一名患有纯红细胞再生障碍性贫血患者的再生障碍性贫血。 - Suppr

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Aplastic anaemia in a patient with pure red cell aplasia.

作者信息

McMahon J N, Egan E L

出版信息

Ir J Med Sci. 1980 May;149(5):212-4. doi: 10.1007/BF02939142.

DOI:10.1007/BF02939142

PMID:7429787

Abstract

摘要

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Aplastic anaemia in a patient with pure red cell aplasia.一名患有纯红细胞再生障碍性贫血患者的再生障碍性贫血。

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本文引用的文献

Studies on red cell aplasia. II. Report of a second patient with an antibody to erythroblast nuclei and a remission after immunosuppressive therapy.

Blood. 1969 Jul;34(1):1-13.

Studies on red cell aplasia. I. Demonstration of a plasma inhibitor to heme synthesis and an antibody to erythroblast nuclei.红细胞再生障碍的研究。I. 血浆血红素合成抑制剂及成红细胞核抗体的证实

Proc Natl Acad Sci U S A. 1967 Aug;58(2):493-500. doi: 10.1073/pnas.58.2.493.

Studies on red cell aplasia. 3. Treatment with horse antihuman thymocyte gamma globulin.红细胞再生障碍的研究。3. 用马抗人胸腺细胞γ球蛋白治疗。

Blood. 1972 Mar;39(3):347-60.

Pure red cell aplasia (PRCA): Response of three patients of cyclophosphamide and/or antilymphocyte globulin (ALG) and demonstration of two types of serum IgG inhibitors to erythropoiesis.

Blood. 1975 Feb;45(2):247-61.

Recovery from aplastic anemia after treatment with cyclophosphamide.环磷酰胺治疗后再生障碍性贫血的恢复情况。

N Engl J Med. 1976 Dec 30;295(27):1522-3. doi: 10.1056/NEJM197612302952708.

Suppression of erythroid-colony formation by lymphocytes from patients with aplastic anemia.

N Engl J Med. 1977 Jan 6;296(1):10-3. doi: 10.1056/NEJM197701062960103.

Diagnosis and treatment of pure red cell aplasia.

Med Clin North Am. 1976 Sep;60(5):945-58. doi: 10.1016/s0025-7125(16)31841-7.

Immune suppression of hematopoiesis.

Am J Med. 1978 Feb;64(2):301-10. doi: 10.1016/0002-9343(78)90060-8.

Autologous bone marrow repopulation following high dose cyclophosphamide and allogeneic marrow transplantation in aplastic anaemia.再生障碍性贫血患者接受大剂量环磷酰胺及异基因骨髓移植后的自体骨髓重建

Br J Haematol. 1977 Jul;36(3):305-12. doi: 10.1111/j.1365-2141.1977.tb00653.x.

Aplastic anaemia: Evidence for an immunological mechanism.再生障碍性贫血：免疫机制的证据。

Lancet. 1976 Mar 27;1(7961):669-71. doi: 10.1016/s0140-6736(76)92780-x.

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