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Differential
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acanthocytosis
adrenoleukodystrophy
adverse drug reaction
alopecia
anisocoria
anosmia
aphasia
areflexia
Argyll Robertson pupil
arrhythmia, cardiac
ataxia
ataxia, cerebellar
ataxic gait
Babinski sign
baclofen
basal ganglia
basal ganglia, calcification of
basal ganglia, lesion of
basal ganglia, lesion, bilateral
Bassen-Kornzweig syndrome
battered child syndrome
behavioral disorder
bladder dysfunction
blepharospasm
blindness
bradykinesia
brain atrophy
brainstem, atrophy
bulbar palsy
cachexia
calcification, intracranial
cardiomyopathy
caries
CAT scan
CAT scan, abnormal
CAT scan, false negative
cataracts
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebral cortical atrophy
cerebro hepato renal syndrome
cerebrospinal fluid, elevated protein of
cerebrovascular accident
cerebrovascular accident, young adult
children
chorea
choreoathetosis
chorioretinitis
chromosomal abnormality
chromosome 20
chronic progressive external ophthalmoplegia
cisterna magna, enlarged
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
Cockayne's syndrome
conjunctival biopsy
consanguinity
contractures, joint
cornea, abnormal
cornea, opacity of
craniopharyngioma
cry, weak
cryptorchidism
cytochrome c oxidase
cytochrome c oxidase, deficiency
deafmute
deafness
deep gray nuclei
degenerative diseases of CNS
dementia
developmental milestones, loss of
developmental retardation
diabetes insipidus
diabetes mellitus
diarrhea
differential diagnosis
diplegia, spastic cerebral
DNA probes
drug induced neurologic disorders
dwarfism
dysarthria
dysmorphic
dysphagia
dystonia
electrocardiogram, abnormal
electroencephalogram, abnormalities of
electron microscopy
electronystagmography
electroretinograph
enzyme, defect
eye injury
eyes, sunken
facial appearance, abnormal
falling
false negative
false negative VDRL
familial
fasciculation
feeding disorder
fingerprint bodies
fluorescein angiography
fluorescent treponema antibody absorption(FTA-ABS)
foot deformity
Friedreich's ataxia
fundus, abnormality of
funduscopic exam
gait disorder
gargoylism
gastrointestinal motility
gene
gene mutation
genetic linkage
genetic neurologic disorders
glaucoma
globus pallidus
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
growth retardation
Hallervorden Spatz disease
Hallervorden Spatz disease, late onset
Hallgren's syndrome
headache
hearing loss
hearing loss, bilateral
hearing loss, congenital
heart block
Hurler's syndrome
hydrocephalus
hyperpigmentation of skin
hyperreflexia
hypocholesterolemia
hypogonadism
hypoparathyroidism
hyposmia
imbalance
immunofluorescence
inclusion bodies
intellectual deficit
intellectual deterioration
intestinal pseudoobstruction
iris, atrophy of
iron, brain
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
light-near dissociation, causes of
macular degeneration
malabsorption
malformation, CNS, congenital
marche a petits pas
Marcus Gunn pupil
MELAS syndrome
memory, impairment of
mental retardation
MERRF syndrome
microcephaly
mitochondrial disease
mitochondrial encephalomyopathy
MNGIE syndrome
molecular genetics
mortality
motor neuron disease
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, eye of tiger sign
MRI, paramagnetic effect
MRI, serial
mucopolysaccharidoses
muscle atrophy, progressive
myelopathy
myoclonus
myopathy
myopathy, mitochondrial
myopia
nausea and vomiting
neuritis
neurocutaneous disease
neuroichthyosis
neurologic complications of, systemic cancer
neurologic disease, diagnoses of
neurologic signs
neuronal ceroid-lipofuscinosis
neuroophthalmology
neuropathology, brain
neuropathy
neuropathy, ataxic
neuropathy, hereditary peripheral
neuropathy, hypertrophic
neuropathy, onion bulb
neuropathy, peripheral
neurosyphilis
night blindness
nystagmus
nystagmus, pendular
obesity
ocular myopathy
ophthalmoplegia
ophthalmoplegia, progressive external
optic atrophy
optic glioma
optic nerve
optic nerve, neoplasm of
optic neuropathy
optical coherence tomography
palilalia
pancytopenia
PANK2 mutation
paraparesis
paraparesis, spastic
Parkinson disease
Parkinsonism syndrome
PAS positive material in the brain
peroxisomal disease
pes cavus
photosensitivity, skin
phytanic acid
pigmentary retinopathy
pleocytosis of cerebrospinal fluid
polydactyly
polyneuropathy
postural abnormality
progeria
prognosis
progressive neurologic disorder
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
ragged-red fibers
rash
refractive errors
Refsum's disease
retina, abnormal
retinal degeneration
retinal detachment
retinal lesion
retinitis pigmentosa
retinoblastoma
retinopathy
review article
rigidity
roving eye movements
schizophrenia
scotoma
scotoma, central
sea-blue histiocytes
sedimentation rate, elevated
seizure
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
spastic diplegia
spasticity
speech disorder
speech disorder, childhood
Spielmeyer Vogt syndrome
spinocerebellar ataxia type 1
spinocerebellar degeneration
steatorrhea
stooped posture
substantia nigra
sudden death
syphilis, diagnosis and treatment
syphilis, neurologic complications with
syphilis, ocular
tabes dorsalis
Tangier's disease
tapetoretinal degeneration
trauma
treatment of neurologic disorder
tremor
Usher's syndrome
uveitis
vision loss, sequential
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
visual loss, slow
vitamin A
vitamin deficiency
vitamin E
vitamin E deficiency
vitamin K
vitritis
walking, difficulty with
weakness
weight loss
white matter disease
Wolfram syndrome
workup
Showing articles 100 to 150 of 175 << Previous Next >>

Mortality in Patients with AIDS Treated with Either Foscarnet or Ganciclovir for CMV Retinitis
AIDS Res Group & AIDS Clin Trials Group, NEJM 326:213-220, 2642., , 1992

Treatment of Aggressive CMV Retinitis with Ganciclovir in Combination with Foscarnet in a Child Infected with HIV
J Pediatr 120:483-486, Butler,K.M.,et al, 1992

Ocular Manifestations of AIDS
JAMA 266:3019-3022, deSmet,M.D.&Nussenbatt,R.B., 1991

A Randomized, Controlled Trial of Foscarnet in the Treatment of Cytomegalovirus Retinitis in Pts with AIDS
Ann Int Med 115:665-673, Palestine,A.G.,et al, 1991

Acute Retinitis 2 Years After Recovery from Herpes Simplex Encephalitis
Neurol 41:456, Sekizawa,T.,et al, 1991

Microangiopathy of the Brain, Retina, and Ear:Improvement without Immunosuppressive Therapy
Stroke 22:933-937, Gordon,D.L.,et al, 1991

Cat Scratch Disease, Acute Encephalopathy & Other Neurologic Manifestations
Am J Dis Child 145:98-101, Carithers,H.A.&Margileth,A.M., 1991

Joubert Syndrome:A Clinico-Radiological Study
Neuroradiology 31:502-506, Kendall,B.,et al, 1990

Carotid-Cavernous Sinus Fistulas
In Glaser, J. S. Neuro-Ophthalmology, Lippincott Co, Phil, 2nd Ed, p. 535, Troost,T.B.&Glaser,J.S., 1990

Spontaneous Visual Phenomena with Visual Loss:104 Patients with Lesions of Retinal and Neural Afferent Pathways
Neurol 40:444-447, Lepore,F.E., 1990

Vision and Hearing During Deferoxamine Therapy
J Pediatr 117:326-330, Cohen,A.,et al, 1990

A Clinical Triad to Diagnose Paraneoplastic Retinopathy
Ann Neurol 28:162-167, Jacobson,D.M.,et al, 1990

A Mitochondrial DNA Mutation as a Cause of Leber's Hereditary Optic Neuropathy
NEJM 320:1300-1305, Singh,G.,et al, 1989

Mitochondrial Myopathies:Clinical & Biochem Features of 30 Patients with Major Deletions of Muscle Mitochondrial DNA
Ann Neurol 26:699-708, Hold,I.J.,et al, 1989

Cancer-Associated Retinopathy (Car Syndrome) with Antibodies Reacting with Retinal, Optic-Nerve, and Cancer Cells
NEJM 321:1589-1594, 1607-16081989., Thirkill,C.E.,et al, 1989

Antiphospholipid Antibodies:A Risk Facor for Occlusive Ocular Vascular Disease in Systemic Lupus Erythematosus and the 'Primary' Antiphospholipid Syndrome
Ann Rheumatic Dis 48:358-361, Asherson,R.A.,et al, 1989

Paraneoplastic Syndromes Involving the Eyes
In Walsh & Hoyt's Clin Neuro-ophthal, 4th ed, Williams & Wilkins, Vol 3, p 1735-1746, Miller,N.R., 1988

Ocular Findings in Infants Treated with Extracorporeal Membrane Oxygenator Support
Pediatrics 82:560-564, Patrias,M.C.,et al, 1988

The Peroxisome:Nervous System Role of a Previously Underrated Organelle, The 1987 Robert Wartenberg Lecture
Neurol 38:1617-1627, Moser,H.W., 1988

Infection of the Retina by Human Immunodeficiency Virus Type I
NEJM 317:1643-1647, Pomerantz,R.J.,et al, 1987

Neurologic Manifestations of AIDS
Medicine 66:407-437, McArthur,J.C., 1987

ABC of AIDS, Neurological Manifestations
BMJ 294:1399-1401, Carne,C.A., 1987

Neurologic Disease as the Presenting Manifestation of Acquired Immunodefieicney Syndrome
South Med J 80:683-686, Berger,J.R.,et al, 1987

Spontaneous Internal Jugular Vein Thrombosis & Venous-Stasis Retinopathy
Stroke 18:808-811, Gutteridge,I.F.,et al, 1987

Optic-Nerve Degeneration in Alzheimer's Disease
NEJM 315:485-487, Hinton,D.R.,et al, 1986

Clinicopath. Conference
Subacute Sclerosing Panencephalitis, Due to Measles Virus, Case 25-1986, NEJM 314:1689-170086., , 1986

Infections with Herpes Simplex Viruses
NEJM 314:686-691, 749-7571986., Corey,L.&Spear,P.G., 1986

Vascular Retinopathy in Migraines
Neurol 36:267-270, Coppeto,F.R.,et al, 1986

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

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

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

Human Cytomegalovirus Infection & Disorders of the Nervous System
Jr. , Arch Neurol 41:310-320984., Bale,J.F., 1984

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

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

Cerebral Toxoplasmosis in Acquired Immune Deficiency Syndrome
Arch Neurol 41:321-323, Alonso,R.,et al, 1984

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

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

Santavuori Disease:Diagnosis by Leukocyte Ultrastructure
Neurol 32:1277-1281, Baumann,R.J.,et al, 1982

Facioscapulohumeral Dystrophy Associated with Hearing Loss & Coats Syndrome
Ann Neurol 12:395-398, Taylor,D.A.,et al, 1982

Ocular Disorders Associated with a New Severe Acquired Cellular Immunodeficiency Syndrome
Am J Ophthalmol 93:393-402, Holland,G.N.,et al, 1982

Retinal Cotton-Wool Spots in a Patient with Pneumocystis Carinii Infection
NEJM 314:184-185, Kwok,S.,et al, 1982

High-Altitude Retinopathy
JAMA 245:581-586, McFadden,D.M.,et al, 1981

Sudden Blindness in Acute Pancreatitis
Arch Int Med 141:134-136, Jacob,H.S.,et al, 1981

Olivopontocerebellar Atrophy in Children:A Report of Seven Cases in Two Families
Ann Neurol 10:355-363, Colan,R.V.,et al, 1981

Ischemic Oculopathy, a Manifestation of Carotid Artery Disease
Arch Neurol 38:358-361, Young,L.H.Y.,et al, 1981

Peripheral Neuropathy in the Cherry-Red Spot-Myoclonus Syndrome (Sialidosis Type I)
Ann Neurol 7:450-456, Steinman,L.,et al, 1980

Neurologic Manifestations in Macroglobulinemia
In Vinken PJ, Bruyn GW, Eds, Handbook of Clin Neurol, Vol 39, North-Holland Publ Co, p. 189, Abramsky,O., 1980

Neurologic Disturbances in Pagets Disease of Bone:Response to Calcitonin
Neurol 29:448-457, Chen,J.R.,et al, 1979

Basal Ganglia Calcification in Kearns-Sayre Syndrome
Arch Neurol 36:711-713, Robertson,W.C.Jr., 1979



Showing articles 100 to 150 of 175 << Previous Next >>