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W. Dressler (1959)
Post-Myocardial Infarction SyndromeArch Intern Med, 103
B. P. Silfverskiold (1951)
Recurrent Uveitis (Beh�et's Syndrome) and EncephalomyelomeningitisActa Psychiat Neurol, 26
R. Chakrabarti, G. Fearnley, E. Hocking (1964)
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R. Asayama , A. Shimizu, T. and Akutagawa (1963)
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G. B. Dowling (1961)
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J. A. Dudgeon (1961)
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A. Garde (1958)
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Polyarthritis in Behçet's Multiple Symptom ComplexAnnals of the Rheumatic Diseases, 22
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J. Becker (1961)
[On the neurological symptomatology of "Behcet's syndrome"].Der Nervenarzt, 32
S. Magni (1951)
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W. Dressler (1959)
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Z. Krzyszton (1959)
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R. Marioni (1960)
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T. Alajouanine (1961)
La meningoencephalite de la maladie de Beh�etRev Neurol, 104
C. Pearson, B. Waksman, J. Sharp (1960)
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H. O. Curth (1946)
Recurrent Genito-Oral Aphthosis and Uveitis With HypopyonArch Derm Syph, 54
G. Fearnley, J. Bunim (1951)
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A. W. Morrison (1959)
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L. Alm (1945)
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N. Sezer (1953)
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H. Curth (1946)
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H. O. Curth (1952)
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[Behçet's disease; clinical and anatomicopathological aspects of a case with encephalitis].Revista clinica espanola, 71 3
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D. L. Phillips (1955)
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N. Sezer (1956)
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P. J. Boolukos (1960)
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H. Bienenstock, M. Margulies (1961)
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B. Waksman, C. Pearson, J. Sharp (1960)
Studies of arthritis and other lesions induced in rats by injection of mycobacterial adjuvant. II. Evidence that the disease is a disseminated immunologic response to exogenous antigen.Journal of immunology, 85
J. Boe , J. Dalgaard, D. and Scott (1958)
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Abstract THE major features of Behçet's syndrome are recurrent oral and genital ulcers and ocular lesions.10 Many types of ocular involvement have been described, including uveitis, iridocyclitis with hypopyon, keratitis, optic neuritis, and inflammation, thrombosis, or hemorrhage of the blood vessels of the retina.57 Other manifestations of the syndrome have included pyoderma, furunculosis, erythema nodosum, thrombophlebitis, pericarditis, arthritis, hepatomegaly, epididymitis, ulcers of the gastrointestinal tract, and central nervous system disease. The etiology is not known. The disease may begin with any one of the triad of symptoms, and the complete syndrome may not appear until several years later.57 Curth23 has suggested that the diagnosis is justified when two of the three classic manifestatations are present; this principle has been accepted by others.26,56,58,90,92 Although the course is variable, the illness often abates in 15 to 20 years. Blindness is a frequent sequel.57 When neurologic complications are References 1. References 1-5, 7-9, 12-14, 16-18, 20, 24, 29, 34, 35, 37, 38, 40-43, 45-49, 51-56, 58, 61, 63-65, 67, 70, 72-74, 77, 80, 81, 87, 89-93. 2. References 1, 3, 7, 9, 16, 24, 37, 67, 73, 74, 79, 87, 94. 3. References 2, 9, 12, 13, 16, 38, 51-53, 55, 64, 74, 77, 79, 89, 90, 94. 4. References 1-3, 7, 9, 13, 16, 18, 35, 37, 38, 40, 43, 49, 51-54, 58, 63-65, 70, 77, 79, 89, 90, 92, 93. 5. References 8, 24, 41, 43, 47, 65, 67, 70, 79, 92. 6. References 2-4, 12, 14, 18, 48, 51, 52, 58, 72, 74, 79. 7. References 2, 3, 12, 18, 48, 51, 52, 58, 72, 74, 79. 8. Aboubeker, G.: Maladie de Behçet, Thesis, Toulouse, 1954. 9. Aksel, I. S.: Au sujet d'une forme confusionnelle encephalitique de la maladie de Behçet: Étude anatomoclinique et electro-encephalographique , Rev Neurol 99:316, 1958. 10. Alajouanine, T., et al: La meningoencephalite de la maladie de Behçet , Rev Neurol 104:62, 1961. 11. 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Archives of Neurology – American Medical Association
Published: Mar 1, 1965
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