Immunodeficiency and general medicine.
作者信息
Denman A M
出版信息
Br Med J. 1980 Nov 22;281(6252):1376-8. doi: 10.1136/bmj.281.6252.1376.
Abstract
摘要
相似文献
1
Immunodeficiency and general medicine.免疫缺陷与普通医学。
Br Med J. 1980 Nov 22;281(6252):1376-8. doi: 10.1136/bmj.281.6252.1376.
2
Immunodeficiency.免疫缺陷
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3
Immunodeficiency diseases: head and neck manifestations.免疫缺陷疾病：头颈部表现
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4
Immunological aberrations in purine nucleoside phosphorylase deficiencies.
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5
Treatment of human immunodeficiencies.人类免疫缺陷的治疗。
Clin Immunol Rev. 1981;1(3):375-408.
6
The lung and primary immunodeficiency.肺部与原发性免疫缺陷
Allergol Immunopathol (Madr). 1988 Nov-Dec;16(6):429-37.
7
Infections in the compromised host.免疫功能低下宿主的感染
Adv Intern Med. 1977;22:73-96.
8
Primary antibody deficiency in adults.成人原发性抗体缺陷
Lancet. 1991 Feb 2;337(8736):281-4. doi: 10.1016/0140-6736(91)90882-p.
9
Gastrointestinal complications of congenital immunodeficiency states. The surgeon's role.先天性免疫缺陷状态的胃肠道并发症。外科医生的作用。
Ann Surg. 1983 Dec;198(6):673-80. doi: 10.1097/00000658-198312000-00001.
10
Purine nucleoside phosphorylase deficiency associated with a fatal lymphoproliferative disorder.与致命性淋巴增殖性疾病相关的嘌呤核苷磷酸化酶缺乏症。
Arch Dis Child. 1981 Jul;56(7):563-5. doi: 10.1136/adc.56.7.563.
引用本文的文献
1
Development of insulin-dependent diabetes in adult-onset hypogammaglobulinaemia.成人期低丙种球蛋白血症患者胰岛素依赖型糖尿病的发生
Br Med J (Clin Res Ed). 1981 May 23;282(6277):1668. doi: 10.1136/bmj.282.6277.1668.
本文引用的文献
1
Hypogammaglobulinemia, depression of delayed-type hypersensitivity, and granuloma formation.低丙种球蛋白血症、迟发型超敏反应抑制及肉芽肿形成。
Am Rev Respir Dis. 1971 Aug;104(2):228-31. doi: 10.1164/arrd.1971.104.2.228.
2
Primary antibody deficiency syndrome of adult onset. Evidence for genetic transmission.成人起病的原发性抗体缺陷综合征。遗传传递的证据。
Am J Med. 1970 Apr;48(4):515-23. doi: 10.1016/0002-9343(70)90053-7.
3
Immune abnormalities associated with chronic mucocutaneous candidiasis.与慢性黏膜皮肤念珠菌病相关的免疫异常。
Cell Immunol. 1973 Mar;6(3):348-61. doi: 10.1016/0008-8749(73)90035-x.
4
X-linked B lymphocyte deficiency. I. Panhypo-gamma-globulinemia and dys-gamma-globulinemia in siblings.X连锁B淋巴细胞缺陷。I. 同胞中的全低丙种球蛋白血症和异常丙种球蛋白血症。
J Pediatr. 1974 Aug;85(2):188-91. doi: 10.1016/s0022-3476(74)80390-2.
5
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.
6
Role of suppressor T cells in pathogenesis of common variable hypogammaglobulinaemia.抑制性T细胞在常见变异型低丙种球蛋白血症发病机制中的作用。
Lancet. 1974 Sep 14;2(7881):609-13. doi: 10.1016/s0140-6736(74)91940-0.
7
Adenosine-deaminase deficiency in two patients with severely impaired cellular immunity.两名细胞免疫严重受损患者的腺苷脱氨酶缺乏症。
Lancet. 1972 Nov 18;2(7786):1067-9. doi: 10.1016/s0140-6736(72)92345-8.
8
[Proceedings: Degenerative encephalopathy in a case of Bruton's disease].[会议论文：一例布鲁顿病患者的退行性脑病]
Arch Fr Pediatr. 1975 Jun-Jul;32(6):581.
9
Enzyme replacement therapy for adenosine deaminase deficiency and severe combined immunodeficiency.腺苷脱氨酶缺乏症和严重联合免疫缺陷的酶替代疗法。
N Engl J Med. 1976 Dec 9;295(24):1337-43. doi: 10.1056/NEJM197612092952402.
10
Autoimmunity in the relatives of patients with immunodeficiency diseases.免疫缺陷疾病患者亲属中的自身免疫现象。
Clin Exp Immunol. 1977 Jun;28(3):375-88.
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