Immunmangel-Krankheiten Pathophysiologie und Klinik

Author:

Hitzig W. H.

Publisher

Springer Berlin Heidelberg

Reference583 articles.

1. Ackerman, B.D.: Dysgammaglobulinemia: Report of a case with a family history of a congenital gamma globulin disorder. Pediatrics 34, 211 (1964).

2. Albertini, R. J., Joo, P., Anderson, J. L., Bortin, M. M.: Bone-marrow transplantation in a patient with the Wiskott-Aldrich Syndrome. Lancet 1968 II, 1364.

3. Albright, F., Bartter, F. C., Forbes, A. P.: The fate of human serum albumin administered intravenously to a patient with idiopathic hypoalbuminemia and hypoglobulinemia. Trans. Assoc. Amer. Phycns 62, 204 (1949).

4. Aldrich, R. A., Steinberg, A. G., Campbell, D. C.: Pedigree demonstrating a sex-linked recessive condition characterized by draining ears, eczematoid dermatitis and bloody diarrhea. Pediatrics 13, 133 (1954).

5. Alexander, W. J., Dunbar, J. S.: Unusual bone changes in thymic alymphoplasia. Ann. Radiol. 11, 389 (1968).

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