Deficit of Anterior Pituitary Function and Variable Immune Deficiency Syndrome: A Novel Mutation.
作者信息
Poowuttikul Pavadee, McGrath Eric, Kamat Deepak
机构信息
Children's Hospital of Michigan, Detroit, MI, USA; Wayne State University, Detroit, MI, USA.
出版信息
Glob Pediatr Health. 2017 Jan 27;4:2333794X16686870. doi: 10.1177/2333794X16686870. eCollection 2017.
Abstract
摘要
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本文引用的文献
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Use and interpretation of diagnostic vaccination in primary immunodeficiency: a working group report of the Basic and Clinical Immunology Interest Section of the American Academy of Allergy, Asthma & Immunology.诊断性疫苗接种在原发性免疫缺陷中的应用和解读：美国过敏、哮喘与免疫学会基础与临床免疫学分会工作组报告。
J Allergy Clin Immunol. 2012 Sep;130(3 Suppl):S1-24. doi: 10.1016/j.jaci.2012.07.002.
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Deficit in anterior pituitary function and variable immune deficiency (DAVID) in children presenting with adrenocorticotropin deficiency and severe infections.儿童促肾上腺皮质激素缺乏伴严重感染时表现为垂体前叶功能减退和可变免疫缺陷（DAVID）。
J Clin Endocrinol Metab. 2012 Jan;97(1):E121-8. doi: 10.1210/jc.2011-0407. Epub 2011 Oct 19.
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Primary immunodeficiencies.原发性免疫缺陷病。
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Primary immunodeficiencies: 2009 update.原发性免疫缺陷病：2009 年更新。
J Allergy Clin Immunol. 2009 Dec;124(6):1161-78. doi: 10.1016/j.jaci.2009.10.013.
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Growth hormone deficiency and antipituitary antibodies in a patient with common variable immunodeficiency.生长激素缺乏和常见变异性免疫缺陷患者的抗垂体抗体。
J Endocrinol Invest. 2009 Sep;32(8):637-40. doi: 10.1007/BF03345733. Epub 2009 May 26.
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Update in understanding common variable immunodeficiency disorders (CVIDs) and the management of patients with these conditions.常见可变免疫缺陷疾病（CVIDs）认识的更新以及这些疾病患者的管理
Br J Haematol. 2009 Jun;145(6):709-27. doi: 10.1111/j.1365-2141.2009.07669.x. Epub 2009 Mar 30.
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Primary B cell immunodeficiencies: comparisons and contrasts.原发性B细胞免疫缺陷：比较与对比
Annu Rev Immunol. 2009;27:199-227. doi: 10.1146/annurev.immunol.021908.132649.
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Thymoma, immunodeficiency, and herpes simplex virus infections.胸腺瘤、免疫缺陷与单纯疱疹病毒感染。
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Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromes.双等位基因与单等位基因TNFRSF13B突变在区分抗体缺陷综合征中致病的TNFRSF13B变异体与增加风险的TNFRSF13B变异体方面的相关性。
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