Elsa Lanke (Former)

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2014
Mark High risk of in-breast tumor recurrence after BRCA1/2-associated breast cancer.
Nilsson, Martin ^LU ; Werner Hartman, Linda ^LU ; Kristoffersson, Ulf ^LU ; Johannsson, Oskar Thor ^LU ; Borg, Åke ^LU ; Henriksson, Karin ^LU ; Lanke, Elsa ^LU ; Olsson, Håkan ^LU and Loman, Niklas ^LU (2014) In Breast Cancer Research and Treatment 147(3). p.571-578
- Contribution to journal › Article
2011
Mark A large deletion identified in a Swedish family with type 1 VWD
Johansson, Anna M. ; Lanke, Elsa ^LU ; Säll, Torbjörn ^LU ; Lethagen, Stefan ^LU and Halldén, Christer ^LU (2011) In Thrombosis and Haemostasis 105(4). p.733-734
- Contribution to journal › Letter
2008
Mark Asn1421Lys mutation in the glycoprotein Ib binding domain impairs - ristocetin and botrocetin - mediated binding of von Willebrand factor to platelets
Lanke, Elsa ^LU ; Kristoffersson, A ; Isaksson, Christina ^LU ; Holmberg, Lars ^LU and Lethagen, Stefan ^LU (2008) XXVIIIth International Congress of the World Federation of Hemophilia, 2008 In Haemophilia 14(s2). p.116-116
- Contribution to journal › Published meeting abstract
Mark Genetic characterization of families with von Willebrand disease
Lanke, Elsa ^LU (2008) In Lund University Faculty of Medicine Doctoral Dissertation Series 2008:89.
- Thesis › Doctoral thesis (compilation)
Mark Patients' and their family members' understanding of the genetics of type 1 von Willebrand disease.
Lanke, Elsa ^LU ; Lanke, Jan ^LU and Lethagen, Stefan ^LU (2008) In Haemophilia 14(5). p.1127-1130
- Contribution to journal › Letter
Mark Characterization of a novel mutation in the von Willebrand factor propeptide in a distinct subtype of recessive von Willebrand disease.
Lanke, Elsa ^LU ; Kristoffersson, Ann-Charlotte ^LU ; Philips, Malou ; Holmberg, Lars ^LU and Lethagen, Stefan ^LU (2008) In Thrombosis and Haemostasis 100(2). p.211-216
- Contribution to journal › Article
Mark N1421K mutation in the glycoprotein Ib binding domain impairs ristocetin- and botrocetin-mediated binding of von Willebrand factor to platelets.
Lanke, Elsa ^LU ; Kristoffersson, Ann-Charlotte ^LU ; Isaksson, Christina ^LU ; Holmberg, Lars ^LU and Lethagen, Stefan ^LU (2008) In European Journal of Haematology 81. p.384-390
- Contribution to journal › Article
Mark Patients’ and their family members’ understanding of the genetics of type 1 von Willebrand disease
Lanke, Jan ^LU and Lanke, Elsa ^LU (2008)
- Working paper/Preprint › Working paper
2005
Mark Genetic analysis of 31 Swedish type 1 von Willebrand disease families reveals incomplete linkage to the von Willebrand factor gene and a high frequency of a certain disease haplotype.
Lanke, Elsa ^LU ; Johansson, Anna ^LU ; Halldén, Christer ^LU and Lethagen, Stefan ^LU (2005) In Journal of Thrombosis and Haemostasis 3(12). p.2656-2663
- Contribution to journal › Article
2004
Mark Co-segregation of the PROS1 locus and protein S deficiency in families having no detectable mutations in PROS1.
Lanke, Elsa ^LU ; Johansson, Anna ^LU ; Hillarp, Andreas ^LU ; Lethagen, Stefan ^LU ; Zöller, Bengt ^LU ; Dahlbäck, Björn ^LU and Halldén, Christer ^LU (2004) In Journal of Thrombosis and Haemostasis 2(11). p.1918-1923
- Contribution to journal › Article