{"title":"低脂蛋白血症。","authors":"J K Lloyd","doi":"10.1136/jcp.s1-5.1.53","DOIUrl":null,"url":null,"abstract":"Hypolipoproteinaemia, resulting from deficiency of one or more of the major serum lipoprotein fractions, may be due to a primary genetically determined condition or may occur as a secondary manifestation in another disease state (table I). This paper will be confined to a discussion of the primary disorders which, although rare, have contributed greatly to our understanding of the normal function of the serum lipoproteins.","PeriodicalId":75995,"journal":{"name":"Journal of clinical pathology. Supplement (Association of Clinical Pathologists)","volume":"5 ","pages":"53-8"},"PeriodicalIF":0.0000,"publicationDate":"1973-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1136/jcp.s1-5.1.53","citationCount":"0","resultStr":"{\"title\":\"Hypolipoproteinaemia.\",\"authors\":\"J K Lloyd\",\"doi\":\"10.1136/jcp.s1-5.1.53\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Hypolipoproteinaemia, resulting from deficiency of one or more of the major serum lipoprotein fractions, may be due to a primary genetically determined condition or may occur as a secondary manifestation in another disease state (table I). This paper will be confined to a discussion of the primary disorders which, although rare, have contributed greatly to our understanding of the normal function of the serum lipoproteins.\",\"PeriodicalId\":75995,\"journal\":{\"name\":\"Journal of clinical pathology. Supplement (Association of Clinical Pathologists)\",\"volume\":\"5 \",\"pages\":\"53-8\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1973-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1136/jcp.s1-5.1.53\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of clinical pathology. Supplement (Association of Clinical Pathologists)\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1136/jcp.s1-5.1.53\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of clinical pathology. Supplement (Association of Clinical Pathologists)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1136/jcp.s1-5.1.53","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Hypolipoproteinaemia, resulting from deficiency of one or more of the major serum lipoprotein fractions, may be due to a primary genetically determined condition or may occur as a secondary manifestation in another disease state (table I). This paper will be confined to a discussion of the primary disorders which, although rare, have contributed greatly to our understanding of the normal function of the serum lipoproteins.