[Spontaneous hemolysis in a patient with glucose-6-p-dehydrogenase deficiency (Mediterranean type) and heterozygote beta thalassemia].
作者信息
Benöhr H C, Usener H, Wagner H, Kleinhauer E, Waller H D
出版信息
Med Welt. 1970 Jun 13;24:1091-5.
PMID:5487689
Abstract
摘要
相似文献
1
2
Hemoglobin A2, E and F levels and the incidence of hemoglobin E, beta-thalassemia, and glucose-6-phosphate dehydrogenase deficiency in lymphoma.
J Med Assoc Thai. 1974 Jan;57(1):3-10.
3
Haemoglobin O Arab, beta-thalassaemia and glucose-6-phosphate dehydrogenase deficiency in a Hungarian family.一个匈牙利家庭中的血红蛋白O阿拉伯型、β地中海贫血和葡萄糖-6-磷酸脱氢酶缺乏症
Folia Haematol Int Mag Klin Morphol Blutforsch. 1980;107(4):654-60.
4
Hereditary hemolytic anemia associated with glucose-6-phosphate dehydrogenase deficiency (Mediterranean type).
Isr J Med Sci. 1969 Sep-Oct;5(5):1053-9.
5
[Thalassemia with glucose-6-phosphate-dehydrogenase deficiency].
Probl Gematol Pereliv Krovi. 1970 Sep;15(9):27-30.
6
Leg ulcer in a patient with beta-thalassemia and glucose-6-phosphate-dehydrogenase deficiency.
Int J Dermatol. 1990 Jul-Aug;29(6):426-7. doi: 10.1111/j.1365-4362.1990.tb03828.x.
7
[Congenital deficiency of intra-erythrocyte glucose-6-phosphate dehydrogenase in a subject affected by Cooley's disease].[一名患库利氏贫血症患者的红细胞内葡萄糖-6-磷酸脱氢酶先天性缺乏]
Riv Clin Pediatr. 1964 Nov;74(5):257-65.
8
[Hemolytic anemia caused by association of a double anomaly: beta-thalassemia and deficiency of G6PD].[由β地中海贫血和葡萄糖-6-磷酸脱氢酶（G6PD）缺乏这一双重异常联合导致的溶血性贫血]
Minerva Pediatr. 1969 Apr 14;21(15):605-10.
9
Thalassemia phenotypes in Sardinia.
Birth Defects Orig Artic Ser. 1982;18(7):165-8.
10
引用本文的文献
1
[Glucose-6-P-dehydrogenase type bodensee (a new enzyme variant)].博登湖型葡萄糖-6-磷酸脱氢酶（一种新的酶变体）
Klin Wochenschr. 1971 Oct 1;49(19):1058-62. doi: 10.1007/BF01732914.
2
Biochemical characterization of a glucose-6-phosphate dehydrogenase variant with favism: G-6-PD Zähringen.伴有蚕豆病的葡萄糖-6-磷酸脱氢酶变异体的生化特征：G-6-PD 察林根
Klin Wochenschr. 1972 Feb 15;50(4):205-9. doi: 10.1007/BF01487145.
Zotero 插件