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Normal erythrocyte osmotic fragility in hereditary spherocytosis.

作者信息

Korones D, Pearson H A

机构信息

Department of Pediatrics, Strong Memorial Hospital, Rochester, New York 14642.

出版信息

J Pediatr. 1989 Feb;114(2):264-6. doi: 10.1016/s0022-3476(89)80794-2.

DOI:10.1016/s0022-3476(89)80794-2
PMID:2915286
Abstract
摘要

相似文献

1
Normal erythrocyte osmotic fragility in hereditary spherocytosis.遗传性球形红细胞增多症中的正常红细胞渗透脆性
J Pediatr. 1989 Feb;114(2):264-6. doi: 10.1016/s0022-3476(89)80794-2.
2
Hereditary spherocytosis with normal osmotic fragility after incubation. Is the autohemolysis test really obsolete?孵育后渗透脆性正常的遗传性球形红细胞增多症。自体溶血试验真的过时了吗？
JAMA. 1979 Jul 6;242(1):63-4.
3
Modified osmotic fragility test for the laboratory diagnosis of hereditary spherocytosis.
Am J Hematol. 1989 Jun;31(2):136-7. doi: 10.1002/ajh.2830310214.
4
[Silent forms of hereditary spherocytosis].[遗传性球形红细胞增多症的隐匿型]
Vnitr Lek. 1999 Oct;45(10):594-7.
5
[Diagnosis of hereditary spherocytosis].
Folia Haematol Int Mag Klin Morphol Blutforsch. 1989;116(5):769-73.
6
Experience with measurement of erythrocyte osmotic fragility by a dialysis technique in congenital hereditary spherocytosis.先天性遗传性球形红细胞增多症中采用透析技术测量红细胞渗透脆性的经验。
J Lab Clin Med. 1969 Feb;73(2):219-28.
7
Abnormality in a specific protein of the erythrocyte membrane in hereditary spherocytosis.遗传性球形红细胞增多症中红细胞膜特定蛋白质的异常。
Biochem Biophys Res Commun. 1974 Apr 23;57(4):1038-44. doi: 10.1016/0006-291x(74)90801-8.
8
Does preincubation of the red blood cells contribute to the capability of the osmotic fragility test to detect very mild forms of hereditary spherocytosis?
Scand J Haematol. 1982 Jul;29(1):89-93. doi: 10.1111/j.1600-0609.1982.tb00568.x.
9
Extramedullary haematopoiesis in hereditary spherocytosis simulating mediastinal tumour.遗传性球形红细胞增多症中模拟纵隔肿瘤的髓外造血
Eur J Haematol. 1997 Feb;58(2):124-6. doi: 10.1111/j.1600-0609.1997.tb00936.x.
10
[Evaluation of the "pink test." Comparison of 2 procedures for the diagnosis of hereditary spherocytosis].["红细胞脆性试验的评估。两种遗传性球形红细胞增多症诊断方法的比较"]
Sangre (Barc). 1993 Oct;38(5):414-5.

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Diagnostic power of laboratory tests for hereditary spherocytosis: a comparison study in 150 patients grouped according to molecular and clinical characteristics.实验室检查对遗传性球形红细胞增多症的诊断价值：根据分子和临床特征对 150 例患者进行分组的对比研究。
Haematologica. 2012 Apr;97(4):516-23. doi: 10.3324/haematol.2011.052845. Epub 2011 Nov 4.
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Time-course investigation of SAGM-stored leukocyte-filtered red bood cell concentrates: from metabolism to proteomics.SAGM 储存的白细胞滤除的红细胞浓缩物的时间进程研究：从代谢组学到蛋白质组学。
Haematologica. 2012 Jan;97(1):107-15. doi: 10.3324/haematol.2011.051789. Epub 2011 Oct 11.
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Hereditary spherocytosis; new guidelines.遗传性球形红细胞增多症；新指南。
Arch Dis Child. 2004 Sep;89(9):809-12. doi: 10.1136/adc.2003.034587.
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The clinical relevance of an isolated increase in the number of circulating hyperchromic red blood cells.循环中高色素红细胞数量单独增加的临床意义。
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Spectrin/band 3 ratio as diagnostic tool in hereditary spherocytosis.血影蛋白/带3比值作为遗传性球形红细胞增多症的诊断工具。
Eur J Pediatr. 1992 Jan;151(1):35-7. doi: 10.1007/BF02073887.