{"title":"(高铁血红蛋白症。细胞色素b5还原酶缺乏症]。","authors":"D T Thu, L Damianova","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>In the paper are considered the basic mechanisms, leading to accumulation of methemoglobin in the red blood cells. The inherited methemoglobinaemia, due to enzymatic failure of cytochrome B5-reductase is considered.</p>","PeriodicalId":11560,"journal":{"name":"Eksperimentalna meditsina i morfologiia","volume":"31 1-2","pages":"42-50"},"PeriodicalIF":0.0000,"publicationDate":"1993-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"[Methemoglobinemias. Cytochrome b5-reductase deficiency].\",\"authors\":\"D T Thu, L Damianova\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>In the paper are considered the basic mechanisms, leading to accumulation of methemoglobin in the red blood cells. The inherited methemoglobinaemia, due to enzymatic failure of cytochrome B5-reductase is considered.</p>\",\"PeriodicalId\":11560,\"journal\":{\"name\":\"Eksperimentalna meditsina i morfologiia\",\"volume\":\"31 1-2\",\"pages\":\"42-50\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1993-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Eksperimentalna meditsina i morfologiia\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Eksperimentalna meditsina i morfologiia","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
In the paper are considered the basic mechanisms, leading to accumulation of methemoglobin in the red blood cells. The inherited methemoglobinaemia, due to enzymatic failure of cytochrome B5-reductase is considered.
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