Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Elsa Lanke"'
Autor:
Linda Werner Hartman, Ulf Kristoffersson, Martin Nilsson, Elsa Lanke, Karin M. Henriksson, Oskar Thor Johannsson, Niklas Loman, Åke Borg, Håkan Olsson
Publikováno v:
Breast Cancer Research and Treatment
Breast Cancer Research and Treatment; 147(3), pp 571-578 (2014)
Breast Cancer Research and Treatment; 147(3), pp 571-578 (2014)
The purpose of the study was to compare breast-conserving therapy (BCT) and mastectomy (M) in BRCA1/2 mutation carriers. Women with invasive breast cancer and a pathogenic mutation in BRCA1 or BRCA2 were included in the study (n = 162). Patients trea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e512a92ad7059c08cbd4fc3355b93db
http://europepmc.org/articles/PMC4174291
http://europepmc.org/articles/PMC4174291
Publikováno v:
Haemophilia. 14:1127-1130
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3675315447b54e4b6871ed12d8de934f
https://doi.org/10.1111/j.1365-2516.2008.01805.x
https://doi.org/10.1111/j.1365-2516.2008.01805.x
Publikováno v:
Thrombosis and Haemostasis. 100:211-216
SummaryvonWillebrand factor (VWF) is a plasma protein that consists of a series of multimers of which the high-molecular-weight VWF multimers are the most potent in platelet adhesion and aggre-gation. The propeptide of theVWF (VWFpp) is known to be e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5133ba7c1ab94c54294bdc4f912b452
https://doi.org/10.1160/th08-03-0187
https://doi.org/10.1160/th08-03-0187
Autor:
Andreas Hillarp, Christer Halldén, Anna Johansson, Björn Dahlbäck, Elsa Lanke, Bengt Zöller, Stefan Lethagen
Publikováno v:
Journal of Thrombosis and Haemostasis; 2(11), pp 1918-1923 (2004)
Inherited deficiency of protein S constitutes an important risk factor of venous thrombosis. Many reports have demonstrated that causative mutations in the protein S gene are found only in approximately 50% of the cases with protein S deficiency. It
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f2a7237765042ffac54112625c895406
https://doi.org/10.1111/j.1538-7836.2004.00950.x
https://doi.org/10.1111/j.1538-7836.2004.00950.x
Publikováno v:
European Journal of Haematology.
von Willebrand disease (VWD) is a common inheritable bleeding disorder caused by deficiency of von Willebrand Factor (VWF), which is involved in platelet adhesion and aggregation. We report a family consisting of three patients with VWD characterized
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::45f56403c0b43a84fe75eadf3773171e
https://doi.org/10.1111/j.1600-0609.2008.01123.x
https://doi.org/10.1111/j.1600-0609.2008.01123.x
Publikováno v:
Journal of Thrombosis and Haemostasis; 3(12), pp 2656-2663 (2005)
Summary. Background: The most common type of von Willebrand disease (VWD), type 1, has in only a few cases been explained by an identified causative mutation in the von Willebrand factor (VWF) gene. The ABO blood group and other modifier loci outside
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ff9f5b73ac2773941a700edd57451a4
http://lup.lub.lu.se/record/148635
http://lup.lub.lu.se/record/148635
Publikováno v:
Thrombosis and Haemostasis. 105:733-734
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea8c2bd9700930e7bb0f9e9dcead351e
https://doi.org/10.1160/th10-08-0556
https://doi.org/10.1160/th10-08-0556