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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.

DOI:10.1136/adc.43.231.585
PMID:4177045
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2020031/
Abstract
摘要

相似文献

1
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.
2
Immunoglobulin E deficiency in ataxia-telangiectasia.共济失调毛细血管扩张症中的免疫球蛋白E缺乏症。
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3
Isolated absence of IgA with autosomal dominant inheritance.
Lancet. 1971 Jul 17;2(7716):124-5. doi: 10.1016/s0140-6736(71)92302-6.
4
[Repeated upper respiratory tract infections among children and immune globulin--study of etiology of recurrent otitis media].[儿童反复上呼吸道感染与免疫球蛋白——复发性中耳炎病因学研究]
Jibiinkoka. 1969 Nov;41(11):845-50.
5
Selective IgA deficiency and autoimmunity.选择性IgA缺乏症与自身免疫
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6
Disaccharidase deficiency in children with immunologic deficits.
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7
Recurrent respiratory infections in a family with immunoglobulin A deficiency.一个患有免疫球蛋白A缺乏症的家庭中的复发性呼吸道感染
Am Rev Respir Dis. 1970 Feb;101(2):245-51. doi: 10.1164/arrd.1970.101.2.245.
8
The IgA system. II. The clinical significance of IgA deficiency: studies in patients with agammaglobulinemia and ataxia-telangiectasia.免疫球蛋白A系统。II. 免疫球蛋白A缺乏的临床意义:对无丙种球蛋白血症和共济失调毛细血管扩张症患者的研究。
Am J Med. 1968 Feb;44(2):168-78. doi: 10.1016/0002-9343(68)90148-4.
9
Chronic pulmonary disease associated with an unusual dysgammaglobulinaemia.与一种罕见的免疫球蛋白异常血症相关的慢性肺部疾病。
Clin Exp Immunol. 1968 Nov;3(9):983-8.
10
Hypogammaglobulinaemia in the United Kingdom. 3. Clinical features of hypogammaglobulinaemia.英国的低丙种球蛋白血症。3. 低丙种球蛋白血症的临床特征。
Spec Rep Ser Med Res Counc (G B). 1971;310:9-34.

引用本文的文献

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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。
Am J Hum Genet. 1999 Apr;64(4):1096-109. doi: 10.1086/302326.
2
Absent IgA and deletions of chromosome 18.IgA缺乏及18号染色体缺失。
J Med Genet. 1970 Mar;7(1):11-9. doi: 10.1136/jmg.7.1.11.
3
Agammaglobulinaemia and co-existent pernicious anaemia.无丙种球蛋白血症与并存的恶性贫血。
Clin Exp Immunol. 1970 Feb;6(2):181-7.
4
Serum immunoglobulin levels in patients suffering from chronic and recurrent chest infections.
Ir J Med Sci. 1972 Oct-Dec;141(10):162-7. doi: 10.1007/BF03004640.
5
Genetic aspects of selective immunoglobulin A deficiency.选择性免疫球蛋白A缺乏症的遗传学方面
J Med Genet. 1972 Sep;9(3):344-7. doi: 10.1136/jmg.9.3.344.
6
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
Proc Natl Acad Sci U S A. 1972 May;69(5):1244-8. doi: 10.1073/pnas.69.5.1244.
7
Immune response in families of children with acute lymphoblastic leukaemia.
Arch Dis Child. 1973 Jun;48(6):441-5. doi: 10.1136/adc.48.6.441.
8
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。
Clin Exp Immunol. 1986 Aug;65(2):434-42.
9
Cellular aspects of selective IgA deficiency.选择性IgA缺乏症的细胞方面
Clin Exp Immunol. 1976 May;24(2):273-9.
10
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。
Eur J Pediatr. 1979 Aug;131(4):263-70. doi: 10.1007/BF00444347.

本文引用的文献

1
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.
2
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.
3
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.