GROMBIŘÍKOVÁ, Hana, Barbora RAVČUKOVÁ, Lucie GRODECKÁ, Pavla HUJOVÁ, Roman HAKL, Pavel KUKLÍNEK, Radana ZACHOVÁ, M. SOBOTKOVÁ, Pavlína KRÁLÍČKOVÁ, Olga KRYŠTŮVKOVÁ, Anna ŠEDIVÁ, Jiří LITZMAN and Tomáš FREIBERGER. A spectrum of SERPING1 mutations and clinical characterisation of Czech Hereditary Angioedema patients. In 12th C1-inhibitor deficiency and angioedema workshop 2021. 2021.
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Basic information
Original name A spectrum of SERPING1 mutations and clinical characterisation of Czech Hereditary Angioedema patients.
Authors GROMBIŘÍKOVÁ, Hana (203 Czech Republic, belonging to the institution), Barbora RAVČUKOVÁ (203 Czech Republic, belonging to the institution), Lucie GRODECKÁ (203 Czech Republic, belonging to the institution), Pavla HUJOVÁ (203 Czech Republic, belonging to the institution), Roman HAKL (203 Czech Republic, belonging to the institution), Pavel KUKLÍNEK (203 Czech Republic, belonging to the institution), Radana ZACHOVÁ (203 Czech Republic), M. SOBOTKOVÁ (203 Czech Republic), Pavlína KRÁLÍČKOVÁ (203 Czech Republic), Olga KRYŠTŮVKOVÁ (203 Czech Republic), Anna ŠEDIVÁ (203 Czech Republic, belonging to the institution), Jiří LITZMAN (203 Czech Republic, belonging to the institution) and Tomáš FREIBERGER (203 Czech Republic, guarantor, belonging to the institution).
Edition 12th C1-inhibitor deficiency and angioedema workshop 2021. 2021.
Other information
Original language English
Type of outcome Conference abstract
Field of Study 30102 Immunology
Country of publisher Switzerland
Confidentiality degree is not subject to a state or trade secret
RIV identification code RIV/00216224:14110/21:00120209
Organization unit Faculty of Medicine
Keywords in English SERPING1 mutations; Czech Hereditary Angioedema patients
Tags rivok
Tags International impact
Changed by Changed by: Mgr. Tereza Miškechová, učo 341652. Changed: 29/4/2022 11:08.
Abstract
A spectrum of SERPING1 mutations and clinical characterisation of Czech Hereditary Angioedema patients - 12th C1-inhibitor deficiency and angioedema workshop 2021 abstract.
Links
MUNI/A/1412/2020, interní kód MUName: Patogenetický význam nespecifické imunity u některých poruch imunitního systému (Acronym: Nespecifická imunita)
Investor: Masaryk University
NV18-05-00330, research and development projectName: Genetická determinace závažnosti otoků podmíněných bradykininem u pacientů s hereditárním angioedémem
Investor: Ministry of Health of the CR, Genetic determination of bradykinin-mediated angioedema severity in patients with hereditary angioedema
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