首页> Clinical and molecular allergy : CMA> Hereditary angioedema due to C1 inhibitor deficiency in Belarus: epidemiology, access to diagnosis and seven novel mutations in SERPING1 gene.

Hereditary angioedema due to C1 inhibitor deficiency in Belarus: epidemiology, access to diagnosis and seven novel mutations in SERPING1 gene.

导出 OA

翻译打印收藏纠错

第一作者： Irina,Guryanova

第一单位： Belarusian Research Center for Pediatric Oncology, Hematology and Immunology, Minsk, Belarus. guryanovairina1985@gmail.com.

作者： Irina,Guryanova ^[1] ; Chiara,Suffritti ^[2] ; Debora,Parolin ^[3] ; Andrea,Zanichelli ^[2] ; Nastassia,Ishchanka ^[4] ; Ekaterina,Polyakova ^[5] ; Mikhail,Belevtsev ^[5] ; Francesca,Perego ^[6] ; Marco,Cicardi ^[6] ; Yulia,Zharankova ^[5] ; Natalya,Konoplya ^[5] ; Sonia,Caccia ^[3] ; Antonio,Gidaro ^[2]

作者单位： Belarusian Research Center for Pediatric Oncology, Hematology and Immunology, Minsk, Belarus. guryanovairina1985@gmail.com. ^[1] General Medicine Department, ASST-Fatebenefratelli-Sacco, Milan, Italy. ^[2] Department of Biomedical and Clinical Sciences Luigi Sacco, Università Degli Studi Di Milano, Milan, Italy. ^[3] ASST Grande Ospedale Metropolitano Niguarda, Milan, Italy. ^[4] Belarusian Research Center for Pediatric Oncology, Hematology and Immunology, Minsk, Belarus. ^[5] Department of Subacute Therapy, IRCCS-Istituti Clinici Scientifici Maugeri, Milan, Italy. ^[6]

关键词 Belarus C1 inhibitor Hereditary angioedema (HAE)Rare disease SERPING1 variants

DOI 10.1186/s12948-021-00141-0

PMID 33827715

发布时间 2021-04-11

基金项目

20190517/Ministry of Health of the Republic of Belarus

翻译满意度评价：

准确一般字义偏差语意偏离译文作用小提交