丙种球蛋白异常血症性抗体缺乏综合征 - Suppr

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Dysgammaglobulinemic antibody deficiency syndrome.

作者信息

Goldman A S, Ritzmann S E, Houston E W, Sidwell S, Bratcher R, Levin W C

出版信息

J Pediatr. 1967 Jan;70(1):16-27. doi: 10.1016/s0022-3476(67)80161-6.

DOI:10.1016/s0022-3476(67)80161-6

PMID:6016801

Abstract

摘要

相似文献

Dysgammaglobulinemic antibody deficiency syndrome.丙种球蛋白异常血症性抗体缺乏综合征

J Pediatr. 1967 Jan;70(1):16-27. doi: 10.1016/s0022-3476(67)80161-6.

Immunoglobulin deficiency in Bloom's syndrome.布卢姆综合征中的免疫球蛋白缺乏症。

Am J Dis Child. 1967 May;113(5):594-6. doi: 10.1001/archpedi.1967.02090200126017.

Immunodeficiency disorders.免疫缺陷疾病

Pediatr Ann. 1976 Jul;5(7):418-29.

Intestinal nodular lymphoid hyperplasia, hypogammaglobulinemia, and hematologic abnormalities in a child with a ring 18 chromosome.

J Pediatr. 1971 Jul;79(1):80-8. doi: 10.1016/s0022-3476(71)80062-8.

Gingivitis in hypogammaglobulinemia.低丙种球蛋白血症中的牙龈炎

J Periodontol. 1973 Mar;44(3):171-4. doi: 10.1902/jop.1973.44.3.171.

Hereditary alterations in the immune response: coexistence of "agammaglobulinemia", acquired hypogammaglobulinemia and selective immunoglobulin deficiency in a sibship.

Pediatr Res. 1968 Mar;2(2):72-84. doi: 10.1203/00006450-196803000-00002.

[Ring-chromosome 18 and IgA deficiency in a 6-year-old girl (46,XX,18r)].

Z Kinderheilkd. 1970;109(1):1-10.

[Lymphoproliferative syndromes with atypical dysglobulinemia and chromosomal anomalies].伴有非典型球蛋白血症和染色体异常的淋巴增殖综合征

Nouv Rev Fr Hematol. 1970 Jul-Aug;10(4):541-51.

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

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Immunoglobulin D in serum, body fluids and lymphoid tissues.血清、体液及淋巴组织中的免疫球蛋白D

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引用本文的文献

Abnormal B cell differentiation and variable increased T cell suppression in immunodeficiency with hyper-IgM.伴有高IgM的免疫缺陷中异常的B细胞分化及可变增加的T细胞抑制。

Clin Exp Immunol. 1980 Apr;40(1):147-56.

[Dysgammaglobulinaemia type I (author's transl)].I型异常丙种球蛋白血症（作者译）

Klin Wochenschr. 1973 Jul 15;51(14):725-9. doi: 10.1007/BF01468364.

Immunoglobulin deficiency with increased immunoglobulin M in three siblings: effect of long-term immunoglobulin therapy.三名同胞患有免疫球蛋白缺乏伴免疫球蛋白M升高：长期免疫球蛋白治疗的效果

Eur J Pediatr. 1988 Dec;148(3):215-7. doi: 10.1007/BF00441406.

Human malignant T cells capable of inducing an immunoglobulin class switch.能够诱导免疫球蛋白类别转换的人类恶性T细胞。

J Exp Med. 1985 Jan 1;161(1):134-44. doi: 10.1084/jem.161.1.134.

X-linked immunodeficiency with hyperimmunoglobulinemia M appears to be linked to the DXS42 restriction fragment length polymorphism locus.

Hum Genet. 1987 May;76(1):96-9. doi: 10.1007/BF00283057.

Analysis of X-chromosome inactivation in X-linked immunodeficiency with hyper-IgM (HIGM1): evidence for involvement of different hematopoietic cell lineages.

Hum Genet. 1991 Dec;88(2):130-4. doi: 10.1007/BF00206059.

Immunological investigations in two brothers with ataxia telangiectasia Louis-Bar.对两名患有共济失调毛细血管扩张症（Louis-Bar 综合征）的兄弟进行的免疫学研究。

Eur J Pediatr. 1976 May 4;122(2):93-102. doi: 10.1007/BF00466267.

Hyper immunoglobulin M immunodeficiency. (Dysgammaglobulinemia). Presence of immunoglobulin M-secreting plasmacytoid cells in peripheral blood and failure of immunoglobulin M-immunoglobulin G switch in B-cell differentiation.高免疫球蛋白M免疫缺陷（异常丙种球蛋白血症）。外周血中存在分泌免疫球蛋白M的浆细胞样细胞，且B细胞分化过程中免疫球蛋白M向免疫球蛋白G的转换失败。

J Clin Invest. 1979 Aug;64(2):385-91. doi: 10.1172/JCI109473.

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