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Thymic dysplasia ("Swiss agammaglobulinemia"). I. Graft versus host reaction following bone-marrow transfusion.

作者信息

Miller M E

出版信息

J Pediatr. 1967 May;70(5):730-6. doi: 10.1016/s0022-3476(67)80323-8.

DOI:10.1016/s0022-3476(67)80323-8
PMID:4164455
Abstract
摘要

相似文献

1
Thymic dysplasia ("Swiss agammaglobulinemia"). I. Graft versus host reaction following bone-marrow transfusion.胸腺发育不全(“瑞士型无丙种球蛋白血症”)。一、骨髓输血后的移植物抗宿主反应。
J Pediatr. 1967 May;70(5):730-6. doi: 10.1016/s0022-3476(67)80323-8.
2
Selective immunoglobulin deficiency associated with thymic alymphoplasia.
Pediatrics. 1967 Apr;39(4):506-15.
3
Sex-linked thymic epithelial hypoplasia in two siblings. Attempt at treatment by transplantation with fetal thymus and adult bone marrow.
J Pediatr. 1968 Jan;72(1):51-62. doi: 10.1016/s0022-3476(68)80400-7.
4
Transplantation of bone-marrow cells and fetal thymus in an infant with lymphopenic immunological deficiency.对一名患有淋巴细胞减少性免疫缺陷的婴儿进行骨髓细胞和胎儿胸腺移植。
Lancet. 1969 Jun 21;1(7608):1223-7. doi: 10.1016/s0140-6736(69)92112-6.
5
The graft versus host reaction in man after bone marrow transplantation: pathology, pathogenesis, clinical features, and implication.人类骨髓移植后的移植物抗宿主反应:病理学、发病机制、临床特征及意义。
Clin Immunol Immunopathol. 1973 Jul;1(4):472-98. doi: 10.1016/0090-1229(73)90005-6.
6
Heterogeneity of phenotypic expression in a family with Swiss-type agammaglobulinemia: observations on the acquisition of agammaglobulinemia.
J Pediatr. 1971 Jun;78(6):968-80. doi: 10.1016/s0022-3476(71)80426-2.
7
Thymic dysplasia.
J Pediatr. 1969 Aug;75(2):229-35. doi: 10.1016/s0022-3476(69)80393-8.
8
Hereditary lymphopenic agammaglobulinemia associated with a distinctive form of short-limbed dwarfism and ectodermal dysplasia.遗传性淋巴细胞减少性无丙种球蛋白血症,伴有一种特殊类型的短肢侏儒症和外胚层发育不良。
J Pediatr. 1969 Oct;75(4):675-84. doi: 10.1016/s0022-3476(69)80465-8.
9
Congenital aplasia of the thymus gland (DiGeorge's syndrome).先天性胸腺发育不全(迪格奥尔格综合征)。
N Engl J Med. 1968 Dec 12;279(24):1295-301. doi: 10.1056/NEJM196812122792401.
10
An autopsy case of lymphopenic hypogammaglobulinemia.
Acta Pathol Jpn. 1967 Nov;17(4):465-73. doi: 10.1111/j.1440-1827.1967.tb02736.x.

引用本文的文献

1
Studies on the immunotherapy of runt disease in rats.大鼠矮小病免疫疗法的研究。
J Exp Med. 1969 Apr 1;129(4):647-61. doi: 10.1084/jem.129.4.647.
2
Lymphocytes in congenital immunological deficiency diseases.先天性免疫缺陷疾病中的淋巴细胞。
Clin Exp Immunol. 1968 Oct;3(8):843-56.
3
Progressive lymphoid system deterioration: a new familial lymphopenic immunological deficiency disease.进行性淋巴系统恶化:一种新的家族性淋巴细胞减少性免疫缺陷病。
Clin Exp Immunol. 1970 Feb;6(2):169-80.
4
Wiskott-Aldrich syndrome, a genetically determined cellular immunologic deficiency: clinical and laboratory responses to therapy with transfer factor.威斯科特-奥尔德里奇综合征,一种由基因决定的细胞免疫缺陷病:对转移因子治疗的临床及实验室反应
Proc Natl Acad Sci U S A. 1970 Oct;67(2):821-8. doi: 10.1073/pnas.67.2.821.
5
Primary immunodeficiencies.原发性免疫缺陷病
Bull World Health Organ. 1971;45(1):125-42.
6
The thymus in immune deficiency.免疫缺陷中的胸腺
Proc R Soc Med. 1968 Sep;61(9):889-90. doi: 10.1177/003591576806100915.
7
Partial immunodeficiency and graft-versus host disease.部分免疫缺陷与移植物抗宿主病。
Arch Dis Child. 1971 Aug;46(248):571-4. doi: 10.1136/adc.46.248.571.
8
Successful bone marrow transplantation in a patient with humoral and cellular immunity deficiency.一名体液和细胞免疫缺陷患者成功进行了骨髓移植。
Clin Exp Immunol. 1970 Sep;7(3):343-53.
9
X-linked severe combined immunodeficiency. Diagnosis in males with sporadic severe combined immunodeficiency and clarification of clinical findings.X连锁重症联合免疫缺陷。散发性重症联合免疫缺陷男性患者的诊断及临床发现的阐明。
J Clin Invest. 1990 May;85(5):1548-54. doi: 10.1172/JCI114603.
10
Histopathologic sequence of events in adult mice undergoing lethal graft-versus-host reaction developed across H-2 and/or non-H-2 histocompatibility barriers.在跨越H-2和/或非H-2组织相容性屏障发生致死性移植物抗宿主反应的成年小鼠中,组织病理学事件的序列。
Am J Pathol. 1979 Jul;96(1):121-42.