关于瑞士型无丙种球蛋白血症（淋巴细胞缺乏症）的进一步观察。同基因骨髓细胞的作用。 - Suppr

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Further observations on the Swiss type of agammaglobulinemia (alymphocytosis). The effect of syngeneic bone-marrow cells.

作者信息

Rosen F S, Gotoff S P, Craig J M, Ritchie J, Janeway C A

出版信息

N Engl J Med. 1966 Jan 6;274(1):18-21. doi: 10.1056/NEJM196601062740104.

DOI:10.1056/NEJM196601062740104

PMID:5322671

Abstract

摘要

相似文献

Further observations on the Swiss type of agammaglobulinemia (alymphocytosis). The effect of syngeneic bone-marrow cells.关于瑞士型无丙种球蛋白血症（淋巴细胞缺乏症）的进一步观察。同基因骨髓细胞的作用。

N Engl J Med. 1966 Jan 6;274(1):18-21. doi: 10.1056/NEJM196601062740104.

Synthesis of donor type gamma-G-globulin following thymus transplantation in hypo-gamma-globulinaemia with severe lymphocytopenia.

Scand J Haematol. 1966;3(5):351-74. doi: 10.1111/j.1600-0609.1966.tb02379.x.

Graft treatment of immunity deficiency.

Lancet. 1969 Feb 1;1(7588):243-5.

Transplantation of bone-marrow cells and fetal thymus in an infant with lymphopenic immunological deficiency.对一名患有淋巴细胞减少性免疫缺陷的婴儿进行骨髓细胞和胎儿胸腺移植。

Lancet. 1969 Jun 21;1(7608):1223-7. doi: 10.1016/s0140-6736(69)92112-6.

[Congenital alymphocytosis. Thymus graft on the 28th day].

Ann Pediatr (Paris). 1966 Dec 2;13(12):804-11.

Sex-linked thymic epithelial hypoplasia in two siblings. Attempt at treatment by transplantation with fetal thymus and adult bone marrow.

J Pediatr. 1968 Jan;72(1):51-62. doi: 10.1016/s0022-3476(68)80400-7.

Heterogeneity of phenotypic expression in a family with Swiss-type agammaglobulinemia: observations on the acquisition of agammaglobulinemia.

J Pediatr. 1971 Jun;78(6):968-80. doi: 10.1016/s0022-3476(71)80426-2.

Alymphocytosis, agammaglobulinaemia, homografts, and delayed hypersen sitivity: study of a case.无淋巴细胞血症、无丙种球蛋白血症、同种移植及迟发型超敏反应：1例研究

Lancet. 1962 Aug 25;2(7252):380-1. doi: 10.1016/s0140-6736(62)90232-5.

Treatment of lymphopenic hypogammaglobulinemia and bone-marrow aplasia by transplantation of allogeneic marrow. Crucial role of histocompatiility matching.

N Engl J Med. 1969 Sep 25;281(13):691-7. doi: 10.1056/NEJM196909252811302.

Thymic dysplasia ("Swiss agammaglobulinemia"). I. Graft versus host reaction following bone-marrow transfusion.胸腺发育不全（“瑞士型无丙种球蛋白血症”）。一、骨髓输血后的移植物抗宿主反应。

J Pediatr. 1967 May;70(5):730-6. doi: 10.1016/s0022-3476(67)80323-8.

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Decoding Immunobiology Through Genetic Errors of Immunity.通过免疫遗传错误解码免疫生物学

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Inborn errors of human JAKs and STATs.人类 JAK 和 STAT 的先天缺陷。

Immunity. 2012 Apr 20;36(4):515-28. doi: 10.1016/j.immuni.2012.03.016.

Quantitative studies of phytohemagglutinin-induced DNA and RNA synthesis in normal and agammaglobulinemic leukocytes.正常和无丙种球蛋白血症白细胞中植物血凝素诱导的DNA和RNA合成的定量研究。

J Exp Med. 1967 May 1;125(5):863-72. doi: 10.1084/jem.125.5.863.

Tissue interaction in the development of thymus lymphocytes.胸腺淋巴细胞发育过程中的组织相互作用。

J Exp Med. 1969 Feb 1;129(2):431-42. doi: 10.1084/jem.129.2.431.

Lymphocytes in congenital immunological deficiency diseases.先天性免疫缺陷疾病中的淋巴细胞。

Clin Exp Immunol. 1968 Oct;3(8):843-56.

Wiskott-Aldrich syndrome, a genetically determined cellular immunologic deficiency: clinical and laboratory responses to therapy with transfer factor.威斯科特-奥尔德里奇综合征，一种由基因决定的细胞免疫缺陷病：对转移因子治疗的临床及实验室反应

Proc Natl Acad Sci U S A. 1970 Oct;67(2):821-8. doi: 10.1073/pnas.67.2.821.

Successful bone marrow transplantation in a patient with humoral and cellular immunity deficiency.一名体液和细胞免疫缺陷患者成功进行了骨髓移植。

Clin Exp Immunol. 1970 Sep;7(3):343-53.

Defective cellular immunity associated with chronic mucocutaneous moniliasis and recurrent staphylococcal botryomycosis: immunological reconstitution by allogeneic bone marrow.与慢性黏膜皮肤念珠菌病和复发性葡萄球菌性足菌肿相关的细胞免疫缺陷：同种异体骨髓进行免疫重建。

Clin Exp Immunol. 1968 Feb;3(2):153-69.

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