蚕豆病：临床与生化数据。 - Suppr

Suppr

超能文献

Favism: clinical and biochemical data.

作者信息

Kattamis C A, Kyriazakou M, Chaidas S

出版信息

J Med Genet. 1969 Mar;6(1):34-41. doi: 10.1136/jmg.6.1.34.

DOI:10.1136/jmg.6.1.34

PMID:5771221

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1468705/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8f9/1468705/1506b4fd9386/jmedgene00372-0042-a.jpg

相似文献

Favism: clinical and biochemical data.蚕豆病：临床与生化数据。

J Med Genet. 1969 Mar;6(1):34-41. doi: 10.1136/jmg.6.1.34.

Some clinical and biochemical aspects of favism in childhood.儿童蚕豆病的一些临床和生化方面

Ann Soc Belges Med Trop Parasitol Mycol. 1969;49(3):298-302.

Favism in GdMediterranean heterozygous females.地中海贫血杂合子女性中的蚕豆病

Pediatr Res. 1979 Jul;13(7):812-6. doi: 10.1203/00006450-197907000-00004.

Favism in the Caspian littoral area of Iran.伊朗里海沿岸地区的蚕豆病

Trop Geogr Med. 1971 Jun;23(2):149-57.

[The significance of heredity in favism, in relation to enzyme activity].[蚕豆病中遗传与酶活性的关系及意义]

Pediatrie. 1971 Jun;26(4):395-9.

On the familial predisposition to favism.关于蚕豆病的家族易感性。

Am J Hum Genet. 1966 May;18(3):253-63.

Family investigations of erythrocyte glucose-6-phosphate dehydrogenase in favism.蚕豆病中红细胞葡萄糖-6-磷酸脱氢酶的家系调查

Pol Med J. 1970;9(5):1093-9.

[Studies on the frequency and distribution of favism in the province of Matera].[关于马泰拉省蚕豆病的发病率和分布情况的研究]

Minerva Med. 1973 Jul 7;64(52):2700-3.

[Family studies of erythrocyte glucose-6-phosphate dehydrogenase in favism].[蚕豆病患者红细胞葡萄糖-6-磷酸脱氢酶的家系研究]

Pol Tyg Lek. 1970 Feb 9;25(6):201-4.

[Favism in Polish families].[波兰家庭中的蚕豆病]

Pol Tyg Lek. 1990;45(38-39):778-81.

引用本文的文献

Monogenic Disorders of ROS Production and the Primary Anti-Oxidative Defense.单基因氧化还原产物异常和主要抗氧化防御异常。

Biomolecules. 2024 Feb 9;14(2):206. doi: 10.3390/biom14020206.

Hyperglycemia and Oxidative Stress: An Integral, Updated and Critical Overview of Their Metabolic Interconnections.高血糖与氧化应激：代谢关联的整体、更新与关键综述。

Int J Mol Sci. 2023 May 27;24(11):9352. doi: 10.3390/ijms24119352.

Dynamics of G6PD activity in patients receiving weekly primaquine for therapy of Plasmodium vivax malaria.接受每周伯氨喹治疗间日疟原虫疟疾患者的 G6PD 活性动力学。

PLoS Negl Trop Dis. 2021 Sep 8;15(9):e0009690. doi: 10.1371/journal.pntd.0009690. eCollection 2021 Sep.

Primaquine Pharmacokinetics in Lactating Women and Breastfed Infant Exposures.哺乳期妇女和母乳喂养婴儿的磷酸氯喹药代动力学暴露情况。

Clin Infect Dis. 2018 Sep 14;67(7):1000-1007. doi: 10.1093/cid/ciy235.

Evaluation of liver and kidney function in favism patients.蚕豆病患者的肝肾功能评估。

Med J Islam Repub Iran. 2013 Feb;27(1):17-22.

Recent progress and clinical importance on pharmacogenetics in cancer therapy.癌症治疗中药物遗传学的最新进展及其临床意义。

Clin Chem Lab Med. 2011 Oct;49(10):1621-32. doi: 10.1515/CCLM.2011.715. Epub 2011 Sep 28.

Glucose-6-phosphate dehydrogenase variants associated with favism in Thai children.与泰国儿童蚕豆病相关的葡萄糖-6-磷酸脱氢酶变体

Int J Hematol. 2006 Feb;83(2):139-43. doi: 10.1532/IJH97.A20513.

Combined erythrocyte glucosephosphate isomerase (GPI) and glucose-6-phosphate dehydrogenase (G6PD) deficiency in an Italian family.意大利一个家族中红细胞磷酸葡萄糖异构酶（GPI）和葡萄糖-6-磷酸脱氢酶（G6PD）联合缺乏症

Hum Genet. 1981;57(2):226-9. doi: 10.1007/BF00282031.

Favism: looking for an autosomal gene associated with glucose-6-phosphate dehydrogenase deficiency.蚕豆病：寻找与葡萄糖-6-磷酸脱氢酶缺乏症相关的常染色体基因。

J Med Genet. 1984 Aug;21(4):278-80. doi: 10.1136/jmg.21.4.278.

On the pathogenesis of favism.论蚕豆病的发病机制。

J Med Genet. 1971 Dec;8(4):462-7. doi: 10.1136/jmg.8.4.462.

本文引用的文献

Glucose-6-phosphate Dehydrogenase Activity Levels in Enzyme-deficient Greek Individuals.希腊酶缺乏个体的葡萄糖-6-磷酸脱氢酶活性水平

Br Med J. 1963 Nov 16;2(5367):1240-3. doi: 10.1136/bmj.2.5367.1240.

DIVERSE CHARACTERISTICS OF GLUCOSE-6-PHOSPHATE DEHYDROGENASE FROM GREEK CHILDREN.希腊儿童葡萄糖-6-磷酸脱氢酶的多样特征

J Lab Clin Med. 1965 Feb;65:212-21.

GENETIC VARIATIONS IN THE QUANTITATIVE CONTROL OF ERYTHROCYTE GLUCOSE-6-PHOSPHATE DEHYDROGENASE ACTIVITY.红细胞葡萄糖-6-磷酸脱氢酶活性定量控制中的基因变异

Ann Hum Genet. 1964 Sep;28:61-70. doi: 10.1111/j.1469-1809.1964.tb00460.x.

MILD GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY IN GREEK MALES.希腊男性中的轻度葡萄糖-6-磷酸脱氢酶缺乏症

Lancet. 1964 Oct 31;2(7366):932-5. doi: 10.1016/s0140-6736(64)90863-3.

Three inherited red-cell abnormalities in a district of Greece. Thalassaemia, sickling, and glucose-6-phosphate-dehydrogenase deficiency.希腊某地区的三种遗传性红细胞异常。地中海贫血、镰状细胞病和葡萄糖-6-磷酸脱氢酶缺乏症。

Lancet. 1963 Apr 27;1(7287):907-9. doi: 10.1016/s0140-6736(63)91688-x.

Deficiency of erythrocyte glucose-6-phosphate dehydrogenase in Greek populations.希腊人群中红细胞葡萄糖-6-磷酸脱氢酶缺乏症

Ann Hum Genet. 1963 Feb;26:237-42. doi: 10.1111/j.1469-1809.1963.tb01980.x.

Neonatal jaundice in glucose-6-phosphate-dehydrogenase-deficient infants.葡萄糖-6-磷酸脱氢酶缺乏婴儿的新生儿黄疸

Br Med J. 1962 Nov 24;2(5316):1359-62. doi: 10.1136/bmj.2.5316.1359.

Primaquine sensitivity. Glucose-6-phosphate dehydrogenase deficiency: an inborn error of metabolism of medical and biological significance.伯氨喹敏感性。葡萄糖-6-磷酸脱氢酶缺乏症：一种具有医学和生物学意义的先天性代谢缺陷。

Arch Intern Med. 1962 Feb;109:209-34. doi: 10.1001/archinte.1962.03620140081013.

Glucose-6-phosphate dehydrogenase deficiency in Greece.希腊的葡萄糖-6-磷酸脱氢酶缺乏症

Blood. 1961 Jul;18:34-47.

A deficiency of glucose-6-phosphate dehydrogenase activity in erythrocytes from patients with favism.蚕豆病患者红细胞中葡萄糖-6-磷酸脱氢酶活性缺乏。

Bull Johns Hopkins Hosp. 1958 Apr;102(4):169-75.

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