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Rapidly fatal familial histiocytosis associated with eosinophilia and primary immunological deficiency.

作者信息

Barth R F, Vergara G G, Khurana S K, Lowman J T, Beckwith J B

出版信息

Lancet. 1972 Sep 9;2(7776):503-6. doi: 10.1016/s0140-6736(72)91904-6.

DOI:10.1016/s0140-6736(72)91904-6
PMID:4115568
Abstract
摘要

相似文献

1
Rapidly fatal familial histiocytosis associated with eosinophilia and primary immunological deficiency.
Lancet. 1972 Sep 9;2(7776):503-6. doi: 10.1016/s0140-6736(72)91904-6.
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[Severe combined immune deficiency with hypereosinophilia. Immunologic study of 5 cases].[伴有嗜酸性粒细胞增多的重症联合免疫缺陷。5例的免疫学研究]
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Expansion of CD3+CD4-CD8- T cell population expressing high levels of IL-5 in Omenn's syndrome.奥门氏综合征中表达高水平白细胞介素-5的CD3⁺CD4⁻CD8⁻T细胞群体的扩增
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Liver lipids in Letterer-Siwe disease.勒-雪病中的肝脏脂质
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A novel eosinophil chemotactic factor derived from a histiocytic lymphoma of the central nervous system.一种源自中枢神经系统组织细胞淋巴瘤的新型嗜酸性粒细胞趋化因子。
Clin Exp Immunol. 1980 May;40(2):249-55.
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Familial haemophagocytic lymphohistiocytosis in two brothers: possible relationship between impaired immune function and clinical picture of graft-versus-host disease.两兄弟患家族性噬血细胞性淋巴组织细胞增生症:免疫功能受损与移植物抗宿主病临床表现之间的可能关系
Eur J Pediatr. 1984 Sep;142(4):306-7. doi: 10.1007/BF00540262.
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Giant cell granulomatosis of lymph nodes with a fatal course.
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Familial hemophagocytic lymphohistiocytosis.家族性噬血细胞性淋巴组织细胞增生症
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Severe pulmonary vascular occlusive disease following bone marrow transplantation in Omenn syndrome.
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