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1
Glucose 6-phosphate dehydrogenase deficiency and cystic fibrosis.葡萄糖-6-磷酸脱氢酶缺乏症与囊性纤维化。
Postgrad Med J. 1981 Jul;57(669):453-4. doi: 10.1136/pgmj.57.669.453.
2
Effect of erythrocyte glucose-6-phosphate dehydrogenase (G-6-PD) deficiency on light-induced riboflavin deficiency in the neonate.
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G-6-PD deficiency and hyperbilirubinemia; in black American full-term infants.葡萄糖-6-磷酸脱氢酶缺乏症与高胆红素血症;美国黑人足月儿的情况
N Y State J Med. 1979 Jan;79(1):22-4.
4
Glucose-6-phosphate dehydrogenase deficiency and hyperbilirubinemia in the newborn.
Med Chir Dig. 1973;2(2):111-7.
5
[Phosphate glucose dehydrogenase deficiency causing hyperbilirubinemia in the newborn].磷酸葡萄糖脱氢酶缺乏导致新生儿高胆红素血症
Ginecol Obstet Mex. 1969 Feb;24(148):203-9.
6
alpha-Thalassaemia and hyperbilirubinaemia in G-6-PD-deficient newborns.葡萄糖-6-磷酸脱氢酶缺乏的新生儿中的α地中海贫血和高胆红素血症。
Arch Dis Child. 1980 Jun;55(6):482-4. doi: 10.1136/adc.55.6.482.
7
[Evolution of some cases of jaundice caused by deficiency of glucose-6-phosphate dehydrogenase. (Partial genealogical tree of an enzymopenic family)].[葡萄糖-6-磷酸脱氢酶缺乏所致黄疸某些病例的演变。(一个酶缺乏家族的部分系谱树)]
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Neonatal hyperbilirubinemia and glucose-6-phosphate dehydrogenase deficiency.新生儿高胆红素血症与葡萄糖-6-磷酸脱氢酶缺乏症
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[Glucose-6-phosphate dehydrogenase deficiency].[葡萄糖-6-磷酸脱氢酶缺乏症]
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10
[Effect of barbituric acid on hyperbilirubinemia in newborn infants with glucosephosphate dehydrogenase deficiency in the erythrocytes].
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引用本文的文献

1
Mitochondrial Stress Responses and "Mito-Inflammation" in Cystic Fibrosis.囊性纤维化中的线粒体应激反应与“线粒体炎症”
Front Pharmacol. 2020 Sep 30;11:581114. doi: 10.3389/fphar.2020.581114. eCollection 2020.
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Glucose-6-Phosphate Dehydrogenase Deficiency Activates Endothelial Cell and Leukocyte Adhesion Mediated via the TGFβ/NADPH Oxidases/ROS Signaling Pathway.葡萄糖-6-磷酸脱氢酶缺乏通过 TGFβ/NADPH 氧化酶/ROS 信号通路激活内皮细胞和白细胞黏附。
Int J Mol Sci. 2020 Oct 10;21(20):7474. doi: 10.3390/ijms21207474.
3
Role of Cystic Fibrosis Bronchial Epithelium in Neutrophil Chemotaxis.囊性纤维化支气管上皮细胞在中性粒细胞趋化中的作用。
Front Immunol. 2020 Aug 4;11:1438. doi: 10.3389/fimmu.2020.01438. eCollection 2020.
4
CFTR activity and mitochondrial function.囊性纤维化跨膜传导调节因子活性与线粒体功能。
Redox Biol. 2013 Feb 5;1(1):190-202. doi: 10.1016/j.redox.2012.11.007.

本文引用的文献

1
Further studies on the properties and assay of glucose 6-phosphate dehydrogenase and 6-phosphogluconate dehydrogenase of rat liver.大鼠肝脏葡萄糖6-磷酸脱氢酶和6-磷酸葡萄糖酸脱氢酶性质及测定的进一步研究。
Biochem J. 1953 Oct;55(3):400-8. doi: 10.1042/bj0550400.
2
Cystic fibrosis of the pancreas in India.印度的胰腺囊性纤维化
J Pediatr. 1969 Sep;75(3):522-3. doi: 10.1016/s0022-3476(69)80288-x.
3
Bilirubin and red cell metabolism in relation to neonatal jaundice.与新生儿黄疸相关的胆红素及红细胞代谢
Postgrad Med J. 1969 Feb;45(520):86-106.
4
Screening for cystic fibrosis by examination of meconium.通过胎粪检查筛查囊性纤维化。
Arch Dis Child. 1974 Aug;49(8):597-601. doi: 10.1136/adc.49.8.597.
5
Increased susceptibility of males to infection.男性对感染的易感性增加。
Lancet. 1969 Oct 18;2(7625):826-7. doi: 10.1016/s0140-6736(69)92278-8.
6
Neutrophil dysfunction, chronic granulomatous disease, and non-spherocytic haemolytic anaemia caused by complete deficiency of glucose-6-phosphate dehydrogenase.中性粒细胞功能障碍、慢性肉芽肿病以及由葡萄糖-6-磷酸脱氢酶完全缺乏引起的非球形细胞溶血性贫血。
Lancet. 1973 Sep 8;2(7828):530-4. doi: 10.1016/s0140-6736(73)92350-7.
7
Hemolytic anemia and edema as the initial signs in infants with cystic fibrosis. Consider this diagnosis even in absence of pulmonary symptoms.
Clin Pediatr (Phila). 1976 Jul;15(7):597-600. doi: 10.1177/000992287601500704.
8
Inherited haemolytic states: glucose-6-phosphate dehydrogenase deficiency.
Clin Haematol. 1975 Feb;4(1):83-108.
9
Research in cystic fibrosis (first of three parts).
N Engl J Med. 1976 Aug 26;295(9):481-5. doi: 10.1056/NEJM197608262950905.
10
A simple method for the quantitative determination of stool trypsin and chymotrypsin.
Clin Chim Acta. 1975 Jul 23;62(2):225-9. doi: 10.1016/0009-8981(75)90231-4.

葡萄糖-6-磷酸脱氢酶缺乏症与囊性纤维化。

Glucose 6-phosphate dehydrogenase deficiency and cystic fibrosis.

作者信息

Congdon P J, Littlewood J M, Aggarwal R K, Shapiro H

出版信息

Postgrad Med J. 1981 Jul;57(669):453-4. doi: 10.1136/pgmj.57.669.453.

DOI:10.1136/pgmj.57.669.453
PMID:7312744
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2424973/
Abstract

A child born to Pakistani parents is described. He had both cystic fibrosis and G-6PD-deficiency. So far as can be ascertained, the occurrence of both these conditions in the same individual has not previously been reported.

摘要

本文描述了一名父母为巴基斯坦人的儿童。他同时患有囊性纤维化和葡萄糖-6-磷酸脱氢酶缺乏症。据目前所知,此前尚未有同一人同时患有这两种疾病的报道。