Abstract
摘要
相似文献
1
[On the clinical picture of favism].
Med Klin. 1967 Oct 6;62(40):1539-41.
2
[Favism in Polish families].[波兰家庭中的蚕豆病]
Pol Tyg Lek. 1990;45(38-39):778-81.
3
4
[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.
5
6
[Considerations on 2 cases of favism].
Minerva Pediatr. 1967 Aug 4;19(31):1453-5.
7
Electrophoretic heterogeneity of erythrocyte and leucocyte glucose-6-phosphate dehydrogenase in Italians from various ethnic groups.
Nature. 1966 Aug 20;211(5051):876-7. doi: 10.1038/211876b0.
8
[Favism - a familial enzymatic defect of the red blood cells in a 7-year-old girl].[蚕豆病——一名7岁女孩红细胞的家族性酶缺陷]
Pediatr Pol. 1982;57(9):731-4.
9
[Red cell enzyme deficiencies - clinical manifestation and pathophysiology (author's transl)].红细胞酶缺乏症——临床表现与病理生理学（作者译）
Monatsschr Kinderheilkd. 1981 Aug;129(8):444-53.
10
Favism in a Portuguese family due to a deficient glucose-phosphate dehydrogenase variant (Canton) or (cpanton-like) type.一个葡萄牙家庭中因葡萄糖-6-磷酸脱氢酶变异体（广东型）或（类广东型）缺乏而导致的蚕豆病。
Acta Haematol. 1976;56(1):58-64. doi: 10.1159/000207919.
Zotero 插件