Selective gamma-A-globulin deficiency, with dominant autosomal inheritance in a Swiss family.
作者信息
Stocker F, Ammann P, Rossi E
出版信息
Arch Dis Child. 1968 Oct;43(231):585-8. doi: 10.1136/adc.43.231.585.
Abstract
摘要
相似文献
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Selective gamma-A-globulin deficiency, with dominant autosomal inheritance in a Swiss family.瑞士一个家族中具有常染色体显性遗传的选择性γ-A球蛋白缺乏症。
Arch Dis Child. 1968 Oct;43(231):585-8. doi: 10.1136/adc.43.231.585.
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Genetic linkage of IgA deficiency to the major histocompatibility complex: evidence for allele segregation distortion, parent-of-origin penetrance differences, and the role of anti-IgA antibodies in disease predisposition.IgA 缺乏症与主要组织相容性复合体的遗传连锁：等位基因分离畸变、亲本来源的外显率差异以及抗 IgA 抗体在疾病易感性中的作用的证据。
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Agammaglobulinaemia and co-existent pernicious anaemia.无丙种球蛋白血症与并存的恶性贫血。
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Serum immunoglobulin levels in patients suffering from chronic and recurrent chest infections.
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Chemical mutagenesis at the phosphoribosyltransferase locus in cultured human lymphoblasts.培养的人淋巴母细胞中磷酸核糖基转移酶基因座的化学诱变
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Immune response in families of children with acute lymphoblastic leukaemia.
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Analysis of IgG subclass production in cell cultures from IgA deficient patients and in normal controls as a function of age.对IgA缺乏患者的细胞培养物以及正常对照中IgG亚类产生情况随年龄变化的分析。
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Cellular aspects of selective IgA deficiency.选择性IgA缺乏症的细胞方面
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Association between HLA-A1,B8 in children with extrinsic asthma and IgA deficiency.外源性哮喘儿童中HLA - A1、B8与IgA缺乏之间的关联。
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本文引用的文献
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CHARACTERISTICS OF AN IMMUNE SYSTEM COMMON TO CERTAIN EXTERNAL SECRETIONS.某些外分泌液共有的免疫系统特征。
J Exp Med. 1965 Jan 1;121(1):101-24. doi: 10.1084/jem.121.1.101.
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SERUM PROTEINS AND ANTIBODY ACTIVITY IN HUMAN NASAL SECRETIONS.人鼻分泌物中的血清蛋白和抗体活性
J Clin Invest. 1964 Aug;43(8):1613-24. doi: 10.1172/JCI105037.
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PRIMARY "ACQUIRED" HYPOGAMMAGLOBULINEMIA; CLINICAL AND GENETIC ASPECTS OF NINE CASES.原发性“获得性”低丙种球蛋白血症；9例患者的临床和遗传学特征
Acta Med Scand. 1964 Jul;176:1-16.
4
ATAXIA TELANGIECTASIS. A DYSGAMMAGLOBULINAEMIA WITH DEFICIENT GAMMA-1-A (BETA-2-A)-GLOBULIN.共济失调毛细血管扩张症。一种伴有γ-1-A（β-2-A）球蛋白缺乏的免疫球蛋白异常血症。
Lancet. 1964 May 30;1(7344):1193-5. doi: 10.1016/s0140-6736(64)91210-3.
5
ATAXIA-TELANGIECTASIA. ITS ASSOCIATION WITH A DEFECTIVE THYMUS, IMMUNOLOGICAL-DEFICIENCY DISEASE, AND MALIGNANCY.共济失调毛细血管扩张症。其与胸腺缺陷、免疫缺陷病及恶性肿瘤的关联。
Lancet. 1964 May 30;1(7344):1189-93. doi: 10.1016/s0140-6736(64)91209-7.
6
BETA-2A AGLOBULINEMIA IN TWO HEALTHY MEN.两名健康男性的β-2A球蛋白血症
J Lab Clin Med. 1964 Feb;63:205-12.
7
Immunoglobulin levels from the newborn period to adulthood and in immunoglobulin deficiency states.从新生儿期到成年期以及免疫球蛋白缺乏状态下的免疫球蛋白水平。
J Clin Invest. 1962 Nov;41(11):2054-64. doi: 10.1172/JCI104663.
8
[The ataxia-telangiectasis syndrome (Louis-Bar syndrome) from the immunologic viewpoint].
Helv Paediatr Acta. 1965 Jun;20(2):137-46.
9
[Quantitative determination of immune globulin maturation by simple radial diffusion method].
Helv Paediatr Acta. 1968 Jun;23(3):242-51.
10
Serum levels of immune globulins in health and disease: a survey.健康与疾病状态下血清免疫球蛋白水平：一项调查
Pediatrics. 1966 May;37(5):715-27.
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