appearance, abnormal

facial nerve palsy

facial nerve palsy, bilateral

failure to thrive

feeding disorder

fever, recurrent

finger nose finger test

flaccid paralysis

flow study, carotid artery

fluorescein angiography

Friedreich's ataxia

frontal bossing

frontal lobe, pathologic signs of

fundus, abnormality of

funduscopic exam

galactocerebrosidase

gangliosidosis GM2

genetic counselling

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic testing

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

granulomatosis with polyangiitis

growth retardation

Hallervorden Spatz disease

head circumference

hearing problems in children

heel-knee-shin test

hemophagocytic lymphohistiocytosis, cerebromeningeal

hemophagocytosis

hepatosplenomegaly

hexosaminidase-A

Horner's syndrome

hydrocephalus, normal pressure

hydrocephalus, normal pressure in children

hydrocephalus, viral induced

hyperostosis corticalis generalisata familiaris

hypertriglyceridemia

hypertrophic intracranial pachymeningitis

hypofibrinogenemia

hypomyelination

hypotonia, infants

immunofluorescence

immunologic disease

inborn errors of metabolism

inclusion bodies

infantile bilateral striatal necrosis

intellectual deficit

intellectual deterioration

intestinal pseudoobstruction

intracerebral hemorrhage

intracerebral hemorrhage, familial

intracranial hypertension, benign

intracranial pressure, increased

Kearns-Sayre syndrome

Krabbe's disease

kyphoscoliosis, neurologic causes of

lactic acidemia

Laurence-Moon-Bardet-Biedl syndrome

Leber's hereditary optic neuropathy

Leigh's disease

Leigh's disease, adult variety

lenticular nucleus, lesion of, bilateral

leukocyte enzyme abnormality

light-near dissociation, causes of

lymphadenopathy

lysosomal storage disease

lysosomes, abnoral

macular degeneration

Marcus Gunn pupil

memory, impairment of

meningitis, aseptic

meningitis, carcinomatous

meningitis, chronic

mental retardation

metabolic acidosis

metabolic disorder, primary

metachromatic leukodystrophy

metachromatic leukodystrophy, juvenile

methylmalonic aciduria

mitochondrial disease

mitochondrial encephalomyopathy

molecular genetics

mononeuropathy multiplex

motor neuron disease

movement disorder

movement disorder, extrapyramidal

movement disorder, hyperkinetic

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, optic nerve

MRI, spinal cord

mucopolysaccharidoses

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, familial

muscle atrophy, progressive

muscle weakness

muscle weakness, proximal

myasthenia gravis, differential diagnosis

myasthenia gravis, misdiagnosis of

myelitis, longitudinal

myelitis, transverse

myoclonic jerks

myoclonus, epilepsy

myopathy, mitochondrial

nausea and vomiting

nerve conduction studies

neuroaxonal dystrophy

neuroendocrinology

neurolipidosis IV

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic examination

neurologic signs

neuromyelitis optica (Devic's disease)

neuromyelitis optica spectrum disorder

neuromyelitis optica, IgG

neuronal ceroid-lipofuscinosis

neuroophthalmology

neuropathology, brain

neuropathy, ataxia, retinitis pigmentosa

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, peripheral

neuropathy, vasculitic, systemic

night blindness

nutritional deficiency

nystagmus, monocular

nystagmus, rotary

nystagmus, upbeating-in primary position of gaze

nystagmus, vertical

ophthalmoplegia

ophthalmoplegia, progressive external

optic atrophy, bilateral

optic atrophy, hereditary

optic chiasm, enlarged

optic chiasm, lesion of

optic disc edema

optic foramina, abnormal

optic nerve, compression of

optic nerve, enhancement

optic nerve, enlarged

optic nerve, lesion of

optic nerve, neoplasm of

optic neuritis, bilateral

optic neuritis, treatment of

optic neuropathy

optic neuropathy, bilateral

optic neuropathy, hereditary

optic neuropathy, ischemic

optic neuropathy, nutritional

optic neuropathy, toxic

optic tract, lesion of

optical coherence tomography

owl's eye sign of spinal cord

palatal myoclonus

paraparesis, familial spastic

paraparesis, spastic

Parkinson disease

Parkinson disease, dystonia with

Parkinsonism syndrome

paroxysmal hemiplegia

paroxysmal neurologic deficits

PAS positive material in the brain

Pelizaeus Merzbacher

peroxisomal disease

personality change

photosensitivity, skin

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

polyneuropathy, familial

posterior leukoencephalopathy syndrome

precipitating factors

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

pretectal syndrome

prisoners of war, neurologic complications in

progressive neurologic disorder

propionic aciduria

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychological testing, neurologic problems

psychomotor retardation

pupil, abnormality in neurologic disorders

pupil, light reflex, abnormal

pyramidal tract

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

ragged-red fibers

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

red free light, fundus exam with

refractive errors

Refsum's disease

release phenomena

respiratory failure

retina, abnormal

retinal degeneration

retinal detachment

retinal ischemia

retinal nerve fiber layer

retinal vasculitis

retinal vasculopathy

retinal vasculopathy with cerebral leukodystrophy

retinitis pigmentosa

scotoma, central

sea-blue histiocytes

sedimentation rate, elevated

seizure, children

seizure, neonatal

sensorineural hearing loss

skin, lesions in neurologic disorders

skull bone, thickening

skull x-ray, abnormal

spastic diplegia

speech disorder

speech disorder, childhood

speech, loss of

spinal cord, compression of

spinal cord, lesion of

spinal cord, pathologic exam of

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 7

spinocerebellar degeneration

spinopontine atrophy, dominant

spongy degeneration of brain

startle myoclonus

startle reaction

status epilepticus

stem cell transplantation

steroid therapy, CNS treatment and complications with

stooped posture

striatonigral degeneration

striatonigral degeneration, infantile

striatum, lesion of

striatum, lesion of, bilateral

strokelike episodes

subarachnoid hemorrhage

subcortical U fibers

substantia nigra

symmetric brain lesions

systemic illness

Tangier's disease

tapetoretinal degeneration

Tay-Sachs disease

thalamus, lesion of

thrombocytopenia

tongue, enlarged

treatment of neurologic disorder

tremor, intention

trigeminal nerve, lesion of

trigeminal neuropathy

trinucleotide repeats

umbilical-cord blood transplantation

upgaze, paralysis of

urea-cycle enzymopathies

urinary incontinence

urine test for metabolic disorders

Usher's syndrome

vestibular function, tests of

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 impairment

visual loss, progressive

visual loss, slow

visual loss, sudden

vitamin deficiency

vitreous opacities

walking, difficulty with

water channel antibodies

white matter disease

white matter disease, subcortical

Wolfram syndrome

Showing articles 800 to 850 of 5752 << Previous Next >>

Acute Optic Neuropathy in Older Patients
Arch Neurol 28:182, Ellenberger,C., 1973

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

Neurosyphilis
JAMA 219:726, Hooshmand,H.,et al, 1972

Genetic Counseling in Retinitis Pigmentosa
MCV Quart 8:283, Noah,V., 1972

Syndrome of Incipient Prechiasmal Optic Nerve Compression
Arch Ophthalmol 87:1, Knight,C., 1972

Medical Approach to Ophthalmopathy of Graves'Disease
Mayo Clin Proc 47:980, Ivy,H., 1972

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

Glaucoma & the Optic Nerve
MCV Quart 8:296, Hoskins,H.D., 1972

Neurologic Manifestations of SLE 1972
Nebraska State Journ Med, Oct 1972, pp 395., Aita,J., 1972

The Glaucomatous Visual Field
Br J Ophthalmol 56:186, Drance,S., 1972

The Changing Management of Acute Optic Neuritis
Neuro Ophth, Chap 5, 6:44, 1972 Ed. J. L. Smith (Book) ., Lubow,M.,et al, 1972

Lymphomatoid Granulomatosis
Human Pathology 3:457, Liebow,A.,et al, 1972

Pituitary Apoplexy in Five Patients with Pituitary Tumors
BMJ 2:267, Epstein,S.,et al, 1971

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

The Nervous System & Diabetes
Joslin's Diabetes Mellitus, 1971, p. 562., Locke,S., 1971

Lymphomatous Leptomeningitis
Am J Med 51:200, Griffin,J.W.,et al, 1971

Encephalomyelopathy of Leigh
Editorial BMJ 238, 1971, May., , 1971

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

Acquired Sixth-Nerve Paresis in Children
Arch Ophthal 83:574-579, Robertson,D.M.,et al, 1970

Sensitivity to Encephalitogenic Protein in Optic Neuritis
Br J Ophthalmol 54:731, Lessell,S.,et al, 1970

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

Polyneroupathies of Undetermined Cause
Acta Neurol Scand (Supp) :5970., Prineas,J., 1970

Acute Intermittent Porphyria
Medicine 49:1, Stein,J.,et al, 1970

Progressive Facial Hemiatrophy (Parry-Romberg Syndrome)
Am J Ophthalmol 67:561, Johnson,R.V.,et al, 1969

Neurologic Manifestations of Bacterial Endocarditis
Ann Int Med 71:21, Jones,H.,et al, 1969

Olfactory Groove Tumor, In Clin. Neuro-ophthalmol
(Ed) , 3rd edition, The Williams & Wilkins Co, Baltimore, 1969, p. 2175-2177., Walsh,F.B., 1969

Intracavernous Carotid Aneur
Clinical Neuro-Ophthalmology, Third Ed. , Baltimore, The Williams & Wilkins Co. , 1969, Vol 2, Chap, 1, ph,F.B.&Hoyt,W.F., 1969

The Carotid-Cavernous Fistula:Spontaneous & Traumatic, In Clinical Neuro-Ophthalmology
3rd Ed, Williams & Wilkins, Baltimore, p. 1714, Walsh,F.B.&Hoyt,W.F., 1969

Papilledema, Optic Neuritis, and Optic Atrophy, in Clinical Neuro-Ophthalmology
3rd Ed, Williams & Wilkins Co, Baltimore 1969, p 623., Walsh,F.B.&Hoyt,W.F., 1969

Aspergillosis of the Orbit, Report of Ten Cases and Review of the Literature
Arch Ophthal 82:302-313, Green,W.R.,et al, 1969

Lower Motor & Primary Sensory Neuron Diseases with Peroneal Muscular Atrophy (II)
Arch Neurol 18:619, Dyck,P.,et al, 1968

Lower Motor & Primary Sensory Neuron Diseases with Peroneal Muscular Atrophy
Arch Neurol 18:603, Dyck,P.,et al, 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

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

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

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

Infectious Mononucleosis:Neurologic & EEG Findings
Medicine 45:5l, Schnell,R.,et al, 1966

Cerebellar Disease in Infectious Monoucleosis
Arch Neurol 15:270, Dowling,M.&Slyck,E., 1966

Causes of Paralysis of the Third, Fourth, & Sixth Cranial Nerves
Am J Ophthalmol 61:353, Rucher,C.W., 1966

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

Unilateral Intracranial Optic Nerve Involvement
Arch Ophthalmol 73:331, Little,H.L.,et al, 1965

Neurological Manifestations of Sarcoidosis
Neurol 15:1147, Wiederholt,W.,et al, 1965

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

Seronegative Ocular Syphilis & Neurosyphilis, Neuro-Ophthalmology Symposium, U. of Miami
(Ed) , St. Louis:C. V. Mosby Co. , 1965, p. 1, Smith,J.L., 1965

The Neurological Sequelae of Electrical Injury
Can Med Assn J 91:195, Silversides,J., 1964

Optic Atrophy in Childhood
Pediatrics 34:670, 1964 (Nov) ., Schwartz,J.F.,et al, 1964

Intracranial Aneurysms Causing Ophthalmoplegia
Arch Ophthal 70:75l, Cogan,D.,et al, 1963

Neurologic Complications of Polycythemia
Ann Int Med 57:909, Silverstein,A.,et al, 1962

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

Tumors Involving the Brain-Stem
Quart J Med 21:265, Barnett,H.J.,et al, 1952

Showing articles 800 to 850 of 5752 << Previous Next >>