Favism in breast-fed infants.
作者信息
Taj-Eldin S
出版信息
Arch Dis Child. 1971 Feb;46(245):121-3. doi: 10.1136/adc.46.245.121.
Abstract
摘要
相似文献
1
Favism in breast-fed infants.母乳喂养婴儿的蚕豆病
Arch Dis Child. 1971 Feb;46(245):121-3. doi: 10.1136/adc.46.245.121.
2
Favism by proxy in nursing glucose-6-phosphate dehydrogenase-deficient neonates.葡萄糖-6-磷酸脱氢酶缺乏的新生儿护理中通过代理导致的蚕豆病
J Perinatol. 1998 Nov-Dec;18(6 Pt 1):477-9.
3
Glucose-6-phosphate-dehydrogenase deficiency and favism.葡萄糖-6-磷酸脱氢酶缺乏症与蚕豆病
Lancet. 1969 Nov 29;2(7631):1177-8.
4
[Favism. Glucose-6-phosphate dehydrogenase deficiency].[蚕豆病。葡萄糖-6-磷酸脱氢酶缺乏症]
Fortschr Med. 1973 Oct;28(11):1097-9.
5
[Favism: hemolytic crisis due to glucose-6-phosphate dehydrogenase deficiency in erythrocytes].[蚕豆病：红细胞葡萄糖-6-磷酸脱氢酶缺乏所致的溶血性危机]
Pol Tyg Lek. 1973 May 14;28(20):744-5.
6
Favism in breast-fed infants.母乳喂养婴儿中的蚕豆病
Arch Dis Child. 1971 Oct;46(249):741. doi: 10.1136/adc.46.249.741.
7
Favism and Glucose-6-Phosphate Dehydrogenase Deficiency.蚕豆病与葡萄糖-6-磷酸脱氢酶缺乏症
N Engl J Med. 2018 Jan 4;378(1):60-71. doi: 10.1056/nejmra1708111.
8
[Pathogenesis of favism].[蚕豆病的发病机制]
Minerva Pediatr. 1967 Jul 28;19(30):1391-4.
9
Hemolytic crises of favism in Sicilian females heterozygous for G-6-PD deficiency.患有G-6-PD缺乏症的西西里岛杂合子女性的蚕豆病溶血危象。
Pediatrics. 1972 Jun;49(6):854-9.
10
Favism: current problems and investigations.蚕豆病：当前问题与研究
J Med Genet. 1973 Jun;10(2):154-7. doi: 10.1136/jmg.10.2.154.
引用本文的文献
1
Favism: Clinical Features at Different Ages.蚕豆病：不同年龄段的临床特征。
Nutrients. 2023 Jan 10;15(2):343. doi: 10.3390/nu15020343.
2
Glucose-6-Phosphate Dehydrogenase Deficiency and Neonatal Hyperbilirubinemia: Insights on Pathophysiology, Diagnosis, and Gene Variants in Disease Heterogeneity.葡萄糖-6-磷酸脱氢酶缺乏症与新生儿高胆红素血症：对疾病异质性的病理生理学、诊断及基因变异的见解
Front Pediatr. 2022 May 24;10:875877. doi: 10.3389/fped.2022.875877. eCollection 2022.
3
Favism in breast-fed infants.母乳喂养婴儿中的蚕豆病
Arch Dis Child. 1971 Oct;46(249):741. doi: 10.1136/adc.46.249.741.
4
Drug therapy in children.儿童药物治疗
J Natl Med Assoc. 1978 Oct;70(10):739-40.
本文引用的文献
1
Favism in Cyprus; analysis of 67 cases admitted to Nicosia General Hospital during the last 3 years.塞浦路斯的蚕豆病；对过去三年间尼科西亚综合医院收治的67例病例的分析。
Cyprus Med J. 1952 Jan;5(3):795-9.
2
Erythrocyte glucose-6-phosphate dehydrogenase deficiency: evidence of differences between Negroes and Caucasians with respect to this genetically determined trait.红细胞葡萄糖-6-磷酸脱氢酶缺乏症：关于这一由基因决定的性状，黑人和白种人之间存在差异的证据。
J Clin Invest. 1959 Dec;38(12):2253-62. doi: 10.1172/JCI104006.
3
FAVISM IN ENGLAND--TWO MORE CASES.
Arch Dis Child. 1965 Jun;40(211):271-3. doi: 10.1136/adc.40.211.271.
4
Peripheral blood and bilirubin values in normal full-term primaquine-sensitive Negro infants: effect of vitamin K.
Pediatrics. 1963 Jun;31:983-95.
5
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.
6
Favism in a nursing infant.哺乳婴儿的蚕豆病
J Pediatr. 1961 Feb;58:263-6. doi: 10.1016/s0022-3476(61)80166-2.
7
Enzyme deficiency in erythrocytes in congenital nonspherocytic hemolytic anemia.先天性非球形红细胞溶血性贫血中的红细胞酶缺乏。
Pediatrics. 1959 Aug;24(2):245-53.
8
Bilateral cortical necrosis of the kidneys in an infant with favism.一名患有蚕豆病的婴儿出现双侧肾皮质坏死。
Am J Clin Pathol. 1956 Jan;26(1):42-7. doi: 10.1093/ajcp/26.1.42.
9
[The hemolytic anemia of premature infants with spontaneous Heinz body formation; a new syndrome observed in 14 cases].
Helv Paediatr Acta. 1953 Dec;8(6):491-529.
10
Favism; report of a case and brief review of the literature.蚕豆病；一例病例报告及文献简要综述
J Pediatr. 1953 Apr;42(4):453-6. doi: 10.1016/s0022-3476(53)80460-9.
Zotero 插件