Skattum L - Search Results

1

Heat differentiated complement factor profiling.

Hamsten C, Skattum L, Truedsson L, von Döbeln U, Uhlén M, Schwenk JM, Hammarström L, Nilsson P, Neiman M. Hamsten C, et al. Among authors: skattum l. J Proteomics. 2015 Aug 3;126:155-62. doi: 10.1016/j.jprot.2015.05.027. Epub 2015 Jun 3. J Proteomics. 2015. PMID: 26047714

2

Complement factor I deficiency associated with recurrent infections, vasculitis and immune complex glomerulonephritis.

Genel F, Sjöholm AG, Skattum L, Truedsson L. Genel F, et al. Among authors: skattum l. Scand J Infect Dis. 2005;37(8):615-618. doi: 10.1080/00365540510034536. Scand J Infect Dis. 2005. PMID: 16138437

3

Antibodies against four proteins from a Streptococcus pyogenes serotype M1 strain and levels of circulating mannan-binding lectin in acute poststreptococcal glomerulonephritis.

Skattum L, Akesson P, Truedsson L, Sjöholm AG. Skattum L, et al. Int Arch Allergy Immunol. 2006;140(1):9-19. doi: 10.1159/000091745. Epub 2006 Feb 27. Int Arch Allergy Immunol. 2006. PMID: 16508336

4

Properdin deficiency in a boy with fulminant meningococcal septic shock.

Genel F, Atlihan F, Gulez N, Sjöholm AG, Skattum L, Truedsson L. Genel F, et al. Among authors: skattum l. Acta Paediatr. 2006 Nov;95(11):1498-1500. doi: 10.1080/08035250600603008. Acta Paediatr. 2006. PMID: 17062484

5

Serum bactericidal activity against Neisseria meningitidis in patients with C3 nephritic factors is dependent on IgG allotypes.

Skattum L, Gullstrand B, Holmström E, Oxelius VA, Truedsson L. Skattum L, et al. Clin Immunol. 2008 Oct;129(1):123-31. doi: 10.1016/j.clim.2008.06.010. Epub 2008 Jul 29. Clin Immunol. 2008. PMID: 18667363

6

Homozygosity for a novel mutation in the C1q C chain gene in a Turkish family with hereditary C1q deficiency.

Gulez N, Genel F, Atlihan F, Gullstrand B, Skattum L, Schejbel L, Garred P, Truedsson L. Gulez N, et al. Among authors: skattum l. J Investig Allergol Clin Immunol. 2010;20(3):255-8. J Investig Allergol Clin Immunol. 2010. PMID: 20635792 Free article.

7

Complement deficiency states and associated infections.

Skattum L, van Deuren M, van der Poll T, Truedsson L. Skattum L, et al. Mol Immunol. 2011 Aug;48(14):1643-55. doi: 10.1016/j.molimm.2011.05.001. Epub 2011 May 31. Mol Immunol. 2011. PMID: 21624663 Review.

8

Molecular basis of hereditary C1q deficiency--revisited: identification of several novel disease-causing mutations.

Schejbel L, Skattum L, Hagelberg S, Åhlin A, Schiller B, Berg S, Genel F, Truedsson L, Garred P. Schejbel L, et al. Among authors: skattum l. Genes Immun. 2011 Dec;12(8):626-34. doi: 10.1038/gene.2011.39. Epub 2011 Jun 9. Genes Immun. 2011. PMID: 21654842

9

Sensitive and specific assays for C3 nephritic factors clarify mechanisms underlying complement dysregulation.

Paixão-Cavalcante D, López-Trascasa M, Skattum L, Giclas PC, Goodship TH, de Córdoba SR, Truedsson L, Morgan BP, Harris CL. Paixão-Cavalcante D, et al. Among authors: skattum l. Kidney Int. 2012 Nov;82(10):1084-92. doi: 10.1038/ki.2012.250. Epub 2012 Aug 1. Kidney Int. 2012. PMID: 22854646 Free PMC article.

10

Primary immunodeficiency in infection-prone children in southern Sweden: occurrence, clinical characteristics and immunological findings.

Brodszki N, Jönsson G, Skattum L, Truedsson L. Brodszki N, et al. Among authors: skattum l. BMC Immunol. 2014 Aug 14;15:31. doi: 10.1186/s12865-014-0031-6. BMC Immunol. 2014. PMID: 25318568 Free PMC article.

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