Zobrazeno 1 - 10
of 2 034
pro vyhledávání: '"G. PILCHER"'
Publikováno v:
South African Medical Journal, Vol 107, Iss 2, Pp 145-148 (2017)
Background. Familial hypercholesterolaemia (FH) is usually caused by mutations in three genes (LDLR, APOB and PCSK9). Objective. To identify the spectrum of FH-causing mutations in black South African (SA) patients. Methods. DNA samples of 16 unrel
Externí odkaz:
https://doaj.org/article/f7cd03e3d4f54c6783727bb90cfc8c66
Autor:
G. Geiseler
Publikováno v:
Berichte der Bunsengesellschaft für physikalische Chemie. 74:727-727
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::765774abac1b279caafe750ad33c8280
https://doi.org/10.1002/bbpc.19700740727
https://doi.org/10.1002/bbpc.19700740727
Autor:
Fu, Chunyi1 (AUTHOR), Luo, Jingchao2 (AUTHOR), Wang, Xiaogang3 (AUTHOR), Xu, Yuan4 (AUTHOR), Liu, Taotao5 (AUTHOR) taotao20022000@163.com
Publikováno v:
Hong Kong Journal of Emergency Medicine. Dec2024, Vol. 31 Issue 6, p331-338. 8p.
Autor:
Zhang, Yijia1 (AUTHOR), Wang, Xueer1 (AUTHOR), Huang, Jianyuan1 (AUTHOR), Zhang, Xinyue1 (AUTHOR), Bu, Lingwei1 (AUTHOR), Zhang, Yarui1 (AUTHOR), Liang, Fengting1 (AUTHOR), Wu, Shenhua1 (AUTHOR), Zhang, Min1 (AUTHOR), Zhang, Lu2 (AUTHOR) zlulu70@126.com, Zhang, Lin1 (AUTHOR) zlilyzh@126.com
Publikováno v:
Aging Cell. Dec2024, Vol. 23 Issue 12, p1-17. 17p.
Autor:
Ghaffari-Bohlouli P; 3BIO-BioMatter, École Polytechnique de Bruxelles, Université Libre de Bruxelles, Avenue F.D. Roosevelt, 50-CP 165/61, Brussels, 1050, Belgium.; Department of Chemistry, McGill University, 801 Sherbrooke Street West, Montréal, Québec, H3A 0B8, Canada., Jafari H; 3BIO-BioMatter, École Polytechnique de Bruxelles, Université Libre de Bruxelles, Avenue F.D. Roosevelt, 50-CP 165/61, Brussels, 1050, Belgium., Nie L; College of Life Sciences, Xinyang Normal University, Xinyang, 464000, China., Kakkar A; Department of Chemistry, McGill University, 801 Sherbrooke Street West, Montréal, Québec, H3A 0B8, Canada., Shavandi A; 3BIO-BioMatter, École Polytechnique de Bruxelles, Université Libre de Bruxelles, Avenue F.D. Roosevelt, 50-CP 165/61, Brussels, 1050, Belgium.
Publikováno v:
Advanced healthcare materials [Adv Healthc Mater] 2024 Dec; Vol. 13 (30), pp. e2401713. Date of Electronic Publication: 2024 Aug 25.
Publikováno v:
South African Medical Journal, Vol 107, Iss 2, Pp 145-148 (2017)
SAMJ: South African Medical Journal, Volume: 107, Issue: 2, Pages: 145-148, Published: FEB 2017
South African Medical Journal; Vol 107, No 2 (2017); 145-148
SAMJ: South African Medical Journal, Volume: 107, Issue: 2, Pages: 145-148, Published: FEB 2017
South African Medical Journal; Vol 107, No 2 (2017); 145-148
Background. Familial hypercholesterolaemia (FH) is usually caused by mutations in three genes ( LDLR , APOB and PCSK9 ). Objective. To identify the spectrum of FH-causing mutations in black South African (SA) patients. Methods. DNA samples of 16 unre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6527a9908a77587d52cc6545a222b5f8
https://doi.org/10.7196/samj.2017.v107i2.12022
https://doi.org/10.7196/samj.2017.v107i2.12022
Autor:
Thille, Arnaud W.1,2 aw.thille@gmail.com, Balen, Frédéric3,4, Carteaux, Guillaume5,6,7, Chouihed, Tahar8,9, Frat, Jean-Pierre1,2, Girault, Christophe10, L'Her, Erwan11, Marjanovic, Nicolas2,12, Nay, Mai-Anh13, Ray, Patrick14, Reffienna, Matthieu15, Retenauer, Leo16, Roch, Antoine17, Thiery, Guillaume18,19, Truchot, Jennifer20
Publikováno v:
Annals of Intensive Care. 10/18/2024, Vol. 14 Issue 1, p1-15. 15p.
Autor:
Helms, Julie1,2 Julie.helms@chru-strasbourg.fr, Catoire, Pierre3, Abensur Vuillaume, Laure4, Bannelier, Héloise5, Douillet, Delphine6,7, Dupuis, Claire8,9, Federici, Laura10, Jezequel, Melissa11, Jozwiak, Mathieu12,13, Kuteifan, Khaldoun14, Labro, Guylaine14, Latournerie, Gwendoline15,16, Michelet, Fabrice17, Monnet, Xavier18, Persichini, Romain19, Polge, Fabien20, Savary, Dominique21,22, Vromant, Amélie23, Adda, Imane24,25, Hraiech, Sami26,27
Publikováno v:
Annals of Intensive Care. 9/5/2024, Vol. 14 Issue 1, p1-15. 15p.
Autor:
Majidazar, Mahdi1, Hamidi, Farzaneh2, Masoudi, Nazanin3, Vand-Rajabpour, Zahra1, Paknezhad, Seyed Pouya1 pooya.paknejad@gmail.com
Publikováno v:
Archives of Iranian Medicine (AIM). Aug2024, Vol. 27 Issue 8, p33-40. 8p.