Lethagen S - Search Results

1

Common and Rare Variants in Genes Associated with von Willebrand Factor Level Variation: No Accumulation of Rare Variants in Swedish von Willebrand Disease Patients.

Manderstedt E, Lind-Halldén C, Lethagen S, Halldén C. Manderstedt E, et al. Among authors: lethagen s. TH Open. 2020 Oct 31;4(4):e322-e331. doi: 10.1055/s-0040-1718885. eCollection 2020 Oct. TH Open. 2020. PMID: 33145474 Free PMC article.

2

Genetic variation in the C-type lectin receptor CLEC4M in type 1 von Willebrand Disease patients.

Manderstedt E, Lind-Halldén C, Lethagen S, Halldén C. Manderstedt E, et al. Among authors: lethagen s. PLoS One. 2018 Feb 1;13(2):e0192024. doi: 10.1371/journal.pone.0192024. eCollection 2018. PLoS One. 2018. PMID: 29389944 Free PMC article.

3

Genetic Variation in the Syntaxin-Binding Protein STXBP5 in Type 1 von Willebrand Disease Patients.

Lind-Halldén C, Manderstedt E, Carlberg D, Lethagen S, Halldén C. Lind-Halldén C, et al. Among authors: lethagen s. Thromb Haemost. 2018 Aug;118(8):1382-1389. doi: 10.1055/s-0038-1661352. Epub 2018 Jul 4. Thromb Haemost. 2018. PMID: 29972863

4

Genetic Variation in the von Willebrand Factor Gene in Swedish von Willebrand Disease Patients.

Manderstedt E, Lind-Halldén C, Lethagen S, Halldén C. Manderstedt E, et al. Among authors: lethagen s. TH Open. 2018 Jan 30;2(1):e39-e48. doi: 10.1055/s-0037-1618571. eCollection 2018 Jan. TH Open. 2018. PMID: 31249928 Free PMC article.

5

Distribution of von Willebrand factor levels in young women with and without bleeding symptoms: influence of ABO blood group and promoter haplotypes.

Lethagen S, Hillarp A, Ekholm C, Mattson E, Halldén C, Friberg B. Lethagen S, et al. Thromb Haemost. 2008 Jun;99(6):1013-8. doi: 10.1160/TH07-06-0419. Thromb Haemost. 2008. PMID: 18521502

6

Variation in the VWF gene in Swedish patients with type 1 von Willebrand Disease.

Johansson AM, Halldén C, Säll T, Lethagen S. Johansson AM, et al. Among authors: lethagen s. Ann Hum Genet. 2011 Jul;75(4):447-55. doi: 10.1111/j.1469-1809.2011.00652.x. Epub 2011 Apr 28. Ann Hum Genet. 2011. PMID: 21534937

7

A large deletion identified in a Swedish family with type 1 VWD.

Johansson AM, Lanke E, Säll T, Lethagen S, Halldén C. Johansson AM, et al. Among authors: lethagen s. Thromb Haemost. 2011 Apr;105(4):733-4. doi: 10.1160/TH10-08-0556. Epub 2011 Jan 12. Thromb Haemost. 2011. PMID: 21225094 No abstract available.

8

Characterization of a novel mutation in the von Willebrand factor propeptide in a distinct subtype of recessive von Willebrand disease.

Lanke E, Kristoffersson AC, Philips M, Holmberg L, Lethagen S. Lanke E, et al. Among authors: lethagen s. Thromb Haemost. 2008 Aug;100(2):211-6. Thromb Haemost. 2008. PMID: 18690339

9

Phenotype and genotype of a cohort of families historically diagnosed with type 1 von Willebrand disease in the European study, Molecular and Clinical Markers for the Diagnosis and Management of Type 1 von Willebrand Disease (MCMDM-1VWD).

Goodeve A, Eikenboom J, Castaman G, Rodeghiero F, Federici AB, Batlle J, Meyer D, Mazurier C, Goudemand J, Schneppenheim R, Budde U, Ingerslev J, Habart D, Vorlova Z, Holmberg L, Lethagen S, Pasi J, Hill F, Hashemi Soteh M, Baronciani L, Hallden C, Guilliatt A, Lester W, Peake I. Goodeve A, et al. Among authors: lethagen s. Blood. 2007 Jan 1;109(1):112-21. doi: 10.1182/blood-2006-05-020784. Epub 2006 Sep 19. Blood. 2007. PMID: 16985174 Free article.

10

Von Willebrand's disease caused by compound heterozygosity for a substitution mutation (T1156M) in the D3 domain of the von Willebrand factor and a stop mutation (Q2470X).

Lethagen S, Isaksson C, Schaedel C, Holmberg L. Lethagen S, et al. Thromb Haemost. 2002 Sep;88(3):421-6. Thromb Haemost. 2002. PMID: 12353070

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