红细胞丙酮酸激酶缺乏症的临床异质性。临床严重形式下ATP利用受损的证据。 - Suppr

Suppr

超能文献

Clinical heterogeneity of erythrocyte pyruvate kinase deficiency. Evidence of an impaired utilization of ATP in a clinically severe form.

作者信息

Schröter W

出版信息

Helv Paediatr Acta. 1972 Nov;27(5):471-88.

PMID:4640902

Abstract

摘要

相似文献

Clinical heterogeneity of erythrocyte pyruvate kinase deficiency. Evidence of an impaired utilization of ATP in a clinically severe form.红细胞丙酮酸激酶缺乏症的临床异质性。临床严重形式下ATP利用受损的证据。

Helv Paediatr Acta. 1972 Nov;27(5):471-88.

[Congenital hemolytic anemia with pyruvate-kinase deficiency].[丙酮酸激酶缺乏所致先天性溶血性贫血]

Arch Fr Pediatr. 1970 Jan;27(1):31-49.

Erythrocyte pyruvate kinase deficiency associated with kinetically aberrant isozyme.与动力学异常同工酶相关的红细胞丙酮酸激酶缺乏症。

Nihon Ketsueki Gakkai Zasshi. 1974 Feb;37(1):17-24.

[Demonstration of an enzyme with abnormal kinetics in 2 new cases of erythrocyte pyruvate kinase deficiency].[2例新的红细胞丙酮酸激酶缺乏症患者中异常动力学酶的证明]

Pathol Biol (Paris). 1969 Jun-Jul;17(11):597-607.

[Erythrocytic pyruvate kinase. II. Enzymatic heterogeneity of deficiencies. Studies concerning 28 cases with congenital hemolytic anemia].[红细胞丙酮酸激酶。II. 缺乏症的酶学异质性。关于28例先天性溶血性贫血的研究]

Nouv Rev Fr Hematol. 1972 Sep-Oct;12(5):569-94.

[Metabolic abnormality in erthyrocytes with atypical pyruvate kinase and potassium deficiency].[伴有非典型丙酮酸激酶和钾缺乏的红细胞代谢异常]

Haematologia (Budap). 1972;6(4):379-94.

[Anomalies of glycolysis during hemolytic anemia due to deficiency of pyruvate kinase in the erythrocytes].红细胞丙酮酸激酶缺乏所致溶血性贫血时糖酵解异常

Clin Chim Acta. 1968 Oct;22(2):165-81. doi: 10.1016/0009-8981(68)90354-9.

Seminars in hematology.血液学研讨会

Semin Hematol. 1971 Oct;8(4):307-10.

Clinical consequences of enzyme deficiencies in the erythrocyte.红细胞中酶缺乏的临床后果。

Ann Clin Lab Sci (1971). 1971 Sep-Oct;1(2):177-83.

The mechanism of mitochondrial extrusion from reticulocytes in the spleen from patients with erythrocyte pyruvate kinase (PK) deficiency.

Nihon Ketsueki Gakkai Zasshi. 1974 Feb;37(1):25-31.

引用本文的文献

Role of the spleen in congenital stomatocytosis associated with high sodium-low potassium erythrocytes.脾脏在与高钠低钾红细胞相关的先天性口形红细胞增多症中的作用。

Klin Wochenschr. 1981 Feb 16;59(4):173-9. doi: 10.1007/BF01477477.

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.

Membrane-localized pyruvate kinase of red blood cells in hemolytic anemia associated with pyruvate kinase deficiency.与丙酮酸激酶缺乏相关的溶血性贫血中红细胞的膜定位丙酮酸激酶

Klin Wochenschr. 1975 Dec 1;53(23):1101-6. doi: 10.1007/BF01614277.

Molecular mechanism of erythrocyte pyruvate kinase deficiency.红细胞丙酮酸激酶缺乏症的分子机制

Humangenetik. 1975 Oct 7;29(4):271-80. doi: 10.1007/BF00394188.

Pyruvate kinase-catalyzed ATP-formation in human red blood cell membranes.

Blut. 1978 Jul 14;37(1):1-5. doi: 10.1007/BF01006547.

[Enzyme deficiencies in glycolysis and nucleotide metabolism of red blood cells in nonspherocytic hemolytic anemia (author's transl)].非球形红细胞性溶血性贫血中红细胞糖酵解及核苷酸代谢的酶缺乏（作者译）

Klin Wochenschr. 1976 Sep 1;54(17):803-21. doi: 10.1007/BF01469302.

Advances in hereditary red cell enzyme anomalies.遗传性红细胞酶异常的进展

Hum Genet. 1979;50(1):1-27. doi: 10.1007/BF00295584.

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验