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Differential
(Click to cross reference)
acanthocytosis
ataxia, cerebellar
Bassen-Kornzweig syndrome
blindness
cataracts
Cockayne's syndrome
consanguinity
cornea, abnormal
deafmute
deafness
dwarfism
electroencephalogram, abnormalities of
Friedreich's ataxia
gargoylism
genetic neurologic disorders
glaucoma
Hallgren's syndrome
heart block
Hurler's syndrome
Kearns-Sayre syndrome
keratoconus
Laurence-Moon-Bardet-Biedl syndrome
malformation, CNS, congenital
mental retardation
mucopolysaccharidoses
myopia
neuritis
obesity
ocular myopathy
polydactyly
pseudoretinitis pigmentosa
psychiatric disorder
retinitis pigmentosa
retinopathy
schizophrenia
seizure
Spielmeyer Vogt syndrome
Usher's syndrome
visual field defect
visual fields, constricted
Showing articles 0 to 8 of 8

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

MR Imaging of Vogt-Koyanagi-Harada Syndrome with Leptomeningeal Enhancement
AJNR 32:E169-E171, Lohman, B.D.,et al, 2011

Treatment of Vogt-Koyanagi-Herada Syndrome with Intravenous Immunoglobulin
Neurol 46:584-585, Helveston,W.R.&Gilmore,R., 1996

Uveomeningoencephalitis in a Human Immunodeficiency Virus Type 2-Seropositive Patient
Ann Neurol 23:308-310, Hormigo,A.,et al, 1988

Chronic Meningitis
Medicine 55:341, Ellner,J.J.,et al, 1976

Internal Ophthalmoplegia, In Ocular Differential Diagnosis
Lea & Febiger, Phila. p 3375., Roy,F.H., 1975

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

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



Showing articles 0 to 8 of 8