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[Clinical studies on hereditary nonspherocytic anemia with erythrocyte pyruvate kinase deficiency].

作者信息

Blume K G, Busch D, Arnold H, Löhr G W

出版信息

Klin Wochenschr. 1971 Feb 15;49(4):228-30. doi: 10.1007/BF01495990.

DOI:10.1007/BF01495990
PMID:5100885
Abstract
摘要

相似文献

1
[Clinical studies on hereditary nonspherocytic anemia with erythrocyte pyruvate kinase deficiency].[红细胞丙酮酸激酶缺乏所致遗传性非球形红细胞贫血的临床研究]
Klin Wochenschr. 1971 Feb 15;49(4):228-30. doi: 10.1007/BF01495990.
2
ERYTHROCYTE PYRUVATE KINASE DEFICIENCY RESULTING IN CONGENITAL NONSPHEROCYTIC HEMOLYTIC ANEMIA.红细胞丙酮酸激酶缺乏导致先天性非球形红细胞溶血性贫血。
N Engl J Med. 1963 Oct 10;269:763-70. doi: 10.1056/NEJM196310102691501.
3
[Familial erythrocyte ATP: pyruvate phosphotransferase deficiency].[家族性红细胞ATP：丙酮酸磷酸转移酶缺乏症]
Acta Haematol Pol. 1982 Jul-Dec;13(3-4):157-63.
4
[A new erythroenzymopathy: congenital non-spherocytic hemolytic anemia and hereditary erythrocytic adenylate kinase deficiency].[一种新的红细胞酶病：先天性非球形细胞溶血性贫血与遗传性红细胞腺苷酸激酶缺乏症]
Presse Med (1893). 1971 Jan 30;79(6):215-8.
5
[Hemolytic congenital non-spherocytic anemia with PK deficiency: destruction of chromium-51 labeled erythrocytes in the spleen].[伴有丙酮酸激酶缺乏的溶血性先天性非球形红细胞贫血：脾脏中铬-51标记红细胞的破坏]
Haematologica. 1973;58(11):803-9.
6
[PYRUVATE KINASE DEFICIENCY HEREDITARY NONSPHEROCYTIC HEMOLYTIC ANEMIA. REPORT OF TWO CASES IN A JAPANESE FAMILY AND REVIEW OF LITERATURE].[丙酮酸激酶缺乏症遗传性非球形细胞溶血性贫血。一个日本家庭中的两例报告及文献复习]
Nihon Ketsueki Gakkai Zasshi. 1965 Feb;28:1-13.
7
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.
8
[Glucosephosphate dehydrogenase deficiency in erythrocytes and leukocytes of patients with congenital nonspherocytic hemolytic anemia and favism].[先天性非球形细胞溶血性贫血和蚕豆病患者红细胞和白细胞中的葡萄糖磷酸脱氢酶缺乏症]
Pol Tyg Lek. 1988 Feb 15;43(7):207-9.
9
[HEREDITARY HEMOLYTIC ANEMIA WITH PYRUVATE-KINASE DEFICIENCY].[遗传性丙酮酸激酶缺乏性溶血性贫血]
Minerva Med. 1964 Jun 27;55:2069-73.
10
[Serum iron in hemolytic anemia (author's transl)].溶血性贫血中的血清铁（作者译）
Klin Wochenschr. 1975 Feb 15;53(4):181-3. doi: 10.1007/BF01466763.

本文引用的文献

1
THE HEREDITARY NON-SPHEROCYTIC HAEMOLYTIC ANAEMIAS.遗传性非球形细胞溶血性贫血
Acta Haematol. 1964 Apr;31:177-86. doi: 10.1159/000209626.
2
EXTREME HEMOLYSIS AND RED-CELL DISTORTION IN ERYTHROCYTE PYRUVATE KINASE DEFICIENCY. I. MORPHOLOGY, ERYTHROKINETICS AND FAMILY ENZYME STUDIES.红细胞丙酮酸激酶缺乏症中的极度溶血与红细胞变形。I. 形态学、红细胞动力学及家族酶学研究。
N Engl J Med. 1964 May 14;270:1023-30. doi: 10.1056/NEJM196405142702001.
3
Hereditary non-spherocytic hemolytic anemia of the pyruvate-kinase deficient type.丙酮酸激酶缺乏型遗传性非球形红细胞溶血性贫血
Ann Intern Med. 1963 Apr;58:567-91. doi: 10.7326/0003-4819-58-4-567.
4
A specific erythrocyte glycolytic enzyme defect (pyruvate kinase) in three subjects with congenital non-spherocytic hemolytic anemia.三名先天性非球形红细胞溶血性贫血患者存在特定的红细胞糖酵解酶缺陷（丙酮酸激酶）。
Trans Assoc Am Physicians. 1961;74:100-10.
5
[Contribution to population genetics of pyruvate kinase from human erythrocytes. ATP-pyruvate phosphotransferase, E.C.2.7.1.40].[对人红细胞丙酮酸激酶群体遗传学的贡献。ATP - 丙酮酸磷酸转移酶，E.C.2.7.1.40]
Humangenetik. 1968;6(3):261-5. doi: 10.1007/BF00291870.
6
[Erythrocyte elimination and erythrocyte turnover in various hereditary hemolytic anemias].[各种遗传性溶血性贫血中的红细胞清除与红细胞更新]
Klin Wochenschr. 1968 May 1;46(9):490-7. doi: 10.1007/BF01810791.
7
[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.
8
[Excessive erythrocyte ATP level feature of a hereditary nonspherocytic hemolytic anemia in disturbed ATP utilization and a red cell metabolic anomaly without disease value].[遗传性非球形红细胞溶血性贫血中红细胞ATP水平过高的特征：ATP利用紊乱及无疾病价值的红细胞代谢异常]
Klin Wochenschr. 1970 May 1;48(9):543-50. doi: 10.1007/BF01488569.
9
[Study of erythrokinetics in 8 cases of homozygote deficiency in pyruvate kinase].8例丙酮酸激酶纯合子缺乏症患者的红细胞动力学研究
Nouv Rev Fr Hematol. 1969 Nov-Dec;9(6):850-9.