{"title":"妇女在科学领域的观点：原发性免疫缺陷的数据共享","authors":"Jessica Willett-Pachul","doi":"10.14785/lymphosign-2023-0006","DOIUrl":null,"url":null,"abstract":"Jessica Willett Pachul is a Clinical Nurse Specialist in the Division of Immunology & Allergy at the Hospital for Sick Children in Toronto, Canada. In this commentary, she discusses the implications that the collection and sharing of health data can have in the diagnosis and treatment of primary immunodeficiency (PID), as well as in research and development in the field.","PeriodicalId":53881,"journal":{"name":"LymphoSign Journal-The Journal of Inherited Immune Disorders","volume":" ","pages":""},"PeriodicalIF":0.3000,"publicationDate":"2023-06-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Perspectives of women in science: data sharing in primary immunodeficiency\",\"authors\":\"Jessica Willett-Pachul\",\"doi\":\"10.14785/lymphosign-2023-0006\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Jessica Willett Pachul is a Clinical Nurse Specialist in the Division of Immunology & Allergy at the Hospital for Sick Children in Toronto, Canada. In this commentary, she discusses the implications that the collection and sharing of health data can have in the diagnosis and treatment of primary immunodeficiency (PID), as well as in research and development in the field.\",\"PeriodicalId\":53881,\"journal\":{\"name\":\"LymphoSign Journal-The Journal of Inherited Immune Disorders\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":0.3000,\"publicationDate\":\"2023-06-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"LymphoSign Journal-The Journal of Inherited Immune Disorders\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.14785/lymphosign-2023-0006\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"IMMUNOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"LymphoSign Journal-The Journal of Inherited Immune Disorders","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.14785/lymphosign-2023-0006","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"IMMUNOLOGY","Score":null,"Total":0}
Perspectives of women in science: data sharing in primary immunodeficiency
Jessica Willett Pachul is a Clinical Nurse Specialist in the Division of Immunology & Allergy at the Hospital for Sick Children in Toronto, Canada. In this commentary, she discusses the implications that the collection and sharing of health data can have in the diagnosis and treatment of primary immunodeficiency (PID), as well as in research and development in the field.
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