Morbus Behçet Klinische und immunpathologische Aspekte

Author:

Djawari D.

Publisher

Springer Berlin Heidelberg

Reference162 articles.

1. Abdaila, M I, Bahgat, N.: Long-lasting remission of Behçet’s disease after chlorambucil therapy. Brit. J. Ophthal. 57, 706–711 (1973).

2. Abdel-Aziz, A H M, Fairburn, E A.: Familial Behçet’s syndrome. Cutis 21, 649–652 (1978).

3. Abdou, A I, Schumacher, H R, Colmann, R W, Sagawa, U, Herbert, J, Pascual, E, Carrol, E T, Miller, M, South, M A, Abdou, N L. Behçet’s disease: Possible role of secretory component deficiency, synovial inclusions and fibrinolytic abnormality in the various manifestations of the disease. J. Lab. clin. Med. 91, 409–422 (1978).

4. Adorno, D, Pivetti-Pezzi, P, Bonini, S, Masala, C, Bonini, S, Amendolea, M A, Casciani, C U.: HLA-B5 and Behçet’s disease. Tissue Antigens 14, 444–448 (1979).

5. Aoki, K, Ohno, S, Ohguchi, M, Sugiura, S.: Familial Behçet’s disease. Jap. J. Ophthal. 22, 72–75 (1978).

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