a 2021

A spectrum of SERPING1 mutations and clinical characterisation of Czech Hereditary Angioedema patients.

GROMBIŘÍKOVÁ, Hana, Barbora RAVČUKOVÁ, Lucie GRODECKÁ, Pavla HUJOVÁ, Roman HAKL et. al.

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

Language

English

Type of outcome

Konferenční abstrakt

Field of Study

30102 Immunology

Country of publisher

Switzerland

Confidentiality degree

není předmětem státního či obchodního tajemství

RIV identification code

RIV/00216224:14110/21:00120209

Organization unit

Faculty of Medicine

Keywords in English

SERPING1 mutations; Czech Hereditary Angioedema patients

Tags

Tags

International impact
Změněno: 29/4/2022 11:08, Mgr. Tereza Miškechová

Abstract

V originále

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 MU
Name: Patogenetický význam nespecifické imunity u některých poruch imunitního systému (Acronym: Nespecifická imunita)
Investor: Masaryk University
NV18-05-00330, research and development project
Name: 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