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Enzyme deficiency in erythrocytes in congenital nonspherocytic hemolytic anemia.

作者信息

SHAHIDI N T, DIAMOND L K

出版信息

Pediatrics. 1959 Aug;24(2):245-53.

PMID:13674822
Abstract
摘要

相似文献

1
Enzyme deficiency in erythrocytes in congenital nonspherocytic hemolytic anemia.先天性非球形红细胞溶血性贫血中的红细胞酶缺乏。
Pediatrics. 1959 Aug;24(2):245-53.
2
Metabolic abnormalities of erythrocytes from patients with congenital nonspherocytic hemolytic anemia.先天性非球形红细胞溶血性贫血患者红细胞的代谢异常。
J Pediatr. 1959 Sep;55:319-36. doi: 10.1016/s0022-3476(59)80228-6.
3
[The anemias].[贫血症]
Vie Med Can Fr. 1973 Apr;2(4):364-9.
4
Nonspherocytic congenital hemolytic anemia.非球形细胞性先天性溶血性贫血
Blood. 1960 Oct;16:1371-97.
5
Congenital nonspherocytic hemolytic anemia. Report of two cases.
Am J Clin Pathol. 1962 Jun;37:608-18. doi: 10.1093/ajcp/37.6.608.
6
Congenital nonspherocytic hemolytic anemia; two nonfamilial cases with red cell survival studies.先天性非球形细胞溶血性贫血；两例非家族性病例及红细胞存活研究
J Pediatr. 1956 Sep;49(3):245-55. doi: 10.1016/s0022-3476(56)80180-7.
7
[CONGENITAL 2,3-DIPHOSPHOGLYCEROMUTASE DEFICIENCY].
Bull Mem Soc Med Hop Paris. 1964;115:493-9.
8
Skull changes in iron deficiency anemia simulating congenital hemolytic anemia.缺铁性贫血时颅骨改变酷似先天性溶血性贫血。
Am J Roentgenol Radium Ther Nucl Med. 1961 Sep;86:447-52.
9
Erythrocyte adenylate kinase deficiency: characterization of recombinant mutant forms and relationship with nonspherocytic hemolytic anemia.红细胞腺苷酸激酶缺乏症：重组突变体形式的特征及其与非球形红细胞溶血性贫血的关系。
Exp Hematol. 2007 Aug;35(8):1182-9. doi: 10.1016/j.exphem.2007.05.004.
10
[The hemolytic anemia of premature infants with spontaneous Heinz body formation; a new syndrome observed in 14 cases].
Helv Paediatr Acta. 1953 Dec;8(6):491-529.

引用本文的文献

1
Effects of sulfhydryl inhibition on red blood cells. I. Mechanism of hemolysis.巯基抑制对红细胞的影响。I. 溶血机制。
J Clin Invest. 1962 Apr;41(4):779-92. doi: 10.1172/JCI104536.
2
[New data on hyperbilirubinemia in the newborn infant].[新生儿高胆红素血症的新数据]
Blut. 1960 Feb;6:35-40. doi: 10.1007/BF01630818.
3
[CHRONIC, NON-SPHEROCYTIC HEMOLYTIC JAUNDICE IN TOTAL ABSENCE OF GLUCOSE-6-PHOSPHATE DEHYDROGENASE ACTIVITY OF THE ERYTHROCYTES].[红细胞葡萄糖-6-磷酸脱氢酶活性完全缺乏所致的慢性非球形细胞溶血性黄疸]
Klin Wochenschr. 1964 Dec 15;42:1250. doi: 10.1007/BF01496761.
4
THE CLINICAL PICTURE OF GLUCOSE 6-PHOSPHATE DEHYDROGENASE DEFICIENCY IN EARLY INFANCY.婴儿早期葡萄糖-6-磷酸脱氢酶缺乏症的临床表现
Arch Dis Child. 1964 Dec;39(208):545-53. doi: 10.1136/adc.39.208.545.
5
Glucose-6-phosphate dehydrogenase deficiency in congenital hemolytic disease. A review.先天性溶血性疾病中的葡萄糖-6-磷酸脱氢酶缺乏症。综述。
J Natl Med Assoc. 1962 Sep;54(5):576-83.
6
Haemolytic mechanisms in health and disease.健康与疾病中的溶血机制。
Br Med J. 1962 Aug 18;2(5302):429-36. doi: 10.1136/bmj.2.5302.429.
7
[Hereditary non-spherocytic hemolytic anemia caused by glucose-6-phosphate dehydrogenase deficiency. Formation of an enzyme protein with modified characteristics in the blood cells of a German family].[葡萄糖-6-磷酸脱氢酶缺乏所致遗传性非球形细胞溶血性贫血。德国家庭血细胞中具有修饰特性的酶蛋白的形成]
Klin Wochenschr. 1966 Feb 1;44(3):122-8. doi: 10.1007/BF01746562.
8
Clinical significance of red-cell structure and metabolism.红细胞结构与代谢的临床意义
Br Med J. 1965 Oct 30;2(5469):1017-20. doi: 10.1136/bmj.2.5469.1017.
9
Glucose-6-phosphate dehydrogenase deficiency in Canadian Negroes.加拿大黑人中的葡萄糖-6-磷酸脱氢酶缺乏症
Can Med Assoc J. 1969 Jun 7;100(21):973-7.
10
[Congenital nonspherocytic hemolytic anemias caused by glucose-6-phosphate dehydrogenase deficiency of the erythrocytes in a Japanese family].[一个日裔家族中由红细胞葡萄糖-6-磷酸脱氢酶缺乏引起的先天性非球形红细胞溶血性贫血]
Blut. 1968 Jun;17(3):143-51. doi: 10.1007/BF01885444.