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Phosphoglycerate kinase (PKG) deficiency hereditary nonspherocytic hemolytic anemia: report of a case found in a Japanese family.

作者信息

Miwa S, Nakashima K, Oda S, Ogawa H, Nagafuji H

出版信息

Nihon Ketsueki Gakkai Zasshi. 1972 Aug;35(4):511-4.

PMID:4676843
Abstract
摘要

相似文献

1
Phosphoglycerate kinase (PKG) deficiency hereditary nonspherocytic hemolytic anemia: report of a case found in a Japanese family.
Nihon Ketsueki Gakkai Zasshi. 1972 Aug;35(4):511-4.
2
Glucosephosphate isomerase (GPI) deficiency hereditary nonspherocytic hemolytic anemia. Report of the first case found in Japanese.葡萄糖磷酸异构酶（GPI）缺乏遗传性非球形细胞溶血性贫血。首例日本病例报告。
Nihon Ketsueki Gakkai Zasshi. 1973 Feb;36(1):65-9.
3
Glucosephosphate isomerase (GPI) deficiency hereditary nonspherocytic hemolytic anemia. Report of the second case found in Japanese.葡萄糖磷酸异构酶（GPI）缺乏遗传性非球形红细胞溶血性贫血。在日本人中发现的第二例病例报告。
Nihon Ketsueki Gakkai Zasshi. 1973 Feb;36(1):70-3.
4
[Pyruvate kinase deficiency in the German Democratic Republic].
Folia Haematol Int Mag Klin Morphol Blutforsch. 1971;96(1):68-72.
5
[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.
6
[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.
7
[Adenosine triphosphatase (ATP-ase) deficiency in a family with nonspherocytic hemolytic anemia].
Nord Med. 1971 Dec 16;86(50):1540.
8
[Erythrocyte and leucocyte 3-phosphoglycerate kinase deficiency. Studies of properties of the enzyme, phagocytic activity of the polymorphonuclear leucoytes and a review of the literature].
Nouv Rev Fr Hematol. 1974 Jul-Aug;14(4):495-508.
9
Hereditary hemolytic anemia with special reference to erythroenzymopathies.
Jpn J Med. 1985 Feb;24(1):68-72. doi: 10.2169/internalmedicine1962.24.68.
10
[Congenital hemolytic anemia associated with phosphoglycerate kinase deficiency in erythrocytes, polynuclear cells and lymphocytes].[先天性溶血性贫血与红细胞、多核细胞及淋巴细胞中磷酸甘油酸激酶缺乏相关]
Nouv Rev Fr Hematol. 1971 Jul-Aug;11(4):565-78.

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A Novel Missense Variant Associated with A Splicing Defect in A Myopathic Form of PGK1 Deficiency in The Spanish Population.一种与西班牙人群中 PGK1 缺乏症肌病形式的剪接缺陷相关的新型错义变异。
Genes (Basel). 2019 Oct 10;10(10):785. doi: 10.3390/genes10100785.
2
[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.