葡萄糖磷酸异构酶缺乏症：一种伴有溶血的酶变体在体内不稳定的证据。 - Suppr

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超能文献

Glucosephosphate isomerase deficiency: evidence for in vivo instability of an enzyme variant with hemolysis.

作者信息

Arnold H, Blume K G, Engelhardt R, Löhr G W

出版信息

Blood. 1973 May;41(5):691-9.

PMID:4694084

Abstract

摘要

相似文献

Glucosephosphate isomerase deficiency: evidence for in vivo instability of an enzyme variant with hemolysis.葡萄糖磷酸异构酶缺乏症：一种伴有溶血的酶变体在体内不稳定的证据。

Blood. 1973 May;41(5):691-9.

Glucose phosphate isomerase deficiency with congenital nonspherocytic hemolytic anemia: a new variant (type Nordhorn). I. Clinical and genetic studies.葡萄糖磷酸异构酶缺乏症伴先天性非球形细胞溶血性贫血：一种新变异型（诺德霍恩型）。I. 临床和遗传学研究。

Pediatr Res. 1974 Jan;8(1):18-25. doi: 10.1203/00006450-197401000-00004.

[Hereditary enzymopenic anemia].

Minerva Med. 1972 Dec 1;63(86):4721-3.

[Laboratory diagnosis of enzymopenic hemolytic anemia].[酶缺乏性溶血性贫血的实验室诊断]

Pediatria (Napoli). 1972;80(2):186-97.

Congenital hemolytic anemias and red cell enzyme deficiencies.先天性溶血性贫血和红细胞酶缺乏症。

Curr Probl Pediatr. 1973 Dec;4(2):1-40. doi: 10.1016/s0045-9380(73)80018-0.

Influence of erythrocyte age on enzyme activity in the bovine.红细胞年龄对牛体内酶活性的影响。

Comp Biochem Physiol B. 1972 Mar 15;41(3):551-8. doi: 10.1016/0305-0491(72)90118-6.

Disorders due to enzyme defects in the red blood cell.红细胞酶缺陷所致疾病

Adv Metab Disord. 1972;60:131-60. doi: 10.1016/b978-0-12-027306-5.50010-3.

[Hereditary non-spherocytic hemolytic anemia caused by glucosephosphate isomerase deficiency: 1. case observed in Switzerland].

Schweiz Med Wochenschr. 1974 Sep 28;104(39):1379-81.

Hereditary deficiency of glucosephosphate isomerase as a cause of nonspherocytic hemolytic anemia.葡萄糖磷酸异构酶遗传性缺乏作为非球形红细胞溶血性贫血的一个病因

Blut. 1973 Jun;26(6):393-8. doi: 10.1007/BF01632749.

Combined glucosephosphate isomerase and glucose-6-phosphate dehydrogenase deficiency of the erythrocytes: a new haemolytic syndrome.红细胞磷酸葡萄糖异构酶和葡萄糖-6-磷酸脱氢酶联合缺乏：一种新的溶血性综合征。

Br J Haematol. 1971 Mar;20(3):249-61. doi: 10.1111/j.1365-2141.1971.tb07036.x.

引用本文的文献

Successful treatment of fetal hemolytic disease due to glucose phosphate isomerase deficiency (GPI) using repeated intrauterine transfusions: a case report.采用反复宫内输血成功治疗葡萄糖磷酸异构酶缺乏症（GPI）所致胎儿溶血病：一例报告

Clin Case Rep. 2015 Oct;3(10):862-5. doi: 10.1002/ccr3.358. Epub 2015 Sep 7.

Augsburg-type glucosephosphate isomerase deficiency. A new variant causing congenital nonspherocytic hemolytic anemia in a German family.

Blut. 1980 Feb;40(2):107-15. doi: 10.1007/BF01013693.

Search for a relationship between molecular anomalies of the mutant erythrocyte pyruvate kinase variants and their pathological expression.探寻突变型红细胞丙酮酸激酶变体的分子异常与其病理表现之间的关系。

Hum Genet. 1981;57(2):172-5. doi: 10.1007/BF00282016.

Properties of arginase from liver of Macaca fascicularis; comparison of normals with red blood cell arginase deficient monkeys.食蟹猴肝脏中精氨酸酶的特性；正常猴与红细胞精氨酸酶缺陷猴的比较

Biochem Genet. 1980 Oct;18(9-10):829-41. doi: 10.1007/BF00500116.

Regulation of expression of genes for enzymes of the mammalian urea cycle in permanent cell-culture lines of hepatic and non-hepatic origin.哺乳动物尿素循环中酶的基因在肝脏和非肝脏来源的永久细胞系中的表达调控。

Mol Cell Biochem. 1983;53-54(1-2):57-76. doi: 10.1007/BF00225246.

[Concerning tissue-specific isoenzymes of glucosephosphate isomerase in man (author's transl)].关于人类磷酸葡萄糖异构酶的组织特异性同工酶（作者译）

Klin Wochenschr. 1974 Feb 1;52(3):149-51. doi: 10.1007/BF01620756.

[Glucose phosphate isomerase type Recklinghausen: a new enzyme variant with haemolytic anaemia (author's transl)].雷克林豪森型磷酸葡萄糖异构酶：一种伴有溶血性贫血的新型酶变体（作者译）

Klin Wochenschr. 1973 Dec 15;51(24):1198-204. doi: 10.1007/BF01468556.

Hereditary deficiency of glucosephosphate isomerase as a cause of nonspherocytic hemolytic anemia.葡萄糖磷酸异构酶遗传性缺乏作为非球形红细胞溶血性贫血的一个病因

Blut. 1973 Jun;26(6):393-8. doi: 10.1007/BF01632749.

Generalised glucosephosphate isomerase (GPI) deficiency causing haemolytic anaemia, neuromuscular symptoms and impairment of granulocytic function: a new syndrome due to a new stable GPI variant with diminished specific activity (GPI Homburg).导致溶血性贫血、神经肌肉症状及粒细胞功能受损的全身性葡萄糖磷酸异构酶（GPI）缺乏症：一种由具有降低的比活性的新型稳定GPI变体（GPI洪堡变体）引起的新综合征

Eur J Pediatr. 1985 Nov;144(4):301-5. doi: 10.1007/BF00441768.

[Immunological studies on glucosephosphate isomerase deficiency: instability and impaired synthesis of the defective enzyme (author's transl)].

Klin Wochenschr. 1975 Dec 1;53(23):1135-6. doi: 10.1007/BF01614284.

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