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Red-cell abnormalities in HEMPAS (hereditary erythroblastic multinuclearity with a positive acidified-serum test).

作者信息

Crookston J H, Crookston M C, Rosse W F

出版信息

Br J Haematol. 1972 Sep;23:Suppl:83-91. doi: 10.1111/j.1365-2141.1972.tb03507.x.

DOI:10.1111/j.1365-2141.1972.tb03507.x
PMID:4567203
Abstract
摘要

相似文献

1
Red-cell abnormalities in HEMPAS (hereditary erythroblastic multinuclearity with a positive acidified-serum test).遗传性红细胞多核伴酸化血清试验阳性(HEMPAS)中的红细胞异常
Br J Haematol. 1972 Sep;23:Suppl:83-91. doi: 10.1111/j.1365-2141.1972.tb03507.x.
2
Mechanisms of immune lysis of the red cells in hereditary erythroblastic multinuclearity with a positive acidified serum test and paroxysmal nocturnal hemoglobinuria.伴有阳性酸化血清试验的遗传性成红细胞多核症及阵发性夜间血红蛋白尿中红细胞免疫溶解的机制
J Clin Invest. 1974 Jan;53(1):31-43. doi: 10.1172/JCI107551.
3
Aberrant regulation of complement by the erythrocytes of hereditary erythroblastic multinuclearity with a positive acidified serum lysis test (HEMPAS).遗传性红细胞多核症伴酸化血清溶血试验阳性(HEMPAS)患者红细胞对补体的异常调节
Blood. 1994 Jan 1;83(1):250-9.
4
Erythrocyte enzymatic abnormalities in HEMPAS (hereditary erythroblastic multinuclearity with a positive acidified-serum test).遗传性红细胞多核伴酸化血清试验阳性(HEMPAS)中的红细胞酶异常
Br J Haematol. 1972 Jul;23(1):107-12. doi: 10.1111/j.1365-2141.1972.tb03464.x.
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[Evaluation and quantification of complement-sensitive red cells in PNH and aplastic anemia-PNH syndrome].[阵发性睡眠性血红蛋白尿症及再生障碍性贫血-阵发性睡眠性血红蛋白尿症综合征中补体敏感红细胞的评估与定量分析]
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6
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Membrane destruction in paroxysmal cold hemoglobinuria.阵发性寒冷性血红蛋白尿中的膜破坏
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[Polyagglutinability due to Hempas antigen].[因Hempas抗原导致的多凝集现象]
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Biological abnormalities in erythroblasts and erythrocytes of acquired idiopathic dyserythropoietic anemia.
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COEXISTENT PAROXYSMAL NOCTURNAL AND COLD HEMOGLOBINURIA PRECEDED BY APLASTIC ANEMIA: A CASE REPORT AND FAMILY STUDY.
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引用本文的文献

1
Mutations affecting the secretory COPII coat component SEC23B cause congenital dyserythropoietic anemia type II.影响分泌性COPII包被组分SEC23B的突变会导致II型先天性红细胞生成异常性贫血。
Nat Genet. 2009 Aug;41(8):936-40. doi: 10.1038/ng.405. Epub 2009 Jun 28.
2
Congenital dyserythropoietic anaemia type II (HEMPAS): a family study.II型先天性红细胞生成异常性贫血(HEMPAS):一项家族研究。
J Clin Pathol. 1980 Dec;33(12):1197-201. doi: 10.1136/jcp.33.12.1197.
3
Mechanisms of immune lysis of the red cells in hereditary erythroblastic multinuclearity with a positive acidified serum test and paroxysmal nocturnal hemoglobinuria.
伴有阳性酸化血清试验的遗传性成红细胞多核症及阵发性夜间血红蛋白尿中红细胞免疫溶解的机制
J Clin Invest. 1974 Jan;53(1):31-43. doi: 10.1172/JCI107551.
4
Congenital dyserythropoietic anemia, type II (Hempas). First five reported cases in Italy.先天性红细胞生成异常性贫血II型(遗传性多核幼红细胞增多症)。意大利首次报告的5例病例。
Blut. 1974 Dec;29(6):391-7. doi: 10.1007/BF01633674.
5
[Congenital dyserythropoietic anemias].
Blut. 1975 Nov;31(5):261-70. doi: 10.1007/BF01634142.
6
[Ultrastructure of erythroid cells in a case of congenital dyserythropoietic anaemia type II (author's transl)].
Blut. 1977 Dec;35(6):437-46. doi: 10.1007/BF00996690.
7
Cell membrane receptors for serological reagents.血清学试剂的细胞膜受体。
J Med Genet. 1975 Jun;12(2):174-84. doi: 10.1136/jmg.12.2.174.