一种淋巴增生综合征、“皮肤营养不良”以及伴有辅助性T细胞因子缺乏的联合免疫缺陷。 - Suppr | 超能文献

A lymphoproliferative syndrome, "cutaneous dystrophy" and combined immune deficiency with lack of helper T-cell factor.

作者信息

Wyss M, von Fliedner V, Jacot-Des-Combes E, Jeannet M, Despont J P, Kapanci Y, Cox J N

出版信息

Clin Immunol Immunopathol. 1982 Apr;23(1):34-49. doi: 10.1016/0090-1229(82)90068-x.

DOI:10.1016/0090-1229(82)90068-x

Abstract

摘要

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引用本文的文献

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The Omenn's syndrome: histological, immunohistochemical and ultrastructural evidence for a partial T cell deficiency evolving in an abnormal proliferation of T lymphocytes and S-100 +/T-6 + Langerhans-like cells.奥门氏综合征：T淋巴细胞和S-100+/T-6+朗格汉斯样细胞异常增殖过程中发生的部分T细胞缺陷的组织学、免疫组织化学及超微结构证据。

Virchows Arch A Pathol Anat Histopathol. 1985;407(1):69-82. doi: 10.1007/BF00701330.

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Restricted heterogeneity of T lymphocytes in combined immunodeficiency with hypereosinophilia (Omenn's syndrome).伴有嗜酸性粒细胞增多的联合免疫缺陷（奥门氏综合征）中T淋巴细胞的限制性异质性。

J Clin Invest. 1991 Apr;87(4):1352-9. doi: 10.1172/JCI115139.