{"title":"[Bernard-Soulier综合征从临床描述(1948)到分子时代(1977)(作者译)]。","authors":"J P Caen, G Tobelem, S Lévy-Tolédano, A Nurden","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>Bernard-Soulier syndrome is a constitutional thrombopathy with an impaired platelet adhesion to the vessel wall. Since the first description in 1948 many works had been reported, and recently a molecular abnormality of the platelet membrane was shown. Interactions between specific membrane sites and platelet functions are now proposed.</p>","PeriodicalId":76247,"journal":{"name":"Nouvelle revue francaise d'hematologie; blood cells","volume":"18 2","pages":"365-70"},"PeriodicalIF":0.0000,"publicationDate":"1977-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"[Bernard-Soulier syndrome from the clinical description (1948) to the molecular era (1977) (author's transl)].\",\"authors\":\"J P Caen, G Tobelem, S Lévy-Tolédano, A Nurden\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Bernard-Soulier syndrome is a constitutional thrombopathy with an impaired platelet adhesion to the vessel wall. Since the first description in 1948 many works had been reported, and recently a molecular abnormality of the platelet membrane was shown. Interactions between specific membrane sites and platelet functions are now proposed.</p>\",\"PeriodicalId\":76247,\"journal\":{\"name\":\"Nouvelle revue francaise d'hematologie; blood cells\",\"volume\":\"18 2\",\"pages\":\"365-70\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1977-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Nouvelle revue francaise d'hematologie; blood cells\",\"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":"Nouvelle revue francaise d'hematologie; blood cells","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
[Bernard-Soulier syndrome from the clinical description (1948) to the molecular era (1977) (author's transl)].
Bernard-Soulier syndrome is a constitutional thrombopathy with an impaired platelet adhesion to the vessel wall. Since the first description in 1948 many works had been reported, and recently a molecular abnormality of the platelet membrane was shown. Interactions between specific membrane sites and platelet functions are now proposed.