| P2093 | author name string | W. H. Perks | |
| | I. S. Petheram | |
| P2860 | cites work | Agammaglobulinemia | Q28244575 |
| | B and T lymphocytes in primary immunodeficiency disease in man. | Q34502743 |
| | Familial hypogammaglobulinemia, splenomegaly and leukopenia. With a review of the etiological factors of the hypogammaglobulinemias | Q35533153 |
| | Lymphocyte purine 5'-nucleotidase edficiency in primary hypogammaglobulinaemia | Q39418919 |
| | Elevation of serum angiotension-converting-enzyme (ACE) level in sarcoidosis | Q39950095 |
| | Elevation of Serum Angiotensin-Converting Enzyme in Gaucher's Disease | Q39991377 |
| | Hereditary alterations in the immune response: coexistence of "agammaglobulinemia", acquired hypogammaglobulinemia and selective immunoglobulin deficiency in a sibship | Q44220660 |
| | Clinical, serologic and leukocyte function studies on patients with idiopathic “acquired” agammaglobulinemia and their families | Q44389491 |
| | Identification and function of T cells in the peripheral blood of patients with hypogammaglobulinaemia. | Q53863272 |
| | Inherited "acquired" hypogammaglobulinaemia | Q59281313 |
| | Sarcoidosis | Q69360974 |
| | Hypogammaglobulinemia, depression of delayed-type hypersensitivity, and granuloma formation | Q71792833 |
| | Agammaglobulinemia | Q73607053 |
| | Agammaglobulinaemia | Q73623158 |
| | Syndrome of hypogammaglobulinemia, splenomegaly and hypersplenism | Q74637830 |
| | PRIMARY "ACQUIRED" HYPOGAMMAGLOBULINEMIA; CLINICAL AND GENETIC ASPECTS OF NINE CASES | Q76916364 |
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 101-105 | |
| P577 | publication date | 1978-02-01 | |
| P1433 | published in | Thorax | Q7796158 |
| P1476 | title | Familial combined cellular and humoral immune defect with multisystem granulomata | |
| P478 | volume | 33 | |